Polymyalgia rheumatica: observations of disease evolution without corticosteroid treatment

Arthur E Brawer Division of Rheumatology, Department of Medicine, Monmouth Medical Center, Long Branch, NJ, USA Objectives: The diagnostic diversity of polymyalgia rheumatica (PMR) can easily be obscured by the widespread use of corticosteroids (CSs) early in the disease course. This study observed...

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Autor principal: Brawer AE
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Publicado: Dove Medical Press 2016
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spelling oai:doaj.org-article:fac9e62500f2409f8a4bc8f1a16b277b2021-12-02T02:54:14ZPolymyalgia rheumatica: observations of disease evolution without corticosteroid treatment1179-156Xhttps://doaj.org/article/fac9e62500f2409f8a4bc8f1a16b277b2016-04-01T00:00:00Zhttps://www.dovepress.com/polymyalgia-rheumatica-observations-of-disease-evolution-without-corti-peer-reviewed-article-OARRRhttps://doaj.org/toc/1179-156XArthur E Brawer Division of Rheumatology, Department of Medicine, Monmouth Medical Center, Long Branch, NJ, USA Objectives: The diagnostic diversity of polymyalgia rheumatica (PMR) can easily be obscured by the widespread use of corticosteroids (CSs) early in the disease course. This study observed the course of PMR without CSs and determined whether alternative medication could be useful. Methods: Seventy patients with new-onset PMR comprised phase 1. Eight were removed with specific diagnoses (four with giant cell arteritis [GCA]). The remaining 62 were treated with nonsteroidal anti-inflammatory drugs (NSAIDs) alone until enough time had elapsed to ascertain whether their PMR had evolved into another rheumatologic inflammatory condition. Hydroxychloroquine (HCQ) was then added to their regimen. Twenty-five additional patients with PMR comprised phase 2. Twenty-two were immediately treated with HCQ prior to the anticipated disease progression. Results: In phase 1, 52/62 developed synovitis in multiple other joints 9 months from PMR onset; 48/52 received HCQ, and 42/48 (87.5%) achieved complete remission. In phase 2, during HCQ induction, 21 patients developed similar synovitis; after 6 months of HCQ use, 80% achieved remission. In 73/95 (77%), a definite diagnosis of rheumatoid arthritis (RA) could be made on average 8.5 months from PMR onset. Only 12/95 (13%) stayed true to form with their PMR and did not develop another specific diagnosis. Conclusion: In this study, true PMR was infrequent in the absence of GCA. PMR in most patients evolved into seronegative RA, which was dramatically responsive to HCQ use. Treatment of acute PMR with HCQ was a rational alternative to CS use even if progressive additive synovitis had not yet occurred. Keywords: polymyalgia rheumatica, rheumatoid arthritis, corticosteroidsBrawer AEDove Medical PressarticlePolymyalgia RheumaticaRheumatoid ArthritisCorticosteroidsDiseases of the musculoskeletal systemRC925-935ENOpen Access Rheumatology: Research and Reviews, Vol 2016, Iss Issue 1, Pp 45-49 (2016)
institution DOAJ
collection DOAJ
language EN
topic Polymyalgia Rheumatica
Rheumatoid Arthritis
Corticosteroids
Diseases of the musculoskeletal system
RC925-935
spellingShingle Polymyalgia Rheumatica
Rheumatoid Arthritis
Corticosteroids
Diseases of the musculoskeletal system
RC925-935
Brawer AE
Polymyalgia rheumatica: observations of disease evolution without corticosteroid treatment
description Arthur E Brawer Division of Rheumatology, Department of Medicine, Monmouth Medical Center, Long Branch, NJ, USA Objectives: The diagnostic diversity of polymyalgia rheumatica (PMR) can easily be obscured by the widespread use of corticosteroids (CSs) early in the disease course. This study observed the course of PMR without CSs and determined whether alternative medication could be useful. Methods: Seventy patients with new-onset PMR comprised phase 1. Eight were removed with specific diagnoses (four with giant cell arteritis [GCA]). The remaining 62 were treated with nonsteroidal anti-inflammatory drugs (NSAIDs) alone until enough time had elapsed to ascertain whether their PMR had evolved into another rheumatologic inflammatory condition. Hydroxychloroquine (HCQ) was then added to their regimen. Twenty-five additional patients with PMR comprised phase 2. Twenty-two were immediately treated with HCQ prior to the anticipated disease progression. Results: In phase 1, 52/62 developed synovitis in multiple other joints 9 months from PMR onset; 48/52 received HCQ, and 42/48 (87.5%) achieved complete remission. In phase 2, during HCQ induction, 21 patients developed similar synovitis; after 6 months of HCQ use, 80% achieved remission. In 73/95 (77%), a definite diagnosis of rheumatoid arthritis (RA) could be made on average 8.5 months from PMR onset. Only 12/95 (13%) stayed true to form with their PMR and did not develop another specific diagnosis. Conclusion: In this study, true PMR was infrequent in the absence of GCA. PMR in most patients evolved into seronegative RA, which was dramatically responsive to HCQ use. Treatment of acute PMR with HCQ was a rational alternative to CS use even if progressive additive synovitis had not yet occurred. Keywords: polymyalgia rheumatica, rheumatoid arthritis, corticosteroids
format article
author Brawer AE
author_facet Brawer AE
author_sort Brawer AE
title Polymyalgia rheumatica: observations of disease evolution without corticosteroid treatment
title_short Polymyalgia rheumatica: observations of disease evolution without corticosteroid treatment
title_full Polymyalgia rheumatica: observations of disease evolution without corticosteroid treatment
title_fullStr Polymyalgia rheumatica: observations of disease evolution without corticosteroid treatment
title_full_unstemmed Polymyalgia rheumatica: observations of disease evolution without corticosteroid treatment
title_sort polymyalgia rheumatica: observations of disease evolution without corticosteroid treatment
publisher Dove Medical Press
publishDate 2016
url https://doaj.org/article/fac9e62500f2409f8a4bc8f1a16b277b
work_keys_str_mv AT brawerae polymyalgiarheumaticaobservationsofdiseaseevolutionwithoutcorticosteroidtreatment
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