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  1. Article ; Online: Significant pain decrease in children with non-systemic Juvenile Idiopathic Arthritis treated to target: results over 24 months of follow up.

    Spekking, Katinka / Anink, Janneke / de Boer, Piroska / Bergstra, Sytske Anne / van den Berg, J Merlijn / Schonenberg-Meinema, Dieneke / van Suijlekom-Smit, Lisette W A / van Rossum, Marion A J / Koopman-Keemink, Yvonne / Cate, Rebecca Ten / Allaart, Cornelia F / Brinkman, Daniëlle M C / Muller, Petra C E Hissink

    Pediatric rheumatology online journal

    2023  Volume 21, Issue 1, Page(s) 90

    Abstract: Background: The aim of this study was to compare pain-scores in three targeted treatment-strategies in JIA-patients and to identify characteristics predicting persistent pain.: Methods: In the BeSt-for-Kids-study 92 DMARD-naïve JIA-patients were ... ...

    Abstract Background: The aim of this study was to compare pain-scores in three targeted treatment-strategies in JIA-patients and to identify characteristics predicting persistent pain.
    Methods: In the BeSt-for-Kids-study 92 DMARD-naïve JIA-patients were randomized in 3 treatment-strategies: 1) initial sequential DMARD-monotherapy 2) initial methotrexate (MTX)/prednisolone-bridging or 3) initial MTX/etanercept. Potential differences in VAS pain scores (0-100 mm) over time between treatment-strategies were compared using linear mixed models with visits clustered within patients. A multivariable model was used to assess the ability of baseline characteristics to predict the chance of high pain-scores during follow-up.
    Results: Pain-scores over time reduced from mean 55.3 (SD 21.7) to 19.5 (SD 25.3) mm after 24 months. On average, pain-scores decreased significantly with β -1.37 mm (95% CI -1.726; -1.022) per month. No significant difference was found between treatment-strategies (interaction term treatment arm*time (months) β (95% CI) arm 1: 0.13 (-0.36; 0.62) and arm 2: 0.37 (-0.12; 0.86) compared to arm 3). Correction for sex and symptom duration yielded similar results. Several baseline characteristics were predictive for pain over time. Higher VAS pain [β 0.44 (95% CI 0.25; 0.65)] and higher active joint count [0.77 (0.19; 1.34)] were predictive of higher pain over time, whereas, low VAS physician [ -0.34 (-0.55; -0.06)], CHQ Physical [ -0.42 (-0.72; -0.11)] and Psychosocial summary Score [ -0.42 (-0.77; -0.06)] were predictive of lower pain.
    Conclusions: Treatment-to-target seems effective in pain-reduction in non-systemic JIA-patients irrespective of initial treatment-strategy. Several baseline-predictors for pain over time were found, which could help to identify patients with a high risk for development of chronic pain.
    Trial registration: Dutch Trial Registry number 1574.
    MeSH term(s) Humans ; Child ; Follow-Up Studies ; Arthritis, Juvenile/complications ; Arthritis, Juvenile/drug therapy ; Chronic Pain ; Antirheumatic Agents/therapeutic use ; Etanercept
    Chemical Substances Antirheumatic Agents ; Etanercept (OP401G7OJC)
    Language English
    Publishing date 2023-08-26
    Publishing country England
    Document type Randomized Controlled Trial ; Journal Article
    ZDB-ID 2279468-2
    ISSN 1546-0096 ; 1546-0096
    ISSN (online) 1546-0096
    ISSN 1546-0096
    DOI 10.1186/s12969-023-00874-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: The provisional Paediatric Rheumatology International Trials Organisation/American College of Rheumatology/European League Against Rheumatism Disease activity core set for the evaluation of response to therapy in juvenile dermatomyositis: a prospective validation study.

    Ruperto, Nicolino / Ravelli, Angelo / Pistorio, Angela / Ferriani, Virginia / Calvo, Immaculada / Ganser, Gerd / Brunner, Jurgen / Dannecker, Guenther / Silva, Clovis Arthur / Stanevicha, Valda / Cate, Rebecca Ten / van Suijlekom-Smit, Lisette W A / Voygioyka, Olga / Fischbach, Michel / Foeldvari, Ivan / Hilario, Odete / Modesto, Consuelo / Saurenmann, Rotraud K / Sauvain, Marie-Josephe /
    Scheibel, Iloite / Sommelet, Danièle / Tambic-Bukovac, Lana / Barcellona, Roberto / Brik, Riva / Ehl, Stephan / Jovanovic, Mirjana / Rovensky, Jozef / Bagnasco, Francesca / Lovell, Daniel J / Martini, Alberto

    Arthritis and rheumatism

    2008  Volume 59, Issue 1, Page(s) 4–13

    Abstract: Objective: To validate a core set of outcome measures for the evaluation of response to treatment in patients with juvenile dermatomyositis (DM).: Methods: In 2001, a preliminary consensus-derived core set for evaluating response to therapy in ... ...

    Abstract Objective: To validate a core set of outcome measures for the evaluation of response to treatment in patients with juvenile dermatomyositis (DM).
    Methods: In 2001, a preliminary consensus-derived core set for evaluating response to therapy in juvenile DM was established. In the present study, the core set was validated through an evidence-based, large-scale data collection that led to the enrollment of 294 patients from 36 countries. Consecutive patients with active disease were assessed at baseline and after 6 months. The validation procedures included assessment of feasibility, responsiveness, discriminant and construct ability, concordance in the evaluation of response to therapy between physicians and parents, redundancy, internal consistency, and ability to predict a therapeutic response.
    Results: The following clinical measures were found to be feasible, and to have good construct validity, discriminative ability, and internal consistency; furthermore, they were not redundant, proved responsive to clinically important changes in disease activity, and were associated strongly with treatment outcome and thus were included in the final core set: 1) physician's global assessment of disease activity, 2) muscle strength, 3) global disease activity measure, 4) parent's global assessment of patient's well-being, 5) functional ability, and 6) health-related quality of life.
    Conclusion: The members of the Paediatric Rheumatology International Trials Organisation, with the endorsement of the American College of Rheumatology and the European League Against Rheumatism, propose a core set of criteria for the evaluation of response to therapy that is scientifically and clinically relevant and statistically validated. The core set will help standardize the conduct and reporting of clinical trials and assist practitioners in deciding whether a child with juvenile DM has responded adequately to therapy.
    MeSH term(s) Child ; Dermatomyositis/diagnosis ; Female ; Humans ; Male ; Practice Guidelines as Topic ; Prospective Studies
    Language English
    Publishing date 2008-01-15
    Publishing country United States
    Document type Journal Article ; Multicenter Study ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Validation Studies
    ZDB-ID 127294-9
    ISSN 1529-0131 ; 0004-3591 ; 2326-5191
    ISSN (online) 1529-0131
    ISSN 0004-3591 ; 2326-5191
    DOI 10.1002/art.23248
    Database MEDical Literature Analysis and Retrieval System OnLINE

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