Factors Associated with an Electronic Health Record-Based Definition of Post-Acute Sequelae of COVID-19 in Patients with Systemic Autoimmune Rheumatic Disease.


Journal

The Journal of rheumatology
ISSN: 1499-2752
Titre abrégé: J Rheumatol
Pays: Canada
ID NLM: 7501984

Informations de publication

Date de publication:
01 Mar 2024
Historique:
medline: 2 3 2024
pubmed: 2 3 2024
entrez: 1 3 2024
Statut: aheadofprint

Résumé

Many individuals with rheumatic disease are at higher risk for severe acute COVID-19. We aimed to evaluate risk factors for Post-Acute Sequelae of COVID-19 (PASC) using an electronic health record (EHR)-based definition. We identified patients with prevalent rheumatic diseases and COVID-19 at Mass General Brigham. PASC was defined by ICD codes, relevant labs, vital signs, and medications, at least 30 days following the first COVID-19 infection. Patients were followed until the earliest of incident PASC, repeat COVID-19 infection, 1 year of follow-up, death, or February 19, 2023. We used multivariable Cox regression to estimate the association of baseline characteristics with PASC risk. Among 2,459 patients (76.37% female, mean age 57.4 years), the most common incident PASC manifestations were cough (14.56%), dyspnea (12.36%), constipation (11.39%), and fatigue (10.70%). Serious manifestations including acute coronary disease (4.43%), thromboembolism (3.09%), hypoxemia (3.09%), stroke (1.75%), and myocarditis (0.12%) were rare. The Delta wave (aHR 0.63, 95% CI: 0.49-0.82) and Omicron era (aHR 0.50, 95% CI: 0.41-0.62) were associated with lower risk of PASC than the early pandemic (March 2020-June 2021). Age, obesity, comorbidity burden, race, and hospitalization for acute COVID-19 infection were associated with greater risk of PASC. Among patients with rheumatic diseases, following their first COVID-19 infection, using an EHR-based definition, we found a decreased risk of PASC over calendar time. Aside from glucocorticoids, no specific immunomodulatory medications were associated with increased risk, and risk factors were otherwise similar to those seen in the general population.

Identifiants

pubmed: 38428964
pii: jrheum.2023-1092
doi: 10.3899/jrheum.2023-1092
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Naomi J Patel (NJ)

Naomi J. Patel, MD, MPH, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston, MA, USA; Harvard Medical School, Boston, MA, USA; Rheumatology and Allergy Clinical Epidemiology Research Center, Mongan Institute.

Xiaosong Wang (X)

Xiaosong Wang MS, Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.

Miao Lin (M)

Miao Lin, MS, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston, MA, USA; Rheumatology and Allergy Clinical Epidemiology Research Center, Mongan Institute.

Emily N Kowalski (EN)

Emily N. Kowalski, BS, Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.

Claire E Cook (CE)

Claire E. Cook, MPH, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston, MA, USA; Rheumatology and Allergy Clinical Epidemiology Research Center, Mongan Institute.

Kathleen M M Vanni (KMM)

Kathleen M.M. Vanni, BA, Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.

Krishan Guzzo (K)

Krishan Guzzo, BA, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston, MA, USA; Rheumatology and Allergy Clinical Epidemiology Research Center, Mongan Institute.

Grace Qian (G)

Grace Qian, BA&Sc, Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.

Katarina J Bade (KJ)

Katarina J. Bade, BS, Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.

Alene Saavedra (A)

Alene Saavedra, BA, Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.

Rathnam Venkat (R)

Rathnam Venkat, BS, Tufts University School of Medicine, Boston, MA, USA.

Shruthi Srivatsan (S)

Shruthi Srivatsan, BS, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston, MA, USA; Rheumatology and Allergy Clinical Epidemiology Research Center, Mongan Institute.

Zachary K Williams (ZK)

Zachary K. Williams, BS, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston, MA, USA; Rheumatology and Allergy Clinical Epidemiology Research Center, Mongan Institute.

Jennifer S Hanberg (JS)

Jennifer S. Hanberg, MD, Harvard Medical School, Boston, MA, USA; Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.

Yumeko Kawano (Y)

Yumeko Kawano, MD, Harvard Medical School, Boston, MA, USA; Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.

Abigail E Schiff (AE)

Abigail E. Schiff, MD, PhD2,6; Jeffrey A. Sparks, MD, MMSc, Harvard Medical School, Boston, MA, USA; Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.

Jeffrey A Sparks (JA)

Zachary S. Wallace, MD, MSc, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston, MA, USA; Harvard Medical School, Boston, MA, USA; Rheumatology and Allergy Clinical Epidemiology Research Center, Mongan Institute.

Classifications MeSH