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Code Red — Obstetric Hemorrhage
Activation, shock classification, management using the 4T's, and therapeutic escalation.
1Definition and criteria
PPH (operational definition): blood loss ≥300 mL with any abnormal hemodynamic sign (HR>100, shock index>1, SBP<100, DBP<60), or blood loss ≥500 mL — whichever occurs first, within 24 h postpartum. Enhanced surveillance during the first 2 h.
Massive hemorrhage: loss/replacement of 50% of blood volume in 3 h, OR ≥150 mL/min, OR ≥1.5 mL/kg/20 min, OR ≥4 units in 24 h.
Activation rule: meet the PPH criterion (≥300 mL with any abnormal sign, or ≥500 mL) or any sign of shock → initiate MOTIVE and ACTIVATE CODE RED. Maternal decompensation signs carry more weight than blood loss volume.
| Definition | Criterion | Status |
|---|---|---|
| WHO/FIGO/ICM 2025 (rec. 22) | ≥300 mL measured + HR >100, SI >1, SBP <100, or DBP <60; or ≥500 mL measured. All modes of delivery, within 24 h, enhanced surveillance during the first 2 h | Current — used by the calculator |
| reVITALize / ACOG PB 183 (2017) | ≥1000 mL cumulative, or blood loss with signs or symptoms of hypovolemia, within 24 h (any mode of delivery) | Variant |
| Classic (WHO 2012 and traditional texts) | ≥500 mL in vaginal delivery; ≥1000 mL in cesarean delivery | No longer current |
The WHO 2025 applies the same criterion to cesarean delivery and warns against normalizing greater blood loss with this route. Always measure objectively (calibrated drape or weighing). Source: WHO/FIGO/ICM, Consolidated guidelines on PPH, 2025.
| Before (classic definition, no longer current) | Now (WHO/FIGO/ICM 2025) | |
|---|---|---|
| Definition | ≥500 mL in vaginal delivery; ≥1000 mL in cesarean delivery | ≥300 mL with any abnormal sign, or ≥500 mL, for all modes of delivery |
| Activation | Code Red with >1000 mL and/or signs of shock | When criteria are met: initiate MOTIVE and activate Code Red |
| Measurement | Visual estimation, which underestimates blood loss | Objective measurement: calibrated drape or weighing |
| What matters more | Volume | The sign of maternal decompensation (HR >100, SI >1, SBP <100, DBP <60) |
Why it changed: with high thresholds and visual estimation, diagnosis was delayed. Objective measurement and action at the first sign of decompensation allow treatment to begin earlier. For cesarean delivery, the WHO advises against normalizing greater blood loss. Source: WHO/FIGO/ICM 2025, recommendation 22 and observations.
Shock index (HR/SBP): >0.9 marker of severity; ≥1.4 urgent need for intervention; ≥1.7 high probability of an adverse outcome.
2Classification and team
Classification of hypovolemic shock (Vélez AG et al., Rev Colomb Obstet Ginecol 2009) — grade is determined by the worst parameter:
| Grade | % vol. | mL | Mental status | Perfusion | Pulse | SBP |
|---|---|---|---|---|---|---|
| Compensated | 10-15% | 500-1000 | Normal | Normal | 60-90 | Normal |
| Mild | 16-25% | 1001-1500 | Normal, agitated | Pallor, cool skin | 91-100 | Normal |
| Moderate | 26-35% | 1501-2000 | Agitated | Pallor, cool skin, sweating | 101-120 | Falls to 80-90 |
| Severe | >35% | >2000 | Lethargic/unconscious | Extreme pallor, coldness | >120 or not palpable | Falls <60 |
CaVeSal® proprietary algorithm · Based on: Vélez AG et al., Rev Colomb Obstet Ginecol 2009 · Colombia Ministry of Health CPG 2013.
Important: Vélez grades shock severity; it does not define hemorrhage. For activation, use WHO 2025: 300 mL with any abnormal sign is already postpartum hemorrhage, even if Vélez classifies it as compensated (500-1000 mL).
Team: Coordinator, Assistant 1, Assistant 2, Circulator (roles defined, Colombia Ministry of Health CPG 2013).
3Flowchart — Golden Hour
Active management of the 3rd/4th stage (6 steps, WHO 2025):
- 1. Drying / initial assessment
- 2. Uterotonic (oxytocin 10 IU IM/IV, or carbetocin 100 µg if cold chain is unavailable, or misoprostol 400-600 µg orally)
- 3. Delayed cord clamping 1-3 min + skin-to-skin contact
- 4. Controlled cord traction + countertraction
- 5. Verify intact placenta + contracted uterus without massage
- 6. Monitoring every 15 min for 2 h
Resuscitation targets: normal mental status, capillary refill <3 s, SBP>90, SpO2≥95%, shock index<0.9, T°>35°C, lactate<2 mmol/L, fibrinogen>200 mg/dL.
23Obstetric Early Warning Scale: EAPO 2025/2022, MAMÁ Score and CaVeSal® Alert
For every patient on admission and at each assessment. EAPO is not a score: each parameter has a color and a single red activates the obstetric emergency, which is then directed to the code according to the cause (hemorrhage → Code Red · hypertension → HDP · infection → Code Yellow — Sepsis · cardiac arrest → Obstetric Code Blue).
| Parameter | Red | Yellow | Green |
|---|---|---|---|
| RR (breaths/min) | ≥22 · ≤11 | 20-21 | 12-19 |
| SpO₂ (%) | <95 | — | 95-100 |
| Temperature (°C) | ≥39 · ≤35 | 38 | 36-37 |
| HR (bpm) | ≥100 · ≤59 | — | 60-99 |
| SBP (mmHg) | ≥160 · ≤70 | 140-159* · 71-99 | 100-139 |
| DBP (mmHg) | ≥110 · 51-59 | 90-109 | 60-89 |
| Neurological | Only responds to pain · unconscious | Disoriented | Alert |
| Appearance | Pale · cyanotic · jaundiced | Diaphoretic | Normal |
| Urine output | No urine output in 6 h or >30 mL/h | — | Yes |
| Proteinuria (dipstick) | +++ or more | — | + / ++ |
| Genital bleeding | Heavy | Spotting | Absent |
| Purulent discharge · headache with visual or auditory disturbance · seizures | Yes | — | No |
| Abdominal pain | With peritoneal irritation | Without irritation | No |
* Note: the 2025 sheet is used, and gaps are supplemented with the 2022 version (the 2025 sheet does not include the SBP 140-159 row).
| Cutoff | 2025 sheet (calculator) | Code Red Guide, 2nd ed. 2022 |
|---|---|---|
| RR red / yellow | ≥22 / 20-21 | ≥25 / 20-24 |
| Temperature red / yellow | ≥39 / 38 | ≥40 / 38-39 |
| SBP 140-159 | No row | Yellow |
| Color | EAPO (MSPBS) | MAMÁ Score (Ecuador MSP) |
|---|---|---|
| Red | Every 5-10 min | ≥5 or any 3: every 30 min |
| Yellow | Every 20-30 min | 2-4: every 1 h |
| Green | Every 1-2 h | 0-1: every 4 h |
| Time | Phase | Data |
|---|---|---|
| Minute 0 | Activation | Stabilize and decide |
| 1-20 min | Resuscitation and diagnosis | The compensatory response lasts about 20-30 min |
| 20 min without compensatory action | Stabilization | Survival 60 % |
| 40-60 min | DIC is assumed | Survival <20 % |
| >60 min | Advanced management | High probability of DIC |
Most deaths from postpartum hemorrhage occur in the first 2-3 h, and WHO calls for treatment to begin within 15 min of diagnosis. The survival figures are from the MSPBS guideline; peer-reviewed literature supports the urgency of the first hour, not those exact percentages.
CaVeSal® Obstetric Alert (EAPO 2025 + MAMÁ Score): the same vital signs are assessed using both scales, and the worse color takes precedence (MAMÁ Score ≥5 or any 3 = red; 2-4 = yellow; 0-1 = green). It adds what EAPO does not measure (oxygen therapy, urine output via catheter, graded level of consciousness), while EAPO adds what the MAMÁ Score does not measure (bleeding, proteinuria, headache, seizures, abdominal pain). Example: SpO₂ 96 % with a mask → green on EAPO for oxygen saturation, MAMÁ Score 3 = red. MAMÁ Score values are in Code Yellow, card 8. Obstetric early warning scales have a median sensitivity of 89 % for severe morbidity (Umar 2019).
CaVeSal® proprietary algorithm · Based on: MSPBS Paraguay, DSSR. Early Obstetric Warning Scale (2025 sheet) · MSPBS. Maternal and Neonatal Code Red Guide, 2nd ed. 2022 · Ecuador MSP. Score MAMÁ and Obstetric Codes Protocol 2025 · Vélez-Álvarez 2009 · Alves 2020 · Mammoliti 2025 (E-MOTIVE) · WHO 2025 (PPH) · Umar 2019The hybrid mode is not validated as an independent scale.
Practice it in the simulator: EAPO case 2025/2022 · CaVeSal® Obstetric Alert case.
4Medications
TXA: 1 g IV over 10 min (1 mL/min), second dose of 1 g if bleeding continues at 30 min or recurs within 24 h. DO NOT use more than 3 h after birth. It is treatment for established PPH; WHO 2025 does not recommend routine prophylaxis (see fact sheet 24).
Heat-stable carbetocin: ONLY for prevention when the cold chain fails — NOT for treatment of established uterine atony.
4 Ts (causes): Tone 70% (atony), Trauma 20% (lacerations), Tissue 10% (retained products), Thrombin 1% (coagulopathy).
E-MOTIVE: Early detection, uterine Massage, Oxytocics, Tranexamic acid, IV fluids, physical Examination and escalation.
24Tranexamic acid: from WOMAN to the present
Key message: TXA is treatment for diagnosed postpartum hemorrhage, given as soon as possible and always within 3 h of birth. The sooner it is given, the greater the benefit: most deaths from PPH occur within the first 2-3 h. It is not used for routine prophylaxis (WHO 2025, recommendations 14 and 15, new).
| Trial | Population | Primary outcome | What changed |
|---|---|---|---|
| WOMAN 2017 | 20,060 women with established PPH, 21 countries | Death from bleeding 1.5 % vs 1.9 % (RR 0.81; CI 0.65-1.00). Within 3 h: 1.2 % vs 1.7 % (RR 0.69; CI 0.52-0.91). No reduction in hysterectomy. No increase in thrombosis | TXA becomes standard treatment when given early |
| TRAAP 2018 | 4,079, vaginal birth, prophylaxis | PPH ≥500 mL 8.1 % vs 9.8 % (RR 0.83; CI 0.68-1.01), not significant | Does not support routine prophylaxis for vaginal birth |
| TRAAP2 2021 | 4,551, cesarean, prophylaxis | Calculated blood loss >1000 mL or transfusion 26.7% vs 31.6% (adjusted RR 0.84; CI 0.75-0.94); no differences in secondary clinical outcomes | Less measured blood loss, no clear clinical benefit |
| MFMU 2023 | 11,000 cesarean deliveries, 31 hospitals in the US | Death or transfusion 3.6% vs 4.3% (adjusted RR 0.89; CI 0.74-1.07) | Does not support prophylaxis at cesarean delivery |
| WOMAN-2 2024 | 15,068 women with moderate or severe anemia, vaginal birth | Clinical PPH 7.0% vs 6.6% (RR 1.05; CI 0.94-1.19). No thromboembolic events | Prophylaxis does not prevent PPH even in women with anemia |
| IPD meta-analysis 2024 | 54,404 women, 5 trials | Life-threatening bleeding 0.65% vs 0.85% (OR 0.77; CI 0.63-0.93), with no increase in thrombosis | Small and safe benefit; still does not change the WHO recommendation |
Administration: 1 g (ampoule 100 mg/mL, 10 mL) IV at 1 mL/min, i.e., over 10 min. Avoid rapid bolus: it may cause hypotension. A second dose of 1 g if bleeding continues at 30 min or recurs within 24 h of the first dose.
Safety: IV route only; never intrathecal or epidural (documented wrong-route error causing seizures and death). No trial showed an increase in thromboembolic events.
Beyond 3 h: no benefit and the estimate points toward harm; the WHO does not recommend it after this time.
CaVeSal® proprietary algorithm · Based on: WOMAN, Lancet 2017 · TRAAP, NEJM 2018 · TRAAP2, NEJM 2021 · Pacheco et al. (MFMU), NEJM 2023 · WOMAN-2, Lancet 2024 · Ker et al., IPD meta-analysis, Lancet 2024 · WHO/FIGO/ICM 2025 (recs. 14, 15 and 27) · FDA Cyklokapron prescribing information 2025 · Presentation by Dr. Rodrigo Rigoni, GyO Conference, Universidad del Pacífico, 2026 (secondary source; figures were taken from the original publications).
54T's, maneuvers and escalation Level 0-3
Tone (70%) — atony: oxytocin 5 U IV over 3 min + infusion 30 U/500 cc at 125 cc/h, methylergonovine, TXA, uterine massage, bimanual compression, balloon.
Trauma (20%) — lacerations: inspect the birth canal, repair, TXA.
Tissue (10%) — retained tissue: inspect the uterine cavity, remove retained tissue/placenta, TXA.
Thrombin (1%) — coagulopathy: coagulation tests, manual clot formation test in a tube for 7 min, correct with plasma/cryoprecipitate/platelets.
Control maneuvers: bimanual compression, external aortic compression, manual removal of the placenta, uterine inversion maneuver, hydrostatic balloon (Bakri), non-pneumatic anti-shock garment.
Escalation of response: Level 0 = E-MOTIVE (early detection); Level 1 = TXA + bimanual uterine compression; Level 2 = 2nd-line pharmacologic agents + intrauterine balloon + transfusion; Level 3 = surgery (B-Lynch, Hayman, Cho sutures; O'Leary, Posadas, Tsirulnikov or hypogastric artery ligations; hysterectomy). The Zea technique (vaginal clamping of the uterine arteries) serves as a bridge, and arterial embolization is an option in the stable patient.
| Medication | Role | Key notes |
|---|---|---|
| Oxytocin | 1st-line uterotonic | Prevention and treatment |
| Methylergonovine | 2nd-line uterotonic | Management of atony (Tone) |
| Tranexamic acid (TXA) | Antifibrinolytic | 1 g IV over 10 min (not as a rapid bolus); 2nd dose at 30 min or if bleeding recurs within 24 h; NOT after 3 h; not for routine prophylaxis |
| Misoprostol | Uterotonic | 400-600 µg orally |
| Heat-stable carbetocin | Uterotonic | FOR PREVENTION ONLY without a cold chain |
| Red blood cells | Blood product | Volume/O2 replacement |
| Fresh frozen plasma | Blood product | Correction of coagulopathy |
| Platelets | Blood product | Thrombin/coagulopathy |
| Cryoprecipitate | Blood product | Low fibrinogen |
| Vasopressors (dopamine, norepinephrine) | Hemodynamic support | Refractory shock |
CaVeSal® proprietary algorithm · Based on: Code Red MSPBS 2022 · WHO 2025 (PPH).
19Perineal tears — classification and repair (RCOG GTG 29)
| Grade | Structures involved |
|---|---|
| 1 | Perineal skin and/or vaginal mucosa |
| 2 | Perineal muscles, without involving the anal sphincter |
| 3a | <50% of the external anal sphincter (EAS) thickness |
| 3b | >50% of the EAS thickness |
| 3c | EAS and internal anal sphincter (IAS) |
| 4 | Anal sphincter (EAS + IAS) and anorectal mucosa |
- If uncertain between 3a and 3b, classify as 3b (higher grade). A rectal buttonhole tear with an intact sphincter is not grade 4: repair it and document it separately.
- Systematic examination with digital rectal examination for every tear before repair.
- Grades 3-4: repair in the operating room under regional or general anesthesia, with good lighting and an assistant; if there is active bleeding, vaginal packing while transferring the patient.
- Full-thickness EAS tear: overlap or end-to-end technique; 3a / partial tear: end-to-end. IAS: separate end-to-end repair. Avoid figure-of-eight (hemostatic) sutures, which cause ischemia.
- Digital rectal examination at the end (to rule out transfixing sutures).
- Postoperative care: broad-spectrum antibiotics, laxatives; avoid suppositories and enemas; follow-up with pelvic floor physiotherapy (6-12 weeks).
- Grades 1-2: continuous layered repair with rapidly absorbing polyglactin 910.
CaVeSal® proprietary algorithm · Based on: RCOG Green-top Guideline No. 29 (2015) · Sultan AH. Obstetric perineal injury and anal incontinence. Clin Risk 1999;5:193-6 · ACSQHC Third and Fourth Degree Perineal Tears Clinical Care Standard.
Sources: WHO Consolidated Guidelines for prevention, diagnosis, treatment of PPH (Geneva, 2025); Macphail & Fitzgerald, Curr Obstet Gynaecol 2001;11:108-114; Vélez AG, Agudelo JB, Gómez GI, Zuleta JJ. Rev Colomb Obstet Ginecol 2009;60(1):34-48; Colombia Ministry of Health CPG 2013; WHO Managing Complications in Pregnancy and Childbirth, 2nd ed. 2017; PAHO 2024.
6Placental abruption with fetal death — mode of delivery and amniotomy
Essential prerequisite: the mother must be hemodynamically stable (no shock or cardiovascular instability). If the mother is unstable → immediate cesarean delivery, regardless of whether the fetus is alive or dead (WHO).
Amniotomy in this context: perform as early as possible (not delayed) — unlike the general rule of delayed amniotomy in the physiological partograph. Objectives: (1) reduce intrauterine pressure (decompress the retroplacental hematoma and potentially halt progressive separation), and (2) allow internal monitoring if vaginal birth is attempted.
| Source | Recommendation |
|---|---|
| WHO | Vaginal delivery (induction with misoprostol) if the mother is stable; cesarean delivery only in the event of maternal hemodynamic instability, regardless of fetal status. |
| RCOG Green-top No. 63 | Attempt vaginal delivery if the maternal condition is stable, with induction of labor. Cesarean delivery only for a maternal indication (uncontrolled hemorrhage, failed induction). |
| MSF Guidelines | Urgent uterine evacuation (vaginal delivery or cesarean delivery) regardless of gestational age; cesarean delivery becomes imperative if labor progresses very slowly, even in the event of fetal demise. |
| PubMed (J Obstet Gynaecol Res, PMID 28370793) | Case series of 16 patients: vaginal delivery was attempted in 15 and achieved in 14 (93.3%). Feasible and safe following fetal demise due to placental abruption, regardless of gestational age, parity, cervical maturity, or duration of labor, when intensive medical resources are available. |
Why vaginal delivery is preferred in this scenario: severe placental abruption with fetal demise is frequently associated with consumptive disseminated intravascular coagulation (DIC)—cesarean delivery in a coagulopathic patient increases the risk of intraoperative hemorrhage due to atony/coagulopathy and peripartum hysterectomy. Vaginal delivery avoids a surgical wound in the presence of a coagulation disorder.
Management protocol:
- Maternal stabilization: two large-bore IV lines (16-18G), Ringer's lactate, consider type and crossmatch, fibrinogen/PT/aPTT/platelet count. Activate the massive obstetric hemorrhage protocol if bleeding is heavy.
- Early amniotomy to decompress the uterus and allow internal monitoring.
- Labor induction: oral or vaginal misoprostol (WHO recommendation for fetal demise/anomaly in the 3rd trimester) + oxytocin if needed.
- Monitor progress: if labor progresses very slowly despite induction, cesarean delivery becomes imperative even in the event of fetal demise. There is no fixed time limit as long as maternal-fetal monitoring shows no progression of the placental abruption.
- Correction of coagulopathy if cesarean delivery is required: thrombocytopenia <50,000/µL or hypofibrinogenemia <100-200 mg/dL with cryoprecipitate/platelets/fresh frozen plasma before or during surgery.
- Postpartum: monitor for PPH and residual coagulopathy; emotional support and bereavement care.
Absolute contraindications to vaginal delivery: uncontrolled hemorrhage, placental abruption with maternal hemodynamic instability, suspected uterine rupture, classic obstetric indication for cesarean delivery (placenta previa, vasa previa).
General note on amniotomy (WHO): amniotomy alone is not recommended as the sole method of labor induction (moderate-quality evidence, weak recommendation)—it is considered only when prostaglandins and oxytocin are unavailable. This is the only documented exception for an emergency maternal hemorrhagic indication.
CaVeSal® proprietary algorithm · Based on: WHO recommendations for induction of labour (2011) · RCOG Green-top Guideline No. 63 — Antepartum Haemorrhage (2011) · MSF Guidelines — Abruptio placentae · PubMed 28370793 (J Obstet Gynaecol Res) · GLOWM — Placental Abruption · Exxcellence — Management of Fetal Demise Caused by Abruption.
7Prevention of Postpartum Hemorrhage — a three-moment framework
Conceptual framework (Pregnancy → Childbirth → Postpartum): PPH results from accumulated factors across 6 categories—social determinants, maternal conditions/diseases, pregnancy factors, childbirth factors, placental factors, and health system factors (antenatal and intrapartum). The pathway to morbidity and mortality progresses as follows: normal/complicated birth → PPH → severe PPH → death/complications—with a specific intervention possible at each stage: preventive measures → early diagnosis → first-response treatment → treatment of refractory cases → post-PPH supportive care.
8Antenatal prevention
Identification and appropriate management of gestational anemia, including the use of intravenous iron when indicated (moderate-to-severe anemia, intolerance or lack of response to oral iron, or advanced gestational age with little time to correct anemia orally). Correcting anemia antenatally reduces morbidity and mortality associated with blood loss during childbirth.
9Intrapartum prevention
Perineal protection during the second stage to reduce trauma and facilitate spontaneous birth, according to the woman's preferences and available options: perineal massage, warm compresses, manual perineal support.
🚫 Avoid routine episiotomy—reserve it for specific indications, not as a routine practice.
Sources: UNFPA / Universidad de Antioquia (Grupo Nacer) — Framework for reducing PPH morbidity and mortality · WHO Consolidated Guidelines for prevention, diagnosis, treatment of PPH (Geneva, 2025) · WHO recommendations for the prevention of postpartum hemorrhage.
10Massive Transfusion Protocol — two valid variants
Activation: anticipated massive hemorrhage (replacement of ≥ 50% of blood volume in 2h) or active bleeding after 4 units of PRBCs in 1-2h.
| Blood component | Effect per unit | Indication / target |
|---|---|---|
| Packed red blood cells (PRBCs) | Increases hematocrit by 3-4% | Based on estimated blood loss |
| Fresh frozen plasma (FFP) | Increases fibrinogen by +10mg/dL | 15mL/kg or 1U/20kg; PT/aPTT>1.5× control |
| Platelets | Increases by 5,000-10,000/µL | Target 50,000-100,000/µL |
| Cryoprecipitate | — | 1-2mL/kg (threshold depends on variant — see below) |
CaVeSal® proprietary algorithm · Based on: Pacheco LD et al. Am J Perinatol 2013;30:1-4 · WHO 2025 (PPH).
11Variant A — Pacheco 2013 protocol (6 rounds, 100mg/dL threshold)
| Round | PRBCs | FFP | Platelets | Cryoprecipitate |
|---|---|---|---|---|
| 1 | 6U | 6U | 6U | 10U |
| 2 | 6U | 6U | — | 20U |
| 3 | Recombinant factor VIIa 40µg/kg | — | ||
| 4 | 6U | 6U | 6U | 10U |
| 5 | 6U | 6U | 10U | — |
| 6 | Recombinant factor VIIa 40µg/kg | — | ||
CaVeSal® proprietary algorithm · Based on: Pacheco LD, Saade GR, Costantine MM, Clark SL, Hankins GD. The Role of Massive Transfusion Protocols in Obstetrics. Am J Perinatol 2013;30(1):1-4.
Cryoprecipitate threshold: fibrinogen <100 mg/dL. If bleeding is not controlled after round 6, restart from round 1.
12Variant B — WHO 2025 protocol (no fixed round table, 200mg/dL threshold)
Fibrinogen replacement threshold: <2 g/L (=200 mg/dL), target ≥ 2g/L.
Typically 3-4g of fibrinogen ≈ 8-10 units of cryoprecipitate.
No fixed round table — guided by ongoing clinical and laboratory assessment (unlike the rigid round-based Pacheco 2013 protocol).
After the 2nd round/reassessment: administer tranexamic acid (TXA) 1g IV if not already administered.
13Other protocol elements
Cell salvage (intraoperative recovery of autologous blood): an option at centers with the technical capacity.
PBM (Patient Blood Management): a patient blood optimization strategy — minimize blood loss, optimize hematopoiesis, tolerate anemia when safe.
Postpartum iron: recommended by WHO 2025 when significant postpartum anemia is present.
14Quantification of blood loss: calibrated drape and visual chart
Operational recommendation: use a calibrated blood collection drape when available (an objective method recognized by WHO 2025); otherwise, use the visual equivalency chart. The chart supplements, but does not replace, objective measurement.
| Item | Estimated volume |
|---|---|
| Stained sanitary pad | 30 mL |
| Saturated sanitary pad | 100 mL |
| Soaked 10×10 cm gauze | 60 mL |
| Incontinence brief | 250 mL |
| 45×45 cm gauze pad | 350 mL |
| Full kidney dish (basin) | 500 mL |
| Spill on floor, 100 cm diameter | 1000 mL |
| PPH confined to the bed | 1500 mL |
| PPH with spill on the floor | 2000 mL |
CaVeSal® proprietary algorithm · Based on: WHO 2025 · Bose et al., BJOG 2006.
Calibrated drape (BRASSS-V drape): simple, low-cost, accurate, and objective; usable in a wide range of settings, with a hygienic surface for childbirth. In its trial, visual estimation underestimated actual blood loss by 33% compared with the calibrated drape (correlation with spectrophotometry 0.92).
15Shock index: bibliographic support for thresholds
| Shock index | Interpretation |
|---|---|
| ≥ 0,9 | Refer to a higher level of care |
| ≥ 1,4 | Urgent intervention at a higher level of care |
| ≥ 1,7 | Greater likelihood of adverse outcomes |
Table adapted (translated) from El Ayadi AM et al. PLoS ONE 2016;11(2):e0148729 · CC BY 4.0 License (use permitted with attribution).
The shock index was evaluated as a predictor of three levels of adverse outcomes: death; severe outcome (death or severe organ dysfunction); and a composite of critical interventions (death, severe end-stage organ dysfunction, ICU admission, transfusion of ≥5 units of red blood cells, emergency hysterectomy).
16Drugs and fluids in PPH: differences that matter (WHO 2025)
| Indication | Dose and route | WHO 2025 recommendation |
|---|---|---|
| Prevention of PPH | 400 or 600 µg ORAL | Recommendation 7.3 — for all births |
| Treatment of PPH (2nd line) | 800 µg SUBLINGUAL | Recommendation 25 — if IV oxytocin is unavailable or bleeding does not respond (with IV ergometrine or an oxytocin+ergometrine combination) |
CaVeSal® proprietary algorithm · Based on: WHO 2025 (PPH) · FIGO 2022 · Zheng 2014 · Chen et al. 2013.
Crystalloids over colloids (Recommendation 28): isotonic crystalloids are recommended over colloids for IV fluid resuscitation in PPH; this applies to the 500 mL boluses of warmed crystalloids in the first 20-minute flowchart. Reaffirmed by FIGO 2022 as part of the PPH care bundle.
Controlled cord traction (Du, Ye & Zheng 2014): meta-analysis of 30,532 patients; reduces manual removal of the placenta (RR 0.70; 95% CI 0.58-0.84) with no difference in severe PPH (RR 0.94; 95% CI 0.88-1.01).
Sustained uterine massage: not routinely recommended after prophylactic oxytocin (Chen et al., ACOG 2013); monitor uterine tone.
Non-pneumatic anti-shock garment (NASG): a temporizing measure while transfer is underway or definitive treatment is being prepared (FIGO 2022, Escobar, Nassar, Theron et al.).
17Balloon tamponade and uterine compression sutures
| Device | Characteristic |
|---|---|
| Bakri | Obstetric-specific design; up to 500 mL |
| Ellavi | Less expensive; similar design to Bakri |
| Condom + Foley/Nelaton catheter | Low-cost adaptation for resource-limited settings |
| Rusch catheter | Adapted hydrostatic balloon |
| Sengstaken-Blakemore | Double balloon (gastric + esophageal); designed for esophageal varices and adapted for uterine tamponade |
| Technique | Particularity |
|---|---|
| B-Lynch | Classic, “suspender” suture; requires open hysterotomy |
| Hayman | Simplified modification; does not require hysterotomy (uterus closed) |
| Pereira | Multiple transverse and vertical sutures; closed uterus |
| Ho-Cho | Multiple square sutures; particularly indicated for placenta accreta |
| Uterine sandwich | Simultaneous intrauterine balloon + external compression suture (B-Lynch + Bakri) |
| Technique | Particularity |
|---|---|
| Zea (vaginal) | Vaginal clamping of the uterine arteries with ring forceps in the lateral parametrium of the cervix; bridging measure while preparing the operating room or addressing the cause. Also useful before evacuating a cervical ectopic pregnancy |
| O'Leary | Bilateral ligation of the uterine arteries via laparotomy; first-line conservative surgical option |
| Posadas | Selective devascularization: posterior ligation of the uterine arteries and internal tubal arteries, without opening the broad ligament; 96.4% success in 750 cases |
| Tsirulnikov | Triple stepwise ligation: round ligaments, utero-ovarian ligaments, and uterine arteries |
| Hypogastric arteries | Internal iliac artery ligation; more complex (ureteral and venous risk), reserved for failure of the preceding procedures |
| Arterial embolization | Interventional radiology in a hemodynamically stable patient; fertility-preserving |
CaVeSal® proprietary algorithm · Based on: INPer — Zea technique · IMSS Clinical Practice Guideline 162 · Ginecol Obstet Méx — Posadas technique · Series of 750 cases.
CaVeSal® proprietary algorithm · Based on: WHO 2021 · MSPBS Code Red 2022.
- Bakri: success rate 79.5-85.9% in systematic reviews; in a meta-analysis of 28 studies, 82% with balloon alone (95% CI 78-86%) and 95% with additional procedures. Lower success after cesarean delivery (69-78%) than after vaginal birth (90%).
- Sutures: no technique demonstrated clear superiority; efficacy ~75% after failure of medical treatment and ~80% as second-line treatment after failed vascular ligation; risk of synechiae 5-10%.
- Combined balloon + suture: success rate >91.7% in refractory PPH; avoids hysterectomy in up to 75% of cases that would otherwise require it.
- Condom/Foley balloon (improvised): WHO 2021 recommends its use only where other treatments, including immediate surgery, are already available. Assembly: 16-18 Foley catheter with the distal tip cut off, inserted into a condom, secured with silk about 5 fingers from the end (without obstructing the lumen); fill with 500 cc of 0.9% normal saline, with vaginal packing to prevent expulsion. In a comparative study of 12 patients (6 per group), the improvised balloon achieved 100% success (6/6), with no complications or associated surgeries, comparable to the SOS Bakri balloon, although time to hemostasis was slightly longer (6.8 vs. 4.6 min, not statistically significant). Source: Jiménez L, Veroes J, Vera M, Colmenares M, Di Muro J, Márquez D. Rev Obstet Ginecol Venez. 2020;80(3):227-235.
Comparative reference; the surgical step-by-step is beyond the scope of a quick-reference guide. Included in the Code Red Level 2-3 escalation — in our setting (Paraguay), where Bakri/Ellavi are not always available, the improvised balloon is the usual and clinically equivalent option.
18“Diamond of Death”: why calcium should be corrected during massive transfusion
Evolution of the classic lethal triad (hypothermia, acidosis, coagulopathy) with a fourth vertex: hypocalcemia. All four components reinforce one another: each worsens the other three.
- Hypothermia ↔ Hypocalcemia ↔ Acidosis ↔ Coagulopathy.
- This is the pathophysiologic framework behind the practical recommendation to replace calcium IV during massive transfusion (see protocol, subcards 10-13).
- In PPH, low ionized calcium is associated with greater bleeding severity (Epstein et al., Br J Anaesth 2021).
20Blood volume, allowable blood loss, and quantification of bleeding
- Estimated blood volume: 100 mL/kg in healthy pregnancy; 70 mL/kg in obesity or volume contraction (severe preeclampsia).
- Maximum allowable blood loss: (initial Hb − minimum Hb) × blood volume ÷ [(initial Hb + minimum Hb) × 0.5]. Usual minimum Hb 7 g/dL.
- Quantify, do not estimate by eye: 1 g = 1 mL. Wet weight − dry weight (pads, gauze, drapes) + suction volume − amniotic fluid − irrigation.
- Separate amniotic fluid before placental delivery (change the canister or record the volume).
- Express blood loss as a % of blood volume and compare it with the Vélez shock classification (subcard 2).
| Method | Use |
|---|---|
| 100 / 70 mL/kg (SOGC 431) | Used by the calculator |
| “Rule of 30”: 100 mL/kg | SA Health PPH |
| 30–60% increase over nonpregnant blood volume | Williams Obstetrics (Pritchard) |
| Nonlinear formula by BMI (obese women have fewer mL/kg) | Lancaster University, nonlinear proposal |
| Nadler (height and weight, nonpregnant) | Nadler, PubMed 30252333 |
CaVeSal® proprietary algorithm · Based on: SOGC Guideline No. 431 (J Obstet Gynaecol Can 2022) · ACOG Committee Opinion No. 794 (2019).
21Coagulopathy based on conventional laboratory tests: thresholds and DIC scores
| Laboratory | Management |
|---|---|
| Fibrinogen <2 g/L | Cryoprecipitate, 2 pools (10 U) or fibrinogen concentrate |
| Platelets <75,000 | 1 pool or apheresis; target >50,000 |
| Prolonged PT / aPTT | FFP 12–15 mL/kg; if >1.5× normal, more is usually required (TACO risk) |
| No active bleeding | Do not transfuse based on an isolated value; repeat |
Concentrate dose (mg/kg) = (target − measured, mg/dL) ÷ 1.7 (RiaSTAP FDA label).
| Score | Variables | Cutoff |
|---|---|---|
| ISTH 2025 (preferred) | Platelets, D-dimer (>3× and >7× ULN), prolonged PT, fibrinogen | ≥5 |
| ISTH 2001 | Same, with a qualitative “fibrin marker” | ≥5 |
| Erez 2014 (pregnancy) | PT difference, platelets, fibrinogen | ≥26 |
| JSOG 2024 (obstetric) | Baseline condition, fibrinogen, FDP or D-dimer | ≥8 |
In pregnancy, normal fibrinogen levels are higher (3.5–6.5 g/L): a “normal” non-pregnant value may already be low. Therefore, obstetric scores give greater weight to fibrinogen.
CaVeSal® proprietary algorithm · Based on: RCOG GTG 52, BJOG 2017;124:e106-49 · Collins P et al. ISTH SSC 2016, J Thromb Haemost 2016;14:205-10 · Iba T et al. ISTH SSC 2025, J Thromb Haemost 2025;23:2356-62 · Taylor FB Jr et al. ISTH 2001 (Thromb Hemost 2001;86:1327-30), included in BCSH 2009 · Morikawa M et al. Sci Rep 2024;14:17677 (JSOG 2024 criteria). Fibrinogen range in pregnancy: RCOG GTG 47. Erez score variables: Table adapted (translated) from Erez O et al. PLoS ONE 2014;9(4):e93240 · CC BY 4.0 License.
22ROTEM in obstetric hemorrhage: quick interpretation
| Parameter | Finding | Management |
|---|---|---|
| FIBTEM A5 | <12 mm with bleeding, or <7 mm | Fibrinogen: g = target increase (mm) × weight ÷ 160 |
| FIBTEM A5 | >12 mm | No fibrinogen required |
| EXTEM CT | >100 s with corrected FIBTEM | FFP 15 mL/kg (or PCC according to protocol) |
| EXTEM A5 | <35 mm with FIBTEM at target | Platelet component: confirm platelet count |
| EXTEM ML | >15 % | Hyperfibrinolysis: tranexamic acid 1 g IV |
- EXTEM reference: CT 38–79 s; ML <15 %. 10 units of cryoprecipitate ≈ 2 g of fibrinogen.
- Threshold variants: FIBTEM A5 >8 mm and EXTEM CT <75 s (All Wales PPH Guideline); EXTEM CT >80 s (Görlinger K et al. Korean J Anesthesiol 2019;72:297-322general algorithm). The calculator lets you choose.
- Repeat ROTEM 10–15 min after each intervention.
CaVeSal® proprietary algorithm · Based on: Curry NS et al. BSH 2018, Br J Haematol 2018;182:789-806 · Collins PW et al. OBS2, Br J Anaesth 2017;119:411-21 · Görlinger K et al. Korean J Anesthesiol 2019;72:297-322 · Drotarova M et al. Diagnostics 2023;13:3219.
Sources subcards 14-18: Bose P, Regan F, Paterson-Brown S. BJOG 2006;113:919-924 · Patel A, Goudar SS, et al. Int J Gynaecol Obstet 2006;93(3):220-224 (BRASSS-V drape; Goudar, Edlavitch, Bellad 2003) · WHO Consolidated Guidelines PPH 2025 (Rec. 7.3, 25, 28) · El Ayadi AM et al. PLoS ONE 2016;11(2):e0148729 · Du Y, Ye M, Zheng F. 2014 · Escobar MF, Nassar AH, Theron G et al. FIGO recommendations on PPH 2022. Int J Gynecol Obstet · PMC7999507 (Bakri) · AJOG 2022 (suturas) · PubMed 35115478 (OMS 2021, balón) · Wray JP et al. Am J Emerg Med 2021;41:104-109 · Epstein D et al. Br J Anaesth 2021;126(5):1022-1028.
Sources: Pacheco LD, Saade GR, Costantine MM, Clark SL, Hankins GD. The Role of Massive Transfusion Protocols in Obstetrics. Am J Perinatol 2013;30:1-4 · WHO 2025 Consolidated Guidelines for prevention, diagnosis and treatment of PPH.
HDP Code — Hypertensive Disorders of Pregnancy
Severe preeclampsia, hypertensive emergency, and eclampsia.
1Definition and criteria
Pregnancy >20 weeks + 2 BP readings 15 min apart if severe (≥160/110) or 4 h apart if mild (140-159/90-109) + evidence of end-organ damage (clinical: headache, visual changes, right upper quadrant pain, pulmonary edema; laboratory: AST/ALT≥70, LDH≥600, platelets<100,000, bilirubin≥1.2) OR proteinuria (≥300 mg/24h, protein/creatinine ratio≥0.3, albumin/creatinine ratio≥0.8, dipstick≥2+) OR angiogenic tests sFlt1/PlGF>38.
Proteinuria is NOT required for the diagnosis of severe preeclampsia.
Prevention: calcium 1-2 g/day in all pregnant patients; aspirin 150 mg/day based on risk factors (1 high-risk factor or 2 moderate-risk factors).
2Classification and team
Code activation: SBP>160 or DBP>110 or eclamptic seizures.
Team: Coordinator, Assistant, Circulating Nurse.
Post-target monitoring: every 10 min for the 1st hour, every 15 min for the 2nd hour, every 30 min for the 3rd hour, every hour from the 4th hour for an additional 4 h.
Sustained severe-range BP for >15 min = life-threatening emergency.
3Flowchart — SSSAO / stepwise algorithm
SSSAO mnemonic: Support, Safety, magnesium sulfate (loading dose 4-6 g IV, maintenance 1-2 g/h until 24 h postpartum), Antihypertensives (reduce by 20-25% over 24-48 h, target 135/85 per NICE), Obstetric management (fetal maturation at 24-34 weeks, fetal well-being, delivery: non-severe PE at 37 weeks, severe PE at 34 weeks).
Stepwise hypertensive emergency algorithm: IV labetalol 20→40 mg / oral nifedipine 10→20→20 mg / IV hydralazine 10 mg, reassessing every 10-20 min.
Fluid management: no bolus, total 80 mL/h or 1 mL/kg/h, max 125 mL/h.
Eclampsia: seizure control with a 4-6 g IV MgSO4 bolus (or 2 g IV if already receiving it), maintenance 2 g/h, second 2 g IV bolus if seizures recur. Intubate if: unconscious after seizure, status epilepticus, aspiration, hypoxia. Continue MgSO4 for at least 24 h postpartum or from the last seizure.
4Medications
All patients with severe PE receive MgSO4; mode of delivery is determined by obstetric factors, NOT automatic cesarean delivery.
5Expanded classification and additional severity criteria (ACOG PB 222 / FIGO / ISSHP)
Chronic hypertension with superimposed preeclampsia: new-onset proteinuria, or sudden loss of blood pressure control, or end-organ dysfunction after 20 weeks of gestation in a patient with hypertension predating pregnancy.
Additional severity criterion — Progressive renal insufficiency: serum creatinine >1.1 mg/dL or doubling of baseline creatinine (not previously included alongside LDH/bilirubin — added as an independent laboratory criterion).
Urine output — alternative weight-based threshold: <0.5 mL/kg/h, as an alternative to the absolute threshold of <30 mL/h already used for MgSO4 toxicity monitoring.
6Chronic/oral maintenance antihypertensives (outside the acute crisis)
| Drug | Dose | Maximum dose |
|---|---|---|
| Oral labetalol | 100-400mg every 8-12h | 2,400mg/day |
| Methyldopa | 250-500mg PO every 6-8h | 2g/day |
| Extended-release nifedipine | 20-60mg PO every 12-24h | 120mg/day |
| 🚫 Contraindicated in pregnancy: ACE inhibitors, ARBs, direct renin inhibitors — teratogenicity, fetal renal failure. |
CaVeSal® proprietary algorithm · Based on: ACOG PB 222 (2020) · NICE NG133 · FIGO 2019 · ISSHP 2021.
7Aspirin prophylaxis — variations in initiation window (2 approaches)
| Source | Dose | Initiation window |
|---|---|---|
| FIGO 2019 / USPSTF | 150mg/night | Weeks 11-14⁺⁶ to 36 |
| ACOG PB 222 (2020) | 100-150mg/day | Weeks 12-16 to 36 |
CaVeSal® proprietary algorithm · Based on: FIGO 2019 · USPSTF 2021 · ACOG PB 222.
High-risk indications (warrant initiation of aspirin): history of preeclampsia, chronic hypertension, type 1 or 2 diabetes, kidney disease, SLE/APS, multiple pregnancy.
Calcium: 1.5-2.0g/day in populations with low dietary calcium intake (<800mg/day) — same FIGO caveat used in Prevention (subcard 1).
8Additional safety notes
- Nifedipine in hypertensive crisis: swallow with water; DO NOT administer sublingually.
- MgSO4 antidote: Calcium gluconate 10% 1g (10mL) slow IV. Two administration-rate options: 3-5 min (MSPBS/CaVeSal regimen) or 10 min (ACOG/WHO).
- Monitoring for MgSO4 toxicity: discontinue if RR <12 breaths/min; some guidelines use <12-16 breaths/min (CaVeSal regimen) and others <12-14 breaths/min (ACOG). Patellar reflex present and urine output ≥30 mL/h in all regimens.
9MgSO4 regimens — Pritchard · Zuspan · IM
The Calculator uses the Pritchard/MSPBS regimen by default. The Zuspan IV regimen is the intravenous alternative and is preferred for neuroprotection; the University of Antioquia uses a larger dilution volume with the same total dose.
| Regimen | Loading dose | Maintenance |
|---|---|---|
| Pritchard / MSPBS | 14 g total: 10 g IM (5 g = 10 cc in each buttock) + 4 g IV (8 cc + 12 cc of NS in a 20 cc syringe, over 20 min) | IV 1-2 g/h in a 100 cc Volutrol, or IM 5 g every 4 h, for 24 h |
| Zuspan (IV) | 4 g IV over 20-30 min | 1-2 g/h IV for 24 h (preeclampsia); for neuroprotection, until delivery or for 12 h |
| University of Antioquia | Same total dose with a larger dilution volume (see source protocol) | |
IM maintenance — how to administer (clarification to prevent underdosing): each dose is 5 g PER SCHEDULED DOSE (10 cc total). Option 1 (official text): 10 cc in one buttock, alternating buttocks at each scheduled dose. Option 2 (administration variant proposed by CaVeSal®): 5 cc (2.5 g) in each buttock at the same scheduled dose, repeated at the next scheduled dose (every 4 h). The frequent error is to administer a TOTAL of 5 cc per scheduled dose (2.5 g): the full dose is 10 cc (5 g).
Typical sequence of toxicity: 1st, decreased urine output (<30 mL/h, risk of accumulation); 2nd, loss of the patellar reflex; 3rd, respiratory depression (RR <12-16 breaths/min). Rescue: calcium gluconate 10%, 1 g (10 cc) slow IV over 3-5 min, in the event of respiratory depression or instability (this is not gram-for-gram neutralization). The regimen may be repeated (repeat regimen) according to clinical course.
CaVeSal® proprietary algorithm · Based on: MSPBS Paraguay, Guía de Código Rojo Materno Neonatal 2ª ed. 2022 (pág. 71) · MSPBS, Manual Nacional de Normas 2018 (neuroprotección) · Universidad de Antioquia/UNFPA.
| Medication | Dose / regimen | Maximum dose |
|---|---|---|
| Nifedipine PO | 10-20-20 mg every 20 min | 180 mg/day |
| Labetalol IV | 20-40-80 mg every 10 min | 300 mg/day |
| Hydralazine IV | 5-10 mg every 20 min | 20 mg/day |
| Magnesium sulfate | 4-6 g bolus + maintenance 1-2 g/h | — |
| Nicardipine (infusion) | 5 mg/h, increasing by 2.5 mg/h every 5 min | 10 mg/h |
| Sodium nitroprusside | 0.2 µg/kg/min, increasing every 5 min | 4 µg/kg/min |
CaVeSal® proprietary algorithm · Based on:
9HELLP syndrome: ACOG, Tennessee, and Mississippi criteria
| System | Platelets | Transaminases | Hemolysis / LDH | Use |
|---|---|---|---|---|
| ACOG PB 222 (2020) | <100.000/µL | AST and ALT >2 times the upper limit of normal | LDH ≥600 U/L | Clinical diagnosis; no subdivision by class |
| Tennessee (Sibai) | <100.000/µL | AST ≥70 U/L | LDH ≥600 U/L (or bilirubin >1.2 mg/dL with abnormal smear: schistocytes) | Complete HELLP = 3 criteria; partial = 1-2 criteria |
| Mississippi — Class 1 (severe) | ≤50.000/µL | AST or ALT ≥70 U/L | LDH ≥600 U/L | Higher risk of DIC and hemorrhage |
| Mississippi — Class 2 (moderate) | >50.000 a ≤100.000/µL | AST or ALT ≥70 U/L | LDH ≥600 U/L | Intermediate risk |
| Mississippi — Class 3 (mild) | >100.000 a ≤150.000/µL | AST or ALT ≥40 U/L | LDH ≥600 U/L | Detects early forms not included in ACOG/Tennessee |
CaVeSal® proprietary algorithm · Based on: ACOG Practice Bulletin No. 222 (2020) · tabla Tennessee vs Mississippi (PMC2654858) · Clin Liver Dis 2019 (PMC6448736) · StatPearls, HELLP Syndrome.
- ACOG management: because of its morbidity and mortality, many authors recommend delivery in HELLP syndrome regardless of gestational age, after maternal stabilization. ACOG considers the evidence insufficient to use corticosteroids to attenuate the disease (they are used for fetal lung maturation according to gestational age).
- Neuraxial anesthesia (ACOG): acceptable with platelets ≥70,000/µL if the count is stable, there is no other coagulopathy, platelet function is normal, and the patient is not taking antiplatelet or anticoagulant agents (risk of epidural hematoma <0.2%).
- Practical difference: ACOG sets the <100,000/µL cutoff for diagnosis; Mississippi subdivides by platelet nadir to grade bleeding risk and guide transfusion planning.
Correction of attribution: bilirubin >1.2 mg/dL and schistocytes belong to the Tennessee criteria (Sibai), not the diagnostic text of ACOG PB 222. In the Calculator the default criterion is Mississippi, with a selector for ACOG and Tennessee. Sources: ACOG Practice Bulletin No. 222 (2020) · tabla Tennessee vs Mississippi (PMC2654858) · Clin Liver Dis 2019 (PMC6448736) · StatPearls, HELLP Syndrome.
10sFlt-1/PlGF ratio: diagnostic and prognostic thresholds
| Ratio | <34 weeks | ≥34 weeks | Interpretation |
|---|---|---|---|
| ≤38 | Rules out | Rules out | Rules out PE in the following week (NPV >99%) |
| 38-85 / 38-110 | 38-85 | 38-110 | Intermediate zone: repeat in 1-2 weeks |
| >85 / >110 | >85 | >110 | High suspicion or diagnostic support for PE |
| >655 / >201 | >655 | >201 | Extreme angiogenic imbalance: high probability of delivery within 48 h |
CaVeSal® proprietary algorithm · Based on: Verlohren S et al. Am J Obstet Gynecol 2012;206(1):58.e1-8 (cited in PMC11012921) · Villalaín C et al. J Am Heart Assoc 2020;9:e015548 (ratio >655) · Sá CPN et al. Rev Bras Ginecol Obstet 2020;42(11).
- Spanish cohort, J Am Heart Assoc 2020 (237 pregnancies with a ratio >655, 20-37 weeks): median time to delivery was 4 days with established PE and 7 days without PE at the time of testing; 60.5% were still pregnant at 48 h with PE (compared with 29.4% in the original series, in which clinicians were blinded to the result). High frequency of FGR (85-90% at delivery) and severe features.
- Some authors propose >1000 as a better predictor of adverse perinatal outcome (Stolz et al.).
- The ratio quantifies the biological severity of placental and systemic disease; it does not replace clinical assessment when deciding timing of delivery.
The Calculator replicates the logic of the CaVeSal prenatal calculator (≤38 / 85 or 110 depending on GA / >655). Sources: Verlohren S et al. Am J Obstet Gynecol 2012;206(1):58.e1-8 (cited in PMC11012921) · Villalaín C et al. J Am Heart Assoc 2020;9:e015548 (ratio >655) · Sá CPN et al. Rev Bras Ginecol Obstet 2020;42(11).
11Maternal ophthalmic artery (OA) Doppler
Key index: systolic peak ratio PSV2/PSV1 (peak ratio). In normal pregnancy it is usually <0.6; in PE, the second peak approaches or exceeds the first.
| PSV2/PSV1 ratio | Interpretation |
|---|---|
| >0,65 | Cutoff for predicting PE (Kalafat 2018 meta-analysis; AUC 0.67 for early-onset PE) |
| <0,70 | Normal (CaVeSal operational cutoff) |
| 0,70-0,77 | Gray zone (CaVeSal operational cutoff) |
| ≥0,78 | Severe vascular compromise (CaVeSal operational cutoff) |
CaVeSal® proprietary algorithm · Based on: Kalafat E et al. UOG 2018;51(6):731-737 · Vaz de Melo PFM et al. BMC Pregnancy Childbirth 2023;23:343 · PMC12844109 review.
Vaz de Melo 2023 meta-analysis (8 studies, 1425 pregnant women): peak ratio and P2 have the best diagnostic performance (PR: sensitivity 84%, specificity 92%).
The 0.70 and 0.78 cutoffs come from the CaVeSal prenatal calculator and do not yet have a single verified primary reference; evidence for specifically predicting eclampsia is limited. Sources: Kalafat E et al. UOG 2018;51(6):731-737 · Vaz de Melo PFM et al. BMC Pregnancy Childbirth 2023;23:343 · PMC12844109 review.
12sFlt-1/PlGF vs ophthalmic artery Doppler in established severe preeclampsia
| Characteristic | sFlt-1/PlGF ratio | Ophthalmic artery Doppler |
|---|---|---|
| Nature | Biochemical marker of antiangiogenesis and placental dysfunction | Functional hemodynamic measurement of the maternal orbital/cerebral vascular territory |
| Strength | Quantifies systemic/multiorgan damage and the severity of placental disease | Reflects in real time the loss of maternal cerebral vascular autoregulation |
| Use in established disease | Helps estimate the urgency of delivery (values >655 associated with delivery within days) | Warning sign in the presence of neurovisual symptoms; supports monitoring of neurological risk |
| Limitation | Cutoffs depend on the platform; availability and cost | Operator-dependent; no universal cutoffs; limited evidence for eclampsia |
CaVeSal® proprietary algorithm · Based on: ACOG PB 222 (2020) · FIGO 2019 · ISSHP 2021 · Kalafat E et al. UOG 2018.
In summary: the ratio quantifies overall biological severity; ophthalmic artery Doppler measures the immediate hemodynamic impact on the maternal cerebral microvasculature. Neither replaces clinical criteria for severe features (BP, symptoms, laboratory findings).
13Mean Arterial Pressure (MAP) — thresholds and variants
Formula: MAP = (SBP + 2 × DBP) / 3.
| Condition | Level | Management | Source cited |
|---|---|---|---|
| MAP ≥105 (any GA) | High — warning sign | Suspected gestational hypertension/preeclampsia, especially >20 weeks. Assess proteinuria, sFlt-1/PlGF, liver and renal function. Close monitoring. | WHO / NICE / ISUOG |
| MAP >90 and GA ≤14 weeks | Moderate | Higher risk of PE. Consider prophylactic aspirin based on combined risk. | FMF / ACOG / Cochrane |
| MAP >90 outside the 1st trimester | Low | Mildly elevated. Routine BP monitoring. | NICE / CDC |
| MAP ≤90 | No alert | — | — |
| Population / measure | Cutoff | Sens. | Spec. | LR+ | LR− |
|---|---|---|---|---|---|
| Low risk — 2nd-trimester MAP (AUC 0.76) | ≥90 mmHg | 62% | 82% | 3,5 | 0,46 |
| High risk — DBP at 13-20 weeks | ≥75 mmHg | — | — | 2,8 | 0,39 |
CaVeSal® proprietary algorithm · Based on: Cnossen JS et al. BMJ 2008;336:1117-20.
MAP predicts PE better than SBP, DBP, or their increase, but alone has modest predictive value: it is used within combined models. In FMF first-trimester screening, MAP is included as MoM in the algorithm along with uterine artery PI and PlGF, not as an absolute cutoff. In sepsis the threshold is different: MAP <65 after fluid resuscitation = septic shock (see Sepsis tab). Source B: Cnossen JS et al. BMJ 2008;336:1117-20.
14Intrahepatic cholestasis of pregnancy (ICP) — liver profile and timing of delivery
Clinical presentation: predominantly nocturnal itching of the palms and soles, in the 2nd-3rd trimester, with no primary skin lesions. Pruritus may precede laboratory abnormalities by days.
| Parameter | Normal | Abnormal | Meaning |
|---|---|---|---|
| AST/ALT | <40 IU/L | >40 IU/L (>70 IU/L: suspect HELLP) | Elevated enzymes = criterion for ICP |
| LDH | — | >400 moderate · >600 IU/L | >600 suggests hemolysis/HELLP, not ICP |
| Total bilirubin | ≤1.2 mg/dL | >1.2 mg/dL | Defines the icteric form |
| Alkaline phosphatase | — | >300 moderate · >500 IU/L high | Poorly specific (placental origin) |
| Total bile acids (TBA) | <10 µmol/L | 10-39 · ≥40 severe · ≥100 very severe | Specific marker; optional (not available at many centers) |
| Form | TBA* | Accessible criterion | Delivery | Risk |
|---|---|---|---|---|
| Normal | <10 µmol/L | No symptoms | — | No risk |
| Anicteric | 10–39 | Pruritus + elevated enzymes · normal bilirubin | 38 weeks | Stillbirth · meconium |
| Icteric | 40–99 | Pruritus + elevated enzymes + bilirubin >1.2 | 36 weeks (36–37 if TBA ≥40 only) | ↑↑ stillbirth · meconium |
| Severe | ≥100 | Any form + severe symptoms | 34–36 weeks | Max. sudden stillbirth risk |
*TBA = total serum bile acids, optional. In all cases: UDCA 10–15 mg/kg/day orally in 2–3 doses (first-line) + oral vitamin K if cholestasis is prolonged. Monitoring: weekly NST from 32 weeks and liver panel every 2 weeks. Deliver if fetal well-being is compromised, regardless of gestational age.
| Source | TBA <40 µmol/L | TBA 40–99 µmol/L | TBA ≥100 µmol/L |
|---|---|---|---|
| RCOG GTG 43 (2022) | 19–39: delivery before 40 weeks | 38–39 weeks | 35–36 weeks |
| SMFM Consult #53 (2021) / ACOG CO 831 | 36+0 to 39+0 (late end) | 36+0 to 39+0 (early end) | 36+0 weeks; 34–36 if refractory pruritus, prior stillbirth <36 weeks due to ICP, or worsening liver disease |
CaVeSal® proprietary algorithm · Based on: SMFM Consult Series #53, AJOG 2021;224:B2-B9 · RCOG Green-top Guideline No. 43 (August 2022) · MINSAL Chile Perinatal Guideline 2015 (chap. 11) · Williamson C et al. Lancet 2018;391:1683-96 · Ovadia C et al. Lancet 2019;393:899-909 · EASL.
SMFM discourages delivery <37 weeks based on clinical diagnosis alone without confirmed bile acids, and recommends corticosteroids if delivery occurs before 37+0. Sources: SMFM Consult Series #53, AJOG 2021;224:B2-B9 · RCOG Green-top Guideline No. 43 (August 2022) · MINSAL Chile Perinatal Guideline 2015 (chap. 11) · Williamson C et al. Lancet 2018;391:1683-96 · Ovadia C et al. Lancet 2019;393:899-909 · EASL.
15Acute fatty liver of pregnancy (AFLP) — Swansea criteria
Diagnosis: ≥6 of the 14 criteria in the absence of another cause to explain them.
| # | Criterion | Cutoff |
|---|---|---|
| 1 | Vomiting | — |
| 2 | Abdominal pain | — |
| 3 | Polydipsia / polyuria | — |
| 4 | Encephalopathy | — |
| 5 | Elevated bilirubin | >0.8 mg/dL (>14 µmol/L) |
| 6 | Hypoglycemia | <72 mg/dL (<4 mmol/L) |
| 7 | Elevated uric acid | >5.7 mg/dL (>340 µmol/L) |
| 8 | Leukocytosis | >11.000/µL |
| 9 | Ascites or bright liver on ultrasound | — |
| 10 | Elevated transaminases (AST/ALT) | >42 IU/L |
| 11 | Elevated ammonia | >47 µmol/L |
| 12 | Renal failure | Creatinine >1.7 mg/dL (>150 µmol/L) |
| 13 | Coagulopathy | PT >14 s or aPTT >34 s |
| 14 | Microvesicular steatosis on liver biopsy | — |
CaVeSal® proprietary algorithm · Based on: Ch'ng CL et al. Gut 2002;51:876-80 · Knight M et al. Gut 2008;57:951-6 · StatPearls — Acute Fatty Liver of Pregnancy · PMC3503387.
Validation (Knight 2008, UKOSS): PPV 85%, NPV 100%, sensitivity ≈100%, specificity 57% versus biopsy. Antithrombin III <65%: suggestive finding, not part of the 14 criteria.
Management: maternal stabilization and immediate delivery, regardless of gestational age; ICU care (monitoring of glucose, coagulopathy, renal and liver function).
Wording variant: some lists (Radiopaedia, NGO) write “urea >340 µmol/L” in criterion 7; the original article refers to urate (uric acid). Sources: Ch'ng CL et al. Gut 2002;51:876-80 · Knight M et al. Gut 2008;57:951-6 · StatPearls — Acute Fatty Liver of Pregnancy · PMC3503387.
16Differential diagnosis: HELLP vs AFLP vs ICP
| Characteristic | HELLP | Acute fatty liver of pregnancy (AFLP) | Cholestasis (ICP) |
|---|---|---|---|
| Timing | >20 weeks / postpartum | 3rd trimester (typically 30-38 weeks) | 2nd-3rd trimester |
| Key symptom | Epigastric/RUQ pain, hypertension | Nausea, vomiting, malaise, polydipsia | Nocturnal palmoplantar pruritus |
| Hypertension / proteinuria | Usual | Up to 50% | No |
| Platelets | <100.000 (↓↓) | Normal or ↓ (due to DIC) | Normal |
| Hemolysis / LDH | LDH ≥600, schistocytes | Mild or absent | No |
| Glucose | Normal | Hypoglycemia | Normal |
| Coagulation | Normal except with DIC | Prolonged PT/aPTT, fibrinogen ↓ | Normal (PT ↑ only with vitamin K deficiency) |
| Bilirubin | Moderately ↑ | ↑↑ | Normal or mildly ↑ |
| Ammonia / creatinine | Creatinine may ↑ | Ammonia and creatinine ↑ | Normal |
| Bile acids | Normal | May ↑ | ↑ (specific marker) |
| Management | Delivery based on gestational age/severity | Immediate delivery + ICU | UDCA + delivery at 34-40 weeks based on TBA levels |
HELLP syndrome and AFLP overlap in up to 20-40% of cases (both may present with hypertension, thrombocytopenia, and elevated enzymes). Hypoglycemia, early coagulopathy, and elevated ammonia suggest AFLP. Sources: ACOG PB 222 · Knight 2008 · StatPearls · RCOG GTG 43.
17MAP/HR index: hemodynamic phenotype in hypertension
MAP ÷ HR approximates peripheral vascular resistance at the bedside, without echocardiography or noninvasive monitoring.
| MAP/HR | Phenotype | Suggested first-line approach |
|---|---|---|
| >1,4 | Hypodynamic: high resistance, normal or low cardiac output; more associated with FGR | Calcium channel blocker (nifedipine) |
| 1,1–1,4 | Normodynamic | Methyldopa |
| <1,1 | Hyperdynamic: high output, low resistance | Labetalol or methyldopa |
- Guides drug selection only for non-severe hypertension or maintenance therapy. Severe hypertension is treated immediately with the available drug.
- Some checklists use a single cutoff of 1.4 (≥1.4 hypodynamic). The calculator uses the three ranges from the systematic review.
CaVeSal® proprietary algorithm · Based on: Novelli GP et al. Ultrasound Obstet Gynecol 2026;68:319-28 · Vasapollo B et al. Position statement AIPE/SIMP, Am J Perinatol 2024;41:1999-2013.
CaVeSal® proprietary algorithm · Based on: Erez, Am J Obstet Gynecol 2022; USPSTF, JAMA 2021; NICE (target 135/85); SSSAO mnemonic and stepped algorithm according to the reference obstetric emergency management guideline · ACOG Practice Bulletin No. 222 (2020) · FIGO Guidelines on Preeclampsia (2019) · ISSHP Classification and Guidelines (2021).
1Definition and criteria
Definition (WHO 2017): "maternal sepsis is a life-threatening condition defined as organ dysfunction resulting from infection during pregnancy, childbirth, postabortion, or the postpartum period."
Suspected or confirmed infection + organ dysfunction = maternal sepsis. Sepsis-3 framework adapted to obstetrics: the focus shifts from the inflammatory response (SIRS) to organ dysfunction. WHO calls for two sets of criteria: early identification ("presumed maternal sepsis") to enable immediate action, and diagnostic confirmation for epidemiological purposes.
Prevention: handwashing, universal urine culture, clean birthing areas, sterile instruments, vector protection, disposal of contaminated materials, vaccination, education, STI screening/treatment.
Criteria for suspected sepsis (WHO GLOSS 2020; labeled "OTAS" in the reference handout, but not the OTAS triage scale): temperature>38°C or <35°C, SpO2<95%, SBP<90, HR>100, RR>25, altered mental status, uterine tenderness with suspected source.
2Classification — California Criteria
Suspected infection + 2 of 4: temp<36 or >38°C, HR>110, RR>24, WBC>15,000 or <4,000 or 10% bands = SEPSIS → start 1-2 L crystalloids + antibiotics + monitoring.
If MAP remains <65 after a 30 mL/kg bolus = SEPTIC SHOCK.
MSPBS, Code Red Guide, 2nd ed. 2022 (p. 76): septic shock = need for vasopressors to maintain MAP ≥65 mmHg with lactate ≥2 mmol/L (18 mg/dL) despite adequate fluid resuscitation.
This set (T, HR>110, RR>24, WBC with >10% bands) is the one used in the UdeA/UNFPA workshop, adapted from the CMQCC Toolkit. It is stricter than classic SIRS (HR>90, RR>20, WBC >12,000; see subcard 10). A slide from the same workshop states "MAP <60"; this is excluded because it lacks its own citation: the current cutoff is 65 (MSPBS + CMQCC + SOMANZ).
Adapted EAPO (MEOWS, reference from the handout): 7 parameters (temp, SBP, DBP, pulse, RR, SpO2, mental status, urine output). Score: 0=routine; 1-3=observation every 4h + notify charge nurse; ≥4 with a single "red 3" or total≥4="THINK SEPSIS" (observation every 4h + urgent notification); ≥6="THINK SEPSIS" (continuous monitoring + emergency notification).
Note: this reference EAPO-MEOWS differs from the official MSPBS EAPO used in the Full module — shown here only as an additional reference; do not confuse them.
3Flowchart — "Sepsis 4-5-3" Bundle (1st hour)
Take 4: cultures, laboratory tests for organ dysfunction + lactate, vital signs, imaging.
Give 5: O2 FiO2≥50%, crystalloids 20-30 mL/kg bolus + maintenance 1-2 mL/kg/h, broad-spectrum antibiotics, treatment of hyper/hypothermia, vasopressors if MAP<65 after bolus.
Consider 3: fetal well-being if >26 weeks, infection source control, thromboprophylaxis.
Targets: urine output>0.5 mL/kg/h or >30 mL/h, MAP ≥65 (MSPBS 2022; Surviving Sepsis Campaign 2021), PaO2>60 or SpO2>95%, Glasgow Coma Scale 15.
UdeA/UNFPA variant (slide "Therapeutic targets"): MAP >60 or SBP >85 mmHg, urine output >0.5 mL/kg/h or >30 mL/h, SpO2 >95%, normal mental status.
Stabilize and refer: review at 3 h (diagnosis/treatment/labs, repeat lactate, reassess source) and at 6 h (review diagnosis/treatment, close monitoring; ideally transfer to a tertiary care center by 6 h).
4Medications — regimens by source
Urinary: piperacillin-tazobactam 4.5 g q8h or gentamicin 3-5 mg/kg q24h.
Respiratory: ampicillin-sulbactam 3g q6h + clarithromycin 500mg q12h (+ oseltamivir if at risk for influenza).
Puerperal infection: clindamycin 900mg q8h + gentamicin 240mg q24h or amikacin 1g q24h; or ampicillin-sulbactam 3g q6h; or crystalline penicillin + metronidazole + gentamicin regimen.
Vasopressor: norepinephrine 0.05 µg/kg/min until MAP ≥65, via central line or 14-16G access. UdeA: dopamine 5 µg/kg/min via peripheral line as an alternative, only after volume repletion.
Sources: WHO GLOSS 2020; CMQCC Quality Improvement Toolkit 2022; Surviving Sepsis Campaign 2021; WHO 2017 (WHO/RHR/17.02); MSPBS Paraguay, Code Red 2nd ed. 2021 (p. 76); University of Antioquia/UNFPA, Obstetric Emergencies Workshop — Maternal Sepsis.
5Obstetric qSOFA (rapid screening)
| Criterion | Points |
|---|---|
| Systolic BP ≤90 mmHg | +1 |
| Respiratory rate ≥25 breaths/min | +1 |
| Altered mental status | +1 |
CaVeSal® proprietary algorithm · Based on: SOMANZ.
≥ 2 points = High Risk (high suspicion of sepsis) — apply the complete Obstetric SOFA. <2 = Low Risk.
Consistent with the SOMANZ omqSOFA (SBP<90, RR≥ 25, mentation not alert) — dual source support. Improves sensitivity from 37.5%→81.2% and specificity from 72.2%→75% compared with standard non-obstetric qSOFA (SBP≤100, RR≥ 22, GCS<15).
6Obstetric SOFA (Modified) — organ dysfunction
| System | 0 points | 1 point | 2 points |
|---|---|---|---|
| Respiration (PaO₂/FiO₂) | ≥400 | 300–<400 | ≤300 |
| Coagulation (platelets ×10³/µL) | ≥150 | 100–150 | <100 |
| Liver (bilirubin mg/dL) | ≤1.2 | 1.2–1.9 | >1.9 |
| Cardiovascular | MAP≥70 | MAP<70 | Requires vasopressors |
| CNS | Alert | Awakens to voice | Awakens to pain |
| Renal (creatinine mg/dL) | ≤1.0 | 1.0–1.4 | >1.4 |
Interpretation: score ≥ 2 = Organ Dysfunction (confirmed sepsis). Increase >2 points from baseline also confirms sepsis (SOMANZ/MFB criterion, same logic in µmol/L).
| SOFA score | Estimated mortality |
|---|---|
| ≥ 12 | >95% |
| ≥ 10 | 50% |
| ≥ 8 | 33% |
| ≥ 6 | 21% |
| ≥ 4 | 20% |
| ≥ 2 | 6% |
| < 2 | <10% |
CaVeSal® proprietary algorithm · Based on: SOMANZ.
7Sepsis in Obstetrics Score (SOS)
Point ladder for: temperature, systolic BP/vasopressor use, heart rate, ventilation/RR/SpO₂, leukocytes, lactate ≥ 4, bands ≥ 10%.
Positive if ≥ 6 points — obstetric sepsis alert.
8Score MAMÁ 2025 (MSP Ecuador, MEOWS-type)
9 variables, each scored from 0 to 3 (0 = normal). Apply every 4 h to all pregnant and postpartum patients.
| Variable | 3 points | 2 points | 1 point |
|---|---|---|---|
| Temperature (°C) | <35 · ≥39 | 38,3-38,9 | 35-35,9 · 37,5-38,2 |
| Systolic BP (mmHg) | ≤70 · ≥160 | 71-79 · 150-159 | 80-89 · 140-149 |
| Diastolic BP (mmHg) | ≥110 | 100-109 | ≤49 · 90-99 |
| Heart rate (bpm) | ≤40 · ≥130 | 41-49 · 110-129 | 100-109 |
| Respiratory rate (breaths/min) | ≤10 · ≥30 | 25-29 | 21-24 |
| SpO₂ (%) | ≤88 | 89-90 | 91-93 |
| Oxygen therapy | Face mask or higher | Nasal cannula | — |
| Consciousness | Unresponsive | Responds to pain | Responds to voice |
| Urine output (mL/h) | ≤10 | ≤30 | — (no catheter = 0) |
| Score | Management | Repeat |
|---|---|---|
| ≥5 or any variable scored 3 | Treat, activate the appropriate code and refer | Every 30 min |
| 2-4 | Treat and refer as indicated | Every 1 h |
| 1 | Assess risk factors | Every 4 h |
| 0 | Assess risk factors, maternal-fetal well-being, and warning signs | Every 4 h |
CaVeSal® proprietary algorithm · Based on: Ministry of Public Health of Ecuador. “MAMÁ Score and Obstetric Codes.” Protocol. Quito: MSP; 2025 (Ministerial Agreement 00042-2025)The colors are from CaVeSal®; the protocol does not assign colors to the levels. In the Full calculator, it can be used alone or in combination with EAPO (CaVeSal® Obstetric Alert, see Code Red, card 23).
Includes embedded sub-calculations for the shock index and preeclampsia screening by BP — does not replace the existing specific modules (Shock Index, HDP); it is an integrated early warning view.
9Hemodynamic mortality indices (screening → severity reinforcement)
| Level | Tool | What it detects |
|---|---|---|
| Rapid screening | Shock Index (SI) = HR/SBP, cutoff ≥ 0.9 | Initial alert for hemodynamic compromise |
| Severity reinforcement | Diastolic Shock Index (DSI) = HR/DBP, cutoff ≥ 2.2 | Vasoplegia / poor prognosis — more sensitive than SI alone in septic shock |
| Reinforcement, only if already receiving a vasopressor | Vasoactive-Diastolic Index (VDI) = DBP ÷ (vasopressor dose × HR), risk if ≤ 6.7 | Degree of vasopressor dependence — refractory shock |
CaVeSal® proprietary algorithm · Based on: MD Antonio Heras G. — Obstetric Coagulopathy and Sepsis Calculator · SOMANZ Sepsis Guidelines 2017 · MDCalc — Diastolic Shock Index.
DSI: general sepsis literature more commonly cites the rounded cutoff ≥2.0; 2.2 is used as the primary cutoff (Heras source), with this note on the variant most cited in the non-obstetric literature. VDI: the classic intensive care formula uses MAP in the denominator (VIS/MAP); the variant recorded here (DBP ÷ dose × HR) is specific to the Heras source.
10SIRS, qSOFA, and maternal early warning in pregnant women — diagnostic performance
| Tool | Activated by | Parameters |
|---|---|---|
| SIRS (Bone 1992) | ≥2 criteria | T >38 or <36 °C · HR >90 · RR >20 or PaCO₂ <32 · leukocytes >12,000 or <4,000 |
| qSOFA (Sepsis-3, Singer 2016) | ≥2 criteria | RR ≥22 · SBP ≤100 · altered mental status |
| Maternal early warning criteria (Mhyre 2014) | 1 criterion is sufficient | SBP <90 or >160 · DBP >100 · HR <50 or >120 · RR <10 or >30 · SpO₂ <95 % on room air · urine output <35 mL/h for ≥2 h · agitation, confusion, or unresponsiveness · preeclampsia with persistent headache or dyspnea |
| Tool | Sens. | Spec. | Use |
|---|---|---|---|
| SIRS ≥2 | 93 % | 63 % | Screen (many false alarms) |
| Maternal early warning criteria (≥1) | 82 % | 87 % | Intermediate |
| qSOFA ≥2 | 50 % | 95 % | Severity (a negative result does not rule it out) |
CaVeSal® proprietary algorithm · Based on: Bauer ME et al. Risk Factors, Etiologies, and Screening Tools for Sepsis in Pregnant Women: A Multicenter Case-Control Study. Anesth Analg 2019;129(6):1613-1620
Most useful individual criteria: HR >90 is almost always present (sensitivity 96 %) but has low specificity (45 %); by contrast, RR >30 and altered mental status are virtually absent in controls (specificity close to 100 %), although they are absent in more than half of sepsis cases.
Clinical interpretation: Use SIRS or maternal early warning criteria for screening; qSOFA to stratify severity; SOFA and lactate to confirm. The operational scores remain those in subcards 5-9.
CaVeSal® proprietary algorithm · Analysis based on Bauer ME et al. Anesth Analg 2019;129(6):1613-1620 (multicenter case-control study: 82 cases, 328 controls). Rounded values; confidence intervals and details by criterion are in the original article. Original definitions: Bone RC et al. Chest 1992;101:1644-55 · Singer M et al. JAMA 2016;315:801-10 · Mhyre JM et al. Obstet Gynecol 2014;124:782-6. The UdeA/UNFPA workshop cites this study for obstetric qSOFA (sensitivity 36-50 %, specificity 70-95 %).
11Causes, pathogens, mortality, and risk factors with ORs
- Most common causes: chorioamnionitis 24.4%; endometritis 23.2%; pneumonia 11.0%.
- Most common pathogens: E. coli 14.6%; other gram-negative bacilli 9.8%; group A Streptococcus 7.3%.
- Mortality: 12.2% overall; 8.3% if antibiotics are started in <1 h versus 20% if >1 h.
| Group | Factor and magnitude of association |
|---|---|
| Childbirth and puerperium | Cesarean delivery during labor ~21 · cesarean delivery before labor ~16 · fetal demise ~15 · retained products of conception ~13 · PROM >24 h ~9 · preterm delivery ~6 · multiple pregnancy ~6 · antenatal corticosteroids ~5 · GBS positive ~2 · nulliparity ~2 |
| Chronic disease | Liver disease ~15 · heart failure ~10 · chronic kidney disease ~10 |
| Other | BMI ≥40 ~4 · smoking ~3 · African American or Asian ethnicity ~4 (US population) |
CaVeSal® proprietary algorithm · Based on: Bauer ME et al., Anesth Analg 2019;129(6):1613-1620 · WHO Statement on Maternal Sepsis (WHO/RHR/17.02)Delivery variables exclude cases of sepsis prior to delivery (reverse causality).
CaVeSal® proprietary algorithm · Analysis based on Bauer ME et al., Anesth Analg 2019;129(6):1613-1620 (rounded ORs; confidence intervals in the original) · WHO Statement on Maternal Sepsis (WHO/RHR/17.02)Delivery variables exclude cases of sepsis prior to delivery (reverse causality).
12Complete 5-level SOFA (0-4)
| System | 0 | 1 | 2 | 3 | 4 |
|---|---|---|---|---|---|
| CNS — Glasgow | 15 | 13-14 | 10-12 | 6-9 | <6 |
| Renal — creatinine (mg/dL) or urine output | <1,2 | 1,2-1,9 | 2-3,4 | 3.5-4.9 or urine output <500 mL/day | >5 or urine output <200 mL/day |
| Liver — bilirubin (mg/dL) | <1,2 | 1,2-1,9 | 2-5,9 | 6-11,9 | >12 |
| Coagulation — platelets (×10³/µL) | >150 | <150 | <100 | <50 | <20 |
| Respiratory — PaO₂/FiO₂ | >400 | <400 | <300 | <200 with support | <100 with support |
| Respiratory — SaO₂/FiO₂ (alternative) | — | 221-301 | 142-220 | 67-141 | <67 |
| Cardiovascular (µg/kg/min) | No hypotension (see note) | MAP <70 mmHg | Dopamine <5 or dobutamine (any dose) | Dopamine 5-15 or norepinephrine/epinephrine ≤0.1 | Dopamine >15 or norepinephrine/epinephrine >0.1 |
Interpretation: an increase ≥2 points above baseline defines organ dysfunction (Sepsis-3). The UdeA/UNFPA workshop expresses it as «> 2».
Cardiovascular 0 points = MAP ≥70 mmHg without vasopressors (Vincent 1996). Subcard 6 shows the modified 3-level obstetric version (0-2) used by Heras/SOMANZ; MSPBS (p. 75) reproduces the same 5-level table. CaVeSal® proprietary algorithm · Based on: Vincent JL et al. Intensive Care Med 1996;22:707-10 · Singer M et al. JAMA 2016 (Sepsis-3) · UdeA/UNFPA «Sepsis» workshop.
13SIRS vs qSOFA: screening vs prognosis
| Tool | Sensitivity | Specificity | Role |
|---|---|---|---|
| SIRS (≥2 criteria) | ≈93% | ≈63% | Screening: detects nearly all, many false positives |
| qSOFA (≥2 criteria) | 50% (Bauer 2019); range 36-50% | 95% (Bauer 2019); range 70-95% | Prognosis / severity: few false alarms, cases are missed |
| SOFA (Δ ≥2) | — | — | Confirmation of organ dysfunction |
| Parameter | Standard qSOFA (Sepsis-3) | Obstetric qSOFA (omqSOFA, SOMANZ) |
|---|---|---|
| Respiratory rate | ≥22 rpm | ≥25 rpm |
| Systolic blood pressure | ≤100 mmHg | ≤90 mmHg |
| Mental status | Abnormal | Altered (any change) |
CaVeSal® proprietary algorithm · Based on: Bauer ME et al. Anesth Analg 2019 (see subcard 10) · UdeA/UNFPA «Sepsis» workshop · SOMANZ 2017.
Suggested sequence: SIRS/MEOWS for screening → qSOFA to stratify severity → SOFA and lactate to confirm. Sources: Bauer ME et al. Anesth Analg 2019 (see subcard 10) · UdeA/UNFPA «Sepsis» workshop · SOMANZ 2017.
14MEOWS — Maternal Early Obstetric Warning Score (complete table)
Cumulative score (0-3 per parameter) for early detection of maternal physiological deterioration — does not diagnose sepsis by itself, but identifies deterioration that warrants escalation of the response, whatever the cause. Complements SIRS/qSOFA/SOFA (subcards 5-13).
| Parameter | 3 | 2 | 1 | 0 | 1 | 2 | 3 |
|---|---|---|---|---|---|---|---|
| Temperature (°C) | ≤35 | 35-35,9 | 36-37,4 | 37,5-37,9 | 38-38,9 | ≥39 | |
| Systolic BP (mmHg) | ≤70 | 71-79 | 80-89 | 90-139 | 140-149 | 150-159 | ≥160 |
| Diastolic BP (mmHg) | ≤49 | 50-89 | 90-99 | 100-109 | ≥110 | ||
| Pulse (bpm) | ≤40 | 40-49 | 50-99 | 100-109 | 110-129 | ≥130 | |
| Respiratory rate (breaths/min) | ≤10 | 11-20 | 21-24 | 25-29 | ≥30 | ||
| O₂ saturation (%) | ≤94 | ≥95 | |||||
| Mental status | Alert | Responds to voice | Responds to pain | Unconscious | |||
| Urine output (mL/h) | ≤10 | ≤30 | Not measured |
| Score | Response level |
|---|---|
| 0 | Routine observation |
| 1-3 | Observation at least every 4 h · call the nurse in charge |
| A single red 3 or aggregate score ≥4 — THINK SEPSIS | Observation at least hourly · urgent call to the responsible medical team and staff with expertise in managing acute illness |
| Aggregate score ≥6 — THINK SEPSIS | Continuous vital sign monitoring · emergency call to the team with critical care expertise and diagnostic skills |
Sensitivity 89%, specificity 79% for severe maternal morbidity (not specific to sepsis). Available as a mini-calculator in the Calculator mode.
CaVeSal® proprietary algorithm · Based on : Norfolk and Norwich University Hospital NHS Trust, MEOWS Development Group, 2022 (scoring table, taken from Universidad de Antioquia/UNFPA, “Sepsis” workshop, p. 17) · Singh S, McGlennan A, England A, Simons R. A validation study of the CEMACH recommended modified early obstetric warning system (MEOWS). Anaesthesia. 2012 Jan;67(1):12-18.
15Clinical chorioamnionitis (Gibbs) and antibiotic regimen
| Criterion | Cutoff |
|---|---|
| Maternal fever (mandatory) | ≥37.8 °C (Gibbs 1982); many guidelines use ≥38.0 °C |
| Maternal tachycardia | >100 bpm |
| Fetal tachycardia | >160 bpm |
| Uterine pain / tenderness | — |
| Foul-smelling / purulent amniotic fluid or discharge | — |
| Maternal leukocytosis | >15,000/mm³ (without recent corticosteroids) |
The current designation «Triple I» (NICHD 2015, ACOG CO 712) is detailed in the PROM tab, subcard 8.
| Drug | Dose |
|---|---|
| Ampicillin | 2 g IV every 6 h |
| + Gentamicin | 2 mg/kg IV loading dose, then 1.5 mg/kg every 8 h, or 5 mg/kg IV every 24 h |
| Mild penicillin allergy | Cefazolin 2 g IV every 8 h + gentamicin |
| Severe allergy | Clindamycin 900 mg IV every 8 h or vancomycin 1 g IV every 12 h + gentamicin |
| If cesarean delivery | Add clindamycin 900 mg IV or metronidazole 500 mg IV (anaerobic coverage) |
CaVeSal® proprietary algorithm · Based on: Chorioamnionitis: An Update on Diagnostic Evaluation (Gibbs 1982, J Infect Dis 145:1-8) · Management of Clinical Chorioamnionitis — PMC8315154 · ACOG Committee Opinion No. 712 (2017).
Heras module sources: Obstetric Coagulopathy and Sepsis Calculator — Md. Antonio Heras G. · SOMANZ Sepsis Guidelines 2017 · Medicina Fetal Barcelona — Sepsis and Septic Shock · DSI: MDCalc — Diastolic Shock Index.
Obstetric Code Blue — CPR / Maternal Cardiac Arrest
Causes of maternal collapse, CABD sequence and perimortem cesarean delivery. Different icon from HDP to avoid confusion.
1Causes of maternal collapse
Mnemonic (Knapp C & Bhatia K, Br J Hosp Med 2022): Accidents/anesthetic complications/asthma; Bleeding (hemorrhages); Cardiovascular; Drugs/medications (magnesium sulfate); Embolic (amniotic fluid, pulmonary); Fever (sepsis, septic shock); General (6Ts and 6Hs); Hypertension (HDP, HELLP).
“Perpetuates cardiac arrest” — 6Hs: Hypoxia, hypo-/hyperkalemia, H+ acidosis, hypothermia, hypovolemia, hypoglycemia.
6Ts: Cardiac tamponade, pulmonary thrombosis, coronary thrombosis, tablets/toxins, pneumothorax, trauma.
2CABD sequence and airway
Unresponsive/unconscious patient → activate Obstetric Code Blue → check pulse for 10 seconds → if no pulse, initiate CABD (Circulation: compressions; Airway: open; Breathing: positive-pressure ventilation; Defibrillate if shockable rhythm).
Chest compressions 30:2, ventilations every 2 min or 5 cycles → aortocaval decompression (left uterine displacement) → open the airway → epinephrine 1mg IV every 3-5 min.
Modifications in pregnancy: deeper chest compressions, left uterine displacement, early endotracheal intubation + cricoid pressure.
Airway: O2 100% at 15L/min → intubation attempt 1 and 2 → if unsuccessful, supraglottic airway device attempt 1 and 2 → if unsuccessful, bag-mask ventilation → if ineffective, cricothyrotomy. 8-10 ventilations/min, monitor CO2, minimize time without compressions, 6.0-7.0mm tube.
3Rhythm and flowchart
VF/pulseless VT: initial shock 150J biphasic or 360J monophasic + 2 min CPR (30:2); if there is no response, another shock + amiodarone 300mg IV (150mg additional if VT persists).
Asystole/PEA: continue compressions and ventilation, verification protocol.
Epinephrine 1mg IV every 3-5 min: for a nonshockable rhythm, administer immediately once IV access is obtained; for a shockable rhythm, after the 2nd shock.
4-minute rule: preparation for hysterotomy begins when cardiac arrest is recognized. If there is no return of spontaneous circulation by minute 4, initiate resuscitative hysterotomy (perimortem cesarean delivery) on site, without transferring the patient or stopping CPR, to achieve delivery by minute 5 → alert the neonatal team if GA>24 weeks. Timer on the calculator, Obstetric Code Blue.
4Perimortem cesarean delivery and MgSO4 toxicity
Perimortem cesarean delivery: <20 weeks NO; 20-24 weeks depending on suspected aortocaval compression; >24 weeks ALWAYS.
Magnesium sulfate toxicity: calcium gluconate 10% 30mL, or calcium chloride 10% 10mL (1g).
5Maternal collapse: sepsis vs PE vs amniotic fluid embolism (POCUS + ROTEM)
| Septic shock | Massive PE | Amniotic fluid embolism | |
|---|---|---|---|
| Context | Progressive onset; fever or source; sudden collapse is rare | Sudden dyspnea, chest pain; VTE risk factors | Labor, cesarean delivery or first 30 min postpartum |
| POCUS: heart | Hyperdynamic LV (or late septic cardiomyopathy) | Dilated RV (RV/LV >1), “D-shaped” septum, McConnell sign; sometimes intracardiac thrombus | Dilated and hypokinetic RV, “D-shaped” septum, small LV; then biventricular failure |
| POCUS: IVC / veins / lung | Small, collapsible IVC; look for a source (consolidation, collections) | Dilated IVC; deep vein thrombosis on lower-extremity compression ultrasound | Dilated IVC; pulmonary edema possible |
| Coagulation / ROTEM | Late coagulopathy; SIC score ≥4 (ISTH 2025) | No inherent consumptive coagulopathy | Early and disproportionate coagulopathy: very low FIBTEM, possible hyperfibrinolysis (high EXTEM ML) |
| Key action | Antibiotics within the first hour, guided crystalloid fluids, norepinephrine | Anticoagulation; thrombolysis if cardiac arrest or shock | High-quality CPR, avoid fluid overload, RV support, early massive transfusion, tranexamic acid |
- A dilated RV does not distinguish PE from AFE. Severe early coagulopathy points to AFE; its absence points to PE.
- No laboratory test confirms AFE: it is a clinical diagnosis of exclusion.
Practice the three cases in the simulator: Septic shock · Massive PE · Amniotic fluid embolism.
CaVeSal® proprietary algorithm · Based on: SMFM Clinical Guideline #9, Pacheco LD et al. Am J Obstet Gynecol 2016 · APSF Newsletter, amniotic fluid embolism · StatPearls, Amniotic Fluid Embolism · POCUS + ROTEM in amniotic fluid embolism (case report, PMC11800665) · Iba T et al. ISTH SSC 2025, J Thromb Haemost 2025;23:2356-62.
Sources: Knapp C & Bhatia K, Br J Hosp Med 2022;83(12):1-12; 2020 AHA Guidelines for CPR and ECC (updated 2025); Bennett Terri-Ann, Critical Care Obstetrics 2024:199-208; Sumer, Emergency Medicine Clinics of North America 2023;41(3):485-508.
Obstetric Thromboprophylaxis — Traffic Light System
Risk scale for venous thromboembolic events (VTE) in pregnancy, labor and puerperium, with 4 risk levels.
1General measures and mandatory anticoagulation
For all patients (pregnancy, labor or postpartum): adequate hydration and early ambulation.
Mandatory anticoagulation (regardless of the risk scale) if there is: active venous thromboembolic disease (DVT, PE, cerebral venous sinus thrombosis), high-risk cardiac conditions (arrhythmias, prosthetic valves, cardiomyopathy with reduced LVEF, intracardiac thrombi, pulmonary hypertension), or known thrombophilia.
24-level scale (traffic light)
| Level | Activated by | Examples of factors |
|---|---|---|
| Very high | 1 factor | Very high-risk inherited thrombophilia, recurrent VTE |
| High | 1 factor | Morbid obesity (BMI>40), APS, single prior VTE |
| Moderate | 2 or more factors | Obesity (BMI 30-39), preeclampsia, cesarean delivery, multiple pregnancy |
| Low | 3-5 factors (non-pharmacological) / 6+ (+pharmacological from week 28) | Age>35, overweight, smoking, chronic hypertension |
CaVeSal® proprietary algorithm · Based on: Grillo-Ardila CF et al. Rev Colomb Obstet Ginecol 2017;68(4):285-304 (rounded values; confidence intervals in the original).
Rule: the most severe level applies when at least one factor is present (factors are not added across levels).
3Weight-based LMWH doses (prophylactic)
| Weight | Enoxaparin | Dalteparin | Nadroparin |
|---|---|---|---|
| <50 kg | 20 mg/day | 2500 U/day | 2850 U/day (0.3 mL) |
| 50-90 kg | 40 mg/day | 5000 U/day | Not specified |
| 91-130 kg | 60 mg/day | 7500 U/day | Not specified |
| 131-170 kg | 80 mg/day | 10000 U/day | Not specified |
| Anticoagulation | 1 mg/kg every 12 h | 5000 U c/12h | 171 U/kg/day |
CaVeSal® proprietary algorithm · Based on: Grillo-Ardila CF et al. Rev Colomb Obstet Ginecol 2017 · MSPBS.
Weight >170 kg — two alternatives: not included in the Colombian CPG table (specialist assessment) · enoxaparin 0.6 mg/kg/day according to the MSPBS Thromboprophylaxis draft (corrected, unpublished version). In the absence of LMWH: unfractionated heparin.
4Contraindications to LMWH
Known bleeding disorder (hemophilia, von Willebrand disease, acquired coagulopathies), active antepartum or postpartum bleeding, risk factors for major obstetric hemorrhage (e.g., placenta previa), thrombocytopenia (<75,000/µL), recent cerebrovascular event (within the last 4 weeks), severe renal disease (GFR<30 mL/min/1.73m²).
Fondaparinux, dabigatran and rivaroxaban are not approved for use during pregnancy. Warfarin and heparins are safe during breastfeeding.
5Epidemiology and relative risk by period (RDI)
Incidence of VTE during pregnancy/postpartum: 0.76-1.72 per 1000 (4× the risk in the general population). Accounts for 14.9% of global maternal mortality.
| Period | Approx. RR |
|---|---|
| Pregnancy (overall) | 3,5 |
| · 1st trimester | 1,6 |
| · 2nd trimester | 2,1 |
| · 3rd trimester | 6,1 |
| Postpartum | 11,9 |
| Hospitalization (overall) | 17,5 |
| · Length of stay ≤3 days | 4,0 |
| · Length of stay ≥4 days | 12,2 |
| · Persists after discharge (28 days) | 6,3 |
CaVeSal® proprietary algorithm · Based on: Grillo-Ardila CF et al. Rev Colomb Obstet Ginecol 2017;68(4):285-304 (rounded values; confidence intervals in the original).
6Antepartum risk factors (adjusted OR, highest to lowest)
| Factor | Approx. OR |
|---|---|
| Previous VTE | 8,0 |
| Ovarian hyperstimulation syndrome | 5,4 |
| ART — multiple pregnancy | 4,4 |
| Pre-existing diabetes | 3,5 |
| Inflammatory bowel disease | 3,5 |
| ART — singleton pregnancy | 2,8 |
| Multiple pregnancy | 2,8 |
| Hyperemesis gravidarum | 2,5 |
| Lower-limb varicose veins | 2,2 |
| Infection during pregnancy | 1,8 |
| Antepartum hemorrhage | 1,3 |
| Maternal age >35 years | 1,3 |
CaVeSal® proprietary algorithm · Based on: Grillo-Ardila CF et al. Rev Colomb Obstet Ginecol 2017;68(4):285-304 (rounded values; confidence intervals in the original).
7Postpartum risk factors (adjusted OR, in descending order)
| Factor | Approx. OR |
|---|---|
| Stillbirth | 7,2 |
| Morbid obesity | 6,4 |
| Previous VTE | 6,1 |
| Preeclampsia/eclampsia | 4,4 |
| Inflammatory bowel disease | 4,1 |
| Lower-limb varicose veins | 4,0 |
| Puerperal systemic infection | 3,7 |
| Elective cesarean delivery | 2,5 |
| Emergency cesarean delivery | 2,2 |
| Preterm birth | 2,1 |
| ≥3 live births | 1,9 |
| Obesity | 1,9 |
| Postpartum hemorrhage | 1,8 |
| Overweight | 1,7 |
| Age 35-44 years | 1,4 |
CaVeSal® proprietary algorithm · Based on: Grillo-Ardila CF et al. Rev Colomb Obstet Ginecol 2017;68(4):285-304 (rounded values; confidence intervals in the original).
8Inherited thrombophilias (OR)
| Thrombophilia | Approx. OR |
|---|---|
| Heterozygous Factor V Leiden | 8,3 |
| Heterozygous prothrombin G20210A | 6,8 |
| Protein C deficiency | 4,8 |
| Antithrombin deficiency | 4,7 |
| Protein S deficiency | 3,2 |
CaVeSal® proprietary algorithm · Based on: Grillo-Ardila CF et al. Rev Colomb Obstet Ginecol 2017;68(4):285-304 (rounded values; confidence intervals in the original).
Homozygous Factor V Leiden and Prothrombin G20210A correspond to the “very high-risk” category of the traffic-light system (subcard 2).
9GRADE recommendations — non-pharmacological measures
- LMWH: strong recommendation in favor, low-quality evidence — no preference for a specific type.
- Unfractionated heparin: alternative when LMWH is not feasible (strong recommendation in favor).
- Fondaparinux: consider only if heparins are contraindicated (good practice point).
- Antiplatelet agents: weak recommendation against use for VTE prevention (very low-quality evidence).
- Intermittent pneumatic compression + pharmacological prophylaxis: weak recommendation against — no clear additional benefit and more bleeding.
- Regional anesthesia preferred over general anesthesia: weak recommendation in favor, associated with lower VTE risk (RR 0.66, 95% CI 0.55-0.79 for DVT).
- Graduated compression stockings: reduce DVT OR 0.33 (0.26-0.41), proximal DVT OR 0.26, PE OR 0.38 — strong recommendation in favor, very low-quality evidence.
- Hydration: “avoid dehydration” is a weak recommendation in favor, with very low-quality evidence. Vigorous hydration/hemodilution increased the risk of postoperative DVT in a controlled trial (RR 4.50, 95% CI 1.06-19.11) — never recommend “aggressive hydration” as a thromboprophylaxis measure.
10Perianesthetic timing and postpartum restart
Last dose before the procedure: 12h before induction/cesarean (prophylactic dose); 24h before if very high risk and receiving anticoagulation doses (therapeutic).
Postpartum restart: 12h after delivery/cesarean if not contraindicated (non-pharmacological measures in the meantime). In patients at high risk of postpartum hemorrhage: non-pharmacological measures only until the bleeding risk is minimal.
Source (traffic-light system, subcards 1-10): Grillo-Ardila CF, Mogollón-Mariño AC, Amaya-Guío J, Molano-Franco D, Correa LP. Guía de práctica clínica para la prevención de eventos tromboembólicos venosos durante la gestación, el parto o el puerperio. Rev Colomb Obstet Ginecol. 2017;68(4):285-304. DOI: 10.18597/rcog.3084.
Alternative system — Puerperal score by points (RCOG/ACOG/ASH/NICE)
Risk stratification system distinct from the Grillo-Ardila traffic-light system — same clinical objective, different source method. Shown here for reference; the Calculator uses the Grillo-Ardila traffic-light system as its sole operational system (see note).
1Points per puerperal risk factor
| Points | Factors |
|---|---|
| 1 | Elevated BMI, smoking, age>35, parity≥3, relative immobility, varicose veins |
| 2 | Cesarean, preeclampsia, medical comorbidity, bed rest >72h |
| 4 | Previous VTE, high-risk thrombophilia, major puerperal surgery, major transfusion |
CaVeSal® proprietary algorithm · Based on: Grillo-Ardila CF et al. Rev Colomb Obstet Ginecol 2017;68(4):285-304 (rounded values; confidence intervals in the original).
2Management according to total score
| Score | Management |
|---|---|
| 0 | No specific prophylaxis — general measures |
| 1-4 | Graduated compression stockings |
| 5-6 | Prophylactic LMWH or intermittent pneumatic compression |
| ≥7 | Prophylactic LMWH + intermittent pneumatic compression (both) |
Additional information: COVID-19 requiring hospitalization → LMWH during hospitalization + for up to 14 days post-discharge (moderate cases) or up to 1 month post-discharge (severe/critical cases).
CaVeSal® proprietary algorithm · Based on (point-based score): Medicina Fetal Barcelona (2021) · RCOG Green-top Guideline No. 37a (2015) · ACOG Practice Bulletin No. 196 (2018) and No. 197 — Inherited Thrombophilias in Pregnancy (2018) · ASH Guidelines for VTE in Pregnancy (2018) · NICE (2018) · NHS Greater Glasgow (2023). Note: this system is NOT implemented in the Calculator — it is shown for documentary reference only; the active calculation uses the Grillo-Ardila 2017 traffic-light system (4 levels).
Diagnosis of VTE, APS, and care protocol
Physiology, DVT, PE (adapted YEARS algorithm), APS, MSPBS screening, and 15-step protocol.
1Physiology of coagulation in pregnancy
VTE risk: pregnancy ×10 vs nonpregnant individuals; postpartum period (6 weeks) ×5, peak in the first week; cesarean delivery ×4 vs vaginal delivery.
| Change | Factors |
|---|---|
| ↑ Procoagulants | Fibrinogen, factors VII, VIII, X, von Willebrand factor, PAI-1, and PAI-2 |
| ↓ Anticoagulants | Protein S |
| No significant changes | Factors II, V, IX, protein C, antithrombin III |
CaVeSal® proprietary algorithm · Based on: Grillo-Ardila CF et al. Rev Colomb Obstet Ginecol 2017;68(4):285-304 (rounded values; confidence intervals in the original).
Anatomic predilection: left lower extremity and proximal iliofemoral veins (May-Thurner phenomenon: compression of the left iliac vein by the right iliac artery, combined with compression of the inferior vena cava by the gravid uterus).
2Deep vein thrombosis (DVT)
Clinical presentation: pain along the course of the vein, unilateral edema, increased local temperature, difference in limb circumference, superficial collateral circulation.
Test of choice: venous Doppler ultrasound of the lower extremities (loss of compressibility or absence of flow). If negative and suspicion persists (especially for iliac vein thrombosis): repeat at 3 and 7 days or consider MRI.
Management: confirmed DVT → therapeutic-dose LMWH (enoxaparin 1 mg/kg every 12 h).
3Pulmonary embolism (PE) — YEARS algorithm adapted for pregnancy
Clinical presentation: sudden or progressive dyspnea, pleuritic chest pain, cough, hemoptysis, tachypnea, tachycardia, cyanosis, syncope.
If leg symptoms are present: Doppler ultrasound first; if DVT is confirmed → anticoagulate without further testing.
| YEARS criteria | D-dimer | Management |
|---|---|---|
| 0 | <1000 ng/mL (1.0 µg/mL) | PE ruled out; do not anticoagulate |
| 0 | ≥1000 ng/mL | CT pulmonary angiography |
| ≥1 | <500 ng/mL (0.5 µg/mL) | PE ruled out |
| ≥1 | ≥500 ng/mL | Pulmonary CT angiography (or V/Q scan) |
CaVeSal® proprietary algorithm · Based on: van der Pol LM et al. NEJM 2019;380:1139-49 (Artemis) · Medicina Fetal Barcelona (2021).
The D-dimer cutoff differs by branch (1000 vs 500 ng/mL); it is not simplified to a single value. This algorithm avoided CT pulmonary angiography in 32-65% of pregnant patients, depending on trimester. Source: van der Pol LM et al. NEJM 2019;380:1139-49 (Artemis) · Medicina Fetal Barcelona (2021).
4Antiphospholipid syndrome (APS) and thrombophilias
Indication for testing: Personal history of VTE or adverse obstetric history (≥3 miscarriages <10 weeks, fetal death ≥10 weeks with a morphologically normal fetus, severe FGR <34 weeks, severe preeclampsia <34 weeks).
Hereditary: factor V Leiden, prothrombin G20210A, protein C, protein S, or antithrombin III deficiency, factor XII mutation. Acquired/mixed: hyperhomocysteinemia, APS.
| Type | Criterion |
|---|---|
| Clinical (≥1) | ≥1 documented vascular thrombosis or ≥1 criterion for obstetric morbidity |
| Laboratory (2 tests 12 weeks apart) | Lupus anticoagulant · anticardiolipin IgG/IgM >40 GPL/MPL · anti-β2-glycoprotein I IgG/IgM |
CaVeSal® proprietary algorithm · Based on: Medicina Fetal Barcelona 2021 · ACOG PB 196 and 197 (2018) · RCOG GTG 37a.
Treatment during pregnancy: Aspirin 100 mg/night from preconception or diagnosis until week 36 + prophylactic LMWH from ultrasound confirmation of fetal heartbeat until delivery. Postpartum: aspirin + prophylactic LMWH for 42 days.
Do not confuse with aspirin 150 mg/night for preeclampsia prevention (HDP tab): these are different indications and doses. Sources: Medicina Fetal Barcelona 2021 · ACOG PB 196 and 197 (2018) · RCOG GTG 37a.
5Risk screening — MSPBS draft
- Normal risk (1/6000): no antepartum thromboprophylaxis, except if hospitalized with ≥4 of: BMI >30 kg/m², age ≥35 years, smoking, preeclampsia, multiple pregnancy, significant varicose veins.
- High risk (>3/1000): rule out APS and thrombophilias; multidisciplinary management.
- COVID-19: thromboprophylaxis if hospitalized for moderate, severe, or critical illness; continue for 14 days after discharge (moderate) or 1 month (severe/critical).
- Postpartum: according to the postpartum score (previous section); continue during hospitalization and decide with hematology whether to continue.
Source: MSPBS draft «Thromboembolism and pregnancy. Thromboprophylaxis» (corrected, unpublished version).
6Protocol for suspected VTE — 15 steps (MSPBS draft)
- Triage: identity, gestational age/postpartum status, reason for presentation, and warning signs (sudden dyspnea, chest pain, tachypnea, cyanosis, syncope, tachycardia, painful and swollen lower limb).
- Assess hemodynamic stability; if there is severe compromise or suspected PE: oxygen, monitoring, and transfer to a higher level of care with referral form and perinatal record.
- Complete the perinatal medical history, with emphasis on thromboembolic risk factors.
- Clear information and emotional support throughout the process.
- Vital signs: BP, HR, RR, temperature, SpO₂.
- Determine gestational age or postpartum day (LMP, delivery date, perinatal record).
- Obstetric assessment: fundal height, FHR, uterine activity, fetal movements.
- Focused history: symptoms, dyspnea, pleuritic pain, cough/hemoptysis, leg pain/swelling, personal or family history of VTE/thrombophilia, immobilization, surgery, cesarean delivery, trauma, obesity.
- Focused physical examination: respiratory and cardiovascular systems, and lower extremities (unilateral edema, pain, warmth, difference in circumference, collateral veins).
- Studies as available: venous duplex ultrasound, ECG, blood gas analysis, chest radiograph with abdominal shielding, CT pulmonary angiography or V/Q scan.
- Presumptive or confirmed diagnosis of DVT/PE.
- Weight-adjusted LMWH (subcard 3 of block 1), unless contraindicated.
- Additional measures: early mobilization, compression stockings >20 mmHg, intermittent pneumatic compression (if LMWH is contraindicated, cesarean delivery/high risk, prior VTE, travel >4 h).
- Education for the patient and family: adherence, warning signs, seek immediate care if symptoms worsen.
- Detailed documentation in the medical record and follow-up scheduling.
Sources: Medicina Fetal Barcelona — Tromboembolismo venoso (2021) · RCOG Green-top 37a (2015) · ACOG Practice Bulletins 196 and 197 (2018) · ASH 2018 · van der Pol LM et al. NEJM 2019 · MSPBS Paraguay draft “Tromboembolismo y embarazo. Tromboprofilaxis” (corrected version).
Shoulder Dystocia — Maneuvers
Obstetric emergency: stepwise management in less than 60 seconds, HELPERR mnemonic, and complications.
1General framework for dystocia (3 Ps)
Risk factors for dystocic labor — maternal: maternal age <18 or >35 years, multiparity/nulliparity, non-gynecoid pelvis, concomitant uterine injury, congenital pelvic defects, maternal history of dystocia, prior cesarean delivery, post-term pregnancy, prior stillbirth, prolonged or instrumented labor, induction with prostaglandins, weight gain >12kg, height <155cm. Fetal: weight >4000g, non-cephalic presentation.
| P | Main causes |
|---|---|
| Power | Inadequate uterine contractions; insufficient pushing effort (maternal exhaustion, sensory and motor effects of epidural anesthesia) |
| Passenger | Abnormal fetal head position (occiput posterior, deep transverse arrest, asynclitism); fetal abnormalities (hydrocephalus, cervical or sacral masses) |
| Pelvis | Pelvic narrowing–uterine dysfunction: the most common cause of dystocia. Cephalopelvic disproportion, pelvic deformities, cervical stenosis |
CaVeSal® proprietary algorithm · Based on: Valenti EA, Andina E, Rey A, et al. Clinical practice guidelines: Shoulder dystocia. Rev Hosp Mat Inf Ramón Sardá 2007;26(1):37-41 · Magnin G, Pierre F. Distocia de hombros. EMC Ginecología-Obstetricia 1999;5-067-A-10 · Romero Gutiérrez G, Ríos López JC, Cortés Salim P, Ponce Ponce de León AL. Risk factors associated with dystocic labor. Ginecol Obstet Mex 2007;75(9):533-8.
2Definition, magnitude, and incidence
Definition: inability of one or both shoulders to pass through the pelvic inlet. It is the obstetric condition most strongly associated with birth trauma (20-50%). Obstetric emergency.
Mechanism: the biparietal diameter exceeds the diameter of the pelvic inlet; pressure at the level of the pubic symphysis from endogenous forces 4-9 times greater than exogenous forces.
| Fetal weight | Incidence |
|---|---|
| 2500-4000 g | 0.3-1% |
| 4000-4500 g | 5-7% |
CaVeSal® proprietary algorithm · Based on: Valenti EA, Andina E, Rey A, et al. Clinical practice guidelines: Shoulder dystocia. Rev Hosp Mat Inf Ramón Sardá 2007;26(1):37-41 · Magnin G, Pierre F. Distocia de hombros. EMC Ginecología-Obstetricia 1999;5-067-A-10 · Romero Gutiérrez G, Ríos López JC, Cortés Salim P, Ponce Ponce de León AL. Risk factors associated with dystocic labor. Ginecol Obstet Mex 2007;75(9):533-8.
⚠️ 50% of cases occur in fetuses with normal weight — macrosomia alone is not predictive; the team must be prepared for every delivery.
3Specific risk factors
| Category | Factors |
|---|---|
| Maternal status | Obesity, multiparity, advanced maternal age, diabetes |
| Current pregnancy | Macrosomia, diabetes, excessive weight gain, post-term pregnancy, pelvic narrowing |
| Obstetric history | Macrosomia, history of shoulder dystocia, history of gestational diabetes |
| Labor | Artificial induction, prolonged second stage, midpelvic forceps |
CaVeSal® proprietary algorithm · Based on: Valenti EA, Andina E, Rey A, et al. Clinical practice guidelines: Shoulder dystocia. Rev Hosp Mat Inf Ramón Sardá 2007;26(1):37-41 · Magnin G, Pierre F. Distocia de hombros. EMC Ginecología-Obstetricia 1999;5-067-A-10 · Romero Gutiérrez G, Ríos López JC, Cortés Salim P, Ponce Ponce de León AL. Risk factors associated with dystocic labor. Ginecol Obstet Mex 2007;75(9):533-8.
4Initial management — first 60 seconds
Turtle sign: retraction of the fetal head toward the perineum after delivery — diagnostic sign.
| 🚫 NO TRACTION |
| 🚫 NO FUNDAL PRESSURE (increases risk of brachial plexus injury/uterine rupture) |
CaVeSal® proprietary algorithm · Based on: Valenti EA, Andina E, Rey A, et al. Clinical practice guidelines: Shoulder dystocia. Rev Hosp Mat Inf Ramón Sardá 2007;26(1):37-41 · Magnin G, Pierre F. Distocia de hombros. EMC Ginecología-Obstetricia 1999;5-067-A-10 · Romero Gutiérrez G, Ríos López JC, Cortés Salim P, Ponce Ponce de León AL. Risk factors associated with dystocic labor. Ginecol Obstet Mex 2007;75(9):533-8.
- Act in less than 60 seconds.
- Wide prophylactic episiotomy.
- McRoberts maneuver (see subcard 6).
- Call for help: obstetrician, pediatrician, anesthesiologist.
5HELPERR mnemonic (30-60 sec per step)
| Letter | Action (English) | Associated maneuver |
|---|---|---|
| H | Call for Help | Ask for help |
| E | Evaluate for Episiotomy | Evaluate episiotomy |
| L | Legs | McRoberts maneuver |
| P | Suprapubic Pressure | Suprapubic pressure |
| E | Enter | Internal maneuvers — Rubin, Woods |
| R | Remove the Posterior Arm | Posterior arm delivery |
| R | Roll the Patient | Rotate the Patient — Gaskin Maneuver |
CaVeSal® proprietary algorithm · Based on: Valenti EA, Andina E, Rey A, et al. Clinical practice guidelines: Shoulder dystocia. Rev Hosp Mat Inf Ramón Sardá 2007;26(1):37-41 · Magnin G, Pierre F. Distocia de hombros. EMC Ginecología-Obstetricia 1999;5-067-A-10 · Romero Gutiérrez G, Ríos López JC, Cortés Salim P, Ponce Ponce de León AL. Risk factors associated with dystocic labor. Ginecol Obstet Mex 2007;75(9):533-8.
6Stepwise maneuvers — first-line
External maneuvers, without additional anesthesia.
| Maneuver | Reported effectiveness |
|---|---|
| McRoberts (hyperflexion and hyperabduction of the maternal hips) | Resolves 90% of cases |
| Suprapubic pressure (on the anterior shoulder, in an oblique direction) | Resolves 40-80% of cases |
| Discontinue oxytocin infusion | Concurrent measure, not a physical maneuver |
CaVeSal® proprietary algorithm · Based on: Valenti EA, Andina E, Rey A, et al. Clinical practice guidelines: Shoulder dystocia. Rev Hosp Mat Inf Ramón Sardá 2007;26(1):37-41 · Magnin G, Pierre F. Distocia de hombros. EMC Ginecología-Obstetricia 1999;5-067-A-10 · Romero Gutiérrez G, Ríos López JC, Cortés Salim P, Ponce Ponce de León AL. Risk factors associated with dystocic labor. Ginecol Obstet Mex 2007;75(9):533-8.
7Stepwise maneuvers — second-line
Internal fetal manipulation, requires regional anesthesia.
- Woods maneuver ("corkscrew" — screw-like rotation of the posterior shoulder, 180°, to an anterior position).
- Rubin maneuver (rotation of the more accessible shoulder toward the oblique diameter, adducting the shoulders).
- Jacquemier maneuver (delivery of the posterior shoulder: the posterior arm is moved backward, the forearm is flexed over the arm, the hand is grasped, and the posterior shoulder is disengaged).
- Posterior axillary traction.
- Gaskin maneuver (maternal position on all fours — changes pelvic geometry without direct fetal manipulation).
8Last-resort maneuvers
Greater fetal morbidity and mortality — use only if the above maneuvers fail.
- Deliberate clavicular fracture (reduces the biacromial diameter).
- Zavanelli maneuver (cephalic replacement and emergency cesarean delivery).
- Abdominal rescue (hysterotomy with disimpaction of the shoulder from the abdomen, followed by assisted vaginal delivery).
- Symphysiotomy (surgical division of the pubic symphysis).
If all the above fail: downward traction on the head + moderate suprapubic pressure, under general anesthesia.
9Documentation and fetal complications
Document (medicolegal): explanation to the patient, severity/complexity, procedures and possible sequelae, maneuvers and timing.
| Brachial plexus injury | ~16.7% (1 in 6 cases) |
| Clavicle or humerus fracture | — |
| Hypoxic-ischemic encephalopathy with neurologic damage | — |
| Erb palsy (C5-C6 roots) | ~50% of brachial plexus palsies — deltoids, biceps, supraspinatus/infraspinatus, brachioradialis |
| Klumpke palsy (C8-T1 roots) | ~40% of brachial plexus palsies — intrinsic hand muscles, flexors and extensors |
CaVeSal® proprietary algorithm · Based on: Valenti EA, Andina E, Rey A, et al. Clinical practice guidelines: Shoulder dystocia. Rev Hosp Mat Inf Ramón Sardá 2007;26(1):37-41 · Magnin G, Pierre F. Distocia de hombros. EMC Ginecología-Obstetricia 1999;5-067-A-10 · Romero Gutiérrez G, Ríos López JC, Cortés Salim P, Ponce Ponce de León AL. Risk factors associated with dystocic labor. Ginecol Obstet Mex 2007;75(9):533-8.
10Maternal complications
| Postpartum hemorrhage | 11% |
| Fourth-degree perineal tears | 3.8% |
| Endometritis | — |
| Uterine rupture | — |
CaVeSal® proprietary algorithm · Based on: Valenti EA, Andina E, Rey A, et al. Clinical practice guidelines: Shoulder dystocia. Rev Hosp Mat Inf Ramón Sardá 2007;26(1):37-41 · Magnin G, Pierre F. Distocia de hombros. EMC Ginecología-Obstetricia 1999;5-067-A-10 · Romero Gutiérrez G, Ríos López JC, Cortés Salim P, Ponce Ponce de León AL. Risk factors associated with dystocic labor. Ginecol Obstet Mex 2007;75(9):533-8.
Assistance with Breech Presentation at Birth — Maneuvers
Epidemiology, types of presentation, ACOG criteria for vaginal delivery, and sequence of maneuvers (MSF/PMC).
1Epidemiology and risk factors
Incidence: 3-4% of births. The frequency increases at lower gestational ages (more common in preterm infants).
Risk factors: prematurity, uterine relaxation/multiparity, pelvic tumor, pelvic narrowing, hydramnios, oligohydramnios, hydrocephalus and anencephaly, history of prior breech delivery, uterine anomalies.
2Types of breech presentation
| English | Spanish | Description |
|---|---|---|
| Frank Breech | Frank breech | Hips flexed, knees extended — legs extended upward alongside the trunk |
| Complete Breech | Complete breech | Hips and knees flexed — "squatting" position |
| Footling Breech | Footling breech / feet first | One or both feet below the buttocks as the presenting part |
CaVeSal® proprietary algorithm · Based on: Williams Obstetrics (Breech Delivery) · ACOG CO 745 (2018) · MSF — Breech presentation.
Only frank or complete breech presentations are candidates for vaginal delivery (see subcard 4); footling breech is excluded.
3Risks to the mother and fetus
| Mother | Fetus |
|---|---|
| Higher incidence of complications and infection | Umbilical cord prolapse |
| Uterine rupture | Femoral, clavicular, and humeral fractures |
| Tears at various levels | Brachial plexus stretch injury |
| Uterine atony | — |
CaVeSal® proprietary algorithm · Based on: Williams Obstetrics (Breech Delivery) · ACOG CO 745 (2018) · MSF — Breech presentation.
4ACOG criteria for attempted vaginal delivery
All criteria must be met — failure to meet any one indicates cesarean delivery:
- Estimated fetal weight <3,500 g.
- Biparietal diameter <96 mm (range 90-100mm, Williams Obstetrics citing Giuliani 2002 and Roman 2008 — not a specific ACOG cutoff).
- Clinically adequate pelvis.
- Frank or complete breech (footling breech excluded).
- Flexed fetal head.
- Absence of fetal anomalies.
- No contraindications to vaginal delivery.
- Absence of concomitant pathology.
This checklist is available as a binary (yes/no) mini-calculator in the Calculator mode.
5Guiding principle — "hands-off"
General management of breech labor, not a specific maneuver: the infant should be delivered by maternal pushing, supported only by the bony parts (hips and sacrum), without traction, without pulling on the legs, without touching the infant until the scapulae appear (to avoid triggering the respiratory reflex before the head is delivered).
⏱️ Once the umbilicus is out: complete delivery within a maximum of 3 minutes (risk of cord compression). Ensure the back does not rotate to a posterior position.
6Maneuvers in order of use
| # | Maneuver | When used |
|---|---|---|
| 1 | Pinard | Breech / incomplete footling breech — bring down the legs |
| 2 | Lovset | Retained shoulders / arms extended above — bring down the arms |
| 3 | Bracht | Entrapped head after releasing the arms — first-line option |
| 4 | Mauriceau-Smellie-Veit | Entrapped head if Bracht fails |
| 5 | Suzor | Retained shoulders if Lovset fails |
| 6 | Forceps for the aftercoming head | Entrapped head if Bracht and Mauriceau fail (experienced operator) |
CaVeSal® proprietary algorithm · Based on: Williams Obstetrics (Breech Delivery) · ACOG CO 745 (2018) · MSF — Breech presentation.
7Detailed technique for each maneuver
Pinard: insert two fingers into the vagina and “hook” the leg from medial to lateral just above the knee; flex at the hip and abduct to release the foot. Repeat with the other leg if the breech is complete.
Lovset: place the thumbs over the sacrum, grasp the hips, and rotate 90°; release the anterior arm; counter-rotate 180° and release the posterior arm.
Bracht: hold the hips and lift with both hands toward the maternal abdomen without traction; the neck pivots over the symphysis. An assistant applies suprapubic pressure.
Mauriceau-Smellie-Veit (modified): kneel at a 45° downward angle; support the infant on the hand and forearm; place the index and middle fingers on the maxilla (NOT inside the mouth — risk of mandibular fracture); place the other hand on either side of the neck; lower the head, bringing the subocciput beneath the symphysis; use a sweeping motion, bringing the back toward the maternal abdomen. Apply suprapubic pressure along the pelvic axis.
Suzor: rotate the back 90°; pull downward; insert one hand along the back to locate the anterior arm; place the thumb in the axilla and the middle finger along the arm; lower the anterior arm; lift by the feet to release the posterior shoulder.
8Complete operational sequence
- Verify the criteria for vaginal delivery (subcard 4) — if not met, cesarean delivery.
- Confirm the type of presentation (subcard 2) — frank/complete breech are candidates; footling breech is highly unfavorable.
- Delivery: hands off — allow descent with maternal pushing.
- Legs (if not delivered spontaneously): Pinard.
- Arms: Lovset (or Suzor if it fails).
- Head: Bracht → if unsuccessful, Mauriceau-Smellie-Veit → if unsuccessful, forceps for the aftercoming head.
- Timer: from delivery of the umbilicus, a maximum of 3 minutes to deliver the head.
- Document maneuvers and times (medicolegal).
Source: Vizcaíno A. “Parto Pélvico.” SlideShare (18/01/10) · ACOG Committee Opinion No. 265/340/745 (qualitative position, no BPD cutoff) · Williams Obstetrics 24th/25th ed. — Breech Delivery (Giuliani 2002; Roman 2008) · MSF Guidelines — Breech presentation · PMC — Footling Breech Delivery.
Preterm Premature Rupture of Membranes (PROM)
Diagnosis, management by gestational age, latency antibiotic regimens, and criteria for immediate delivery.
1Diagnosis
Clinical: clear fluid leaking from the vagina — reliability >90% if visualized at the external cervical os on speculum examination.
Confirmatory tests:
- Fern test.
- Nitrazine test (pH>6.5 turns blue).
- Commercial biomarkers (PAMG-1/AmniSure, IGFBP-1/Actim PROM).
- Measurement of urea and creatinine in vaginal secretions — urea 94%/82% and creatinine 98%/90% (sensitivity/specificity, Alao 2023); low cost, useful in resource-limited settings. See comparative table in subcard 7.
Diagnostic amniocentesis (gold standard in equivocal cases): ultrasound-guided instillation of indigo carmine, vaginal tampon, confirmation of staining at 20-30 min.
| Methylene blue CONTRAINDICATED for intra-amniotic use — teratogenic; causes neonatal jejunal/ileal atresia, severe hyperbilirubinemia, fetal methemoglobinemia, and hemolysis. Safe alternatives: indigo carmine or fluorescein. |
CaVeSal® proprietary algorithm · Based on: Alao AI et al. Arch Gynecol Obstet 2023;307(2):447-452.
Microbiological analysis of amniotic fluid: Gram stain, culture (aerobes/anaerobes/Mycoplasma/Ureaplasma), amniotic fluid glucose (<14 mg/dL suggests intra-amniotic infection), leukocyte count.
2Management by gestational age
| Gestational age | Management |
|---|---|
| Previable (<22-24 wk) | Expectant management as an outpatient/inpatient; counseling on the risk of pulmonary hypoplasia, deformities, and stillbirth. No corticosteroids, tocolysis, or routine antibiotics. |
| Preterm, remote from term (24⁰/⁷-33⁶/⁷ wk) | Expectant inpatient management; complete course of antenatal corticosteroids (betamethasone/dexamethasone); magnesium sulfate for neuroprotection if delivery is imminent and GA<32 wk; mandatory latency antibiotic prophylaxis; tocolysis contraindicated or limited to 48h to complete corticosteroid treatment (if no infection). |
| Late preterm (34⁰/⁷-36⁶/⁷ wk) | ACOG/FIGO recommendation: delivery/induction at diagnosis. Exception: expectant management until 37 weeks only if there are no signs of infection + close monitoring. |
| At term (≥37⁰/⁷ wk) | Induction (oxytocin or misoprostol if the cervix is unfavorable) within 12-24h to reduce the risk of intrauterine infection. |
CaVeSal® proprietary algorithm · Based on: ACOG · FIGO.
3Latency antibiotic regimens (24-34 wk)
Standard ACOG/NICHD regimen (7 days):
- Days 1-2 IV: Ampicillin 2g q6h + erythromycin 250mg q6h (or azithromycin 1g PO as a single dose).
- Days 3-7 PO: Amoxicillin 250mg q8h + erythromycin base 333mg q8h (MSPBS 2018 uses amoxicillin 500mg; see card 17).
Alternative regimen (with azithromycin, widely used):
- Ampicillin 2g IV q6h x48h → amoxicillin 250mg PO q8h x5 days + azithromycin 1g PO as a single dose at admission (ACOG: an appropriate substitute for erythromycin).
| Avoid amoxicillin + clavulanic acid — risk of neonatal necrotizing enterocolitis (NEC). |
CaVeSal® proprietary algorithm · Based on: ACOG.
4Criteria for immediate delivery
Contraindicate expectant management at any gestational age:
- Clinical chorioamnionitis / confirmed intra-amniotic infection (Gibbs criteria).
- Placental abruption.
- Acute fetal compromise (non-reassuring FHR / abnormal biophysical profile).
- Established labor.
- Fetal death.
5Fetal lung maturation and neuroprotection (submodule shared with TPL)
These therapies are shared with the Threatened Preterm Labor (TPL) module — same regimen, same table of recommendations by guideline:
| Guideline | GA window |
|---|---|
| ACOG | 24⁰/⁷-33⁶/⁷ weeks (consider “late preterm” 34⁰/⁷-36⁶/⁷ if no prior course was given) |
| FIGO/WHO | 24⁰/⁷-34⁶/⁷ weeks (in settings with adequate neonatal care capacity) |
| NICE | Offer 24⁰/⁷-33⁶/⁷; consider 34⁰/⁷-35⁶/⁷ |
Regimens: Betamethasone 12mg IM every 24h (2 doses total); Dexamethasone 6mg IM every 12h (4 doses total). Rescue dose: a single dose or repeat course if >14 days since the initial course, GA<34 weeks, and imminent risk of delivery within 7 days.
| Guideline | GA cutoff |
|---|---|
| ACOG | <32⁰/⁷ weeks |
| NICE | <30⁰/⁷ weeks; consider 30⁰/⁷-33⁶/⁷ |
| FIGO/WHO | <32⁰/⁷ weeks (some consensus statements extend to <34 weeks if delivery is imminent) |
CaVeSal® proprietary algorithm · Based on: ACOG · FIGO · WHO · NICE.
Regimen: loading dose 4g IV over 20-30min; maintenance 1g/h IV until delivery or for a total of 24h; antidote: Calcium Gluconate 10% 1g IV.
In the Calculator, the single cutoff used is that of MSPBS Paraguay (corticosteroids: 24⁰/⁷ to 34⁰/⁷ weeks, not from 34¹/⁷ onward · MgSO4: less than 32 weeks); ACOG/FIGO/NICE variations are listed in this guide — see Calculator Mode.
6Definitions and subtypes of rupture
- PROM: rupture of membranes occurring at least 2 hours before the onset of labor, regardless of GA (FASGO 2018 consensus).
- Latency period: time between rupture and onset of labor; inversely proportional to GA (longer when rupture occurs earlier).
| Subtype | Characteristic |
|---|---|
| High rupture of membranes | Rupture above the internal cervical os; scant or intermittent fluid leakage. |
| Low rupture of membranes | Rupture near the internal cervical os; frank fluid leakage. |
| False rupture of membranes | Rupture of only one membrane (amniochorion) with persistence of the other; difficult to diagnose, with confirmatory tests that may yield false-negative results. |
CaVeSal® proprietary algorithm · Based on: FASGO. 2018 Obstetrics Consensus: Premature rupture of membranes.
These subtypes are not included in the 2018 FASGO Consensus and are presented without specific attribution to that source.
7Diagnostic performance of confirmatory tests
| Method | Sensitivity | Specificity | Note |
|---|---|---|---|
| Nitrazine (pH >6.5) | 90-97% | 16-70% | Low specificity: false positives with blood, semen, and bacterial vaginosis. |
| Crystallization (Fern test) | 55-98% | 30-88% | Wide range; depends on the operator. |
| PAMG-1 (AmniSure) | 98-99% | 98-100% | Considered the best commercial biomarker (reference standard in SOGOCEP/FLASOG); some studies report sensitivity of 95.7-97.3%. |
| IGFBP-1 (Actim PROM) | 74-97% | 74-97% | Commercial alternative to PAMG-1; individual studies show ~89-90% sensitivity and ~83-87% specificity. |
| Vaginal urea (cutoff 1.25 mg/dL) | 94% | 82% | Low cost; useful in resource-limited settings (Alao 2023). |
| Vaginal creatinine (cutoff 0.23 mg/dL) | 98% | 90% | Low cost; useful in resource-limited settings (Alao 2023). |
CaVeSal® proprietary algorithm · Based on: Chalurkar U, Andallu R. Int J Contemp Med Res 2017;4(5):1118-21 (IGFBP-1 vs. ferning) · Khooshideh M et al. Iran J Reprod Med 2015;13(6):355-60 (PAMG-1) · Abdelazim IA, Makhlouf HH. Arch Gynecol Obstet 2012;285(4):985-9 (AmniSure®) · Alao AI et al. Arch Gynecol Obstet 2023;307(2):447-452.
8Triple I (clinical chorioamnionitis): criteria for suspected infection
“Triple I” (Intrauterine Inflammation, Infection or both) is the modern term proposed by the 2015 NICHD workshop and adopted by ACOG/SMFM; it replaces “clinical chorioamnionitis” (classic Gibbs 1982 criteria: fever ≥37.8 °C + ≥2 signs; many guidelines use ≥38.0 °C).
| Category | Criterion |
|---|---|
| Suspected intra-amniotic infection (Triple I) — highest priority | Maternal temperature ≥39.0 °C isolated, or 38.0-38.9 °C sustained (confirmed on repeat measurement at 30 min) plus 1 additional factor: maternal leukocytosis, purulent cervical drainage, or fetal tachycardia. |
| Isolated maternal fever | Temperature 38.0-38.9 °C without other factors, whether persistent or not. |
| Management of Triple I: broad-spectrum antibiotics, delivery, and maternal resuscitation. In PROM, monitoring uses the same obstetric qSOFA (SBP <90, RR ≥25, altered mental status) used in the sepsis module; ≥2 points = high risk of deterioration. |
CaVeSal® proprietary algorithm · Based on: ACOG Committee Opinion No. 712 (2017) · Medicina Fetal Barcelona — Chorioamnionitis or Triple I.
9Risk stratification for multidrug-resistant bacteria (MDR)
Patient at risk of MDR = 1 major criterion or 2 or more minor criteria (comorbidities count as one criterion).
- Major criterion: previous infection or colonization with MDR bacteria.
- Minor criterion 1: comorbidity (CKD, pregestational diabetes, heart disease, COPD) or immunosuppression (neutropenia, transplant, corticosteroids >20 mg/day of prednisone or equivalent for >2 weeks, immunosuppressants/cytotoxic agents, HIV with CD4 <200, primary immunodeficiencies).
- Minor criterion 2: indwelling urinary catheter.
- Minor criterion 3: hospital admission in the previous 3 months, regardless of duration.
- Minor criterion 4: systemic antibiotic (oral or IV) in the previous 3 months, regardless of duration (common in recurrent UTIs).
- Minor criterion 5: origin from an endemic area (Latin America, the Caribbean, Asia, non-EU Mediterranean) and <6 months in the country, or >6 months in the country but travel to or visits from family from that country in the previous 6 months.
| Situation | Regimen |
|---|---|
| Initial | Ampicillin 2 g q/6 h IV + Ertapenem 1 g q/24 h IV + Clarithromycin 500 mg q/12 h PO |
| De-escalation (negative rectal MDR screening swab) | Ampicillin 2 g q/6 h IV + Ceftriaxone 1 g q/12 h IV + Clarithromycin 500 mg q/12 h PO (or other options susceptible according to the antibiogram) |
| Penicillin/beta-lactam allergy | Teicoplanin 600 mg q/12 h IV (2 initial doses, then q/24 h) + Aztreonam 1 g q/8 h IV + Clarithromycin 500 mg q/12 h PO |
CaVeSal® proprietary algorithm · Based on: Medicina Fetal Barcelona protocol, preterm and term PROM (09/2025).
In the absence of suspected multidrug-resistant bacteria, the standard regimen in subcard 3 is maintained. Source: Medicina Fetal Barcelona protocol, preterm and term PROM (09/2025).
10Erythromycin vs azithromycin: meta-analysis
Seaman et al., AJOG 2022 (5 studies, 1289 patients):
- Latency: no difference (6.6 vs 6.7 days; mean difference 0.07 days, 95% CI −0.45 to 0.60).
- Clinical chorioamnionitis: OR 0.53 (95% CI 0.39-0.71) with azithromycin; median prevalence 14% vs 25% with erythromycin (approximately 47% relative reduction).
Azithromycin is not intended to achieve longer latency: it aims for equal efficacy with better tolerability and less chorioamnionitis (FLASOG 2026 pearl). Source: Seaman AN et al. Am J Obstet Gynecol 2022;226(6):794-801.
11Decision tree: immediate delivery vs expectant management
Triple I / clinical chorioamnionitis · placental abruption · acute fetal compromise · cord prolapse · active labor · active maternal bleeding
Counseling (pulmonary hypoplasia, deformities, fetal demise). No routine corticosteroids, tocolysis, or antibiotics.
Inpatient expectant management; corticosteroids, latency antibiotics, magnesium sulfate if <32 wk and delivery is imminent.
Delivery at diagnosis (ACOG/FIGO); expectant management until 37 wk only in the absence of infection and with close monitoring.
Induction within 12-24 h.
References: FIGO 2023 (Ubom et al., Int J Gynecol Obstet 163 Suppl 2:40-50) · SMFM Consult Series #71 (2024) · NICE NG25 (2022) · ACOG PB 217 (2020) · RCOG Green-top No. 73 (2022) · FASGO Consensus 2018 · Manual of Obstetric Standards and Procedures 2021, INPer Mexico (generic attribution) · Ghafoor S. Malays J Med Sci 2021;28(3):5-17.
12Surveillance during expectant management
| Scope | What to monitor | Frequency |
|---|---|---|
| Maternal | Temperature, pulse, blood pressure; uterine pain (intensity, frequency, hypertonia); fluid characteristics (color, odor, amount); CBC ± CRP according to clinical course | Temperature, pulse, and FHR every 4-8 h (RCOG) |
| Fetal | Cardiotocography/NST; biophysical profile; ultrasound (growth, AFI, placenta); umbilical and middle cerebral artery Doppler if indicated | Daily NST or according to clinical condition; BPP and ultrasound every 24-48 h (usual practice, no consensus on frequency) |
| BPP | Interpretation | Management |
|---|---|---|
| 6 | Equivocal | ≥37 weeks: strongly consider delivery. <37 weeks: repeat BPP within 24 h. |
| ≤4 | Abnormal | ≥32 weeks: delivery recommended. <32 weeks: extended surveillance may be considered. |
| 2 | Very abnormal | Delivery recommended in most cases. |
CaVeSal® proprietary algorithm · Based on: RCOG Green-top No. 73 · StatPearls (NBK537123).
RCOG: biophysical profile and Doppler are not first-line tests for diagnosing fetal infection. ACOG: there is no consensus on the optimal frequency of assessment during expectant management. Sources: RCOG Green-top No. 73 · StatPearls (NBK537123).
13Regional context: outpatient management vs continuous hospitalization
| Conditional golden rule: without active remote monitoring (continuous temperature sensor, outpatient CTG with remote transmission) or emergency access to a hospital within <15 min, continuous hospitalization is the only standard that safeguards the mother and fetus and provides medico-legal safety. |
CaVeSal® proprietary algorithm · Based on: RCOG · ACOG · NICE.
Outpatient management should only be considered if all these requirements are met:
- Patient at low risk of infection, strictly selected.
- Guaranteed maternal adherence and stable connectivity.
- 24/7 monitoring by a specialized team.
- Immediate access to obstetric and neonatal ICU care.
- Response in <15 min to a critical alarm.
Recommendation to use regional clinical judgment, consistent with RCOG #73, ACOG, and NICE NG25 (inpatient expectant management by default).
14Interventions: magnitude of benefit (NNT)
| Intervention | Effect | NNT / measure |
|---|---|---|
| Antenatal corticosteroids | Neonatal death (Cochrane 2020: RR 0.78; 95% CI 0.70-0.87; 10,609 infants) | NNT 38; for RDS, varies by gestational age: 19 (<28 weeks) to 55 (>34 weeks) |
| Latency antibiotics | Chorioamnionitis RR 0.66 (0.46-0.96); delivery <48 h RR 0.71; delivery <7 days RR 0.79 (Kenyon, Cochrane 2013) | No consolidated NNT |
| MgSO4 for neuroprotection | Cerebral palsy RR 0.68 (0.54-0.87); relative reduction ~30-40% | NNT 46-63 (95% CI 39-172) |
| GBS prophylaxis | Neonatal sepsis due to group B streptococcus | NNT 47 (screening + risk factors), 140 (screening only), 222 (risk factors only) |
CaVeSal® proprietary algorithm · Based on: Cochrane 2020 (corticosteroids) · Kenyon, Cochrane 2013 · SciELO Argentina (MgSO4) · Universiteit Leiden (GBS).
Low-cost, high-evidence interventions (corticosteroids, antibiotics, MgSO4, GBS prophylaxis) provide greater benefit than costly technology without infrastructure. Sources: Cochrane 2020 (corticosteroids) · Kenyon, Cochrane 2013 · SciELO Argentina (MgSO4) · Universiteit Leiden (GBS).
15Horizon and innovation (educational content)
- Emerging molecular biomarkers: proteomics, metabolomics, microRNA, IL-6, IL-8, TNF-α; detect intra-amniotic inflammation before clinical manifestations.
- QuantusFLM® (AI-based fetal lung texture analysis) in PROM: sensitivity 60%, specificity 79.5%, negative predictive value 89.7% (Palacio M et al. Fetal Diagn Ther 2020).
- Cervical elastography and amniotic sludge as emerging risk markers.
Not an acute management protocol. AI does not replace clinical judgment; it enhances its analytical capacity to support better decision-making (FLASOG 2026).
16Stepwise diagnostic algorithm
| Step | What to do | If positive | If negative or equivocal |
|---|---|---|---|
| 0. Established labor | Do not test for PROM | Labor management | Proceed to step 1 |
| 1. History | Time of fluid loss, color, odor, amount; reliable gestational age; serologies | Always proceed to step 2 | |
| 2. Sterile speculum examination | Valsalva or Tarnier maneuver; samples for culture; no digital vaginal examination | Visible fluid: PROM confirmed, no further testing needed | Step 3 |
| 3. Vaginal fluid test | PAMG-1 or IGFBP-1; if unavailable: urea/creatinine, crystallization, or nitrazine | PROM likely: integrate with clinical findings | Step 4 |
| 4. Ultrasound | Single deepest pocket (preferred) or AFI | Oligohydramnios (MVP <2 cm or AFI ≤5 cm): supportive, not diagnostic | Normal fluid: PROM unlikely; no antibiotics; consider differential diagnoses |
| 5. Amniocentesis with dye | Indigo carmine or fluorescein + vaginal tampon | Dye staining at 30-60 min: PROM confirmed | Rules out PROM |
| Point | MSPBS 2018 | NICE NG25 |
|---|---|---|
| Nitrazine | Accepted (pH >6.5), before digital examination | Do not use |
| IGFBP-1 / PAMG-1 | If the case is uncertain and available | If no fluid is seen on speculum examination |
| Ultrasound | Useful adjunct, not diagnostic | Not listed as a diagnostic test |
| Negative test | Suspect urinary tract infection, vulvovaginitis, or oligohydramnios of another cause | PROM unlikely: do not offer antibiotics |
Vaginal urea and creatinine: the reference study (Alao 2023) was conducted in Nigeria as an inexpensive alternative to AmniSure®; it is not standard practice in the UK, where NICE recommends IGFBP-1 or PAMG-1. Ultrasound: oligohydramnios cutoffs are the same as those in the prenatal calculator (AIUM/ACOG/SMFM).
CaVeSal® proprietary algorithm · Based on: MSPBS Paraguay 2018, chapter 29 · NICE NG25, section 1.3 · Alao AI et al. Arch Gynecol Obstet 2023.
17MSPBS 2018 protocol by gestational age (Paraguay)
| GA | Management | Antibiotics |
|---|---|---|
| Less than 24 weeks (previable) | Expectant management; decision made jointly with the parents. No group B streptococcus prophylaxis, corticosteroids, tocolysis, or MgSO4 before viability | Consider from 20⁰/⁷ weeks |
| 24⁰/⁷ a 33⁶/⁷ | Inpatient expectant management (or refer to a Level III facility); IV crystalloids; CBC and CRP every 48 h; temperature monitoring. Corticosteroids at 24-34 weeks; MgSO4 if <32 weeks and delivery is likely within 24 h; tocolysis only to complete corticosteroid administration or for 48 h. Deliver if contractions, infection, or fetal compromise persist | One of: ampicillin 2 g IV, then 1 g every 4 h · amoxicillin 500 mg PO every 8 h · clindamycin 900 mg IV every 8 h (allergy) · erythromycin 250 mg PO every 6 h · amoxicillin + sulbactam 1.5 g every 8 h; 7 days or until delivery + azithromycin 1 g PO once |
| 34⁰/⁷ a 36⁶/⁷ | Consider delivery by the most appropriate route | Same options. Alternative if available: ampicillin 1-2 g IV every 6 h + erythromycin 500 mg PO every 6 h (48 h), then amoxicillin 500 mg PO every 6 h + erythromycin 500 mg PO every 8 h (5 days) |
| 37⁰/⁷ or more | Deliver by the most appropriate route according to cervical status | Group B streptococcus positive: ampicillin 2 g IV q4 h until delivery. More than 18 h without infection: penicillin G 5 M IU, then 2.5 M q4 h, or ampicillin 2 g, then 1 g q4 h |
| Chorioamnionitis (any GA) | Delivery regardless of GA; notify neonatology | Ampicillin 2 g IV q6 h + gentamicin 2 mg/kg, then 1.5 mg/kg q8 h (or 5 mg/kg q24 h); for cesarean delivery, add metronidazole 500 mg q8 h or clindamycin 900 mg q8 h; until 48 h without signs |
Difference from ACOG PB 217 (2020): amoxicillin 250 mg q8 h + erythromycin 333 mg q8 h during the oral phase, and no latency antibiotics from 34⁰/⁷ onward (only Group B streptococcus prophylaxis). The calculator uses ACOG as the preferred regimen at 24-33⁶/⁷ and allows selection of the MSPBS and NICE regimens.
CaVeSal® proprietary algorithm · Based on: MSPBS Paraguay, National Manual of Standards for Care of Major Obstetric Conditions 2018, ch. 29, pp. 217-224.
18Corticosteroids after 34 weeks: benefit versus harm
| CaVeSal® approach: antenatal corticosteroids are suggested from 24⁰/⁷ to 34⁰/⁷ (MSPBS), in the absence of chorioamnionitis. Other guidelines extend the limit: ACOG through 36⁶/⁷ and NICE to consider through 35⁶/⁷. |
| Study | Design | Outcome |
|---|---|---|
| ALPS (NEJM 2016) | Randomized trial, 34⁰/⁷-36⁵/⁷ | Benefit: composite respiratory outcome 11.6% vs 14.4% (RR 0.80; 95% CI 0.66-0.97). Harm: neonatal hypoglycemia 24.0% vs 15.0% (RR 1.60; 1.37-1.87) |
| ALPS follow-up (JAMA 2024) | 949 children, median age 7 years | No difference in cognitive impairment (17.1% vs 18.5%; adjusted RR 0.94; 0.73-1.22) |
| Ninan (JAMA Pediatr 2022) | Observational cohort, more than 1.25 million children | Among late preterm and term infants exposed: more neurocognitive visits (HR 1.12) and mental or behavioral disorders in infants born at term (HR 1.47). Low certainty: does not prove causality |
| Aviram (Arch Dis Child Fetal Neonatal Ed 2022) | Population-based retrospective cohort (Ontario), 25,668 infants born at 34⁰/⁷ to 36⁶/⁷; 2,689 exposed to corticosteroids before 34⁰/⁷ | At 5 years: higher suspicion of neurocognitive disorder (adjusted HR 1.12; 95% CI 1.05-1.20) and more audiometric assessments (adjusted HR 1.20) and vision assessments (adjusted HR 1.06). Observational: does not prove causality |
| Guideline | Limit | Conditions |
|---|---|---|
| MSPBS 2018 (calculator) | 24⁰/⁷-34⁰/⁷ | No chorioamnionitis |
| NICE NG25 | Consider through 35⁶/⁷ | Risk of preterm birth |
| ACOG CO 713 | Up to 36⁶/⁷ | Delivery likely within 7 days, no prior course, no chorioamnionitis; caution in pregestational diabetes |
| European guideline on perinatal care 2023 | 34⁰/⁷-34⁶/⁷ only in selected cases; 35⁰/⁷-36⁶/⁷ only in trials | At 35-36⁶/⁷, reduces transient tachypnea, with no effect on RDS and more hypoglycemia |
If corticosteroids are given after 34 weeks: neonatal glucose monitoring. Chorioamnionitis: ALPS showed no increase in chorioamnionitis or sepsis, and neither did a meta-analysis (RR 0.86) (WAPM, J Perinat Med 2022). The citation "Li G et al. Lancet Neurol 2022;21:948-962" (>16,000 women) does not exist in PubMed or Lancet Neurology; the title corresponds to Aviram 2022, whose data are shown above.
CaVeSal® proprietary algorithm · Based on: Gyamfi-Bannerman C et al. NEJM 2016;374:1311-20 · Gyamfi-Bannerman C et al. JAMA 2024;331:1629-37 · Ninan K et al. JAMA Pediatr 2022;176:e220483 · Aviram A et al. Arch Dis Child Fetal Neonatal Ed 2022;107:250-255 · Daskalakis G et al. J Matern Fetal Neonatal Med 2023 (European guideline) · WAPM, J Perinat Med 2022 · ACOG CO 713 · NICE NG25.
19Tocolysis in PROM: an evidence-based option
| Source | Recommendation |
|---|---|
| MSPBS 2018 | Only to complete lung maturation or for 48 h (24-34 weeks) |
| Cochrane 2014 (8 trials, 408 women) | Latency +73 h and fewer deliveries within 48 h (RR 0.55), but more chorioamnionitis before 34 weeks (RR 1.79; 1.02-3.14); no benefit in perinatal mortality |
| RCOG GTG 73 | Not recommended |
If used: no signs of infection, maximum 48 h, discontinue if fever or tachycardia occurs. Drugs and timer in the calculator (Tocolysis card).
CaVeSal® proprietary algorithm · Based on: MSPBS 2018 · Mackeen AD et al. Cochrane 2014 (CD007062) · RCOG Green-top No. 73.
20Fetal lung maturity
| Test | Sample | Mature | Comment |
|---|---|---|---|
| L/E ratio | AF (amniocentesis) | 2.0 or more | Blood and meconium alter it |
| Phosphatidylglycerol | Amniotic fluid or vaginal pool | Present | Blood and meconium do not alter it; its absence does not predict fetal distress |
| Lamellar bodies | Amniotic fluid | More than 50,000/µL (immature <15,000) | Intermediate: supplement with another test; cutoff depends on the analyzer |
| quantusFLM® | Ultrasound: axial chest section at the four-chamber level, AI-based texture analysis | «Low risk» | Sensitivity 74.3%, specificity 88.6%, PPV 51%, NPV 95.5% (730 cases). In PROM: sensitivity 60%, specificity 79.5%, NPV 89.7% |
All predict maturity well and immaturity poorly. If delivery is indicated, the result does not change management (2011 consensus). In PROM before 34 weeks, it may guide the decision.
CaVeSal® proprietary algorithm · Based on: Varner S et al. Rev Obstet Gynecol 2013;6(3-4):126-134 · Palacio M et al. Am J Obstet Gynecol 2017 · Palacio M et al. Fetal Diagn Ther 2020.
Subcards 6-20: content from the RPM-SOGOCEP 2025 and RPM-FLASOG 2026 presentations (Dr. Carlos Vera Salerno), verified against the sources cited in each subcard.
Source: ACOG Practice Bulletin No. 217 (2020) · FIGO Guidelines on PROM Management (2021) · Cowles et al. Obstet Gynecol 1993 (Indigo Carmine vs Methylene Blue) · ACOG Practice Bulletin No. 171 (2016, reaffirmed 2020) · NICE Guideline NG25 (2019, updated 2022) · FIGO Recommendations on Preterm Birth (2021).
Threatened Preterm Labor (TPL)
Diagnosis, tocolysis, and shared fetal lung maturation/neuroprotection submodule (see also PROM tab).
1Diagnosis and clinical criteria
Definition: regular uterine activity (≥4 contractions/20min or ≥8/60min) + cervical changes, between 22⁰/⁷ and 36⁶/⁷ weeks.
Transvaginal cervical ultrasound (TVUS):
- Cervical length (CL) >30mm → high negative predictive value (rules out active preterm labor).
- CL <25mm (or <20mm) → short cervix / elevated risk.
Biomarkers if CL 20-30mm: fetal fibronectin (fFN) or PAMG-1 (PartoSure) — if negative, avoids unnecessary tocolysis.
2Tocolysis — complete regimens
Objective: delay delivery 48-72h to complete fetal lung maturation, provide neuroprotection, and transfer to a Level III center. Use: weeks 22/24 to 33⁶/⁷.
| Drug | Regimen | Maintenance schedule |
|---|---|---|
| Nifedipine (1st-line ACOG/FIGO) | Loading dose 10-20mg orally every 20min (max 40mg in 1st hour); maintenance 10-20mg orally every 6-8h for 48h. | c/6-8h |
| Atosiban (NICE/RCOG first line) | 6.75mg IV bolus over 1min; infusion 300mcg/min for 3h, then 100mcg/min until 48h are completed. | Continuous infusion (0-3h / 3-48h phases) |
| Indomethacin (preferred before week 32) | 50-100mg rectal/oral initial dose, then 25-50mg orally every 6h for a maximum of 48h. | c/6h |
| Isoxsuprine (beta-agonist) | 100 mg (10 ampoules of 10 mg) in 500 cc of 5% dextrose or normal saline; start at 10 drops/min (100 mcg/min), increase by 10 drops every 15 min up to 40 drops/min (400 mcg/min); 12 h (max 24 h). | Continuous infusion; monitor HR/BP with each adjustment |
| ⚠️ Nifedipine + MgSO4: DO NOT combine — risk of severe hypotension/cardiovascular collapse. |
| ⚠️ Indomethacin: DO NOT use after week 32 — premature closure of the ductus arteriosus, oligohydramnios. |
Progesterone (prevention, not acute tocolysis): micronized vaginal progesterone 200 mg/day, started between 16-24 weeks and continued until at least 34 weeks, for a short cervix (≤25 mm) or history of preterm birth (NICE NG25 · SOGC 398).
CaVeSal® proprietary algorithm · Based on: ACOG · FIGO · NICE · RCOG.
3Tocolysis hours timer (concept — calculation in Calculator Mode)
The Calculator includes a single timer, reusable for all 3 drugs, with an internal cadence parameterized according to the active drug:
- Manual trigger: starts when “tocolysis initiated” is selected — not assumed automatically.
- Active alerts at dose milestones: alert at each hour corresponding to the next maintenance dose for the drug (see table above).
- Pause/stop button: preserves the accumulated time (e.g., “tocolysis stopped at 18h 40min”) without resetting to zero.
- End of window: alert at 48h (or 72h) — “tocolysis target reached; reassess continuation/transfer.”
- Joint display with the uterine activity record (contractions/20-60min) to assess clinical response.
4Fetal lung maturation (antenatal corticosteroids)
Submodule shared with PROM — same 3 guideline positions:
| Guideline | GA window |
|---|---|
| ACOG | 24⁰/⁷-33⁶/⁷ weeks (consider “late preterm” 34⁰/⁷-36⁶/⁷ if no prior course was given) |
| FIGO/WHO | 24⁰/⁷-34⁶/⁷ weeks |
| NICE | Offer 24⁰/⁷-33⁶/⁷; consider 34⁰/⁷-35⁶/⁷ |
CaVeSal® proprietary algorithm · Based on: ACOG · FIGO · WHO · NICE.
Regimens: Betamethasone 12mg IM every 24h (2 doses); dexamethasone 6mg IM every 12h (4 doses).
Single cutoff in Calculator: NICE.
5Fetal neuroprotection with MgSO4
Submodule shared with PROM — same 3 guideline positions:
| Guideline | GA cutoff |
|---|---|
| ACOG | <32⁰/⁷ weeks |
| NICE | <30⁰/⁷ weeks; consider 30⁰/⁷-33⁶/⁷ |
| FIGO/WHO | <32⁰/⁷ weeks (some consensus statements extend to <34 weeks if delivery is imminent) |
CaVeSal® proprietary algorithm · Based on: ACOG · NICE · FIGO · WHO.
Regimen: loading dose 4g IV over 20-30min; maintenance 1g/h IV until delivery or for a total of 24h; antidote: Calcium Gluconate 10% 1g IV.
Single cutoff in Calculator: FIGO/WHO.
6Fetal lung maturation: comparison of 5 guidelines (Wynne 2020)
| Guidelines (year) | Gestational age | Steroid |
|---|---|---|
| RCOG / NICE (2015) | 24⁰/⁷-33⁶/⁷ weeks; consider 23⁰/⁷-23⁶/⁷ and 34⁰/⁷-35⁶/⁷ | Not specified |
| ACOG (2017) | 24⁰/⁷-36⁶/⁷ weeks with risk of delivery within 7 days; consider 23⁰/⁷-23⁶/⁷ based on family decision | Betamethasone or dexamethasone |
| RANZCOG (2015) | 24⁰/⁷-34⁶/⁷ weeks; up to 39⁰/⁷ if pulmonary immaturity is confirmed (amniocentesis, L/E ratio) | Betamethasone or dexamethasone |
| FIGO (2019) | 24-34 weeks; <24 weeks to be discussed with the family/clinician; consider 34⁰/⁷-36⁶/⁷ | Betamethasone or dexamethasone |
| WHO (2015) | 24⁰/⁷-34⁰/⁷ weeks, without evidence of maternal infection and with care available for delivery/newborn | Betamethasone or dexamethasone |
Table adapted (translated) from Wynne K et al. F1000Research 2020;9:F1000 Faculty Rev-219 (Table 1) · CC BY 4.0 License (use permitted with attribution). Single cutoff in Calculator: NICE.
7Rescue course, benefits and long-term risks of corticosteroids
- Do not repeat routinely. Single rescue course if risk of delivery recurs, the previous course was >14 days ago, and gestational age is <34 weeks (risk of delivery within 7 days).
- Benefits: reduces neonatal RDS by 34%, neonatal mortality by 31%, intraventricular hemorrhage by 46%, and necrotizing enterocolitis by 54%.
- Betamethasone vs dexamethasone (ASTEROID, Crowther 2019): no difference in the primary outcome (death or neurodevelopmental disability at 2 years: 33% vs 32%; RR 0.97). With dexamethasone: fewer cesarean deliveries (43% vs 52%; RR 0.84) and less hypertension at 2 years (32% vs 41%; RR 0.78). Intraventricular hemorrhage did not differ (RR 1.09; p=0.72).
| Group | Outcome | Measure |
|---|---|---|
| Extremely preterm | ↓ neurodevelopmental impairment | aOR 0.69 (0.57-0.84) — ~31% lower |
| Extremely preterm | ↓ cerebral palsy | aOR 0.60 (0.43-0.83) — ~40% lower |
| Late preterm | ↑ neurocognitive disorders | aHR 1.12 (1.05-1.20) — ~12% higher |
| Term (≥37 weeks) | ↑ mental/behavioral disorders | aHR 1.47 (1.36-1.60) — ~47% more |
| Term (≥37 weeks) | ↑ neurocognitive disorders | aHR 1.16 (1.10-1.21) — ~16% more |
CaVeSal® proprietary algorithm · Based on: Crowther CA et al. ASTEROID, Lancet Child Adolesc Health 2019;3(11):769-780 · Ninan K et al. JAMA Pediatr 2022;176(6):e220483.
Supports the rule against routine use of corticosteroids in late preterm/term infants or repeating courses. Räikkönen et al., JAMA 2020 (670,097 children): HR 1.33 (1.26-1.41) for any mental/behavioral disorder.
8Cerebral palsy: risk by gestational age at birth
| Gestational age at birth | Relative risk |
|---|---|
| 34-36 weeks | ~3× |
| 30-33 weeks | ~8× |
| 28-30 weeks | ~46× |
| <28 weeks | ~80× |
CaVeSal® proprietary algorithm · Based on: Petrini JR et al. Increased risk of adverse neurological development for late preterm infants. J Pediatr 2009;154(2):169-76 · Stanley FJ. Survival and cerebral palsy in low birthweight infants: implications for perinatal care. Paediatr Perinat Epidemiol 1992;6:298-310 · Moster D et al. NEJM 2008;359(3):262-273.
Prevalence of cerebral palsy: 2-2.5/1000 live births, inversely proportional to gestational age. Prematurity accounts for 75% of perinatal deaths and 50% of neurological abnormalities (excluding malformations).
Justifies prioritizing neuroprotection at the earliest gestational ages. Citation chain: Petrini 2009 (J Pediatr; HR 3.39 at 34-36 weeks), Stanley 1992 (Paediatr Perinat Epidemiol), Moster 2008 (NEJM; RR 78.9 at 23-27 weeks). The 8× value has no specific primary reference identified.
9MgSO4: regimens by author and neuroprotection protocol
| Regimen | Loading dose | Maintenance |
|---|---|---|
| Pritchard | 4 g IV over 5 min + 5 g IM in each buttock | 5 g IM every 4 h for 24 h after birth or the last seizure |
| Zuspan | 4 g IV over 20 min | 1-2 g IV per hour |
| Sibai | 6 g IV over 20-30 min | 2 g IV per hour (some educational sources: 2-3 g/h) |
| Regimen | Loading and maintenance | Timing |
|---|---|---|
| A — standard (FIGO 2021, SOGC 2019, NICE) — used in the calculator | 4 g IV over 20-30 min + 1 g/h | Start as close as possible to 4 h before delivery; continue until delivery or 24 h; do not repeat the loading dose |
| B — high dose (Sibai / Rouse) | 6 g over 20-30 min + 2 g/h | Stop at 12 h if delivery is no longer imminent; if risk recurs after ≥6 h, repeat the loading bolus |
CaVeSal® proprietary algorithm · Based on: Doyle, Cochrane 2007 · SOGC · FIGO 2021 · SOGC 2019 · NICE · Martínez Gallegos 2024.
The sequence “4 h before, 12 h, repeat at 6 h” mixes the two regimens. Alternative dose (Martínez Gallegos 2024): loading dose 5 g IV in 100-200 cc of 5% dextrose over 30 min; maintenance 20 g in 500 cc of 5% dextrose at 7 drops/min.
10Magnesium toxicity: correlation with serum magnesium concentration
| Level | mmol/L | mEq/L | mg/dL | Effect |
|---|---|---|---|---|
| Therapeutic | 2-3,5 | 4-7 | 5-9 | Therapeutic range |
| Early toxicity | >3,5 | >7 | >9 | Loss of deep tendon reflexes |
| Moderate toxicity | >5 | >10 | >12 | Respiratory paralysis |
| Severe toxicity | >12,5 | >25 | >30 | Cardiac arrest |
Hourly monitoring: blood pressure and pulse, respiratory rate, deep tendon reflexes, and urine output. Antidote: calcium gluconate 1 g IV slowly (over 3-4 min; some sources indicate up to 10 min).
Serum magnesium measurement is optional, depending on availability; clinical monitoring remains the mainstay. Thresholds vary slightly between sources (e.g., StatPearls places respiratory paralysis at 12-15 mg/dL).
CaVeSal® proprietary algorithm · Based on: subcards 6-10: Wynne K et al. F1000Research 2020 · Crowther CA et al. ASTEROID, Lancet Child Adolesc Health 2019;3(11):769-780 · Ninan K et al. JAMA Pediatr 2022;176(6):e220483 · Räikkönen K et al. JAMA 2020;323(19):1924-1933 · Petrini JR et al. J Pediatr 2009 · Moster D et al. NEJM 2008;359(3):262-273 · Stanley FJ. Paediatr Perinat Epidemiol 1992;6(2):298-310 · Sibai BM et al. Am J Obstet Gynecol 1984;150(6):728-733 · SOGC No. 376, Magee et al. 2019 · FIGO, Shennan et al. 2021 · Doyle LW et al. Cochrane 2007 · ACOG Practice Bulletin No. 222 (2020).
Source: ACOG Practice Bulletin No. 171 (2016, reaffirmed 2020) · NICE Guideline NG25 (2019, updated 2022) · FIGO Recommendations on Preterm Birth (2021).
Hyperemesis Gravidarum and PUQE Scale
Differential diagnosis, PUQE scale, stepwise pharmacologic treatment, and safe rehydration. This module is also available in Calculator Mode with interactive PUQE.
1Diagnosis and differentiation
NVP (Nausea and Vomiting of Pregnancy): physiological/mild, affecting up to 80% of pregnant patients, onset at weeks 4-9, resolution at weeks 16-20.
HG (Hyperemesis Gravidarum): severe and intractable form, 0.3-2% of pregnancies. Classic triad:
- Intractable vomiting.
- Weight loss >5% of prepregnancy weight.
- Ketonuria/ketonemia + electrolyte abnormalities (hypokalemia, hypochloremia, metabolic alkalosis).
2PUQE Scale (assesses the previous 24h — 3 questions, 1-5 points each, total range 3-15)
| Question | 1 point | 5 points |
|---|---|---|
| P1 — Duration of nausea | None | >6 hours |
| P2 — Episodes of retching without vomiting | None | ≥7 |
| P3 — Episodes of vomiting | None | ≥7 |
| Total score | Classification | Management |
|---|---|---|
| ≤6 | Mild NVP | Outpatient / dietary |
| 7-12 | Moderate NVP | Outpatient pharmacologic treatment |
| ≥13 | Severe HG | Hospital care / parenteral hydration |
CaVeSal® proprietary algorithm · Based on: Koren G et al. 2002 y 2005 (PUQE scale) · ACOG PB 189 (2018).
3Stepwise pharmacologic treatment
| Line | Scenario | Medications and doses |
|---|---|---|
| 1st line | Mild to moderate, outpatient | Pyridoxine (B6) 10-25mg orally q6-8h; preferred combination: Doxylamine 10mg + Pyridoxine 10mg (2 tablets at bedtime, up to 4 tablets/day). |
| 2nd line | Persistent / moderate to severe | Dimenhydrinate 50-100mg orally or rectally q4-6h; Metoclopramide 10mg IV/orally q8h (avoid >5 days, risk of extrapyramidal effects); Promethazine 12.5-25mg orally/IV/rectally q4-6h. |
| 3rd line | Severe HG / hospitalized | Ondansetron 4-8mg IV/orally q8h (preferably from week 10 because of debate about cleft palate); Methylprednisolone 16mg IV/orally q8h x3 days, then taper (restricted to >10 weeks, risk of orofacial cleft). |
CaVeSal® proprietary algorithm · Based on: ACOG PB 189 (2018, reaffirmed 2021) · RCOG GTG 69 (2016).
4Rehydration and hospital safety
0.9% Normal Saline or Lactated Ringer’s solution.
| 🚫 Golden safety rule: Thiamine (B1) 100mg IV BEFORE or WITH the first infusion of glucose-containing fluids — never administer dextrose alone to a malnourished patient without prior thiamine (prevents Wernicke encephalopathy/osmotic demyelination). |
KCl replacement according to the electrolyte panel.
CaVeSal® proprietary algorithm · Based on: ACOG Practice Bulletin No. 189 (2018, reaffirmed 2021) · Koren G. et al. (2002, 2005) — validation of the PUQE scale · RCOG Green-top Guideline No. 69 (2016).
Labor Progress — Preventing the First Cesarean Delivery
Three partograph models (Ministry CLAP, WHO 2020, ACOG 2024) with usage flowcharts, arrest criteria, and prevention of the first cesarean delivery.
1Active-phase onset — three sources, not combined
| Source | Active-phase onset | Expected progression |
|---|---|---|
| Ministry CLAP — MSPBS partograph (PAHO/WHO-CLAP) | 4 cm | Alert line (1 cm/h) and action line 4 h later |
| WHO 2020 — Labour Care Guide | 5 cm | Maximum time per centimeter; no 1 cm/h rule if mother and fetus are well |
| ACOG 2024 — CPG 8 (ratifies the ACOG/SMFM 2014 consensus) | 6 cm | Hours without cervical change, no fixed cm/h |
CaVeSal® proprietary algorithm · Based on: MSPBS · WHO · CLAP · FIGO · Labour Care Guide 2018 · ACOG.
The three sources are shown separately, without merging. The Calculator’s dynamic partograph (Childbirth tab) lets you choose the model: Ministry CLAP (default), WHO 2020 or ACOG 2024. How to use each: cards 9 to 12.
2Key ACOG/SMFM recommendations 2014 (Grade 1B — strong recommendation)
- Prolonged latent phase (>20h nulliparous, >14h multiparous in the 2014 consensus; ACOG 2024: >16 h in nulliparous patients) should NOT be an indication for cesarean delivery on its own.
- Slow but progressive active phase (not arrested) should not be an indication for cesarean delivery.
- Operative vaginal delivery (forceps/vacuum) in the 2nd stage by trained personnel: a reasonable alternative to cesarean delivery — training should be encouraged.
- Fetal monitoring: appropriate use of CTG categories (ACOG/NICHD classification) to reduce unnecessary cesarean deliveries for suspected fetal compromise, including intrauterine resuscitation measures before cesarean delivery.
- External cephalic version for breech presentation from 36 0/7 weeks, when there is no contraindication.
- Elective induction only with a favorable cervix, or after considering the risk of failure if the cervix is unfavorable.
- Fetal macrosomia: elective cesarean delivery for suspected macrosomia should be limited to an estimated fetal weight ≥ 5000g (or ≥ 4500g if diabetes is present) — do not perform routine cesarean delivery for suspected macrosomia without reaching that threshold (weak recommendation, lower-quality evidence).
3Active-phase arrest (1st stage) — ACOG 2024
Diagnose only if:
- Dilation ≥ 6 cm, AND
- Ruptured membranes, AND
- No cervical progress despite ≥ 4 h of adequate uterine activity (more than 200 MVUs with an intrauterine pressure catheter), or ≥ 6 h of inadequate activity with oxytocin
Source: ACOG CPG 8 (2024). Detail and flowchart in sheet 11.
4Prolonged second stage (pushing) — ACOG 2024
| Parity | ACOG 2024 (current) | Traditional definition (no longer current) |
|---|---|---|
| Nulliparous | More than 3 h of pushing | 3 h with an epidural · 2 h without an epidural |
| Multiparous | More than 2 h of pushing | 2 h with epidural · 1 h without epidural |
CaVeSal® proprietary algorithm · Based on: ACOG CPG 8 (2024) · ACOG/SMFM Obstetric Care Consensus No. 1 (2014).
Beyond these time limits, ACOG recommends an individualized approach (progress of descent, epidural, occiput posterior position, patient preference) before diagnosing arrest. The traditional definition is shown for historical reference only.
5Ministry CLAP Partograph — MSPBS Paraguay model
| Parameter | Official MSPBS value |
|---|---|
| Latent phase | <4 cm |
| Active phase / start of the partograph | ≥4 cm |
| Expected dilatation | ≥1 cm/hour |
| Recording | Above the alert line from 4 cm; normal progress on or to its left |
| Alert line → action line | 4 hours (time to refer, reassess and correct causes) |
| Upon reaching the action line | Final assessment and decision on the safest mode of delivery |
CaVeSal® proprietary algorithm · Based on: MSPBS — Standards for Preconception, Prenatal, Labor, Birth and Postpartum Care · WHO partograph, Lancet 1994;343:1399-404 · CLAP/SMR 1577 (2011).
Recording frequency: FHR, contractions and maternal pulse every 30 min · temperature every 2 h · BP every 4 h · at each vaginal examination: dilatation, descent and molding. Amniotomy: not routine; only for abnormal progress.
The manual does not name Friedman: it is cited as the WHO/CLAP partograph (alert/action line, 1994). Sources: MSPBS — Standards for Preconception, Prenatal, Labor, Birth and Postpartum Care · WHO partograph, Lancet 1994;343:1399-404 · CLAP/SMR 1577 (2011).
6WHO 2020 Labour Care Guide
- Active phase from 5 cm; do not apply the 1 cm/h rule to justify interventions if the mother and fetus are stable.
- Companion of choice and freedom of position.
- Vaginal examination every 4 h in uncomplicated active labor.
- Intermittent auscultation (Pinard/Doppler): every 15-30 min during dilatation, every 5 min or after each contraction during the second stage.
- Second stage: non-supine positions, spontaneous pushing, perineal protection or warm compresses, restrictive episiotomy.
- Third stage: oxytocin 10 IU IM/IV, controlled cord traction, cord clamping at 1-3 min.
- Newborn: skin-to-skin contact for 60-90 min, breastfeeding in the first hour; defer anthropometric measurements, eye prophylaxis and vitamin K; bathing after 24 h.
Practices NOT routinely recommended: enema, pubic shaving, admission pelvimetry, prophylactic IV access in low-risk patients, early amniotomy, oxytocin to shorten labor, routine episiotomy, Kristeller maneuver (prohibited).
Sources: WHO Intrapartum care for a positive childbirth experience (2018) · WHO Labour Care Guide (2020) · FIGO 2019 (third stage, IJGO 145:256-8) · Lalonde A. IJGO 2012;119:84-7.
7Birth positions
| Recommendation | Benefit |
|---|---|
| Semi-sitting / obstetric chair | Less blood loss and PPH; comfortable for the clinician |
| Upright / standing with support | More effective contractions, improved fetal oxygenation |
| Classic lithotomy | Fewer perineal lacerations (according to the source) |
| Seated on a birth stool | More effective contractions, pain relief |
| All fours | Less perineal trauma, facilitates descent |
| Supported squatting | Increases pelvic diameters |
CaVeSal® proprietary algorithm · Based on: Lugones Botell M, Ramírez Bermúdez M. El parto en diferentes posiciones a través de la ciencia, la historia y la cultura. Rev Cubana Obstet Ginecol 2012;38(1):134-45 (cited in the UdeA/UNFPA workshop).
WHO recommends free choice of position, not one mandatory position. Source: Lugones MB. Rev Cubana Obstet Ginecol 2012;38(1) (UdeA workshop).
8Labor pain, analgesia, cord clamping, and bonding
- Labor pain is physiological; nonpharmacological pain relief: warm water, movement, breathing, massage, and continuous support.
- In the absence of contraindications, maternal request alone is a sufficient indication for an epidural.
- Delayed cord clamping (1-3 min): less neonatal anemia and fewer transfusions, improved transition, and placental blood transfer (Edmonds 2013).
- Skin-to-skin contact: warmth, bonding and attachment, greater breastfeeding success; requires continuous support from the team.
Sources: WHO 2018 · Edmonds P. Midwifery Today 2013;(108):58-62 · UdeA workshop.
9How to use the Ministry CLAP Partograph — flowchart
Do not open the partograph. Ambulation, oral hydration, monitoring of FHR and contractions; reassess according to progress.
Mark the first point (X for dilation) on the alert line; the action line is 4 h to the right.
Normal progress: continue the plan (ambulation, oral hydration, light meals, position changes).
Assess causes (uterine activity, fetal position, possible cephalopelvic disproportion) and correct them. The 4 h until the action line are for timely referral if birth is not imminent.
Final assessment and decision on the safest mode of delivery.
| Intensity | Duration | CaVeSal® Calculator | Classic paper form |
|---|---|---|---|
| Mild | Less than 20 s | Light shading | Points |
| Moderate | 20 a 40 s | Medium shading | Dashed |
| Bold | Greater than 40 s | Dark tone | Solid shading |
CaVeSal® proprietary algorithm · Based on: MSPBS — Care Standards (PAHO/WHO-CLAP partograph) · MSPBS — Safe Birth Protocol · shading by duration: Bettercare — Maternal Care y J Obstet Gynecol India.
Descent: the calculator allows it to be recorded in Hodge planes (default) or in palpable fifths by abdominal examination. In the calculator: Labor → Dynamic partograph → “Ministry CLAP” model.
10How to use the WHO 2020 Guide (Labour Care Guide) — flowchart
Do not open the guide; do not apply active-phase thresholds.
One column per assessment: supportive care, baby, woman, labor, medication, plan.
Continue care. Progress slower than 1 cm/h, by itself, does not indicate intervention.
Circle it, notify the most experienced obstetrician or physician, document the assessment and plan, and share them with the woman.
| Section | Alert if… |
|---|---|
| Cervix (time at the same cm) | 5 cm ≥6 h · 6 cm ≥5 h · 7 cm ≥3 h · 8 cm ≥2,5 h · 9 cm ≥2 h |
| Second stage | ≥3 h nulliparous · ≥2 h multiparous |
| Baby | Baseline FHR <110 or ≥160 · late decelerations (L) · amniotic fluid M+++ or blood-stained (B) · occiput posterior or transverse position · caput +++ · molding +++ |
| Woman | Pulse <60 or ≥120 · SBP <80 or ≥140 · DBP ≥90 · temperature <35 or ≥37,5 °C · protein or acetone in urine ++ |
| Contractions | ≤2 or >5 in 10 min · duration <20 or >60 s |
| Supportive care | No birth companion, no pain relief, or no oral fluids (N) · supine position (SP) |
CaVeSal® proprietary algorithm · Based on: WHO Labour Care Guide (2020) · Jhpiego — LCG Participant ManualOriginal design; does not reproduce the form (CC BY-NC-SA).
Variable decelerations (V) are recorded but are not alerts. The guide has no alert or action lines. In the calculator: Labor → Dynamic partograph → “WHO 2020” model (dynamic table with alerts marked).
11ACOG 2024 (CPG 8) — active phase begins at 6 cm and criteria for arrest
Do not apply active-phase criteria. Prolonged latent phase: >16 h (nulliparous women). There is no definition of latent-phase arrest: avoid cesarean delivery for this reason if the mother and fetus are well.
Yes: count the time without cervical change.
No cervical change for ≥4 h → active-phase arrest.
No cervical change for ≥6 h → active-phase arrest.
Consider augmentation before measuring.
| Item | What ACOG says |
|---|---|
| Onset of the active phase | 6 cm (strong recommendation). There may be a range between 4 and 6 cm, but active-phase standards do not apply before 6 cm. |
| Active-phase arrest | ≥6 cm with ruptured membranes and no progress despite 4 h of adequate uterine activity, or 6 h of inadequate activity with oxytocin. |
| Adequate contractions | More than 200 Montevideo units (MVU) measured with an intrauterine pressure catheter. |
| Prolonged second stage | More than 3 h of pushing in nulliparous patients and more than 2 h in multiparous patients. Beyond these time limits, use an individualized approach (descent progress, epidural, occiput posterior position, patient preference). |
CaVeSal® proprietary algorithm · Based on: ACOG Clinical Practice Guideline No. 8 — First and Second Stage Labor Management (2024).
In the calculator the “ACOG 2024” model has a selector: with a catheter (textual criterion, MVU >200) or without a catheter, with a contraction counter (clinical adaptation: strong contractions every 3 min or less, according to FPQC/USF PROVIDE). Intensity is marked as mild, moderate, or strong by palpation.
12Comparison of the three calculator models
| Item | Ministry CLAP (default) | WHO 2020 | ACOG 2024 |
|---|---|---|---|
| Dilation | 4 cm, over the alert line | 5 cm | 6 cm (active phase) |
| How progress is assessed | Alert line (1 cm/h) and action line 4 h later | Maximum time at each centimeter | Hours without cervical change (4 h or 6 h) |
| Contractions | Number in 10 min + intensity on a 3-level scale (mild, moderate, strong) | Number in 10 min + duration in seconds | Number + mild, moderate, or strong; adequacy with or without a catheter |
| Membranes | Recorded | Recorded (M+ to M+++, B) | Ruptured: required to diagnose arrest |
| Second stage | Up to 2 h | Alert ≥3 h for nulliparous women, ≥2 h for multiparous women | Prolonged: >3 h of pushing for nulliparous women, >2 h for multiparous women |
| If deviation | Assess causes, correct them, and refer in a timely manner; decide the mode of delivery during management | Alert: notify, assess, and agree on a shared plan | Arrest: assess for cesarean delivery or operative vaginal delivery |
CaVeSal® original table · sources in cards 9, 10, and 11.
Variant (reference only, not in the calculator): the partograph with CLAP alert curves (Schwarcz et al.) uses five curves according to parity, maternal position (upright or horizontal), and membrane status, constructed using the 10th percentile of 1188 normal births. Source: Ministry of Health of Argentina — Resolution 647/2003, Chapter 2. The Ministry of Paraguay uses the alert and action line model described in card 9.
Source: ACOG/SMFM Obstetric Care Consensus No. 1 (2014) — Safe Prevention of the Primary Cesarean Delivery. · ACOG CPG 8 (2024) · MSPBS — Standards of Care · WHO Labour Care Guide (2020).
First-Half Bleeding — Miscarriage, Ectopic Pregnancy, Cervical Insufficiency/Cerclage
Differential diagnosis <20-22 weeks, luteal support, anti-D prophylaxis, and cervical insufficiency with cerclage.
1Differential diagnosis (<20-22 weeks)
| Condition | Bleeding | Pain / uterine activity | Internal os | Key findings |
|---|---|---|---|---|
| Threatened miscarriage | Scant/moderate | Mild cramping | CLOSED | Viability confirmed by ultrasound |
| Miscarriage in progress/inevitable | Heavy | Progressive contractions | OPEN ± protruding tissue/PROM | — |
| Incomplete miscarriage | Persistent active | Partial expulsion | Patent | Ultrasound: heterogeneous endometrial thickness >15mm |
| Complete miscarriage | Bleeding stops | Pain resolves, complete expulsion | Closed | Homogeneous endometrial stripe <10-15mm |
| Missed miscarriage | No active bleeding | No cervical changes | Closed | Retained embryonic/fetal demise |
| Ectopic pregnancy | Dark, scant | Adnexal pelvic pain + amenorrhea (triad) | — | β-hCG above the discriminatory zone >1500-2000 IU/L without an intrauterine gestational sac |
| Gestational trophoblastic disease / hydatidiform mole | With "bunch of grapes" vesicles | — | — | Uterus larger than expected for gestational age, β-hCG >100.000 IU/L, "snowstorm" appearance on ultrasound |
CaVeSal® proprietary algorithm · Based on: ACOG PB 200 (2018) · NICE NG126 (2019/2023).
2Management of threatened miscarriage
General measures: relative rest, sexual abstinence, avoid repeated vaginal examinations.
Progesterone — CaVeSal recommends: micronized progesterone 400 mg vaginally every 12 h until week 16, even without a history of miscarriage.
Variants: MSPBS 2018 not routinely indicated · NICE NG126 only with ≥1 prior miscarriage (PRISM trial) · in favor: RANZCOG, FOGSI 2024, Cochrane 2018 y Cochrane 2021.
- Micronized progesterone 400mg vaginally every 12h until week 16.
- Alternative: Dydrogesterone 40mg orally initially, then 10mg every 8h.
Anti-D prophylaxis: if Rh-negative, unsensitized, with clinically significant bleeding → anti-D immunoglobulin 120-300mcg IM within the first 72h.
3Cervical insufficiency (CI) and cerclage
Definition: inability of the cervix to retain the pregnancy in the absence of contractions/clinical abruption, with painless dilation/effacement in the 2nd trimester (16-24 weeks) → recurrent fetal loss or extreme preterm birth.
Types:
- History-indicated (prophylactic/elective): ≥2-3 prior unexplained painless 2nd-trimester losses or preterm births. Timing: week 12⁺⁰-14⁺⁶ (after confirming viability and ruling out aneuploidy).
- Ultrasound-indicated (therapeutic): prior spontaneous preterm birth <34 weeks + cervical length <25mm on transvaginal ultrasound surveillance before week 24.
- Emergency/rescue: painless dilation with membranes protruding into the vagina/external cervical os between weeks 16-24, without active labor, chorioamnionitis, or placental abruption.
Classification: primary (congenital, malformations, collagen disorders) or secondary (conization, dilations, lacerations). Prophylactic cerclage (based on history), therapeutic cerclage (based on ultrasound), or emergency cerclage (based on physical examination) (Ginecol Obstet Méx 2020).
By history — variants: RCOG GTG 75: ≥3 losses or preterm births in the 2nd trimester; with 1-2, serial ultrasound at 16-24 weeks and cerclage if ≤25 mm. ACOG: may be offered after 1 typical loss.
Short cervix without prior history (≤20 mm): vaginal progesterone; cerclage is not indicated.
| Technique | Particularity |
|---|---|
| McDonald | Submucosal purse-string without dissection, nonabsorbable suture (Mersilene); most commonly used |
| Shirodkar | Vesicocervical dissection, higher suture placement |
| Espinosa Flores (Mexico, 1966) | Simple transcardinal ligature without mucosal dissection; short procedure and easy removal |
| Abdominal (Benson-Durfee) | By laparotomy or laparoscopy, preconceptionally or at 10-14 weeks, after failed vaginal cerclage or with a very short cervix; delivery by cesarean |
CaVeSal® proprietary algorithm · Based on: GPC IMSS 539 · UNAM (Espinosa Flores) · FASGO 2021 · ACOG PB 142.
Contraindications: active labor, intra-amniotic infection, active bleeding, PROM, placental abruption, lethal fetal anomaly, or fetal demise.
Fetal fibronectin: does not diagnose cervical insufficiency; predicts preterm birth in preterm labor (high negative predictive value).
Cerclage removal: scheduled electively at 36-37 weeks (or immediately if active labor/chorioamnionitis).
4Abortion: classification and evacuation
| Type | <13 weeks | 13-22 weeks |
|---|---|---|
| Threatened miscarriage (incipient) | Expectant ± progesterone (see card 2); anti-D if Rh(-) | |
| In progress: imminent (dilated cervix) or inevitable (PROM) | MVA | Expulsion (oxytocin/misoprostol) + D&C |
| Incomplete | MVA, or misoprostol 600 µg PO / 400 µg SL (WHO); MSPBS: 400-800 µg vaginally | D&C after cervical preparation |
| Complete | No evacuation; clinical follow-up | |
| Missed (fetal demise confirmed on ultrasound) | Misoprostol 800 µg vaginally every 3 h ×2 or 600 µg SL every 3 h ×2 → MVA | Misoprostol 200 µg every 4-6 h up to 5 doses (every 6 h with uterine scar); oxytocin 16-22 wk → D&C |
CaVeSal® proprietary algorithm · Based on: MSPBS 2018 (p. 63) · WHO 2022 · NICE NG126.
Evacuation: WHO recommends aspiration and advises against sharp curettage before 14 weeks; MSPBS uses MVA before 13 and D&C from 13 to 22. The calculator ends at 13 weeks.
5Infected and septic abortion
- With sepsis or septic shock: IV antibiotics within the 1st hour + immediate evacuation for source control (Code Yellow — Sepsis, Rule 4-5-3; SSC 2021).
- Without sepsis: IV antibiotics and evacuation 6-8 h after initiation (Clinical Practice Guideline IMSS-088, Ecuador Clinical Practice Guideline). Other guidelines: 12 h or 24-48 h.
- MSPBS regimens (72 h): ampicillin + metronidazole · cefazolin + metronidazole · ceftriaxone + metronidazole · gentamicin + metronidazole · gentamicin + clindamycin · ampicillin/sulbactam + clindamycin · ampicillin 2 g + gentamicin 5 mg/kg + metronidazole.
6Recurrent pregnancy loss
- WHO / RCOG GTG 17: 3 consecutive losses.
- ESHRE 2022 / ASRM: ≥2, not necessarily consecutive.
- National literature (Acosta, Paraguay): 3 consecutive or 5 nonconsecutive losses.
Management: genetic counseling and gynecologic-obstetric and reproductive evaluation.
7Pregnancy of unknown location and ectopic pregnancy
PUL: do not treat without ultrasound confirmation; βhCG at 48 h with a minimum rise of 49 % (<1500), 40 % (1500-3000) or 33 % (>3000) (AAFP 2020).
Complicated (free fluid, severe pain, instability): emergency surgery + Code Red; salpingectomy is preferred.
| Management | CaVeSal (calculator) | MSPBS 2018 | NICE NG126 |
|---|---|---|---|
| Expectant | β-hCG <1000 and declining, no criteria | β-hCG <5000, mass ≤35 mm, fluid ≤300 mL, no heartbeat | ≤1000 offer; 1000-1500 consider |
| Methotrexate 50 mg/m² IM | β-hCG 1000-<5000, mass <35 mm, no heartbeat | β-hCG <6000, mass ≤40 mm | <1500 first-line; 1500-5000 either option |
| Surgery | ≥5000, mass ≥35 mm, heartbeat or pain | Outside criteria; salpingectomy | ≥5000, ≥35 mm, heartbeat or pain |
CaVeSal® proprietary algorithm · Based on: MSPBS 2018 · NICE NG126 (ectopic pregnancy).
Methotrexate follow-up: β-hCG on days 4 and 7; decline ≥15 % → weekly until negative; otherwise, second dose or surgery. Anti-D if Rh(-).
Non-tubal ectopics (RCOG GTG 21): cervical → methotrexate; for evacuation, uterine artery embolization or vaginal uterine artery clamping (Zea technique) · cesarean scar → neither expectant management nor systemic methotrexate alone; aspiration or resection · interstitial/cornual → methotrexate or cornual resection · abdominal → early laparoscopy; advanced, laparotomy with the placenta left in situ.
8Hydatidiform mole
Diagnosis: complete (snowstorm appearance, enlarged uterus, very high β-hCG, diploid) vs. partial (fetus, placenta with cysts, triploid). Chest X-ray in all cases.
Treatment: suction evacuation with oxytocin started at the time of aspiration; histopathology in all cases; contraception.
| Source | Regimen |
|---|---|
| Ministry (MSPBS) — by default | Weekly → every 2 weeks → monthly until 3 negative results; monthly for 6 months and every 2 months for 6 months (1 year). Chest X-ray at 14 days, 6 and 12 months |
| RCOG 2020 | Complete: normal before 56 days → 6 months from evacuation; otherwise, 6 months from normalization. Partial: 2 normal samples 4 weeks apart |
CaVeSal® proprietary algorithm · Based on: MSPBS 2018 · RCOG 2020.
Sources: ACOG Practice Bulletin No. 200 — Early Pregnancy Loss (2018, reaffirmed 2021) · ACOG Practice Bulletin No. 142 — Cerclage for the Management of Cervical Insufficiency (2014, reaffirmed 2021) · NICE Guideline NG126 — Ectopic pregnancy and miscarriage (2019, updated 2023).
Second-half hemorrhage — placental abruption, placenta previa, uterine rupture, vasa previa
Differential diagnosis of the 4 main causes, ACOG/RCOG management, MSPBS/SPGO variant + 2021 Code Red, and emergency protocols.
1Differential diagnosis of the 4 main causes
| Cause | Bleeding | Pain / uterine tone | Fetal status | Context |
|---|---|---|---|---|
| Placental abruption | Dark | Sudden, severe abdominal pain, uterine hypertonia/boardlike uterus | Rapid onset of acute fetal distress | Common with preeclampsia/trauma |
| Placenta previa | Bright red, painless | Normal uterine tone (soft uterus) | Fetal heart rate initially normal | Insidious onset |
| Uterine rupture | Variable | Acute, lacerating intrapartum pain, abrupt cessation of uterine contractions | Maternal shock + extreme fetal bradycardia | History of cesarean delivery/myomectomy common; loss of fetal station |
| Vasa previa | Immediately after rupture of membranes, 100% of fetal origin | — | Bradycardia/severe decelerations | High immediate fetal mortality |
| 🚫 DIGITAL VAGINAL EXAMINATION IS PROHIBITED if placenta previa is suspected — it may precipitate massive hemorrhage. |
CaVeSal® proprietary algorithm · Based on: ACOG PB 183 (2017) · RCOG GTG 63 · MSPBS/SPGO 2018 · MSPBS Code Red 2022.
2Management of Placenta Previa and Placental Abruption (ACOG/RCOG)
Placenta previa: Diagnosis by transvaginal ultrasound — placenta previa if it covers the internal os; low-lying placenta if <20mm from the internal os.
- Stable/no active bleeding: fetal lung maturation at 34-36⁺⁶ weeks; elective cesarean delivery at 36⁺⁰-37⁺⁶.
- Severe active hemorrhage: stabilization + immediate emergency cesarean delivery, regardless of gestational age.
Placental abruption: immediate delivery.
- Emergency cesarean delivery: general rule if the fetus is alive with compromise or the mother is unstable.
- Fetal demise: MSPBS recommends cesarean delivery for grades II and III; RCOG GTG 63 and the 2013 Colombian CPG accept vaginal delivery with a stable mother, early amniotomy, and oxytocin (see card 9).
3Paraguayan variant: MSPBS/SPGO + Code Red 2021 (additional variant)
Timing definition: bleeding in the second half of pregnancy = vaginal bleeding from 22.0 weeks until before birth.
Initial stabilization protocol:
- O2 via non-rebreather mask at 10 L/min, target SpO2 >95%.
- 2 large-bore peripheral IV lines (14G or 16G).
- Tube color code: blue (coagulation: PT/aPTT/fibrinogen), red/brown (chemistry), lavender (CBC + crossmatch/blood bank).
- Warm crystalloids at 37-39°C in 250-500 mL boluses, target SBP ≥90 mmHg while avoiding fluid overload.
- Check vital signs every 15 min with EAPO + Foley catheter, target urine output ≥30 mL/h.
Expectant management (placenta previa only) — eligibility: GA <34 weeks + scant/self-limited bleeding + stable mother + normal fetal well-being.
- Strict bed rest in the left lateral position.
- Lung maturation: Betamethasone 12mg IM every 24h ×2 doses or dexamethasone 6mg IM every 12h ×4 doses (if <34 weeks).
- Neuroprotection with MgSO4 if preterm labor is threatened at <32 weeks.
- Serial CBCs + strict monitoring of blood loss.
Indications for emergency cesarean delivery (regardless of GA): active moderate-to-severe bleeding unresponsive to conservative measures; hemodynamic instability/shock; acute fetal distress; confirmed placental abruption or uterine rupture/strong suspicion; complete placenta previa at term ≥37.0 weeks.
| Point | ACOG/RCOG | MSPyBS/SPGO |
|---|---|---|
| Elective cesarean delivery for stable placenta previa | 36⁺⁰-37⁺⁶ weeks | ≥37.0 weeks (at term) |
| Temporal definition of the condition | >20-22 weeks | ≥22.0 exact weeks |
CaVeSal® proprietary algorithm · Based on: MSPBS/SPGO · Code Red 2021 · ACOG · RCOG · SPGO.
4Uterine rupture: immediate management
- Activate the obstetric emergency team + notify the obstetrician on call.
- Left lateral position + supplemental oxygen by face mask; stop oxytocin infusion if running.
- 2 large-bore IV lines (16G), samples for CBC + coagulation studies + crossmatch for 6 units.
- Crystalloids/blood products as needed; continuous monitoring of vital signs + CTG.
- Prepare the operating room for emergency cesarean delivery — birth within 30 minutes of the decision (Category 1), anticipating neonatal resuscitation.
- In hemodynamic instability: fluid resuscitation/transfusion in parallel with surgical preparation, without waiting for complete stabilization before operating.
5Uterine rupture: intraoperative surgical management
Incision: Pfannenstiel incision provides good exposure of the lower uterine segment/pelvis; a vertical midline incision provides better exposure for exploring the entire abdominal cavity (including the uterine fundus)—preferred when fetal distress and maternal instability coexist.
Repair vs. hysterectomy: depends on the extent of the injury, patient stability, desire for future fertility, and surgeon experience — if adequate closure and hemostasis cannot be achieved → hysterectomy (usually subtotal).
Complications to manage: concomitant uterine atony (uterotonics + hemostatic sutures + intrauterine balloon); bladder injury if the laceration extends to the bladder, or suspected ureteral injury → consult urology.
Hemorrhage control after delivery if bleeding persists: abdominal packing, uterine artery ligation, internal iliac artery ligation, topical hemostatic agents, cesarean hysterectomy as a last resort.
General anesthesia is usual; regional/spinal anesthesia is contraindicated in cases of severe bleeding diathesis.
6Vasa previa: management
Antenatal diagnosis by ultrasound (color Doppler along the cervical route) allows elective cesarean delivery to be scheduled before the onset of labor — fetal survival >95% with antenatal diagnosis + planned cesarean delivery, vs. fetal mortality ≥60% when diagnosed intrapartum.
- Timing of elective cesarean delivery: SMFM Consult Series #37 recommends scheduled cesarean delivery between 34⁺⁰ and 37⁺⁶ weeks (GRADE 2C).
- Antenatal corticosteroids: consider between 28-32 weeks if there is a risk of urgent preterm delivery (GRADE 2C), not routinely in asymptomatic patients; a 2023 review suggests administering them within the 7 days before scheduled delivery.
- Antenatal hospitalization: proposed from 30-34 weeks in some series (GRADE 2C), but evidence is insufficient to make it a mandatory standard — individualized decision.
| 🚫 Undiagnosed vasa previa: high risk of rupture when membranes rupture — immediate emergency cesarean delivery in the event of bleeding + bradycardia/acute deceleration after amniotomy. |
CaVeSal® proprietary algorithm · Based on: SMFM.
7Placenta accreta spectrum (PAS)
| Grade | Intraoperative finding |
|---|---|
| 1 | Adherent placenta (creta): no myometrial invasion |
| 2 | Increta: myometrial invasion, without reaching the serosa |
| 3a | Percreta limited to the uterine serosa |
| 3b | Percreta with bladder invasion |
| 3c | Percreta with invasion of other pelvic tissues or organs |
| Cesarean delivery | 1ª | 2ª | 3ª | 4ª | ≥5ª |
|---|---|---|---|---|---|
| Risk of PAS | 3% | 11% | 40% | 61% | 67% |
Without placenta previa, risk ranges from 0.24% to 6.74% according to the number of cesarean deliveries.
Ultrasound signs (ISUOG 2016): loss of the retroplacental clear zone, placental lacunae, myometrial thinning <1 mm, disruption of the bladder line, placental bulge, focal exophytic mass; Doppler: uterovesical or subplacental hypervascularity and bridging vessels.
| Source | Window |
|---|---|
| ACOG/SMFM Obstetric Care Consensus No. 7 (2018) | 34+0 to 35+6 weeks |
| RCOG Green-top 27b (2018) | 35+0 to 36+6 weeks |
Management: level III-IV center with a multidisciplinary team and blood bank; corticosteroids if <37 weeks; tranexamic acid at onset; uterine incision away from the placenta and cesarean hysterectomy with the placenta in situ (do not attempt placental separation). Activate Code Red in the event of bleeding.
CaVeSal® proprietary algorithm · Based on: Jauniaux E et al. FIGO classification, Int J Gynaecol Obstet 2019 · FIGO — Classification of PAS disorders · Silver RM et al. Obstet Gynecol 2006;107:1226-32 · ACOG/SMFM OCC No. 7 · RCOG GTG 27b · ISUOG/EW-AIP 2016.
8Placenta previa — MSPBS details
- Classification: complete, partial, marginal, lateral (>2 cm from the internal os). Definitive diagnosis from 32 weeks.
- Expectant management <34+0 weeks with mild bleeding; from 34+0, cesarean delivery with recurrent bleeding. MSPBS mentions 35 weeks in one chapter; CaVeSal uses 34+0 for consistency.
- Asymptomatic complete previa: admission at 36 and cesarean at 37 (ACOG/SMFM: 36+0-37+6).
- Marginal previa in labor: amniotomy and trial of vaginal birth with the operating room ready; lateral previa: vaginal delivery may be possible.
- Tocolysis (hybrid): nifedipine only with preterm labor, light bleeding, and stability; avoid with heavy bleeding, instability, or fetal compromise (RCOG GTG 63).
- Prior cesarean: rule out placenta accreta (calculation in the CaVeSal prenatal calculator).
9Placental abruption — grades and management
| Grade | Findings | Management |
|---|---|---|
| I | <11 %, normal FHR | <34 weeks: monitored expectant management + antenatal corticosteroids; ≥34: delivery |
| II | ~50 %, uterine hypertonus, fetal compromise | Emergency cesarean delivery |
| III | >50 %, tetany, fetal death, shock, DIC | Cesarean delivery (MSPBS) + correction of coagulopathy |
CaVeSal® proprietary algorithm · Based on: MSPBS 2018 (p. 83).
- Fetal death — expectant management: RCOG GTG 63, Colombia CPG 2013 y Universidad Nacional de Colombia: vaginal delivery if the mother is stable, with early amniotomy and oxytocin.
- Tocolysis: optional in mild abruption <34 weeks with a stable mother and no fetal compromise, at the discretion of the senior obstetrician, to complete fetal maturation (observational studies).
- ≥34 weeks in advanced labor: vaginal delivery may be possible with amniotomy and continuous monitoring (NHS Worcestershire).
10Impending uterine rupture
| Sign | Description |
|---|---|
| Bandl | Pathological retraction ring rising toward the umbilicus (hourglass uterus) |
| Frommel | Taut round ligaments, palpable like cords |
| Pinard | Scant, dark vaginal bleeding (Paraguayan and classical literature); some sources describe it as cervical edema |
| Other | Uterine hyperactivity (oxytocin/misoprostol), hematuria, abnormal FHR |
CaVeSal® proprietary algorithm · Based on: Clínica Universidad de Navarra · Medway.
Impending: discontinue uterotonics, initiate acute uterine inhibition, and perform urgent cesarean delivery. Established: laparotomy; uterine repair if the rupture is not extensive and the patient is stable, hysterectomy if irreparable; evaluate the bladder if hematuria occurred.
11PAS and vasa previa — timing and conservative management
| Table | MSPBS | ACOG/SMFM | FIGO/RCOG |
|---|---|---|---|
| SBP | Hospitalization at 32 weeks; delivery at 36-37 | 34+0-35+6 | 35+0-36+6 |
| Vasa previa | — | 34+0-37+0; hospitalization at 30-34 individualized | — |
CaVeSal® proprietary algorithm · Based on: MSPBS 2018 · ACOG/SMFM · SMFM CS 44 · FIGO 2018.
- Planned PAS: TXA 1 g, incision away from the placenta, no traction or uterotonics, cesarean hysterectomy with the placenta left in situ.
- Conservative (focal, in centers with experience): placenta in situ, one-stage resection, arterial embolization (FIGO 2018 conservative management). MSPBS includes methotrexate; FIGO does not recommend it. Prophylactic iliac balloons: not routinely.
- Vasa previa with bleeding after PROM or a sinusoidal pattern: immediate cesarean delivery.
Sources: ACOG Practice Bulletin No. 183 — Postpartum Hemorrhage and Placenta Accreta Spectrum (2017) · RCOG Green-top Guideline No. 63 — Antepartum Haemorrhage (2018) · National Manual of Standards for the Care of Major Obstetric Conditions MSPBS+SPGO (2018) · Maternal and Neonatal Code Red Guide MSPBS, 2nd ed. (2021) · Queenan, Spong, Lockwood — Protocols for High-Risk Pregnancies, 7th ed. (2021) · RCOG Green-top Guideline No. 27b — Vasa Praevia · SMFM Consult Series #37 (Sinkey, Odibo, Dashe, Am J Obstet Gynecol 2015;213:615-619).
Normal Puerperium
Chronological classification, third stage of labor (Schultze and Duncan, timing), monitoring during the first 2 hours, uterine involution, lochia, and maternal supplementation.
1Chronological classification
- Immediate (first 24h): highest risk of PPH/4Ts — monitor vital signs, uterine tone (Pinard’s safety globe) and bleeding every 15 min for the first 2 h (MSPBS), then every 6 h — see flowchart in sheet 5.
- Early (day 2 to 7-10): onset of lactogenesis II, progressive intra-pelvic uterine involution (~1cm/day), red/serous lochia.
- Late (day 11 to 42/6 weeks): return of the genital organs to the pre-pregnancy state, resolution of lochia (alba), resumption of ovulation if not exclusively breastfeeding.
2Clinical checks and care
Uterine involution: the uterine fundus should not be palpable above the pubic symphysis from postpartum day 10-12.
| Type | Days | Characteristics |
|---|---|---|
| Red / bloody | 1-3/4 | Blood + decidual remnants |
| Serous | 4-10 | Pink/brown, exudate + leukocytes |
| White / alba | 10-28/42 | Whitish/yellowish, mucus + epithelial cells |
| ⚠️ Warning sign: foul odor (suspected puerperal endometritis) or persistent heavy bloody lochia after day 14 (suspected retained placental tissue/subinvolution). |
CaVeSal® proprietary algorithm · Based on: WHO 2022 (postnatal care) · ACOG CO 736 (2018).
Perineal/surgical wound care: wash with water and mild soap, pat dry, monitor for infection/dehiscence of episiotomy repair or cesarean incision.
4Third stage of labor — placental delivery
Definition (MSPBS): from the birth of the newborn until expulsion of the placenta. A period with potential risk of hemorrhage.
| Phase | What happens | Median duration |
|---|---|---|
| Latent | From birth until the onset of placental separation; myometrial-placental blood flow ceases. This phase determines the total duration | ~2 min (5 s – 13 min) |
| Separation | The placenta separates from the myometrium | ~50 s |
| Expulsion | From complete separation to passage through the vagina | ~80 s |
Signs of placental separation: lengthening of the cord · sudden gush of blood · the uterus rises and becomes globular (Schröder) · the cord does not retract with suprapubic pressure (Küstner). Both signs were positive in 98 % of placentas with ultrasound-confirmed separation.
| Mechanism | How it is expelled | Frequency and implications |
|---|---|---|
| Schultze | Central separation, expelled like an inverted umbrella: fetal surface first; the clot remains within the membranes | ~80 % · less visible bleeding before expulsion |
| Duncan | Separation from the edge, expelled sideways: maternal surface first | ~20 % · more bleeding and risk of retained membranes: inspect carefully |
Ultrasound shows that separation usually begins at the lower pole; the observed mechanism is determined as the placenta exits through the vulva.
Check placental and membrane integrity · uterine massage · checks every 15 min for 2 h
Controlled cord traction, mobilize or squat, empty the bladder. Monitor bleeding
| Source | Criterion | Status |
|---|---|---|
| WHO/FIGO/ICM 2025 (rec. 30) | Without PPH: intervene at 15 min; at 30 min, prepare for manual removal. With PPH: uterotonic and removal | Used by the calculator |
| NICE NG235 (1.10.20) | Prolonged: >30 min with active management; >60 min with physiological management | Variant |
| MSPBS 2022 | Active management: oxytocin 10 IU IM <1 min, controlled cord traction, massage; no routine intrauterine examination | National guideline |
CaVeSal® original table · Based on: MSPBS, Normas de Cuidados 2022, p. 69 · WHO/FIGO/ICM 2025, rec. 16, 30 and 31 · NICE NG235 (2023) · Herman et al., ultrasound and clinical findings in the third stage · El-Mowafi, GFMER — Schultze 80 % / Duncan 20 %. Third-stage timer in the calculator →
5Immediate postpartum period — first 2 hours and beyond
Postpartum hemorrhage: MOTIVE and Code Red. Do not transfer until stabilized
Mother and newborn to the inpatient ward (no bleeding, no infection, normal vital signs, nonhemorrhagic, non-foul-smelling lochia)
| Source | Frequency and parameters | Length of stay |
|---|---|---|
| MSPBS 2022 | Every 15 min for 2 h (uterus, Pinard, EAPO); then every 6 h | Discharge from 48 h onward |
| WHO 2018 (rec. 52 and 55) | Uterine tone in all women; routine assessment of bleeding, uterine contraction, fundal height, temperature, and pulse during the first 24 h, starting in the first hour; BP shortly after birth and, if normal, again within 6 h; documented urination within 6 h | Minimum 24 h after uncomplicated vaginal birth (rec. 56) |
| WHO/FIGO/ICM 2025 (rec. 22) | PPH criterion within 24 h, with special monitoring during the first 2 h | — |
CaVeSal® proprietary algorithm · Based on: MSPBS, Normas de Cuidados 2022, pp. 69-71 · WHO 2018, intrapartum care, rec. 52, 55 and 56 · WHO/FIGO/ICM 2025, rec. 22. Dynamic 2 h monitoring in the calculator →
6Maternal supplementation during the postpartum period/lactation
| Supplement | Dose | Notes |
|---|---|---|
| Elemental iron | 60-100mg/day PO | At least 3 months postpartum — especially in cases of peripartum blood loss or Hb<11g/dL |
| Folic acid | 400mcg/day PO | Together with iron |
| Calcium | 1000-1200mg/day | Diet or supplement if dairy intake is inadequate |
| Iodine | 150-200mcg/day | — |
| Vitamin D | 600-1000 IU/day | Maternal |
CaVeSal® proprietary algorithm · Based on: WHO — Recommendations on Maternal and Newborn Care for a Positive Postnatal Experience (2022) · ACOG Committee Opinion No. 736 — Optimizing Postpartum Care (2018, reaffirmed 2021).
Breastfeeding and Postpartum Mastitis
Physiology, diagnosis, and stepwise decision tree for mastitis, breast abscess, and drainage techniques.
1Physiology and basic technique
Hormonal axis: prolactin (production through suckling) + oxytocin (milk ejection through myoepithelial contraction).
Correct latch: mouth wide open, lower lip everted, covering most of the lower areola, chin against the breast, nose unobstructed.
Physiological breast engorgement: manually express a few drops beforehand to soften the areola, frequent on-demand feeds, brief warm compresses before feeding + local cold after feeding.
2Diagnosis of postpartum mastitis
Etiology: milk stasis + bacterial superinfection; most common pathogen Staphylococcus aureus (and S. epidermidis).
Clinical presentation: severe unilateral breast pain, wedge-shaped/well-demarcated erythema, local warmth, induration, fever ≥38.5°C, flu-like symptoms.
3Management decision tree
- Initial management (ALL cases):
- NEVER stop breastfeeding — frequent and effective emptying of the affected breast is the mainstay; breast milk poses no infectious risk to a term infant.
- Warm compresses before feeding + cold after feeding.
- Analgesia: Ibuprofen 400-600mg orally every 8h or acetaminophen 500-1000mg orally every 6-8h.
- Maternal hydration and rest.
- Reassess at 12-24h — start antibiotics ONLY IF there are systemic symptoms (fever >38.5°C, chills, myalgia) OR there is no clinical improvement after 12-24h of optimized nonpharmacological management.
- Antibiotic regimen (10-14 days) if the above criterion is met:
Scenario Medications and doses 1st line (methicillin-susceptible, outpatient) Cephalexin 500mg orally every 6h; Cloxacillin/Dicloxacillin 500mg orally every 6h; Amoxicillin + Clavulanic acid 875/125mg orally every 8-12h Penicillin/beta-lactam allergy Clindamycin 300mg orally every 6h; Erythromycin 500mg orally every 6h Suspected MRSA Trimethoprim/sulfamethoxazole 160/800mg orally every 12h (avoid if infant is <1 month old with jaundice) or IV vancomycin if hospitalization is required CaVeSal® proprietary algorithm · Based on: ABM Clinical Protocol #36 (2022) · WHO — Mastitis.
4Breast abscess: suspicion and ultrasound diagnosis
Clinical suspicion: persistent painful fluctuant mass with erythema that does not resolve after 48-72h of antibiotics.
Criteria for referral to the emergency department/surgery:
- Treatment failure (persistence/worsening after 48-72h of appropriate antibiotics + effective milk drainage).
- Signs of a collection (fluctuant mass, induration, overlying skin thinned/shiny).
- Severe systemic involvement (refractory fever >38.5°C, tachycardia, hypotension, marked leukocytosis, suspected sepsis/SIRS).
- Local complications (ischemia, skin necrosis, rapid spread of erythema, suspected granulomatous mastitis/inflammatory breast cancer — oncologic red flag).
- Technical difficulty (image-guided percutaneous drainage not feasible at the facility).
Ultrasound diagnosis (gold standard): hypoechoic/anechoic collection, irregular/microlobulated margins, thickened wall with Doppler hypervascularity; heterogeneous contents with mobile internal echoes, septa, sometimes fluid-fluid levels or gas bubbles; posterior acoustic enhancement; color Doppler shows no flow in the center with increased peripheral vascularity (inflammatory halo); perilesional edema.
5Stepwise drainage techniques
- Ultrasound-guided fine-/large-bore needle aspiration (first line): collections <3-5cm, intact skin without necrosis. 16G-18G needle + 10-20mL syringe under ultrasound guidance, complete aspiration + saline irrigation. May be repeated every 48-72h if recurrence (success rate >85-90%). Always send for culture (aerobes, anaerobes, susceptibility testing).
- Percutaneous catheter drainage: abscesses ≥3-5cm or rapid recurrence after simple aspiration. Ultrasound-guided 8-12Fr pigtail catheter, daily irrigation, removal when output is <10-15mL/24h and the cavity has collapsed.
- Open surgical incision and drainage: failure of percutaneous drainage/repeated aspiration, extensive multiloculated abscesses, or skin compromise with necrosis/ischemia. Curvilinear incision respecting Langer’s lines (or periareolar), gentle digital debridement, irrigation + passive drainage (Penrose drain or iodoform gauze) for healing by secondary intention.
6Breastfeeding during abscess treatment
Do not stop breastfeeding; continue emptying the affected breast.
- If the infant’s mouth does NOT come into direct contact with the wound/drain/infected area → direct breastfeeding is safe.
- If the incision/drainage involves the areola or nipple → express milk mechanically/by hand; breastfeed from the unaffected breast while visible pus contamination persists.
Sources: Academy of Breastfeeding Medicine (ABM) Clinical Protocol #36 — The Mastitis Spectrum (revised 2022) · WHO — Mastitis: Causes and Management · ABM Clinical Protocol #4 (PMC 2014).
ICT Model and Resuscitation — ABCDE Code Red
Identify-Compensate-Treat, response to crystalloids, sequence of hemorrhage control, uterotonics, and time-based task allocation.
1Quick access: 3 basic steps by code
| Root cause | Step 1 | Step 2 | Step 3 | Step 4 |
|---|---|---|---|---|
| Severe hemorrhage / hypovolemic shock | Fluid resuscitation | Control the hemorrhage | Etiologic treatment | — |
| Severe hypertensive disorders | Fluid resuscitation | Anticonvulsant | Antihypertensive | — |
| Severe obstetric infections | Fluid resuscitation | Antibiotic | Antipyretic | Remove the septic focus |
CaVeSal® proprietary algorithm · Based on: MSPBS/DGPS Paraguay, “Time is life” (ICT model, training material) · MSPBS Maternal and Neonatal Code Red Guide, 2nd ed. (2021).
2“Time is life”: survival curve and 3 delays
| Timing | Survival |
|---|---|
| Time zero (identify) | 100% |
| 1-20 min (stabilize) | ~60% |
| 20-60 min (treat/transfer) | <15% |
| >60 min | <10% |
CaVeSal® proprietary algorithm · Based on: Cresswell et al., Lancet Glob Health 2025 · WHO, Trends in Maternal Mortality 2000-2023
- Delay 1: in seeking help.
- Delay 2: in reaching care.
- Delay 3: in receiving appropriate treatment.
- They correspond to delays in identifying, stabilizing and treating/transferring, each associated with declining survival.
- Pathophysiology: hypovolemic shock with DIC and peripheral redistribution (cardiothoracic due to sympathetic activity; peripheral due to parasympathetic activity).
Global context: causes of maternal death — hemorrhage ~27%, hypertensive disorders ~14%, sepsis ~11% (Cresswell et al., Lancet Glob Health 2025). In 2023, there were ~260,000 maternal deaths (≈1 every 2 minutes), global MMR 197/100,000 live births, 40% lower than in 2000 (WHO, Trends in Maternal Mortality 2000-2023).
Three-delays model: Thaddeus & Maine 1994. Official graphic version, MSPBS/DGPS Paraguay.
3ICT — Stage 1: Identify
- Apply the Early Obstetric Warning Score (EAPO) and start the timer.
- Look for signs of MODS (multiple organ dysfunction syndrome): severe, acquired functional abnormality of at least 2 organ systems; an early detection criterion for extreme maternal morbidity/near-miss.
- Determine the cause: hemorrhage (4 Ts), severe hypertensive disorder, or infection.
Definition of MODS adopted from the Latin American obstetric literature (Rev Méd IMSS).
4ICT — Stage 2: Stabilize (basic care)
5 basic steps: call for help · 2 peripheral IV lines · oxygen therapy · urinary catheterization · prevent hypothermia.
Detailed version (8 steps):
- Call for help.
- Ensure airway patency.
- Administer oxygen.
- Insert 2 intravenous catheters, No. 14, 16, or 18 gauge.
- Parenteral hydration with normal saline: maintain systolic BP >90 mmHg and urine output >30 mL/h (or >0.5 mL/kg/h); in hypertension, maintain diastolic BP >90 mmHg.
- Urinary catheter and urine output monitoring.
- Cover with a blanket to prevent hypothermia.
- Monitor vital signs using the Code Red Alert Scale every 5-10 min.
Urine output target: >0.5 mL/kg/h (international clinical standard, WHO/StatPearls) or >30 mL/h (MSPBS/DGPS); both are shown with their source.
5Response to the initial crystalloid bolus (500 mL boluses)
| Response | Clinical findings | % blood loss / volume | Transfusion requirement |
|---|---|---|---|
| Rapid | Returns to normal | 10-25% or 500-1500 mL (compensated/mild shock) | Transfusion unlikely; type-compatible blood with crossmatch testing (45-60 min) |
| Transient | Recurrent hypotension (SBP <90), impaired mental status, weak radial pulse, tachycardia | 26-40% or 1500-2000 mL (moderate shock) | Likely: emergency packed red blood cell package, 2 units PRBCs, or emergency transfusion package, 4 units PRBCs / 6 units FFP / 6 units platelets, ABO-compatible |
| No response | Abnormal parameters or targets not achieved at any time | >40% or >2000 mL (severe shock) | Immediate: group-specific packed red blood cells without crossmatch (15 min), or O-/O+ if unavailable; O-/O+ FFP; O Rh-compatible platelets |
CaVeSal® proprietary algorithm · Based on: ATLS · Plaat F (classification adapted to obstetrics) · WHO 2025.
Intervention according to response: sustained improvement → no further intervention; partial improvement → fluid challenges; no improvement → blood products + surgery; no response → immediate surgical control.
Do not administer predetermined 1-2 L fluid loads or use replacement formulas. IV isotonic crystalloid boluses of 500 mL at 39 °C; assess radial pulse and mental status. Isotonic crystalloids over colloids (WHO 2025, Rec. 28).
6ICT — Stage 3: Treat/Transfer. Control bleeding by Tone (sequence 1-5)
- Continuous external uterine massage throughout management, until bleeding stops.
- Bimanual massage for ≥20 min or until bleeding stops if external massage is ineffective; additional uterotonics, Pinard safety balloon, and tranexamic acid.
- Continue bimanual compression until bleeding stops (no bleeding when compression is released and uterus is contracted).
- Abdominal aortic compression: closed fist (thumb out), pressing downward just above the umbilicus and slightly to the left.
- Immediate surgical intervention if uterine tone is not restored: B-Lynch compression suture or obstetric hysterectomy.
Technique consistent with WHO, Managing Complications in Pregnancy and Childbirth, 2nd ed. 2017.
7Oxytocin for atony (microdrip) and ergometrine as second-line treatment
- Oxytocin IM: 10 IU if no IV line is in place.
- Oxytocin IV: 5 IU slowly over 5 min; may be repeated after 5 min up to a maximum of 10 IU.
- IV maintenance: 20 IU in 500 cc of normal saline over 4 h (80 mIU/min = 42 drops/min = 126 cc/h by pump).
- Misoprostol 800 µg SL as a 3rd option if oxytocin or ergonovine is unavailable.
| Variant | Interval to 2nd dose | Continuation | Maximum |
|---|---|---|---|
| WHO (2012 / MCPC 2017) — IM or slow IV | 15 min | 0.2 mg every 4 h | 5 doses (1 mg) in 24 h |
| FIGO 2022 / ACOG / FDA — IM or slow IV | No intermediate dose | 0.2 mg every 2-4 h | 5 doses (1 mg) in 24 h |
| Regional adaptation for Latin America (Colombia/Peru/Panama) — IM | 20 min (one additional dose only) | 0.2 mg every 4-6 h | 5 ampoules in 24 h |
CaVeSal® proprietary algorithm · Based on: WHO · FIGO 2022 · ACOG.
Contraindicated in hypertension, preeclampsia/eclampsia, and heart disease. Indicated if oxytocin is unavailable or the response is insufficient after 30 min.
8Uterine inversion and surgical hierarchy
Antibiotic prophylaxis after correction (single dose, together with oxytocin to prevent recurrence):
- Ampicillin 2 g IV + metronidazole 500 mg IV, or
- Cefazolin 1 g IV + metronidazole 500 mg IV (penicillin allergy).
Vascular ligation: bilateral uterine artery ligation (O'Leary) is the first-choice conservative surgical option (simpler, faster, immediate efficacy ~80-90%); internal iliac artery ligation is more complex (ureteral/venous risk, efficacy ~65-70%) and is reserved for failure of the former. Variants: Posadas technique (posterior selective devascularization of the uterine and internal tubal arteries, Series of 750 cases) and Tsirulnikov (triple ligation of the round ligaments, utero-ovarian and uterine arteries). Vaginal bridge: Zea technique (INPer — Zea technique).
The hierarchy reflects technical ease and risk profile, not absolute superiority in efficacy (FIGO/WHO).
9Hemostatic resuscitation
- 1:1:1 ratio — RBCs 6 U : FFP 6 U : 1 apheresis unit (or 6 U) of platelets.
- Cryoprecipitate 10-20 units.
- Fibrinogen concentrate 2 g.
- Tranexamic acid 1 g.
- Fibrinogen <2 g/L: independent risk factor for massive PPH, OR 12.0 (95% CI 2.6-56.1) (Cortet et al., Br J Anaesth 2012); between 2 and 3 g/L, OR 1.90 (1.16-3.09).
Supporting reviews: Butwick, Int J Obstet Anesth 2013;22:87-91 · Pacheco et al., AJOG 2011;205(6):526-532.
10“Golden Hour of Resuscitation”: role- and time-based allocation
| Block | Obstetrician | Anesthesiologist |
|---|---|---|
| 0-30 min | Diagnosis using the 4 Ts, uterine massage, medical management | Monitoring, labs, 2 IV lines, fluid boluses |
| 30-60 min | Balloon tamponade, non-pneumatic antishock garment, hemostatic sutures | Invasive monitoring, transfusion, vasopressors |
| 60-90 min | Hysterectomy, damage control | Massive transfusion, coagulation factors |
CaVeSal® original table · Original content by Dr. Carlos Vera Salerno (“Emergencias Obstétricas 2025”).
Original content: Dr. Carlos Vera Salerno, “Emergencias Obstétricas 2025”. Complements the allocation by body area.
11Primary xABCDE survey adapted for the pregnant patient
Assess and treat in order; if the patient deteriorates, return to “x”. Tasks are carried out simultaneously by team members.
| Step | What to assess/do | Adjustment in the pregnant patient |
|---|---|---|
| x Exsanguinating hemorrhage | Massive, compressible external bleeding: direct pressure, packing, tourniquet if involving an extremity (record the time) | For obstetric bleeding: activate Code Red and follow the sequence for control by Tone (card 6) |
| A Airway | Patency; cervical spine protection if trauma occurred | Consider earlier intubation: the pregnant patient desaturates faster. Higher risk of failed intubation: it should be performed by the most experienced operator |
| B Breathing | RR, SpO₂, symmetry, auscultation | O₂ for SpO₂ 94-98 %. If a chest drain is placed, 1-2 spaces higher (3rd-4th intercostal space) because of diaphragm elevation |
| C Circulation | Pulse, BP, capillary refill, 2 large-bore IV lines, labs, bleeding control | From 20 weeks: manual left uterine displacement (preferred in the unstable patient) or 15-30° left lateral tilt. The pregnant patient may show no signs until losing around 30% of blood volume; tachycardia with normal BP = early sign |
| D Disability (neurologic deficit) | Glasgow or AVPU, pupils, blood glucose | Rule out a metabolic cause (blood glucose) before attributing the presentation to trauma |
| E Exposure | Undress and examine the entire body | Prevent hypothermia: warmed fluids, warm environment, temperature >36.5 °C |
| Variant | Difference | Source |
|---|---|---|
| ABCDE | Classic scheme, without an initial “x” | ATLS through the 10th ed.; maternal collapse guidelines |
| <C>ABCDE | “C” for catastrophic hemorrhage before A | Victorian State Trauma System; NICE NG39 |
| xABCDE | “x” for exsanguinating hemorrhage before A | ATLS 11th ed. (ACS, 2025) |
| XABCDE-F | Adds “F”: fetal assessment after stabilizing the mother | Obstetric emergency checklist (Heras). The “F” is supported by: fetal monitoring from 24 weeks, once the mother is stable; “the best treatment for the fetus is to resuscitate the mother well” (StatPearls; Victoria obstetric guideline) |
CaVeSal® proprietary algorithm · Based on: StatPearls — Trauma Assessment (xABCDE, ATLS 11th ed.) · ACS — ATLS 11 launch · Victorian State Trauma System — Obstetric Trauma Guideline v2.0, pp. 7-9 and 11 · Krywko DM et al. StatPearls — Pregnancy Trauma · Frimley Health — Maternal Collapse in Pregnancy and the Puerperium (ABCDE) · Heras A. — Preeclampsia Checklist.
12FAST / eFAST in pregnant and postpartum patients
| Window | Search |
|---|---|
| Subxiphoid | Pericardial effusion / tamponade |
| Hepatorenal (Morrison) | Free fluid. In preeclampsia/HELLP with epigastric or right upper quadrant pain: subcapsular hepatic hematoma (hypoechoic crescent beneath the capsule) |
| Perisplenic | Free fluid |
| Suprapubic / pelvis | Free fluid; uterus: fetal heartbeat, placenta, amniotic fluid |
| Pulmonary (eFAST) | Pneumothorax, pleural effusion. B-pattern (≥3 B-lines per field) = pulmonary edema |
- Positive FAST in an unstable pregnant patient = significant finding. If stable, it can be performed during the secondary survey, ideally by a second operator.
- Performance for free fluid: sensitivity 61 % and specificity 94 % in pregnant patients (compared with 71 % and 97 % in nonpregnant patients). A negative FAST does not rule out bleeding.
- Ultrasound has low sensitivity for placental abruption: it cannot be used to rule it out.
- Severe preeclampsia: B-pattern was associated with elevated filling pressures. Restrict fluids (pilot study, n = 20).
- Subcapsular hematoma: bedside ultrasound in the unstable patient; CT if stable.
CaVeSal® proprietary algorithm · Based on: Victorian Obstetric Trauma Guideline v2.0, pp. 8 and 15 · OpenAnesthesia — Obstetric Trauma · Zieleskiewicz L et al. Anesthesiology 2014;120(4):906-914 · Hepatic rupture in HELLP, case report (PMC) · Subcapsular hepatic hematoma in HELLP (PMC).
13Monitoring during the emergency
| Parameter | Target / frequency |
|---|---|
| Vital signs (EAPO) | Every 5-10 min during the Compensate and Treat stages. Communicate to the team using colors (red / yellow / green) |
| Urine output (urinary catheter with collection bag) | Normal: 50 cc/h or 0.5 cc/kg/h. Compensated hemorrhage: SBP >90 mmHg + urine output >30 cc/h. Sepsis: >0.5 cc/kg/h. Also assess urine characteristics |
| Lactate / base deficit | Initial level and its clearance: identifies incomplete resuscitation even if BP has normalized |
| Temperature | Avoid hypothermia (lethal triad: hypoperfusion/acidosis, hypothermia, coagulopathy) |
| Fetus (trauma, ≥24 weeks) | CTG for at least 4 h after trauma, once the mother is stabilized |
| Monitoring | MSPBS 2022 | WHO (product information) |
|---|---|---|
| Respiratory rate | <12/min | <16/min |
| Patellar reflex | Decreased or absent | Absent |
| Urine output | <30 cc/h | <30 mL/h in the previous 4 h |
| Antidote | 10% calcium gluconate, 1 g (10 cc) IV over 3 min (MSPBS) | |
CaVeSal® proprietary algorithm · Based on: MSPBS Maternal and Neonatal Code Red Guide, 2nd ed. (2021), pp. 32-33, 39, 70 and 124-126 · WHO-PQ — magnesium sulfate technical information (RH086) · Victorian Obstetric Trauma Guideline v2.0, p. 11.
Sources: MSPBS/DGPS Paraguay, «El Tiempo es Vida» (ICT model) · Manual Nacional de Normas de Atención de las Principales Patologías Obstétricas (MSPBS) · Thaddeus & Maine 1994 · Plaat F; Pacheco LD et al. AJOG 2011;205(6):526-532 · ATLS (ACS) · WHO MCPC 2nd ed. 2017 · WHO Consolidated Guidelines PPH 2025 · FIGO 2022 (Escobar et al.) · FDA Methergine · PubMed 37480294 (antibiotics after uterine exploration) · Cortet M et al. Br J Anaesth 2012;108(6):984-989 · IMSS Med J — MODS.
Mode of Delivery — Robson Classification, Bishop Score, and Maternal-Fetal Biometry
Robson classification at admission with management by group, cesarean audit (WHO/PAHO), cervical ripening, and cesarean alert criteria for macrosomia, SGA/FGR, and maternal height.
1Robson Classification — 10 groups (WHO 2015, FIGO 2016)
| Group | Definition |
|---|---|
| 1 | Nulliparous, singleton, cephalic, ≥37 weeks, spontaneous labor |
| 2 | Nulliparous, singleton, cephalic, ≥37 weeks, induced labor (2a) or cesarean before labor (2b) |
| 3 | Multiparous with no previous cesarean, singleton, cephalic, ≥37 weeks, spontaneous labor |
| 4 | Multiparous with no previous cesarean, singleton, cephalic, ≥37 weeks, induced labor (4a) or cesarean before labor (4b) |
| 5 | At least one previous cesarean, singleton, cephalic, ≥37 weeks (5.1: one cesarean; 5.2: two or more) |
| 6 | All nulliparous women with a singleton breech fetus |
| 7 | All multiparous women with a singleton breech fetus (including previous cesarean) |
| 8 | All multiple pregnancies (including previous cesarean) |
| 9 | Singleton fetus in transverse or oblique lie (including previous cesarean) |
| 10 | Singleton cephalic fetus <37 weeks (including previous cesarean) |
CaVeSal® proprietary algorithm · Based on: PAHO/WHO — Robson Classification: application manual (2018).
It is classified using 6 variables: parity, prior cesarean delivery, onset of labor, number of fetuses, presentation/lie, and GA. Groups are mutually exclusive. Groups 1, 2 and 5 usually account for most cesarean deliveries and are the target of reduction strategies. Source: PAHO/WHO — Robson Classification: application manual (2018).
| Variable | Options | Note |
|---|---|---|
| Parity | Nulliparous · Multiparous | Multiparous: at least one previous birth, vaginal or cesarean |
| Previous cesarean | No · 1 · 2 or more | Defines subgroups 5.1 and 5.2 |
| Onset of labor | Spontaneous · Induced · Cesarean before labor | As found at admission, regardless of what was planned. An emergency cesarean before labor starts counts as «before labor» |
| Number of fetuses | Singleton · Multiple | |
| Presentation / lie | Cephalic · Breech · Transverse or oblique | |
| Gestational age | Weeks | Cut-off at 37+0 |
CaVeSal® proprietary table · Based on: PAHO/WHO — Robson Classification: application manual (2018).
Classification at admission and real-time use
- It is applied to every woman admitted for birth, prospectively: each woman is assigned a group at admission and followed to the outcome (WHO — Robson Platform; WHO implementation manual).
- Real-time use is institutional: each birth is recorded as it happens to track the cesarean rate by group and plan actions (quality improvement experience). WHO provides a platform where hospitals upload these data (WHO Bulletin).
- Standard report by group: number of cesareans, number of women, group size, group cesarean rate, absolute and relative contribution to the overall rate (Robson report table).
- Robson does not assess whether a cesarean was appropriately indicated: that requires an audit of indications.
- In CaVeSal®: the Prenatal Calculator shows the probable group (prognosis); the Emergency calculator assigns the group at admission with intrapartum management (Labor tab).
2Robson — intrapartum management by group
| Group | Management | Sources |
|---|---|---|
| 1 | Prolonged latent phase and slow but progressive labor are not indications for cesarean. Partograph according to the chosen model (Ministry CLAP from 4 cm, WHO 2020 from 5 cm, ACOG from 6 cm). Active-phase arrest: ≥6 cm with ruptured membranes and no change with ≥4 h of adequate contractions or ≥6 h of oxytocin with inadequate contractions. Second stage: ≥3 h of pushing before diagnosing arrest (longer with epidural, individualized). Continuous support. | WHO — Labour Care Guide 2020 · ACOG/SMFM — Safe prevention of the primary cesarean delivery (2014) |
| 2a / 4a | Induce only with a clear indication; from 41+0 weeks induction is recommended. Bishop ≤6: cervical ripening (oral misoprostol 25 µg q2h or vaginal 25 µg q6h, balloon, or balloon + oxytocin). Do not diagnose failed induction in the latent phase before ≥24 h of induction and ≥12-18 h of oxytocin after membrane rupture. Never unsupervised; induce where an operating room is available. | WHO — Induction of labour at or beyond term (2022) · WHO — Induction of labour (2011) · WHO — Mechanical methods (2022) · ACOG/SMFM — Safe prevention of the primary cesarean delivery (2014) |
| 2b / 4b | Verify and document the indication. Without a medical indication, do not schedule before 39 weeks. | ACOG CO 765 (2019) · ACOG/SMFM — Safe prevention of the primary cesarean delivery (2014) |
| 3 | Same criteria as Group 1 with multiparous standards. Second stage: ≥2 h of pushing. Lowest cesarean rate group: a cesarean here deserves review of the indication. | WHO — Labour Care Guide 2020 · ACOG/SMFM — Safe prevention of the primary cesarean delivery (2014) |
| 5.1 | VBAC if: low transverse (or low vertical) incision, no previous rupture and no contraindication to vaginal birth. Contraindicated: classical cesarean, T or J incision, previous rupture. Only with 24-h emergency cesarean, blood bank and NICU. Continuous fetal monitoring and one-to-one care (abnormal FHR is the most common sign of rupture). Induction with mechanical methods; misoprostol contraindicated; oxytocin with caution. Epidural not contraindicated. Interval under 18 months: higher risk. EFW >4500 g: cesarean (FIGO). | FIGO — VBAC (2025) · ACOG PB 205 (2019) · RCOG GTG 45 · WHO — Induction of labour (2011) |
| 5.2 | Two cesareans: FIGO generally does not recommend VBAC (only with a previous vaginal birth, senior obstetrician counseling and a high-complexity center); RCOG and ACOG allow it with counseling. Three or more: cesarean. With placenta previa or low anterior placenta, rule out accreta. | FIGO — VBAC (2025) · ACOG PB 205 (2019) · RCOG GTG 45 |
| 6 | Offer external cephalic version (ECV) from 36 weeks. Without ECV: planned cesarean from 39 weeks, or vaginal breech birth only with an institutional protocol, trained operator and written consent. In labor: ultrasound (type of breech, head flexion, EFW) and continuous monitoring; inadequate progress → cesarean. Imminent delivery: hands-off assistance. | ACOG CO 745 (2018, reaf. 2023) · RCOG GTG 20b |
| 7 | Same as Group 6, with ECV from 37 weeks. With one previous low transverse cesarean, ECV may be attempted if she is a good VBAC candidate. | ACOG CO 745 (2018, reaf. 2023) · RCOG GTG 20b · FIGO — VBAC (2025) |
| 8 | Uncomplicated dichorionic or monochorionic diamniotic twins, >32 weeks, first twin cephalic, no significant discordance: vaginal birth and cesarean are equally safe. First twin non-cephalic: cesarean. Monoamniotic: cesarean (32+0-33+6). Triplets: cesarean. One previous low transverse cesarean does not contraindicate VBAC. Active third stage due to higher hemorrhage risk. | NICE NG137 (2019) · ACOG PB 231 (2021) · ACOG/SMFM — Safe prevention of the primary cesarean delivery (2014) · FIGO — VBAC (2025) |
| 9 | In labor or with ruptured membranes: cesarean (cord prolapse, uterine rupture). Before labor and without contraindications: ECV from 37 weeks. Ultrasound to rule out a mechanical cause (placenta previa, fibroids, anomalies). With back down, consider a vertical uterine incision. | GLOWM · StatPearls — ECV |
| 10 | Lung maturation, neuroprotection, tocolysis and PROM according to the preterm labor and PROM cards in this guide. Notify neonatology. Prematurity alone does not determine the mode of birth; it is decided by obstetric conditions. | ACOG CO 831 (2021) |
CaVeSal® proprietary algorithm · Based on: sources listed for each group · PAHO/WHO — Robson Classification (2018).
Fetal lung maturation, magnesium sulfate neuroprotection, tocolysis and PROM follow the management already set in their cards in this guide and in the calculator. Does not replace clinical judgment.
3Bishop Score
| Parameter | 0 | 1 | 2 | 3 |
|---|---|---|---|---|
| Dilation (cm) | 0 | 1-2 | 3-4 | ≥5 |
| Effacement (%) | 0-30 | 40-50 | 60-70 | ≥80 |
| Fetal station | −3 | −2 | −1, 0 | +1, +2 |
| Consistency | Firm | Medium | Soft | — |
| Cervical position | Posterior | Medium | Anterior | — |
| Source | Cutoff |
|---|---|
| NICE | >6 |
| ACOG | >8 (probability of vaginal birth similar to spontaneous labor) |
| CMQCC | ≥6 multiparous · ≥8 nulliparous |
| Simplified Bishop score (dilation, effacement, station) | >5 |
CaVeSal® proprietary algorithm · Based on: StatPearls — Bishop Score.
Variant: the modified Bishop score (Calder) replaces effacement with cervical length (cm). Unfavorable cervix → cervical ripening (misoprostol, Foley balloon) before oxytocin. Source: StatPearls — Bishop Score.
4SGA vs FGR (Delphi consensus)
| Category | Criterion |
|---|---|
| SGA | EFW and/or AC p3-p10, normal anatomy and normal Doppler; follow-up every 2 weeks |
| FGR | EFW/AC <p3 (with any Doppler finding), or <p10 with abnormal Doppler (UA PI >p95, mean uterine artery PI >p95, CPR/MCA <p5), or a drop of >2 quartiles over ≥2 weeks (late-onset FGR) |
CaVeSal® proprietary algorithm · Based on: Gordijn SJ et al. Consensus definition of fetal growth restriction: a Delphi procedure. Ultrasound Obstet Gynecol 2016;48(3):333-9 · Hospital Universitario Virgen de las Nieves — FGR Protocol (2025) · Valenti EA et al. 2017 FASGO Consensus Update: FGR · Sardá Maternity Hospital — Clinical Practice Guideline for Fetal Growth Restriction.
It is subdivided into early-onset (<32 weeks) and late-onset (≥32 weeks). Sources: Delphi consensus (Gordijn 2016) · HUVN FGR protocol · FASGO 2017 · SARDA.
5Macrosomia and cesarean delivery alert (ACOG PB 216)
| Glycemic status | EFW | Management |
|---|---|---|
| No diabetes | ≥5000 g | Planned cesarean delivery justified |
| No diabetes | 4000-4999 g | Trial of labor with monitoring of the second stage; avoid midpelvic instrumental delivery |
| Gestational or pregestational diabetes | ≥4500 g | Planned cesarean delivery justified |
| Diabetes | 4000-4499 g | Trial of labor with monitoring |
CaVeSal® proprietary algorithm · Based on: ACOG PB 216 (2020) · RCOG GTG 42 (2018, shoulder dystocia).
Macrosomia: ≥4000 g (some guidelines reserve the term for ≥4500 g); LGA: EFW ≥p90. In our setting, consider a history of birth weight ≥4000 g. Sources: ACOG PB 216 (2020) · RCOG GTG 42 (2018, shoulder dystocia).
6Short maternal stature and cephalopelvic disproportion (CPD)
- Height <145-150 cm is not an indication for cesarean delivery (WHO 2018, FIGO, ACOG): it is a biomechanical risk factor; allow a trial of labor with a strict partograph and, if available, intrapartum ultrasound.
- MSPBS: height <145 cm → referral to orthopedics and genetics (possible skeletal dysplasia), not a criterion for mode of delivery.
- CPD is diagnosed intrapartum: adequate uterine activity (3-5/10 min, >2-4 h), dilation ≥5-6 cm, and lack of progress in dilation or descent. Signs: cervical edema, marked caput with overlapping sutures, persistent asynclitism. Once confirmed → cesarean delivery.
- Estimated fetal weight ≥4000 g + short stature → heightened alert for surveillance of CPD, not automatic cesarean delivery.
Sources: WHO Intrapartum care 2018 · MSPBS Manual Nacional Prenatal · ACOG PB 216 · Williams Obstetrics 26.ª ed. (2022) · Caldwell-Moloy 1933 (tipos de pelvis).
Sources: OPS/OMS Clasificación de Robson (2018) · StatPearls Bishop Score · ACOG PB 216 (2020) · RCOG GTG 42 · Consenso Delphi de RCIU · WHO 2018 · MSPBS Paraguay · WHO Robson Platform · FIGO VBAC 2025 · ACOG/SMFM 2014 · WHO Induction 2011/2022 · ACOG CO 745, 765, 831 · ACOG PB 205, 231 · RCOG GTG 45, 20b · NICE NG137.
