Nakajima Atsushi, Fujimaki Mio, Arai Yuki, Emori Kento
Department of Gastroenterology and Hepatology, Yokohama City University School of Medicine, Yokohama, Japan.
Medical Department, EA Pharma Co, Ltd, Tokyo, Japan.
J Neurogastroenterol Motil. 2022 Jul 30;28(3):431-441. doi: 10.5056/jnm20263.
BACKGROUND/AIMS: Elobixibat, an ileal bile acid transporter (apical sodium-dependent bile acid transporter) inhibitor, was recently launched in Japan for the treatment of chronic idiopathic constipation. We conducted an interim analysis of post-marketing surveillance to evaluate the safety and efficacy of elobixibat in elderly patients with chronic constipation and compared the efficacy according to administration time.
Safety and efficacy outcomes were evaluated through patient interviews for 4 weeks.
Adverse drug reactions (ADRs) were observed in 5.24% of the 1049 patients analyzed; diarrhea (2.19%) and abdominal pain (1.81%) were the most common. A serious ADR of death was reported in one patient (0.10%). The incidence of ADRs in the ≥ 65-year old or ≥ 75-year-old subpopulation was similar to that in the total patient population. Mean bowel movements per week significantly increased from 2.9 ± 2.5 at baseline to 5.0 ± 3.1 ( < 0.001) at Week 2 and 5.3 ± 2.6 ( < 0.001) at Week 4. The mean Bristol Stool Form Scale score significantly increased from 2.3 ± 1.4 at baseline to 3.8 ± 1.3 ( < 0.001) at Week 2 and 3.9 ± 1.1 at Week 4 ( < 0.001). Bowel movements significantly increased in the elderly population and subpopulations receiving elobixibat before breakfast, lunch, or dinner. The median time to bowel movement was 5 hours.
The results suggested that elobixibat was well-tolerated and efficacious in elderly patients with chronic constipation and can be administered before any meals.
背景/目的:依洛比昔巴特是一种回肠胆汁酸转运体(顶端钠依赖性胆汁酸转运体)抑制剂,最近在日本获批用于治疗慢性特发性便秘。我们进行了一项上市后监测的中期分析,以评估依洛比昔巴特在老年慢性便秘患者中的安全性和有效性,并比较不同给药时间的疗效。
通过对患者进行4周的访谈来评估安全性和有效性结果。
在分析的1049例患者中,5.24%出现药物不良反应(ADR);腹泻(2.19%)和腹痛(1.81%)最为常见。有1例患者(0.10%)报告了严重的ADR死亡。≥65岁或≥75岁亚组的ADR发生率与总体患者人群相似。每周平均排便次数从基线时的2.9±2.5显著增加到第2周时的5.0±3.1(<0.001)和第4周时的5.3±2.6(<0.001)。布里斯托大便性状量表平均得分从基线时的2.3±1.4显著增加到第2周时的3.8±1.3(<0.001)和第4周时的3.9±1.1(<0.001)。在早餐、午餐或晚餐前接受依洛比昔巴特治疗的老年人群和亚组中,排便次数显著增加。排便的中位时间为5小时。
结果表明,依洛比昔巴特在老年慢性便秘患者中耐受性良好且有效,可在任何餐前给药。