Tack Jan, Wyndaele Jean-Jacques, Ligozio Greg, Egermark Mathias
University of Leuven, Gastroenterology Section, Leuven.
Drug Healthc Patient Saf. 2012;4:127-39. doi: 10.2147/DHPS.S26580. Epub 2012 Sep 27.
Constipation is a common side effect of antimuscarinic treatment for overactive bladder (OAB). This review evaluates the incidence and impact of constipation on the lives of patients with OAB being treated with darifenacin.
Constipation data from published Phase III and Phase IIIb/IV darifenacin studies were reviewed and analyzed. Over 4000 patients with OAB (aged 18-89 years; ≥80% female) enrolled in nine studies (three Phase III [data from these fixed-dose studies were pooled and provide the primary focus for this review], three Phase IIIb, and three Phase IV). The impact of constipation was assessed by discontinuations, use of concomitant laxatives, patient-reported perception of treatment, and a bowel habit questionnaire.
In the pooled Phase III trials, 14.8% (50/337) of patients on darifenacin 7.5 mg/day and 21.3% (71/334) on 15 mg/day experienced constipation compared with 12.6% (28/223) and 6.2% (24/388) with tolterodine and placebo, respectively. In addition, a few patients discontinued treatment due to constipation (0.6% [2/337], 1.2% [4/334], 1.8% [4/223], and 0.3% [1/388] in the darifenacin 7.5 mg/day or 15 mg/day, tolterodine, and placebo groups, respectively), or required concomitant laxatives (3.3% [11/337], 6.6% [22/334], 7.2% [16/223], and 1.5% [6/388] in the darifenacin 7.5 mg/day or 15 mg/day, tolterodine, and placebo groups, respectively). Patient-reported perception of treatment quality was observed to be similar between patients who experienced constipation and those who did not. During the long-term extension study, a bowel habit questionnaire showed only small numerical changes over time in frequency of bowel movements, straining to empty bowels, or number of days with hard stools.
While constipation associated with darifenacin was reported in ≤21% of the patient population, it only led to concomitant laxative use in approximately one-third of these patients and a low incidence of treatment discontinuation. These data suggest that constipation did not impact patient perception of treatment quality.
便秘是治疗膀胱过度活动症(OAB)的抗毒蕈碱药物常见的副作用。本综述评估了服用达非那新治疗的OAB患者便秘的发生率及其对生活的影响。
对已发表的达非那新III期和IIIb/IV期研究中的便秘数据进行回顾和分析。9项研究纳入了4000多名OAB患者(年龄18 - 89岁;女性≥80%)(3项III期研究[这些固定剂量研究的数据进行了汇总并为本综述提供主要重点],3项IIIb期研究和3项IV期研究)。通过停药情况、同时使用泻药的情况、患者报告的治疗感受以及排便习惯问卷来评估便秘的影响。
在汇总的III期试验中,服用7.5毫克/天达非那新的患者中有14.8%(50/337)出现便秘,服用15毫克/天的患者中有21.3%(71/334)出现便秘,而服用托特罗定和安慰剂的患者中这一比例分别为12.6%(28/223)和6.2%(24/388)。此外,有少数患者因便秘停药(7.5毫克/天或15毫克/天达非那新组分别为0.6%[2/337]、1.2%[4/334],托特罗定组为1.8%[4/223],安慰剂组为0.3%[1/388]),或需要同时使用泻药(7.5毫克/天或15毫克/天达非那新组分别为3.3%[11/337]、6.6%[22/334],托特罗定组为7.2%[16/223],安慰剂组为1.5%[6/388])。观察发现,出现便秘的患者和未出现便秘的患者报告的治疗质量感受相似。在长期延长期研究中,一份排便习惯问卷显示,随着时间推移,排便频率、排便费力程度或硬便天数仅有微小的数值变化。
虽然报告显示服用达非那新的患者中便秘发生率≤21%,但其中只有约三分之一的患者因此同时使用泻药,且停药发生率较低。这些数据表明便秘并未影响患者对治疗质量的感受。