What is the management of postpartum hemorrhage (PPH)?

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Management of Postpartum Hemorrhage

Immediate First-Line Management

Administer intravenous tranexamic acid 1 g over 10 minutes within 3 hours of birth alongside oxytocin 5-10 IU (IV or IM), initiate uterine massage and bimanual compression, and begin fluid resuscitation with physiologic electrolyte solutions. 1, 2, 3

Critical Time-Sensitive Actions

  • Tranexamic acid must be given within 3 hours of birth—effectiveness decreases by approximately 10% for every 15-minute delay, and administration beyond 3 hours may be harmful 1, 2
  • A second dose of TXA 1 g IV can be given if bleeding continues after 30 minutes or restarts within 24 hours 1, 4
  • TXA should be administered in all cases of PPH regardless of etiology (uterine atony, trauma, retained tissue) 1

Oxytocin Administration Protocol

  • First-line uterotonic: Oxytocin 5-10 IU slow IV or IM immediately after placental delivery 1, 2, 3
  • For ongoing bleeding control: 10-40 units oxytocin in 1,000 mL non-hydrating diluent, infused at rate necessary to control atony (not exceeding 40 IU cumulative dose) 2, 3
  • Slow IV infusion (<2 U/min) prevents systemic hypotension 5

Simultaneous Non-Pharmacological Interventions

  • Perform uterine massage and bimanual compression (fist in vagina against anterior lower uterine segment with abdominal counter-pressure) 2
  • Manual uterine examination with antibiotic prophylaxis 6
  • Careful visual assessment of lower genital tract for lacerations 6
  • Use calibrated blood collection drape for accurate measurement—visual estimation is unreliable 4

Second-Line Pharmacological Management

If oxytocin fails to control bleeding within 30 minutes:

  • Carboprost tromethamine (prostaglandin F2α): Indicated for uterine atony unresponsive to oxytocin and uterine massage 7
  • Methylergonovine 0.2 mg IM: For routine management of uterine atony 8
    • CONTRAINDICATED in hypertensive patients (>10% risk of vasoconstriction and severe hypertension) 5, 1
    • Avoid in women with asthma due to bronchospasm risk 4

Mechanical and Surgical Interventions

Non-Surgical Approaches (if pharmacological management fails)

  • Intrauterine balloon tamponade: Implement before proceeding to surgery or interventional radiology 1, 2, 6
  • Pelvic pressure packing: Effective for acute uncontrolled hemorrhage stabilization, can remain for 24 hours 2
  • Non-pneumatic antishock garment: For temporary stabilization while arranging definitive care 1

Surgical and Interventional Options

  • Uterine compression sutures (B-Lynch or similar brace sutures) 1, 2
  • Arterial embolization: Particularly useful when no single bleeding source identified, requires hemodynamic stability for transfer 5, 2
  • Uterine or internal iliac artery ligation 1, 2
  • Hysterectomy: Last resort when all other measures fail 1, 2

Resuscitation and Blood Product Management

Fluid and Transfusion Protocol

  • Initiate massive transfusion protocol if blood loss exceeds 1,500 mL 2, 9
  • Transfuse packed RBCs, fresh frozen plasma, and platelets in fixed ratio 2
  • Do not delay transfusion waiting for laboratory results in severe bleeding 2, 4, 6
  • Target hemoglobin >8 g/dL and fibrinogen ≥2 g/L during active hemorrhage 2, 6

Critical Laboratory Monitoring

  • Obtain baseline CBC, coagulation profile, fibrinogen level, and crossmatch 2
  • Hypofibrinogenemia (fibrinogen <2 g/L) is the most common factor deficiency and predicts progression to massive hemorrhage 4, 6
  • Point-of-care viscoelastic testing (FIBTEM A5 <12 mm) can predict severe hemorrhage 4
  • Platelet transfusion rarely required unless PPH exceeds 5,000 mL or platelet count <75 × 10⁹/L 4

Essential Supportive Measures

  • Maintain normothermia: Warm all infusion solutions and blood products; use active skin warming (clotting factors function poorly at lower temperatures) 2, 6
  • Administer oxygen in severe PPH 6
  • Re-dose prophylactic antibiotics if blood loss exceeds 1,500 mL 2
  • Continue hemodynamic monitoring for at least 24 hours post-delivery due to significant fluid shifts that may precipitate heart failure in women with structural heart disease 5, 1

Common Pitfalls to Avoid

  • Delaying TXA administration: Every 15-minute delay reduces effectiveness by 10% 1, 2
  • Visual estimation of blood loss: Consistently underestimates actual loss—use calibrated measurement tools 4
  • Waiting for laboratory results before initiating blood products: In severe bleeding, transfuse empirically 2, 4
  • Failing to maintain normothermia and normal pH: Impairs clotting cascade 2
  • Using methylergonovine in hypertensive patients: High risk of severe vasoconstriction 5, 1
  • Manual placental removal without severe indication: Should not be routine except in severe uncontrollable PPH 1

Special Considerations

Anticoagulated Patients with Mechanical Heart Valves

  • Switch from oral anticoagulants to LMWH/UFH from 36 weeks gestation 5
  • Discontinue UFH 4-6 hours before planned delivery 5
  • If emergent delivery required on therapeutic anticoagulation, consider protamine (partially reverses LMWH) 5
  • Caesarean delivery preferred to reduce fetal intracranial hemorrhage risk 5

Post-Acute Monitoring

  • Monitor for complications: renal failure, liver failure, infection, Sheehan syndrome 2
  • Early ambulation with elastic support stockings to reduce thromboembolism risk 5
  • Consider thromboprophylaxis after bleeding controlled, especially with additional VTE risk factors 4

References

Guideline

Management of Postpartum Hemorrhage

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Postpartum Hemorrhage

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Bleeding After Cesarean Section

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Postpartum Hemorrhage: Prevention and Treatment.

American family physician, 2017

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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