Update on pain assessment in sick neonates and infants
M Van Dijk, D Tibboel - Pediatric Clinics, 2012 - pediatric.theclinics.com
To understand how complicated pain assessment in neonates and young infants is, this
article presents 3 scenarios: a 25-week-old neonate with sepsis in the neonatal intensive …
article presents 3 scenarios: a 25-week-old neonate with sepsis in the neonatal intensive …
Pharmacokinetics of drugs in neonates: pattern recognition beyond compound specific observations
A Smits, A Kulo, JN de Hoon… - Current pharmaceutical …, 2012 - ingentaconnect.com
Although the principles of drug disposition also apply in neonates, their specific
characteristics warrant focussed assessment. Children display maturation in drug …
characteristics warrant focussed assessment. Children display maturation in drug …
Body weight-dependent pharmacokinetics of busulfan in paediatric haematopoietic stem cell transplantation patients: towards individualized dosing
I Bartelink, JJ Boelens, RGM Bredius… - Clinical …, 2012 - Springer
Abstract Background and Objectives: The wide variability in pharmacokinetics of busulfan in
children is one factor influencing outcomes such as toxicity and event-free survival. A meta …
children is one factor influencing outcomes such as toxicity and event-free survival. A meta …
[HTML][HTML] A bodyweight-dependent allometric exponent for scaling clearance across the human life-span
C Wang, MYM Peeters, K Allegaert… - Pharmaceutical …, 2012 - Springer
Purpose To explore different allometric equations for scaling clearance across the human
life-span using propofol as a model drug. Methods Data from seven previously published …
life-span using propofol as a model drug. Methods Data from seven previously published …
Pharmacokinetic behavior and appraisal of intravenous busulfan dosing in infants and older children: the results of a population pharmacokinetic study from a large …
Background Intravenous (IV) busulfan (Bu) dosing approved in Europe based on 5 body
weight (BW) strata has been validated for targeting Bu exposures in children undergoing …
weight (BW) strata has been validated for targeting Bu exposures in children undergoing …
Prediction of codeine toxicity in infants and their mothers using a novel combination of maternal genetic markers
J Sistonen, P Madadi, CJ Ross… - Clinical …, 2012 - Wiley Online Library
Substantial variation exists in response to standard doses of codeine ranging from poor
analgesia to life‐threatening central nervous system (CNS) depression. We aimed to …
analgesia to life‐threatening central nervous system (CNS) depression. We aimed to …
Prediction of morphine dose in humans
NHG Holford, SC Ma, BJ Anderson - Pediatric Anesthesia, 2012 - Wiley Online Library
Background: Morphine is widely used throughout the human life span. Several
pharmacokinetic models have been proposed to predict how morphine clearance changes …
pharmacokinetic models have been proposed to predict how morphine clearance changes …
[HTML][HTML] First dose in children: physiological insights into pharmacokinetic scaling approaches and their implications in paediatric drug development
Dose selection for “first in children” trials often relies on scaling of the pharmacokinetics from
adults to children. Commonly used approaches are physiologically-based pharmacokinetic …
adults to children. Commonly used approaches are physiologically-based pharmacokinetic …
Ontogeny of hepatic glucuronidation; methods and results
E HJ Krekels, M Danhof, D Tibboel… - Current drug …, 2012 - ingentaconnect.com
The onset and maturation, or so-called ontogeny, of hepatic glucuronidation is important for
the clearance of a number of drugs in children. The current review discusses methods for …
the clearance of a number of drugs in children. The current review discusses methods for …
Critical illness is a major determinant of midazolam clearance in children aged 1 month to 17 years
I Ince, SN De Wildt, MYM Peeters… - Therapeutic drug …, 2012 - journals.lww.com
Background: In children, a large variability in pharmacokinetics of midazolam, a cytochrome
P450 3A4/5 (CYP3A4/5) enzyme substrate, has been described, which cannot be explained …
P450 3A4/5 (CYP3A4/5) enzyme substrate, has been described, which cannot be explained …