Schöni M, Kraemer R, Rossi E
Helv Paediatr Acta. 1981 Sep;36(4):359-69.
Under controlled clinical observation we administered Cimetidine (600 mg/m2/day) in 10 children with cystic fibrosis. All patients received identical diets (40% fat, 45% carbohydrate, 15% protein) as well as same standardized enzyme preparation (lyophilised whole pancreas). 3-day fecal fat and nitrogen excretion analyses were performed. After 6 days of Cimetidine therapy, an improvement of fat and nitrogen absorption could be detected in 5 patients. Statistical analysis of the group as a whole showed no improvement in fat absorption coefficients. We conclude that this drug therapy should only be recommended for routine clinical use after long-term trials have shown a real improvement of absorption.
在对照临床观察中,我们对10名囊性纤维化患儿给予西咪替丁(600毫克/平方米/天)。所有患者均接受相同的饮食(40%脂肪、45%碳水化合物、15%蛋白质)以及相同的标准化酶制剂(冻干全胰腺)。进行了为期3天的粪便脂肪和氮排泄分析。西咪替丁治疗6天后,5名患者的脂肪和氮吸收有所改善。对整个组进行的统计分析显示脂肪吸收系数没有改善。我们得出结论,只有在长期试验表明吸收有真正改善之后,这种药物治疗才应推荐用于常规临床使用。