Ketamine potentiates analgesic effect of morphine in postoperative epidural pain control.

Regional anesthesia Pub Date : 1996-11-01
C S Wong, W J Liaw, C S Tung, Y F Su, S T Ho
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Abstract

Background and objectives: Ketamine is currently the only N-methyl-D-aspartate receptor channel blocker in clinical use. This study evaluated the analgesic efficacy of epidurally coadministered ketamine and morphine in postoperative pain control.

Methods: The patient population consisted of ASA class I and II patients undergoing major joint replacement. Epidural lidocaine was used as the primary anesthesia for the surgery. In phase I of the study, either ketamine (10-30 mg) or morphine (0.5-2 mg) was administered via epidural catheter immediately after surgery. This was done to evaluate the dose-response effect of these drugs when used for postoperative pain relief, and the results were applied to phase II of the study, in which all patients received ketamine pretreatment (total 30 mg) with each dose of lidocaine administered before and during surgery. Forty patients were randomly divided into four groups, each of which received one of three different pain control regimens mixed with 10 ml of saline: group B received 10 mg ketamine, group C 2 mg morphine, and group D 10 mg ketamine plus 0.5 mg morphine while the control group A received 10 mL of saline with no additive. The intensity of pain expressed by patients, as well as the number of intramuscular meperidine (1 mg/kg) injections administered and any side effects that may have occurred, were recorded.

Results: Ketamine produced no significant pain relief. A 2-mg morphine dose did produce significant analgesia but was accompanied by a high incidence of side effects. Co-administration of subanalgesic doses of ketamine, 10 mg and morphine, 0.5 mg, however, also produced a strong analgesic effect.

Conclusions: Ketamine, although not itself an epidural analgesic agent, potentiates the analgesic effect of morphine, especially when administered as a pretreatment. The resulting lowered dosage of epidural morphine needed for postoperative pain relief reduces, in turn, the incidence of side effects. Pretreatment of patients with ketamine epidurally, followed by injections of combined morphine and ketamine could be a promising new analgesic regimen.

氯胺酮增强吗啡在术后硬膜外疼痛控制中的镇痛作用。
背景和目的:氯胺酮是目前临床使用的唯一n -甲基- d -天冬氨酸受体通道阻滞剂。本研究评估硬膜外氯胺酮和吗啡在术后疼痛控制中的镇痛效果。方法:ASA I级和II级患者行大关节置换术。术中以硬膜外利多卡因为主麻。在I期研究中,手术后立即通过硬膜外导管给予氯胺酮(10-30毫克)或吗啡(0.5-2毫克)。这项研究是为了评估这些药物在用于术后疼痛缓解时的剂量反应效应,结果应用于该研究的II期,在该研究中,所有患者在手术前和术中接受氯胺酮预处理(总剂量为30 mg)和每次剂量的利多卡因。40例患者随机分为4组,每组接受3种不同的疼痛控制方案中的一种,每组使用10 ml生理盐水:B组使用10 mg氯胺酮,C组使用2 mg吗啡,D组使用10 mg氯胺酮加0.5 mg吗啡,而对照组A组使用10 ml生理盐水,不添加任何添加剂。记录患者表达的疼痛强度,肌肉注射哌替啶(1mg /kg)的次数以及可能发生的任何副作用。结果:氯胺酮对疼痛无明显缓解作用。2毫克吗啡剂量确实能产生明显的镇痛作用,但伴随有高发生率的副作用。同时给予亚镇痛剂量氯胺酮(10mg)和吗啡(0.5 mg)也能产生很强的镇痛效果。结论:氯胺酮虽然本身不是硬膜外镇痛剂,但可以增强吗啡的镇痛作用,特别是作为预处理时。因此,术后镇痛所需的硬膜外吗啡剂量降低,反过来也减少了副作用的发生。硬膜外氯胺酮预处理后再联合注射吗啡和氯胺酮可能是一种很有前景的新镇痛方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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