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Pediatric patient dosages diverge from adults due to disparities in body surface area, total body water, and extracellular fluid per kilogram of body weight. The dosing regimen considers the variations in pharmacokinetics and pharmacology across distinct age groups, encompassing preterm newborns, infants, young children, older children, and adolescents. Calculation of pediatric patient doses is predicated on determining body surface area, which exhibits a superior correlation with the child's...

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Related Experiment Video

Updated: Feb 27, 2026

Defining the Role Of Language in Infants' Object Categorization with Eye-tracking Paradigms

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Published on: February 8, 2019

The INFANT trial

Peter Brocklehurst¹, David J Field², Ed Juszczak³

¹Birmingham Clinical Trials Unit, College of Medical and Dental Sciences, University of Birmingham, Birmingham B15 2TT, UK.

Lancet (London, England)

|July 6, 2017

Summary

No abstract available in PubMed .

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