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Long‐Term Outcomes Following Achievement of Clinically Inactive Disease in Juvenile Idiopathic Arthritis: The Importance of Definition

OBJECTIVE: Potential targets for treat‐to‐target strategies in juvenile idiopathic arthritis are minimal disease activity (MDA) and clinically inactive disease (CID). We undertook this study to compare short‐ and long‐term outcomes following achievement of MDA and CID on the 10‐joint clinical Juveni...

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Autores principales: Shoop‐Worrall, Stephanie J. W., Verstappen, Suzanne M. M., McDonagh, Janet E., Baildam, Eileen, Chieng, Alice, Davidson, Joyce, Foster, Helen, Ioannou, Yiannis, McErlane, Flora, Wedderburn, Lucy R., Thomson, W., Hyrich, Kimme L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175118/
https://www.ncbi.nlm.nih.gov/pubmed/29648683
http://dx.doi.org/10.1002/art.40519
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author Shoop‐Worrall, Stephanie J. W.
Verstappen, Suzanne M. M.
McDonagh, Janet E.
Baildam, Eileen
Chieng, Alice
Davidson, Joyce
Foster, Helen
Ioannou, Yiannis
McErlane, Flora
Wedderburn, Lucy R.
Thomson, W.
Hyrich, Kimme L.
author_facet Shoop‐Worrall, Stephanie J. W.
Verstappen, Suzanne M. M.
McDonagh, Janet E.
Baildam, Eileen
Chieng, Alice
Davidson, Joyce
Foster, Helen
Ioannou, Yiannis
McErlane, Flora
Wedderburn, Lucy R.
Thomson, W.
Hyrich, Kimme L.
author_sort Shoop‐Worrall, Stephanie J. W.
collection PubMed
description OBJECTIVE: Potential targets for treat‐to‐target strategies in juvenile idiopathic arthritis are minimal disease activity (MDA) and clinically inactive disease (CID). We undertook this study to compare short‐ and long‐term outcomes following achievement of MDA and CID on the 10‐joint clinical Juvenile Arthritis Disease Activity Score (cJADAS10) and following achievement of CID on Wallace et al's preliminary criteria. METHODS: Children recruited to the Childhood Arthritis Prospective Study, a UK multicenter inception cohort, were selected if they were recruited prior to January 2011 and diagnosed as having oligoarthritis or rheumatoid factor–negative or –positive polyarthritis. One year following diagnosis, children were assessed for MDA on the cJADAS10 and for CID on both Wallace et al's preliminary criteria and the cJADAS10. Associations were tested between those disease states and functional ability, absence of joints with limited range of motion, psychosocial health, and pain at 1 year and annually to 5 years. RESULTS: Of 832 children, 70% were female and the majority had oligoarthritis (68%). At 1 year, 21% had achieved CID according to both definitions, 7% according to Wallace et al's preliminary criteria alone, and 16% according to the cJADAS10 alone; 56% had not achieved CID. Only 10% of children in the entire cohort achieved MDA without also achieving CID. Achieving either early CID state was associated with a greater absence of joints with limited range of motion. However, only CID according to the cJADAS10 was associated with improved functional ability and psychosocial health. Achieving CID was superior to achieving MDA in terms of short‐ and long‐term pain and the absence of joints with limited range of motion. CONCLUSION: CID on the cJADAS10 may be preferable as a treatment target to CID on Wallace et al's preliminary criteria in terms of both feasibility of application and long‐term outcomes.
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spelling pubmed-61751182018-10-15 Long‐Term Outcomes Following Achievement of Clinically Inactive Disease in Juvenile Idiopathic Arthritis: The Importance of Definition Shoop‐Worrall, Stephanie J. W. Verstappen, Suzanne M. M. McDonagh, Janet E. Baildam, Eileen Chieng, Alice Davidson, Joyce Foster, Helen Ioannou, Yiannis McErlane, Flora Wedderburn, Lucy R. Thomson, W. Hyrich, Kimme L. Arthritis Rheumatol Pediatric Rheumatology OBJECTIVE: Potential targets for treat‐to‐target strategies in juvenile idiopathic arthritis are minimal disease activity (MDA) and clinically inactive disease (CID). We undertook this study to compare short‐ and long‐term outcomes following achievement of MDA and CID on the 10‐joint clinical Juvenile Arthritis Disease Activity Score (cJADAS10) and following achievement of CID on Wallace et al's preliminary criteria. METHODS: Children recruited to the Childhood Arthritis Prospective Study, a UK multicenter inception cohort, were selected if they were recruited prior to January 2011 and diagnosed as having oligoarthritis or rheumatoid factor–negative or –positive polyarthritis. One year following diagnosis, children were assessed for MDA on the cJADAS10 and for CID on both Wallace et al's preliminary criteria and the cJADAS10. Associations were tested between those disease states and functional ability, absence of joints with limited range of motion, psychosocial health, and pain at 1 year and annually to 5 years. RESULTS: Of 832 children, 70% were female and the majority had oligoarthritis (68%). At 1 year, 21% had achieved CID according to both definitions, 7% according to Wallace et al's preliminary criteria alone, and 16% according to the cJADAS10 alone; 56% had not achieved CID. Only 10% of children in the entire cohort achieved MDA without also achieving CID. Achieving either early CID state was associated with a greater absence of joints with limited range of motion. However, only CID according to the cJADAS10 was associated with improved functional ability and psychosocial health. Achieving CID was superior to achieving MDA in terms of short‐ and long‐term pain and the absence of joints with limited range of motion. CONCLUSION: CID on the cJADAS10 may be preferable as a treatment target to CID on Wallace et al's preliminary criteria in terms of both feasibility of application and long‐term outcomes. John Wiley and Sons Inc. 2018-07-22 2018-09 /pmc/articles/PMC6175118/ /pubmed/29648683 http://dx.doi.org/10.1002/art.40519 Text en © 2018 The Authors. Arthritis & Rheumatology published by Wiley Periodicals, Inc. on behalf of American College of Rheumatology. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Pediatric Rheumatology
Shoop‐Worrall, Stephanie J. W.
Verstappen, Suzanne M. M.
McDonagh, Janet E.
Baildam, Eileen
Chieng, Alice
Davidson, Joyce
Foster, Helen
Ioannou, Yiannis
McErlane, Flora
Wedderburn, Lucy R.
Thomson, W.
Hyrich, Kimme L.
Long‐Term Outcomes Following Achievement of Clinically Inactive Disease in Juvenile Idiopathic Arthritis: The Importance of Definition
title Long‐Term Outcomes Following Achievement of Clinically Inactive Disease in Juvenile Idiopathic Arthritis: The Importance of Definition
title_full Long‐Term Outcomes Following Achievement of Clinically Inactive Disease in Juvenile Idiopathic Arthritis: The Importance of Definition
title_fullStr Long‐Term Outcomes Following Achievement of Clinically Inactive Disease in Juvenile Idiopathic Arthritis: The Importance of Definition
title_full_unstemmed Long‐Term Outcomes Following Achievement of Clinically Inactive Disease in Juvenile Idiopathic Arthritis: The Importance of Definition
title_short Long‐Term Outcomes Following Achievement of Clinically Inactive Disease in Juvenile Idiopathic Arthritis: The Importance of Definition
title_sort long‐term outcomes following achievement of clinically inactive disease in juvenile idiopathic arthritis: the importance of definition
topic Pediatric Rheumatology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175118/
https://www.ncbi.nlm.nih.gov/pubmed/29648683
http://dx.doi.org/10.1002/art.40519
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