Open AccessNeurological Adverse Effects Associated With Anti‐tumor Necrosis Factor Alpha Antibodies in Pediatric Inflammatory Bowel Diseases
Author(s) -
Bertrand Valérie,
Massy Nathalie,
Pigneur Bénédicte,
Coopman Stéphanie,
Durrieu Geneviève,
Gaboriau Louise,
Langlois Vincent,
GowerRousseau Corinne,
Hugot JeanPierre,
Ruemmele Frank M.
Publication year - 2020
Publication title -
journal of pediatric gastroenterology and nutrition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.206
H-Index - 131
eISSN - 1536-4801
pISSN - 0277-2116
DOI - 10.1097/mpg.0000000000002654
Subject(s) - medicine , inflammatory bowel disease , incidence (geometry) , transverse myelitis , adverse effect , ulcerative colitis , myelitis , optic neuritis , infliximab , population , pediatrics , gastroenterology , tumor necrosis factor alpha , immunology , disease , multiple sclerosis , physics , environmental health , psychiatry , spinal cord , optics
Objectives: Neurological adverse effects (NAEs) induced by biotherapies have been reported in the literature mainly in adult patients with inflammatory bowel disease (IBD), rheumatic diseases, or psoriasis. There are scant data in children. Aims of this study are to report and describe noninfective NAE associated with anti‐TNFα antibodies in pediatric IBD, and to evaluate their incidence. Methods: We retrospectively collected all reports of NAE in pediatric IBD treated with anti‐TNFα antibodies recorded in the French Pharmacovigilance Database. To estimate the national incidence of NAEs, we extrapolated data from the French regional inception population‐based cohort EPIMAD. Results: Between 2000 and 2018, 231 adverse events in pediatric IBD exposed to anti‐TNFα antibodies were reported to this Database. Seventeen NAEs (7.36%) were collected: 8 severe NAE (1 demyelinating neuropathy, 1 optic neuritis, 1 acute transverse myelitis, 1 polyradiculoneuritis, 1 sensorineural hearing loss, 1 seizure, 1 stroke, and 1 glioma), 7 moderate NAE (headaches), and 2 neuropsychic events. The median delay between anti‐TNFα start and NAE occurrence was 6 months (range: 13 days to 26 months). In 10 of 17 patients, anti‐TNFα antibodies were stopped. Nine of 17 patients had a complete resolution (including 2 severe NAE) and 8 of 17 a partial resolution (including 6 severe NAE). We estimate the incidence of severe NAE in pediatric IBD treated with anti‐TNFα antibodies at 1 case for 10,000 patients‐year in France. Conclusions: NAE associated with anti‐TNFα antibodies in pediatric IBD are rare. In severe NAE, we recommend to discontinue anti‐TNFα therapy and to consider alternative treatment.