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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:
  1. Underestimation of blood loss
  2. Inadequate volume replacement
  3. 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

SourceDefinition
WHO, 1998Blood loss ≥ 500 ml after childbirth
ACOG, 2001≥10% change in haematocrit, or need for erythrocyte transfusion
McCormick ML et al, 2002Any 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:
  1. Oxytocin 10 IU IM within 1 minute of birth of the baby
  2. Controlled cord traction to deliver the placenta
  3. Uterine massage until contracted

Uterotonic Options

DrugDoseNotes
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/sublingualStable storage; no refrigeration needed

5. Principles of Management (SOGC, 2000)

  1. Early recognition
  2. Initial assessment and treatment
  3. Identification of aetiology and direct therapy
  4. 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
TonusUterine atony
TissueRetained placental fragments
TraumaLacerations of uterus/lower genital tract; uterine inversion
ThrombinPre-existing or acquired coagulation abnormalities

Vaginal Bleeding Management by Placental Status

Placenta not yet delivered:
  1. Oxytocin 10 IU IM (if not already given)
  2. Massage uterus; attempt controlled cord traction if contracted
  3. If unsuccessful → vaginal exam; remove from cervix if present
  4. If not in vagina/cervix → manual removal
  5. 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
AdvantagesDisadvantages
Low costDoes NOT reduce maternal mortality
No refrigeration neededDoes NOT reduce hysterectomy rate
Easy to administerDoes NOT reduce blood transfusion need
Suitable for low-resource settingsAssociated 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:
  1. Call for help
  2. Inform Blood Bank and ICU
  3. 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):
  1. B-Lynch suture (haemostatic compression suture) — first described 1997; >1300 cases reported; prevented hysterectomy in most; no serious complications; fertility preserved
  2. Bilateral ligation of uterine arteries — effectiveness 80–96%
  3. Bilateral ligation of internal iliac arteries
  4. 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
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