TY - JOUR
T1 - Awake Prone Positioning in Adults With COVID-19
T2 - An Individual Participant Data Meta-Analysis
AU - Awake Prone Positioning Meta-Analysis Group
AU - Luo, Jian
AU - Pavlov, Ivan
AU - Tavernier, Elsa
AU - Perez, Yonatan
AU - Kharat, Aileen
AU - McNicholas, Bairbre
AU - Roca, Oriol
AU - Vines, David L
AU - Ibarra-Estrada, Miguel
AU - Alhazzani, Waleed
AU - Lewis, Kimberley
AU - Simpson, Steven Q
AU - Rampon, Garrett
AU - Liu, Ling
AU - Sun, Qin
AU - Qiu, Haibo
AU - Yang, Yi
AU - Lapadula, Giuseppe
AU - Qian, Edward Tang
AU - Gatto, Cheryl L
AU - Rice, Todd W
AU - Parhar, Ken Kuljit S
AU - Weatherald, Jason
AU - Walkey, Allan J
AU - Bosch, Nicholas A
AU - Nay, Mai-Anh
AU - Boulain, Thierry
AU - Fossat, Guillaume
AU - Harris, Tim R E
AU - Thwaites, C Louise
AU - Phong, Nguyen Thanh
AU - Bonfanti, Paolo
AU - Yarahmadi, Sajad
AU - Hashemian, Seyed Mohammadreza
AU - Jayakumar, Devachandran
AU - Taylor, Stephanie Parks
AU - Johnson, Stacy A
AU - Guerin, Claude
AU - Laffey, John G
AU - Ehrmann, Stephan
AU - Li, Jie
PY - 2025/5/1
Y1 - 2025/5/1
N2 - IMPORTANCE: The impact of awake prone positioning (APP) on clinical outcomes in patients with COVID-19 and acute hypoxemic respiratory failure (AHRF) remains uncertain.OBJECTIVE: To assess the association of APP with improved clinical outcomes among patients with COVID-19 and AHRF, and to identify potential effect modifiers.DATA SOURCES: PubMed, Embase, the Cochrane Library, and ClinicalTrials.gov were searched through August 1, 2024.STUDY SELECTION: Randomized clinical trials (RCTs) examining APP in adults with COVID-19 and AHRF that reported intubation rate or mortality were included.DATA EXTRACTION AND SYNTHESIS: Individual participant data (IPD) were extracted according to PRISMA-IPD guidelines. For binary outcomes, logistic regression was used and odds ratio (OR) and 95% CIs were reported, while for continuous outcomes, linear regression was used and mean difference (MD) and 95% CIs were reported.MAIN OUTCOMES AND MEASURES: The primary outcome was survival without intubation. Secondary outcomes included intubation, mortality, death without intubation, death after intubation, escalation of respiratory support, intensive care unit (ICU) admission, time from enrollment to intubation and death, duration of invasive mechanical ventilation, and hospital and ICU lengths of stay.RESULTS: A total of 14 RCTs involving 3019 patients were included; 1542 patients in the APP group (mean [SD] age, 59.3 [14.1] years; 1048 male [68.0%]) and 1477 in the control group (mean [SD] age, 59.9 [14.1] years; 979 male [66.3%]). APP improved survival without intubation (OR, 1.42; 95% CI, 1.20-1.68), and it reduced the risk of intubation (OR, 0.70; 95% CI, 0.59-0.84) and hospital mortality (OR, 0.77; 95% CI, 0.63-0.95). APP also extended the time from enrollment to intubation (MD, 0.93 days; 95% CI, 0.43 to 1.42 days). In exploratory subgroup analyses, improved survival without intubation was observed in patients younger than age 68 years, as well as in patients with a body mass index of 26 to 30, early implementation of APP (ie, less than 1 day from hospitalization), a pulse saturation to inhaled oxygen fraction ratio of 155 to 232, respiratory rate of 20 to 26 breaths per minute (bpm), and those receiving advanced respiratory support at enrollment. However, none of the subgroups had significant interaction with APP treatment. APP duration 10 or more hours/d within the first 3 days was associated with increased survival without intubation (OR, 1.85; 95% CI, 1.37-2.49).CONCLUSIONS AND RELEVANCE: This IPD meta-analysis found that in adults with COVID-19 and AHRF, APP was associated with increased survival without intubation and with reduced risks of intubation and mortality, including death after intubation. Prolonged APP duration (10 or more hours/d) was associated with better outcomes.
AB - IMPORTANCE: The impact of awake prone positioning (APP) on clinical outcomes in patients with COVID-19 and acute hypoxemic respiratory failure (AHRF) remains uncertain.OBJECTIVE: To assess the association of APP with improved clinical outcomes among patients with COVID-19 and AHRF, and to identify potential effect modifiers.DATA SOURCES: PubMed, Embase, the Cochrane Library, and ClinicalTrials.gov were searched through August 1, 2024.STUDY SELECTION: Randomized clinical trials (RCTs) examining APP in adults with COVID-19 and AHRF that reported intubation rate or mortality were included.DATA EXTRACTION AND SYNTHESIS: Individual participant data (IPD) were extracted according to PRISMA-IPD guidelines. For binary outcomes, logistic regression was used and odds ratio (OR) and 95% CIs were reported, while for continuous outcomes, linear regression was used and mean difference (MD) and 95% CIs were reported.MAIN OUTCOMES AND MEASURES: The primary outcome was survival without intubation. Secondary outcomes included intubation, mortality, death without intubation, death after intubation, escalation of respiratory support, intensive care unit (ICU) admission, time from enrollment to intubation and death, duration of invasive mechanical ventilation, and hospital and ICU lengths of stay.RESULTS: A total of 14 RCTs involving 3019 patients were included; 1542 patients in the APP group (mean [SD] age, 59.3 [14.1] years; 1048 male [68.0%]) and 1477 in the control group (mean [SD] age, 59.9 [14.1] years; 979 male [66.3%]). APP improved survival without intubation (OR, 1.42; 95% CI, 1.20-1.68), and it reduced the risk of intubation (OR, 0.70; 95% CI, 0.59-0.84) and hospital mortality (OR, 0.77; 95% CI, 0.63-0.95). APP also extended the time from enrollment to intubation (MD, 0.93 days; 95% CI, 0.43 to 1.42 days). In exploratory subgroup analyses, improved survival without intubation was observed in patients younger than age 68 years, as well as in patients with a body mass index of 26 to 30, early implementation of APP (ie, less than 1 day from hospitalization), a pulse saturation to inhaled oxygen fraction ratio of 155 to 232, respiratory rate of 20 to 26 breaths per minute (bpm), and those receiving advanced respiratory support at enrollment. However, none of the subgroups had significant interaction with APP treatment. APP duration 10 or more hours/d within the first 3 days was associated with increased survival without intubation (OR, 1.85; 95% CI, 1.37-2.49).CONCLUSIONS AND RELEVANCE: This IPD meta-analysis found that in adults with COVID-19 and AHRF, APP was associated with increased survival without intubation and with reduced risks of intubation and mortality, including death after intubation. Prolonged APP duration (10 or more hours/d) was associated with better outcomes.
KW - Humans
KW - COVID-19/therapy
KW - Prone Position
KW - SARS-CoV-2
KW - Respiratory Insufficiency/therapy
KW - Patient Positioning/methods
KW - Respiration, Artificial
KW - Wakefulness
KW - Adult
KW - Intubation, Intratracheal/statistics & numerical data
KW - Male
U2 - 10.1001/jamainternmed.2025.0011
DO - 10.1001/jamainternmed.2025.0011
M3 - Article
C2 - 40063016
SN - 2168-6106
VL - 185
SP - 572
EP - 581
JO - JAMA Internal Medicine
JF - JAMA Internal Medicine
IS - 5
ER -