The relationship between coagulation disorders and the risk of bleeding in cirrhotic patients

Ann Hepatol. 2019 Jul-Aug;18(4):627-632. doi: 10.1016/j.aohep.2018.12.007. Epub 2019 May 6.

Abstract

Introduction and objectives: For long, bleeding in cirrhotic patients has been associated with acquired coagulation disorders. The aim of our study was to investigate the impact of acquired coagulation disorders on bleeding risk in cirrhotic patients.

Materials and methods: Blood samples were collected from 51 cirrhotic patients with (H+) or without (H-) bleeding events and 50 controls matched by age and sex. Thrombin generation was assessed as endogenous thrombin potential (ETP). Hemostatic balance was assessed by means of ratios of pro- to anticoagulant factors and by ETP ratio with/without protein C (PC) activator (ETP ratio).

Results: Bleeding events occurred in 9 patients (17.6%). Compared with controls, VIII/anticoagulant factors, VII/PC and XII/PC were significantly higher in (H+) patients. No significant difference as regards all ratios across patient groups was detected. ETP ratio was significantly higher in (H+) patients than in controls (p=0.017). However, there was no significant difference between patient groups as regards ETP ratio.

Conclusion: Hemostatic balance is shifted toward a hypercoagulability state even in cirrhotic patients who experienced bleeding. These findings provide evidence against traditional concept of hemostasis-related bleeding tendency in cirrhotic patients.

Keywords: Gastrointestinal hemorrhage; Hypercoagulability; Liver; Prothrombin time; Thrombosis.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Blood Coagulation Disorders / blood*
  • Blood Coagulation Tests
  • Case-Control Studies
  • Factor VII / metabolism
  • Factor VIII / metabolism
  • Factor XII / metabolism
  • Hemorrhage / blood*
  • Humans
  • Liver Cirrhosis / blood*
  • Middle Aged
  • Partial Thromboplastin Time
  • Protein C / metabolism
  • Prothrombin Time
  • Risk
  • Thrombin / metabolism
  • Thrombophilia / blood*
  • Young Adult

Substances

  • Protein C
  • Factor VII
  • Factor VIII
  • Factor XII
  • Thrombin