Impact of Blood Product Transfusions on the Risk of
ICU-Acquired Infections in Septic Shock*
by Péju, Edwige; Llitjos, Jean-François; Charpentier,
Julien; François, Anne; Marin, Nathalie; Cariou, Alain; Chiche, Jean-Daniel;
Mira, Jean-Paul; Lambert, Jérôme; Jamme, Matthieu; Pène, Frédéric
Critical Care
Medicine: June 2021 -
Volume 49 - Issue 6 - p 912-922
OBJECTIVES:
Transfusions of blood products are common in critically ill
patients and have a potential for immunomodulation. The aim of this study is to
address the impact of transfusion of blood products on the
susceptibility to ICU-acquired infections in the high-risk patients with septic
shock.
DESIGN:
A single-center retrospective study over a 10-year period
(2008–2017).
SETTING:
A medical ICU of a tertiary-care center.
PATIENTS:
All consecutive patients diagnosed for septic shock within
the first 48 hours of ICU admission were included. Patients who were discharged
or died within the first 48 hours were excluded.
INTERVENTIONS:
RBC, platelet, and fresh frozen plasma transfusions
collected up to 24 hours prior to the onset of ICU-acquired infection.
MEASUREMENTS AND MAIN RESULTS:
During the study period, 1,152 patients were admitted for
septic shock, with 893 patients remaining alive in the ICU after 48 hours of
management. A first episode of ICU-acquired infection occurred in 28.3% of the
48-hour survivors, with a predominance of pulmonary infections (57%). Patients
with ICU-acquired infections were more likely to have received RBC, platelet,
and fresh frozen plasma transfusions. In a multivariate Cox cause-specific
analysis, transfusions of platelets (cause-specific hazard ratio = 1.55
[1.09–2.20]; p = 0.01) and fresh frozen plasma (cause-specific hazard
ratio = 1.38 [0.98–1.92]; p = 0.05) were independently associated
with the further occurrence of ICU-acquired infections.
CONCLUSIONS:
Transfusions of platelets and fresh frozen plasma account
for risk factors of ICU-acquired infections in patients recovering from septic
shock. The occurrence of ICU-acquired infections should be considered as a
relevant endpoint in future studies addressing the indications of transfusions
in critically ill patients.
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