Seizures and quinolone antibiotics in children: a systematic review of adverse events.


Journal

European journal of hospital pharmacy : science and practice
ISSN: 2047-9956
Titre abrégé: Eur J Hosp Pharm
Pays: England
ID NLM: 101578294

Informations de publication

Date de publication:
03 2020
Historique:
received: 12 11 2018
revised: 29 11 2018
accepted: 13 12 2018
entrez: 6 3 2020
pubmed: 7 3 2020
medline: 7 3 2020
Statut: ppublish

Résumé

Quinolone antibiotics have a broad spectrum of activity including against Gram-negative organisms (especially We conducted a systematic review of the MEDLINE, EMBASE and CENTRAL databases. Any studies reporting the administration of quinolones to children and including a methodology for identifying or reporting adverse events were identified by two authors who worked independently. Data relating to study characteristics (including population, intervention, comparison and outcome data) and study quality (including the quality of adverse event reporting) were extracted. We identified 140 studies involving 21 884 children. No studies reported involving children with epilepsy and 21 studies reported the involvement of 317 children with CNS disorders. 2/317 (0.63%) children with CNS disorders developed seizures and at least 4/21 567 (0.023%) children without CNS pathology were reported to have developed seizures. The quality of adverse event reporting in included studies was low. Only 8/140 (5.71%) included studies provided details of a methodology for actively identifying adverse neurological events. Even for children with CNS disorders the risk of developing seizures in association with the use of quinolones seems to be low. Further evaluations of quinolone use in children should include methodologies for actively identifying and reporting adverse neurological events.

Sections du résumé

Background
Quinolone antibiotics have a broad spectrum of activity including against Gram-negative organisms (especially
Method
We conducted a systematic review of the MEDLINE, EMBASE and CENTRAL databases. Any studies reporting the administration of quinolones to children and including a methodology for identifying or reporting adverse events were identified by two authors who worked independently. Data relating to study characteristics (including population, intervention, comparison and outcome data) and study quality (including the quality of adverse event reporting) were extracted.
Results
We identified 140 studies involving 21 884 children. No studies reported involving children with epilepsy and 21 studies reported the involvement of 317 children with CNS disorders. 2/317 (0.63%) children with CNS disorders developed seizures and at least 4/21 567 (0.023%) children without CNS pathology were reported to have developed seizures. The quality of adverse event reporting in included studies was low. Only 8/140 (5.71%) included studies provided details of a methodology for actively identifying adverse neurological events.
Discussion
Even for children with CNS disorders the risk of developing seizures in association with the use of quinolones seems to be low. Further evaluations of quinolone use in children should include methodologies for actively identifying and reporting adverse neurological events.

Identifiants

pubmed: 32133130
doi: 10.1136/ejhpharm-2018-001805
pii: ejhpharm-2018-001805
pmc: PMC7043247
doi:

Substances chimiques

Anti-Bacterial Agents 0
Quinolones 0

Types de publication

Case Reports Journal Article Research Support, Non-U.S. Gov't Systematic Review

Langues

eng

Pagination

60-64

Subventions

Organisme : Medical Research Council
ID : MR/L006758/1
Pays : United Kingdom

Informations de copyright

© European Association of Hospital Pharmacists 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Références

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Auteurs

Matthew Neame (M)

Alder Hey Children's Hospital, Liverpool, UK.

Charlotte King (C)

Department of Women's and Children's Health, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.

Andrew Riordan (A)

Alder Hey Children's Hospital, Liverpool, UK.

Anand Iyer (A)

Alder Hey Children's Hospital, Liverpool, UK.

Rachel Kneen (R)

Alder Hey Children's Hospital, Liverpool, UK.

Ian Sinha (I)

Alder Hey Children's Hospital, Liverpool, UK.

Daniel B Hawcutt (DB)

Department of Women's and Children's Health, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
NIHR Alder Hey Clinical Research Facility, University of Liverpool, Liverpool, UK.

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Classifications MeSH