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How children's responses to drugs differ from adults
Open accessAbstract
Children are not small adults. However, the main thesis of this review will be that children's responses to drugs have much in common with the responses in adults and indeed in other mammals. Often, it is assumed that drug effects differ in children but in reality this perception often arises because the drugs have not been adequately studied in paediatric populations of different ages and with different diseases. There may also be difficulties in measuring small but significant effects because the outcome measures are more difficult to assess in children. In some cases, stage of development can alter the action of, and response to, a drug – a truly age‐dependent difference in pharmacodynamics. This may be true of both the desired action and adverse events. Examples are given. Programming by drugs is also a phenomenon almost exclusive to early life, i.e. permanent effects result from a stimulus applied at a sensitive point in development (‘critical window’), often in fetal or neonatal life. Again, examples are discussed. Different pathophysiology, different disease variants, different pharmacodynamics, different ‘host’ response and different adverse drug reactions can all explain why some drugs behave differently in children. However, we need to explore ways to avoid re‐inventing the wheel by determining how data from adult animal and human models can help inform research and practice for children.
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Of the included studies, 5 were pilot trials with insufficient power to detect small treatment effect sizes.
“Of the included studies, 5 were pilot trials,37,38,39,40,43 with insufficient power to detect small treatment effect sizes.”
From Safety Planning Interventions for Suicide Prevention in Children and Adolescents: A Systematic Review and Meta-Analysis (2025) · cites this paper as [37]
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Haakenstad, A., Yearwood, J. A., Fullman, N., Bintz, C., Bienhoff, K., Weaver, M. R., Nandakumar, V., LeGrand, K. E., Knight, M., Abbafati, C., et al. (2022) · The Lancet Global Health · doi:10.1016/s2214-109x(22)00429-6 · Cited by 258
Investigating the pharmacodynamics of ketamine in children
HERD, D. W., ANDERSON, B. J., KEENE, N. A., & HOLFORD, N. H. G. (2008) · Pediatric Anesthesia · doi:10.1111/j.1460-9592.2007.02384.x · Cited by 103
Albaum, C., Irwin, S. H., Muha, J., Schumacher, A., Clarissa, S., Finkelstein, Y., Bridge, J. A., & Korczak, D. J. (2025) · JAMA Pediatrics · doi:10.1001/jamapediatrics.2025.1012 · Cited by 40
Metadata
- Authors
- Stephenson, T.
- Affiliations
- University of Nottingham (GB)
- Corresponding author
- Stephenson, Terence
- ORCID
- Stephenson, Terence
- Venue
- British Journal of Clinical Pharmacology
- Publisher
- Wiley
- Published
- 2005-06
- Volume
- 59
- Issue
- 6
- Pages
- 670-673
- ISSN
- 0306-5251 (ISSN-L)
- 1365-2125
- PMC
- PMC1884865
- OpenAlex
- W2114907395
- Cited by
- 178
- References
- 0
- Citations by year
- 2026: 4 · 2025: 15 · 2024: 6 · 2023: 10 · 2022: 12 · 2021: 7 · 2020: 7 · 2019: 11 · 2018: 9 · 2017: 7 · 2016: 12 · 2015: 7 · 2014: 12 · 2013: 4 · 2012: 9
- FWCI
- 4.94
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- British Journal of Clinical Pharmacology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Topics
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Pharmaceutical studies and practices
- Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods in Clinical Trials
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Child and Adolescent Health
- Keywords
- pediatric pharmacology, developmental programming, critical window, adverse drug reactions in children
- MeSH terms
- Adult, Aging, Bayes Theorem, Child, Clinical Trials as Topic, Humans, Pharmacogenetics, Pharmacokinetics, Research Design
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