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Reported transfusion-related acute lung injury associated with solvent/detergent plasma - A case series.
Klanderman, Robert B; Bulle, Esther B; Heijnen, Josephine W M; Allen, Judith; Purmer, Ilse M; Kerkhoffs, Jean-Louis H; Wiersum-Osselton, Johanna C; Vlaar, Alexander P J.
Afiliação
  • Klanderman RB; Department of Intensive Care, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Bulle EB; Laboratory of Experimental Intensive Care and Anesthesiology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Heijnen JWM; Department of Anesthesiology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Allen J; Department of Intensive Care, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Purmer IM; Laboratory of Experimental Intensive Care and Anesthesiology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Kerkhoffs JH; TRIP Hemovigilance and Biovigilance Office, Leiden, The Netherlands.
  • Wiersum-Osselton JC; Department of Quality and Security, HagaZiekenhuis, The Hague, The Netherlands.
  • Vlaar APJ; Department of Intensive Care, HagaZiekenhuis, The Hague, The Netherlands.
Transfusion ; 62(3): 594-599, 2022 03.
Article em En | MEDLINE | ID: mdl-35174882
ABSTRACT

BACKGROUND:

Antibody-mediated transfusion-related acute lung injury (TRALI) is caused by donor HLA or HNA antibodies in plasma-containing products. In the Netherlands 55,000 units of solvent/detergent plasma (SDP), a pooled plasma product, are transfused yearly. It's produced by combining plasma from hundreds of donors, diluting harmful antibodies. Due to a lack of reported cases following implementation, some have labeled SDP as "TRALI safe". STUDY DESIGN AND

METHODS:

Pulmonary transfusion reactions involving SDP reported to the Dutch national hemovigilance network in 2016-2019 were reviewed. Reporting hospitals were contacted for additional information, cases with TRALI and imputability definite, probable, or possible were included and informed consent was sought.

RESULTS:

A total of three TRALI and nine TACO cases were reported involving SDP. The imputability of one TRALI case was revised from possible to unlikely and excluded; in one case no informed consent was obtained. We present a case description of TRALI following SDP transfusion in a 69-year-old male, 3 days following endovascular aortic aneurysm repair. The patient received one unit of SDP to correct a heparin-induced coagulopathy, prior to removal of a spinal catheter post-operatively. Within five hours he developed hypoxemic respiratory failure requiring intubation, hypotension, bilateral chest infiltrates, and leucopenia. The patient made a full recovery.

CONCLUSION:

This case of TRALI, following transfusion of a single unit of SDP to a patient without ARDS risk factors, demonstrates that TRALI can occur with this product. Clinicians should remain vigilant and continue to report suspected cases, to help further understanding of SDP-associated TRALI.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Lesão Pulmonar Aguda / Reação Transfusional / Lesão Pulmonar Aguda Relacionada à Transfusão Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Aged / Humans / Male Idioma: En Revista: Transfusion Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Lesão Pulmonar Aguda / Reação Transfusional / Lesão Pulmonar Aguda Relacionada à Transfusão Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Aged / Humans / Male Idioma: En Revista: Transfusion Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Holanda