COVID-19 versus Non-COVID-19 Acute Respiratory Distress Syndrome Comparison of Demographics, Physiologic Parameters, Inflammatory Biomarkers, and Clinical Outcomes

被引:110
作者
Bain, William [1 ,2 ,3 ]
Yang, Haopu [1 ,2 ,4 ]
Shah, Faraaz Ali [1 ,2 ,3 ]
Suber, Tomeka [1 ,2 ]
Drohan, Callie [5 ]
Al-Yousif, Nameer [5 ]
DeSensi, Rebecca S. [1 ,2 ]
Bensen, Nicole [6 ]
Schaefer, Caitlin [1 ,2 ]
Rosborough, Brian R. [1 ,2 ]
Somasundaram, Ashwin [7 ,8 ,10 ]
Workman, Creg J. [8 ,10 ]
Lampenfeld, Caleb [8 ,10 ]
Cillo, Anthony R. [8 ,10 ]
Cardello, Carly [8 ,10 ]
Shan, Feng [8 ,10 ]
Bruno, Tullia C. [8 ,10 ]
Vignali, Dario A. A. [8 ,9 ,10 ]
Ray, Prabir [1 ,2 ,10 ]
Ray, Anuradha [1 ,2 ,10 ]
Zhang, Yingze [1 ,2 ]
Lee, Janet S. [1 ,2 ]
Methe, Barbara [1 ,2 ,11 ]
McVerry, Bryan J. [1 ,2 ,11 ]
Morris, Alison [1 ,2 ,11 ]
Kitsios, Georgios D. [1 ,2 ,11 ]
机构
[1] Univ Pittsburgh, Acute Lung Injury Ctr Excellence, Dept Med, Sch Med,Div Pulm Allergy & Crit Care Med, Pittsburgh, PA USA
[2] Univ Pittsburgh, Med Ctr, Pittsburgh, PA USA
[3] Vet Affairs Pittsburgh Hlth Syst, Pittsburgh, PA USA
[4] Tsinghua Univ, Sch Med, Beijing, Peoples R China
[5] Univ Pittsburgh, Med Ctr, Dept Med, Pittsburgh, PA USA
[6] Univ Pittsburgh, Med Ctr, Dept Crit Care Med, Pittsburgh, PA USA
[7] Univ Pittsburgh, Med Ctr, Hillman Canc Ctr, Dept Med,Div Hematol Oncol, Pittsburgh, PA USA
[8] Univ Pittsburgh, Med Ctr, Hillman Canc Ctr, Tumor Microenvironm Ctr, Pittsburgh, PA USA
[9] Univ Pittsburgh, Med Ctr, Hillman Canc Ctr, Canc Immunol & Immunotherapy Program, Pittsburgh, PA USA
[10] Univ Pittsburgh, Sch Med, Dept Immunol, Pittsburgh, PA USA
[11] Univ Pittsburgh, Sch Med, Ctr Med & Microbiome, Pittsburgh, PA USA
基金
美国国家卫生研究院;
关键词
pneumonia; acute respiratory distress syndrome; SARS-CoV-2; COVID-19; SUBPHENOTYPES; EPIDEMIOLOGY; MECHANICS;
D O I
10.1513/AnnalsATS.202008-1026OC
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Rationale: There is an urgent need for improved understanding of the mechanisms and clinical characteristics of acute respiratory distress syndrome (ARDS) due to coronavirus disease (COVID-19). Objectives: To compare key demographic and physiologic parameters, biomarkers, and clinical outcomes of COVID-19 ARDS and ARDS secondary to direct lung injury from other etiologies of pneumonia. Methods: We enrolled 27 patients with COVID-19 ARDS in a prospective, observational cohort study and compared them with a historical, pre-COVID-19 cohort of patients with viral ARDS (n 5 14), bacterial ARDS (n 5 21), and ARDS due to culturenegative pneumonia (n 5 30). We recorded clinical demographics; measured respiratory mechanical parameters; collected serial peripheral blood specimens for measurement of plasma interleukin (IL)-6, IL-8, and IL-10; and followed patients prospectively for patient-centered outcomes. We conducted between-group comparisons with nonparametric tests and analyzed time-to-event outcomes with Kaplan-Meier and Cox proportional hazards models. Results: Patients with COVID-19 ARDS had higher body mass index and were more likely to be Black, or residents of skilled nursing facilities, compared with those with non-COVID-19 ARDS (P, 0.05). Patients with COVID-19 had lower delivered minute ventilation compared with bacterial and culture-negative ARDS (post hoc P, 0.01) but not compared with viral ARDS. We found no differences in static compliance, hypoxemic indices, or carbon dioxide clearance between groups. Patients with COVID-19 had lower IL-6 levels compared with bacterial and culture-negative ARDS at early time points after intubation but no differences in IL-6 levels compared with viral ARDS. Patients with COVID-19 had longer duration of mechanical ventilation but similar 60-day mortality in both unadjusted and adjusted analyses. Conclusions: COVID-19 ARDS bears several similarities to viral ARDS but demonstrates lower minute ventilation and lower systemic levels of IL-6 compared with bacterial and culturenegative ARDS. COVID-19 ARDS was associated with longer dependence on mechanical ventilation compared with non- COVID-19 ARDS. Such detectable differences of COVID-19 do not merit deviation from evidence-based management of ARDS but suggest priorities for clinical research to better characterize and treat this new clinical entity.
引用
收藏
页码:1202 / 1210
页数:9
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