Safety of Medical Interventions in Children Versus Adults
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Summary
Comparing the risk of harm from pharmacologic interventions in pediatric versus adult randomized controlled trials (RCTs) and the relative odds ratio (ROR) in adults versus children per meta-analysis shows large uncertainty in available evidence on harms/harm-related end points.
- Type
- article
- Published
- 2014-03-01
- Cited by
- 28
- References
- 48
- OpenAlex
- https://openalex.org/W24567023
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:1618199
Keywords
Exhibition, Sculpture, Architecture, Recreation, Vernacular
References
- Children Are Not Just Small Adults: The Urgent Need for High-Quality Trial Evidence in Children
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- HETEROGI: Stata module to quantify heterogeneity in a meta-analysis
- Stimulation programs for pediatric drug research – do children really benefit?
- Uncertainty in heterogeneity estimates in meta-analyses
- Quantitative Synthesis in Systematic Reviews
- Availability of large-scale evidence on specific harms from systematic reviews of randomized trials.
- Better Reporting of Harms in Randomized Trials: An Extension of the CONSORT Statement
- Meta-analyses of Adverse Effects Data Derived from Randomised Controlled Trials as Compared to Observational Studies: Methodological Overview
- A literature review on off-label drug use in children
- Adverse events in randomized trials: neglected, restricted, distorted, and silenced.
- Postmarketing surveillance--lack of vigilance, lack of trust.
- Adverse Drug Reactions Among Children Over a 10-Year Period
- Retrospective hospital based surveillance of intussusception in children in a sentinel paediatric hospital: benefits and pitfalls for use in post-marketing surveillance of rotavirus vaccines.
- Comparative effectiveness of medical interventions in adults versus children.
- Pediatric information in drug product labeling.
- Intussusception following rotavirus vaccine administration: post-marketing surveillance in the National Immunization Program in Australia.
- Challenges in meta-analysis of randomized clinical trials for rare harmful cardiovascular events: the case of rosiglitazone.
Cited by
- Pharmacovigilance in pediatrics.
- Adult and paediatric cough guidelines: Ready for an overhaul?
- Clinical trials in pediatrics
- Effect of bivalent human papillomavirus vaccination on pregnancy outcomes: long term observational follow-up in the Costa Rica HPV Vaccine Trial
- PRISMA harms checklist: improving harms reporting in systematic reviews
- Comparative rates of harms in randomized trials from more developed versus less developed countries may be different.
- Empirical evaluation of which trial characteristics are associated with treatment effect estimates.
- Design and conduct of early phase drug studies in children: challenges and opportunities
- Insomnia From Drug Treatments: Evidence From Meta‐analyses of Randomized Trials and Concordance With Prescribing Information
- Are child-centric aspects in newborn and child health systematic review and meta-analysis protocols and reports adequately reported?—two systematic reviews
- Do systematic reviews on pediatric topics need special methodological considerations?
- Justification de la prescription hors-AMM d’antibiotiques chez l’enfant hospitalisé
- The rational use of available evidence before extrapolating the benefit risk ratio from adults to children
- Comparative evidence on harms in pediatric randomized clinical trials from less developed versus more developed countries is limited.
- Comparison of nuisance parameters in pediatric versus adult randomized trials: a meta-epidemiologic empirical evaluation
- (In)-Equality in the Allocation of R&D Resources for Rare Diseases
- High prevalence of off-label and unlicensed paediatric prescribing in a hospital in Indonesia during the period Aug.—Oct. 2014
- Co-morbid chronic pain and opioid misuse in youth: Knowns, unknowns, and implications for behavioral treatment
- Supportive interventions for childhood cancer: An umbrella review of randomized evidence.
- Off-label prescription: developing a guideline and validating an instrument to measure physicians’ and clinical pharmacists’ knowledge and attitudes toward off-label medication use
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