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考来烯胺与洛哌丁胺治疗门诊婴儿急性腹泻的对比试验。

A comparative trial of cholestyramine and loperamide for acute diarrhoea in infants treated as outpatients.

作者信息

Vesikari T, Isolauri E

出版信息

Acta Paediatr Scand. 1985 Sep;74(5):650-4. doi: 10.1111/j.1651-2227.1985.tb10006.x.

Abstract

Infants aged 4 to 36 months with acute diarrhoea (rotavirus 66%) were treated as outpatients with oral fluids and a rapid return to full feedings. In addition, the infants were randomized to receive for 3 days either cholestyramine 2 g twice daily (N = 10), an equivalent placebo 2 g twice daily (N = 15), or loperamide 0.10 mg/kg divided in three doses (N = 16). The duration of watery diarrhoea from the beginning of treatment was 0.9 +/- 1.0 days in the cholestyramine group, 2.5 +/- 1.3 days in the loperamide group, and 3.3 +/- 1.6 days in the placebo group (p less than 0.001 cholestyramine vs. placebo, p less than 0.005 cholestyramine vs. loperamide). The infants receiving cholestyramine also had a better weight gain than those receiving the placebo, and their metabolic acidosis was corrected sooner. There was no hyperchloraemia associated with the cholestyramine treatment. It is concluded that cholestyramine 2 g twice daily for 3 days can be safely used to shorten the course of acute diarrhoea. The use of loperamide in acute infantile diarrhoea does not appear justified.

摘要

年龄在4至36个月的急性腹泻婴儿(轮状病毒感染占66%)作为门诊患者接受口服补液治疗,并迅速恢复全量喂养。此外,这些婴儿被随机分为三组,分别接受为期3天的以下治疗:每天两次,每次2克考来烯胺(N = 10);每天两次,每次2克等效安慰剂(N = 15);或洛哌丁胺0.10毫克/千克,分三次服用(N = 16)。从治疗开始计算,考来烯胺组水样腹泻的持续时间为0.9±1.0天,洛哌丁胺组为2.5±1.3天,安慰剂组为3.3±1.6天(考来烯胺组与安慰剂组相比,p<0.001;考来烯胺组与洛哌丁胺组相比,p<0.005)。接受考来烯胺治疗的婴儿体重增加情况也优于接受安慰剂的婴儿,且其代谢性酸中毒得到更快纠正。考来烯胺治疗未出现高氯血症。结论是,每天两次,每次2克考来烯胺,连用3天可安全用于缩短急性腹泻病程。在急性婴儿腹泻中使用洛哌丁胺似乎没有依据。

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