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Risks and treatment related aspects of COVID-19 infection in patients with ANCA-associated vasculitis.
Antovic, A; Bruchfeld, A; Ekland, J; Lövström, B; Hugelius, A; Börjesson, O; Knight, A; Gunnarsson, I.
  • Antovic A; Division of Rheumatology, Department of Medicine, Karolinska Institutet, Solna, Sweden.
  • Bruchfeld A; Unit of Rheumatology, Karolinska University Hospital, Stockholm, Sweden.
  • Ekland J; Department of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden.
  • Lövström B; Department of Renal Medicine, CLINTEC, Karolinska Institutet at Karolinska University Hospital, Stockholm, Sweden.
  • Hugelius A; Rheumatology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
  • Börjesson O; Division of Rheumatology, Department of Medicine, Karolinska Institutet, Solna, Sweden.
  • Knight A; Unit of Rheumatology, Karolinska University Hospital, Stockholm, Sweden.
  • Gunnarsson I; Division of Rheumatology, Department of Medicine, Karolinska Institutet, Solna, Sweden.
Scand J Rheumatol ; : 1-6, 2022 Sep 20.
Article in English | MEDLINE | ID: covidwho-20232498
ABSTRACT

OBJECTIVE:

Patients with anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) require immunosuppressive therapy for disease control and relapse prevention and may be at risk for severe coronavirus disease 2019 (COVID-19). The study objective was to analyse risk factors and outcomes of COVID-19 in well-characterized AAV patients.

METHOD:

Data were retrieved from March 2020 to May 2021 from medical records of AAV cohorts in Stockholm and Uppsala, Sweden. COVID-19 was confirmed by positive PCR test or by ELISA. Severe COVID-19 was defined as need for non-invasive ventilation, intensive care unit care, and/or death. Age, gender, ANCA antibody type, ongoing immunosuppressive medication, and estimated glomerular filtration rate were recorded.

RESULTS:

The cohort comprised 310 AAV patients, of whom 29 (9%) were diagnosed with COVID-19. Four deaths were attributed to COVID-19. Fifteen patients (52%) were on prednisolone in the COVID-19 group and 130 (46%) in the non-COVID group, with significantly higher doses in COVID-19 patients (p < 0.01). Ongoing induction therapy was more prevalent in the COVID-19 group (p < 0.01). Severe COVID-19 was diagnosed in 9/29 (31%). Significant risk factors for severe COVID-19 were impaired kidney function (p = 0.01) and more intense immunosuppressive therapy (p = 0.02), with a trend for age (p = 0.07). Maintenance therapy with rituximab was not associated with severe COVID-19.

CONCLUSIONS:

Our findings highlight risks and suggest that more attention should be given to optimal AAV treatment in a pandemic situation. They also emphasize the need for continued shielding, mitigation strategies, and effective vaccination of AAV patients.

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Language: English Journal: Scand J Rheumatol Year: 2022 Document Type: Article Affiliation country: 03009742.2022.2109337

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Language: English Journal: Scand J Rheumatol Year: 2022 Document Type: Article Affiliation country: 03009742.2022.2109337