Obstetric Haemorrhages — Study Notes
Effective Perinatal Care (EPC) Programme | WHO/USAID
1. Magnitude of the Problem
- ~14 million pregnancy-related haemorrhages per year worldwide
- At least 128,000 women bleed to death annually
- Risk of death from PPH:
- 1:100,000 deliveries in the UK/USA
- 1:1,000 births in some developing countries (100× higher)
2. Management Flaws — Why Women Die
The main reasons for PPH death:
- Underestimation of blood loss
- Inadequate volume replacement
- Delayed operative interventions
These are often linked to:
- Lack of back-up services (blood bank, surgical services)
- Lack of referral system
3. Definitions of PPH
| Source | Definition |
|---|
| WHO, 1998 | Blood loss ≥ 500 ml after childbirth |
| ACOG, 2001 | ≥10% change in haematocrit, or need for erythrocyte transfusion |
| McCormick ML et al, 2002 | Any blood loss that cannot be compensated physiologically → tissue damage |
Most Appropriate Definition (WHO 1998 / Cunningham 2001)
- Early PPH: ≥500 ml after vaginal delivery, or ≥1000 ml after caesarean — occurring within 24 hours
- Late PPH: 24 hours up to 6 weeks after childbirth
4. Prevention — Active Management of the Third Stage of Labour (AMTSL)
Reduces PPH risk by 60% (Prendiville WJ et al, 2007)
Three steps:
- Oxytocin 10 IU IM within 1 minute of birth of the baby
- Controlled cord traction to deliver the placenta
- Uterine massage until contracted
Uterotonic Options
| Drug | Dose | Notes |
|---|
| Oxytocin (first choice) | 10 IU IM/IV within 1 min | — |
| Ergometrine (if oxytocin unavailable) | 0.2 mg IM within 1 min | — |
| Misoprostol (if injectables unavailable) | 600 mcg oral/sublingual | Stable storage; no refrigeration needed |
5. Principles of Management (SOGC, 2000)
- Early recognition
- Initial assessment and treatment
- Identification of aetiology and direct therapy
- Replacement of blood loss
6. Step 1 — Early Recognition
Routine post-delivery observation:
- Check uterine tone (should be hard and round)
- Every 15 min for the first hour
- At end of 2nd, 3rd, 4th hour, then every 4 hours
- Estimate blood loss — clinical + quantitative methods
7. Step 2 — Initial Assessment and Treatment
Assess and monitor:
- Respiration, BP, HR, skin colour, urine output
- Coagulation screen, ABO type & cross-match
Initiate resuscitation:
- Insert 1–2 large-bore IV lines (size 16 or larger)
- Bolus infusion: 1 litre crystalloid in 15 minutes (ratio 3 ml:1 ml blood loss)
If signs of shock:
- Tilt head down
- Clear airways
- Oxygen by mask 6–8 L/min
Search for the cause of bleeding:
- Explore uterus: atony, retained placental fragments, rupture
- Explore lower genital tract: trauma
- Observe clots
8. Step 3 — Identification of Aetiology: The 4 "T"s
| "T" | Cause |
|---|
| Tonus | Uterine atony |
| Tissue | Retained placental fragments |
| Trauma | Lacerations of uterus/lower genital tract; uterine inversion |
| Thrombin | Pre-existing or acquired coagulation abnormalities |
Vaginal Bleeding Management by Placental Status
Placenta not yet delivered:
- Oxytocin 10 IU IM (if not already given)
- Massage uterus; attempt controlled cord traction if contracted
- If unsuccessful → vaginal exam; remove from cervix if present
- If not in vagina/cervix → manual removal
- If placenta accreta → surgical treatment
Placenta delivered but incomplete:
- Remove fragments by hand, ovum forceps, or large curette
- If bleeding persists → bedside clotting test (clot failure at 7 min = coagulopathy)
- If fragments cannot be removed (accreta) → surgical treatment
Placenta delivered and complete:
- Check for uterine atony
- Check for trauma
Bleeding Due to Uterine Atony — Drug Treatment
First-line: Oxytocin
- Initial: 10 IU IM/IV or 20 IU in 1000 mL saline at 60 drops/min
- Continuing: repeat 10 IU after 20 min if heavy bleeding, or 10 IU in 1000 mL saline at 30 drops/min
Second-line (if oxytocin fails): Ergometrine
- Initial: 0.2 mg IM/IV slowly
- Continuing: 0.2 mg IM every 15 min; up to 5 doses (total 1.0 mg)
- Onset: 2–5 min IM; duration ~3 hours
Third-line: Carboprost (15-methyl PGF₂α)
- Initial: 0.25 mg deep IM or intramyometrial
- Continuing: 0.25 mg every 15 min; up to 8 doses (2 mg total)
- Success rate: 86–96%; majority need only one dose
Misoprostol — Advantages vs. Disadvantages
| Advantages | Disadvantages |
|---|
| Low cost | Does NOT reduce maternal mortality |
| No refrigeration needed | Does NOT reduce hysterectomy rate |
| Easy to administer | Does NOT reduce blood transfusion need |
| Suitable for low-resource settings | Associated with maternal pyrexia and shivering |
Bleeding Due to Trauma
- Uterine rupture → laparotomy
- Vaginal/cervical lacerations → careful complete examination and repair
9. Refractory Haemorrhage
When initial treatment fails:
- Call for help
- Inform Blood Bank and ICU
- Assign roles: one midwife monitors/records; one manages blood preparation; one physician manages transfusion
Ongoing management:
- Continue IV crystalloids
- Prepare for surgery — BETTER SOONER THAN LATER
Temporary arrest of bleeding:
- Bimanual compression of the uterus (one fist vaginally, one hand abdominally)
- Compression of the aorta (external pressure above umbilicus)
10. Surgical Haemostasis — Arresting Bleeding
Key principle: Too late recourse to surgical haemostasis is a leading factor contributing to poor outcomes.
Sequence of interventions (until bleeding stops):
- B-Lynch suture (haemostatic compression suture) — first described 1997; >1300 cases reported; prevented hysterectomy in most; no serious complications; fertility preserved
- Bilateral ligation of uterine arteries — effectiveness 80–96%
- Bilateral ligation of internal iliac arteries
- Hysterectomy — incidence 7–13/10,000 births; most common indication now is placenta accreta/percreta (49.6%)
Total vs. Subtotal Hysterectomy:
- Subtotal is preferred in most PPH cases
- Total (with cervix) needed when bleeding source is in lower segment/cervix (rupture, placenta praevia, increta)
- Do not delay hysterectomy while attempting less familiar procedures
11. Step 4 — Replacement of Blood Loss
Crystalloids vs. Colloids
- First-line: Normal saline (crystalloid), ratio 3:1
- Colloids have no survival advantage over crystalloids and are more expensive
- Albumin: RR mortality 1.02; HES: 1.16; Dextran: 1.24 (Roberts & Alderson, 2004)
Red-Cell Transfusion Indications
- Only when there is decreased oxygen-carrying capacity (clinical hypoxia)
- Transfusion threshold individually determined:
- Critical Hb level: 70 g/L, but clinical signs of anaemia/hypoxia are equally important
- If blood loss ≥1000 mL and continuing → red cells should be readily available
Fresh-Frozen Plasma (FFP)
- Indicated only for replacement of coagulation factors in clotting disorders
- Give if PT and APTT exceed 1.5× control level in the presence of continued bleeding
12. Conclusions
Prevention:
- Each facility must have local PPH protocols
- Routine AMTSL reduces PPH risk by 60%
- Ensure availability of equipment, drugs, and trained personnel
Management:
- Early recognition and resuscitation are vital
- Oxytocin (up to 40 IU) and prostaglandins effective for uterine atony
- Bimanual compression and aorta compression are recommended for temporary arrest
- Surgical intervention must not be delayed — BETTER SOONER THAN LATER
- Hysterectomy is not always necessary; it need not be total in every case
Volume replacement:
- Crystalloids are first-line
- Blood transfusion is vital in severe PPH but must be used judiciously
- Strict indications for red-cell and FFP transfusion