首页> 外文期刊>Health technology assessment: HTA >Sugammadex for the reversal of muscle relaxation in general anaesthesia: A systematic review and economic assessment
【24h】

Sugammadex for the reversal of muscle relaxation in general anaesthesia: A systematic review and economic assessment

机译:Sugammadex逆转的肌肉放松在全身麻醉:系统回顾和经济评估

获取原文
           

摘要

Background: Sugammadex (Bridion ?) is a newly developed agent for the reversal of neuromuscular blockade (NMB) induced by rocuronium or vecuronium. Sugammadex can reverse profound blockade and can be given for immediate reversal and its use would avoid the potentially serious adverse effects of the currently used agent, succinylcholine. Also, sugammadex can reverse NMB more quickly and predictably than existing agents. Objectives: To determine the clinical effectiveness and cost-effectiveness of sugammadex for the reversal of muscle relaxation after general anaesthesia in UK practice following routine or rapid induction of NMB. Data sources: Medical databases [including MEDLINE, EMBASE, CINAHL, Science Citation Index, BIOSIS and Cochrane Central Register of Controlled Trials (CENTRAL), conference proceedings, internet sites and clinical trials registers] were searched to identify published and unpublished studies. The main searches were carried out in May 2008 and supplemented by current awareness updates up until November 2008. Review methods: For the clinical effectiveness review, randomised controlled trials of sugammadex against placebo or an active comparator (neostigmine + glycopyrrolate) for the reversal of moderate or profound NMB and for immediate reversal (spontaneous recovery from succinylcholineinduced blockade) were included. The primary effectiveness outcome was speed of recovery from NMB, as measured by objective monitoring of neuromuscular function. For the cost-effectiveness review, a de novo economic assessment considered the routine induction of NMB and the rapid induction and/or reversal of NMB, and threshold analyses were carried out on a series of pairwise comparisons to establish how effective sugammadex needs to be to justify its cost. Results: The review of clinical effectiveness included four randomised active-control trials of sugammadex, nine randomised placebo-controlled trials and five studies in special populations. A total of 2132 titles and abstracts and 265 full-text publications were screened. The included trials indicated that sugammadex produces more rapid recovery from moderate or profound NMB than placebo or neostigmine. Median time to recovery from moderate blockade was 1.3-1.7 minutes for rocuronium + sugammadex, 21-86 minutes for rocuronium + placebo and 17.6 minutes for rocuronium + neostigmine. In profound blockade, median time to recovery was 2.7 minutes for rocuronium + sugammadex, 30 to 90 minutes for rocuronium + placebo, and 49 minutes for rocuronium + neostigmine. Results for vecuronium were similar. In addition, recovery from NMB was faster with rocuronium reversed by sugammadex 16 mg/kg after 3 minutes (immediate reversal) than with succinylcholine followed by spontaneous recovery (median time to primary outcome 4.2 versus 7.1 minutes). The evidence base for modelling costeffectiveness is very limited. However, assuming that the reductions in recovery times seen in the trials can be achieved in routine practice and can be used productively, sugammadex [2 mg/kg (4 mg/kg)] is potentially cost-effective at its current list price for the routine reversal of rocuronium-induced moderate (profound) blockade, if each minute of recovery time saved can be valued at approximately £2.40 (£1.75) or more. This is more likely to be achieved if any reductions in recovery time are in the operating room (estimated value of £4.44 per minute saved) rather than the recovery room (estimated value of £0.33 per minute saved). The results were broadly similar for rocuronium- and vecuronium-induced blockade. For rapid reversal of NMB it appeared that any reduction in morbidity from adopting sugammadex is unlikely to result in significant cost savings. Limitations: The evidence base was not large and many of the published trials were dose-finding and safety studies with very small sample sizes. Also, some relevant outcomes, in particular patient experience/ quality of life and resources/costs
机译:背景:Sugammadex (Bridion ?)是一个新开发代理的逆转神经肌肉(NMB)由rocuronium或封锁维库。封锁,可以立即逆转和它的使用可以避免潜在的严重不利影响的当前使用的代理,琥珀酰胆碱。更快,比现有的预测代理。效率和成本效益的sugammadex逆转的肌肉放松全身麻醉后英国的实践后常规或NMB快速感应。来源:医学数据库(MEDLINE、CINAHL EMBASE,科学引文索引,生命现象和Cochrane中央控制寄存器试验(中央),会议论文集,网站和临床试验注册)确定发布和搜索吗未发表的研究。在2008年5月进行补充当前意识更新直到2008年11月。检查方法:临床疗效审查,随机对照试验sugammadex反对安慰剂或积极比较器(新斯的明+胃长宁)温和的或深刻的NMB和逆转立即逆转(自发的复苏包括succinylcholineinduced封锁)。主要结果有效性的速度从NMB复苏,以目标监测神经肌肉功能。成本效益评估,新创的经济评估的常规感应NMB和快速诱导和/或逆转NMB,阈值进行分析一系列成对的比较建立如何sugammadex需要证明其有效成本。有效性包括四个随机的主动控制试验sugammadex, 9随机安慰剂对照试验和5在特殊人群的研究。标题和摘要,265全文出版物筛选。表明sugammadex产生更迅速从温和的或深刻的NMB复苏安慰剂或新斯的明。从温和的封锁是1.3 - -1.7分钟rocuronium + sugammadex, 21 - 86分钟rocuronium +安慰剂和17.6分钟rocuronium +新斯的明。平均恢复时间为2.7分钟rocuronium + sugammadex 30比;rocuronium +安慰剂,49分钟rocuronium +新斯的明。是相同的。快与rocuronium逆转sugammadex 16毫克/公斤3分钟后(立即逆转)与琥珀酰胆碱自发紧随其后恢复(平均时间4.2主要结果和7.1分钟)。造型costeffectiveness非常有限。然而,假设减少复苏次试验中可以实现常规练习,可以高效地使用,sugammadex[2毫克/公斤(4毫克/公斤))是可能的成本效益以当前价格列表常规的逆转rocuronium-induced温和(深刻)封锁,如果复苏的每分钟节省时间可以在大约价值£2.40(£1.75)或更多。是否有减少恢复时间在手术室(估计价值£4.44每分钟保存),而不是恢复室(估计价值£0.33每分钟保存)。结果rocuronium——大体相似vecuronium-induced封锁。的NMB看来任何减少发病率从采用sugammadex不太可能带来巨大的成本节省。的证据基础并不大,很多发表的试验研究和安全研究非常小的样本大小。相关成果,特别是病人经验/生活质量和资源/成本

著录项

相似文献

  • 外文文献
  • 中文文献
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