Yadav Monu, Durga Padmaja, Gopinath R
Department of Anesthesiology and Critical Care, Nizam's Institute of Medical Sciences, Hyderabad, India.
J Anaesthesiol Clin Pharmacol. 2011 Oct;27(4):470-4. doi: 10.4103/0970-9185.86582.
Pain following intravenous injection of propofol continues to be an intriguing problem. None of the commonly used methods completely attenuate the pain. Inflammatory response to propofol contributes to the pain. Role of hydrocortisone in attenuating pain has not been evaluated. This study was conducted to compare the efficacy of lignocaine and hydrocortisone in attenuation of pain following intravenous injection of propofol.
A prospective randomized double-blind, placebo-controlled study was conducted on 72 adult patients belonging to American Society of Anesthesiologists (ASA) physical status I or II, scheduled to undergo elective surgery. They were randomly assigned to four groups of 18 each. Group NS, group LG, group HC10, and group HC25. The groups received 2 ml normal saline, 2 ml 2% lignocaine, 10 mg/2 ml hydrocortisone, and 25 mg/2 ml hydrocortisone, respectively, as pretreatment. Propofol was injected 30 sec later. A blinded researcher assessed the patient's pain level using a four point verbal rating scale.
The four groups were comparable in respect to patient's characteristics. There was no significant difference of hemodynamics changes during propofol induction between all the groups. There was no statistically significant difference in the incidence of pain between patients who received hydrocortisone and the placebo group. The incidence of pain was significantly less in group LG than other three groups.
Use of intravenous low dose hydrocortisone pretreatment of the vein does not attenuate pain following propofol injection.
静脉注射丙泊酚后出现的疼痛仍是一个引人关注的问题。目前常用的方法均无法完全减轻这种疼痛。丙泊酚引发的炎症反应会导致疼痛。氢化可的松在减轻疼痛方面的作用尚未得到评估。本研究旨在比较利多卡因和氢化可的松在减轻静脉注射丙泊酚后疼痛方面的疗效。
对72例美国麻醉医师协会(ASA)身体状况为I或II级、计划接受择期手术的成年患者进行了一项前瞻性随机双盲、安慰剂对照研究。他们被随机分为四组,每组18人。分别为生理盐水组(NS组)、利多卡因组(LG组)、10mg/2ml氢化可的松组(HC10组)和25mg/2ml氢化可的松组(HC25组)。各组分别接受2ml生理盐水、2ml 2%利多卡因、10mg/2ml氢化可的松和25mg/2ml氢化可的松作为预处理。30秒后注射丙泊酚。一名不知情的研究人员使用四点语言评定量表评估患者的疼痛程度。
四组患者在特征方面具有可比性。所有组在丙泊酚诱导期间的血流动力学变化无显著差异。接受氢化可的松治疗的患者与安慰剂组之间的疼痛发生率无统计学显著差异。LG组的疼痛发生率明显低于其他三组。
静脉注射低剂量氢化可的松预处理静脉并不能减轻丙泊酚注射后的疼痛。