4.2 Article

Early and out-of-hospital use of COVID-19 convalescent plasma: An international assessment of utilization and feasibility

Journal

VOX SANGUINIS
Volume 117, Issue 10, Pages 1202-1210

Publisher

WILEY
DOI: 10.1111/vox.13347

Keywords

convalescent plasma; COVID-19; home transfusion

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This study summarizes trials of early use of convalescent plasma in the treatment of COVID-19 and explores its feasibility in different countries. The results show that some countries are conducting trials on early convalescent plasma transfusion, and home transfusion has been implemented in several countries. However, many institutions and countries still lack such programs, and barriers to implementation include existing legislation and lack of policies and resources.
Background and Objectives: The use of coronavirus disease 2019 (COVID-19) convalescent plasma (CCP) in the treatment of patients with severe acute respiratory syndrome-2 infection has been controversial. Early administration of CCP before hospital admission offers a potential advantage. This manuscript summarizes current trials of early use of CCP and explores the feasibility of this approach in different countries. Materials and Methods: A questionnaire was distributed to the International Society of Blood Transfusion (ISBT) CCP working group. We recorded respondents' input on existing trials on early/outpatient CCP and out-of-hospital (OOH)/home transfusion (HT) practices in their countries and feedback on challenges in initiating home CCP infusion programmes. In addition, details of existing trials registered on clinicaltrials.gov were summarized. Results: A total of 31 country representatives participated. Early/OOH CCP transfusion studies were reported in the United States, the Netherlands, Spain and Brazil. There were a total of six published and five ongoing trials on the prophylactic and therapeutic early use of CCP. HT was practised in Australia, the UK, Belgium, France, Japan, Nigeria, the Netherlands, Spain, Italy, Norway, the United States and some provinces in Canada. Thirty-four representatives indicated a lack of OOH CCP or HT in their institutions and countries. Barriers to implementation of OOH/HT included existing legislation, lack of policies pertaining to outpatient transfusion, and associated logistical challenges, including lack of staffing and resources. Conclusion: Early administration of CCP remains a potential option in COVID-19 management in countries with existing OOH/HT programmes. Legislation and regulatory bodies should consider OOH/HT practice for transfusion in future pandemics.

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