Morselli P L
Department of Clinical Research, Synthélabo Recherche (LERS), Paris, France.
Clin Pharmacokinet. 1989;17 Suppl 1:13-28. doi: 10.2165/00003088-198900171-00004.
A consistent body of data, acquired in the last 20 years, indicates that at birth most of the physiological variables regulating drug kinetics are immature, thus conditioning modified kinetic profiles in the neonate. The situation may be greatly complicated by the possible 'in utero' exposure to agents capable of altering the activity of liver and/or kidney excretory functions, and/or the presence of severe pathological conditions capable of significantly altering regional or general haemodynamics. The different variables mature at different rates depending on the gestational age and physiopathological conditions. A review of the available information on drug kinetics in the neonate and early infancy is presented here. Therapeutic drug monitoring appears to be the only possible way to assure a safer therapy for at-risk populations.
过去20年积累的一系列连贯数据表明,出生时大多数调节药物动力学的生理变量尚未成熟,因此决定了新生儿的药物动力学特征会有所改变。若胎儿在子宫内可能接触到能够改变肝脏和/或肾脏排泄功能活性的物质,和/或存在能够显著改变局部或全身血流动力学的严重病理状况,情况可能会变得极为复杂。不同变量依据胎龄和生理病理状况以不同速率成熟。本文对新生儿和婴儿早期药物动力学的现有信息进行了综述。治疗药物监测似乎是确保为高危人群提供更安全治疗的唯一可行方法。