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氯胺酮缓解神经性疼痛的疗效:动物研究的系统评价和荟萃分析。

Efficacy of ketamine in relieving neuropathic pain: a systematic review and meta-analysis of animal studies.

机构信息

Department of Anesthesiology, Leiden University Medical Center, Leiden, the Netherlands.

Amsterdam University Medical Center, location AMC, Amsterdam, the Netherlands.

出版信息

Pain. 2021 Sep 1;162(9):2320-2330. doi: 10.1097/j.pain.0000000000002231.

Abstract

In humans, proof of long-term efficacy of ketamine treatment in neuropathic pain is lacking. To improve our understanding of ketamine behavior under various administration conditions, we performed a systematic review and meta-analyses of controlled studies on the efficacy of ketamine in mice and rats with a disease model of nerve injury on relief of allodynia. Searches in PubMed and EMBASE identified 31 unique studies. Four meta-analyses were conducted. The first analysis included 19 comparisons on a single ketamine dose and measurement of effect within 3 hours of dosing and showed an appreciable effect (standardized mean difference 1.6, 95% confidence interval 1.1-2.1). Subgroup analyses showed no effect of species, administration route, or dose. A single administration was insufficient to sustain relief of allodynia at 24 or 72 hours after dosing, as observed in our second analysis (7 comparisons) with similar effects in ketamine-treated and control animals. Chronic ketamine administration (9 comparisons) caused profound relief of allodynia when tested during ketamine exposure (effect size 5.1, 3.7-6.5). The final analysis (6 comparisons) showed that chronic administration caused a slow loss of relief of allodynia with 70% loss of effect 24 days after end of treatment. No subgroups analyses were possible in the last 3 meta-analyses due to small group sizes. These results indicate long-term ketamine anti-allodynic effects after chronic exposure (>3 days) but not after a single administration. Given several limitations, extrapolation of the animal data to the human condition is tenuous.

摘要

在人类中,缺乏氯胺酮治疗神经性疼痛的长期疗效的证据。为了更好地了解氯胺酮在各种给药条件下的行为,我们对使用疾病模型(神经损伤)的小鼠和大鼠进行了氯胺酮疗效的对照研究进行了系统评价和荟萃分析,以评估氯胺酮对痛觉过敏的缓解作用。在 PubMed 和 EMBASE 中进行了搜索,共确定了 31 项独特的研究。进行了四项荟萃分析。第一项分析包括 19 项关于单次氯胺酮剂量的比较,并在给药后 3 小时内测量了效果,结果显示氯胺酮具有明显的效果(标准化均数差 1.6,95%置信区间 1.1-2.1)。亚组分析显示,物种、给药途径或剂量均无影响。单次给药不足以维持 24 或 72 小时后痛觉过敏的缓解,这在我们的第二项分析(7 项比较)中得到了观察,氯胺酮治疗组和对照组动物的效果相似。慢性氯胺酮给药(9 项比较)在暴露于氯胺酮时会引起明显的痛觉过敏缓解(效应大小 5.1,3.7-6.5)。最后一项分析(6 项比较)表明,慢性给药导致痛觉过敏缓解缓慢丧失,治疗结束后 24 天效应丧失 70%。由于组内样本量较小,最后三项荟萃分析中无法进行亚组分析。这些结果表明,慢性暴露(>3 天)后氯胺酮具有长期的抗痛觉过敏作用,但单次给药后没有。鉴于存在一些局限性,将动物数据外推到人类状况是不确定的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0177/8374709/381447cbe9ec/jop-162-2320-g001.jpg

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