Longitudinal respiratory subphenotypes in patients with COVID-19-related acute respiratory distress syndrome: results from three observational cohorts

被引:83
|
作者
Bos, Lieuwe D. J. [1 ,2 ]
Sjoding, Michael [3 ]
Sinha, Pratik [4 ]
Bhavani, Sivasubramanium, V [5 ,6 ]
Lyons, Patrick G. [4 ]
Bewley, Alice F. [4 ]
Botta, Michela [1 ,2 ]
Tsonas, Anissa M. [1 ,2 ]
Neto, Ary Serpa [1 ,2 ,7 ,8 ,9 ,10 ]
Schultz, Marcus J. [1 ,2 ,11 ,12 ]
Dickson, Robert P. [3 ]
Paulus, Frederique [1 ,2 ]
机构
[1] Amsterdam UMC, Dept Intens Care, NL-1105 AZ Amsterdam, Netherlands
[2] Amsterdam UMC, Lab Expt Intens Care & Anaesthesiol LEICA, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Michigan, Div Pulm & Crit Care Med, Ann Arbor, MI 48109 USA
[4] Washington Univ, Sch Med, St Louis, MO USA
[5] Univ Chicago, Dept Med, 5841 S Maryland Ave, Chicago, IL 60637 USA
[6] Emory Univ, Dept Med, Atlanta, GA 30322 USA
[7] Monash Univ, Australian & New Zealand Intens Care Res Ctr ANZI, Melbourne, Vic, Australia
[8] Hosp Israelita Albert Einstein, Dept Crit Care Med, Sao Paulo, Brazil
[9] Ctr Austin Hosp, Melbourne, Vic, Australia
[10] Univ Melbourne, Melbourne, Vic, Australia
[11] Univ Oxford, Nuffield Dept Med, Oxford, England
[12] Mahidol Univ, Mahidol Oxford Trop Med Res Unit MORU, Bangkok, Thailand
来源
LANCET RESPIRATORY MEDICINE | 2021年 / 9卷 / 12期
关键词
D O I
10.1016/S2213-2600(21)00365-9
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background Patients with COVID-19-related acute respiratory distress syndrome (ARDS) have been postulated to present with distinct respiratory subphenotypes. However, most phenotyping schema have been limited by sample size, disregard for temporal dynamics, and insufficient validation. We aimed to identify respiratory subphenotypes of COVID-19-related ARDS using unbiased data-driven approaches. Methods PRoVENT-COVID was an investigator-initiated, national, multicentre, prospective, observational cohort study at 22 intensive care units (ICUs) in the Netherlands. Consecutive patients who had received invasive mechanical ventilation for COVID-19 (aged 18 years or older) served as the derivation cohort, and similar patients from two ICUs in the USA served as the replication cohorts. COVID-19 was confirmed by positive RT-PCR. We used latent class analysis to identify subphenotypes using clinically available respiratory data cross-sectionally at baseline, and longitudinally using 8-hourly data from the first 4 days of invasive ventilation. We used group-based trajectory modelling to evaluate trajectories of individual variables and to facilitate potential clinical translation. The PRoVENT-COVID study is registered with ClinicalTrials.gov, NCT04346342. Findings Between March 1, 2020, and May 15, 2020, 1007 patients were admitted to participating ICUs in the Netherlands, and included in the derivation cohort. Data for 288 patients were included in replication cohort 1 and 326 in replication cohort 2. Cross-sectional latent class analysis did not identify any underlying subphenotypes. Longitudinal latent dass analysis identified two distinct subphenotypes. Subphenotype 2 was characterised by higher mechanical power, minute ventilation, and ventilatory ratio over the first 4 days of invasive mechanical ventilation than subphenotype 1, but PaO2/FiO(2), pH, and compliance of the respiratory system did not differ between the two subphenotypes. 185 (28%) of 671 patients with subphenotype 1 and 109 (32%) of 336 patients with subphenotype 2 had died at day 28 (p=0.10). However, patients with subphenotype 2 had fewer ventilator-free days at day 28 (median 0, IQR 0-15 vs 5, 0-17; p=0.016) and more frequent venous thrombotic events (109[32%] of 336 patients vs 176 [26%] of 671 patients; p=0.048) compared with subphenotype 1. Group-based trajectory modelling revealed trajectories of ventilatory ratio and mechanical power with similar dynamics to those observed in latent class analysis-derived trajectory subphenotypes. The two trajectories were: a stable value for ventilatory ratio or mechanical power over the first 4 days of invasive mechanical ventilation (trajectory A) or an upward trajectory (trajectory B). However, upward trajectories were better independent prognosticators for 28-day mortality (OR 1.64, 95% CI 1.17-2.29 for ventilatory ratio; 1.82, 1.24-2.66 for mechanical power). The association between upward ventilatory ratio trajectories (trajectory B) and 28-day mortality was confirmed in the replication cohorts (OR 4.65, 95% CI 1. 87-11 6 for ventilatory ratio in replication cohort 1; 1-89, 1.05-3-37 for ventilatory ratio in replication cohort 2). Interpretation At baseline, COVID-19-related ARDS has no consistent respiratory subphenotype. Patients diverged from a fairly homogenous to a more heterogeneous population, with trajectories of ventilatory ratio and mechanical power being the most discriminatory. Modelling these parameters alone provided prognostic value for duration of mechanical ventilation and mortality. Copyright (C) 2021 Published by Elsevier Ltd. All rights reserved.
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收藏
页码:1377 / 1386
页数:10
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