Race against clots: the challenges of managing antithrombin deficiency in the ICU

BMJ Case Rep. 2024 Dec 22;17(12):e263287. doi: 10.1136/bcr-2024-263287.

Abstract

We present the case of a man in his 50s with a history of recurrent unprovoked venous thromboembolism who developed haemorrhagic shock due to venous intestinal ischaemia. Despite anticoagulation and monitoring of anti-Xa levels, the thrombosis progressed, leading to complete necrosis and perforation of the small bowel wall, persistent septic shock and ultimately death. The clinical course and family history raised suspicion for hereditary antithrombin deficiency, a rare but potentially catastrophic thrombophilia. This case highlights the importance of considering inherited thrombophilia in critically ill patients with progressive thrombosis despite adequate anticoagulation, and the challenges of managing these conditions in the intensive care unit.

Keywords: Adult intensive care; GI bleeding; Genetics; Haematology (incl blood transfusion); Venous thromboembolism.

Publication types

  • Case Reports

MeSH terms

  • Anticoagulants / therapeutic use
  • Antithrombin III Deficiency* / complications
  • Antithrombin III Deficiency* / diagnosis
  • Fatal Outcome
  • Humans
  • Intensive Care Units
  • Male
  • Middle Aged
  • Shock, Septic / etiology
  • Thrombophilia* / complications
  • Thrombophilia* / drug therapy
  • Venous Thromboembolism* / complications
  • Venous Thromboembolism* / drug therapy
  • Venous Thromboembolism* / etiology

Substances

  • Anticoagulants