Department of Anaesthesiology and Reanimation, Faculty of Medicine, Gazi University, Ankara, Turkey.
Clinics (Sao Paulo). 2011;66(5):811-5. doi: 10.1590/s1807-59322011000500017.
To evaluate the effects of three different target-controlled remifentanil infusion rates during target-controlled propofol infusion on hemodynamic parameters, pain, sedation, and recovery score during oocyte retrieval.
Sixty-nine women were scheduled for oocyte retrieval. Target-controlled propofol infusion at an effect-site concentration of 1.5 μg/mL was instituted. The patients were randomly allocated to receive remifentanil at an effect-site concentration of either 1.5 (group I, n = 23), 2 (group II, n = 23) or 2.5 ng/mL (group III, n = 23). Hemodynamic variables, sedation, pain, the Aldrete recovery score, and side effects were recorded.
Hemodynamic variables, sedation and pain scores and the number of patients with the maximum Aldrete recovery score 10 min after the procedure were comparable among the groups. The number of patients in group III with the maximum Aldrete recovery score 5 min after the procedure was significantly lower than that in groups I and II. One patient in group II and one patient in group III suffered from nausea.
Similar pain-free conscious sedation conditions without significant changes in hemodynamic parameters were provided by all three protocols. However, target controlled infusion of remifentanil at 1.5 or 2 ng/mL proved superior at providing early recovery compared to 2.5 ng/mL.
评估在目标控制丙泊酚输注期间给予三种不同靶控瑞芬太尼输注率对取卵过程中血流动力学参数、疼痛、镇静和恢复评分的影响。
69 名妇女拟行取卵术。给予效应室浓度为 1.5μg/ml 的目标控制丙泊酚输注。患者随机分为三组,分别接受效应室浓度为 1.5(I 组,n=23)、2(II 组,n=23)或 2.5ng/ml(III 组,n=23)的瑞芬太尼。记录血流动力学变量、镇静、疼痛、Aldrete 恢复评分和不良反应。
三组间血流动力学变量、镇静和疼痛评分以及术后 10min 达到最大 Aldrete 恢复评分 10 的患者数无差异。术后 5min 时,III 组达到最大 Aldrete 恢复评分 10 的患者数明显低于 I 组和 II 组。II 组和 III 组各有 1 例患者出现恶心。
所有三种方案均能提供无痛清醒镇静条件,且血流动力学参数无明显变化。然而,与 2.5ng/ml 相比,1.5 或 2ng/ml 的瑞芬太尼靶控输注能更早地恢复。