Department of Anaesthesia and Intensive Care, Robert Debre University Hospital, Paris, France.
Paris Diderot University, France.
Eur J Pain. 2018 Apr;22(4):632-646. doi: 10.1002/ejp.1153. Epub 2017 Nov 26.
Ketamine has been suggested to be efficient in relieving chronic pain. However, there is inconsistency across studies investigating the effect of ketamine for chronic pain management. We aimed to perform a meta-analysis in order to assess the efficacy of this compound during chronic non-cancer pain conditions.
The study consisted in a meta-analysis of clinical trials comparing ketamine to a placebo during chronic non-cancer pain. The primary endpoint of this study was pain relief 4 weeks after the beginning of treatment. Secondary outcomes were: pain relief 1, 2, 8 and 12 weeks after the beginning of treatment and incidence of psychedelic manifestations.
Six studies were included in this meta-analysis. Overall, 99 patients received ketamine and 96 received placebo. Ketamine did not decrease pain intensity at 4 weeks (MD (on a 0 to 10 scale) = -1.12 [-2.33, 0.09], GRADE evidence: very low). However, analysing studies with no high-risk bias found ketamine to decrease pain intensity at 4 weeks and increased the level of GRADE evidence to moderate. Trial sequential analysis confirmed the overall result and revealed the lack of power of this meta-analysis. Ketamine also decreased pain intensity at all other evaluated points in time. Ketamine increased the incidence of psychedelic manifestations in comparison to placebo.
Results of this meta-analysis found moderate evidence suggesting the efficacy of ketamine during chronic pain. Further studies are warranted to conclude about the effect of ketamine during chronic pain conditions and to determine optimal administration regimes of this agent during this condition.
Ketamine has been found interesting for managing chronic pain. We performed a meta-analysis aiming to confirm those results. Ketamine was found efficient in alleviating pain up to 12 weeks after the beginning of treatment. However, overall evidence favouring the use of this compound was very low.
氯胺酮已被证明在缓解慢性疼痛方面有效。然而,在研究氯胺酮治疗慢性疼痛管理的效果时,研究结果并不一致。我们旨在进行荟萃分析,以评估该化合物在慢性非癌性疼痛情况下的疗效。
该研究是一项比较慢性非癌性疼痛患者使用氯胺酮和安慰剂的临床试验荟萃分析。该研究的主要终点是治疗开始后 4 周时的疼痛缓解情况。次要结局包括:治疗开始后 1、2、8 和 12 周时的疼痛缓解情况以及出现致幻表现的发生率。
共有 6 项研究纳入本荟萃分析。共有 99 名患者接受氯胺酮治疗,96 名患者接受安慰剂治疗。氯胺酮不能在 4 周时降低疼痛强度(MD(0 至 10 分制)=-1.12[-2.33,0.09],GRADE 证据:极低)。然而,分析无高风险偏倚的研究发现,氯胺酮能在 4 周时降低疼痛强度,并将 GRADE 证据的等级提高到中度。试验序贯分析证实了总体结果,并显示出该荟萃分析缺乏效力。氯胺酮还能降低所有其他评估时间点的疼痛强度。与安慰剂相比,氯胺酮增加了致幻表现的发生率。
本荟萃分析结果发现中度证据表明氯胺酮在慢性疼痛中的疗效。需要进一步的研究来确定氯胺酮在慢性疼痛情况下的效果,并确定在这种情况下该药物的最佳给药方案。
氯胺酮已被证明对治疗慢性疼痛有效。我们进行了一项荟萃分析,旨在证实这些结果。氯胺酮在治疗开始后 12 周内缓解疼痛的效果显著。然而,总体上支持使用该化合物的证据非常低。