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SARS-CoV-2 breakthrough infections among vaccinated individuals with rheumatic disease: results from the COVID-19 Global Rheumatology Alliance provider registry.
Liew, Jean; Gianfrancesco, Milena; Harrison, Carly; Izadi, Zara; Rush, Stephanie; Lawson-Tovey, Saskia; Jacobsohn, Lindsay; Ja, Clairissa; Hyrich, Kimme L; Gossec, Laure; Strangfeld, Anja; Carmona, Loreto; Schäfer, Martin; Frãzao-Mateus, Elsa; Bulina, Inita; Stafford, Frances; Tufan, Abdurrahman; Graver, Christine; Yardimci, Gözde Kübra; Zepa, Julija; Al Emadi, Samar; Cook, Claire; Abutiban, Fatemah; Dey, Dfiza; Katigbak, Genevieve; Kaufman, Lauren; Kowalski, Emily; Martínez-Martínez, Marco Ulises; Patel, Naomi J; Reyes-Cordero, Greta; Salido, Evelyn; Smith, Ellison; Snow, David; Sparks, Jeffrey; Wise, Leanna; Bhana, Suleman; Gore-Massy, Monique; Grainger, Rebecca; Hausmann, Jonathan; Sirotich, Emily; Sufka, Paul; Wallace, Zachary; Machado, Pedro M; Robinson, Philip C; Yazdany, Jinoos.
  • Liew J; Medicine, Section of Rheumatology, Boston University, Boston, Massachusetts, USA liew.jw@gmail.com.
  • Gianfrancesco M; Department of Medicine, Division of Rheumatology, University of California, San Francisco, San Francisco, California, USA.
  • Harrison C; LupusChat, New York, New York, USA.
  • Izadi Z; Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, California, USA.
  • Rush S; Division of Rheumatology, Department of Medicine, University of California, San Francisco, San Francisco, California, USA.
  • Lawson-Tovey S; Centre for Genetics and Genomics Versus Arthritis, The University of Manchester, Manchester, UK.
  • Jacobsohn L; National Institute for Health Research Manchester Biomedical Research Centre, Manchester University NHS Foundation Trust, Manchester, UK.
  • Ja C; Department of Medicine, Division of Rheumatology, University of California, San Francisco, San Francisco, California, USA.
  • Hyrich KL; Division of Rheumatology, Department of Medicine, University of California, San Francisco, California, USA.
  • Gossec L; University of Manchester, Manchester, UK.
  • Strangfeld A; INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, INSERM, Sorbonne Universite, Paris, France.
  • Carmona L; APHP, Rheumatology Department, Hopital Universitaire Pitie Salpetriere, Paris, France.
  • Schäfer M; Forschungsbereich Epidemiologie, Deutsches Rheuma-Forschungszentrum Berlin, Berlin, Germany.
  • Frãzao-Mateus E; Instituto de Salud Musculoesquelética (INMUSC), Madrid, Spain.
  • Bulina I; Epidemiology and Health Services Research, German Rheumatism Research Center Berlin, Berlin, Germany.
  • Stafford F; Portuguese League Against Rheumatic Diseases (LPCDR), Lisbon, Portugal.
  • Tufan A; Paul Stradins Clinical University Hospital, Riga, Latvia.
  • Graver C; Blackrock Clinic, Blackrock, Ireland.
  • Yardimci GK; Gazi University, Ankara, Turkey.
  • Zepa J; Royal Hampshire County Hospital, Winchester, UK.
  • Al Emadi S; Department of Internal Medicine, Hacettepe University, Ankara, Turkey.
  • Cook C; Hacettepe University, Ankara, Turkey.
  • Abutiban F; Paul Stradins Clinical University Hospital, Riga, Latvia.
  • Dey D; Hamad Medical Corporation, Doha, Qatar.
  • Katigbak G; Rheumatology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Kaufman L; Jaber Al Ahmed Al Jaber Al Sabah Hospital, Surra, Kuwait.
  • Kowalski E; University of Ghana Medical School, Accra, Ghana.
  • Martínez-Martínez MU; Korle Bu Teaching Hospital, Accra, Ghana.
  • Patel NJ; Makati Medical Center, Makati City, Philippines.
  • Reyes-Cordero G; Rheumatology Associates Louisville, Louisville, Kentucky, USA.
  • Salido E; Inflammation and Immunity, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Smith E; Rheumatology, Hospital Central "Dr Ignacio Morones Prieto", San Luis Potosí, Mexico.
  • Snow D; Faculty of Medicine, Universidad Autónoma de San Luis Potosí, San Luis, Mexico.
  • Sparks J; Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Wise L; Autonomous University of Chihuahua, Chihuahua, Mexico.
  • Bhana S; University of the Philippines Manila, Manila, Philippines.
  • Gore-Massy M; University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.
  • Grainger R; Asheville Arthritis & Osteoporosis Center, Asheville, North Carolina, USA.
  • Hausmann J; Cape Fear Arthritis Care, Leland, North Carolina, USA.
  • Sirotich E; Department of Medicine, Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Sufka P; Department of Internal Medicine, Division of Rheumatology, University of Southern California, Los Angeles, California, USA.
  • Wallace Z; Crystal Run Healthcare, Middletown, New York, USA.
  • Machado PM; Lupus Foundation of America, Washington, DC, USA.
  • Robinson PC; Department of Medicine, University of Otago, Wellington, Wellington, New Zealand.
  • Yazdany J; University Of Otago, Wellington, New Zealand.
RMD Open ; 8(1)2022 04.
Article in English | MEDLINE | ID: covidwho-1779411
ABSTRACT

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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Full text: Available Collection: International databases Database: MEDLINE Main subject: Rheumatology / Rheumatic Diseases / COVID-19 Type of study: Observational study / Prognostic study Topics: Long Covid / Vaccines Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: English Year: 2022 Document Type: Article Affiliation country: Rmdopen-2021-002187

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Rheumatology / Rheumatic Diseases / COVID-19 Type of study: Observational study / Prognostic study Topics: Long Covid / Vaccines Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: English Year: 2022 Document Type: Article Affiliation country: Rmdopen-2021-002187