TextbookObstetrics & GynaecologyPostpartum Haemorrhage

Postpartum Haemorrhage

Postpartum haemorrhage is blood loss of ≥500mL after vaginal delivery or ≥1000mL after CS, and remains the leading cause of maternal death worldwide.

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Key Facts

Primary PPH: blood loss within 24 hours of delivery; secondary PPH: 24 hours to 12 weeks postpartum 4 T's of PPH causes: Tone (70%), Trauma (20%), Tissue (10%), Thrombin (<1%) Uterine atony is the most common cause (70% of PPH) Oxytocin 10 IU IM for active management of third stage reduces PPH risk by 60% Major PPH defined as >1000 mL; massive PPH >2000 mL or requiring >4 units blood Tranexamic acid 1g IV within 3 hours of delivery reduces death from bleeding (WOMAN trial) Stepwise approach: uterotonics → tamponade → compression sutures → arterial ligation → hysterectomy PPH complicates 5-10% of all deliveries; maternal mortality approximately 1 per 100,000 in UK

Overview

Key Facts

Postpartum haemorrhage is the leading cause of maternal mortality worldwide and remains a significant cause of morbidity in the UK. Early recognition and a systematic stepwise approach to management are crucial.

Epidemiology

  • Primary PPH (within 24 hours): complicates 5-10% of deliveries
  • Minor PPH (500-1000 mL): ~5%
  • Major PPH (>1000 mL): ~1-3%
  • Secondary PPH (24 hours - 12 weeks): ~1%
  • Leading cause of maternal death globally; approximately 1 per 100,000 maternities in the UK

Aetiology (4 T's)

  • Tone (70%): uterine atony - overdistended uterus (macrosomia, polyhydramnios, multiple pregnancy), prolonged labour, oxytocin use, chorioamnionitis, grand multiparity
  • Trauma (20%): perineal tears, cervical tears, uterine rupture, episiotomy extension
  • Tissue (10%): retained placenta, retained products, placenta accreta
  • Thrombin (<1%): coagulopathy (DIC, pre-eclampsia, HELLP, inherited bleeding disorders, anticoagulant therapy)

Pathophysiology

  • After placental separation, myometrial contraction compresses spiral arteries (living ligatures)
  • Failure of uterine contraction (atony) leaves vessels open, causing rapid haemorrhage
  • Blood loss can be rapid (up to 500 mL/min from the placental bed)
  • Concealed haemorrhage (haematoma formation) may mask true blood loss

Clinical Presentation

Primary PPH

  • Visible vaginal bleeding (may be underestimated by 30-50%)
  • Boggy, poorly contracted uterus on palpation (atony)
  • Tachycardia, hypotension, pallor (signs of hypovolaemia)
  • Continuous trickle of blood despite contracted uterus (suggests trauma or retained tissue)

Secondary PPH

  • Abnormal vaginal bleeding >24 hours postpartum
  • Offensive lochia (infection)
  • Uterine tenderness
  • Fever

Red Flags

  • Blood loss >1000 mL
  • Haemodynamic instability (tachycardia >120, systolic BP <90 mmHg)
  • Altered consciousness
  • Inability to achieve a contracted uterus
  • Ongoing bleeding despite uterotonics
  • Signs of DIC (oozing from IV sites, widespread petechiae)

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Uterine atonySoft boggy uterus, most commonBimanual palpation
Genital tract traumaBleeding despite contracted uterusSystematic inspection
Retained placenta/productsIncomplete placenta, uterus not contracting fullyExamine placenta, USS
Uterine rupturePrevious CS scar, severe pain, shockClinical, laparotomy
Uterine inversionFundus not palpable, mass at introitus, shockClinical
CoagulopathyGeneralised oozing, no clot formationCoagulation screen
Broad ligament haematomaLateral uterine mass, shock, may not bleed PVUSS, CT

Diagnosis / Investigation

Bedside

  • ABCDE assessment
  • Weigh swabs and measure blood in suction (quantitative blood loss)
  • Bimanual uterine assessment
  • Inspect placenta for completeness
  • Systematic inspection of genital tract for tears
  • Urinary catheter (hourly urine output)

Bloods

  • FBC (haemoglobin, platelet count)
  • Coagulation screen (PT, APTT, fibrinogen)
  • Crossmatch (4-6 units for massive PPH)
  • U&Es, LFTs
  • ABG/VBG (lactate, base excess)
  • Point-of-care testing: ROTEM/TEG if available

Imaging

  • Ultrasound: retained products, uterine inversion, broad ligament haematoma
  • CT angiography if considering embolisation

Special Tests

  • Kleihauer test if RhD-negative
  • Blood bank: activate massive transfusion protocol if needed

Management

Non-pharmacological

  • Call for help early (obstetric emergency team)
  • ABCDE approach with simultaneous resuscitation
  • Two large-bore IV cannulae (14G)
  • Uterine massage (rubbing up a contraction)
  • Empty bladder (catheterise)
  • Bimanual uterine compression if severe
  • Keep patient warm (prevent hypothermia)

Pharmacological

  • First-line: Oxytocin 10 IU slow IV or 40 IU in 500 mL saline infusion
  • Second-line: Ergometrine 500mcg IM/IV (avoid in hypertension/pre-eclampsia)
  • Third-line: Carboprost (Hemabate) 250mcg IM every 15 min (max 8 doses; avoid in asthma)
  • Misoprostol 800mcg sublingual/rectal (if other agents unavailable)
  • Tranexamic acid 1g IV (give within 3 hours - WOMAN trial: reduced death from bleeding by 19%)
  • Blood products: packed red cells, FFP, platelets, cryoprecipitate (target fibrinogen >2 g/L)
  • Massive transfusion protocol: 1:1:1 ratio of RBC:FFP:platelets

Surgical/Interventional

  • Intrauterine balloon tamponade (Bakri balloon, Rusch catheter)
  • B-Lynch compression suture (uterine compression suture)
  • Uterine artery ligation (bilateral)
  • Internal iliac artery ligation
  • Uterine artery embolisation (interventional radiology if available and patient stable)
  • Peripartum hysterectomy (life-saving last resort)
  • Manual removal of placenta under regional/GA if retained

Referral Criteria

  • All major PPH requires consultant obstetrician attendance
  • Interventional radiology for uterine artery embolisation
  • Haematology for massive transfusion/DIC
  • ITU for haemodynamic instability
  • Debrief and psychological support post-event

Prognosis

  • Active management of third stage reduces PPH by 60%
  • Maternal mortality from PPH in UK: approximately 1 per 100,000 maternities
  • Tranexamic acid within 3 hours: reduces death from bleeding by 19% (WOMAN trial)
  • Hysterectomy rate for massive PPH: ~1 per 2,000 deliveries
  • Sheehan syndrome (postpartum hypopituitarism): rare long-term complication of massive PPH
  • Recurrence risk: 8-15% in subsequent pregnancies
  • Psychological impact: PTSD, postnatal depression, fear of subsequent pregnancy

Other Relevant Information

4 T's of PPH

CauseFrequencyExamples
Tone70%Uterine atony, overdistension
Trauma20%Perineal/cervical tears, rupture
Tissue10%Retained placenta/products
Thrombin<1%DIC, coagulopathy

WOMAN Trial Summary

FeatureDetail
Population20,060 women with PPH
InterventionTXA 1g IV vs placebo
Result19% reduction in death from bleeding
Key findingBenefit greatest when given within 3 hours
NNT~250 to prevent one death

Massive Transfusion Targets

ParameterTarget
Haemoglobin>80 g/L
Platelets>50 × 10⁹/L
Fibrinogen>2 g/L
PT/APTT ratio<1.5