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本文引用的文献

1
Implementation of a Nurse-Driven Sedation Protocol in a PICU Decreases Daily Doses of Midazolam.在儿科重症监护病房实施护士主导的镇静方案可降低咪达唑仑的每日剂量。
Pediatr Crit Care Med. 2017 Jan;18(1):e9-e17. doi: 10.1097/PCC.0000000000000998.
2
National survey and point prevalence study of sedation practice in UK critical care.英国重症监护镇静实践的全国性调查与时点患病率研究
Crit Care. 2016 Oct 27;20(1):355. doi: 10.1186/s13054-016-1532-x.
3
Staff education, regular sedation and analgesia quality feedback, and a sedation monitoring technology for improving sedation and analgesia quality for critically ill, mechanically ventilated patients: a cluster randomised trial.医护人员教育、常规镇静和镇痛质量反馈以及镇静监测技术可提高重症机械通气患者的镇静和镇痛质量:一项整群随机试验。
Lancet Respir Med. 2016 Oct;4(10):807-817. doi: 10.1016/S2213-2600(16)30178-3. Epub 2016 Jul 26.
4
Protocolized sedation vs usual care in pediatric patients mechanically ventilated for acute respiratory failure: a randomized clinical trial.程序化镇静与机械通气治疗急性呼吸衰竭患儿的常规护理比较:一项随机临床试验。
JAMA. 2015 Jan 27;313(4):379-89. doi: 10.1001/jama.2014.18399.
5
Protocol-directed sedation versus non-protocol-directed sedation to reduce duration of mechanical ventilation in mechanically ventilated intensive care patients.在机械通气的重症监护患者中,采用方案指导镇静与非方案指导镇静以缩短机械通气时间的比较。
Cochrane Database Syst Rev. 2015 Jan 7;1:CD009771. doi: 10.1002/14651858.CD009771.pub2.
6
Protocolized versus non-protocolized weaning for reducing the duration of mechanical ventilation in critically ill adult patients.标准化与非标准化撤机对缩短危重症成年患者机械通气时间的影响
Cochrane Database Syst Rev. 2014 Nov 6;2014(11):CD006904. doi: 10.1002/14651858.CD006904.pub3.
7
Daily sedation interruption versus no daily sedation interruption for critically ill adult patients requiring invasive mechanical ventilation.对于需要有创机械通气的成年重症患者,每日中断镇静与不中断镇静的比较。
Cochrane Database Syst Rev. 2014 Jul 9;2014(7):CD009176. doi: 10.1002/14651858.CD009176.pub2.
8
The implementation of an analgesia-based sedation protocol reduced deep sedation and proved to be safe and feasible in patients on mechanical ventilation.基于镇痛的镇静方案的实施减少了深度镇静,并被证明在机械通气患者中是安全可行的。
Rev Bras Ter Intensiva. 2013 Jul-Sep;25(3):188-96. doi: 10.5935/0103-507X.20130034.
9
Implementation of a protocol for integrated management of pain, agitation, and delirium can improve clinical outcomes in the intensive care unit: a randomized clinical trial.实施疼痛、躁动和谵妄的综合管理方案可改善重症监护病房的临床转归:一项随机临床试验。
J Crit Care. 2013 Dec;28(6):918-22. doi: 10.1016/j.jcrc.2013.06.019. Epub 2013 Sep 4.
10
Patient comfort in the intensive care unit: a multicentre, binational point prevalence study of analgesia, sedation and delirium management.重症监护病房患者舒适度:一项多中心、两国镇痛、镇静和谵妄管理的现况调查研究。
Crit Care Resusc. 2013 Sep;15(3):213-9.

机械通气的成人及儿童重症监护患者中,方案指导镇静与非方案指导镇静的比较

Protocol-directed sedation versus non-protocol-directed sedation in mechanically ventilated intensive care adults and children.

作者信息

Aitken Leanne M, Bucknall Tracey, Kent Bridie, Mitchell Marion, Burmeister Elizabeth, Keogh Samantha J

机构信息

School of Health Sciences, City, University of London, Myddelton Street, London, UK, EC1V 0HB.

出版信息

Cochrane Database Syst Rev. 2018 Nov 12;11(11):CD009771. doi: 10.1002/14651858.CD009771.pub3.

DOI:10.1002/14651858.CD009771.pub3
PMID:30480753
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6516800/
Abstract

BACKGROUND

The sedation needs of critically ill patients have been recognized as a core component of critical care that is vital to assist recovery and ensure humane treatment. Evidence suggests that sedation requirements are not always optimally managed. Suboptimal sedation, both under- and over-sedation, have been linked to short-term (e.g. length of stay) and long-term (e.g. psychological recovery) outcomes. Strategies to improve sedation assessment and management have been proposed. This review was originally published in 2015 and updated in 2018.

OBJECTIVES

To assess the effects of protocol-directed sedation management compared to usual care on the duration of mechanical ventilation, intensive care unit (ICU) and hospital mortality and other patient outcomes in mechanically ventilated ICU adults and children.

SEARCH METHODS

We used the standard search strategy of the Cochrane Anaesthesia, Critical and Emergency Care Group (ACE). We searched the Cochrane Central Register of Controlled trials (CENTRAL) (December 2017), MEDLINE (OvidSP) (2013 to December 2017), Embase (OvidSP) (2013 to December 2017), CINAHL (BIREME host) (2013 to December 2017), LILACS (2013 to December 2017), trial registries and reference lists of articles. (The original search was run in November 2013).

SELECTION CRITERIA

We included randomized controlled trials (RCTs) and quasi-randomized controlled trials conducted in ICUs comparing management with and without protocol-directed sedation in intensive care adults and children.

DATA COLLECTION AND ANALYSIS

Two authors screened the titles and abstracts and then full-text reports identified from our electronic search. We assessed seven domains of potential risk of bias for the included studies. We examined clinical, methodological and statistical heterogeneity and used the random-effects model for meta-analysis where we considered it appropriate. We calculated the mean difference (MD) for duration of mechanical ventilation and risk ratio (RR) for mortality across studies, with 95% confidence intervals (CIs).

MAIN RESULTS

We included four studies with a total of 3323 participants (864 adults and 2459 paediatrics) in this update. Three studies were single-centre, patient-level RCTs and one study was a multicentre cluster-RCT. The settings were in metropolitan centres and included general, mixed medical-surgical, medical only and a range of paediatric units. All four included studies compared the use of protocol-directed sedation, specifically protocols delivered by nurses, with usual care. We rated the risk of selection bias due to random sequence generation low for two studies and unclear for two studies. The risk of bias was highly variable across the domains and studies, with the risk of selection and performance bias generally rated high and the risk of detection and attrition bias generally rated low.When comparing protocol-directed sedation with usual care, there was no clear evidence of difference in duration of mechanical ventilation in hours for the entire duration of the first ICU stay for each patient (MD -28.15 hours, 95% CI -69.15 to 12.84; I = 85%; 4 studies; adjusted sample 2210 participants; low-quality evidence). There was no clear evidence of difference in ICU mortality (RR 0.77, 95% CI 0.39 to 1.50; I = 67%; 2 studies; 513 participants; low-quality evidence), or hospital mortality (RR 0.90, 95% CI 0.72 to 1.13; I = 10%; 3 studies; adjusted sample 2088 participants; low-quality evidence). There was no clear evidence of difference in ICU length of stay (MD -1.70 days, 95% CI-3.71 to 0.31; I = 82%; 4 studies; adjusted sample of 2123 participants; low-quality of evidence), however there was evidence of a significant reduction in hospital length of stay (MD -3.09 days, 95% CI -5.08 to -1.10; I = 2%; 3 studies; adjusted sample of 1922 participants; moderate-quality evidence). There was no clear evidence of difference in the incidence of self-extubation (RR 0.88, 95% CI 0.55 to 1.42; I = 0%; 2 studies; adjusted sample of 1687 participants; high-quality evidence), or incidence of tracheostomy (RR 0.67, 95% CI 0.35 to 1.30; I = 66%; 3 studies; adjusted sample of 2008 participants; low-quality evidence). Only one study examined incidence of reintubation, therefore we could not pool data; there was no clear evidence of difference (RR 0.65, 95% CI 0.35 to 1.24; 1 study; 321 participants; low-quality evidence).

AUTHORS' CONCLUSIONS: There is currently limited evidence from RCTs evaluating the effectiveness of protocol-directed sedation on patient outcomes. The four included RCTs reported conflicting results and heterogeneity limited the interpretation of results for the primary outcomes of duration of mechanical ventilation and mortality. Further studies, taking into account differing contextual characteristics, are necessary to inform future practice. Methodological strategies to reduce the risk of bias need to be considered in future studies.

摘要

背景

重症患者的镇静需求已被视为重症监护的核心组成部分,这对于促进康复和确保人道治疗至关重要。有证据表明,镇静需求的管理并非总能达到最佳状态。镇静不足和过度镇静这两种不理想的镇静状态,都与短期(如住院时间)和长期(如心理恢复)预后相关。已有人提出改善镇静评估和管理的策略。本综述最初发表于2015年,并于2018年更新。

目的

评估与常规护理相比,采用方案导向的镇静管理对机械通气的成年和儿童重症监护病房(ICU)患者机械通气时长、ICU及医院死亡率以及其他患者预后的影响。

检索方法

我们采用了Cochrane麻醉、重症和急诊护理组(ACE)的标准检索策略。检索了Cochrane对照试验中心注册库(CENTRAL)(2017年12月)、MEDLINE(OvidSP)(2013年至2017年12月)、Embase(OvidSP)(2013年至2017年12月)、护理学与健康领域数据库(CINAHL)(BIREME平台)(2013年至2017年12月)、拉丁美洲及加勒比地区健康科学数据库(LILACS)(2013年至2017年12月)、试验注册库以及文章的参考文献清单。(最初的检索于2013年11月进行)。

入选标准

我们纳入了在ICU中进行的随机对照试验(RCT)和半随机对照试验,这些试验比较了对成年和儿童重症监护患者采用与不采用方案导向镇静管理的情况。

数据收集与分析

两位作者筛选了标题和摘要,然后对通过电子检索识别出的全文报告进行筛选。我们评估了纳入研究中七个潜在偏倚风险领域。我们检查了临床、方法学和统计学异质性,并在认为合适的情况下使用随机效应模型进行荟萃分析。我们计算了各研究中机械通气时长的平均差(MD)和死亡率的风险比(RR),并给出95%置信区间(CI)。

主要结果

本次更新纳入了四项研究,共有3323名参与者(864名成人和2459名儿童)。三项研究为单中心、患者层面的RCT,一项研究为多中心整群RCT。研究地点均位于大城市中心,包括综合、内科外科混合、仅内科以及一系列儿科病房。所有四项纳入研究均比较了采用方案导向镇静,特别是由护士实施的方案,与常规护理的情况。我们将两项研究中因随机序列产生导致的选择偏倚风险评为低,两项研究评为不清楚。各领域和研究的偏倚风险差异很大,选择和实施偏倚风险通常评为高,检测和失访偏倚风险通常评为低。在比较方案导向镇静与常规护理时,对于每位患者在首个ICU住院期间的机械通气时长(MD -28.15小时,95%CI -69.15至12.84;I² = 85%;4项研究;调整样本2210名参与者;低质量证据),没有明确证据表明存在差异。在ICU死亡率(RR 0.77,95%CI 0.39至1.50;I² = 67%;2项研究;513名参与者;低质量证据)或医院死亡率(RR 0.90,95%CI 0.72至1.13;I² = 10%;3项研究;调整样本2088名参与者;低质量证据)方面,也没有明确证据表明存在差异。在ICU住院时长(MD -1.70天,95%CI -3.71至0.31;I² = 82%;4项研究;调整样本2123名参与者;低质量证据)方面,没有明确证据表明存在差异,然而有证据表明医院住院时长显著缩短(MD -3.09天,95%CI -5.08至-1.10;I² = 2%;3项研究;调整样本1922名参与者;中等质量证据)。在自行拔管发生率(RR 0.88,95%CI 0.55至1.42;I² = 0%;2项研究;调整样本1687名参与者;高质量证据)或气管切开发生率(RR 0.67,95%CI 0.35至1.30;I² = 66%;3项研究;调整样本2008名参与者;低质量证据)方面,没有明确证据表明存在差异。只有一项研究考察了再次插管发生率,因此我们无法汇总数据;没有明确证据表明存在差异(RR 0.65,95%CI 0.35至1.24;1项研究;321名参与者;低质量证据)。

作者结论

目前来自RCT的证据有限,难以评估方案导向镇静对患者预后的有效性。纳入的四项RCT报告了相互矛盾的结果,异质性限制了对机械通气时长和死亡率等主要结局结果的解释。需要进一步开展考虑不同背景特征的研究,为未来实践提供参考。未来研究需要考虑采用方法学策略来降低偏倚风险。