Definitions of massive transfusion in adults with critical
bleeding: a systematic review
by Victor S. Lin,
Emily Sun, Serine Yau, Chathuri Abeyakoon, Georgia Seamer, Simran Bhopal,
Harriet Tucker, Carolyn Doree, Susan J. Brunskill, Zoe K. McQuilten, Simon J.
Stanworth, Erica M. Wood and Laura Green
Critical Care volume 27,
Article number: 265 Published: 05
July 2023
Background
Definitions for massive transfusion (MT) vary widely between
studies, contributing to challenges in interpretation of research findings and
practice evaluation. In this first systematic review, we aimed to identify all
MT definitions used in randomised controlled trials (RCTs) to date to inform
the development of consensus definitions for MT.
Methods
We systematically searched the following databases for RCTs
from inception until 11 August 2022: MEDLINE, Embase, Cochrane Central Register
of Controlled Trials (CENTRAL), PubMed, Cumulative Index to Nursing and Allied
Health Literature, and Transfusion Evidence Library. Ongoing trials were sought
from CENTRAL, ClinicalTrials.gov, and World Health Organisation International
Clinical Trials Registry Platform. To be eligible for inclusion, studies had to
fulfil all the following three criteria: (1) be an RCT; (2) include an adult
patient population with major bleeding who had received, or were anticipated to
receive, an MT in any clinical setting; and (3) specify a definition for MT as
an inclusion criterion or outcome measure.
Results
Of the 8,458 distinct references identified, 30 trials were
included for analysis (19 published, 11 ongoing). Trauma was the most common
clinical setting in published trials, while for ongoing trials, it was
obstetrics. A total of 15 different definitions of MT were identified across
published and ongoing trials, varying greatly in cut-offs for volume transfused
and time period. Almost all definitions specified the number of red blood cells
(RBCs) within a set time period, with none including plasma, platelets or other
haemostatic agents that are part of contemporary transfusion resuscitation. For
completed trials, the most commonly used definition was transfusion of ≥ 10 RBC
units in 24 h (9/19, all in trauma), while for ongoing trials it was 3–5
RBC units (n = 7), with the timing for transfusion being poorly defined, or in
some trials not provided at all (n = 5).
Conclusions
Transfusion of ≥ 10 RBC units within 24 h was the most
commonly used definition in published RCTs, while lower RBC volumes are being
used in ongoing RCTs. Any consensus definitions should reflect the need to
incorporate different blood components/products for MT and agree on whether a
‘one-size-fits-all’ approach should be used across different clinical settings.
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