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O&G SAQsAntenatal care — obstetric haemorrhage

O&G SAQs · Antenatal care — obstetric haemorrhage

Antepartum haemorrhage — structured SAQ (15 marks)

FRANZCOG-format structured SAQ on undifferentiated antepartum haemorrhage at 32 weeks: parallel resuscitation and fetal assessment, the discriminating differential, anti-D and Kleihauer with ANZ doses, and disposition by gestation and severity. Per-sub-part marking rubric included.

15 marks20 min4 min readSource-verified ·

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FRANZCOGMRCOGABOG
Prompt
You are the on-call registrar. A 29-year-old G2P1 (previous caesarean) presents at 32+3 weeks with a sudden painless bright red vaginal bleed of approximately 400 mL. She is RhD negative with no preformed antibodies. Observations: HR 112 bpm, BP 108/64 mmHg, RR 18, alert. The uterus is soft and non-tender; the presenting part is high. She has not had a mid-pregnancy scan. (a) Outline your immediate assessment and resuscitation in the first fifteen minutes, with the reasoning for each step. (5 marks) (b) State the differential diagnosis with the feature that discriminates each. (4 marks) (c) She is RhD negative. Detail your rhesus management, including agent, dose, route, timing and laboratory testing. (3 marks) (d) The bleeding settles and the CTG is normal. Outline your ongoing management and disposition to birth. (3 marks)

How this SAQ is marked

Twelve SAQs, 180 marks, two 2-hour papers — roughly 15 marks and 20 minutes each. Marks come from specifics: the named drug, the dose, the route, the threshold, the time window. Write labelled short points, answer the sub-part you were asked, and never spend a mark restating the stem. [1]

Reveal model answer and mark schemeShowHide

(a) Immediate assessment and resuscitation, first fifteen minutes (5 marks)

One mark per point, maximum five. A mark is available for stating that maternal resuscitation and fetal assessment happen in parallel. [1][2]

  • Call for help and declare the emergency — obstetric consultant, anaesthetist, midwifery coordinator, blood bank; escalate to the massive obstetric haemorrhage protocol if loss exceeds 1000 mL or she becomes shocked.[1]
  • Mother: left lateral tilt, oxygen if hypoxic, two large-bore cannulae, warmed crystalloid then blood; quantify loss rather than estimate it; compute the shock index (112 divided by 108 equals 1.04, already above the 1.0 threshold despite a reassuring blood pressure).[1][2]
  • Bloods: full blood count, coagulation profile with fibrinogen, group and antibody screen, crossmatch, U&E and liver function, and a Kleihauer because she is RhD negative.[3][4]
  • Fetus: auscultate then apply continuous CTG — at 32+3 weeks the trace determines whether this pregnancy continues tonight.[2]
  • No digital vaginal examination until the placental site is known. Arrange urgent ultrasound for placental localisation; a speculum examination is acceptable once the site is known or in a setting where immediate caesarean is possible.[1]
  • Catheterise, warm, and document a running quantitative loss total.[1]

(b) Differential diagnosis with discriminators (4 marks)

One mark per cause with its discriminating feature. No mark for a bare list. [1][2]

CauseThe feature that discriminates it
Placenta praeviaPainless bright red bleeding, soft non-tender uterus, high or unengaged presenting part — fits this woman
Placental abruptionPain usually precedes the bleeding, dark loss, tense tender uterus that will not relax, early CTG abnormality
Vasa praeviaBleeding at rupture of membranes with immediate fetal bradycardia while the mother stays well
Uterine rupture or scar dehiscencePrevious caesarean, scar pain, loss of station, fetal bradycardia, maternal collapse
Local genital tract causeCervical ectropion, polyp, cervicitis or malignancy — found on speculum, not on scan
Unknown originA diagnosis of exclusion, still associated with preterm birth and adverse perinatal outcome
[1][2][8]

A mark is available for stating that a normal ultrasound does not exclude abruption because sonographic sensitivity is low. [7]

(c) Rhesus management (3 marks)

One mark each for the agent with dose and route, the timing, and the laboratory testing with its purpose. [3][4]

  • Give Rh D immunoglobulin 625 IU IM in Australia and New Zealand (500 IU IM is the United Kingdom dose after 20 weeks) as soon as possible, ideally within 72 hours; a dose given up to 10 days later still offers some protection.[3]
  • Do not wait for the laboratory. The first dose is given on clinical grounds; testing determines whether an additional dose is required, not whether to give the first one.[3][4]
  • Send a maternal sample for fetomaternal haemorrhage quantification — Kleihauer acid-elution screening, with flow cytometry as the more accurate confirmatory method — and give a calculated top-up dose on laboratory advice if the bleed is large.[4][3]
  • Repeat with repeat bleeds at approximately six-weekly intervals with re-quantification, and continue routine antenatal prophylaxis at 28 and 34 weeks in addition to sensitising-event doses.[3]

(d) Ongoing management and disposition (3 marks)

One mark each for corticosteroids with the correct regimen, neuroprotection with the correct threshold, and a defensible plan for the place and timing of birth. [5][6]

  • Admit. A 400 mL bleed is a major antepartum haemorrhage; she stays until stable, and given the previous caesarean the placental site report must comment explicitly on accreta features if she has a praevia.[1]
  • Betamethasone 11.4 mg IM, two doses 24 hours apart (or dexamethasone 6 mg IM for four doses 12 hours apart) — a single course reduces perinatal death, respiratory distress syndrome and intraventricular haemorrhage.[5]
  • Magnesium sulphate 4 g IV over 20 to 30 minutes then 1 g/h for fetal neuroprotection only if birth under 30 weeks is anticipated in Australia and New Zealand — at 32+3 weeks she is above the ANZ threshold, and saying so earns the mark.[6]
  • Ongoing surveillance: serial growth scans, fetal wellbeing assessment, iron optimisation, a valid group and screen maintained, and a documented plan for the place and timing of birth with a third-stage plan written in advance.[1][8]
  • Discharge criteria if she settles: no further bleeding, normal CTG, anti-D given, close to hospital with reliable transport and a companion, and explicit instructions to return immediately with any further loss.[1]
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References8ShowHide
  1. [1]Jauniaux E, Bhide A, Hussein AM, et al. Placenta Praevia and Placenta Accreta Spectrum: Diagnosis and Management: Green-Top Guideline No. 27a BJOG, 2026.PMID 42374711
  2. [2]Oyelese Y, Ananth CV Placental abruption Obstet Gynecol, 2006.PMID 17012465
  3. [3]Qureshi H, Massey E, Kirwan D, et al. BCSH guideline for the use of anti-D immunoglobulin for the prevention of haemolytic disease of the fetus and newborn Transfus Med, 2014.PMID 25121158
  4. [4]Porter L, Hazell M, Eggington J, et al. BSH guideline for the estimation of fetomaternal haemorrhage Transfus Med, 2026.PMID 42286430
  5. [5]McGoldrick E, Stewart F, Parker R, Dalziel SR Antenatal corticosteroids for accelerating fetal lung maturation for women at risk of preterm birth Cochrane Database Syst Rev, 2020.PMID 33368142
  6. [6]Shepherd ES, Goldsmith S, Doyle LW, et al. Magnesium sulphate for women at risk of preterm birth for neuroprotection of the fetus Cochrane Database Syst Rev, 2024.PMID 38726883
  7. [7]Glantz C, Purnell L Clinical utility of sonography in the diagnosis and treatment of placental abruption J Ultrasound Med, 2002.PMID 12164566
  8. [8]Bhandari S, Raja EA, Shetty A, Bhattacharya S Maternal and perinatal consequences of antepartum haemorrhage of unknown origin BJOG, 2014.PMID 24125550
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