Antepartum Haemorrhage — Placenta Praevia & Abruption

Comprehensive Nursing Guide for GCC Obstetric Practice

GCC Nursing CPD Obstetric Emergencies ≥24 Weeks Gestation Evidence-Based 2025
Definition — Antepartum Haemorrhage (APH) Bleeding from the genital tract of ≥24 weeks gestation and before the onset of labour. Any visible APH warrants immediate assessment. Do NOT perform a vaginal examination until placenta praevia has been excluded by ultrasound.
📋Causes of APH
  • Placenta praevia — low-lying placenta covering or adjacent to os
  • Placental abruption — premature separation of normally sited placenta
  • Vasa praevia — fetal vessels crossing internal os
  • Bloody show (cervical mucus plug) — not true APH
  • Cervical lesion (polyp, ectropion, carcinoma)
  • Trauma (domestic violence — always consider)
  • Undiagnosed / idiopathic (~50% of APH cases)
NEVER Perform Vaginal Examination

Until placenta praevia has been excluded by ultrasound

  • Digital VE with praevia can provoke catastrophic haemorrhage
  • Speculum examination ONLY after USS clearance
  • USS (transabdominal ± transvaginal) must confirm placental location first
  • If no USS available — treat as praevia until proven otherwise
Initial ABCDE Assessment
ABCDE Primary Survey & Immediate Actions

Airway & Breathing

  • Assess airway patency
  • O₂ saturation — target ≥95%
  • High-flow O₂ if compromised
  • Respiratory rate, auscultate

Circulation

  • HR, BP, capillary refill
  • IV access × 2 (14–16G)
  • Blood: FBC, coagulation, G&S, crossmatch
  • UEC, LFTs, fibrinogen
  • Left lateral tilt (aortocaval relief)

Disability & Exposure

  • GCS / AVPU
  • Uterine tenderness, tone
  • Pad count — estimate blood loss
  • CTG for fetal wellbeing
  • Fetal parts palpable?
📅Blood Loss Estimation
  • Pad count — weigh saturated pads (1g ≈ 1mL blood)
  • Clot weight — estimate in addition to free blood
  • Minor APH: <50mL, haemodynamically stable
  • Major APH: 50–1000mL without clinical shock
  • Massive APH: >1000mL OR haemodynamic instability
  • Note: concealed abruption underestimates true loss
📊Fetal Assessment — CTG
  • Commence CTG immediately on all APH presentations
  • Bradycardia — sustained <100bpm = fetal emergency
  • Late decelerations — uteroplacental insufficiency
  • Reduced variability — assess in clinical context
  • Pathological CTG + APH = emergency delivery assessment
  • CTG normal does NOT exclude significant abruption
🔍Placental Localisation
  • Routine 20-week anomaly scan identifies low-lying placenta
  • Low-lying = placenta within 20mm of internal os
  • ~90% of low-lying placentas at 20 weeks resolve by 36 weeks (due to lower uterine segment development)
  • Repeat USS at 32 weeks if low-lying at 20 weeks
  • Transvaginal USS is safe and more accurate than transabdominal for placental localisation
  • MRI useful for accreta spectrum assessment
🧪Anti-D Immunoglobulin

All Rh-negative women with APH require anti-D

  • Kleihauer-Betke test — quantifies feto-maternal haemorrhage (FMH) volume
  • Standard dose anti-D: 250IU (<20 weeks) / 500IU (≥20 weeks)
  • Large FMH on Kleihauer → additional anti-D doses needed
  • Administer within 72 hours of bleed
  • Document blood group on all APH presentations
Shock Index Reference
Shock Index (HR ÷ SBP)InterpretationAction
<0.9NormalContinue monitoring
0.9–1.0Mild compromiseIncreased vigilance, fluid challenge
1.0–1.7Significant haemorrhageActive resuscitation, team alert
>1.7Critical — life-threateningMTP activation, immediate senior obstetric & anaesthetic review
Placenta Praevia — Key Principle Painless, bright red vaginal bleeding with a soft uterus. The placenta lies in the lower uterine segment, partially or completely covering the internal os. NEVER perform digital vaginal examination.
Classification of Placenta Praevia
GradeDescriptionClinical Significance
Grade IPlacenta encroaches lower uterine segment but does not reach osMinor — vaginal birth possible
Grade IIPlacenta reaches internal os but does not cover itMarginal — individualised management
Grade IIIPlacenta partially covers the internal osMajor praevia — Caesarean section required
Grade IVPlacenta completely covers the internal osMajor praevia — elective LSCS mandatory
Major Praevia = Grade III or IV Always plan delivery by elective lower segment Caesarean section (LSCS). Prepare for potential accreta spectrum.
Clinical Features — Placenta Praevia
  • PAINLESS bright red (fresh) vaginal bleeding
  • Uterus soft and non-tender
  • Fetal parts palpable (normal fetal lie/presentation OR malpresentation due to praevia)
  • Abnormal fetal lie (transverse/oblique) common
  • Fetal compromise less common than abruption unless massive haemorrhage
  • Recurrent bleeds — sentinel bleed often precedes major haemorrhage
  • Haemodynamic instability with large bleed
Antepartum Management
  • Hospitalisation from 34 weeks for major praevia
  • Complete bed rest; no pelvic (sexual) rest
  • IV access × 2, group and crossmatch 4–6 units
  • Corticosteroids if <34 weeks (betamethasone 12mg IM × 2 doses, 24h apart)
  • MgSO₄ neuroprotection if <34 weeks and delivery anticipated
  • Tocolysis controversial — only if benefits outweigh risks (not for abruption)
  • Iron supplementation for chronic anaemia from repeated bleeds
  • Platelet target >80 × 10⁹/L for LSCS; crossmatch available in theatre
Delivery Planning
  • Major praevia (III/IV): Elective LSCS at 36–38 weeks gestation
  • Minor praevia (I/II): Vaginal birth possible if ≥20mm from os — senior decision
  • Delivery location: tertiary centre with blood bank, level 3 NICU, interventional radiology
  • Theatre immediately available for all praevia patients
  • Senior obstetrician to perform LSCS (risk of torrential haemorrhage)
  • Cell salvage consideration (autologous blood)
  • Paediatric team at delivery
Accreta Spectrum (PAS)
  • Accreta: villi adhere to myometrium (no decidua)
  • Increta: villi invade into myometrium
  • Percreta: villi penetrate through uterus (bladder/bowel)
  • Highest risk: praevia + previous Caesarean section
  • Risk increases with each prior CS — up to 67% with ≥3 prior CS + praevia
  • MRI ± USS with colour Doppler for diagnosis
  • Interventional radiology pre-operatively (balloon occlusion / UAE)
  • Planned hysterectomy may be required — consent includes fertility loss
Interventional Radiology in GCC Major GCC tertiary centres (SKMC Abu Dhabi, Cleveland Clinic Abu Dhabi, KFSH Riyadh) have active interventional radiology teams capable of internal iliac artery balloon occlusion and uterine artery embolisation for accreta spectrum haemorrhage. Ensure referral pathway is established antenatally.
Placental Abruption — Key Principle Premature separation of a normally sited placenta. Can be CONCEALED (no external bleeding but severe pain and shock) or REVEALED (visible dark bleeding). DIC risk is high. Fetal compromise is common.
Clinical Features — Abruption
  • PAINFUL — sudden onset severe abdominal pain
  • Dark red (old) blood — or concealed (no visible bleed)
  • Hypertonic, board-like uterus — tender on palpation
  • Fetal parts difficult to palpate (uterine rigidity)
  • Fetal compromise — CTG abnormalities common
  • Maternal shock disproportionate to visible blood loss (concealed)
  • Uterine tenderness localised or generalised
  • Passage of clots
Revealed vs Concealed
FeatureRevealedConcealed
External bleedingPresentAbsent / minimal
Pain severityModerateSevere
Shock indexCorrelates with lossDisproportionate
Uterine tendernessPresentMarked
DIC riskModerateHigh
Fetal compromiseVariableHigh
Disseminated Intravascular Coagulation (DIC)

Pathophysiology

  • Retroplacental haematoma releases tissue thromboplastin
  • Activates extrinsic coagulation cascade
  • Consumptive coagulopathy — fibrinogen falls rapidly
  • Fibrinogen <2g/L is critically low in obstetrics (<4g/L = early warning)
  • Thrombocytopaenia develops
  • PT / APTT prolonged

Management of DIC

  • ROTEM / TEG point-of-care testing guides component therapy
  • Cryoprecipitate (fibrinogen source) — target fibrinogen >2g/L
  • FFP (1:1 ratio with RBCs in MTP)
  • Platelet transfusion — target >75 × 10⁹/L
  • Tranexamic acid 1g IV (antifibrinolytic)
  • Calcium gluconate 10mL 10% with each 4 units FFP (chelation prevention)
  • Haematology team involvement essential
Kleihauer-Betke Test
  • Detects fetal red cells in maternal circulation
  • Quantifies feto-maternal haemorrhage (FMH) volume
  • Used to calculate additional anti-D dose in Rh-negative women
  • Positive result with abruption — significant FMH possible
  • Flow cytometry increasingly used as alternative
  • Perform on all significant APH in Rh-negative women
Couvelaire Uterus
  • Extravasation of blood into uterine myometrium
  • Uterus appears purple/bruised at Caesarean section
  • Impairs uterine contractility → increases PPH risk
  • May prevent response to uterotonics
  • Hysterectomy may be required to control haemorrhage
  • ICU admission post-operatively
Abruption Management by Severity
SeverityFeaturesManagement
Minor / StableSmall bleed, stable vitals, normal CTG, no coagulopathyContinuous CTG monitoring, IV access, bloods, senior review, consider steroids if <34/40
ModerateModerate bleed, maternal tachycardia, suspicious CTG, early coagulopathyActive resuscitation, crossmatch 4–6U, haematology alert, delivery assessment
Severe / MajorMassive haemorrhage, shock, fetal compromise, DIC, concealedMTP activation, emergency delivery (LSCS vs instrumental depending on stage), HDU/ICU
Abruption in Pre-eclampsia Up to 25% of severe pre-eclampsia cases are complicated by placental abruption. Concurrent hypertension worsens outcomes — vasospasm reduces uteroplacental flow. MgSO₄ should continue for seizure prophylaxis while managing the abruption. Anti-hypertensives must be maintained. These patients have significantly worse maternal and fetal outcomes.
Vasa Praevia — Definition Fetal blood vessels, unsupported by placenta or umbilical cord, run across or near the internal cervical os. Rupture of these vessels at membrane rupture causes rapid FETAL exsanguination. Fetal mortality 60–75% if undiagnosed.
Risk Factors
  • Velamentous cord insertion (cord inserts into membranes not placental disc)
  • Bilobed or succenturiate placenta (accessory lobe with bridging vessels)
  • IVF / ART — significantly higher risk of velamentous insertion
  • Multiple pregnancy
  • Low-lying placenta in second trimester
  • Placenta praevia in previous pregnancy
Clinical Features
  • Painless bright fresh bleeding at membrane rupture
  • Sudden fetal bradycardia — sinusoidal CTG pattern
  • Fetal tachycardia (compensatory) before bradycardia
  • Blood loss is FETAL — small volume causes fetal shock
  • Normal maternal haemodynamics (maternal blood not lost)
  • Fetal mortality 60–75% if undiagnosed and vessels rupture
  • Survival approaches 97% with antenatal diagnosis and planned delivery
Diagnosis
  • Colour Doppler ultrasound at 16–20 weeks anomaly scan
  • Transvaginal USS with Doppler — vessels overlying os
  • Screen all high-risk women (IVF, velamentous insertion, succenturiate lobe)
  • MRI can confirm in difficult cases
  • Apt test (blood diluted in water — fetal Hb resistant to alkali denaturation) — rarely used, rapid but imprecise
  • Confirm placental cord insertion at anomaly scan in all pregnancies
Antenatal Management (Diagnosed)
  • Diagnosis at 28–32 weeks → planned hospitalisation
  • Corticosteroids for fetal lung maturity (34 weeks if not given earlier)
  • Planned elective LSCS at 34–36 weeks — BEFORE spontaneous labour / membrane rupture
  • Avoid amniotomy, membrane sweep, or sexual intercourse
  • Education — warn of emergency symptoms (bleeding + bradycardia = call emergency)
  • Tertiary centre delivery with immediate surgical capability
  • Neonatal team present at delivery
Emergency Management — Suspected Vasa Praevia Rupture
  • Call emergency team immediately — obstetrician, anaesthetist, neonatologist
  • Rush patient to theatre — every minute counts (fetal exsanguination rate is rapid)
  • Emergency LSCS under general anaesthesia if fetal bradycardia present
  • Alert neonatal team — neonate will likely require immediate resuscitation
  • Prepare O-negative blood for neonate — exchange transfusion may be required
  • Maternal IV access and bloods — maternal haemodynamics usually stable
  • Neonatal team to manage fetal haemorrhagic shock: volume resuscitation, blood transfusion
  • 🚨

    MAJOR APH — ACTIVATE EMERGENCY RESPONSE

    Blood loss >500mL, haemodynamic instability, OR fetal compromise. Every minute matters — simultaneous team activation and resuscitation.

    Immediate Emergency Steps (First 5 Minutes)
  • Call for help: Obstetric registrar/consultant + Anaesthetist + Midwife coordinator + Haematology + Neonatal team (if viable fetus)
  • Position: Left lateral tilt 15° (reduces aortocaval compression, improves cardiac output)
  • Airway & Breathing: High-flow O₂ 15L/min via non-rebreather mask; target SpO₂ ≥95%
  • IV Access × 2: 14–16G large-bore cannulae; draw bloods simultaneously (FBC, coag, fibrinogen, G+S, crossmatch, UEC, LFT, glucose, ABG)
  • Fluid resuscitation: Crystalloid 500mL bolus × 2 while awaiting blood; do NOT over-dilute coagulation factors
  • Urinary catheter: Monitor urine output hourly — target ≥0.5mL/kg/hr (reflects organ perfusion)
  • CTG: Continuous fetal monitoring — pathological CTG = emergency delivery
  • Massive Transfusion Protocol (MTP)
    • Activate MTP when ≥4U pRBCs in 4 hours OR haemodynamic instability despite resuscitation
    • 1:1:1 ratio: pRBCs : FFP : Platelets (empirical until ROTEM available)
    • Tranexamic acid (TXA) 1g IV over 10 minutes — within 3 hours of bleeding onset; repeat 1g if ongoing at 30 minutes
    • Calcium gluconate 10mL 10% IV with every 4 units of FFP (citrate chelation)
    • Fibrinogen concentrate 2–4g IV if fibrinogen <2g/L
    • Aim: Hb ≥80g/L, Platelets ≥75×10⁹/L, Fibrinogen ≥2g/L, INR <1.5
    Point-of-Care Coagulation Testing
    • ROTEM (Rotational Thromboelastometry) or TEG (Thromboelastography)
    • Guides targeted component therapy — avoids empirical over-transfusion
    • EXTEM/FIBTEM: fibrinogen function assessment
    • APTEM: detects hyperfibrinolysis (responds to TXA)
    • Results available within 10–15 minutes
    • Available in most GCC tertiary obstetric centres
    • Repeat every 30–60 minutes during active haemorrhage
    Perimortem Caesarean Section
    • Maternal cardiac arrest in pregnancy — standard CPR ineffective after 20 weeks (aortocaval compression)
    • Perimortem CS must be initiated within 4 minutes of maternal cardiac arrest
    • Delivery by 5 minutes optimises maternal AND fetal outcome
    • Do NOT delay for theatre — perform at bedside in resuscitation room
    • CPR continues throughout and after delivery
    • Most common cause of perimortem CS = APH / haemorrhagic shock
    Post-Operative / HDU Care
    • Minimum HDU care × 24h post major APH
    • DIC monitoring: coagulation profile 4-hourly × 24h
    • Fluid balance — strict hourly documentation
    • Urine output ≥0.5mL/kg/hr — alert if less than this for ≥2 hours
    • Serial Hb (6h and 12h post-surgery)
    • Wound inspection × 4h post-delivery
    • VTE prophylaxis when safe (post-DIC resolution)
    • Psychological debrief — traumatic birth experience support
    • Neonatal unit liaison for maternal-infant bonding support
    Praevia vs Abruption — Key Comparison
    Feature
    Placenta Praevia
    Placental Abruption
    Pain
    PAINLESS
    PAINFUL (severe)
    Blood colour
    Bright red (fresh)
    Dark red / concealed
    Uterine tone
    Soft, non-tender
    Hard, hypertonic, tender
    Fetal parts
    Palpable
    Difficult to palpate
    Fetal compromise
    Less common
    Common / early
    DIC risk
    Low (unless accreta)
    HIGH — early feature
    VE safety
    NEVER without USS
    Avoid until assessed
    Delivery route
    LSCS (major praevia)
    Emergency LSCS if fetal compromise
    GCC-Specific Context for APH Management The Gulf Cooperation Council region has unique demographic, cultural, and healthcare system factors that directly affect APH incidence, presentation, and management. GCC nurses must understand this context.
    30–50%
    CS rate in some GCC hospitals (vs 20–25% global recommendation)
    4–7
    Average lifetime births per woman in some GCC populations (grand multiparity)
    ↑67%
    Accreta risk with praevia + ≥3 prior Caesarean sections
    Placenta Accreta Spectrum Rising in GCC
    • High CS rates (30–50% in many GCC hospitals) create scarred uteri at younger maternal ages
    • Multiple CSections in the same patient at younger age — earlier and more severe accreta
    • Grand multiparity common in GCC → increased uterine surgeries → accreta spectrum risk multiplied
    • Praevia + scarred uterus = highest accreta risk combination
    • Accreta spectrum may be diagnosed incidentally at anomaly scan in GCC tertiary centres
    • Dedicated placenta accreta clinics established in SKMC, KFSH, Cleveland Clinic Abu Dhabi
    Antenatal Care Access Variation
    • Private clinic antenatal care prevalent — high-quality surveillance in major cities
    • Expatriate workers — variable antenatal care quality; late presentation possible
    • Remote/rural GCC areas — limited access to specialist obstetric care
    • Some patients present for first time in active haemorrhage with no USS on record
    • Language barriers (South Asian, Filipino, African expatriate workers)
    • Ensure translated patient information available in Arabic, Urdu, Tagalog, Hindi
    Cultural & Religious Considerations
    • Female-only care preference: Many GCC women prefer female obstetricians and nurses for intimate examinations — organise when possible; document when unavailable in emergency
    • Fertility significance: Hysterectomy carries profound cultural weight — Arabic language informed consent essential; involve family spokesperson per patient wishes
    • Mahram presence: Male guardian (husband/father) may wish to be involved in major decisions — respect while ensuring patient autonomy
    • Ramadan fasting: Dehydration during Ramadan can trigger small APH bleeds; educate patients that medical exemptions apply
    • Consanguineous marriage: Higher rates of rare blood group antibodies in some populations — early blood group and antibody screen essential
    Blood Products & Specialist Resources
    • Blood banks well-stocked in GCC tertiary centres — 24/7 crossmatch capability
    • O-negative blood available for emergency release without crossmatch
    • Cell salvage (intraoperative autotransfusion) available in major centres
    • ROTEM/TEG point-of-care coagulation testing widely available in GCC Level 1 hospitals
    • Interventional radiology (IR) teams for PAS management:
    SKMC Abu Dhabi Cleveland Clinic ABD KFSH Riyadh KHMC Qatar KKUH Jeddah
    Ramadan & Seasonal APH Considerations

    Ramadan Risk Factors

    • Dehydration from prolonged fasting → uterine irritability → can trigger small bleeds or preterm labour
    • Hypoglycaemia may mask / mimic haemodynamic compromise
    • Delayed hospital attendance — patients may fear breaking fast for non-emergency
    • Educate: Islamic jurisprudence permits breaking fast for medical emergencies — reinforce this clearly
    • Increase hydration advice during non-fasting hours

    Staff & System Considerations

    • Reduced staffing possible during Ramadan night shifts in GCC — ensure safe staffing ratios maintained
    • Blood product availability unchanged — blood bank staff on rotation
    • Emergency drills recommended before and during Ramadan
    • Summer heat (UAE/Saudi/Qatar) — dehydration risk year-round for outdoor workers' partners
    Arabic-Language Consent — Hysterectomy
    🤔 APH Assessment & Classification Tool
    Enter clinical features to classify likely APH cause and generate immediate management steps

    📋 Most Likely Diagnosis

    ▶ Immediate Management Steps