慢性子宫内接触氯丙嗪后新生儿的排泄。

H C Nielsen, S Wiriyathian, R Rosenfeld, K Leveno, J C Garriott
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引用次数: 0

摘要

氯丙嗪在新生儿体内的药代动力学尚未见报道。我们研究了氯丙嗪从婴儿血浆中去除的动力学,其母亲在怀孕的最后三个月接受了高剂量的氯丙嗪和锂治疗。婴儿表现出严重的神经系统抑郁症状,在出生后的前9天逐渐减轻。血浆氯丙嗪去除动力学用双室模型描述,其快速半衰期为1.46天,慢半衰期为3.19天。这两种半衰期都比在成人中描述的快半衰期和慢半衰期长得多。胎儿或新生儿接触氯丙嗪时应谨慎。需要进一步了解新生儿氯丙嗪的分布和排泄情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chlorpromazine excretion by the neonate following chronic in utero exposure.

The pharmacokinetics of chlorpromazine in the newborn have not been reported. We studied the kinetics of removal of chlorpromazine from plasma in an infant whose mother was treated with high doses of chlorpromazine and lithium throughout the last trimester of pregnancy. The infant exhibited symptoms of severe neurologic depression that slowly abated over the first 9 days of life. The kinetics of plasma chlorpromazine removal were described with a two-compartment model, exhibiting a rapid half-life of 1.46 days and a slow half-life of 3.19 days. Both half-lives are considerably longer than the rapid and slow half-lives described in adults. Caution in exposing the fetus or newborn to chlorpromazine is warranted. Further information on the distribution and excretion of chlorpromazine by the newborn is needed.

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