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Model-based PEEP titration versus standard practice in mechanical ventilation: a randomised controlled trial

机译:基于模型的窥视滴定与机械通风的标准实践:随机对照试验

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BACKGROUND:Positive end-expiratory pressure (PEEP) at minimum respiratory elastance during mechanical ventilation (MV) in patients with acute respiratory distress syndrome (ARDS) may improve patient care and outcome. The Clinical utilisation of respiratory elastance (CURE) trial is a two-arm, randomised controlled trial (RCT) investigating the performance of PEEP selected at an objective, model-based minimal respiratory system elastance in patients with ARDS.METHODS AND DESIGN:The CURE RCT compares two groups of patients requiring invasive MV with a partial pressure of arterial oxygen/fraction of inspired oxygen (PaO2/FiO2) ratio?≤?200; one criterion of the Berlin consensus definition of moderate (≤?200) or severe (≤?100) ARDS. All patients are ventilated using pressure controlled (bi-level) ventilation with tidal volume?=?6-8?ml/kg. Patients randomised to the control group will have PEEP selected per standard practice (SPV). Patients randomised to the intervention will have PEEP selected based on a minimal elastance using a model-based computerised method. The CURE RCT is a single-centre trial in the intensive care unit (ICU) of Christchurch hospital, New Zealand, with a target sample size of 320 patients over a maximum of 3?years. The primary outcome is the area under the curve (AUC) ratio of arterial blood oxygenation to the fraction of inspired oxygen over time. Secondary outcomes include length of time of MV, ventilator-free days (VFD) up to 28?days, ICU and hospital length of stay, AUC of oxygen saturation (SpOsub2/sub)/FiOsub2/sub during MV, number of desaturation events (SpOsub2/sub??88%), changes in respiratory mechanics and chest x-ray index scores, rescue therapies (prone positioning, nitric oxide use, extracorporeal membrane oxygenation) and hospital and 90-day mortality.DISCUSSION:The CURE RCT is the first trial comparing significant clinical outcomes in patients with ARDS in whom PEEP is selected at minimum elastance using an objective model-based method able to quantify and consider both inter-patient and intra-patient variability. CURE aims to demonstrate the hypothesized benefit of patient-specific PEEP and attest to the significance of real-time monitoring and decision-support for MV in the critical care environment.TRIAL REGISTRATION:Australian New Zealand Clinical Trial Registry, ACTRN12614001069640. Registered on 22 September 2014. (https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=366838&isReview=true) The CURE RCT clinical protocol and data usage has been granted by the New Zealand South Regional Ethics Committee (Reference number: 14/STH/132).
机译:背景:急性呼吸窘迫综合征(ARDS)患者的机械通风(MV)期间的正末端呼气压力(PEEP)可能改善患者护理和结果。呼吸弹性(固化)试验的临床利用是一种双臂,随机对照试验(RCT)调查在ARDS的患者患者的目的,基于模型的最小呼吸系统系统弹性时选择的窥视性能。方法和设计:治愈RCT比较了两组患者,需要侵入式MV,其中动脉氧的分压/氧气(PAO2 / FIO2)比率的分数(PAO2 / FIO2)比例Δ≤≤200;柏林共识定义的一个标准适度(≤α100)或严重(≤≤100)ARDS。所有患者均使用潮气量的压力控制(Bi-Level)通气通风Δ=Δ= 6-8?ml / kg。随机向对照组患者每标准做法选择窥视(SPV)。随机随机化的患者将根据基于模型的计算机化方法基于最小的弹性来选择窥视。固化RCT是新西兰基督城医院密集护理单位(ICU)的单一中心试验,目标样本大小为320名患者,最多3年。主要结果是动脉血氧曲线(AUC)比率在动脉血氧随时间随时间的氧气分数的比例。二次结果包括MV的时间长度,无呼吸机的天(VFD)高达28?天,ICU和医院住院时间,氧饱和度(SPO 2 )/ FIO 2 在MV期间,去饱和事件的数量(SPO 2 ?<?88%),呼吸力学和胸部X射线指数分数的变化,救援疗法(易于定位,一氧化氮使用,体外膜氧合)和医院和90天死亡率。探讨:治愈RCT是使用能够量化和考虑的目标模型的方法在最小弹性中选择窥视患者的第一次试验。患者间和患者内部变异性。治疗方法旨在展示患者特异性窥视的假设益处,并证明在关键护理环境中对MV的实时监测和决策支持的重要性.TTIAL注册:澳大利亚新西兰临床试验登记处,ACTRN12614001069640。 2014年9月22日注册。(https://www.anzctr.org.au/trier/registration/trialreview.aspx?id=366838&isreview=true)Cure RCT临床协议和数据使用量由新西兰南部地区授予道德委员会(参考号:14 / StH / 132)。

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