World Health Organization · 1st edition, 2025 · 116 pages
First consolidated WHO/FIGO/ICM guidelines on PPH prevention, diagnosis and treatment across antenatal, intrapartum and postpartum care
- Issuer
- World Health Organization
- Edition
- 1st edition, 2025
- Audience
- Midwives, obstetricians, nurses, anaesthesiologists, general practitioners, maternal health programme managers, national guideline developers
- Evidence
- GRADE-rated systematic reviews and individual participant data meta-analysis; evidence-to-decision frameworks
- Reviewed
- 14 Oct 2026 · GMJ
What this guideline says
GMJ summary
These consolidated guidelines present 51 evidence-based recommendations addressing postpartum haemorrhage (PPH), the leading cause of maternal death in most low-income countries. Developed jointly by WHO, FIGO and ICM, they integrate prevention strategies from pregnancy through the immediate postpartum period, diagnostic criteria and treatment protocols for both first-response and refractory PPH.
Key preventive measures include antenatal treatment of iron-deficiency anaemia, universal prophylactic uterotonic use (oxytocin 10 IU intramuscularly/intravenously, heat-stable carbetocin 100 μg, or misoprostol 400–600 μg orally), objective blood loss measurement and early detection. For diagnosis, the guidelines introduce new criteria: objectively measured blood loss ≥300 mL with abnormal haemodynamic signs or ≥500 mL, whichever occurs first. First-response treatment includes uterotonic agents, early tranexamic acid (within 3 hours), uterine massage and intravenous fluids delivered as a standardized bundle.
The guidelines explicitly do not recommend tranexamic acid for PPH prevention, ergometrine/methylergometrine for prophylaxis, or routine episiotomy. They emphasize health systems strengthening through formal protocols, simulation training and supply chain reliability for quality-assured medicines.
Key points
For clinicians — doses and thresholds as stated in the guideline
- Diagnose PPH when objectively measured blood loss ≥300 mL with any abnormal haemodynamic sign (pulse >100 bpm, shock index >1, systolic BP <100 mmHg or diastolic BP <60 mmHg), or ≥500 mL, whichever occurs first within 24 hours after birth
- Give prophylactic uterotonic to all women: oxytocin 10 IU IM/IV (preferred), carbetocin 100 μg IM/IV (heat-stable formulation where cold chain unreliable), or misoprostol 400–600 μg orally, administered within 1 minute of birth
- For PPH treatment, give intravenous oxytocin plus tranexamic acid 1 g IV slowly within 3 hours of birth, uterine massage, isotonic crystalloids and examine genital tract
- Do NOT use tranexamic acid for PPH prevention at vaginal or caesarean birth; reserve it for treatment only
- Do NOT use ergometrine/methylergometrine or oxytocin-ergometrine combination for PPH prevention because of hypertension risk
- Use intravenous iron therapy (not oral) for iron-deficiency anaemia in pregnancy when rapid correction needed or oral iron not tolerated, with monitoring for anaphylaxis (ferritin <30 mg/mL threshold)
- Implement uterine balloon tamponade for atonic PPH unresponsive to first-line treatment only where immediate surgical backup and blood products available
- Initiate blood transfusion based on continuous clinical and haematological assessment, not fixed thresholds alone
Summary of recommendations for prevention, diagnosis and treatment of postpartum haemorrhage
Table extracted from the guideline
| Context | Recommendation | Category |
|---|---|---|
| Antenatal prevention | Full blood count for anaemia diagnosis; if unavailable, haemoglobinometer over haemoglobin colour scale | Context-specific |
| Antenatal prevention | Daily oral iron 30–60 mg elemental + folic acid 400 μg | Recommended |
| Antenatal prevention | Intravenous iron therapy when oral not tolerated or rapid correction needed (with anaphylaxis monitoring) | Context-specific |
| Postpartum prevention | Oxytocin 10 IU IM/IV for all births | Recommended |
| Postpartum prevention | Carbetocin 100 μg IM/IV; heat-stable formulation where cold chain unreliable | Recommended |
| Postpartum prevention | Misoprostol 400 μg or 600 μg orally for all births | Recommended |
| Postpartum prevention | Ergometrine/methylergometrine NOT recommended | Not recommended |
| Postpartum prevention | Tranexamic acid NOT recommended for prevention at vaginal birth | Not recommended |
| Postpartum prevention | Tranexamic acid NOT recommended for prevention at caesarean birth | Not recommended |
| Diagnosis | Blood loss ≥300 mL + abnormal vital signs OR ≥500 mL, whichever first within 24 hours | Recommended |
| First-response treatment | Intravenous oxytocin | Recommended |
| First-response treatment | Tranexamic acid 1 g IV within 3 hours of birth | Recommended |
| First-response treatment | Treatment bundle: uterine massage, oxytocic, tranexamic acid, IV fluids, genital exam, escalation | Recommended |
| Refractory treatment | Uterine balloon tamponade (when surgical backup and blood available) | Context-specific |
Source: World Health Organization, Consolidated guidelines for the prevention, diagnosis and treatment of postpartum haemorrhage. Reproduced in summary form.
What changed in this edition
Versus the previous edition
- First consolidated PPH guidelines integrating antenatal, intrapartum and postpartum care; previously fragmented across 12 WHO documents (2012–2023)
- New diagnostic criteria introduced: blood loss ≥300 mL with abnormal haemodynamics OR ≥500 mL (replacing sole reliance on 500-mL threshold)
- Tranexamic acid explicitly NOT recommended for PPH prevention at vaginal or caesarean birth (despite previous interest); reserved for treatment only
- Ergometrine/methylergometrine and oxytocin-ergometrine combination no longer recommended for PPH prevention (previously context-specific options in 2018 WHO guidelines) because of hypertension risks
- Heat-stable carbetocin added as recommended uterotonic option for settings without reliable cold chain
- Intravenous iron therapy newly recommended for antenatal iron-deficiency anaemia when oral not tolerated or rapid correction needed
- Updated recommendation on techniques to reduce perineal trauma including perineal massage and warm compresses
From the guideline
Verbatim
“Oxytocin (10 IU, intramuscularly/intravenously) is the recommended uterotonic agent of choice for the prevention of postpartum haemorrhage for all births.”
Editor’s perspective
Why this matters for Georgia and the region
Prof. Giorgi Pkhakadze, MD, MPH, PhD
Editor-in-Chief, Georgian Medical Journal · Chair, Public Health Institute of Georgia · WHO consultant, health and migration
As Editor-in-Chief of the Georgian Medical Journal and Chair of the Public Health Institute, I view these consolidated PPH guidelines as critical for Georgia, where maternal mortality from haemorrhage persists despite our UHC programme's success in reducing overall maternal deaths. The recommendation I would stress to Georgian obstetricians and midwives is the new diagnostic threshold: ≥300 mL blood loss with any abnormal vital sign triggers treatment, not waiting for 500 mL. Our 2019 national confidential enquiry into maternal deaths showed that delayed recognition of PPH severity contributed to seven preventable deaths in Imereti and Samtskhe-Javakheti regions. The realistic implementation caveat is cold-chain reliability: many rural facilities in Racha-Lechkhumi and mountainous Kakheti lack consistent refrigeration, yet heat-stable carbetocin procurement remains beyond Ministry of Health budgets without GAVI or UNFPA support. We must prioritize ensuring that at least misoprostol 600 μg is universally available at rural birthing centres, where our 2021 reproductive health survey documented that 18% of births still occur with only feldshers present.
ORCID 0000-0001-7609-4515 · Perspective written for the GMJ Guidelines Library, 14 Oct 2026
Applicability
Georgia and the South Caucasus
Georgia has made substantial progress in maternal health through its Universal Health Care Programme (since 2013), yet maternal mortality from haemorrhage remains a concern, particularly in rural Adjara, Kakheti and mountainous regions where access to skilled birth attendants and quality-assured uterotonics may be inconsistent. The National Center for Disease Control and Public Health reports that many rural facilities lack continuous cold-chain capacity for oxytocin, making heat-stable carbetocin a practical option if procurement costs can be addressed through international mechanisms. Georgian national protocols will need updating to reflect the new diagnostic criteria (≥300 mL + abnormal vitals OR ≥500 mL) and to remove ergometrine from routine prophylaxis lists while ensuring tranexamic acid is reserved for treatment. The prohibition on prophylactic tranexamic acid will require clear communication to obstetricians in Tbilisi teaching hospitals where off-label use has occasionally been reported. Simulation training recommendations align well with Georgia’s existing perinatal centre network but require investment in calibrated drapes and provider education on objective blood-loss measurement.
Questions this guideline answers
Quick answers
What are the new diagnostic criteria for postpartum haemorrhage?
Initiate first-response treatment when objectively measured blood loss reaches ≥300 mL with ANY abnormal haemodynamic sign (pulse >100 bpm, shock index >1, systolic BP <100 mmHg, or diastolic BP <60 mmHg), OR when blood loss reaches ≥500 mL, whichever occurs first within 24 hours after birth. This replaces reliance solely on the 500-mL threshold.
Which uterotonic should I use for PPH prevention if I have multiple options?
Oxytocin 10 IU IM/IV is the recommended first choice when multiple uterotonics are available. If the oxytocin cold chain cannot be consistently maintained, use heat-stable carbetocin 100 μg IM/IV; if heat-stable carbetocin is unavailable, use misoprostol 400–600 μg orally. Do NOT use ergometrine, methylergometrine or oxytocin-ergometrine combinations for prevention.
Should I give tranexamic acid to prevent PPH during caesarean section?
No. Tranexamic acid is NOT recommended for PPH prevention at either vaginal or caesarean birth. It provides no additional benefit over standard prophylactic measures and carries a small risk of thromboembolic events. Reserve tranexamic acid (1 g IV) for treatment of PPH, administered within 3 hours of birth onset.
What should the first-response treatment bundle for PPH include?
Rapidly institute: (1) uterine massage, (2) uterotonic agent (intravenous oxytocin preferred), (3) tranexamic acid 1 g IV (within 3 hours of birth), (4) intravenous isotonic crystalloids, (5) examination of the genital tract for trauma, and (6) escalation of care if bleeding continues. Administer the full bundle within 15 minutes of PPH diagnosis.
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- Issuer
- World Health Organization
- Type
- Guideline
- Edition
- 1st edition, 2025
- Replaces
- Consolidates 12 previous WHO guidelines (2012–2023) on PPH and routine maternal care
- Status
- Current
- Published
- 2025-09-30
- Languages
- English
- Scope
- Antenatal, intrapartum and postpartum interventions for prevention, diagnosis and treatment of PPH in all settings
- Audience
- Midwives, obstetricians, nurses, anaesthesiologists, general practitioners, maternal health programme managers, national guideline developers
- Pages
- 116
- Licence
- CC BY-NC-SA 3.0 IGO
- ISBN
- 978-92-4-011563-7
- Evidence
- GRADE-rated systematic reviews and individual participant data meta-analysis; evidence-to-decision frameworks
- Next review
- Not specified
- Record history
- Created 14 Oct 2026 · updated 14 Oct 2026 · next check Apr 2027
World Health Organization. Consolidated guidelines for the prevention, diagnosis and treatment of postpartum haemorrhage. Geneva: World Health Organization; 2025. Licence: CC BY-NC-SA 3.0 IGO.GMJ Guidelines Library records are original summaries written by the GMJ editorial team from the issuer’s published document and reviewed by a physician. They do not replace the full guideline. The document is the copyright of its issuer and is linked, not hosted. Spotted an error or a newer edition? Tell the Guidelines Desk.
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