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Comparative risk of pulmonary adverse events with transfusion of pathogen reduced and conventional platelet components.
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.
Afiliação
  • Snyder EL; Yale University School of Medicine, New Haven, Connecticut, USA.
  • Wheeler AP; Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Refaai M; University of Rochester Medical Center, Rochester, New York, USA.
  • Cohn CS; University of Minnesota Medical Center, Minneapolis, Minnesota, USA.
  • Poisson J; Duke University Medical Center, Durham, North Carolina, USA.
  • Fontaine M; University of Maryland Medical Center, Baltimore, Maryland, USA.
  • Sehl M; UCLA Medical Center, Los Angeles, California, USA.
  • Nooka AK; Emory University Medical Center, Atlanta, Georgia, USA.
  • Uhl L; Harvard University - Beth Israel Deaconess Hospital, Boston, Massachusetts, USA.
  • Spinella P; University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
  • Fenelus M; Memorial-Sloan Kettering Medical Center, New York, New York, USA.
  • Liles D; East Carolina University Medical Center, Greenville, North Carolina, USA.
  • Coyle T; Trihealth Medical Center, Cincinnati, Ohio, USA.
  • Becker J; Roswell Park Medical Center, Buffalo, New York, USA.
  • Jeng M; Stanford Medical School, Palo Alto, California, USA.
  • Gehrie EA; Johns-Hopkins Medical Institute, Baltimore, Maryland, USA.
  • Spencer BR; American Red Cross Scientific Affairs, Dedham, Massachusetts, USA.
  • Young P; Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Johnson A; University of Minnesota Medical Center, Minneapolis, Minnesota, USA.
  • O'Brien JJ; Mayo Clinic Florida, Jacksonville, Florida, USA.
  • Schiller GJ; UCLA Medical Center, Los Angeles, California, USA.
  • Roback JD; Emory University Medical Center, Atlanta, Georgia, USA.
  • Malynn E; Harvard University - Beth Israel Deaconess Hospital, Boston, Massachusetts, USA.
  • Jackups R; Washington University St. Louis, St. Louis, Missouri, USA.
  • Avecilla ST; Memorial-Sloan Kettering Medical Center, New York, New York, USA.
  • Lin JS; Cerus Corporation, Concord, California, USA.
  • Liu K; Cerus Corporation, Concord, California, USA.
  • Bentow S; Cerus Corporation, Concord, California, USA.
  • Peng HL; Cerus Corporation, Concord, California, USA.
  • Varrone J; Cerus Corporation, Concord, California, USA.
  • Benjamin RJ; Cerus Corporation, Concord, California, USA.
  • Corash LM; Cerus Corporation, Concord, California, USA.
Transfusion ; 62(7): 1365-1376, 2022 07.
Article em En | MEDLINE | ID: mdl-35748490
ABSTRACT

BACKGROUND:

Platelet 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

DESIGN:

An 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.

RESULTS:

By 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.

DISCUSSION:

PRPC demonstrated reduced TEAMV with no excess treatment-related pulmonary morbidity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Desconforto Respiratório / Reação Transfusional Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Transfusion Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Desconforto Respiratório / Reação Transfusional Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Transfusion Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos
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