Pc. Hebert et al., TRANSFUSION REQUIREMENTS IN CRITICAL CARE - A PILOT-STUDY, JAMA, the journal of the American Medical Association, 273(18), 1995, pp. 1439-1444
Objective.-To evaluate the effects of a restrictive and a liberal red
blood cell (RBC) transfusion strategy on mortality and morbidity in cr
itically ill patients. Study Design.-Multicenter, prospective, randomi
zed clinical trial. Patient Population.-Sixty-nine normovolemic critic
ally ill patients admitted to one of five tertiary level intensive car
e units with hemoglobin values less than 90 g/L within 72 hours of adm
ission. Interventions.-Patients were randomly allocated to one of two
RBC transfusion strategies. Hemoglobin values were maintained between
100 and 120 g/L in the liberal transfusion group and between 70 and 90
g/L in the restrictive group. Results.-Primary diagnosis and mean+/-S
D age (58.6+/-15 vs 59.0+/-21 years) and Acute Physiology and Chronic
Health Evaluation II score (20+/-6.2 vs 21 +/-7.2) were similar in the
restrictive and liberal groups, respectively. Daily hemoglobin values
averaged 90 g/L in the restrictive group vs 109 g/L in the liberal gr
oup (P<.001). The restrictive group received 2.5 U per patient compare
d with 4.8 U per patient in the liberal group. This represents a 48% r
elative decrease (P<.001) in RBC units transfused per patient. The 30-
day mortality rate was 24% in the restrictive group compared with 25%
in the liberal group; the 95% confidence interval around the absolute
difference was -19% to 21%. Similar observations were noted for intens
ive care unit mortality (P=.76) and 120-day mortality (P>.99). In addi
tion, survival analysis comparing time until death in both groups did
not reveal any significant difference (P=.93) between groups. Organ dy
sfunction scores were also similar (P=.44). Conclusion.-In this small
randomized trial, neither mortality nor the development of organ dysfu
nction was affected by the transfusion strategy, which suggests that a
more restrictive approach to the transfusion of RBCs may be safe in c
ritically ill patients. However, the study lacked power to detect smal
l but clinically significant differences. Therefore, further investiga
tions of RBC transfusion strategies are warranted.