WHO 2025 Guidelines for Postpartum Hemorrhage Management
First-Line Treatment
The WHO strongly recommends early intravenous tranexamic acid (1 g over 10 minutes) within 3 hours of birth, combined with oxytocin (5-10 IU IV or IM), as first-line treatment for all women with clinically diagnosed postpartum hemorrhage. 1, 2
Tranexamic Acid Administration
- Administer 1 g IV over 10 minutes as soon as PPH is diagnosed 2, 3
- Must be given within 3 hours of birth - effectiveness decreases by 10% for every 15 minutes of delay 1, 2, 3
- Do NOT administer beyond 3 hours postpartum - evidence suggests potential harm rather than benefit 1, 2, 3
- A second 1 g dose can be given if bleeding continues after 30 minutes or restarts within 24 hours 2, 4
- Use in all cases of PPH regardless of etiology (uterine atony, genital tract trauma, or other causes) 2
- Number needed to treat: 276 to prevent one bleeding-related death 4
Oxytocin Administration
- Administer 5-10 IU slow IV or IM immediately upon PPH diagnosis 2, 3, 5
- Follow with maintenance infusion of 10-40 IU in 1000 mL at a rate necessary to control atony, not exceeding 40 IU cumulative dose 3, 5
- Higher doses (up to 80 IU total) are associated with 47% reduction in PPH compared to lower doses 2
- Can be given as IV bolus (5-10 IU over 1-2 minutes) for active hemorrhage 5
Critical Timing Considerations
- Tranexamic acid is time-critical: loses 10% effectiveness every 15 minutes after birth 1, 2, 3
- Absolute contraindication: TXA beyond 3 hours postpartum 1, 2, 3, 4
- At 24 hours postpartum, TXA is contraindicated if not already administered 3
Second-Line Pharmacotherapy
If bleeding persists after oxytocin and tranexamic acid, proceed sequentially through second-line uterotonics within 30 minutes of PPH diagnosis. 3, 6
Methylergonovine
- Dose: 0.2 mg IM 3, 7
- Absolute contraindication in hypertensive patients - risk of severe vasoconstriction and hypertensive crisis 2, 3, 4
- May increase nausea, vomiting, and diarrhea 8
Misoprostol (Rectal)
- Dose: 800-1000 mcg rectally for active hemorrhage unresponsive to oxytocin 3, 4
- Achieves sustained uterine contraction within 3 minutes 3
- Hemorrhage control rate of 63% within 10 minutes 3
- May increase nausea, vomiting, fever, and diarrhea 8
Carboprost (Prostaglandin F2α)
- First-line prostaglandin for PPH treatment despite side effects 9
- Do not delay administration while waiting for laboratory results during active hemorrhage 3
Mechanical Interventions
If pharmacotherapy fails, proceed to intrauterine balloon tamponade before surgical intervention. 2, 3
Intrauterine Balloon Tamponade
- Success rate: 79.4-88.2% for uterine atony 2, 3
- Implement after failure of uterotonics but before interventional radiology or surgery 2
- Can temporarily control active PPH while preparing for definitive intervention 10
Other Non-Surgical Interventions
Surgical and Interventional Procedures
When conservative measures fail, proceed to definitive interventions based on available resources and patient stability. 3, 10
Uterine Artery Embolization
- Particularly useful when no single bleeding source is identified 3
- Hospital-to-hospital transfer possible if hemoperitoneum ruled out and patient hemodynamically stable 6
Surgical Options
- Uterine compression sutures (B-Lynch or similar) 3
- Arterial ligation 2
- Hysterectomy as last resort 2
- Sequential approach: start with least invasive, progress as needed 2, 4
Supportive Care Requirements
Fluid Resuscitation
- Initiate for PPH persistent after first-line uterotonics or with clinical signs of severity 6
- Use physiologic electrolyte solutions 2, 5
- Maintain normothermia - clotting factors function poorly at lower temperatures 3
- Warm infusion solutions and blood products 6
Transfusion Thresholds
- Maintain hemoglobin >8 g/dL 6
- Maintain fibrinogen ≥2 g/L during active hemorrhage 6
- May administer RBC, fibrinogen, and FFP without awaiting laboratory results 6
- Initiate massive transfusion protocol if blood loss exceeds 1500 mL 3
Additional Measures
- Administer oxygen in severe PPH 6
- Manual uterine examination with antibiotic prophylaxis 6
- Re-dose prophylactic antibiotics if blood loss exceeds 1500 mL 3
- Continue hemodynamic monitoring for at least 24 hours after delivery 2, 3
Common Pitfalls to Avoid
- Never delay TXA administration - every 15 minutes reduces effectiveness by 10% 1, 2, 3
- Never give TXA beyond 3 hours postpartum - potentially harmful 1, 2, 3
- Never use methylergonovine in hypertensive patients - risk of hypertensive crisis 2, 3, 4
- Never delay carboprost while awaiting labs during active hemorrhage 3
- Never perform routine manual placental removal before 30 minutes - increases infection and hemorrhage risk 3, 4
- Avoid visual estimation of blood loss - use clinical markers (signs/symptoms) instead 10