Intravenous and subcutaneous immunoglobulins-associated eczematous reactions occur with a broad range of immunoglobulin types: A French national multicenter study.


Journal

Journal of the American Academy of Dermatology
ISSN: 1097-6787
Titre abrégé: J Am Acad Dermatol
Pays: United States
ID NLM: 7907132

Informations de publication

Date de publication:
02 2023
Historique:
received: 09 06 2022
revised: 27 09 2022
accepted: 01 10 2022
pubmed: 18 10 2022
medline: 17 1 2023
entrez: 17 10 2022
Statut: ppublish

Résumé

Human immunoglobulins are used for treating diverse inflammatory and autoimmune disorders. Eczema is an adverse event reported but poorly described. To describe the clinical presentation, severity, outcome, and therapeutic management of immunoglobulin-associated eczema. This retrospective and descriptive study included a query of the French national pharmacovigilance database, together with a national call for cases among dermatologists. We included 322 patients. Eczema occurred preferentially in men (78.9%) and in patients treated for neurological pathologies (76%). The clinical presentation consisted mainly of dyshidrosis (32.7%) and dry palmoplantar eczema (32.6%); 5% of cases exhibited erythroderma. Sixty-two percent of the eczema flares occurred after the first immunoglobulin course. Eczema was observed with 13 intravenous or subcutaneous immunoglobulin types and recurred in 84% of patients who maintained the same treatment and in 68% who switched the immunoglobulin type. After immunoglobulin discontinuation, 30% of patients still had persistent eczema. Retrospective study, with possible missing data or memory bias. Immunoglobulin-associated eczema occurred with all immunoglobulin types, preferentially in patients with neurologic diseases who required prolonged immunoglobulin treatment. Recurrence was frequent, even after switching the immunoglobulin type, which can lead to a challenging therapeutic situation when immunoglobulin maintenance is required.

Sections du résumé

BACKGROUND
Human immunoglobulins are used for treating diverse inflammatory and autoimmune disorders. Eczema is an adverse event reported but poorly described.
OBJECTIVES
To describe the clinical presentation, severity, outcome, and therapeutic management of immunoglobulin-associated eczema.
METHODS
This retrospective and descriptive study included a query of the French national pharmacovigilance database, together with a national call for cases among dermatologists.
RESULTS
We included 322 patients. Eczema occurred preferentially in men (78.9%) and in patients treated for neurological pathologies (76%). The clinical presentation consisted mainly of dyshidrosis (32.7%) and dry palmoplantar eczema (32.6%); 5% of cases exhibited erythroderma. Sixty-two percent of the eczema flares occurred after the first immunoglobulin course. Eczema was observed with 13 intravenous or subcutaneous immunoglobulin types and recurred in 84% of patients who maintained the same treatment and in 68% who switched the immunoglobulin type. After immunoglobulin discontinuation, 30% of patients still had persistent eczema.
LIMITATIONS
Retrospective study, with possible missing data or memory bias.
CONCLUSION
Immunoglobulin-associated eczema occurred with all immunoglobulin types, preferentially in patients with neurologic diseases who required prolonged immunoglobulin treatment. Recurrence was frequent, even after switching the immunoglobulin type, which can lead to a challenging therapeutic situation when immunoglobulin maintenance is required.

Identifiants

pubmed: 36252685
pii: S0190-9622(22)02886-9
doi: 10.1016/j.jaad.2022.10.015
pii:
doi:

Substances chimiques

Immunoglobulins 0
Immunoglobulins, Intravenous 0

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

380-387

Informations de copyright

Copyright © 2022 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest None disclosed.

Auteurs

Pauline Voland (P)

Dermatology Department, Robert-Debré Hospital, Reims-Champagne Ardennes University, IRMAIC, EA7509, Reims, France.

Camille Barthel (C)

Department of Dermatology, Nantes University Hospital, Nantes, France.

Brahim Azzouz (B)

Regional Pharmacovigilance Center of Reims, Reims-Champagne Ardennes University, Reims, France.

Nadia Raison-Peyron (N)

Department of Dermatology, Montpellier University Hospital, Montpellier, France.

Aurélie Du-Thanh (A)

Department of Dermatology, Montpellier University Hospital, Montpellier, France.

Delphine Staumont-Sallé (D)

Department of Dermatology, Lille University Hospital Center, University of Lille, Lille, France.

Marie Jachiet (M)

University of Paris, Faculty of Medicine, Assistance Publique-Hôpitaux de Paris (APHP), Department of Dermatology, Saint-Louis Hospital, Paris, France.

Angèle Soria (A)

Sorbonne Université, Department of Dermatology and Allergy, Tenon Hospital, AP-HP, Paris, France.

Audrey Nosbaum (A)

Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, Service d'Allergologie et Immunologie Clinique, Pierre-Bénite, France.

Aude Valois (A)

Dermatology Department, Army training hospital Sainte Anne, Toulon, France.

Camille Leleu (C)

Dermatology Department, Dijon University Hospital Center, Dijon, France.

Bénédicte Lebrun-Vignes (B)

Regional Pharmacovigilance Center, Pitié Salpétrière Hospital, Assistance Publique-Hôpitaux de Paris (APHP), Paris, France.

Thierry Trenque (T)

Regional Pharmacovigilance Center of Reims, Reims-Champagne Ardennes University, Reims, France.

Dominique Hettler (D)

Pharmacy and Pharmacovigilance Unit, Robert-Debré Hospital, Reims-Champagne Ardennes University, Reims, France.

Claire Bernier (C)

Department of Dermatology, Nantes University Hospital, Nantes, France.

Manuelle Viguier (M)

Dermatology Department, Robert-Debré Hospital, Reims-Champagne Ardennes University, IRMAIC, EA7509, Reims, France. Electronic address: mviguier@chu-reims.fr.

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Classifications MeSH