SECONDARY PPH

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Secondary Postpartum Hemorrhage (Secondary PPH)

Definition

Secondary (late) PPH is excessive genital tract blood loss occurring more than 24 hours after delivery up to 6–12 weeks postpartum. The onset threshold that distinguishes it from primary PPH is 24 hours post-delivery.
Operationally defined as:
  • Blood loss causing hemodynamic instability, or
  • A 10% drop in hematocrit, or
  • Requirement for packed red blood cell transfusion
Incidence: approximately 1–2% of all postpartum women.

Causes ("4 T's" framework applied to secondary PPH)

CauseDetails
Tissue (most common)Retained placental fragments / products of conception
ToneSubinvolution of the placental site (failure of uterine lining to contract at former placental implantation)
ThrombinInherited coagulopathies (e.g., von Willebrand disease — women with Type 3 vWD have markedly reduced Factor VIII and are at risk for recurrent secondary PPH)
Trauma/InfectionUterine/genital tract infection (endometritis); genital tract wounds; dehiscence of caesarean section scar
Additional/rarer causes:
  • Uterine vascular malformations (arteriovenous malformations)
  • Submucosal fibroids / infected polyp
  • Choriocarcinoma
  • Undiagnosed cervical carcinoma
  • Placenta accreta spectrum (accreta/increta/percreta) — retained morbidly adherent placenta
Suspect endometritis if: septic shock post-CS, prolonged membrane rupture, multiple vaginal examinations, internal monitoring, manual placental removal, or prolonged labor.

Clinical Features

  • Heavy vaginal bleeding (24 hrs – 12 weeks postpartum)
  • Uterine tenderness / subinvolution (uterus larger and softer than expected for the postpartum stage)
  • Fever and offensive lochia if infective cause
  • Signs of hypovolemic shock in severe cases (tachycardia, hypotension, altered mentation)
Key point: Hematologic adaptations of pregnancy (plasma volume +40%, RBC volume +25%) can mask signs of hemorrhage. Up to 30% blood volume loss may occur before blood pressure drops.

Investigations

InvestigationPurpose
FBC / CBCHemoglobin, hematocrit, platelets
Coagulation screenPT, aPTT, fibrinogen, fibrin split products
Group & crossmatchTransfusion preparation
Transvaginal ultrasoundIdentify retained placental tissue, intrauterine clots, endometritis, scar dehiscence, AV malformation
HVS / endometrial swabIf infection suspected
Serum β-hCGRule out choriocarcinoma / gestational trophoblastic disease if bleeding is atypical

Management

Step 1: Resuscitation

  • Call for senior help immediately
  • High-flow O₂ via face mask
  • 2 large-bore IV access lines
  • IV crystalloid (lactated Ringer's); prepare for blood product transfusion
  • Monitor vital signs closely (pulse is the first sign to change)
  • Foley catheter to monitor urine output

Step 2: Identify and Treat the Cause

A. Retained Products of Conception

  • Uterotonics (first-line medical):
    • Oxytocin: 20–30 units in 1 L IV fluid (infusion rate ≤100 mU/min); avoid IV bolus (risk of hypotension)
    • Methylergonovine (Methergine): 0.2 mg IM every 2–4 hours; contraindicated in hypertensive disorders (causes vasoconstriction → severe hypertension)
    • Carboprost (15-methyl PGF₂α, Hemabate): 250 μg IM, repeat every 15–90 min (max 8 doses); use with caution in asthma/cardiovascular disease
    • Misoprostol: 800–1000 μg rectally/transvaginally (intrauterine route reported) — useful when conventional pharmacotherapy fails
  • Surgical evacuation: Suction curettage / ERPC (evacuation of retained products of conception) under ultrasound guidance

B. Infection / Endometritis

  • Broad-spectrum antibiotics (e.g., clindamycin + gentamicin ± metronidazole)
  • If retained products co-exist, evacuate after antibiotic cover

C. Subinvolution of Placental Site

  • Uterotonics as above
  • Uterine massage (bimanual compression if needed)

D. Coagulopathy

  • Fresh frozen plasma (FFP), cryoprecipitate, platelet transfusion as appropriate
  • Tranexamic acid (TXA) — antifibrinolytic; increasingly used, evidence from WOMAN trial extends to secondary hemorrhage
  • Target fibrinogen >2 g/L

Step 3: If Hemorrhage Continues Despite Medical Management

  • Uterine balloon tamponade: Bakri balloon or large Foley catheter balloon (especially for low placental site bleeding)
  • Uterine cavity packing with sterile gauze
  • Selective uterine artery embolization (UAE): preferred in hemodynamically stable patients where angiography suite is available — fertility-sparing
  • Laparotomy options (stepwise):
    1. Uterine/B-Lynch compression sutures
    2. Uterine artery ligation (O'Leary sutures)
    3. Internal iliac artery ligation
    4. Peripartum hysterectomy — last resort, definitive

Differential Diagnosis

ConditionDistinguishing Feature
Gestational trophoblastic diseaseElevated β-hCG, irregular bleeding
Cervical/vaginal lacerationVisible on speculum exam
Uterine AV malformationPelvic US / Doppler; sudden massive hemorrhage
Scar dehiscence post-CSPelvic pain, US/MRI findings

Key Points Summary

  1. Secondary PPH = haemorrhage >24 hours to 12 weeks postpartum
  2. Most common causes: retained products, subinvolution, endometritis
  3. First-line management: resuscitate → uterotonics → evacuate retained tissue → treat infection
  4. Methylergonovine is contraindicated in hypertensive disorders
  5. Surgical escalation follows a stepwise approach; hysterectomy is the definitive last resort
  6. Always rule out gestational trophoblastic disease with serum β-hCG if presentation is atypical
  7. Women with von Willebrand disease are at particular risk for recurrent secondary PPH

Sources: Tintinalli's Emergency Medicine (9e); Textbook of Family Medicine (9e); Creasy & Resnik's Maternal-Fetal Medicine (9e); StatPearls (2025)
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