Hypersensitivity transfusion reactions to fresh frozen plasma: a retrospective analysis of the French hemovigilance network.


Journal

Transfusion medicine reviews
ISSN: 1532-9496
Titre abrégé: Transfus Med Rev
Pays: United States
ID NLM: 8709027

Informations de publication

Date de publication:
04 2022
Historique:
received: 10 02 2022
revised: 08 04 2022
accepted: 08 04 2022
pubmed: 3 5 2022
medline: 25 5 2022
entrez: 2 5 2022
Statut: ppublish

Résumé

Few data are currently available on hypersensitivity transfusion reactions (HTRs) after exposure to fresh frozen plasma (FFP). Between 2000 and 2018, three different FFP production strategies have been used in France, leading to the concomitant use of different types of FFP. The objective of this study was to describe the rate of FFP-related HTRs and to assess the relative risk of each type of FFP. HTR following FFP transfusion between 2000 and 2018 were retrospectively extracted from the national hemovigilance database of the French National Agency for Medicines and Health Products Safety (ANSM). Temporal evolution of the incidence of reactions was modeled using logistic regression. During the study period, the overall rate of FFP-related HTRs was 52.0 (95% CI 50.2-53.9) reactions per 100,000 units of FFP issued. The rate of FFP-related HTRs progressively increased over the study period, from 28.7 (95% CI 22.8-36.0) in 2000 to 88.9 (78.8-100.3) reactions per 100,000 units of FFP issued in 2018 (OR 1.08 [1.07 - 1.09], P < .001), whereas the rate of other types of adverse transfusion reactions (ATRs) decreased. Between 2000 and 2014, its period of use, Solvent-Detergent-treated Apheresis FFP (SD-APH) was associated with the lowest risk of HTR. Our results indicate that although the rate of HTRs to FFP is low in France, the risk of having such a reaction has steadily increased between 2000 and 2018. A declarative bias is unlikely as the rate of other type of FFP-related ATRs decreased over the same period. The risk of HTRs to FFP is suggested to differ according to the processing of the FFP with a lower risk for SD-APH.

Identifiants

pubmed: 35501216
pii: S0887-7963(22)00010-4
doi: 10.1016/j.tmrv.2022.04.002
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

77-81

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest The authors have no conflict of interest to disclose in relation to the submitted review.

Auteurs

Charles Tacquard (C)

CHU de Strasbourg, Service d'anesthésie-réanimation du Nouvel Hôpital Civil, Strasbourg, France. Electronic address: charlesambroise.tacquard@chru-strasbourg.fr.

Georges Andreu (G)

Retired Hospital Practitioner, Dijon, France.

Nicolas Meyer (N)

CHU de Strasbourg, GMRC, Service de santé publique, Strasbourg, France; I-Cube - UMR 7357, Laboratoire des sciences de l'ingénieur, de l'informatique et de l'imagerie, Université de Strasbourg, Strasbourg, France.

Monique Carlier (M)

Agence Régionale de Santé Grand Est, Châlons en Champagne, France.

Jean-Yves Py (JY)

Etablissement Français du Sang Centre-Pays de la Loire, Orléans, France.

Christian Drouet (C)

Institut Cochin, INSERM UMR1016, Université de Paris, Paris, France; University Grenoble-Alpes and Centre Hospitalier Universitaire de Grenoble, Grenoble, France.

Jacques Bienvenu (J)

Claude Bernard University, Lyon, France.

Paul Michel Mertes (PM)

CHU de Strasbourg, Service d'anesthésie-réanimation du Nouvel Hôpital Civil, Strasbourg, France.

Karim Boudjedir (K)

French National Agency for Medicines and Health Products Safety (ANSM), Saint Denis, France.

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Classifications MeSH