Efficacy and safety of elobixibat in combination with or switched from conventional treatments of chronic constipation: A retrospective observational study

IF 1.7 Q3 GASTROENTEROLOGY & HEPATOLOGY JGH Open Pub Date : 2024-08-26 DOI:10.1002/jgh3.70019
Takaaki Eguchi, Osamu Inatomi, Shuhei Shintani, Kenji Momose, Tomoya Sako, Megumi Takagi, Daiki Fumihara, Kazuki Inoue, Norio Katayama, Toshiyuki Morisawa, Takumi Ota, Yoshihisa Tsuji
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Abstract

Background and Aim

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.

Methods

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.

Results

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 (P < 0.0001). The BSFS score improved significantly from 3.2 ± 1.7 to 4.4 ± 1.4 (P < 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 (P < 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.

Conclusion

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.

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依洛昔巴特与慢性便秘的常规治疗方法联合使用或转换使用的疗效和安全性:回顾性观察研究
背景和目的 依洛昔巴特是一种三重作用模式的泻药,可增加结肠的水分分泌、促进结肠蠕动并重建排便欲望。本研究旨在评估依洛昔巴特对常规泻药难治性慢性便秘(CC)患者的有效性和安全性。 方法 在2018年4月至2022年6月期间,大阪济生会中津医院对根据罗马IV标准诊断并接受了依洛昔巴特治疗的难治性CC患者进行了一项单中心回顾性观察研究。研究收集了自发性肠蠕动(SBM)、布里斯托粪便形态量表(BSFS)评分、腹部症状和不良事件的数据。 结果 筛选出符合条件的 311 名患者进行分析。为期两周的艾洛昔巴特治疗可显著增加排便次数(次数/周),从 2.9 ± 1.9 增加到 4.3 ± 1.9(P < 0.0001)。BSFS 评分从 3.2 ± 1.7 显著提高到 4.4 ± 1.4(P < 0.0001)。大便变硬的患者比例下降,大便正常的患者比例上升。腹部症状(排便不尽感、拉稀、腹痛、腹胀和排便困难)也有显著改善(P < 0.05)。这些便秘症状都得到了改善,与患者的特征或之前使用的泻药无关。43.9%的患者在开始接受依洛昔巴特治疗时或治疗后停用了以前使用的泻药。观察到少数不良反应,依洛昔巴特的耐受性良好。 结论 依洛昔巴特对其他泻药难治的患者有效,与既往治疗或患者特征无关。依洛昔巴特可能有助于解决单一作用模式泻药的多重药理作用。
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来源期刊
JGH Open
JGH Open GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
3.40
自引率
0.00%
发文量
143
审稿时长
7 weeks
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