1. Duration of prone position sessions: a prospective cohort study.
- Author
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Jochmans, Sebastien, Mazerand, Sandie, Chelly, Jonathan, Pourcine, Franck, Sy, Oumar, Thieulot-Rolin, Nathalie, Ellrodt, Olivier, Mercier Des Rochettes, Emmanuelle, Michaud, Gaël, Serbource-Goguel, Jean, Vinsonneau, Christophe, Vong, Ly Van Phach, and Monchi, Mehran
- Subjects
LONGITUDINAL method ,COHORT analysis ,SUPINE position ,ADULT respiratory distress syndrome - Abstract
Background: Prone position (PP) is highly recommended in moderate-to-severe ARDS. However, the optimal duration of PP sessions remains unclear. We searched to evaluate the time required to obtain the maximum physiological effect, and to search for parameters related to patient survival in PP. Methods and results: It was a prospective, monocentric, physiological study. We included in the study all prone-positioned patients in our ICU between June 2016 and January 2018. Pulmonary mechanics, data from volumetric capnography and arterial blood gas were recorded before prone positioning, 2 h after proning, before return to a supine position (SP) and 2 h after return to SP. Dynamic parameters were recorded before proning and every 30 min during the session until 24 h. 103 patients (ARDS 95%) were included performing 231 PP sessions with a mean length of 21.5 ± 5 h per session. They presented a significant increase in pH, static compliance and P
a O2 /Fi O2 with a significant decrease in Pa CO2 , Pplat , phase 3 slope of the volumetric capnography, Pet CO2 , VD /VT-phy and ΔP. The beneficial physiological effects continued after 16 h of PP and at least up to 24 h in some patients. The evolution of the respiratory parameters during the first session and also during the pooled sessions did not find any predictor of response to PP, whether before, during or 2 h after the return in SP. Conclusions: PP sessions should be prolonged at least 24 h and be extended in the event that the Pa O2 /Fi O2 ratio at 24 h remains below 150, especially since no criteria can predict which patient will benefit or not from it. Trial registration The trial has been registered on 28 June 2016 in ClinicalTrials.gov (NCT 02816190) (https://clinicaltrials.gov/ct2/show/NCT02816190?term=propocap&rank=1). [ABSTRACT FROM AUTHOR]- Published
- 2020
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