Gryboski J D, Hillemeier A C, Grill B, Kocoshis S
Am J Gastroenterol. 1985 Nov;80(11):871-6.
Twenty-nine infants and children, age 2-70 months with chronic diarrhea, were admitted to a double-blind, parallel clinical trial. The subjects were randomly assigned to receive either a bismuth subsalicylate liquid or a placebo liquid formulation. Treatment was given for 7 days with dosage varied according to age. Analysis of the results showed that the subjects in the bismuth subsalicylate-treated group gained significantly more weight (p less than 0.05), had significantly fewer (p less than 0.01) and firmer (p less than 0.01) stools with less water content (p less than 0.01) during the course of the study than did the placebo-treated group. Response to treatment, as graded by nursing staff, family, and physicians was moderate to excellent in 86% of the treated group while none of the placebo group received such a rating (p less than 0.01). No differences were noted between stool weights or bile acid excretion.
29名年龄在2至70个月、患有慢性腹泻的婴幼儿被纳入一项双盲平行临床试验。受试者被随机分配接受碱式水杨酸铋液剂或安慰剂液剂。治疗为期7天,剂量根据年龄有所不同。结果分析显示,在研究过程中,碱式水杨酸铋治疗组的受试者体重显著增加(p<0.05),粪便数量显著减少(p<0.01)、质地更硬(p<0.01)且含水量更低(p<0.01),优于安慰剂治疗组。经护理人员、家属和医生评定,治疗组86%的受试者治疗反应为中度至极佳,而安慰剂组无一获得该评定(p<0.01)。粪便重量或胆汁酸排泄方面未发现差异。