PMID- 35549809 OWN - NLM STAT- MEDLINE DCOM- 20230614 LR - 20230615 IS - 1502-7732 (Electronic) IS - 0300-9742 (Linking) VI - 52 IP - 4 DP - 2023 Jul TI - Risk of severe COVID-19 in patients with inflammatory rheumatic diseases treated with immunosuppressive therapy in Scotland. PG - 412-417 LID - 10.1080/03009742.2022.2063376 [doi] AB - OBJECTIVE: To investigate the association of severe coronavirus disease 2019 (COVID-19) in patients with inflammatory rheumatic diseases (IRDs) treated with immunosuppressive drugs. METHOD: A list of 4633 patients on targeted - biological or targeted synthetic - DMARDs in March 2020 was linked to a case-control study that includes all cases of COVID-19 in Scotland. RESULTS: By 22 November 2021, 433 of the 4633 patients treated with targeted DMARDS had been diagnosed with COVID-19, of whom 58 had been hospitalized. With all those in the population not on DMARDs as the reference category, the rate ratio for hospitalized COVID-19 associated with DMARD treatment was 2.14 [95% confidence interval (CI) 2.02-2.26] in those on conventional synthetic (cs) DMARDs, 2.01 (95% CI 1.38-2.91) in those on tumour necrosis factor (TNF) inhibitors as the only targeted agent, and 3.83 (95% CI 2.65-5.56) in those on other targeted DMARDs. Among those on csDMARDs, rate ratios for hospitalized COVID-19 were lowest at 1.66 (95% CI 1.51-1.82) in those on methotrexate and highest at 5.4 (95% CI 4.4-6.7) in those on glucocorticoids at an average dose > 10 mg/day prednisolone equivalent. CONCLUSION: The risk of hospitalized COVID-19 is elevated in IRD patients treated with immunosuppressive drugs compared with the general population. Of these drugs, methotrexate, hydroxychloroquine, and TNF inhibitors carry the lowest risk. The highest risk is associated with prednisolone. A larger study is needed to estimate reliably the risks associated with each class of targeted DMARD. FAU - McKeigue, P M AU - McKeigue PM AUID- ORCID: 0000-0002-5217-1034 AD - Usher Institute, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh, UK. AD - Public Health Scotland, Glasgow, UK. FAU - Porter, D AU - Porter D AUID- ORCID: 0000-0001-8481-5204 AD - Department of Rheumatology, Gartnavel General Hospital, Glasgow, UK. FAU - Hollick, R J AU - Hollick RJ AUID- ORCID: 0000-0001-6558-7189 AD - Aberdeen Centre for Arthritis and Musculoskeletal Health (Epidemiology Group), School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, UK. FAU - Ralston, S H AU - Ralston SH AUID- ORCID: 0000-0002-2804-7586 AD - Institute of Genetics and Cancer, College of Medicine and Veterinary Medicine, University of Edinburgh, Western General Hospital Campus, Edinburgh, UK. FAU - McAllister, D A AU - McAllister DA AUID- ORCID: 0000-0003-3550-1764 AD - Public Health Scotland, Glasgow, UK. AD - Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK. FAU - Colhoun, H M AU - Colhoun HM AUID- ORCID: 0000-0002-8345-3288 AD - Public Health Scotland, Glasgow, UK. AD - Institute of Genetics and Cancer, College of Medicine and Veterinary Medicine, University of Edinburgh, Western General Hospital Campus, Edinburgh, UK. LA - eng PT - Journal Article DEP - 20220512 PL - England TA - Scand J Rheumatol JT - Scandinavian journal of rheumatology JID - 0321213 RN - YL5FZ2Y5U1 (Methotrexate) RN - 0 (Antirheumatic Agents) RN - 0 (Immunosuppressive Agents) RN - 9PHQ9Y1OLM (Prednisolone) SB - IM MH - Humans MH - Methotrexate/therapeutic use MH - *Arthritis, Rheumatoid/drug therapy MH - Case-Control Studies MH - *COVID-19 MH - *Antirheumatic Agents/therapeutic use MH - Immunosuppressive Agents/therapeutic use MH - Immunosuppression Therapy MH - Prednisolone/therapeutic use MH - *Rheumatic Diseases/drug therapy EDAT- 2022/05/14 06:00 MHDA- 2023/06/14 06:42 CRDT- 2022/05/13 12:08 PHST- 2023/06/14 06:42 [medline] PHST- 2022/05/14 06:00 [pubmed] PHST- 2022/05/13 12:08 [entrez] AID - 10.1080/03009742.2022.2063376 [doi] PST - ppublish SO - Scand J Rheumatol. 2023 Jul;52(4):412-417. doi: 10.1080/03009742.2022.2063376. Epub 2022 May 12.