首页> 外文期刊>Journal of the Canadian Association of Gastroenterology >The Benefit of Fentanyl in Effective Sedation and Quality of Upper Endoscopy: A Double-Blinded Randomized Trial of Fentanyl Added to Midazolam Versus Midazolam Alone for Sedation
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The Benefit of Fentanyl in Effective Sedation and Quality of Upper Endoscopy: A Double-Blinded Randomized Trial of Fentanyl Added to Midazolam Versus Midazolam Alone for Sedation

机译:芬太尼对有效镇静作用和上内镜检查质量的益处:咪达唑仑和咪达唑仑单独镇静的芬太尼双盲随机试验

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Aims Our goals were to compare the effect of adding fentanyl to midazolam in a double-blinded, randomized, placebo-controlled trial and determine if fentanyl enhances sedation, increases adverse events or effects time of the procedure or discharge. Methods Patients 18 to 65 years scheduled for outpatient upper endoscopy were eligible for the study. Patients were randomized to receive either 100 mcg/2 mL of Fentanyl or 2 mL of placebo IV with a double-blinded protocol. All patients received 2 mg of intravenous midazolam initially. Additional midazolam could be given to achieve adequate sedation. Results There were 68 patients randomized to the Fentanyl group and 69 patients to the placebo group. The mean dose of midazolam was 4.0 mg for the Fentanyl group and 5.2 mg for placebo group ( P =0.003). Both endoscopist and nurse independently rated sedation to be better in the fentanyl group ( P =0001). The patient did not perceive any difference in sedation ( P =0.4). Procedure time was significantly shorter in the Fentanyl group (8.5 versus 11.1 minutes, P =0.001), with no difference in the discharge time. There was significantly less retching observed in patients in the fentanyl group ( P 0.001). There were no major complications. Conclusions Endoscopists and nurses found adding fentanyl significantly improved sedation, led to a shorter procedure time, and allowed for less midazolam to be used per case. It did not affect the patient experience of sedation and was safe. Fentanyl use for routine outpatient upper endoscopy should be considered as a safe option to improve procedural sedation. NCT:01514695 ( www.clinicaltrials.gov ) Accepted as an abstract for the Canadian Digestive Diseases Week meeting in February 2014.
机译:目的我们的目标是在一项双盲,随机,安慰剂对照试验中比较将芬太尼添加到咪达唑仑中的效果,并确定芬太尼是否增强镇静作用,增加不良事件或影响手术时间或出院时间。方法对18至65岁的门诊上内镜患者进行了研究。采用双盲方案,患者随机接受100 mcg / 2 mL的芬太尼或2 mL的安慰剂IV。所有患者最初均接受2 mg静脉注射咪达唑仑。可以给予其他咪达唑仑以达到足够的镇静作用。结果随机分为芬太尼组68例和安慰剂组69例。芬太尼组咪达唑仑的平均剂量为4.0 mg,安慰剂组为5.2 mg(P = 0.003)。内镜医生和护士均对芬太尼组的镇静效果进行了独立评估(P = 0001)。患者在镇静方​​面未见任何差异(P = 0.4)。芬太尼组的手术时间明显缩短(8.5比11.1分钟,P = 0.001),放电时间无差异。在芬太尼组中观察到的患者的ret痒明显减少(P <0.001)。没有重大并发症。结论内镜医师和护士发现,加入芬太尼可显着改善镇静作用,缩短手术时间,并减少每例患者的咪达唑仑使用量。它不会影响患者的镇静效果,并且很安全。常规门诊上内镜检查中使用芬太尼应被视为改善手术镇静的安全选择。 NCT:01514695(www.clinicaltrials.gov)被接受为2014年2月的加拿大消化系统疾病周会议的摘要。

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