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Latent Class Analysis Reveals COVID-19-related Acute Respiratory Distress Syndrome Subgroups with Differential Responses to Corticosteroids.
Sinha, Pratik; Furfaro, David; Cummings, Matthew J; Abrams, Darryl; Delucchi, Kevin; Maddali, Manoj V; He, June; Thompson, Alison; Murn, Michael; Fountain, John; Rosen, Amanda; Robbins-Juarez, Shelief Y; Adan, Matthew A; Satish, Tejus; Madhavan, Mahesh; Gupta, Aakriti; Lyashchenko, Alexander K; Agerstrand, Cara; Yip, Natalie H; Burkart, Kristin M; Beitler, Jeremy R; Baldwin, Matthew R; Calfee, Carolyn S; Brodie, Daniel; O'Donnell, Max R.
  • Sinha P; Department of Anesthesiology, Washington University Medical School, Saint Louis, Missouri.
  • Furfaro D; Division of Pulmonary, Allergy, and Critical Care Medicine.
  • Cummings MJ; Division of Pulmonary, Allergy, and Critical Care Medicine.
  • Abrams D; Division of Pulmonary, Allergy, and Critical Care Medicine.
  • Delucchi K; Department of Psychiatry & Behavioral Sciences.
  • Maddali MV; Department of Medicine.
  • He J; Department of Anesthesiology, Washington University Medical School, Saint Louis, Missouri.
  • Thompson A; Division of Pulmonary, Allergy, and Critical Care Medicine.
  • Murn M; Division of Pulmonary, Allergy, and Critical Care Medicine.
  • Fountain J; Department of Internal Medicine, and.
  • Rosen A; Department of Internal Medicine, and.
  • Robbins-Juarez SY; Vagelos College of Physicians and Surgeons, Columbia University, New York, New York.
  • Adan MA; Vagelos College of Physicians and Surgeons, Columbia University, New York, New York.
  • Satish T; Vagelos College of Physicians and Surgeons, Columbia University, New York, New York.
  • Madhavan M; Division of Cardiology, Department of Medicine.
  • Gupta A; Division of Cardiology, Department of Medicine.
  • Lyashchenko AK; Department of Pathology and Cell Biology, Columbia University Irving Medical Center and NewYork-Presbyterian Hospital, New York, New York.
  • Agerstrand C; Division of Pulmonary, Allergy, and Critical Care Medicine.
  • Yip NH; Division of Pulmonary, Allergy, and Critical Care Medicine.
  • Burkart KM; Division of Pulmonary, Allergy, and Critical Care Medicine.
  • Beitler JR; Division of Pulmonary, Allergy, and Critical Care Medicine.
  • Baldwin MR; Division of Pulmonary, Allergy, and Critical Care Medicine.
  • Calfee CS; Department of Medicine, Division of Pulmonary, Critical Care, Allergy and Sleep Medicine.
  • Brodie D; Cardiovascular Research Institute, and.
  • O'Donnell MR; Department of Anesthesia, University of California, San Francisco, San Francisco, California; and.
Am J Respir Crit Care Med ; 204(11): 1274-1285, 2021 12 01.
Article in English | MEDLINE | ID: covidwho-1546620
ABSTRACT
Rationale Two distinct subphenotypes have been identified in acute respiratory distress syndrome (ARDS), but the presence of subgroups in ARDS associated with coronavirus disease (COVID-19) is unknown.

Objectives:

To identify clinically relevant, novel subgroups in COVID-19-related ARDS and compare them with previously described ARDS subphenotypes.

Methods:

Eligible participants were adults with COVID-19 and ARDS at Columbia University Irving Medical Center. Latent class analysis was used to identify subgroups with baseline clinical, respiratory, and laboratory data serving as partitioning variables. A previously developed machine learning model was used to classify patients as the hypoinflammatory and hyperinflammatory subphenotypes. Baseline characteristics and clinical outcomes were compared between subgroups. Heterogeneity of treatment effect for corticosteroid use in subgroups was tested. Measurements and Main

Results:

From March 2, 2020, to April 30, 2020, 483 patients with COVID-19-related ARDS met study criteria. A two-class latent class analysis model best fit the population (P = 0.0075). Class 2 (23%) had higher proinflammatory markers, troponin, creatinine, and lactate, lower bicarbonate, and lower blood pressure than class 1 (77%). Ninety-day mortality was higher in class 2 versus class 1 (75% vs. 48%; P < 0.0001). Considerable overlap was observed between these subgroups and ARDS subphenotypes. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RT-PCR cycle threshold was associated with mortality in the hypoinflammatory but not the hyperinflammatory phenotype. Heterogeneity of treatment effect to corticosteroids was observed (P = 0.0295), with improved mortality in the hyperinflammatory phenotype and worse mortality in the hypoinflammatory phenotype, with the caveat that corticosteroid treatment was not randomized.

Conclusions:

We identified two COVID-19-related ARDS subgroups with differential outcomes, similar to previously described ARDS subphenotypes. SARS-CoV-2 PCR cycle threshold had differential value for predicting mortality in the subphenotypes. The subphenotypes had differential treatment responses to corticosteroids.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Distress Syndrome / Adrenal Cortex Hormones / Latent Class Analysis / COVID-19 Drug Treatment Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Long Covid Limits: Aged / Female / Humans / Male / Middle aged Language: English Journal: Am J Respir Crit Care Med Journal subject: Critical Care Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Distress Syndrome / Adrenal Cortex Hormones / Latent Class Analysis / COVID-19 Drug Treatment Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Long Covid Limits: Aged / Female / Humans / Male / Middle aged Language: English Journal: Am J Respir Crit Care Med Journal subject: Critical Care Year: 2021 Document Type: Article