Abstract

BackgroundDisseminated intravascular coagulopathy (DIC) relates to the consumption of coagulation factors and platelets with bleeding and micro thrombosis events.AimThe aim of this study was to compare haemostasis parameters in critically ill patients with DIC versus patients without DIC, and in survivors versus non-survivors over time. Correlations between the DIC-score, the degree of organ failure and the haemostasis were assessed.MethodPatients admitted to the intensive care unit with a condition known to be associated with DIC and with an expected length of stay of >3 days were included. Routine laboratory tests, prothrombin time, activated partial thromboplastin time, platelet count, fibrinogen concentration and D-dimer were measured. Coagulation and platelet function were assessed with two point-of-care devices; Multiplate and ROTEM. DIC scores were calculated according to the International Society on Thrombosis and Haemostasis and Japanese Association for Acute Medicine.ResultsBlood was sampled on days 0–1, 2–3 and 4–10 from 136 patients with mixed diagnoses during 290 sampling events. The point-of-care assays indicated a hypocoagulative response (decreased platelet aggregation and reduced clot strength) in patients with DIC and, over time, in non-survivors compared to survivors. Patients with DIC as well as non-survivors had decreased fibrinolysis as shown by ROTEM. DIC scores were higher in non-survivors than in survivors.ConclusionsPatients with DIC displayed signs of a hypocoagulative response and impaired fibrinolysis, which was also evident over time in non-survivors. Patients with DIC had a higher mortality rate than non-DIC patients, and DIC scores were higher in non-survivors than in survivors.

Highlights

  • Coagulopathy is common in patients in the intensive care unit (ICU)

  • Patients with disseminated intravascular coagulopathy (DIC) displayed signs of a hypocoagulative response and impaired fibrinolysis, which was evident over time in non-survivors

  • The number of patients included in the study categorised into 5 diagnosis groups, estimated mortality risk (EMR), the number and percentage of patients with actual 30-day mortality, the percentage of patients with overt disseminated intravascular coagulopathy (DIC) determined by International Society on Thrombosis and Haemostasis (ISTH)-score and JAAMscore as well as percentage of patients on anticoagulants and platelet inhibitors and transfused within 24h of blood collection

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Summary

Introduction

There are multiple contributing factors, such as impaired synthesis or increased consumption of coagulation factors and platelets due to massive bleeding, for example, as well as platelet dysfunction [1] and derangement of fibrinolysis This can lead to a serious condition with microvascular thrombosis: disseminated intravascular coagulopathy (DIC) and can result in multiple organ failure and mortality. DIC is associated with a prolongation of activated partial thromboplastin time (aPTT) and prothrombin time (PT) [3,4,5], which are two methods routinely used to monitor coagulation Neither of these tests nor the measurement of fibrinogen or platelet count are adequate to detect coagulopathy and DIC [6]. Disseminated intravascular coagulopathy (DIC) relates to the consumption of coagulation factors and platelets with bleeding and micro thrombosis events

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