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西沙必利治疗胃食管反流病

Cisapride in the treatment of gastro-oesophageal reflux disease.

作者信息

Robertson C S, Evans D F, Ledingham S J, Atkinson M

机构信息

Department of Surgery, University Hospital, Queen's Medical Centre, Nottingham, UK.

出版信息

Aliment Pharmacol Ther. 1993 Apr;7(2):181-90. doi: 10.1111/j.1365-2036.1993.tb00088.x.

Abstract

Prokinetic agents are being used increasingly in medical therapy for gastro-oesophageal reflux disease (GERD). This study examined the effect of 10 mg q.d.s., oral cisapride, or placebo, taken for 12 weeks, on 48 patients with symptoms and endoscopic evidence of GERD. Objective evaluation of benefit was obtained by endoscopy and biopsy, oesophageal manometry, acid reflux provocation test and 24-h oesophageal pH monitoring. Cisapride significantly increased lower oesophageal sphincter pressure (P = 0.003) against baseline and also against placebo, in patients (n = 9) with an hypotensive lower oesophageal sphincter pressure (P < 0.01). The frequency of dyspeptic symptoms was significantly improved in the cisapride group (P = 0.03). Antacid intake, global evaluation of symptoms and a VAS score for symptoms were all better than placebo but failed to reach significance (global evaluation by patients, P = 0.07). Overall, there was no significant improvement in oesophagitis at either 6 weeks (P < 0.05 > 0.3) or 12 weeks (P = 0.07). However, if patients with grades I and II oesophagitis at entry were excluded, cisapride had a significantly greater effect than placebo, 6 weeks (P = 0.05), 12 weeks (P = 0.04). In those with oesophageal ulceration, cisapride was significantly more effective than placebo in inducing healing. Gastro-oesophageal reflux was very variable on both 24-h pH monitoring and acid reflux provocation test. In spite of a 50% decrease in acid exposure on 24-h pH monitoring (cisapride group, mean % pH < 4 day: entry 18.9%, 12 weeks 9.6%), there were no significant intra- or intergroup differences for percentage of time < pH 4, or frequency and duration of episodes, neither pre- or post-prandially, day or night, except for the number of post-prandial episodes during acid reflux provocation tests, which decreased significantly more with cisapride than with placebo (P < 0.05). Thus, oral cisapride when taken for 12 weeks promoted healing of oesophagitis and improved symptoms in patients with GERD; although an increase in lower oesophageal sphincter pressure was observed and a reduction in acid reflux was measured, no significant decrease of acid exposure was seen.

摘要

促动力药在胃食管反流病(GERD)的医学治疗中应用越来越广泛。本研究考察了48例有GERD症状及内镜证据的患者,口服10毫克西沙必利每日4次或安慰剂,持续服用12周的效果。通过内镜检查和活检、食管测压、酸反流激发试验及24小时食管pH监测对疗效进行客观评估。西沙必利可使食管下括约肌压力较基线水平显著升高(P = 0.003),在食管下括约肌压力降低的患者(n = 9)中,与安慰剂相比也显著升高(P < 0.01)。西沙必利组消化不良症状的频率显著改善(P = 0.03)。抗酸剂的摄入量、症状的总体评估及症状的视觉模拟评分均优于安慰剂,但未达到显著差异(患者总体评估,P = 0.07)。总体而言,6周时(P < 0.05 > 0.3)或12周时(P = 0.07)食管炎均无显著改善。然而,如果排除入组时患有I级和II级食管炎的患者,西沙必利在6周时(P = 0.05)和12周时(P = 0.04)的疗效显著优于安慰剂。在患有食管溃疡的患者中,西沙必利在促进愈合方面显著比安慰剂更有效。在24小时pH监测和酸反流激发试验中,胃食管反流情况差异很大。尽管24小时pH监测显示西沙必利组酸暴露减少了50%(平均pH < 4的天数:入组时18.9%,12周时9.6%),但在pH < 4的时间百分比、发作频率和持续时间方面,组内和组间均无显著差异,无论餐前还是餐后、白天还是晚上,除了酸反流激发试验中餐后发作次数外,西沙必利组较安慰剂组显著减少更多(P < 0.05)。因此,口服西沙必利12周可促进GERD患者食管炎的愈合并改善症状;尽管观察到食管下括约肌压力升高且测量到酸反流减少,但酸暴露无显著降低。

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