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更安全的镇静实践可能无法转化为内镜治疗结果的改善。

Safer sedation practice may not translate into improvements in endoscopic outcomes.

机构信息

Department of Gastroenterology, Digestive Diseases Centre, University Hospital Aintree, Liverpool, UK.

出版信息

Eur J Gastroenterol Hepatol. 2009 May;21(5):534-43. doi: 10.1097/MEG.0b013e32831bed96.

Abstract

INTRODUCTION

Although the literature surrounding sedation practice and endoscopic outcomes remains sparse and controversial, there have been a number of stringent guidelines issued regarding sedation use in endoscopy.

AIMS

To assess the impact of changes to enhance safer sedation practice on endoscopic outcomes.

METHODS

Sedation practice was audited in 7234 consecutive gastrointestinal endoscopic procedures in 2004 and protocols for enhancing safer sedation practice were introduced. These included; introduction of a unit sedation policy, exchange of midazolam 10 mg vials to 5 mg repacked syringes, adverse events recording of midazolam use of greater than 5 mg and reversal agents, more stringent patient monitoring procedures and endoscopists education and feedback. A reaudit of 7071 procedures was performed in 2006. Outcomes audited the included midazolam doses, patient intolerance, 30-day postprocedure mortality, reversal agent use and total adverse events.

RESULTS

Sedation doses were reduced substantially after intervention [mean midazolam dose (SD): 4.9 mg (2.5) in 2004 vs. 2.9 mg (1.2) in 2006; P<0.0001] with no endoscopist using a mean greater than 5 mg in 2006 compared with 19% in 2004 (P=0.005). The use of reversal agents (0.6 vs. 0.7% for 2004 and 2006, respectively; P=0.74), mortality (1.0 vs. 1.3%; P=0.23) and the adverse events (1.7 vs. 2%; P=0.44) were similar. Unsuccessful procedures because of patient intolerance increased from 0.1 to 1.9% (P<0.0001).

CONCLUSION

Although protocols to enhance safer sedation practice substantially reduced sedation doses used; this did not, however, translate into improved endoscopic outcomes. Moreover, incomplete procedures because of poor tolerance increased.

摘要

简介

尽管有关镇静实践和内镜结果的文献仍然很少且存在争议,但已经发布了许多关于内镜镇静使用的严格指南。

目的

评估增强更安全镇静实践对内镜结果的影响。

方法

2004 年对 7234 例连续胃肠道内镜检查中的镇静实践进行了审核,并引入了增强更安全镇静实践的方案。这些方案包括:引入单位镇静政策、将咪达唑仑 10mg 小瓶更换为 5mg 重新包装的注射器、记录咪达唑仑使用量超过 5mg 和逆转剂的不良事件、更严格的患者监测程序以及内镜医师的教育和反馈。2006 年对 7071 例进行了重新审核。审核的结果包括咪达唑仑剂量、患者不耐受、30 天术后死亡率、逆转剂使用和总不良事件。

结果

干预后镇静剂量显著降低[2004 年平均咪达唑仑剂量(SD):4.9mg(2.5),2006 年 2.9mg(1.2);P<0.0001],2006 年没有内镜医师使用平均大于 5mg 的剂量,而 2004 年为 19%(P=0.005)。逆转剂的使用(2004 年和 2006 年分别为 0.6%和 0.7%;P=0.74)、死亡率(1.0%和 1.3%;P=0.23)和不良事件(1.7%和 2%;P=0.44)相似。由于患者不耐受而导致的手术不成功从 0.1%增加到 1.9%(P<0.0001)。

结论

尽管增强更安全镇静实践的方案大大降低了使用的镇静剂量;但这并没有转化为内镜结果的改善。此外,由于耐受性差导致的不完整手术增加。

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