Patil Pavan M, Patil Seema P
Department of Oral and Maxillofacial Surgery, Sharda University, School of Dental Sciences, Greater Noida, Uttar Pradesh, India.
J Oral Maxillofac Surg. 2012 Feb;70(2):257-62. doi: 10.1016/j.joms.2011.07.011. Epub 2011 Sep 21.
To evaluate the safety and efficacy of an admixture of lidocaine with clonidine with regard to the anesthetic abilities, hemodynamic parameters, and postoperative pain control and to compare the results with those obtained with a lidocaine-epinephrine solution.
A total of 50 patients with poorly controlled, moderate hypertension (American Society of Anesthesiologists class II) who presented for uncomplicated upper third molar extraction were included in a double-blind study. The time of onset of action, duration, and intensity of anesthesia and the vasoconstrictor properties were evaluated. The hemodynamic changes (ie, systolic blood pressure, diastolic blood pressure, mean arterial pressure, heart rate, ST-segment depression of 1 mm or greater, and cardiac arrhythmias) were recorded. The presence of postoperative pain and analgesic requirements were also compared. The results were analyzed using an unpaired, type sample equal-variance t test with the Bonferroni correction.
Of the 50 patients with hypertension (American Society of Anesthesiologists class II), 25 received 2 mL of 2% lidocaine with clonidine (15 μg/mL) and 25 received lidocaine with epinephrine (12.5 μg/mL). There were no significant differences between the 2 agents with regard to the time of onset of action, duration or intensity of anesthesia, or the vasoconstrictor properties. The clonidine group showed better hemodynamic parameters compared with the epinephrine group. The clonidine group showed significantly lesser postoperative pain and, therefore, had lesser analgesic consumption.
Clonidine could be a useful and safe alternative to epinephrine for intraoral block anesthesia with lidocaine in patients with hypertension and American Society of Anesthesiologists class II.
评估利多卡因与可乐定混合液在麻醉能力、血流动力学参数及术后疼痛控制方面的安全性和有效性,并将结果与利多卡因 - 肾上腺素溶液的结果进行比较。
共有50例控制不佳的中度高血压患者(美国麻醉医师协会II级)因单纯性上颌第三磨牙拔除前来就诊,纳入一项双盲研究。评估麻醉起效时间、持续时间、强度以及血管收缩特性。记录血流动力学变化(即收缩压、舒张压、平均动脉压、心率、ST段压低1毫米或更大以及心律失常)。还比较了术后疼痛的存在情况和镇痛需求。结果采用未配对、等方差t检验并进行Bonferroni校正进行分析。
在50例高血压患者(美国麻醉医师协会II级)中,25例接受了2毫升含可乐定(15微克/毫升)的2%利多卡因,25例接受了含肾上腺素(12.5微克/毫升)的利多卡因。两种药物在麻醉起效时间、持续时间或强度以及血管收缩特性方面无显著差异。与肾上腺素组相比,可乐定组显示出更好的血流动力学参数。可乐定组术后疼痛明显较轻,因此镇痛药物消耗较少。
对于美国麻醉医师协会II级的高血压患者,可乐定可能是利多卡因口腔阻滞麻醉中肾上腺素的一种有用且安全的替代品。