...
首页> 外文期刊>Hand surgery: an international journal devoted to hand and upper limb surgery and related research : journal of the Asia-Pacific Federation of Societies for Surgery of the Hand >Wide-Awake Local Anesthesia No Tourniquet (WALANT) versus Local or Intravenous Regional Anesthesia with Tourniquet in Atraumatic Hand Cases in Orthopedics: A Systematic Review and Meta-Analysis
【24h】

Wide-Awake Local Anesthesia No Tourniquet (WALANT) versus Local or Intravenous Regional Anesthesia with Tourniquet in Atraumatic Hand Cases in Orthopedics: A Systematic Review and Meta-Analysis

机译:宽令局部麻醉没有止血带(WALANT)与朝向矫形器中的止血带(Walant)与脑矫形器中的止血带(Walant)的区域麻醉:系统性评论和荟萃分析

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Background: To compare outcomes of atraumatic hand surgeries using the WALANT technique versus intravenous regional anesthesia or local anesthesia with tourniquet. Methods: We conducted a comprehensive literature search using PubMed, MEDLINE, Embase, and Cochrane Library from inception to October 2018. All randomized or quasi-randomized trials and cohort studies comparing WALANT procedure versus local anesthesia or intravenous regional anesthesia with tourniquet among atraumatic hand surgeries were included. Methodological quality and risk of bias of eligible studies were assessed by three independent reviewers. The random effects model was used due to both statistical and clinical heterogeneity among studies. Results: The search yielded 496 records, of which 9 studies were included in the systematic review. We were able to pool findings for operative time, post-operative pain scores, patient satisfaction, and complication rates. On the average, the WALANT group had longer operative times by 2.06 minutes (pooled mean difference, random effects, 95% confidence interval 0.46 to 3.67 minutes, p = 0.01,I~2 0%, p = 0.66). The post-operative pain scores were lower in the WALANT group by an average of two VAS points (random effects, pooled mean difference -2.40, 95% confidence interval -3.41 to -1.38, p < 0.00001; I~2 0%p = 0.99). We had insufficient evidence to demonstrate a difference in terms of patient satisfaction (random effects, pooled risk ratio 0.98,95% confidence interval 0.93 to 1.03,p = 0.36,I~2 0%,p = 0.64) and complication rates (random effects, pooled risk ratio 0.40,95% confidence interval 0.07 to 2.18,p = 0.29,I~2 60%p = 0.08) between WALANT versus conventional methods. Conclusions: The WALANT group reported lower post-operative pain scores, but had slightly longer operative times. There are no significant differences between WALANT and conventional methods in terms of patient satisfaction and complication rates.
机译:背景:使用Walant Technology与静脉内麻醉或局部麻醉与止血带,比较Atraumatic手术手术的结果。方法:采用2018年10月,使用PubMed,Medline,Embase和Cochrane图书馆进行了全面的文学搜索。所有随机或准随机试验和队列研究将Walant手术与局部麻醉或静脉内区域麻醉与Atraumatic手术手术中的止血带相比包括在内。三名独立审查员评估了三项独立审稿人的方法论质量和符合条件研究偏差的风险。由于研究中的统计和临床异质性,使用随机效应模型。结果:搜索收出了496条记录,其中9项研究包括在系统审查中。我们能够为手术时间,术后疼痛评分,患者满意度和并发症率进行汇集结果。在平均水平上,Walant组的操作时间更长2.06分钟(合并平均差异,随机效应,95%置信区间0.46至3.67分钟,P = 0.01,I〜2 0%,P = 0.66)。在术后疼痛分数较低,瓦尔美组较低,平均两个VAS点(随机效应,合并平均差异-2.40,95%置信区间-3.41至-1.38,P <0.00001; I〜2 0%P = 0.99)。我们证据不足以证明患者满意度的差异(随机效应,汇总风险比0.98,95%置信区间0.93至1.03,P = 0.36,I〜2 0%,P = 0.64)和并发症率(随机效应,汇集风险比0.40.95%置信区间0.07至2.18,p = 0.29,瓦雅与常规方法之间的达0〜2 60%p = 0.08)。结论:Walant Group报告较低的术后疼痛评分,但操作时间稍长。 Walant与常规方法在患者满意度和并发症率方面没有显着差异。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号