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Active surveillance of serious adverse events following transfusion of COVID-19 convalescent plasma.
Swenson, Erica; Wong, Lisa Kanata; Jhaveri, Perrin; Weng, Yingjie; Kappagoda, Shanthi; Pandey, Suchitra; Pritchard, Angelica; Rogers, Angela; Ruoss, Stephen; Subramanian, Aruna; Shan, Hua; Hollenhorst, Marie.
  • Swenson E; Department of Pathology, Stanford University, Stanford, California, USA.
  • Wong LK; Department of Pathology, Stanford University, Stanford, California, USA.
  • Jhaveri P; Department of Hematology, Kaiser Permanente, Renton, Washington, USA.
  • Weng Y; Department of Medicine, Quantitative Sciences Unit, Stanford University, Stanford, California, USA.
  • Kappagoda S; Department of Medicine, Division of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, California, USA.
  • Pandey S; Department of Pathology, Stanford University, Stanford, California, USA.
  • Pritchard A; Stanford Blood Center, Stanford, California, USA.
  • Rogers A; Department of Emergency Medicine, Stanford University, Stanford, California, USA.
  • Ruoss S; Department of Medicine, Division of Pulmonary, Allergy and Critical Care Medicine, Stanford University, Stanford, California, USA.
  • Subramanian A; Department of Medicine, Division of Pulmonary, Allergy and Critical Care Medicine, Stanford University, Stanford, California, USA.
  • Shan H; Department of Medicine, Division of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, California, USA.
  • Hollenhorst M; Department of Pathology, Stanford University, Stanford, California, USA.
Transfusion ; 62(1): 28-36, 2022 01.
Article in English | MEDLINE | ID: covidwho-1480228
ABSTRACT

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.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: Blood Component Transfusion / COVID-19 Type of study: Observational study / Prognostic study Limits: Humans Language: English Journal: Transfusion Year: 2022 Document Type: Article Affiliation country: Trf.16711

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Blood Component Transfusion / COVID-19 Type of study: Observational study / Prognostic study Limits: Humans Language: English Journal: Transfusion Year: 2022 Document Type: Article Affiliation country: Trf.16711