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Comparative risk of pulmonary adverse events with transfusion of pathogen reduced and conventional platelet components.

Authors :
Snyder, Edward L
Snyder, Edward L
Wheeler, Allison P
Refaai, Majed
Cohn, Claudia S
Poisson, Jessica
Fontaine, Magali
Sehl, Mary
Nooka, Ajay K
Uhl, Lynne
Spinella, Philip
Fenelus, Maly
Liles, Darla
Coyle, Thomas
Becker, Joanne
Jeng, Michael
Gehrie, Eric A
Spencer, Bryan R
Young, Pampee
Johnson, Andrew
O'Brien, Jennifer J
Schiller, Gary J
Roback, John D
Malynn, Elizabeth
Jackups, Ronald
Avecilla, Scott T
Lin, Jin-Sying
Liu, Kathy
Bentow, Stanley
Peng, Ho-Lan
Varrone, Jeanne
Benjamin, Richard J
Corash, Laurence M
Snyder, Edward L
Snyder, Edward L
Wheeler, Allison P
Refaai, Majed
Cohn, Claudia S
Poisson, Jessica
Fontaine, Magali
Sehl, Mary
Nooka, Ajay K
Uhl, Lynne
Spinella, Philip
Fenelus, Maly
Liles, Darla
Coyle, Thomas
Becker, Joanne
Jeng, Michael
Gehrie, Eric A
Spencer, Bryan R
Young, Pampee
Johnson, Andrew
O'Brien, Jennifer J
Schiller, Gary J
Roback, John D
Malynn, Elizabeth
Jackups, Ronald
Avecilla, Scott T
Lin, Jin-Sying
Liu, Kathy
Bentow, Stanley
Peng, Ho-Lan
Varrone, Jeanne
Benjamin, Richard J
Corash, Laurence M
Source :
Transfusion; vol 62, iss 7, 1365-1376; 0041-1132
Publication Year :
2022

Abstract

BackgroundPlatelet transfusion carries risk of transfusion-transmitted infection (TTI). Pathogen reduction of platelet components (PRPC) is designed to reduce TTI. Pulmonary adverse events (AEs), including transfusion-related acute lung injury and acute respiratory distress syndrome (ARDS) occur with platelet transfusion.Study designAn open label, sequential cohort study of transfusion-dependent hematology-oncology patients was conducted to compare pulmonary safety of PRPC with conventional PC (CPC). The primary outcome was the incidence of treatment-emergent assisted mechanical ventilation (TEAMV) by non-inferiority. Secondary outcomes included: time to TEAMV, ARDS, pulmonary AEs, peri-transfusion AE, hemorrhagic AE, transfusion reactions (TRs), PC and red blood cell (RBC) use, and mortality.ResultsBy modified intent-to-treat (mITT), 1068 patients received 5277 PRPC and 1223 patients received 5487 CPC. The cohorts had similar demographics, primary disease, and primary therapy. PRPC were non-inferior to CPC for TEAMV (treatment difference -1.7%, 95% CI: (-3.3% to -0.1%); odds ratio = 0.53, 95% CI: (0.30, 0.94). The cumulative incidence of TEAMV for PRPC (2.9%) was significantly less than CPC (4.6%, p = .039). The incidence of ARDS was less, but not significantly different, for PRPC (1.0% vs. 1.8%, p = .151; odds ratio = 0.57, 95% CI: (0.27, 1.18). AE, pulmonary AE, and mortality were not different between cohorts. TRs were similar for PRPC and CPC (8.3% vs. 9.7%, p = .256); and allergic TR were significantly less with PRPC (p = .006). PC and RBC use were not increased with PRPC.DiscussionPRPC demonstrated reduced TEAMV with no excess treatment-related pulmonary morbidity.

Details

Database :
OAIster
Journal :
Transfusion; vol 62, iss 7, 1365-1376; 0041-1132
Notes :
application/pdf, Transfusion vol 62, iss 7, 1365-1376 0041-1132
Publication Type :
Electronic Resource
Accession number :
edsoai.on1367457933
Document Type :
Electronic Resource