Khan Khurram J, Fergani Houssein, Ganguli Subhas C, Jalali Subash, Spaziani Robert, Tsoi Keith, Morgan David G
Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
J Can Assoc Gastroenterol. 2019 May;2(2):86-90. doi: 10.1093/jcag/gwy041. Epub 2018 Aug 9.
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.
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.
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 (=0.003). Both endoscopist and nurse independently rated sedation to be better in the fentanyl group (=0001). The patient did not perceive any difference in sedation (=0.4). Procedure time was significantly shorter in the Fentanyl group (8.5 versus 11.1 minutes, =0.001), with no difference in the discharge time. There was significantly less retching observed in patients in the fentanyl group (<0.001). There were no major complications.
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.
在一项双盲、随机、安慰剂对照试验中,比较在咪达唑仑中添加芬太尼的效果,并确定芬太尼是否能增强镇静作用、增加不良事件或影响操作时间或出院时间。
计划进行门诊上消化道内镜检查的18至65岁患者符合本研究条件。患者通过双盲方案随机接受100 mcg/2 mL芬太尼或2 mL安慰剂静脉注射。所有患者最初均接受2 mg静脉注射咪达唑仑。可给予额外的咪达唑仑以达到充分镇静。
68例患者被随机分配至芬太尼组,69例患者被分配至安慰剂组。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)。内镜医师和护士均独立评定芬太尼组的镇静效果更好(P=0.001)。患者并未感觉到镇静方面有任何差异(P=0.4)。芬太尼组的操作时间显著更短(8.5分钟对11.1分钟,P=0.001),出院时间无差异。芬太尼组患者的干呕明显更少(P<0.001)。无重大并发症。
内镜医师和护士发现添加芬太尼可显著改善镇静效果,缩短操作时间,且每例患者使用的咪达唑仑更少。它不影响患者的镇静体验且安全。在常规门诊上消化道内镜检查中使用芬太尼应被视为改善操作镇静的一种安全选择。临床试验编号:NCT:01514695(www.clinicaltrials.gov)被接受作为2014年2月加拿大消化系统疾病周会议的摘要。