Jaakola M L
Department of Anesthesiology, Turku University Hospital, Finland.
J Clin Anesth. 1994 May-Jun;6(3):204-11. doi: 10.1016/0952-8180(94)90060-4.
To assess the efficacy and safety of intravenous (i.v.) dexmedetomidine, an alpha-2 agonist, as a premedication before i.v. regional anesthesia.
Randomized, double-blind, placebo-controlled study with two parallel groups.
Day-case surgery unit, Department of Surgery, Turku University Hospital, Turku, Finland.
30 healthy ASA physical status I outpatients scheduled for minor hand surgery with i.v. regional anesthesia.
Patients were assigned to one of two groups to receive either dexmedetomidine 1 microgram/kg i.v. (n = 15) or saline placebo i.v. (n = 15) 10 minutes before exsanguination and inflation of a tourniquet. Regional blockade was induced with 0.5% lidocaine 3 mg/kg (maximum 200 mg). Additional fentanyl 1 microgram/kg intraoperatively and oxycodone 0.05 mg/kg postoperatively were administered for analgesia if needed.
Dexmedetomidine preoperatively induced 16% to 20% decreases in systolic blood pressure (p < 0.001), diastolic blood pressure (p < 0.001), and heart rate (p < 0.001), which were mainly abolished within the 4-hour postoperative follow-up period. A clinically significant decrease in arterial oxygen saturation was not observed. The subjective intensity of pain during tourniquet inflation was similar in both groups, but fewer intraoperative (p = 0.009) opioid analgesics were needed in the dexmedetomidine group. Dexmedetomidine decreased sympathoadrenal responses: plasma norepinephrine concentration decreased to one-fourth of the baseline level (p < 0.001), and one of its main metabolites, 3,4-dihydroxyphenylglycol, decreased by 27% (p < 0.001). Dexmedetomidine also prevented an increase in plasma epinephrine concentration following tourniquet inflation (p = 0.003). Dexmedetomidine induced subjective sedation (p = 0.002), but the Maddox Wing test did not show any statistically significant differences between the groups. General effectiveness was graded superior in the dexmedetomidine group (p < 0.001).
Dexmedetomidine is an effective premedication before i.v. regional anesthesia because it reduces patient anxiety, sympathoadrenal responses, and opioid analgesic requirements.
评估α-2激动剂静脉注射右美托咪定作为静脉区域麻醉前用药的有效性和安全性。
随机、双盲、安慰剂对照研究,分为两个平行组。
芬兰图尔库图尔库大学医院外科日间手术病房。
30例美国麻醉医师协会(ASA)身体状况I级的健康门诊患者,计划接受静脉区域麻醉下的手部小手术。
患者被分为两组,在驱血和扎止血带前10分钟,一组静脉注射右美托咪定1微克/千克(n = 15),另一组静脉注射生理盐水安慰剂(n = 15)。用0.5%利多卡因3毫克/千克(最大200毫克)诱导区域阻滞。术中根据需要追加芬太尼1微克/千克,术后追加羟考酮0.05毫克/千克用于镇痛。
术前右美托咪定使收缩压(p < 0.001)、舒张压(p < 0.001)和心率(p < 0.001)下降了16%至20%,这些下降在术后4小时随访期内基本消失。未观察到动脉血氧饱和度有临床意义上的下降。两组在止血带充气期间的主观疼痛强度相似,但右美托咪定组术中所需的阿片类镇痛药较少(p = 0.009)。右美托咪定降低了交感肾上腺反应:血浆去甲肾上腺素浓度降至基线水平的四分之一(p < 0.001),其主要代谢产物之一3,4-二羟基苯乙二醇下降了27%(p < 0.001)。右美托咪定还可防止止血带充气后血浆肾上腺素浓度升高(p = 0.003)。右美托咪定引起主观镇静(p = 0.002),但两组间马多克斯翼试验未显示出任何统计学上的显著差异。右美托咪定组的总体有效性评分更高(p < 0.001)。
右美托咪定是一种有效的静脉区域麻醉前用药,因为它可减轻患者焦虑、交感肾上腺反应并减少阿片类镇痛药的需求。