Consumptive coagulopathy is associated with a disturbed host response in patients with sepsis

J Thromb Haemost. 2021 Apr;19(4):1049-1063. doi: 10.1111/jth.15246. Epub 2021 Feb 17.

Abstract

Background: A prolonged prothrombin time (PT) is a common feature in sepsis indicating consumptive coagulopathy.

Objectives: To determine the association between a prolonged PT and aberrations in other host response mechanisms in sepsis.

Methods: Patients admitted to the intensive care unit with sepsis were divided in quartiles according to the highest PT value measured within 24 h after admission. The host response was evaluated by measuring 19 plasma biomarkers reflecting pathways implicated in sepsis pathogenesis and by blood leukocyte gene expression profiling.

Measurements and main results: Of 1524 admissions for sepsis, 386 (25.3%) involved patients with a normal PT (≤12.7 s); the remaining quartiles entailed 379 (24.9%) patients with a slightly prolonged PT (12.8 ≤ PT ≤ 15.0 s), 383 (25.1%) with an intermediately prolonged PT (15.1 ≤ PT ≤ 17.2 s), and 376 (24.7%) with an extremely prolonged PT (≥17.3 s). While patients with an extremely prolonged PT showed an increased crude mortality up to 1 year after admission, none of the prolonged PT groups was independently associated with 30-day adjusted mortality. Comparison of the host response between patients with a normal PT or an extremely prolonged PT matched for baseline characteristics including severity of disease showed that an extremely prolonged PT was associated with impaired anticoagulant mechanisms, a more disturbed endothelial barrier integrity and increased systemic inflammation, and blood leukocyte transcriptomes indicating more prominent metabolic reprogramming and protein catabolism.

Conclusion: A prolonged PT is associated with stronger anomalies in pathways implicated in the pathogenesis of sepsis, suggesting that activation of coagulation impacts other host response mechanisms.

Keywords: endothelium inflammation; host response; intensive care unit; prothrombin time; sepsis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers
  • Blood Coagulation Disorders*
  • Disseminated Intravascular Coagulation* / diagnosis
  • Humans
  • Intensive Care Units
  • Sepsis* / diagnosis

Substances

  • Biomarkers