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首页> 外文期刊>Atencion Primaria >A systematic review and meta-analysis of the effectiveness and adverse events of gabapentin and pregabalin for sciatica pain
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A systematic review and meta-analysis of the effectiveness and adverse events of gabapentin and pregabalin for sciatica pain

机译:系统评价和荟萃分析加巴彭素和普瑞巴林的巩膜疼痛的效果和不良事件

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AimThis SR aims to assess the effectiveness of pregabalin and gabapentin on pain and disability caused by acute sciatica and the adverse events associated with their clinical use.DesignSystematic review.DatabasesElectronic databases of Cochrane Central Register of Controlled Trials, MEDLINE, EMBASE, and Clinical Trials.gov were searched from their inception until March 1st of 2021.Selection criteriaRandomized trials (RCT) with adults>18 years old with acute sciatica for a minimum of 1 week and a maximum of 1 year (at least moderate pain).Data treatmentThe outcomes were pain, disability and adverse events. Data was summarized using odds ratio and mean difference. GRADE was used to calculate the level of evidence.ResultsEight RCT involving 747 participants were included. The effect of pregabalin was assessed in 3 RCT and in one three-arm trial (pregabalin vs limaprost vs a combination of limaprost and pregabalin). Two trials assessed the effect of gabapentin compared with placebo and one compared with tramadol. One study assessed the effect of gabapentin vs pregabalin in a crossover head-to-head trial.A statistically significant improvement on leg pain at 2 weeks and leg pain with movement at 3 and 4 months was found in a RCT comparing gabapentin with placebo. There were no statistically differences on the remaining time periods assessed for leg pain, low back pain and functional disability.ConclusionsThis SR provides clear evidence for lack of effectiveness of pregabalin and gabapentin for sciatica pain management. In view of this, its routine clinical use cannot be supported.
机译:AIMTHIS SR旨在评估Pragabalin和加巴彭素对由急性坐骨神经痛和与其临床使用相关的不良事件引起的疼痛和残疾的有效性.Designsystemication评论。Cochrane中央寄存器的控制试验,Medline,Embase和临床试验。从他们的初始搜索到2021年3月1日的研究。选择标准治疗试验(RCT)与成人> 18岁,急性坐骨神经痛至少为1周,最多1年(至少疼痛).Data治疗结果疼痛,残疾和不良事件。数据总结了使用赔率比和平均差异。级别用于计算证据水平。包括涉及747名参与者的RCT。普瑞巴林的效果在3 rct中评估,并在三个手臂试验中(Praetabalin Vs Limaprost与Limaprost和Praetabalin的组合)。两项试验评估了加布普坦与安慰剂相比的影响,与曲马多相比。一项研究评估了加巴彭素对普雷巴林在交叉头脑中的作用。在一个RCT与安慰剂的RCT比较加州氏植物的RCT中,在腿部疼痛和腿部疼痛的统计学上显着改善。对腿部疼痛评估的剩余时间段没有统计学差异,低腰疼痛和功能性残疾.Clusionsthis SR提供明确的证据表明缺乏普瑞巴林和加巴文顿缺乏坐骨神经痛疼痛管理的效果。鉴于此,不能支持其常规临床使用。

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