Evans B W, Clark W K, Moore D J, Whorwell P J
University of Hertfordshire, School of Pharmacy, College Lane Campus, Hatfield, UK, AL10 9AB.
Cochrane Database Syst Rev. 2007 Oct 17(4):CD003960. doi: 10.1002/14651858.CD003960.pub3.
IBS is a complex disorder that encompasses a wide profile of symptoms. The symptoms of chronic constipation frequently resemble those of constipation-predominant IBS. Current drug treatments for irritable bowel syndrome (IBS) are of limited value. Many target specific symptoms only. Tegaserod, a 5HT(4) partial agonist, represents a novel mechanism of action in the treatment of IBS and chronic constipation.
The objective of this review was to evaluate the efficacy and tolerability of tegaserod for the treatment of IBS and chronic constipation in adults and adolescents aged 12 years and above.
MEDLINE 1966-December 2006 and EMBASE 1980 to December 2006 were searched. The text and key words used included "tegaserod", "HTF 919", "irritable bowel", "constipation" and "colonic diseases, functional". The Cochrane Central Register of Controlled Trials, and the Inflammatory Bowel Disease Review Group Specialized Trials Register were also searched. Searches stopped on 15th December 2006. Relevant articles were retrieved, and their reference lists were also reviewed.
Randomised or quasi-randomised controlled trials comparing tegaserod with placebo, no treatment or any other intervention (pharmacological or non-pharmacological) in subjects aged 12 years and above with a diagnosis of IBS or chronic constipation, focusing on clinical endpoints were considered for review.
Study inclusion and exclusion, data extraction and quality assessment was undertaken by two authors independently. Meta-analysis was performed where study populations, designs, outcomes, and statistical reporting allowed combination of data in a valid way, using the summary statistics relative risk for dichotomous data and weighted mean difference for continuous data, both with 95% CI. Thirteen short-term placebo-controlled studies fulfilled the inclusion criteria. These were predominantly conducted in women. Ten studies evaluated the efficacy of tegaserod on global gastrointestinal (GI) symptoms in patients with constipation-predominant IBS (C-IBS). One small study evaluated safety in patients with diarrhoea-predominant IBS. Two studies evaluated the effectiveness of tegaserod for the treatment of chronic constipation.
In patients with C-IBS, the relative risk (RR) of being a responder in terms of global relief of GI symptoms during the last 4 weeks of treatment was significantly higher with both tegaserod 12 mg and 4 mg doses compared with placebo. Although the pooled results indicate statistically significant benefit with tegaserod, the a priori minimal clinically important differences set in two of three studies were not reached. The responder rate for this endpoint was also higher when considered for the first 4 weeks of treatment (tegaserod 12 mg only). Tegaserod did not significantly improve the patients' individual symptoms of abdominal pain and discomfort although bowel habit showed a statistically significant improvement with tegaserod 4 mg and there was a non-significant trend in this outcome in favour of tegaserod 12 mg. In patients with chronic constipation, the RR of being a responder in terms of complete spontaneous bowel movements per week with tegaserod 12 mg was 1.54 (95% CI 1.35 to 1.75), WMD for this endpoint compared with placebo 0.6 (95% CI 0.42 to 0.78). Differences between tegaserod and placebo in increases in frequency of bowel movements were small (less than one per week). The proportion of patients with either diagnosis who experienced diarrhea was significantly higher in the tegaserod 12 mg group compared with placebo (RR 2.80, 95% CI 2.13 to 3.68), with a number needed to harm (NNH) of 20. Effects of tegaserod on GI symptoms such as bloating, stool consistency, and straining were not consistent across the studies.
AUTHORS' CONCLUSIONS: Tegaserod appears to improve the overall symptomatology of IBS, and the frequency of bowel movements in those with chronic constipation. The clinical importance of these modest improvements is not clear. There are currently few data on its effect on quality of life. In addition, more information is needed about its efficacy in men. It would also be of interest to know whether treatment with tegaserod leads either directly, or indirectly, to changes in visceral sensitivity or psychopathology, which are also considered important in the pathophysiology of these conditions.
肠易激综合征(IBS)是一种复杂的疾病,症状表现多样。慢性便秘的症状常与以便秘为主型的肠易激综合征相似。目前用于治疗肠易激综合征(IBS)的药物疗效有限,许多药物仅针对特定症状。替加色罗是一种5HT(4)部分激动剂,代表了治疗IBS和慢性便秘的一种新作用机制。
本综述旨在评估替加色罗治疗12岁及以上成人和青少年IBS及慢性便秘的疗效和耐受性。
检索了MEDLINE 1966年至2006年12月以及EMBASE 1980年至2006年12月的数据。使用的文本和关键词包括“替加色罗”、“HTF 919”、“肠易激”、“便秘”和“结肠疾病,功能性”。还检索了Cochrane对照试验中心注册库以及炎症性肠病综述小组专门试验注册库。检索于2006年12月15日停止。检索出相关文章,并对其参考文献列表进行了审查。
纳入12岁及以上诊断为IBS或慢性便秘的受试者,比较替加色罗与安慰剂、不治疗或任何其他干预措施(药物或非药物)的随机或半随机对照试验,重点关注临床终点,纳入综述。
由两位作者独立进行研究纳入与排除、数据提取和质量评估。在研究人群、设计、结局和统计报告允许以有效方式合并数据的情况下,进行荟萃分析,使用二分数据的汇总统计相对危险度和连续数据的加权均数差,两者均带有95%可信区间。13项短期安慰剂对照研究符合纳入标准。这些研究主要在女性中进行。10项研究评估了替加色罗对以便秘为主型肠易激综合征(C-IBS)患者总体胃肠道(GI)症状的疗效。一项小型研究评估了腹泻为主型肠易激综合征患者的安全性。两项研究评估了替加色罗治疗慢性便秘的有效性。
在C-IBS患者中,与安慰剂相比,替加色罗12毫克和4毫克剂量在治疗最后4周胃肠道症状总体缓解方面的应答者相对危险度(RR)显著更高。尽管汇总结果表明替加色罗有统计学显著益处,但三项研究中的两项设定的先验最小临床重要差异未达到。在治疗的前4周(仅替加色罗12毫克)考虑该终点时,应答率也更高。替加色罗虽未显著改善患者的腹痛和不适等个体症状,但肠道习惯方面,替加色罗4毫克有统计学显著改善,替加色罗12毫克在该结局上有不显著的改善趋势。在慢性便秘患者中,替加色罗12毫克每周完全自主排便的应答者RR为1.54(95%可信区间1.35至1.75),该终点与安慰剂相比的加权均数差为0.6(95%可信区间0.42至0.78)。替加色罗与安慰剂在排便频率增加方面的差异较小(每周少于一次)。与安慰剂相比,替加色罗12毫克组中任一诊断的患者发生腹泻的比例显著更高(RR 2.80,95%可信区间2.13至3.68),伤害所需人数(NNH)为20。替加色罗对诸如腹胀、大便性状和用力排便等胃肠道症状的影响在各研究中不一致。
替加色罗似乎可改善IBS的总体症状以及慢性便秘患者的排便频率。这些适度改善的临床重要性尚不清楚。目前关于其对生活质量影响的数据很少。此外,关于其对男性疗效的更多信息也需要。了解替加色罗治疗是否直接或间接导致内脏敏感性或精神病理学改变也会很有意义,这些在这些疾病的病理生理学中也被认为很重要。