西沙必利用于糖尿病患者胃排空:疗效和安全性的荟萃分析。

Yifan Lu, Yixuan Xie, Xinyi Yang, Lijuan Nie, Zhe Cheng, Yixian He, Tiansu Lv, Qibiao Wu, Xiqiao Zhou
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引用次数: 0

摘要

背景:糖尿病性胃轻瘫是糖尿病常见的并发症,以胃排空延迟为特征,严重影响患者的生活质量。目前的治疗方案有限,往往导致不满意的结果。本荟萃分析旨在评价西沙必利对糖尿病胃轻瘫患者的疗效和安全性。方法:系统的文献检索确定了13项研究,涉及185名参与者。提取并分析了胃排空率、症状缓解和安全性的数据。通过胃排空半衰期(T1/2,以分钟计)、120分钟胃排空率(以百分比计)和不良事件来衡量有效性。关键结果:分析显示,与安慰剂相比,西沙必利显著改善胃排空,T1/2的平均差异(MD)为-33.74 (95% CI: -68.84至-2.65,P = 0.03)。此外,120分钟胃排空率提高了-25.84 (95% CI: -16.80 ~ -25.84)。结论和推论:西沙利在改善糖尿病胃轻瘫患者胃排空方面有显著疗效,安全性一般可接受。临床医生应考虑西沙必利作为可行的治疗方案,同时监测患者的任何潜在的副作用。需要进一步的研究来探索长期的安全性和有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cisapride for gastric emptying in diabetic patients: a meta-analysis on its efficacy and safety.

Background: Diabetic gastroparesis is a common complication of diabetes, characterized by delayed gastric emptying, significantly impacting patients' quality of life. Current treatment options are limited often resulting in unsatisfactory outcomes. This meta-analysis aims to evaluate the efficacy and safety of cisapride in diabetic patients suffering from gastroparesis.

Methods: A systematic literature search identified 13 studies involving 185 participants. Data on gastric emptying rates, symptom relief, and safety profiles were extracted and analyzed. Effectiveness was measured through gastric emptying half-life (T1/2, measured in min), 120-min gastric emptying rate (measured as a percentage), and adverse events.

Key results: The analysis revealed that cisapride significantly improved gastric emptying compared to placebo, with a mean difference (MD) of -33.74 for T1/2 (95% CI: -68.84 to -2.65, P = 0.03). Additionally, the 120-min gastric emptying rate improved by -25.84 (95% CI: -16.80 to -25.84, P < 0.001). The occurrence of adverse events was low, with most patients tolerating the treatment well.

Conclusion and inferences: Cisapride demonstrates notable efficacy in improving gastric emptying in diabetic gastroparesis, with a generally acceptable safety profile. Clinicians should consider cisapride as a viable treatment option while monitoring patients for any potential side effects. Further research is warranted to explore long-term safety and effectiveness.

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