Influence of the end inspiratory pause on respiratory mechanics and tidal gas distribution of surgical patients ventilated under a tailored open lung approach strategy: A randomised, crossover trial

高原压力 医学 潮气量 交叉研究 呼吸生理学 平均气道压 麻醉 最大吸气压力 机械通风 呼气末正压 气道 肺顺应性 通风(建筑) 呼吸系统 呼吸频率 内科学 血压 心率 病理 替代医学 工程类 机械工程 安慰剂
作者
Daniel López-Herrera,Manuel de la Matta
出处
期刊:Anaesthesia, critical care & pain medicine [Elsevier BV]
卷期号:41 (2): 101038-101038 被引量:6
标识
DOI:10.1016/j.accpm.2022.101038
摘要

The effect of modifying the end inspiratory pause (EIP) on respiratory mechanics and gas distribution of surgical patients ventilated with an open lung approach (OLA) has not been addressed before.Prospective, randomised, crossover study carried out in a tertiary hospital. Subjects were assigned to receive an initial EIP of 10% or 30% of the total inspiratory time. We compared standard ventilation [time 0: tidal volume (VT) 7 mL × kg-1, respiratory rate (RR) 13, inspiratory:expiratory (I:E) rate 1:2, positive end-expiratory pressure (PEEP) 5 cm H2O and EIP 10% and 30% for groups 1 and 2, respectively) with tailored OLA (similar parameters except for a tailored PEEP after a stepwise recruitment manoeuvre), followed by a crossover assignment sequence between groups (times 2-4).We included 32 adult subjects undergoing major surgery. Tailored OLA strategy was associated with a significant increase in PEEP, plateau pressure (Pplat), PaO2, and compliance of the respiratory system (CRS) with a significant decrease in driving pressure (Pdriv) and PaCO2, and a more homogeneous gas distribution in both groups. A significantly lower PEEP (p < 0.001), Pdriv (5 [5-6] versus 6.5 [6-8] cmH2O; p < 0.001) and mean airway pressure (Pmean; p < 0.001) together with a higher CRS (77 [67-87] versus 58 [52-70] ml*cmH2O-1; p < 0.001) were observed when an EIP of 30% was applied as compared to an EIP of 10%.The use of a tailored OLA strategy combined with a longer EIP is associated with a higher CRS, and a lower Pdriv, Pmean and PEEP. Additional studies are necessary to assess if the improved ventilatory conditions observed with a longer EIP are associated with better patients' outcomes. Trial registration at clinicaltrials.gov with identifier: NCT03568786.
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