What is the treatment for postpartum hemorrhage (PPH) after a cesarean section (C-section)?

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Management of Bleeding After Cesarean Section

The first-line treatment for postpartum hemorrhage (PPH) after cesarean section is uterine massage and administration of oxytocin (5-10 IU slow IV or IM), followed by a maintenance infusion not exceeding a cumulative dose of 40 IU. 1

Initial Management

  • Uterine atony is the most common cause of PPH after cesarean section, occurring in >75% of cases 2
  • Initial management includes:
    • Manual uterine massage 1
    • Oxytocin administration: 5-10 IU slow IV or IM, followed by maintenance infusion 3, 1
    • Visual assessment of the lower genital tract to identify lacerations or trauma 1
    • Antibiotic prophylaxis if manual exploration is performed 1

Pharmacological Management Algorithm

First-line treatment:

  • Oxytocin 5-10 IU slow IV/IM bolus, followed by infusion (10-40 units in 1000 mL of non-hydrating solution) 3, 1
  • Higher infusion doses (up to 80 IU/500 mL) appear more effective than lower doses for cesarean deliveries 4
  • Bolus administration of oxytocin is more effective than continuous infusion alone 5

Second-line treatment (if bleeding persists after 30 minutes):

  • Prostaglandin analogues such as sulprostone or carboprost tromethamine 6, 1
  • Carboprost tromethamine (Hemabate) 250 μg IM can be administered when conventional methods including oxytocin have failed 6
  • Methergine (ergometrine) can be used for postpartum atony and hemorrhage 7
    • Caution: Ergometrine may cause bronchospasm, particularly with general anesthetics, and should be avoided in women with asthma 2

Third-line treatment:

  • Tranexamic acid 1 g IV (over 10 minutes) within 3 hours of bleeding onset 2
  • If bleeding continues after 30 minutes or restarts within 24 hours, a second dose of 1 g IV can be given 2

Mechanical and Surgical Interventions

  • Intrauterine balloon tamponade if pharmacological management fails 1
  • If bleeding continues despite medical management:
    • Uterine compression sutures (during cesarean section) 2, 8
    • Uterine or ovarian artery ligation (during cesarean section) 2, 8
    • Arterial embolization (if patient is stable enough for transfer to interventional radiology) 2, 1
    • Hysterectomy as last resort when all other measures fail 8

Blood Component Therapy

  • Fluid resuscitation is recommended for persistent PPH 1
  • Maintain hemoglobin concentration >8 g/dL 1
  • Maintain fibrinogen level ≥2 g/L during active hemorrhage 1
  • For severe bleeding:
    • Red blood cells, fibrinogen, and fresh frozen plasma may be administered without awaiting laboratory results 1
    • If coagulation results are unavailable and bleeding is ongoing after 4 units of RBC, administer 4 units of FFP and maintain 1:1 ratio until coagulation results are available 2
    • Point-of-care testing is recommended in this setting 2

Additional Considerations

  • Hypofibrinogenemia (fibrinogen <2 g/L) with ongoing bleeding is associated with progression to massive obstetric hemorrhage 2
  • Cell salvage can be used during cesarean section with excessive bleeding (use a leukocyte filter for autotransfusion) 2
  • Prevent and treat hypothermia by warming infusion solutions, blood products, and active skin warming 1
  • Administer oxygen in women with severe PPH 1

Common Pitfalls and Caveats

  • Blood loss during cesarean section is frequently underestimated 8
  • Delay in recognizing and treating PPH increases morbidity and mortality 1
  • Prostaglandin F2α (carboprost) may cause bronchoconstriction and should be used with caution in women with asthma 2
  • Protocol-led use of blood products without laboratory guidance may lead to overtransfusion of FFP in many cases 2
  • Consider thromboprophylaxis after bleeding is controlled, especially in women with additional risk factors for VTE 2

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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