New-Onset Rheumatic Immune-Mediated Inflammatory Diseases Following SARS-CoV-2 Vaccinations until May 2023: A Systematic Review.
Albert Selva-O'CallaghanVictor DurkowskiS Sujitha PillayBhupen BarmanHelen ElwellKaustubh BoraSyed BilgramiSajid MahmoodNasarulla BabajanSrinivasan VenkatachalamLesley OttewellCiro ManzoPublished in: Vaccines (2023)
A comprehensive, up-to-date systematic review (SR) of the new-onset rheumatic immune-mediated inflammatory diseases (R-IMIDs) following COVID-19 vaccinations is lacking. Therefore, we investigated the demographics, management, and prognosis of new R-IMIDs in adults following SARS-CoV-2 vaccinations. A systematic literature search of Medline, Embase, Google Scholar, LitCovid, and Cochrane was conducted. We included any English-language study that reported new-onset R-IMID in adults following the post-COVID-19 vaccination. A total of 271 cases were reported from 39 countries between January 2021 and May 2023. The mean age of patients was 56 (range 18-90), and most were females (170, 62.5%). Most (153, 56.5%) received the Pfizer BioNTech COVID-19 vaccine. Nearly 50% of patients developed R-IMID after the second dose of the vaccine. Vasculitis was the most prevalent clinical presentation (86, 31.7%), followed by connective tissue disease (66, 24.3%). The mean duration between the vaccine's 'trigger' dose and R-IMID was 11 days. Most (220, 81.2%) received corticosteroids; however, 42% (115) received DMARDs such as methotrexate, cyclophosphamide, tocilizumab, anakinra, IV immunoglobulins, plasma exchange, or rituximab. Complete remission was achieved in 75 patients (27.7%), and 137 (50.6%) improved following the treatment. Two patients died due to myositis. This SR highlights that SARS-CoV-2 vaccines may trigger R-IMID; however, further epidemiology studies are required.
Keyphrases
- sars cov
- systematic review
- end stage renal disease
- ejection fraction
- newly diagnosed
- coronavirus disease
- prognostic factors
- rheumatoid arthritis
- respiratory syndrome coronavirus
- randomized controlled trial
- autism spectrum disorder
- patient reported outcomes
- high resolution
- mass spectrometry
- systemic sclerosis
- risk factors
- patient reported
- idiopathic pulmonary fibrosis
- hodgkin lymphoma