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术中及术后极低剂量静脉注射氯胺酮输注并不能增加术前使用阿片类镇痛药患者大脊柱手术后的疼痛缓解。

Intra- and postoperative very low dose intravenous ketamine infusion does not increase pain relief after major spine surgery in patients with preoperative narcotic analgesic intake.

机构信息

Beth Israel Deaconess Medical Center, Boston, MA, USA.

出版信息

Pain Med. 2011 Aug;12(8):1276-83. doi: 10.1111/j.1526-4637.2011.01144.x. Epub 2011 Jun 13.

Abstract

OBJECTIVE

This study aims to demonstrate the analgesic efficacy and opioid-sparing effect of low dose ketamine in patients with preoperative narcotic intake undergoing major spine surgery.

DESIGN

The study used a prospective, randomized, double-blinded, and placebo-controlled clinical trial.

SETTINGS AND PATIENTS

We evaluated the analgesic efficacy and safety of low dose IV ketamine infusion after major spine surgery in patients with preoperative narcotic analgesic intake. Ketamine group received IV ketamine infusion (2 µg/kg/min) and saline group received saline intraoperatively and the first 24 hours postoperatively. In addition, all patients received IV patient-controlled hydromorphone and epidural bupivacaine.

OUTCOME MEASURES

Pain scores, narcotic requirement, and side effects were compared between the groups for 48 hours postoperatively.

RESULTS

Thirty patients completed the study (N = 15 in each group). No difference in pain scores at rest and movement was noted between the groups (P > 0.05). Patients in ketamine group received 40.42 ± 32.86 mg IV hydromorphone at 48 hours compared with 38.24 ± 26.19 mg in saline group (P = 0.84). Central nervous system side effects were observed in five (33%) ketamine group patients compared with nine (60%) in saline group (P = 0.29).

CONCLUSION

The addition of IV very low dose ketamine infusion regimen did not improve postoperative analgesia. Side effects were not increased with low dose ketamine.

摘要

目的

本研究旨在证明术前使用阿片类药物的患者在接受大脊柱手术后使用小剂量氯胺酮的镇痛效果和阿片类药物节省效应。

设计

本研究采用前瞻性、随机、双盲、安慰剂对照临床试验。

设置和患者

我们评估了术前使用阿片类药物镇痛的大脊柱手术后患者接受小剂量 IV 氯胺酮输注的镇痛效果和安全性。氯胺酮组接受 IV 氯胺酮输注(2 µg/kg/min),生理盐水组在术中及术后前 24 小时内接受生理盐水。此外,所有患者均接受 IV 患者自控氢吗啡酮和硬膜外布比卡因。

观察指标

术后 48 小时比较两组的疼痛评分、阿片类药物需求和不良反应。

结果

30 例患者完成了研究(每组 15 例)。两组患者静息和活动时的疼痛评分无差异(P>0.05)。氯胺酮组患者在 48 小时内接受 40.42±32.86mg IV 氢吗啡酮,而生理盐水组为 38.24±26.19mg(P=0.84)。氯胺酮组有 5 例(33%)患者出现中枢神经系统不良反应,生理盐水组有 9 例(60%)(P=0.29)。

结论

添加 IV 极低剂量氯胺酮输注方案并未改善术后镇痛效果。小剂量氯胺酮不会增加副作用。

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