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BNT162b2 mRNA COVID-19 vaccine and booster in patients with autoimmune rheumatic diseases: a national cohort study.
Bieber, Amir; Sagy, Iftach; Novack, Lena; Brikman, Shay; Abuhasira, Ran; Ayalon, Snait; Novofastovski, Irina; Abu-Shakra, Mahmoud; Mader, Reuven.
  • Bieber A; Rheumatology, Emek Medical Center, Afula, Northern, Israel amir.bieber@gmail.com.
  • Sagy I; Clinical Research Center, Soroka University Medical Center, Beer Sheva, Israel.
  • Novack L; Rheumatology, Soroka Medical Center, Beer Sheva, Israel.
  • Brikman S; Faculty of Medicine, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
  • Abuhasira R; Clinical Research Center, Soroka University Medical Center, Beer Sheva, Israel.
  • Ayalon S; Rheumatology, Emek Medical Center, Afula, Northern, Israel.
  • Novofastovski I; Technion Israel Institute of Technology The Ruth and Bruce Rappaport Faculty of Medicine, Haifa, Israel.
  • Abu-Shakra M; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Mader R; Department Medicine B, Rabin Medical Center Beilinson Hospital, Petah Tikva, Israel.
Ann Rheum Dis ; 81(7): 1028-1035, 2022 07.
Article in English | MEDLINE | ID: covidwho-1788924
ABSTRACT

INTRODUCTION:

Emerging evidence supports the immunogenic response to mRNA COVID-19 vaccine in patients with autoimmune rheumatic diseases (ARD). However, large-scale data about the association between vaccination, and COVID-19 outcomes in patients with ARD is limited.

METHODS:

We used data from Clalit Health Services, which covers more than half of the population in Israel. Patients with ARD older than 18 were included between 20 December 2020 and 30 September 2021, when the BNT162b2 mRNA COVID-19 vaccine, and later a third booster dose, were available. The primary outcome was a documented positive SARS-CoV-2 PCR test. We used a Cox regression models with vaccination status as time-dependent covariate and calculated the HR for the study outcome.

RESULTS:

We included 127 928 patients with ARD, of whom, by the end of the study follow-up, there were 27 350 (21.3%) unvaccinated patients, 31 407 (24.5%) vaccinated patients and 69 171 (54.1%) patients who also received a third booster-dose. We identified 8470 (6.6%) patients with a positive SARS-CoV-2 PCR test during the study period. The HR for SARS-CoV-2 infection among the vaccination group was 0.143 (0.095 to 0.214, p<0.001), and among the booster group was 0.017 (0.009 to 0.035, p<0.001). Similar results were found regardless of the type of ARD group or antirheumatic therapy.

CONCLUSION:

Our results indicate that both the BNT162b2 mRNA COVID-19 vaccine and the booster are associated with better COVID-19 outcomes in patients with ARD.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Autoimmune Diseases / Rheumatic Diseases / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Ann Rheum Dis Year: 2022 Document Type: Article Affiliation country: Annrheumdis-2021-221824

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Autoimmune Diseases / Rheumatic Diseases / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Ann Rheum Dis Year: 2022 Document Type: Article Affiliation country: Annrheumdis-2021-221824