Best PEEP trials are dependent on tidal volume
© The Author(s). 2018
Received: 11 April 2018
Accepted: 17 April 2018
Published: 2 May 2018
Determining the optimal positive end-expiratory pressure (PEEP) in patients with acute respiratory distress syndrome remains an area of active investigation. Most trials individualizing PEEP optimize one physiologic parameter (e.g., driving pressure) by titrating PEEP while holding other ventilator settings constant. Optimal PEEP, however, may depend on the tidal volume, and changing the tidal volume with which a best PEEP trial is performed may lead to different best PEEP settings in the same patient.
ClinicalTrials.gov, NCT02871102. Registered on 12 August 2016.
Positive end-expiratory pressure (PEEP) may mitigate ventilator-induced lung injury in acute respiratory distress syndrome (ARDS) by recruiting collapsed alveolar units, thereby reducing stress raisers and minimizing atelectrauma . Excessive PEEP, however, may cause barotrauma and biotrauma from alveolar hyperdistension. Many studies have attempted to identify the best PEEP for individual patients , including the recent Alveolar Recruitment for ARDS Trial (ART) which reported a higher mortality with use of a recruitment maneuver and titrated PEEP compared with use of lower PEEP .
Our findings suggest one possible mechanism for the ART results. The ART intervention utilized a decremental PEEP trial at a VT of 5 ml/kg predicted body weight (PBW), and then set PEEP at 2 cmH2O above the PEEP level found to have the maximal CRS. If multiple PEEP levels had CRS measures within 1 ml/cmH2O, the highest PEEP level was chosen. This protocol likely resulted in the use of PEEP levels in the intervention arm associated with a stress index of > 1.05, suggesting the presence of tidal hyperinflation , as demonstrated in our patient by the vertical lines in Fig. 1. Moreover, the curves predict an even greater degree of tidal hyperinflation for patients whose highest PEEP based on maximal compliance was set at one VT, but who then received a higher VT for clinical management. Indeed, in the ART trial, intervention patients had a day 1 mean VT of 5.6 ml/kg PBW, implying that many received a VT above that used to select the optimum PEEP.
How to individualize PEEP for patients with ARDS remains a conundrum. Our finding is important because it implies that carefully titrated PEEP may not apply outside of the ventilator parameters with which PEEP was tested and that changes in tidal volume likely influence optimal PEEP.
ACM was supported by the Vanderbilt Institute for Clinical and Translational Research (UL1 TR000445 from NCATS/NIH). MWS was supported by a National Heart, Lung, and Blood Institute (NHLBI) K12 award (K12HL133117). ACM and TWR received nonmonetary support from Maquet in the form of access to ServoTracker software and the ventilator Stress Index module for research purposes only. The funding institutions had no role in the conception, design, or conduct of the study; the collection, management, analysis, interpretation, or presentation of the data; or the preparation of the manuscript.
Availability of data and materials
The datasets generated during the current study are available from the corresponding author on reasonable request.
ACM, MWS, and TWR contributed to the study concept and design. ACM was responsible for acquisition of data. ACM, MWS, and TWR analyzed and interpreted the data. ACM and MWS drafted the manuscript. TWR critically revised the manuscript for important intellectual content. All authors read and approved the final manuscript.
Ethics approval and consent to participate
The study was approved by the Vanderbilt University Institutional Review Board (IRB# 160770) with informed consent obtained by patient surrogate.
Maquet was given the opportunity to review the manuscript prior to submission to ensure the absence of Maquet Confidential Information. The authors declare that they have no potential conflicts of interest.
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