Journal article
Phenotypes of disease severity in a cohort of hospitalized COVID-19 patients: Results from the IMPACC study
EBioMedicine, v 83, pp 104208-104208
01 Sep 2022
PMID: 35952496
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
Background Better understanding of the association between characteristics of patients hospitalized with coronavirus disease 2019 (COVID-19) and outcome is needed to further improve upon patient management. Methods Immunophenotyping Assessment in a COVID-19 Cohort (IMPACC) is a prospective, observational study of 1164 patients from 20 hospitals across the United States. Disease severity was assessed using a 7-point ordinal scale based on degree of respiratory illness. Patients were prospectively surveyed for 1 year after discharge for post -acute sequalae of COVID-19 (PASC) through quarterly surveys. Demographics, comorbidities, radiographic findings, clinical laboratory values, SARS-CoV-2 PCR and serology were captured over a 28-day period. Multivariable logistic regression was performed. Findings The median age was 59 years (interquartile range [IQR] 20); 711 (61%) were men; overall mortality was 14%, and 228 (20%) required invasive mechanical ventilation. Unsupervised clustering of ordinal score over time revealed distinct disease course trajectories. Risk factors associated with prolonged hospitalization or death by day 28 included age > 65 years (odds ratio [OR], 2.01; 95% CI 1.28-3.17), Hispanic ethnicity (OR, 1.71; 95% CI 1.13-2.57), elevated baseline creatinine (OR 2.80; 95% CI 1.63- 4.80) or troponin (OR 1.89; 95% 1.03-3.47), base-line lymphopenia (OR 2.19; 95% CI 1.61-2.97), presence of infiltrate by chest imaging (OR 3.16; 95% CI 1.96-5.10), and high SARS-CoV2 viral load (OR 1.53; 95% CI 1.17-2.00). Fatal cases had the lowest ratio of SARS-CoV-2 antibody to viral load levels compared to other trajectories over time (p=0.001). 589 survivors (51%) completed at least one survey at follow-up with 305 (52%) having at least one symptom consistent with PASC, most commonly dyspnea (56% among symptomatic patients). Female sex was the only associated risk factor for PASC. Interpretation Integration of PCR cycle threshold, and antibody values with demographics, comorbidities, and laboratory/radiographic findings identified risk factors for 28-day outcome severity, though only female sex was associ-ated with PASC. Longitudinal clinical phenotyping offers important insights, and provides a framework for immunophenotyping for acute and long COVID-19.
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Details
- Title
- Phenotypes of disease severity in a cohort of hospitalized COVID-19 patients: Results from the IMPACC study
- Creators
- Al Ozonoff - Clinical & Data Coordinating Center (CDCC); Precision Vaccines Program, Boston Children's Hospital, Boston, MA, United States.Joanna Schaenman - University of California, Los AngelesNaresh Doni Jayavelu - Benaroya Research InstituteCarly E. Milliren - Clinical & Data Coordinating Center (CDCC); Precision Vaccines Program, Boston Children's Hospital, Boston, MA, United States.Carolyn S. Calfee - University of California, San FranciscoCharles B. Cairns - Drexel UniversityMonica Kraft - University of ArizonaLindsey R. Baden - Brigham and Women's HospitalAlbert C. Shaw - Yale UniversityFlorian Krammer - Icahn School of Medicine at Mount SinaiHarm van Bakel - Icahn School of Medicine at Mount SinaiDenise A. Esserman - Yale UniversityShanshan Liu - Clinical & Data Coordinating Center (CDCC); Precision Vaccines Program, Boston Children's Hospital, Boston, MA, United States.Ana Fernandez Sesma - Icahn School of Medicine at Mount SinaiViviana Simon - Icahn School of Medicine at Mount SinaiDavid A. Hafler - Yale UniversityRuth R. Montgomery - Yale UniversitySteven H. Kleinstein - Yale UniversityOfer Levy - Brigham and Women's HospitalChristian Bime - University of ArizonaElias K. Haddad - Drexel UniversityDavid J. Erle - University of California, San FranciscoBali Pulendran - Stanford UniversityKari C. Nadeau - Stanford UniversityMark M. Davis - Stanford UniversityCatherine L. Hough - Oregon Health & Science UniversityWilliam B. Messer - Oregon Health & Science UniversityNelson I. Agudelo Higuita - University of Oklahoma Health Sciences CenterJordan P. Metcalf - University of Oklahoma Health Sciences CenterMark A. Atkinson - University of South FloridaScott C. Brakenridge - University of South FloridaDavid Corry - Michael E. DeBakey VA Medical CenterFarrah Kheradmand - Michael E. DeBakey VA Medical CenterLauren I. R. Ehrlich - The University of Texas at AustinEsther Melamed - The University of Texas at AustinGrace A. McComsey - Case Western Reserve UniversityRafick Sekaly - Case Western Reserve UniversityJoann Diray-Arce - Clinical & Data Coordinating Center (CDCC); Precision Vaccines Program, Boston Children's Hospital, Boston, MA, United States.Bjoern Peters - La Jolla Institute For Allergy & ImmunologyAlison D. Augustine - National Institute of Allergy and Infectious DiseasesElaine F. Reed - University of California, Los AngelesMatthew C. Altman - Benaroya Research InstitutePatrice M. Becker - National Institute of Allergy and Infectious DiseasesNadine Rouphael - Emory UniversityIMPACC Study Grpthe IMPACC study group membersBarry Brent Simmons - Family (Community and Preventive) Medicine
- Publication Details
- EBioMedicine, v 83, pp 104208-104208
- Publisher
- Elsevier
- Number of pages
- 16
- Grant note
- 5R01AI135803-03; 5U19AI118608-04; 5U19 AI128910-04; 4U19AI090023-11; 4U19AI118610-06; R01AI145835-01A1S1; 5U19AI062 6 2 9-17; 5U19AI05722 9-17; 5U19AI125357-05; 5U19AI128913-03; 3U19AI077439-13; 5U54AI142766-03; 5R01AI104870-07; 3U19AI089992-09; 3U19AI128913-03 / United States National Insti-tutes of Health; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- College of Medicine; Infectious Diseases (and HIV Medicine); Family (Community and Preventive) Medicine
- Web of Science ID
- WOS:000848658800005
- Scopus ID
- 2-s2.0-85135716647
- Other Identifier
- 991019184178304721
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- Collaboration types
- Domestic collaboration
- Web of Science research areas
- Medicine, Research & Experimental