RISK FACTORS FOR INFECTION AND HEALTH IMPACTS OF THE COVID-19 PANDEMIC IN PEOPLE WITH AUTOIMMUNE DISEASES.


Journal

medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986

Informations de publication

Date de publication:
05 Feb 2021
Historique:
pubmed: 11 2 2021
medline: 11 2 2021
entrez: 10 2 2021
Statut: epublish

Résumé

People with autoimmune or inflammatory conditions who take immunomodulatory/suppressive medications may have a higher risk of novel coronavirus disease 2019 (COVID-19). Chronic disease care has also changed for many patients, with uncertain downstream consequences. Assess whether COVID-19 risk is higher among those on immunomodulating or suppressive agents and characterize pandemic-associated changes to care. Longitudinal registry study. 4666 individuals with autoimmune or inflammatory conditions followed by specialists in neurology, rheumatology, cardiology, pulmonology or gastroenterology at Johns Hopkins. Periodic surveys querying comorbidities, disease-modifying medications, exposures, COVID-19 testing and outcomes, social behaviors, and disruptions to healthcare. A total of 265 (5.6%) developed COVID-19 over 9 months of follow-up (April-December 2020). Patient characteristics (age, race, comorbidity, medication exposure) were associated with differences in social distancing behaviors during the pandemic. Glucocorticoid exposure was associated with higher odds of COVID-19 in multivariable models incorporating behavior and other potential confounders (OR: 1.43; 95%CI: 1.08, 1.89). Other medication classes were not associated with COVID-19 risk. Diabetes (OR: 1.72; 95%CI: 1.08, 2.73), cardiovascular disease (OR: 1.68; 95%CI: 1.24, 2.28), and chronic kidney disease (OR: 1.76; 95%CI: 1.04, 2.97) were each associated with higher odds of COVID-19. Pandemic-related disruption to care was common. Of the 2156 reporting pre-pandemic utilization of infusion, mental health or rehabilitative services, 975 (45.2%) reported disruptions. Individuals experiencing changes to employment or income were at highest odds of care disruption. Results may not be generalizable to all patients with autoimmune or inflammatory conditions. Information was self-reported. Exposure to glucocorticoids may increase risk of COVID-19 in people with autoimmune or inflammatory conditions. Disruption to healthcare and related services was common. Those with pandemic-related reduced income may be most vulnerable to care disruptions.

Sections du résumé

Background UNASSIGNED
People with autoimmune or inflammatory conditions who take immunomodulatory/suppressive medications may have a higher risk of novel coronavirus disease 2019 (COVID-19). Chronic disease care has also changed for many patients, with uncertain downstream consequences.
Objective UNASSIGNED
Assess whether COVID-19 risk is higher among those on immunomodulating or suppressive agents and characterize pandemic-associated changes to care.
Design UNASSIGNED
Longitudinal registry study.
Participants UNASSIGNED
4666 individuals with autoimmune or inflammatory conditions followed by specialists in neurology, rheumatology, cardiology, pulmonology or gastroenterology at Johns Hopkins.
Measurements UNASSIGNED
Periodic surveys querying comorbidities, disease-modifying medications, exposures, COVID-19 testing and outcomes, social behaviors, and disruptions to healthcare.
Results UNASSIGNED
A total of 265 (5.6%) developed COVID-19 over 9 months of follow-up (April-December 2020). Patient characteristics (age, race, comorbidity, medication exposure) were associated with differences in social distancing behaviors during the pandemic. Glucocorticoid exposure was associated with higher odds of COVID-19 in multivariable models incorporating behavior and other potential confounders (OR: 1.43; 95%CI: 1.08, 1.89). Other medication classes were not associated with COVID-19 risk. Diabetes (OR: 1.72; 95%CI: 1.08, 2.73), cardiovascular disease (OR: 1.68; 95%CI: 1.24, 2.28), and chronic kidney disease (OR: 1.76; 95%CI: 1.04, 2.97) were each associated with higher odds of COVID-19. Pandemic-related disruption to care was common. Of the 2156 reporting pre-pandemic utilization of infusion, mental health or rehabilitative services, 975 (45.2%) reported disruptions. Individuals experiencing changes to employment or income were at highest odds of care disruption.
Limitations UNASSIGNED
Results may not be generalizable to all patients with autoimmune or inflammatory conditions. Information was self-reported.
Conclusions UNASSIGNED
Exposure to glucocorticoids may increase risk of COVID-19 in people with autoimmune or inflammatory conditions. Disruption to healthcare and related services was common. Those with pandemic-related reduced income may be most vulnerable to care disruptions.

Identifiants

pubmed: 33564774
doi: 10.1101/2021.02.03.21251069
pmc: PMC7872366
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIMH NIH HHS
ID : K01 MH121582
Pays : United States
Organisme : NIAMS NIH HHS
ID : K23 AR075898
Pays : United States

Commentaires et corrections

Type : UpdateIn

Auteurs

Kathryn C Fitzgerald (KC)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.

Christopher A Mecoli (CA)

Division of Rheumatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Morgan Douglas (M)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Samantha Harris (S)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Berna Aravidis (B)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Jemima Albayda (J)

Division of Rheumatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Elias S Sotirchos (ES)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Ahmet Hoke (A)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Ana-Maria Orbai (AM)

Division of Rheumatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Michelle Petri (M)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Lisa Christopher-Stine (L)

Division of Rheumatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Alan N Baer (AN)

Division of Rheumatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Julie J Paik (JJ)

Division of Rheumatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Brittany L Adler (BL)

Division of Rheumatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Eleni Tiniakou (E)

Division of Rheumatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Homa Timlin (H)

Division of Rheumatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Pavan Bhargava (P)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Scott D Newsome (SD)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Arun Venkatesan (A)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Vinay Chaudhry (V)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Thomas E Lloyd (TE)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Carlos A Pardo (CA)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Barney J Stern (BJ)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Mark Lazarev (M)

Division of Gastroenterology and Hepatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Brindusa Truta (B)

Division of Gastroenterology and Hepatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Shiv Saidha (S)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Edward S Chen (ES)

Division of Pulmonary and Critical Care Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Michelle Sharp (M)

Division of Pulmonary and Critical Care Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Nisha Gilotra (N)

Department of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Edward K Kasper (EK)

Department of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Allan C Gelber (AC)

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Division of Rheumatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Clifton O Bingham (CO)

Division of Rheumatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Ami A Shah (AA)

Division of Rheumatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Ellen M Mowry (EM)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.

Classifications MeSH