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Published in: Intensive Care Medicine 1/2018

01-01-2018 | Original

A prospective international observational prevalence study on prone positioning of ARDS patients: the APRONET (ARDS Prone Position Network) study

Authors: C. Guérin, P. Beuret, J. M. Constantin, G. Bellani, P. Garcia-Olivares, O. Roca, J. H. Meertens, P. Azevedo Maia, T. Becher, J. Peterson, A. Larsson, M. Gurjar, Z. Hajjej, F. Kovari, A. H. Assiri, E. Mainas, M. S. Hasan, D. R. Morocho-Tutillo, L. Baboi, J. M. Chrétien, G. François, L. Ayzac, L. Chen, L. Brochard, A. Mercat, for the investigators of the APRONET Study Group, the REVA Network, the Réseau recherche de la Société Française d’Anesthésie-Réanimation (SFAR-recherche) and the ESICM Trials Group

Published in: Intensive Care Medicine | Issue 1/2018

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Abstract

Introduction

While prone positioning (PP) has been shown to improve patient survival in moderate to severe acute respiratory distress syndrome (ARDS) patients, the rate of application of PP in clinical practice still appears low.

Aim

This study aimed to determine the prevalence of use of PP in ARDS patients (primary endpoint), the physiological effects of PP, and the reasons for not using it (secondary endpoints).

Methods

The APRONET study was a prospective international 1-day prevalence study performed four times in April, July, and October 2016 and January 2017. On each study day, investigators in each ICU had to screen every patient. For patients with ARDS, use of PP, gas exchange, ventilator settings and plateau pressure (Pplat) were recorded before and at the end of the PP session. Complications of PP and reasons for not using PP were also documented. Values are presented as median (1st–3rd quartiles).

Results

Over the study period, 6723 patients were screened in 141 ICUs from 20 countries (77% of the ICUs were European), of whom 735 had ARDS and were analyzed. Overall 101 ARDS patients had at least one session of PP (13.7%), with no differences among the 4 study days. The rate of PP use was 5.9% (11/187), 10.3% (41/399) and 32.9% (49/149) in mild, moderate and severe ARDS, respectively (P = 0.0001). The duration of the first PP session was 18 (16–23) hours. Measured with the patient in the supine position before and at the end of the first PP session, PaO2/FIO2 increased from 101 (76–136) to 171 (118–220) mmHg (P = 0.0001) driving pressure decreased from 14 [11–17] to 13 [10–16] cmH2O (P = 0.001), and Pplat decreased from 26 [23–29] to 25 [23–28] cmH2O (P = 0.04). The most prevalent reason for not using PP (64.3%) was that hypoxemia was not considered sufficiently severe. Complications were reported in 12 patients (11.9%) in whom PP was used (pressure sores in five, hypoxemia in two, endotracheal tube-related in two ocular in two, and a transient increase in intracranial pressure in one).

Conclusions

In conclusion, this prospective international prevalence study found that PP was used in 32.9% of patients with severe ARDS, and was associated with low complication rates, significant increase in oxygenation and a significant decrease in driving pressure.
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Metadata
Title
A prospective international observational prevalence study on prone positioning of ARDS patients: the APRONET (ARDS Prone Position Network) study
Authors
C. Guérin
P. Beuret
J. M. Constantin
G. Bellani
P. Garcia-Olivares
O. Roca
J. H. Meertens
P. Azevedo Maia
T. Becher
J. Peterson
A. Larsson
M. Gurjar
Z. Hajjej
F. Kovari
A. H. Assiri
E. Mainas
M. S. Hasan
D. R. Morocho-Tutillo
L. Baboi
J. M. Chrétien
G. François
L. Ayzac
L. Chen
L. Brochard
A. Mercat
for the investigators of the APRONET Study Group, the REVA Network, the Réseau recherche de la Société Française d’Anesthésie-Réanimation (SFAR-recherche) and the ESICM Trials Group
Publication date
01-01-2018
Publisher
Springer Berlin Heidelberg
Published in
Intensive Care Medicine / Issue 1/2018
Print ISSN: 0342-4642
Electronic ISSN: 1432-1238
DOI
https://doi.org/10.1007/s00134-017-4996-5

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