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O&G TopicsCritical care in obstetrics and gynaecology

O&G · Critical care in obstetrics and gynaecology

Massive obstetric haemorrhage: transfusion, ROTEM-guided replacement and DIC

Also known as Massive obstetric haemorrhage · Massive transfusion in obstetrics · Obstetric coagulopathy · Obstetric DIC · ROTEM-guided transfusion · Viscoelastic haemostatic testing · Major obstetric haemorrhage protocol

Exam-exhaustive FRANZCOG fellowship reference on massive obstetric haemorrhage — definitions and activation triggers, ratio-based versus viscoelastic-guided replacement, the fibrinogen and FIBTEM A5 thresholds with the three negative randomised trials, calcium and temperature, the lethal triad, ISTH DIC scoring in pregnancy, cell salvage evidence, and post-event AKI and Sheehan syndrome. Companion to the primary postpartum haemorrhage topic, which carries the uterotonic and surgical ladders.

high24 referencesUpdated 26 July 202621 min readVerification in progress

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Practise this topic10 MCQs with explanations

Target exams

FRANZCOGMRCOGABOGFRCSCMRCPI

Red flags

  • Activating the protocol without also naming the surgical decision point — products do not close a bleeding vessel
  • A fibrinogen of 3 g/L in a woman who started pregnancy at 6 g/L is a falling fibrinogen, not a normal one
  • Ionised hypocalcaemia in rapid transfusion — an independent, concentration-dependent mortality factor, not a footnote
  • Cold products and a cold patient: hypothermia below 35 degrees Celsius is a coagulation diagnosis
  • Litres of crystalloid before blood — dilutional coagulopathy you created yourself
  • Delaying fibrinogen replacement beyond 3 hours from the start of red cell transfusion
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Your progress

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Practise this topic10 MCQs with explanations

Target exams

FRANZCOGMRCOGABOGFRCSCMRCPI

Red flags

  • Activating the protocol without also naming the surgical decision point — products do not close a bleeding vessel
  • A fibrinogen of 3 g/L in a woman who started pregnancy at 6 g/L is a falling fibrinogen, not a normal one
  • Ionised hypocalcaemia in rapid transfusion — an independent, concentration-dependent mortality factor, not a footnote
  • Cold products and a cold patient: hypothermia below 35 degrees Celsius is a coagulation diagnosis
  • Litres of crystalloid before blood — dilutional coagulopathy you created yourself
  • Delaying fibrinogen replacement beyond 3 hours from the start of red cell transfusion
One-line fellowship answer

Massive obstetric haemorrhage is bleeding that outruns the laboratory, so you activate a protocol, give tranexamic acid early, warm everything, replace calcium, and switch from formulaic packs to viscoelastic-guided replacement the moment a point-of-care result is back — while somebody else names the surgical decision point, because products do not close a bleeding vessel.[1][13][16]

She has lost 2600 mL, she has had four uterotonics and a balloon, and the field is now oozing from everywhere you have touched. Somebody hands you a coagulation result from 40 minutes ago. That is the moment this topic exists for — when the problem stops being the uterus and becomes the clot.[14][12]

The uterotonic ladder, the 4 T's, balloon tamponade and the surgical ladder live in the primary postpartum haemorrhage topic. This topic is the transfusion, coagulopathy and protocol science that sits underneath them.[1]

Overview and definition

There is no single definition, and examiners know it. Give the family of thresholds, then say which one you would use to act. [1][2]

  • Volume: loss of 2500 mL or more; or one whole blood volume in 24 hours; or 50% of blood volume within 3 hours.[1][2]
  • Transfusion: 4 or more units of red cells (many obstetric protocols use 5 or more, which is the threshold the Welsh national cohort applied alongside a 2500 mL loss).[14][1]
  • Rate: ongoing loss of about 150 mL/min, which is where the laboratory can no longer keep pace with you.[2][1]
  • Physiology: any bleeding with hypovolaemic compromise, regardless of the measured number.[2][1]
Say this instead of a number"Massive haemorrhage is bleeding at a rate at which a formulaic response is safer than waiting for a laboratory result." That sentence covers every published definition and tells the examiner you understand why the thresholds exist.[2][14]

Classify the coagulopathy, not just the volume. Four mechanisms, and they demand different products: [20][7]

  • Dilutional — crystalloid and red cells without factor replacement.
  • Consumptive (DIC) — tissue factor exposure driving thrombin generation and fibrinogen consumption.
  • Hyperfibrinolytic — excess plasmin activity; the target of tranexamic acid.
  • Pre-existing — inherited bleeding disorder, anticoagulant effect, liver disease.[20][3]
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References24ShowHide
  1. [1]Royal College of Obstetricians and Gynaecologists (RCOG) Prevention and Management of Postpartum Haemorrhage: Green-top Guideline No. 52 BJOG, 2017.PMID 27981719
  2. [2]Robinson D, Basso M, Chan WS, et al. Guideline No. 431: Postpartum Hemorrhage and Hemorrhagic Shock J Obstet Gynaecol Can, 2022.PMID 36567097
  3. [3]WOMAN Trial Collaborators Effect of early tranexamic acid administration on mortality, hysterectomy, and other morbidities in women with post-partum haemorrhage (WOMAN): an international, randomised, double-blind, placebo-controlled trial Lancet, 2017.PMID 28456509
  4. [4]Gayet-Ageron A, Prieto-Merino D, Ker K, et al. Effect of treatment delay on the effectiveness and safety of antifibrinolytics in acute severe haemorrhage: a meta-analysis of individual patient-level data from 40 138 bleeding patients Lancet, 2018.PMID 29126600
  5. [5]Holcomb JB, Tilley BC, Baraniuk S, et al. Transfusion of plasma, platelets, and red blood cells in a 1:1:1 vs a 1:1:2 ratio and mortality in patients with severe trauma: the PROPPR randomized clinical trial JAMA, 2015.PMID 25647203
  6. [6]Charbit B, Mandelbrot L, Samain E, et al. The decrease of fibrinogen is an early predictor of the severity of postpartum hemorrhage J Thromb Haemost, 2007.PMID 17087729
  7. [7]Collins PW, Lilley G, Bruynseels D, et al. Fibrin-based clot formation as an early and rapid biomarker for progression of postpartum hemorrhage: a prospective study Blood, 2014.PMID 25024304
  8. [8]Collins PW, Cannings-John R, Bruynseels D, et al. Viscoelastometric-guided early fibrinogen concentrate replacement during postpartum haemorrhage: OBS2, a double-blind randomized controlled trial Br J Anaesth, 2017.PMID 28969312
  9. [9]Wikkelsø AJ, Edwards HM, Afshari A, et al. Pre-emptive treatment with fibrinogen concentrate for postpartum haemorrhage: randomized controlled trial Br J Anaesth, 2015.PMID 25586727
  10. [10]Ducloy-Bouthors AS, Mercier FJ, Grouin JM, et al. Early and systematic administration of fibrinogen concentrate in postpartum haemorrhage following vaginal delivery: the FIDEL randomised controlled trial BJOG, 2021.PMID 33713384
  11. [11]Mallaiah S, Barclay P, Harrod I, et al. Introduction of an algorithm for ROTEM-guided fibrinogen concentrate administration in major obstetric haemorrhage Anaesthesia, 2015.PMID 25289791
  12. [12]McNamara H, Kenyon C, Smith R, et al. Four years' experience of a ROTEM-guided algorithm for treatment of coagulopathy in obstetric haemorrhage Anaesthesia, 2019.PMID 30950521
  13. [13]Bell SF, Collis RE, Pallmann P, et al. Reduction in massive postpartum haemorrhage and red blood cell transfusion during a national quality improvement project, Obstetric Bleeding Strategy for Wales, OBS Cymru: an observational study BMC Pregnancy Childbirth, 2021.PMID 33992094
  14. [14]Bell SF, Collis RE, Bailey C, et al. The incidence, aetiology, and coagulation management of massive postpartum haemorrhage: a two-year national prospective cohort study Int J Obstet Anesth, 2021.PMID 33994274
  15. [15]Deleu F, Deneux-Tharaux C, Chiesa-Dubruille C, et al. Fibrinogen concentrate and maternal outcomes in severe postpartum hemorrhage: A population-based cohort study with a propensity score-matched analysis J Clin Anesth, 2022.PMID 35662057
  16. [16]Ho KM, Leonard AD Concentration-dependent effect of hypocalcaemia on mortality of patients with critical bleeding requiring massive transfusion: a cohort study Anaesth Intensive Care, 2011.PMID 21375089
  17. [17]Kander T, Schött U Effect of hypothermia on haemostasis and bleeding risk: a narrative review J Int Med Res, 2019.PMID 31475619
  18. [18]Taylor FB Jr, Toh CH, Hoots WK, et al. Towards definition, clinical and laboratory criteria, and a scoring system for disseminated intravascular coagulation Thromb Haemost, 2001.PMID 11816725
  19. [19]Iba T, Levy JH, Maier CL, et al. Updated definition and scoring of disseminated intravascular coagulation in 2025: communication from the ISTH SSC Subcommittee on Disseminated Intravascular Coagulation J Thromb Haemost, 2025.PMID 40216223
  20. [20]Erez O, Mastrolia SA, Thachil J Disseminated intravascular coagulation in pregnancy: insights in pathophysiology, diagnosis and management Am J Obstet Gynecol, 2015.PMID 25840271
  21. [21]Dey T, Brown D, Cole MG, et al. Cell salvage for the management of postpartum haemorrhage Cochrane Database Syst Rev, 2024.PMID 39704317
  22. [22]Khan KS, Moore PAS, Wilson MJ, et al. Cell salvage and donor blood transfusion during cesarean section: A pragmatic, multicentre randomised controlled trial (SALVO) PLoS Med, 2017.PMID 29261655
  23. [23]Prick BW, Jansen AJ, Steegers EA, et al. Transfusion policy after severe postpartum haemorrhage: a randomised non-inferiority trial BJOG, 2014.PMID 24405687
  24. [24]Karaca Z, Kelestimur F Sheehan syndrome: a current approach to a dormant disease Pituitary, 2025.PMID 39863703

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