Active surveillance of serious adverse events following transfusion of COVID-19 convalescent plasma.


Journal

Transfusion
ISSN: 1537-2995
Titre abrégé: Transfusion
Pays: United States
ID NLM: 0417360

Informations de publication

Date de publication:
01 2022
Historique:
revised: 07 10 2021
received: 30 04 2021
accepted: 07 10 2021
pubmed: 23 10 2021
medline: 28 1 2022
entrez: 22 10 2021
Statut: ppublish

Résumé

The reported incidence of adverse reactions following Coronavirus disease 2019 (COVID-19) convalescent plasma (CCP) transfusion has generally been lower than expected based on the incidence of transfusion reactions that have been observed in studies of conventional plasma transfusion. This raises the concern for under-reporting of adverse events in studies of CCP that rely on passive surveillance strategies. Our institution implemented a protocol to actively identify possible adverse reactions to CCP transfusion. In addition, we retrospectively reviewed the charts of inpatients who received CCP at Stanford Hospital between May 13, 2020 and January 31, 2021. We determined the incidence of adverse events following CCP transfusion. A total of 49 patients received CCP. Seven patients (14%) had an increased supplemental oxygen requirement within 4 h of transfusion completion, including one patient who was intubated during the transfusion. An additional 11 patients (total of 18, 37%) had increased oxygen requirements within 24 h of transfusion, including 3 patients who were intubated. Six patients (12%) fulfilled criteria for transfusion-associated circulatory overload (TACO). Using an active surveillance strategy, we commonly observed adverse events following the transfusion of CCP to hospitalized patients. It was not possible to definitively determine whether or not these adverse events are related to CCP transfusion. TACO was likely over-diagnosed given overlap with the manifestations of COVID-19. Nevertheless, these results suggest that the potential adverse effects of CCP transfusion may be underestimated by reports from passive surveillance studies.

Sections du résumé

BACKGROUND
The reported incidence of adverse reactions following Coronavirus disease 2019 (COVID-19) convalescent plasma (CCP) transfusion has generally been lower than expected based on the incidence of transfusion reactions that have been observed in studies of conventional plasma transfusion. This raises the concern for under-reporting of adverse events in studies of CCP that rely on passive surveillance strategies.
MATERIALS AND METHODS
Our institution implemented a protocol to actively identify possible adverse reactions to CCP transfusion. In addition, we retrospectively reviewed the charts of inpatients who received CCP at Stanford Hospital between May 13, 2020 and January 31, 2021. We determined the incidence of adverse events following CCP transfusion.
RESULTS
A total of 49 patients received CCP. Seven patients (14%) had an increased supplemental oxygen requirement within 4 h of transfusion completion, including one patient who was intubated during the transfusion. An additional 11 patients (total of 18, 37%) had increased oxygen requirements within 24 h of transfusion, including 3 patients who were intubated. Six patients (12%) fulfilled criteria for transfusion-associated circulatory overload (TACO).
CONCLUSION
Using an active surveillance strategy, we commonly observed adverse events following the transfusion of CCP to hospitalized patients. It was not possible to definitively determine whether or not these adverse events are related to CCP transfusion. TACO was likely over-diagnosed given overlap with the manifestations of COVID-19. Nevertheless, these results suggest that the potential adverse effects of CCP transfusion may be underestimated by reports from passive surveillance studies.

Identifiants

pubmed: 34677830
doi: 10.1111/trf.16711
pmc: PMC8661846
doi:

Substances chimiques

Oxygen S88TT14065

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

28-36

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR003142
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1TR003142
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1TR003142
Pays : United States

Informations de copyright

© 2021 AABB.

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Auteurs

Erica Swenson (E)

Department of Pathology, Stanford University, Stanford, California, USA.

Lisa Kanata Wong (LK)

Department of Pathology, Stanford University, Stanford, California, USA.

Perrin Jhaveri (P)

Department of Hematology, Kaiser Permanente, Renton, Washington, USA.

Yingjie Weng (Y)

Department of Medicine, Quantitative Sciences Unit, Stanford University, Stanford, California, USA.

Shanthi Kappagoda (S)

Department of Medicine, Division of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, California, USA.

Suchitra Pandey (S)

Department of Pathology, Stanford University, Stanford, California, USA.
Stanford Blood Center, Stanford, California, USA.

Angelica Pritchard (A)

Department of Emergency Medicine, Stanford University, Stanford, California, USA.

Angela Rogers (A)

Department of Medicine, Division of Pulmonary, Allergy and Critical Care Medicine, Stanford University, Stanford, California, USA.

Stephen Ruoss (S)

Department of Medicine, Division of Pulmonary, Allergy and Critical Care Medicine, Stanford University, Stanford, California, USA.

Aruna Subramanian (A)

Department of Medicine, Division of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, California, USA.

Hua Shan (H)

Department of Pathology, Stanford University, Stanford, California, USA.

Marie Hollenhorst (M)

Department of Pathology, Stanford University, Stanford, California, USA.
Department of Medicine, Division of Hematology, Stanford University, Stanford, California, USA.
Chemistry, Engineering, & Medicine for Human Health Institute (ChEM-H), Stanford University, Stanford, California, USA.

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