What is the management of postpartum hemorrhage (PPH)?

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Management of Postpartum Hemorrhage

Administer tranexamic acid 1 g IV over 10 minutes immediately upon diagnosis of PPH (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

Immediate First-Line Pharmacological Management

Tranexamic Acid (Critical Time-Sensitive Intervention)

  • TXA 1 g IV over 10 minutes must be given within 3 hours of birth—this is non-negotiable. 1, 2, 3
  • Effectiveness decreases by approximately 10% for every 15-minute delay, and administration beyond 3 hours may be harmful rather than beneficial. 1, 2, 3
  • Administer TXA in all cases of PPH regardless of etiology (uterine atony, trauma, retained tissue, or coagulopathy). 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, 2, 3

Oxytocin Administration

  • Administer oxytocin 5-10 IU slow IV or IM immediately after delivery of the anterior shoulder or placenta. 4, 1, 2
  • The IV route is more effective than IM for PPH prevention and treatment. 5
  • For active PPH treatment, use 10-40 units of oxytocin in 1,000 mL of non-hydrating diluent (physiologic electrolyte solution) run at a rate necessary to control uterine atony. 6
  • Higher oxytocin doses (up to 80 IU) are associated with a 47% reduction in PPH compared to lower doses (10 IU), with moderate doses (30 IU) showing intermediate benefit. 2, 7

Mechanical Interventions (Sequential Approach)

Immediate Physical Maneuvers

  • Initiate uterine massage and bimanual compression immediately upon diagnosis. 1, 2
  • These maneuvers should be performed while pharmacological agents are being prepared and administered. 2

Intrauterine Balloon Tamponade

  • Implement intrauterine balloon tamponade before proceeding to surgery or interventional radiology. 1, 2
  • Success rate is 90% when properly placed, with 79.4-88.2% effectiveness in uterine atony cases. 2
  • Pelvic pressure packing can remain in place for 24 hours for acute uncontrolled hemorrhage stabilization. 1

Second-Line Pharmacological Agents

Methylergonovine

  • Administer methylergonovine 0.2 mg IM only if oxytocin fails and patient is normotensive. 1, 8
  • Methylergonovine is absolutely contraindicated in hypertensive patients (>10% risk of severe vasoconstriction and hypertensive crisis). 1, 2, 3
  • Also avoid in women with asthma due to bronchospasm risk. 1

Carboprost Tromethamine

  • Use carboprost for postpartum hemorrhage due to uterine atony that has not responded to oxytocin and uterine massage. 9
  • Prior treatment should include IV oxytocin and manipulative techniques before carboprost administration. 9

Resuscitation and Blood Product Management

Fluid Resuscitation

  • Begin immediate fluid resuscitation with physiologic electrolyte solutions. 1, 2
  • Warm all infusion solutions and blood products to maintain normothermia (clotting factors function poorly at lower temperatures). 1

Massive Transfusion Protocol

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

Surgical and Interventional Options

Conservative Surgical Interventions

  • Uterine compression sutures (B-Lynch or similar brace sutures) can be used to control bleeding when medical management and balloon tamponade fail. 1, 2
  • Non-pneumatic antishock garment can be used for temporary stabilization while arranging definitive care. 1, 2

Arterial Embolization

  • Arterial embolization is particularly useful when no single bleeding source is identified. 1
  • Requires hemodynamic stability for transfer to interventional radiology. 1

Critical Pitfalls to Avoid

Manual Removal of Placenta

  • Do not perform manual removal of placenta routinely to reduce PPH risk. 4, 3
  • Manual removal should only be performed in cases of severe and uncontrollable PPH, not as a preventive measure. 4, 3
  • Spontaneous placental delivery should occur within 30 minutes; retained placenta beyond this increases PPH risk. 3

Time-Sensitive Errors

  • Never delay TXA administration—every 15 minutes of delay reduces effectiveness by 10%. 1, 2, 3
  • Never administer TXA beyond 3 hours postpartum as it may cause harm. 1, 2, 3

Monitoring and Supportive Care

Hemodynamic Monitoring

  • 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. 1, 2
  • Monitor for complications including renal failure, liver failure, infection, and Sheehan syndrome. 1

Oxygen and Antibiotics

  • Administer oxygen in severe PPH. 1
  • Re-dose prophylactic antibiotics if blood loss exceeds 1,500 mL. 1

Thromboprophylaxis

  • Consider thromboprophylaxis after bleeding is controlled, especially with additional VTE risk factors. 1
  • Early ambulation with elastic support stockings can reduce thromboembolism risk. 1

Special Populations

Anticoagulated Patients

  • Active management of third stage with uterotonics (oxytocin) is critical, as the primary mechanism of placental bed hemostasis is myometrial contraction, not coagulation. 2
  • Switch from oral anticoagulants to LMWH/UFH from 36 weeks gestation. 1
  • Discontinue UFH 4-6 hours before planned delivery. 1
  • If emergent delivery is required on therapeutic anticoagulation, consider protamine (partially reverses LMWH). 1

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 Third Stage of Labour

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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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