Evidence map›Paper›PMID 42049472›Full record

Observational studyBritish journal of clinical pharmacology2026

Contraindicated drug-drug interactions and associated adverse drug reactions in an observational cohort study of 4543 paediatric hospitalized patients.

Emilie Laval, Sylvain Goutelle, Inesse Boussaha, Xavier Dode, Yanis Mimouni, Kim An Nguyen, Behrouz Kassai

Abstract readObservational Study
In one paragraph

Observational study in British journal of clinical pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Emilie LavalDepartment of Pharmacotoxicology, Hospices Civils de Lyon, CIC 1407 de Lyon, INSERM, CHU-Lyon, Bron, France.ORCID https://orcid.org/0009-0009-3897-5325
Sylvain GoutelleUMR CNRS 5558, Laboratoire de Biométrie et Biologie Humaine, Equipe Evaluation et Modélisation des Effets Thérapeutiques, Lyon, France.
Inesse BoussahaDepartment of Pharmacotoxicology, Hospices Civils de Lyon, CIC 1407 de Lyon, INSERM, CHU-Lyon, Bron, France.
Xavier DodeDepartment of Pharmacy, Hospices Civils de Lyon, CHU-Lyon, Bron, France.
Yanis MimouniThematic Institute of Genetics, Genomics & Bioinformatics, INSERM, Paris, France.
Kim An NguyenDepartment of Pharmacotoxicology, Hospices Civils de Lyon, CIC 1407 de Lyon, INSERM, CHU-Lyon, Bron, France.
Behrouz KassaiDepartment of Pharmacotoxicology, Hospices Civils de Lyon, CIC 1407 de Lyon, INSERM, CHU-Lyon, Bron, France.

Funding

Agence Nationale de Sécurité du Médicament et des Produits de Santé AAP 2012
6 · The paper itself

Abstract

background and purposeDrug-drug interactions (DDIs) are associated with an increased risk of adverse drug reactions (ADRs). Hospitalized children are particularly vulnerable to DDIs and ADRs due to polypharmacy, frequent use of unlicensed or off-label medications, and dosing regimens often extrapolated from adult data. The aims of this study were to characterize contraindicated DDIs detected in paediatric hospital wards and to assess whether these interactions were associated with ADRs. EXPERIMENTAL APPROACH: Medication and ADR data were prospectively collected over a 2-year observational period in hospitalized children. Patients aged ≤15 years, hospitalized for >3 days and receiving at least two medication during their stay were eligible. Potential contraindicated DDIs were identified using the algorithm implemented in the Thériaque database, based on the official DDI Thesaurus issued by the French National Agency for the Safety of Medicines and Health Products (ANSM). KEY

resultsA total of 4543 hospitalized children were included; 12.5% experienced at least one DDI, and 4.3% had at least one contraindicated DDI. Overall, 4225 DDIs were identified, including 709 classified as contraindicated. Thus 72% of the contraindicated DDIs occurred in three departments: paediatric cardiology, developmental psychopathology ward and pulmonology/allergology/cystic fibrosis. Most contraindicated DDIs (80%) were observed in children aged 2-11 years and 12-15 years. CONCLUSION AND IMPLICATIONS: Although a large number of DDIs were detected in hospitalized paediatric patients, contraindicated DDIs were rarely associated with clinically relevant ADRs. These findings highlight the need to improve the specificity and clinical relevance of DDI alert systems in paediatric inpatient settings.

Indexed as

Child, HospitalizedContraindications, DrugDrug-Related Side Effects and Adverse ReactionsAdolescentChildChild, PreschoolCohort StudiesDrug InteractionsFemaleFranceHospitalizationHumansInfantInfant, NewbornMalePolypharmacyadverse drug reactionsdrug interactionsmedication safetypaediatricspharmacoepidemiologypharmacovigilance

Identifiers

PMID42049472
PMCPMC13420905

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.