ArticleRheumatology international2025
The mortality and acute complications of large vessel vasculitis patients hospitalized with COVID-19 in the US: a nationwide inpatient sample analysis (2020).
Article in Rheumatology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Vasculitis syndromes: the pathogenic roles of COVID-19 and related vaccinations.Virology journal · 2025Review
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
COVID-19 was an emerging pandemic in 2020 which resulted in millions of deaths worldwide. It has been known that COVID-19 can cause secondary vasculitis. However, the impact of large vessel vasculitis, giant cell arteritis (GCA) and Takayasu (TAK), on COVID-19 infection is not known. This retrospective analysis used data from the US National Inpatient Survey 2020. Patients of all ages hospitalized due to COVID-19 in 2020 were identified on the database. A primary diagnosis of COVID-19 and a secondary diagnosis of LVV were included. Characteristics of patients, comorbidities, and clinical outcomes were compared. The primary outcome was the mortality rate. Secondary outcomes included resource utilization and acute in-hospital complications of COVID-19 infection. Multivariate logistic regression and univariate logistic regression analyses were conducted, with P values < 0.05 considered statistically significant. A total of 675 patients hospitalized with COVID-19 had concurrent LVV. Patients with LVV were older (73.70 vs 62.61; P < 0.001) and more likely female (75.00% vs 48.20%; p < 0.001). There is no difference in in-hospital mortality of COVID patients with and without LVV (aOR 0.95, p = 0.834), GCA (aOR 0.94, p = 0.827), or TAK (aOR 2.30, p = 0.394). There is an increase in the in-hospital risk of developing acute MI in COVID patients with LVV (aOR = 1.54; p = 0.04) but not with subgroup GCA and TAK. There were no significant differences in resource utilization and other acute in-hospital complications. Hospitalized COVID-19 patients with LVV and GCA were more likely to develop acute MI than those without. Further studies are required to minimize confounders to better explore the causal relationship of COVID-19 and LVV.
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