How donor selection criteria can be evaluated with limited scientific evidence: lessons learned from the TRANSPOSE project.

blood safety donor health donor safety donor selection donor vigilance donors haemovigilance

Journal

Vox sanguinis
ISSN: 1423-0410
Titre abrégé: Vox Sang
Pays: England
ID NLM: 0413606

Informations de publication

Date de publication:
Mar 2021
Historique:
revised: 21 10 2020
received: 29 05 2020
accepted: 21 10 2020
pubmed: 17 11 2020
medline: 21 5 2021
entrez: 16 11 2020
Statut: ppublish

Résumé

Donor selection criteria (DSC) are a vital link in the chain of supply of Substances of Human Origin (SoHO) but are also subject to controversy and differences of opinion. Traditionally, DSC have been based on application of the precautionary principle. From 2017 to 2020, TRANSPOSE (TRANSfusion and transplantation PrOtection and SElection of donors), a European research project, aimed to identify discrepancies between current DSC by proposing a standardized risk assessment method for all SoHO (solid organs excluded) and all levels of evidence. The current DSC were assessed using a modified risk assessment method based on the Alliance of Blood Operators' Risk-based decision-making framework for blood safety. It was found that with limited or diverging scientific evidence, it was difficult to reach consensus and an international standardized method for decision-making was lacking. Furthermore, participants found it hard to disregard their local guidelines when providing expert opinion, which resulted in substantial influence on the consensus-based decision-making process. While the field of donation-safety research is expanding rapidly, there is an urgent need to formalize the decision-making process regarding DSC. This includes the need for standardized methods to increase transparency in the international decision-making process and to ensure that this is performed consistently. Our framework provides an easy-to-implement approach for standardizing risk assessments, especially in the context of limited scientific evidence.

Sections du résumé

BACKGROUND AND OBJECTIVE OBJECTIVE
Donor selection criteria (DSC) are a vital link in the chain of supply of Substances of Human Origin (SoHO) but are also subject to controversy and differences of opinion. Traditionally, DSC have been based on application of the precautionary principle.
MATERIALS AND METHODS METHODS
From 2017 to 2020, TRANSPOSE (TRANSfusion and transplantation PrOtection and SElection of donors), a European research project, aimed to identify discrepancies between current DSC by proposing a standardized risk assessment method for all SoHO (solid organs excluded) and all levels of evidence.
RESULTS RESULTS
The current DSC were assessed using a modified risk assessment method based on the Alliance of Blood Operators' Risk-based decision-making framework for blood safety. It was found that with limited or diverging scientific evidence, it was difficult to reach consensus and an international standardized method for decision-making was lacking. Furthermore, participants found it hard to disregard their local guidelines when providing expert opinion, which resulted in substantial influence on the consensus-based decision-making process.
CONCLUSIONS CONCLUSIONS
While the field of donation-safety research is expanding rapidly, there is an urgent need to formalize the decision-making process regarding DSC. This includes the need for standardized methods to increase transparency in the international decision-making process and to ensure that this is performed consistently. Our framework provides an easy-to-implement approach for standardizing risk assessments, especially in the context of limited scientific evidence.

Identifiants

pubmed: 33191514
doi: 10.1111/vox.13028
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

342-350

Subventions

Organisme : European Union's Health Programme (2014-2020).
ID : '738145 / TRANSPOSE'

Informations de copyright

© 2020 International Society of Blood Transfusion.

Références

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Auteurs

Christina Mikkelsen (C)

Department of Clinical Immunology, Copenhagen University Hospital, Copenhagen, Denmark.

Gaia Mori (G)

Sanquin Blood Supply Foundation, Amsterdam, the Netherlands.

Suzanna M van Walraven (SM)

Sanquin Blood Supply Foundation, Amsterdam, the Netherlands.

Johanna Castrén (J)

Finnish Red Cross, Blood Service, Helsinki, Finland.

Sharon Zahra (S)

Scottish National Blood Transfusion Service, Edinburgh, Scotland.

Sheila MacLennan (S)

National Health Service Blood and Transplant, UK.

Kirsten Seidel (K)

CSL Plasma GmbH, Marburg, Germany.

Stefano Fontana (S)

Interregional Blood Transfusion Service SRC, University of Lausanne, Berne, Switzerland.

Eva Veropalumbo (E)

Centro Nazionale Sangue, Istituto Superiore di Sanità, Rome, Italy.

Livia Cannata (L)

Centro Nazionale Sangue, Istituto Superiore di Sanità, Rome, Italy.

Simonetta Pupella (S)

Centro Nazionale Sangue, Istituto Superiore di Sanità, Rome, Italy.

Maria Kvist (M)

Department of Clinical Immunology and Transfusion Medicine, Karolinska University Hospital, Solna, Sweden.

Marjan Happel (M)

TRIP Hemovigilance and Biovigilance Office, Leiden, the Netherlands.

Piia Korkalainen (P)

Finnish Red Cross, Blood Service, Helsinki, Finland.

Akila Chandrasekar (A)

National Health Service Blood and Transplant, UK.

Ulrike Paulus (U)

National Health Service Blood and Transplant, UK.

Arlinke Bokhorst (A)

TRIP Hemovigilance and Biovigilance Office, Leiden, the Netherlands.

Birgit Wulff (B)

Institute of Legal Medicine, University Medical Center Hamburg, Hamburg, Germany.

Jesus Fernandez-Sojo (J)

Banc de Sang I Teixits, Barcelona, Spain.

Cristina Eguizabal (C)

Bioef-Fundacion Vasca de Innovacion e Investigation Sanitarias-Osakidetza-Centro Vasco de Transfusión y Tejidos Humanos, Galdakao, Spain.

Fernando Urbano (F)

Bioef-Fundacion Vasca de Innovacion e Investigation Sanitarias-Osakidetza-Centro Vasco de Transfusión y Tejidos Humanos, Galdakao, Spain.

Miguel Angel Vesga (MA)

Bioef-Fundacion Vasca de Innovacion e Investigation Sanitarias-Osakidetza-Centro Vasco de Transfusión y Tejidos Humanos, Galdakao, Spain.

Marian van Kraaij (M)

Sanquin Blood Supply Foundation, Amsterdam, the Netherlands.

Eva-Maria Merz (EM)

Sanquin Research, Department of Donor Medicine Research - Donor Studies, Amsterdam, the Netherlands.
Department of Sociology, Vrije Universiteit, Amsterdam, the Netherlands.

Katja van den Hurk (K)

Sanquin Research, Department of Donor Medicine Research - Donor Studies, Amsterdam, the Netherlands.

Morten Bagge Hansen (MB)

Department of Clinical Immunology, Copenhagen University Hospital, Copenhagen, Denmark.

Ed Slot (E)

Sanquin Blood Supply Foundation, Amsterdam, the Netherlands.

Henrik Ullum (H)

Department of Clinical Immunology, Copenhagen University Hospital, Copenhagen, Denmark.

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