Morise Takashi, Fukuzawa Masakatsu, Sugimoto Mitsushige, Nagata Naoyoshi, Kono Shin, Yamauchi Yoshiya, Sugimoto Akihiko, Uchida Kumiko, Koyama Yohei, Madarame Akira, Yamaguchi Hayato, Matsumoto Taisuke, Kagawa Yasuyuki, Kawai Takashi, Itoi Takao
Department of Gastroenterology and Hepatology, Tokyo Medical University Hospital, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo 160-0023, Japan.
Endoscopy Center, Tokyo Medical University Hospital, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo 160-0023, Japan.
J Clin Biochem Nutr. 2023 Jul;73(1):91-96. doi: 10.3164/jcbn.22-24. Epub 2023 May 16.
The prevalence of chronic constipation in Japan is increasing, and is presently almost 1 in 5 people. Because constipation is common, especially in older patients, to avoid adverse events and polypharmacy, simple treatments at low doses are generally desired. Although the chloride channel activator lubiprostone is candidate drug that may solve these problems, factors associated with the long-term efficacy of lubiprostone monotherapy for chronic constipation in treatment-naive patients remain unclear. We here retrospectively investigated the clinical characteristics and factors of patients who achieved long-term constipation improvement with lubiprostone monotherapy. Seventy-four patients with chronic constipation treated with lubiprostone monotherapy (24 or 48 μg/day) from January 2017 to August 2018 were reviewed. Patient characteristics and clinical time-courses were compared between those who sustained improvement for 6 months, and those who became refractory to treatment. In 54 patients (76.1%), constipation improved by lubiprostone administration for 6 months. On multivariate analysis, a significant clinical factor associated with sustained improvement was a starting lubiprostone dose of 24 μg/day (odds ratio: 5.791; 95% confidence interval: 1.032-32.498; = 0.046). A starting lubiprostone dose of 24 μg/day has efficacy to improve chronic constipation and to prevent adverse events of nausea and diarrhea in Japanese patients.
日本慢性便秘的患病率正在上升,目前几乎每5人中就有1人患病。由于便秘很常见,尤其是在老年患者中,为避免不良事件和多重用药,通常希望采用低剂量的简单治疗方法。尽管氯离子通道激活剂鲁比前列酮是一种可能解决这些问题的候选药物,但鲁比前列酮单药治疗初治慢性便秘患者的长期疗效相关因素仍不清楚。我们在此回顾性研究了接受鲁比前列酮单药治疗并实现长期便秘改善的患者的临床特征和相关因素。回顾了2017年1月至2018年8月期间接受鲁比前列酮单药治疗(24或48μg/天)的74例慢性便秘患者。比较了持续改善6个月的患者和治疗无效的患者的患者特征和临床病程。54例患者(76.1%)通过服用鲁比前列酮6个月后便秘得到改善。多因素分析显示,与持续改善相关的一个显著临床因素是鲁比前列酮起始剂量为24μg/天(比值比:5.791;95%置信区间:1.032 - 32.498;P = 0.046)。对于日本患者,鲁比前列酮起始剂量为24μg/天具有改善慢性便秘以及预防恶心和腹泻等不良事件的疗效。