Koshy G, Nair S, Norkus E P, Hertan H I, Pitchumoni C S
Division of Gastroenterology, Our Lady of Mercy Medical Center, New York Medical College, Bronx 10466, USA.
Am J Gastroenterol. 2000 Jun;95(6):1476-9. doi: 10.1111/j.1572-0241.2000.02080.x.
Propofol (2,6-diisopropyl phenol) is a relatively new intravenous sedative hypnotic with an ideal pharmacokinetic profile for conscious sedation. In this study, we compared the safety and efficacy of propofol versus the conventional regimen of midazolam and meperidine for conscious sedation in GI endoscopy.
In this prospective study, 274 patients that included many elderly patients with multiple comorbid conditions underwent GI endoscopic procedures at our hospital. A total of 150 patients received propofol (20-120 mg) and fentanyl (0.25-1.5 mg). The control group of 124 patients was given midazolam (2-6 mg) and meperidine (25-75 mg). The dose of medication was titrated according to patient need and the duration of the procedure. A "comfort score" on a scale of 1-4 assessed the efficacy of the drugs based on pain or discomfort to the patient and ease of endoscopy. A "sedation score" was used to assess the degree of sedation on a scale of 1-5. The Aldrete score was used to measure recovery from anesthesia at 5 and 10 min after the procedure.
After controlling for age, American Society of Anesthesiologists' Physical Status Classification (ASA grade), and type and duration of procedure, logistic regression analysis determined that propofol resulted in 2.04 times better patient comfort (p = 0.033, 95% CI = 1.058-3.923). Propofol was 1.84 times more likely to produce deeper sedation than the regimen of midazolam and meperidine (p = 0.027, 95% CI = 1.071-3.083). The recovery from sedation was faster in patients receiving propofol, although this did not reach statistical significance. The safety parameters between the two groups were comparable.
Propofol was associated with a statistically significant improvement in comfort and sedation score when compared to midazolam and meperidine.
丙泊酚(2,6 - 二异丙基苯酚)是一种相对新型的静脉镇静催眠药,具有用于清醒镇静的理想药代动力学特征。在本研究中,我们比较了丙泊酚与咪达唑仑和哌替啶传统方案用于胃肠内镜检查清醒镇静的安全性和有效性。
在这项前瞻性研究中,274例患者(包括许多患有多种合并症的老年患者)在我院接受了胃肠内镜检查。总共150例患者接受了丙泊酚(20 - 120毫克)和芬太尼(0.25 - 1.5毫克)。124例患者的对照组给予咪达唑仑(2 - 6毫克)和哌替啶(25 - 75毫克)。根据患者需求和检查持续时间调整药物剂量。基于患者的疼痛或不适以及内镜检查的难易程度,采用1 - 4分的“舒适度评分”来评估药物疗效。采用1 - 5分的“镇静评分”来评估镇静程度。采用Aldrete评分在检查后5分钟和10分钟测量麻醉恢复情况。
在控制年龄、美国麻醉医师协会身体状况分类(ASA分级)以及检查类型和持续时间后,逻辑回归分析确定丙泊酚使患者舒适度提高2.04倍(p = 0.033,95%可信区间 = 1.058 - 3.923)。丙泊酚产生深度镇静的可能性比咪达唑仑和哌替啶方案高1.84倍(p = 0.027,95%可信区间 = 1.071 - 3.083)。接受丙泊酚的患者镇静恢复更快,尽管这未达到统计学显著性。两组之间的安全参数具有可比性。
与咪达唑仑和哌替啶相比,丙泊酚在舒适度和镇静评分方面有统计学显著改善。