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首页> 外文期刊>Gastrointestinal Endoscopy >Electroacupuncture-reduced sedative and analgesic requirements for diagnostic EUS: a prospective, randomized, double-blinded, sham-controlled study
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Electroacupuncture-reduced sedative and analgesic requirements for diagnostic EUS: a prospective, randomized, double-blinded, sham-controlled study

机译：诊断EUS的电针降低镇静和镇痛要求：前瞻性，随机，双盲，假手术研究

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摘要

Background and Aims The role of electroacupuncture (EA) in reducing sedative and analgesic requirements during EUS is uncertain. The aim of this study was to investigate the efficacy of EA in reducing procedure-related pain and discomfort during EUS. Methods This was a double-blinded randomized controlled study conducted between March 2014 and July 2016. Consecutive patients who were scheduled for diagnostic EUS were recruited and randomized to receive EA or sham-electroacupuncture (SA). The primary outcome was the dosage of propofol used. Other outcome measurements included pain scores, anxiety scores, satisfaction scores, patients’ willingness to repeat the procedure, total procedure time, and adverse events. Results A total of 128 patients were recruited to the study. The patients who received EA had significantly fewer requirements for patient-controlled sedation and analgesia (PCA). The median (interquartile range) number of demands for PCA (2 [1-5] vs 16.5 [8.5-33.8]; P ? P ? P ? P ? P ? P ? P ? P ? P ?= .009, respectively). Conclusions In conclusion, the use of EA reduced sedative and analgesia demands, improved patient experience, and was associated with a low risk of adverse events during diagnostic EUS. (Clinical trial registration number: NCT02066194 .) Graphical abstract Display Omitted
机译：背景和旨在在EUS期间降低镇压和镇痛要求的电灭绝（EA）的作用是不确定的。本研究的目的是探讨EA在减少eus期间与过程相关的疼痛和不适的疗效。方法这是2014年3月至2016年7月至2016年7月之间进行的一项双盲随机对照研究。招募并随机招募并随机预定诊断EUS的患者接受EA或假电针（SA）。主要结果是使用异丙酚的剂量。其他结果测量包括疼痛评分，焦虑分数，满意度评分，患者重复程序的意愿，总程序时间和不良事件。结果共有128名患者招募到该研究。收到EA的患者对患者控制的镇静和镇痛（PCA）的要求显着较少。中位数（四分位数范围）PCA的需求数量（2 [1-5] Vs 16.5 [8.5-33.8]; p？p？p≤p≤p≤p≤p≤p≤p≤x.009） 。结论总之，EA减少镇静剂和镇痛需求，改善患者体验，并与诊断EUS期间不良事件的风险有关。 （临床试验登记号码：NCT02066194。）省略图形抽象显示

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  • 来源
    《Gastrointestinal Endoscopy》 |2018年第2期|共10页
  • 作者

    Anthony Yuen Bun Teoh; Charing Ching Ning Chong; Wing Wa Leung; Simon Kin Cheong Chan; Yee Kit Tse; Enders Kwok Wai Ng; Paul Bo San Lai; Justin Che Yuen Wu; James Yun Wong Lau;

  • 作者单位

    Department of Surgery Prince of Wales Hospital The Chinese University of Hong Kong;

    Department of Surgery Prince of Wales Hospital The Chinese University of Hong Kong;

    Department of Surgery Prince of Wales Hospital The Chinese University of Hong Kong;

    Department of Anaesthesia and Intensive Care Prince of Wales Hospital The Chinese University of;

    Institute of Digestive Disease Prince of Wales Hospital The Chinese University of Hong Kong;

    Department of Surgery Prince of Wales Hospital The Chinese University of Hong Kong;

    Department of Surgery Prince of Wales Hospital The Chinese University of Hong Kong;

    Institute of Digestive Disease Prince of Wales Hospital The Chinese University of Hong Kong;

    Department of Surgery Prince of Wales Hospital The Chinese University of Hong Kong;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 消化系及腹部疾病;
  • 关键词

  • 入库时间 2022-08-20 03:04:13

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