4.5 Article

SARS-CoV-2 breakthrough infections among vaccinated individuals with rheumatic disease: results from the COVID-19 Global Rheumatology Alliance provider registry

期刊

RMD OPEN
卷 8, 期 1, 页码 -

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/rmdopen-2021-002187

关键词

COVID-19; vaccination; antirheumatic agents

资金

  1. National Institutes of Health, NIAMS
  2. NIHR Manchester Biomedical Research Centre
  3. National Institute of Arthritis and Musculoskeletal and Skin Diseases [R01 AR077607, P30 AR070253, P30 AR072577]
  4. Rheumatology Research Foundation
  5. National Institutes of Health [K24 AR074534, P30 AR070155]
  6. National Institute for Health Research (NIHR) University College London Hospitals (UCLH) Biomedical Research Centre (BRC)

向作者/读者索取更多资源

This study analyzed the clinical characteristics of patients with rheumatic disease who developed breakthrough COVID-19 after receiving the SARS-CoV-2 vaccine. The results showed that more than half of fully vaccinated patients who required hospitalization were receiving B cell-depleting therapy or mycophenolate.
Objective While COVID-19 vaccination prevents severe infections, poor immunogenicity in immunocompromised people threatens vaccine effectiveness. We analysed the clinical characteristics of patients with rheumatic disease who developed breakthrough COVID-19 after vaccination against SARS-CoV-2. Methods We included people partially or fully vaccinated against SARS-CoV-2 who developed COVID-19 between 5 January and 30 September 2021 and were reported to the Global Rheumatology Alliance registry. Breakthrough infections were defined as occurring >= 14 days after completion of the vaccination series, specifically 14 days after the second dose in a two-dose series or 14 days after a single-dose vaccine. We analysed patients' demographic and clinical characteristics and COVID-19 symptoms and outcomes. Results SARS-CoV-2 infection was reported in 197 partially or fully vaccinated people with rheumatic disease (mean age 54 years, 77% female, 56% white). The majority (n=140/197, 71%) received messenger RNA vaccines. Among the fully vaccinated (n=87), infection occurred a mean of 112 (+/- 60) days after the second vaccine dose. Among those fully vaccinated and hospitalised (n=22, age range 36-83 years), nine had used B cell-depleting therapy (BCDT), with six as monotherapy, at the time of vaccination. Three were on mycophenolate. The majority (n=14/22, 64%) were not taking systemic glucocorticoids. Eight patients had pre-existing lung disease and five patients died. Conclusion More than half of fully vaccinated individuals with breakthrough infections requiring hospitalisation were on BCDT or mycophenolate. Further risk mitigation strategies are likely needed to protect this selected high-risk population.

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