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Ketamine for chronic non‐cancer pain: A meta‐analysis and trial sequential analysis of randomized controlled trials

机译:慢性非癌症疼痛的氯胺酮:随机对照试验的荟萃分析和试验顺序分析

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Abstract Background 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. Methods 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. Results 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. Conclusion 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. Significance 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.
机译:摘要背景氯胺酮提出效率缓解慢性疼痛。然而,研究跨研究调查氯胺酮对慢性疼痛管理的影响不一致。我们的目标是进行荟萃分析,以评估慢性非癌症疼痛病症期间该化合物的疗效。方法研究与临床试验的荟萃分析,将氯胺酮与安慰剂进行比较慢性非癌症疼痛。本研究的主要终点是疼痛缓解4?治疗开始后的周数。二次结果是:疼痛浮雕1,2,8和12?在治疗开始和迷幻表现的发病率之后的时间。结果该荟萃分析中包括六项研究。总体而言,99名患者接受氯胺酮和96名接受安慰剂。氯胺酮在4?周(MD(0到10刻度上)?= ?? 1.12 [?2.33,0.09],等级证据:非常低)。然而,没有高风险偏见的分析研究发现氯胺酮在4?周内降低疼痛强度,并增加了等级证据的水平。试验顺序分析证实了整体结果,并揭示了该荟萃分析的缺乏力量。氯胺酮在所有其他评估的时间点也降低了疼痛强度。氯胺酮与安慰剂相比增加了迷幻表现的发病率。结论该荟萃分析的结果发现中度证据表明氯胺酮在慢性疼痛期间的疗效。进一步的研究是关于缩酮在慢性疼痛条件下的作用以及在此条件下确定该试剂的最佳给药制度的影响。对于管理慢性疼痛,发现氯胺酮的意义有趣。我们进行了一个旨在确认这些结果的Meta分析。在治疗开始后,氯胺酮的效率有效地减轻了12次疼痛。然而,有利于使用这种化合物的总体证据非常低。

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  • 来源
    《European journal of pain :》 |2018年第4期|共15页
  • 作者单位

    Department of Anaesthesia and Intensive CareRobert Debre University HospitalParis France;

    Department of Anaesthesia and Pain ManagementRoyal Children's HospitalMelbourne Australia;

    Department of Anaesthesia and Intensive CareRobert Debre University HospitalParis France;

    Department of Anaesthesia and Intensive CareRobert Debre University HospitalParis France;

    Department of Anaesthesia and Intensive CareRobert Debre University HospitalParis France;

    Department of Anaesthesia and Intensive CareRobert Debre University HospitalParis France;

    Paris Diderot UniversityFrance;

    Department of Anaesthesia and Intensive CareRobert Debre University HospitalParis France;

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  • 正文语种 eng
  • 中图分类 诊断学;
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