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.
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
| Diagnosis | Key Features | Investigation |
|---|---|---|
| Uterine atony | Soft boggy uterus, most common | Bimanual palpation |
| Genital tract trauma | Bleeding despite contracted uterus | Systematic inspection |
| Retained placenta/products | Incomplete placenta, uterus not contracting fully | Examine placenta, USS |
| Uterine rupture | Previous CS scar, severe pain, shock | Clinical, laparotomy |
| Uterine inversion | Fundus not palpable, mass at introitus, shock | Clinical |
| Coagulopathy | Generalised oozing, no clot formation | Coagulation screen |
| Broad ligament haematoma | Lateral uterine mass, shock, may not bleed PV | USS, 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
| Cause | Frequency | Examples |
|---|---|---|
| Tone | 70% | Uterine atony, overdistension |
| Trauma | 20% | Perineal/cervical tears, rupture |
| Tissue | 10% | Retained placenta/products |
| Thrombin | <1% | DIC, coagulopathy |
WOMAN Trial Summary
| Feature | Detail |
|---|---|
| Population | 20,060 women with PPH |
| Intervention | TXA 1g IV vs placebo |
| Result | 19% reduction in death from bleeding |
| Key finding | Benefit greatest when given within 3 hours |
| NNT | ~250 to prevent one death |
Massive Transfusion Targets
| Parameter | Target |
|---|---|
| Haemoglobin | >80 g/L |
| Platelets | >50 × 10⁹/L |
| Fibrinogen | >2 g/L |
| PT/APTT ratio | <1.5 |