A multicenter, postmarketing surveillance of elobixibat in patients with chronic constipation in Japan: A final analysis report.

IF 2.3 Q2 MEDICINE, GENERAL & INTERNAL
SAGE Open Medicine Pub Date : 2025-02-25 eCollection Date: 2025-01-01 DOI:10.1177/20503121251321659
Atsushi Nakajima, Minami Umeyama, Masaaki Higashikawa, Yusuke Shimada, Yuki Arai
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Abstract

Objective: An interim analysis of postmarketing surveillance reported the safety and efficacy of elobixibat, a laxative medication that inhibits the ileal bile acid transporter, at 4 weeks in approximately 1000 patients with chronic constipation in Japan. However, its long-term safety and efficacy in elderly patients remain unclear. This study aimed to conclude and report the final analysis of postmarketing surveillance, including 52-week safety and efficacy profiles in a clinical practice setting, using approximately 3000 patients.

Methods: The overall survey period spanned from June 2018 to May 2022. Observation periods were set at 4 weeks (4-week treatment period) and 52 weeks (52-week treatment period). Adverse drug reactions and efficacy outcomes, including defecation frequency, Bristol Stool Form Scale scores, and patient satisfaction, were analyzed.

Results: The 4-week safety analysis set included 3638 patients with a mean age of 70.8 years, and 73.7% were aged ⩾65 years. Most patients (62.5%) were treated with elobixibat alone, while the rest received concomitant laxatives. In total, 231 patients (6.35%) experienced adverse drug reactions, with gastrointestinal disorders (6.02%) such as diarrhea (3.35%) and abdominal pain (2.06%), being the most common adverse drug reaction. The adverse drug reaction incidence in elderly patients aged ⩾65, ⩾75, and ⩾85 years was 5.49%, 4.85%, and 2.80%, respectively. In the 52-week treatment period, adverse drug reaction incidence was 5.40% (71/1315 patients), similar to that in the 4-week treatment period. Regarding efficacy, defecation frequency and Bristol Stool Form Scale scores significantly improved from week 2 onward, regardless of the age group and administration timing (before breakfast, lunch, or dinner). Most patients reported satisfaction from week 2 onward (6.0%, 66.9%, 78.6%, and 90.4% at baseline, weeks 2, 4, and 52, respectively).

Conclusion: This study confirmed the long-term safety and efficacy of elobixibat in patients with chronic constipation, including many elderly ones, in routine clinical practice.

在日本对慢性便秘患者进行的一项多中心上市后监测:最终分析报告。
目的:一项上市后监测的中期分析报告了elobixbat的安全性和有效性,elobixbat是一种抑制回肠胆汁酸转运体的泻药,在日本约1000名慢性便秘患者4周后使用。然而,其在老年患者中的长期安全性和有效性尚不清楚。该研究旨在总结和报告上市后监测的最终分析,包括在临床实践环境中使用约3000例患者的52周安全性和有效性概况。方法:整体调查时间为2018年6月至2022年5月。观察期分别为4周(治疗期4周)和52周(治疗期52周)。分析药物不良反应和疗效结果,包括排便次数、布里斯托大便量表评分和患者满意度。结果:4周的安全性分析集包括3638名患者,平均年龄为70.8岁,73.7%的患者年龄大于或等于65岁。大多数患者(62.5%)单独使用依洛比西他治疗,其余患者同时使用泻药。共有231例(6.35%)患者发生药物不良反应,其中腹泻(3.35%)、腹痛(2.06%)等胃肠道紊乱(6.02%)是最常见的药物不良反应。年龄大于或等于65岁、大于或等于75岁和大于或等于85岁的老年患者的药物不良反应发生率分别为5.49%、4.85%和2.80%。52周治疗期间,药物不良反应发生率为5.40%(71/1315例),与4周治疗期间相似。关于疗效,排便频率和布里斯托大便形式量表评分从第2周起显著改善,无论年龄组和给药时间(早餐,午餐或晚餐前)。大多数患者从第2周开始报告满意度(基线、第2周、第4周和第52周分别为6.0%、66.9%、78.6%和90.4%)。结论:本研究在常规临床实践中证实了依洛比昔巴特治疗慢性便秘患者,包括许多老年便秘患者的长期安全性和有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
SAGE Open Medicine
SAGE Open Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
3.50
自引率
4.30%
发文量
289
审稿时长
12 weeks
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