Eguchi Takaaki, Inatomi Osamu, Shintani Shuhei, Momose Kenji, Sako Tomoya, Takagi Megumi, Fumihara Daiki, Inoue Kazuki, Katayama Norio, Morisawa Toshiyuki, Ota Takumi, Tsuji Yoshihisa
Department of Gastroenterology and Hepatology Osaka Saiseikai Nakatsu Hospital Osaka Japan.
Department of General Medicine Shiga University of Medical Science Hospital Shiga Japan.
JGH Open. 2024 Aug 26;8(8):e70019. doi: 10.1002/jgh3.70019. eCollection 2024 Aug.
Elobixibat is a triple mode of action laxative that increases water secretion into the colon, promotes colonic motility, and reestablishes the defecation desire. This study aims to evaluate the effectivity and safety of elobixibat in chronic constipation (CC) patients refractory to conventional laxatives.
A single-center retrospective observational study was conducted in refractory CC patients diagnosed according to the Rome IV criteria and received elobixibat between April 2018 and June 2022 at Osaka Saiseikai Nakatsu Hospital. Data were collected for spontaneous bowel movement (SBM), Bristol stool form scale (BSFS) scores, abdominal symptoms, and adverse events.
Eligible 311 patients were selected for the analysis. Two-week Elobixibat treatment significantly increased SBM (times/week) from 2.9 ± 1.9 to 4.3 ± 1.9 ( < 0.0001). The BSFS score improved significantly from 3.2 ± 1.7 to 4.4 ± 1.4 ( < 0.0001). The percentages of patients with hard stool were decrease and that with normal stools were increase. Improvements in abdominal symptoms (sensation of incomplete bowel evacuation, straining, abdominal pain and distention, and difficulty defecating) were also significant ( < 0.05). These constipation symptoms were improved irrespective of patient characteristics or previous laxatives. The 43.9% of previous laxatives were discontinued at the start of or after starting elobixibat treatment. A few adverse events were observed, elobixibat was well tolerated.
Elobixibat was effective in patients who were refractory to other laxatives, irrespective of previous therapy or patient characteristics. Elobixibat may contribute to resolving polypharmacy with single mode of action laxatives.
埃洛必利是一种具有三重作用模式的泻药,可增加结肠水分分泌、促进结肠蠕动并恢复排便欲望。本研究旨在评估埃洛必利对常规泻药难治的慢性便秘(CC)患者的有效性和安全性。
在大阪济生会中津医院对2018年4月至2022年6月期间根据罗马IV标准诊断并接受埃洛必利治疗的难治性CC患者进行了单中心回顾性观察研究。收集了自发排便(SBM)、布里斯托大便形态量表(BSFS)评分、腹部症状和不良事件的数据。
选取311例符合条件的患者进行分析。两周的埃洛必利治疗使SBM(次/周)从2.9±1.9显著增加至4.3±1.9(<0.0001)。BSFS评分从3.2±1.7显著改善至4.4±1.4(<0.0001)。硬便患者的百分比下降,正常大便患者的百分比增加。腹部症状(排便不尽感、用力排便、腹痛和腹胀以及排便困难)的改善也很显著(<0.05)。无论患者特征或先前使用的泻药如何,这些便秘症状均得到改善。43.9%的先前使用的泻药在开始或开始埃洛必利治疗后停用。观察到少数不良事件,埃洛必利耐受性良好。
埃洛必利对其他泻药难治的患者有效,无论先前的治疗或患者特征如何。埃洛必利可能有助于解决多种单一作用模式泻药的联合使用问题。