与 lubiprostone 治疗慢性便秘的长期疗效相关的因素
Takashi Morise1, Masakatsu Fukuzawa1, Mitsushige Sugimoto2
1Department of Gastroenterology and Hepatology, Tokyo Medical University Hospital, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo 160-0023, Japan.
Journal of clinical biochemistry and nutrition
|August 3, 2023
概括
起始剂量为24μg/天的 lubiprostone 有效地治疗日本患者的慢性便秘. 这种低剂量改善了长期的疗效,并减少了恶心和腹等不良事件.
科学领域:
- 胃肠病学 胃肠病学
- 药理学 药理学是指药理学的学科.
背景情况:
- 在日本,慢性便秘的患病率正在上升,影响近20%的人口.
- 老年患者通常需要简单的低剂量治疗,以尽量减少不良事件和多药.
研究的目的:
- 在未经治疗的慢性便秘患者中研究与 lubiprostone 单一治疗的长期疗效相关的因素.
- 为了确定预测 lubiprostone 持续改善的临床特征.
主要方法:
- 74名慢性便秘患者的回顾性评估,这些患者接受了 lubiprostone (24或48μg/天) 治疗.
- 患者特征和持续改善 (≥6个月) 和耐火患者之间的临床结果的比较.
- 多变量分析以确定持续改善的重要预测因素.
主要成果:
- 在6个月的时间里,lubiprostone在76.1%的患者中改善了便秘.
- 每天24μg的起始剂量与持续改善显著相关 (OR:5.791,p=0.046).
- 24微克/天剂量在改善慢性便秘和预防恶心和腹方面表现出有效性.
结论:
- 在日本患者的长期慢性便秘管理中,24μg/天的起始剂量是有效的.
- 较低的lubiprostone初始剂量可以提高治疗坚持性,减少副作用.
- 进一步的研究应该探索在不同患者群体中对 lubiprostone 的最佳剂量策略.
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