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在急诊科有严重疼痛的患者中,使用低剂量氯胺酮和低剂量氢吗啡酮实现有效镇痛。

Effective analgesia with low-dose ketamine and reduced dose hydromorphone in ED patients with severe pain.

机构信息

Department of Emergency Medicine, Alameda County Medical Center, Highland Hospital, Oakland, CA 94602-1018, USA.

出版信息

Am J Emerg Med. 2013 May;31(5):847-51. doi: 10.1016/j.ajem.2013.02.008. Epub 2013 Apr 18.

Abstract

OBJECTIVE

We assessed the analgesic effect and feasibility of low-dose ketamine combined with a reduced dose of hydromorphone for emergency department (ED) patients with severe pain.

METHODS

This was a prospective observational study of adult patients with severe pain at an urban public hospital. We administered 0.5 mg of intravenous (IV) hydromorphone and 15 mg of IV ketamine, followed by optional 1 mg hydromorphone IV at 15 and 30 minutes. Pain intensity was assessed at 12 intervals over 120 minutes using a 10-point verbal numerical rating scale (NRS). Patients were monitored throughout for adverse events. Dissociative side effects were assessed using the side effects rating scale for dissociative anesthetics.

RESULTS

Of 30 prospectively enrolled patients with severe pain (initial mean NRS, 9), 14 reported complete pain relief (NRS, 0) at 5 minutes; the mean reduction in NRS pain score was 6.0 (SD, 3.2). At 15 minutes, the mean reduction in NRS pain score was 5.0 (SD, 2.8). The summed pain intensity difference and percent summed pain intensity difference scores were 25 (95% confidence interval [CI], 21-30) and 58% (95% CI, 49-68) at 30 minutes and 41 (95% CI, 34-48) and 50% (95% CI, 42-58) at 60 minutes, respectively. Most patients (80%) reported only weak or modest side effects. Ninety percent of patients reported that they would have the medications again. No significant adverse events occurred.

CONCLUSIONS

Low-dose ketamine combined with a reduced dose hydromorphone protocol produced rapid, profound pain relief without significant side effects in a diverse cohort of ED patients with acute pain.

摘要

目的

评估小剂量氯胺酮联合低剂量氢吗啡酮用于急诊科(ED)重度疼痛患者的镇痛效果和可行性。

方法

这是一项在城市公立医院进行的成人重度疼痛患者的前瞻性观察性研究。我们给予 0.5mg 静脉(IV)氢吗啡酮和 15mg IV 氯胺酮,然后在 15 分钟和 30 分钟时可选择给予 1mg IV 氢吗啡酮。在 120 分钟内通过 10 点数字评分量表(NRS)评估 12 个时间点的疼痛强度。整个过程中监测患者的不良反应。使用分离麻醉剂副作用评分量表评估分离副作用。

结果

30 例重度疼痛(初始 NRS 均值为 9)的前瞻性纳入患者中,14 例患者在 5 分钟时报告完全疼痛缓解(NRS 为 0);NRS 疼痛评分平均降低 6.0(SD,3.2)。在 15 分钟时,NRS 疼痛评分平均降低 5.0(SD,2.8)。30 分钟时,总和疼痛强度差和总和疼痛强度差异百分比评分分别为 25(95%置信区间[CI],21-30)和 58%(95% CI,49-68),41(95% CI,34-48)和 50%(95% CI,42-58)在 60 分钟时。大多数患者(80%)仅报告轻微或中度副作用。90%的患者表示他们会再次使用这些药物。没有发生明显的不良事件。

结论

小剂量氯胺酮联合低剂量氢吗啡酮方案在急性疼痛的不同队列 ED 患者中产生了快速、显著的镇痛效果,且无明显副作用。

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