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Association between blood transfusion and ventilator-associated events: a nested case-control study
by
Ji, Peng
, Zong, Zhiyong
, Zhu, Shichao
, Zou, Kang
, Sun, Xin
, Kang, Yan
, Wang, Wen
, Zhang, Rui
, Wang, Mingqi
, He, Qiao
in
Blood transfusions
/ Case studies
/ Demographics
/ Disease control
/ Hospitals
/ Infections
/ Intensive care
/ Missing data
/ Original Article
/ Patients
/ Pneumonia
/ Surveillance
/ Transfusion
/ Ventilators
2022
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Association between blood transfusion and ventilator-associated events: a nested case-control study
by
Ji, Peng
, Zong, Zhiyong
, Zhu, Shichao
, Zou, Kang
, Sun, Xin
, Kang, Yan
, Wang, Wen
, Zhang, Rui
, Wang, Mingqi
, He, Qiao
in
Blood transfusions
/ Case studies
/ Demographics
/ Disease control
/ Hospitals
/ Infections
/ Intensive care
/ Missing data
/ Original Article
/ Patients
/ Pneumonia
/ Surveillance
/ Transfusion
/ Ventilators
2022
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Association between blood transfusion and ventilator-associated events: a nested case-control study
by
Ji, Peng
, Zong, Zhiyong
, Zhu, Shichao
, Zou, Kang
, Sun, Xin
, Kang, Yan
, Wang, Wen
, Zhang, Rui
, Wang, Mingqi
, He, Qiao
in
Blood transfusions
/ Case studies
/ Demographics
/ Disease control
/ Hospitals
/ Infections
/ Intensive care
/ Missing data
/ Original Article
/ Patients
/ Pneumonia
/ Surveillance
/ Transfusion
/ Ventilators
2022
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Association between blood transfusion and ventilator-associated events: a nested case-control study
Journal Article
Association between blood transfusion and ventilator-associated events: a nested case-control study
2022
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Overview
The association between blood transfusion and ventilator-associated events (VAEs) has not been fully understood. We sought to determine whether blood transfusion increases the risk of a VAE.
Nested case-control study.
This study was based on a registry of healthcare-associated infections in intensive care units at West China Hospital system.
1,657 VAE cases and 3,293 matched controls were identified.
For each case, 2 controls were randomly selected using incidence density sampling. We defined blood transfusion as a time-dependent variable, and we used weighted Cox models to calculate hazard ratios (HRs) for all 3 tiers of VAEs.
Blood transfusion was associated with increased risk of ventilator-associated complication-plus (VAC-plus; HR, 1.47; 95% CI, 1.22-1.77; P <.001), VAC-only (HR, 1.29; 95% CI, 1.01-1.65; P = .038), infection-related VAC-plus (IVAC-plus; HR, 1.78; 95% CI, 1.33-2.39; P < .001), and possible ventilator-associated pneumonia (PVAP; HR, 2.10; 95% CI, 1.10-3.99; P = .024). Red blood cell (RBC) transfusion was also associated with increased risk of VAC-plus (HR, 1.34; 95% CI, 1.08-1.65; P = .007), IVAC-plus (HR, 1.70; 95% CI, 1.22-2.36; P = .002), and PVAP (HR, 2.49; 95% CI, 1.17-5.28; P = .018). Compared to patients without transfusion, the risk of VAE was significantly higher in patients with RBC transfusions of >3 units (HR, 1.73; 95% CI, 1.25-2.40; P = .001) but not in those with RBC transfusions of 0-3 units.
Blood transfusions were associated with increased risk of all tiers of VAE. The risk was significantly higher among patients who were transfused with >3 units of RBCs.
Publisher
Cambridge University Press
Subject
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