Abstract

IntroductionFresh frozen plasma (FFP) is widely used, but few studies have described patterns of plasma use in critical care. We carried out a multicentre study of coagulopathy in intensive care units (ICUs) and here describe overall FFP utilisation in adult critical care, the indications for transfusions, factors indicating the doses used and the effects of FFP use on coagulation.MethodsWe conducted a prospective, multicentre, observational study of all patients sequentially admitted to 29 adult UK general ICUs over 8 weeks. Daily data throughout ICU admission were collected concerning coagulation, relevant clinical outcomes (including bleeding), coagulopathy (defined as international normalised ratio (INR) >1.5, or equivalent prothrombin time (PT)), FFP and cryoprecipitate use and indications for transfusion.ResultsOf 1,923 admissions, 12.7% received FFP in the ICU during 404 FFP treatment episodes (1,212 FFP units). Overall, 0.63 FFP units/ICU admission were transfused (0.11 units/ICU day). Reasons for FFP transfusion were bleeding (48%), preprocedural prophylaxis (15%) and prophylaxis without planned procedure (36%). Overall, the median FFP dose was 10.8 ml kg-1, but doses varied widely (first to third quartile, 7.2 to 14.4 ml kg-1). Thirty-one percent of FFP treatments were to patients without PT prolongation, and 41% were to patients without recorded bleeding and only mildly deranged INR (<2.5). Higher volumes of FFP were administered when the indication was bleeding (median doses: bleeding 11.1 ml kg-1, preprocedural prophylaxis 9.8 ml kg-1, prophylaxis without procedure 8.9 ml kg-1; P = 0.009 across groups) and when the pretransfusion INR was higher (ranging from median dose 8.9 ml kg-1 at INR ≤1.5 to 15.7 ml kg-1 at INR >3; P < 0.001 across ranges). Regression analyses suggested bleeding was the strongest predictor of higher FFP dose. Pretransfusion INR was more frequently normal when the transfusion indication was bleeding. Overall, posttransfusion corrections of INR were consistently small unless the pretransfusion INR was >2.5, but administration during bleeding was associated with greater INR corrections.ConclusionsThere is wide variation in FFP use by ICU clinicians, and a high proportion of current FFP transfusions are of unproven clinical benefit. Better evidence from clinical trials could significantly alter patterns of use and modify current treatment costs.

Highlights

  • Fresh frozen plasma (FFP) is widely used, but few studies have described patterns of plasma use in critical care

  • We previously reported a large national study of coagulopathy in UK intensive care units (ICUs), which showed that 30% of all critical care admissions had at least one episode of prothrombin time (PT) prolongation [18]

  • (1) What reasons do clinicians give for administering FFP, and how does the presence of bleeding and coagulopathy influence the dose? (2) What PT or international normalised ratio (PT/INR) triggers are currently used by clinicians, and how do these relate to the doses administered? (3) What changes in PT/INR occur following FFP administration? We describe the current use of cryoprecipitate in UK critical care, since it is often prescribed with or as an alternative to FFP

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Summary

Introduction

Fresh frozen plasma (FFP) is widely used, but few studies have described patterns of plasma use in critical care. Fresh frozen plasma (FFP) and cryoprecipitate are used widely in hospital practice across a range of clinical specialties, especially in critical care units [1,2,3,4,5]. We described risk factors for the development of coagulopathy and showed an association with higher ICU mortality, but did not describe the use of FFP in detail. The aim of this analysis of the study database was to describe plasma use in detail, with the following research questions. The aim of this analysis of the study database was to describe plasma use in detail, with the following research questions. (1) What reasons do clinicians give for administering FFP, and how does the presence of bleeding and coagulopathy influence the dose? (2) What PT or international normalised ratio (PT/INR) triggers are currently used by clinicians, and how do these relate to the doses administered? (3) What changes in PT/INR occur following FFP administration? We describe the current use of cryoprecipitate in UK critical care, since it is often prescribed with or as an alternative to FFP

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