Skin Manifestations in Pediatric Patients Treated With a TNF-Alpha Inhibitor for Inflammatory Bowel Disease: A Retrospective Study [Formula: see text].


Journal

Journal of cutaneous medicine and surgery
ISSN: 1615-7109
Titre abrégé: J Cutan Med Surg
Pays: United States
ID NLM: 9614685

Informations de publication

Date de publication:
Historique:
pubmed: 13 6 2020
medline: 16 6 2021
entrez: 13 6 2020
Statut: ppublish

Résumé

Tumor necrosis factor (TNF) alpha inhibitors (anti-TNF) are effective in the treatment of inflammatory bowel disease (IBD) as well as psoriasis. Their increasing use has raised the identification of cutaneous side effects (CSEs). Evidence in children is limited. The objective of this study is to describe CSEs of anti-TNF treatment in a pediatric population with IBD. This is a retrospective single-center study of children with IBD under anti-TNF treatment between 2013 and 2016. A total of 40 patients with CSEs related to anti-TNF were referred to our pediatric dermatology clinic. A control group was randomly selected from patients receiving anti-TNF for IBD, who were referred to the dermatology clinic for other conditions unrelated to anti-TNF. Of 343 patients with IBD, 40 (11.3%) presented CSEs potentially related to the treatment. No differences in sex, age, and underlying disease were found between those with and without CSEs. The most frequent CSEs were psoriasiform eruptions (41%) which were more exudative than usual, located especially in skin folds and on the scalp; skin infections (20%); and eczematous eruptions (10%). Only 5% of patients changed or discontinued the current anti-TNF because of CSEs. This is one of the largest pediatric cohorts of IBD patients with CSEs. Psoriasiform eruptions were the most common CSEs, with predilection for skin folds and scalp, and frequent superimposed bacterial infection. Topical and/or systemic antibiotics were required in addition to topical corticosteroids in 25% of patients. The rate of discontinuation of anti-TNF therapy due to CSEs was low.

Sections du résumé

BACKGROUND BACKGROUND
Tumor necrosis factor (TNF) alpha inhibitors (anti-TNF) are effective in the treatment of inflammatory bowel disease (IBD) as well as psoriasis. Their increasing use has raised the identification of cutaneous side effects (CSEs). Evidence in children is limited.
OBJECTIVES OBJECTIVE
The objective of this study is to describe CSEs of anti-TNF treatment in a pediatric population with IBD.
METHODS METHODS
This is a retrospective single-center study of children with IBD under anti-TNF treatment between 2013 and 2016. A total of 40 patients with CSEs related to anti-TNF were referred to our pediatric dermatology clinic. A control group was randomly selected from patients receiving anti-TNF for IBD, who were referred to the dermatology clinic for other conditions unrelated to anti-TNF.
RESULTS RESULTS
Of 343 patients with IBD, 40 (11.3%) presented CSEs potentially related to the treatment. No differences in sex, age, and underlying disease were found between those with and without CSEs. The most frequent CSEs were psoriasiform eruptions (41%) which were more exudative than usual, located especially in skin folds and on the scalp; skin infections (20%); and eczematous eruptions (10%). Only 5% of patients changed or discontinued the current anti-TNF because of CSEs.
CONCLUSION CONCLUSIONS
This is one of the largest pediatric cohorts of IBD patients with CSEs. Psoriasiform eruptions were the most common CSEs, with predilection for skin folds and scalp, and frequent superimposed bacterial infection. Topical and/or systemic antibiotics were required in addition to topical corticosteroids in 25% of patients. The rate of discontinuation of anti-TNF therapy due to CSEs was low.

Identifiants

pubmed: 32527153
doi: 10.1177/1203475420917387
doi:

Substances chimiques

Tumor Necrosis Factor Inhibitors 0
Infliximab B72HH48FLU
Adalimumab FYS6T7F842

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

333-339

Auteurs

María-Laura Cossio (ML)

Division of Dermatology, CHU Sainte-Justine, University of Montreal, QC, Canada.
28033Department of Dermatology, Faculty of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.

Annie Genois (A)

Division of Dermatology, CHU Sainte-Justine, University of Montreal, QC, Canada.

Prévost Jantchou (P)

25461Division of Gastroenterology, CHU Sainte-Justine, University of Montreal, QC, Canada.

Afshin Hatami (A)

Division of Dermatology, CHU Sainte-Justine, University of Montreal, QC, Canada.

Colette Deslandres (C)

25461Division of Gastroenterology, CHU Sainte-Justine, University of Montreal, QC, Canada.

Catherine McCuaig (C)

Division of Dermatology, CHU Sainte-Justine, University of Montreal, QC, Canada.

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Classifications MeSH