PHARMACOKINETICS IN THE INFANT

被引:77
作者
MILSAP, RL [1 ]
JUSKO, WJ [1 ]
机构
[1] SUNY BUFFALO, SCH PHARM, DEPT PHARMACEUT, BUFFALO, NY 14260 USA
关键词
PHARMACOKINETICS; ABSORPTION; DISTRIBUTION; METABOLISM; EXCRETION; PHARMACODYNAMICS;
D O I
10.1289/ehp.94102s11107
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Processes controlling the absorption, distribution. metabolism excretion, and pharmacologic effects of drugs are likely to be immature or altered in neonates and infants. Absorption may be affected by differences in gastric pH and stomach emptying rate. Low serum protein concentrations and higher body water composition can change drug distribution. Drug metabolism enzyme activity is typically reduced in the neonate, but rapidly develops over the first year oi life. Renal excretion mechanisms are low at birth, but mature over a few months. Limited data are available on the pharmacodynamics of drugs; infants show greater sensitivity to d-tubocurarine. Developmental changes are rapid during the first weeks and months of life, thus requiring continual modification of drug dosage regimens designed for treating pediatric patients.
引用
收藏
页码:107 / 110
页数:4
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