Altabas Karmela, Bilić Ante, Jurcić Dragan, Dorosulić Zdravko, Mihanović Mate, Sunić-Omejc Martina, Restek-Petrović Branka, Tolj Nikolina
Department of Hepatogastroenterology, University Department of Medicine, General Hospital Sveti Duh, Zagreb, Croatia.
Coll Antropol. 2003 Jun;27(1):197-204.
The effects of cisapride (10 mg three times daily) on the stool evacuation characteristics, laxative consumption (symptom diary) and motility pattern (rectoanal manometry) were assessed in patients with chronic idiopathic constipation who fulfilled Rome II criteria. After a 14-day basal period on a diet rich in fiber (phase I), patients were treated with placebo (n = 20) or cisapride (n = 19) (phase II). Anorectal manometry was performed at the end of each phase. The study was controlled, randomized and double blind. Side effects related to the use of cisapride were noted and found to be mild. Cisapride and placebo increased stool frequency from 4 (1-11) to 7 (14-12) (p < 0.001) and from 4 (2-10) to 6 (2-11) (p < 0.05) per week, respectively. Straining was decreased from 69.0% to 39.7% in the cisapride (p < 0.0001) group, and from 79% to 35% (p < 0.0001) in the placebo group. Both cisapride and placebo decreased the feeling of incomplete evacuation from 91.7% to 37.5% (p < 0.0001) and from 82.7% to 39.2% (p < 0.0001), respectively. Cisapride reduced the need of laxatives and showed a tendency to normalize stool consistency but did not influence any other symptom or bowel motility parameter.
在符合罗马II标准的慢性特发性便秘患者中,评估了西沙必利(每日三次,每次10毫克)对粪便排出特征、泻药使用情况(症状日记)和动力模式(直肠肛门测压)的影响。在富含纤维的饮食基础期(第一阶段)14天后,患者接受安慰剂治疗(n = 20)或西沙必利治疗(n = 19)(第二阶段)。在每个阶段结束时进行肛门直肠测压。该研究为对照、随机和双盲研究。记录了与使用西沙必利相关的副作用,发现副作用较轻。西沙必利和安慰剂分别使每周排便次数从4次(1 - 11次)增加到7次(1 - 14次)(p < 0.001)和从4次(2 - 10次)增加到6次(2 - 11次)(p < 0.05)。西沙必利组用力排便的比例从69.0%降至39.7%(p < 0.0001),安慰剂组从79%降至35%(p < 0.0001)。西沙必利和安慰剂均使排便不尽感分别从91.7%降至37.5%(p < 0.0001)和从82.7%降至39.2%(p < 0.0001)。西沙必利减少了泻药的需求,并显示出使粪便稠度正常化的趋势,但未影响任何其他症状或肠道动力参数。