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同步机械通气用于新生儿呼吸支持

Synchronized mechanical ventilation for respiratory support in newborn infants.

作者信息

Greenough A, Milner A D, Dimitriou G

机构信息

Dept of Child Health, King's College School of Medicine and Dentistry, Bessemer Road, London, UK, SE5 9PJ.

出版信息

Cochrane Database Syst Rev. 2004 Oct 18(4):CD000456. doi: 10.1002/14651858.CD000456.pub2.

Abstract

BACKGROUND

During synchronized mechanical ventilation, positive airway pressure and spontaneous inspiration coincide. Thus, if synchronous ventilation is provoked, adequate gas exchange should be achieved at lower peak airway pressures, potentially reducing barotrauma and hence airleak and chronic lung disease. Synchronous ventilation can be achieved by manipulation of rate and inspiratory time during conventional ventilation and employment of patient assisted ventilation.

OBJECTIVES

To compare (i) the efficacy of synchronized mechanical ventilation, delivered as high frequency positive pressure ventilation or triggered ventilation (patient triggered ventilation (PTV) or synchronous intermittent mandatory ventilation (SIMV)) with conventional ventilation(ii) different types of triggered ventilation

SEARCH STRATEGY

Searches from 1985-2004 of the Cochrane Central Register of Controlled Trials (CENTRAL, The Cochrane Library, Issue 3, 2004), Oxford Database of Perinatal Trials, MEDLINE, previous reviews, abstracts and symposia proceedings; hand searches of journals in the English language and contact with expert informants.

SELECTION CRITERIA

Randomized or quasi randomized clinical trials comparing synchronized ventilation delivered as high frequency positive pressure ventilation (HFPPV) or triggered ventilation (PTV/SIMV) to conventional mechanical ventilation (CMV) in neonates. Randomized trials comparing different triggered ventilation modes (PTV and SIMV) in neonates.

DATA COLLECTION AND ANALYSIS

Data regarding clinical outcomes including mortality, airleaks (pneumothorax or pulmonary interstitial emphysema (PIE)), severe intracerebral haemorrhage (grades 3 and 4), chronic lung disease (oxygen dependency beyond 28 days) and duration of weaning/ventilation. Three comparisons were made: (i) HFPPV vs CMV; (ii) PTV/SIMV vs CMV; (iii) PTV vs SIMV. Data analysis was conducted using relative risk for categorical outcomes, weighted mean difference for outcomes measured on a continuous scale.

MAIN RESULTS

Eleven studies were eligible for inclusion. The meta-analysis demonstrate that HFPPV compared to CMV was associated with a reduction in the risk of airleak (typical relative risk for pneumothorax was 0.69, 95% CI 0.51, 0.93). PTV/SIMV compared to CMV was associated with a shorter duration of ventilation (weighted mean difference -34.8 hours, 95% CI -62.1, -7.4). PTV compared to SIMV was associated with a trend to a shorter duration of weaning (weighted mean difference -42.4 hours, 95% CI -94.4, 9.6). Neither HFPPV nor triggered ventilation was associated with a significant reduction in the incidence of chronic lung disease. There was a non-significant trend towards a lower mortality rate using HFPPV versus CMV, but a non-significant trend towards a higher mortality rate using triggered ventilation versus CMV. No disadvantage of HFPPV or triggered ventilation was noted regarding other outcomes.

REVIEWERS' CONCLUSIONS: Compared to conventional ventilation, benefit is demonstrated for both HFPPV and triggered ventilation with regard to a reduction in airleak and a shorter duration of ventilation, respectively. In none of the trials was complex respiratory monitoring undertaken and thus it is not possible to conclude that the mechanism of producing those benefits is by provocation of synchronized ventilation. Further trials are needed to determine whether synchronized ventilation is associated with other benefits, but optimization of trigger and ventilator design with respect to respiratory diagnosis is encouraged before embarking on further trials.

摘要

背景

在同步机械通气期间,气道正压与自主吸气同时发生。因此,如果诱发同步通气,应能在较低的气道峰压下实现充分的气体交换,从而有可能减少气压伤,进而减少气漏和慢性肺病。通过在传统通气过程中调整频率和吸气时间以及采用患者辅助通气可实现同步通气。

目的

比较(i)作为高频正压通气或触发通气(患者触发通气(PTV)或同步间歇指令通气(SIMV))的同步机械通气与传统通气的疗效;(ii)不同类型的触发通气。

检索策略

检索1985年至2004年的Cochrane对照试验中央注册库(CENTRAL,Cochrane图书馆,2004年第3期)、牛津围产期试验数据库、MEDLINE、既往综述、摘要和研讨会论文集;手工检索英文期刊并与专家信息提供者联系。

入选标准

比较作为高频正压通气(HFPPV)或触发通气(PTV/SIMV)的同步通气与新生儿传统机械通气(CMV)的随机或半随机临床试验。比较新生儿不同触发通气模式(PTV和SIMV)的随机试验。

数据收集与分析

有关临床结局的数据,包括死亡率、气漏(气胸或肺间质气肿(PIE))、重度脑室内出血(3级和4级)、慢性肺病(28天以上的氧依赖)以及撤机/通气时间。进行了三项比较:(i)HFPPV与CMV;(ii)PTV/SIMV与CMV;(iii)PTV与SIMV。使用分类结局的相对风险、连续量表测量结局的加权均数差进行数据分析。

主要结果

11项研究符合纳入标准。荟萃分析表明,与CMV相比,HFPPV与气漏风险降低相关(气胸的典型相对风险为0.69,95%可信区间0.51,0.93)。与CMV相比,PTV/SIMV与通气时间缩短相关(加权均数差-34.8小时,95%可信区间-62.1,-7.4)。与SIMV相比,PTV与撤机时间缩短趋势相关(加权均数差-42.4小时,95%可信区间-94.4,9.6)。HFPPV和触发通气均与慢性肺病发病率显著降低无关。使用HFPPV与CMV相比,死亡率有非显著降低趋势,但使用触发通气与CMV相比,死亡率有非显著升高趋势。在其他结局方面未发现HFPPV或触发通气有不利之处。

综述作者结论

与传统通气相比,HFPPV和触发通气分别在减少气漏和缩短通气时间方面显示出益处。在任何一项试验中均未进行复杂的呼吸监测,因此无法得出产生这些益处的机制是通过诱发同步通气的结论。需要进一步试验来确定同步通气是否与其他益处相关,但在开展进一步试验之前,鼓励在呼吸诊断方面优化触发和呼吸机设计。

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