Lung Ultrasound to Determine the Effect of Lower vs. Higher PEEP on Lung Aeration in Patients without ARDS—A Substudy of a Randomized Clinical Trial

Claudio Zimatore, Anna Geke Algera, Michela Botta, Charalampos Pierrakos, Ary Serpa Neto, Salvatore Grasso, Marcus J. Schultz, Luigi Pisani, Frederique Paulus, on behalf of the RELAx–Investigators

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Abstract

Background: Ventilation with lower positive end–expiratory pressure (PEEP) may cause loss of lung aeration in critically ill invasively ventilated patients. This study investigated whether a systematic lung ultrasound (LUS) scoring system can detect such changes in lung aeration in a study comparing lower versus higher PEEP in invasively ventilated patients without acute respiratory distress syndrome (ARDS). Methods: Single center substudy of a national, multicenter, randomized clinical trial comparing lower versus higher PEEP ventilation strategy. Fifty–seven patients underwent a systematic 12–region LUS examination within 12 h and between 24 to 48 h after start of invasive ventilation, according to randomization. The primary endpoint was a change in the global LUS aeration score, where a higher value indicates a greater impairment in lung aeration. Results: Thirty–three and twenty–four patients received ventilation with lower PEEP (median PEEP 1 (0–5) cm H2O) or higher PEEP (median PEEP 8 (8–8) cm H2O), respectively. Median global LUS aeration scores within 12 h and between 24 and 48 h were 8 (4 to 14) and 9 (4 to 12) (difference 1 (–2 to 3)) in the lower PEEP group, and 7 (2–11) and 6 (1–12) (difference 0 (–2 to 3)) in the higher PEEP group. Neither differences in changes over time nor differences in absolute scores reached statistical significance. Conclusions: In this substudy of a randomized clinical trial comparing lower PEEP versus higher PEEP in patients without ARDS, LUS was unable to detect changes in lung aeration.
Original languageEnglish
Article number1989
Number of pages11
JournalDiagnostics
Volume13
Issue number12
DOIs
Publication statusPublished - Jun 2023

Funding

The parent study was supported by a grant from ZonMW, the Netherlands Organization for Health Research and Development (Nederlandse organisatie voor gezondheidsonderzoek en zorginnovatie) and the Amsterdam University Medical Centers, Location AMC. The funding sources had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; or decision to submit the manuscript for publication. The parent study and this substudy were supported by a grant from ZonMW (the Netherlands Organization for Health Research and Development) and the Amsterdam University Medical Centers, Location AMC. The funders had neither a role in the design and conduct of RELAx, nor in the interpretation of the data and the preparation of the final report.

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