Evidence & references
Every quantity displayed anywhere on this site, with the publication it came from, plus a full account of what was merged and what was deliberately left out.
Numbers used in this tool
| Quantity | Value | Source | Evidence type |
|---|---|---|---|
| Incidence of AFE | ~2–6 per 100,000 births | SMFM 2026, citing refs 4 and 6 | Narrative review / cohort |
| Case fatality, “classic” cases | ~20–40% or more | SMFM 2026, citing refs 4 and 6 | Narrative review / cohort |
| DIC accompanying AFE | >80% of cases | SMFM 2026, citing ref 2 | Guideline |
| Onset window | During labour or within 30 min of delivery of the placenta | Ref 5 | Research case definition |
| Time to delivery if no ROSC | 4 minutes | Figure 1; refs 3, 7 | Guideline / expert review |
| Maximum acceptable OR transfer | Under 2 minutes (text: 1–2 min) | Figure 1 and text | Expert consensus |
| Initial comprehensive labs | Within 5 minutes of CPR initiation | Figure 2 | Expert consensus |
| Timekeeper interval | 1 minute | Figure 1; Figure 2 | Expert consensus |
| ECMO, pooled case reports | 72% maternal survival; 6% major neurologic sequelae; n = 79 | Ref 9 | Systematic review of case reports |
| Tranexamic acid | 1 g IV over 10 min | Figure 1; ref 11 | Expert consensus / cohort |
| Norepinephrine | 0.05–3.3 mcg/kg/min | Figure 1; ref 20 | Expert consensus |
| Dobutamine | 2.5–5.0 mcg/kg/min | Figure 1 | Expert consensus |
| Milrinone | 0.25–0.75 mcg/kg/min | Figure 1 | Expert consensus |
| Inhaled epoprostenol | 10–50 ng/kg/min | Figure 1 | Expert consensus |
| IV epoprostenol | 1–2 ng/kg/min via central line | Figure 1 | Expert consensus |
| Inhaled nitric oxide | 5–40 ppm | Figure 1 | Expert consensus |
| Sildenafil | 20 mg orally, if awake and alert | Figure 1 | Expert consensus |
| Oxygenation target | SpO2 94–98% | Figure 1 | Expert consensus |
| Fluid bolus size | 500 mL, then reassess | Figure 1 | Expert consensus |
A note on the norepinephrine unit
Figure 1 of the 2026 statement prints the vasopressor range in mg/kg/min. This tool uses mcg/kg/min, the unit in which the identical 0.05–3.30 range is published elsewhere (ref 20) and the unit used for the two inotropes in the same figure. Doses throughout this site are computed on that basis.
What this tool merged, and what it left alone
Merged. The statement publishes the same response twice, as a text checklist (Figure 1) and as a cardiac-arrest flow chart (Figure 2), and the two are not identical. Four items appear only in Figure 2: activation of the obstetrical emergency response team with its named disciplines; ensuring intravenous or intraosseous access; requesting the resuscitative cesarean delivery kit to the patient's location; and initial comprehensive laboratory assessment within 5 minutes of CPR initiation. All four are included here, each labelled with its figure. A clinician working from the printed checklist alone would not have them.
Left alone. No dose, threshold, interval or recommendation has been added, rounded, converted or inferred, with the single exception of the norepinephrine unit noted above. Where the source gives no dose — oxytocin and the other uterotonics — none is supplied. Where the source declares something out of scope, this tool says so rather than filling the gap: comprehensive cardiac arrest management in pregnancy, including defibrillation timing and drug dosing, belongs to a separate pregnancy-specific flowsheet (ref 7), and post-stabilization ICU management is outside the statement's scope.
Added as clearly labelled annotation. Two safety items appear on the live checklist that are not in the SMFM statement and are marked as LiveEvidence annotations: a warning against tocolysis for the hypertonus of a suspected AFE, and a note to stop an oxytocin infusion already running at the moment of collapse before restarting it for atony prophylaxis after delivery. The reasoning is on the hyperstimulation page.
Not attempted. No risk score, no probability estimate, no prediction. AFE is a clinical diagnosis of exclusion; the statement offers no scoring system and this tool invents none.
Full reference list
References transcribed from source records and publisher pages; individual fields have not each been verified against PubMed. Refs 21–28 support the hyperstimulation analysis and are not cited by the SMFM statement.