Pharmacokinetic and pharmacodynamic considerations of general anesthesia in pediatric subjects
Introduction: The target concentration strategy uses PKPD information for dose
determination. Models have also quantified exposure-response relationships, improved …
determination. Models have also quantified exposure-response relationships, improved …
Pharmacokinetics in neonatal prescribing: evidence base, paradigms and the future
K O'Hara, IMR Wright, JJ Schneider… - British journal of …, 2015 - Wiley Online Library
Paediatric patients, particularly preterm neonates, present many pharmacological
challenges. Due to the difficulty in conducting clinical trials in these populations dosing …
challenges. Due to the difficulty in conducting clinical trials in these populations dosing …
The clinical pharmacology of short acting analgo-sedatives in neonates
K Allegaert - Current clinical pharmacology, 2011 - ingentaconnect.com
Effective pain management remains an important indicator of the quality of care provided to
neonates, not only from an ethical, but also from a clinical outcome perspective. Significant …
neonates, not only from an ethical, but also from a clinical outcome perspective. Significant …
Pharmacokinetic and pharmacodynamic principles: unique considerations for optimal design of neonatal clinical trials
CHT Yeung, RHJ Verstegen, R Greenberg… - Frontiers in …, 2024 - frontiersin.org
Core clinical pharmacology principles must be considered when designing and executing
neonatal clinical trials. In this review, the authors discuss important aspects of drug dose …
neonatal clinical trials. In this review, the authors discuss important aspects of drug dose …
Pharmacological sedation management in the paediatric intensive care unit
MA Baarslag, K Allegaert, CAJ Knibbe… - Journal of Pharmacy …, 2017 - academic.oup.com
Objective This review addresses sedation management on paediatric intensive care units
and possible gaps in the knowledge of optimal sedation strategies. We present an overview …
and possible gaps in the knowledge of optimal sedation strategies. We present an overview …
Bioanalytical aspects and challenges in supporting pediatric drug development
K Heinig, E Zwanziger, J Potter, D Fraier - Bioanalysis, 2020 - Taylor & Francis
Historically, many commercially available drugs were not investigated sufficiently and/or
authorized for pediatric use (children age from 0 to 16 years)[1]. Consequently, physicians …
authorized for pediatric use (children age from 0 to 16 years)[1]. Consequently, physicians …
The path to perfect pediatric posology—drug development in pediatrics
JM Korth‐Bradley - The Journal of Clinical Pharmacology, 2018 - Wiley Online Library
Reluctance to enroll pediatric subjects in clinical trials has left gaps in information about
dosing, safety, and efficacy of medications. Pharmacotherapeutic information for pediatric …
dosing, safety, and efficacy of medications. Pharmacotherapeutic information for pediatric …
Prediction of clearance and dose of midazolam in preterm and term neonates: a comparative study between allometric scaling and physiologically based …
N Mansoor, T Ahmad, RA Khan… - American journal of …, 2019 - journals.lww.com
Children are not small adults because besides size there are subtle physiological and
biochemical differences between children and adults. Like adults, children also require …
biochemical differences between children and adults. Like adults, children also require …
Physiologically based pharmacokinetic modeling in neonates: Current status and future perspectives
Rational drug use in special populations is a clinical problem that doctors and pharma-cists
must consider seriously. Neonates are the most physiologically immature and vulnerable to …
must consider seriously. Neonates are the most physiologically immature and vulnerable to …