Kelsaka Ebru, Karakaya Deniz, Sarihasan Binnur, Baris Sibel
Department of Anesthesiology, Faculty of Medicine, Ondokuz Mayis University, Samsun 55139, Turkey.
J Clin Anesth. 2006 Mar;18(2):83-6. doi: 10.1016/j.jclinane.2005.05.004.
The aim of the study was to compare the effect of pretreatment with remifentanil 1 microg/kg and the effect of gender on the incidence of myoclonus after anesthesia induction with etomidate.
This was a randomized, double-blind study.
The study was conducted at a university hospital.
Sixty patients were pretreated in a randomized double-blinded fashion with remifentanil 1 microg/kg or placebo. Two minutes after remifentanil or placebo injection, etomidate 0.3 mg/kg was given.
Myoclonus was recorded with a scale of 0 to 3. The grade of sedation (none, mild, moderate, severe), nausea, pruritus, and apnea were recorded after injection of both drugs.
The incidence of myoclonus was significantly lower in the remifentanil group (6.7%) than in the placebo group (70%) (P < 0.001). None of the patients experienced sedation, apnea, nausea, or pruritus after injection of both drugs. In the placebo group, male patients were associated with significantly increased incidence of myoclonus after etomidate administration.
Pretreatment with remifentanil 1 microg/kg reduced myoclonus after etomidate induction without side effects such as sedation, apnea, nausea, or pruritus. Men experience increased incidence of myoclonus than women after etomidate administration.
本研究旨在比较1微克/千克瑞芬太尼预处理的效果以及性别对依托咪酯麻醉诱导后肌阵挛发生率的影响。
这是一项随机、双盲研究。
研究在一家大学医院进行。
60例患者以随机双盲方式接受1微克/千克瑞芬太尼或安慰剂预处理。注射瑞芬太尼或安慰剂两分钟后,给予0.3毫克/千克依托咪酯。
肌阵挛采用0至3级评分记录。注射两种药物后记录镇静程度(无、轻度、中度、重度)、恶心、瘙痒和呼吸暂停情况。
瑞芬太尼组肌阵挛发生率(6.7%)显著低于安慰剂组(70%)(P<0.001)。注射两种药物后,所有患者均未出现镇静、呼吸暂停、恶心或瘙痒。在安慰剂组中,男性患者依托咪酯给药后肌阵挛发生率显著增加。
1微克/千克瑞芬太尼预处理可降低依托咪酯诱导后的肌阵挛,且无镇静、呼吸暂停、恶心或瘙痒等副作用。依托咪酯给药后,男性肌阵挛发生率高于女性。