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Efficacy and safety of inhaled anaesthetic for postoperative sedation during mechanical ventilation in adult cardiac surgery patients: a systematic review and meta-analysis

机译:成人心脏手术患者机械通风中吸入麻醉剂术后镇静的功效和安全性:系统综述和荟萃分析

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摘要

The aim was to evaluate the efficacy and safety of volatile anaesthetic for postoperative sedation in adult cardiac surgery patients through a systematic review and meta-analysis. We retrieved randomized controlled trials from MEDLINE, EMBASE, CENTRAL, Web of Science, clinical trials registries, conference proceedings, and reference lists of included articles. Independent reviewers extracted data, including patient characteristics, type of intraoperative anaesthesia, inhaled anaesthetic used, comparator sedation, and outcomes of interest, using pre-piloted forms. We assessed risk of bias using the Cochrane Tool and evaluated the strength of the evidence using the GRADE approach. Eight studies enrolling 610 patients were included. Seven had a high and one a low risk of bias. The times to extubation after intensive care unit (ICU) admission and sedation discontinuation were, respectively, 76 [95% confidence interval (CI) -150 to -2, I-2 = 79%] and 74 min (95% CI -126 to -23, I-2 = 96%) less in patients who were sedated using volatile anaesthetic. There was no difference in ICU or hospital length of stay. Patients who received volatile anaesthetic sedation had troponin concentrations that were 0.71 ng ml(-1) (95% CI 0.23-1.2) lower than control patients. Reporting on other outcomes was varied and not suitable for meta-analysis. Volatile anaesthetic sedation may be associated with a shorter time to extubation after cardiac surgery but no change in ICU or hospital length of stay. It is associated with a significantly lower postoperative troponin concentration, but the impact of this on adverse cardiovascular outcomes is uncertain. Blinded randomized trials using intention-to-treat analysis are required. PROSPERO registry number: 2016: CRD42016033874. Available from http://www.crd.york.ac.uk/PROSPERO/display_record.asp?ID=CRD42016033874.
机译:目的是通过系统审查和荟萃分析评估成人心脏手术患者术后镇静的挥发性麻醉剂的疗效和安全性。我们检索来自Medline,Embase,Central,Scient的随机对照试验,临床试验登记处,会议诉讼程序以及包括条款的参考名单。独立审查员提取数据,包括患者特征,术中麻醉的类型,使用预先驾驶形式,吸入的麻醉剂,比较的麻醉剂,比较的麻醉剂和感兴趣的结果。我们评估了使用Cochrane工具的偏差风险,并使用等级方法评估证据的强度。纳入610名患者的八项研究。七有一个高,偏差风险很低。在重症监护单元(ICU)入院和镇静中断后的时间分别为76 [95%置信区间(CI)-150至-2,I-2 = 79%]和74分钟(95%CI -126使用挥发性麻醉剂镇静的患者少于-23,I-2 = 96%。 ICU或医院的住宿时间没有差异。接受挥发性麻醉镇静的患者具有比对照患者低0.71 ng(-1)(95%CI 0.23-1.2)的肌钙蛋白浓度。关于其他结果的报告是不同的,不适合Meta分析。挥发性麻醉镇静可能与心脏手术后延伸的较短时间相关联,但ICU或医院住院时间没有变化。它与显着降低的肌钙蛋白浓度显着降低,但这种对不良心血管结果的影响是不确定的。需要使用意向治疗分析的盲目的随机试验。 Prospero注册表号:2016:CRD42016033874可从http://www.crd.york.ac.uk/prospero/display_record.asp?id=crd42016033877获得。

著录项

  • 来源
    《British journal of anaesthesia》 |2017年第5期|共12页
  • 作者单位

    McMaster Univ Populat Hlth Res Inst Dept Anaesthesia &

    Crit Care Hamilton ON Canada;

    McMaster Univ Populat Hlth Res Inst Dept Anaesthesia &

    Crit Care Hamilton ON Canada;

    McMaster Univ Populat Hlth Res Inst Dept Anaesthesia &

    Crit Care Hamilton ON Canada;

    McMaster Univ Populat Hlth Res Inst Dept Anaesthesia &

    Crit Care Hamilton ON Canada;

    McMaster Univ Populat Hlth Res Inst Dept Anaesthesia &

    Crit Care Hamilton ON Canada;

    McGill Univ Div Cardiac Surg Dept Surg Montreal PQ Canada;

    Populat Hlth Res Inst Div Cardiac Surg Dept Surg Hamilton ON Canada;

    McMaster Univ Populat Hlth Res Inst Dept Clin Epidemiol &

    Biostat Hamilton ON Canada;

    McMaster Univ Populat Hlth Res Inst Dept Clin Epidemiol &

    Biostat Hamilton ON Canada;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 麻醉学;
  • 关键词

    anaesthetics; inhalation; cardiac surgical procedures; postoperative care;

    机译:麻醉剂;吸入;心脏外科手术;术后护理;

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