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      Proposal for a definition for response to treatment, inactive disease and damage for JIA associated uveitis based on the validation of a uveitis related JIA outcome measures from the Multinational Interdisciplinary Working Group for Uveitis in Childhood (MIWGUC)

      research-article
      1 , , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 , 21 , 11 , 12 , 23 , 24 , 13 , 14 , 15 , 16 , 16 , 2 , 17 , 18 , 19 , 7 , 2 , 13 , 10 , 14 , 20 , 10 , 21 , 22 , 10 , 21
      Pediatric Rheumatology Online Journal
      BioMed Central
      Anterior uveitis, Uveitis, Juvenile idiopathic arthritis, Response, Damage, Inactive disease, Outcome measures

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          Abstract

          Background

          JIA-associated uveitis (JIAU) is a serious, sight-threatening disease with significant long-term complications and risk of blindness, even with improved contemporary treatments. The MIWGUC was set up in order to propose specific JIAU activity and response items and to validate their applicability for clinical outcome studies.

          Methods

          The group consists of 8 paediatric rheumatologists and 7 ophthalmologists. A consensus meeting took place on November 2015 in Barcelona (Spain) with the objective of validating the previously proposed measures. The validation process was based on the results of a prospective open, international, multi-centre, cohort study designed to validate the outcome measures proposed by the initial MIWGUC group meeting in 2012. The meeting used the same Delphi and nominal group technique as previously described in the first paper from the MIWGUC group (Arthritis Care Res 64:1365–72, 2012). Patients were included with a diagnosis of JIA, aged less than 18 years, and with active uveitis or an uveitis flare which required treatment with a disease-modifying anti-rheumatic drug. The proposed outcome measures for uveitis were collected by an ophthalmologist and for arthritis by a paediatric rheumatologist. Patient reported outcome measures were also measured.

          Results

          A total of 82 patients were enrolled into the validation cohort. Fifty four percent ( n = 44) had persistent oligoarthritis followed by rheumatoid factor negative polyarthritis ( n = 15, 18%). The mean uveitis disease duration was 3.3 years (SD 3.0). Bilateral eye involvement was reported in 65 (79.3%) patients.

          The main findings are that the most significant changes, from baseline to 6 months, are found in the AC activity measures of cells and flare. These measures correlate with the presence of pre-existing structural complications and this has implications for the reporting of trials using a single measure as a primary outcome. We also found that visual analogue scales of disease activity showed significant change when reported by the ophthalmologist, rheumatologist and families.

          The measures formed three relatively distinct groups. The first group of measures comprised uveitis activity, ocular damage and the ophthalmologists’ VAS. The second comprised patient reported outcomes including disruption to school attendance. The third group consisted of the rheumatologists’ VAS and the joint score.

          Conclusions

          We propose distinctive and clinically significant measures of disease activity, severity and damage for JIAU. This effort is the initial step for developing a comprehensive outcome measures for JIAU, which incorporates the perspectives of rheumatologists, ophthalmologists, patients and families.

          Electronic supplementary material

          The online version of this article (10.1186/s12969-019-0345-2) contains supplementary material, which is available to authorized users.

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          Most cited references20

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          Measurement of health status in children with juvenile rheumatoid arthritis.

          To develop and validate a self- or parent-administered instrument for measuring functional status in children with juvenile rheumatoid arthritis (JRA). We adapted the Stanford Health Assessment Questionnaire (HAQ) for use in children ages 1-19 years, by adding several new questions, such that for each functional area, there was at least 1 question relevant to children of all ages. The face validity of the instrument was evaluated by a group of 20 health professionals and parents of 22 healthy children. The questionnaire was then administered to parents of 72 JRA patients (mean age 9.1 years, onset type systemic in 16, polyarticular in 21, pauciarticular in 35). The instrument showed excellent internal reliability (Cronbach's alpha = 0.94), with a mean inter-item correlation of 0.6. The convergent validity was demonstrated by strong correlations of the Disability Index (average of scores on all functional areas) with Steinbrocker functional class (Kendall's tau b = 0.77, P 8 years) was 0.84 (n = 29; P 0.9 by paired t-test; Spearman's correlation coefficient = 0.8, P < 0.002). The Childhood HAQ, which takes less than 10 minutes to complete, is a valid, reliable, and sensitive instrument for measuring functional status in children with JRA.
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            Preliminary criteria for clinical remission for select categories of juvenile idiopathic arthritis.

            To develop preliminary criteria for inactive disease and clinical remission for select categories of juvenile idiopathic arthritis (JIA), and to decide what such clinical states should predict in terms of probability of disease recurrence. A Delphi serial questionnaire consensus-formation approach was used initially to gather criteria in use by pediatric rheumatologists (PR) for defining clinical remission in oligoarticular (persistent and extended), rheumatoid factor (RF) positive and negative polyarticular, and systemic JIA. Results from sequential questionnaires provided an agenda for a nominal group technique (NGT) conference to reach consensus on unresolved questions. One hundred and thirty PR from 34 countries responded to the questionnaires and 20 PR from 9 countries attended the conference. Draft criteria for inactive disease include the following: no active arthritis; no fever, rash, serositis, splenomegaly, or generalized lymphadenopathy attributable to JIA; no active uveitis; normal erythrocyte sedimentation rate or C-reactive protein; and a physician's global assessment of disease activity rated at the best score possible for the instrument used. According to consensus vote, 6 continuous months of inactive disease on medication defines clinical remission on medication, while 12 months of inactive disease off all anti-arthritis (and anti-uveitis) medications defines clinical remission off medication. The finalized criteria for remission off medication ideally should predict that a patient has
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              Application of random-effects pattern-mixture models for missing data in longitudinal studies.

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                Author and article information

                Contributors
                040 2092 3697 , foeldvari@t-online.de
                Jens.Klotsche@drfz.de
                gabriele.simonini@unifi.it
                edelsten@easynet.co.uk
                Sheila.Angeles-Han@cchmc.org
                regitze.bangsgaard@regionh.dk
                jboer@umcutrecht.nl
                dr.gabrielebrumm@gmx.de
                rbou@sjdhospitalbarcelona.org
                tamasconstantin@gmail.com
                c.delibero@meyer.it
                jdiazc@sjdhospitalbarcelona.org
                ValeriaMaria.Gerloni@gpini.it
                margguedes@gmail.com
                arnd.heiligenhaus@uveitis-zentrum.de
                kaisumkotaniemi@gmail.com
                sanna.t.leinonen@khshp.fi
                minden@drfz.de
                +351 22 207 7500 , vm.miranda@gmail.com
                miserocchi.elisabetta@hsr.it
                Susan.Nielsen@regionh.dk
                niewerth@drfz.de
                irene.pontikaki@gpini.it
                cgvicuna@sjdhospitalbarcelona.org
                +351 22 207 7500 , carlazilhao@gmail.com
                steven.yeh@emory.edu
                JAnton@sjdhospitalbarcelona.org
                Journal
                Pediatr Rheumatol Online J
                Pediatr Rheumatol Online J
                Pediatric Rheumatology Online Journal
                BioMed Central (London )
                1546-0096
                1 October 2019
                1 October 2019
                2019
                : 17
                : 66
                Affiliations
                [1 ]Head of the Hamburg Centre for Pediatric and Adolescence Rheumatology Centre for Treatment of Scleroderma and Uveitis in Childhood and Adolescence Teaching Unit of the Asklepios Campus of the Semmelweis Medical School, Budapest An der Schön Klinik Hamburg Eilbek Dehnhaide, 120 22081 Hamburg, Germany
                [2 ]ISNI 0000 0000 9323 8675, GRID grid.418217.9, German Rheumatism Research Centre, ; 10117 Berlin, Germany
                [3 ]ISNI 0000 0001 2218 4662, GRID grid.6363.0, Institute for Social Medicine, Epidemiology, and Health Economics, , Charité Universitaetsmedizin Berlin, ; Berlin, Germany
                [4 ]ISNI 0000 0004 1757 2304, GRID grid.8404.8, Rheumatology Unit- A. Meyer Children’s Hospital- NEUROFARBA Department, , University of Florence, ; Florence, Italy
                [5 ]GRID grid.420468.c, Dept Rheumatology, Great Ormond Street Hospital, ; Great Ormond Street, London, UK
                [6 ]Division of Rheumatology, Cincinnati Children’s Hospital Medical Center, 3333 Burnett Avenue, Cincinnati, OH 45229; Department of Pediatrics, University of Cincinnati, Cincinnati, OH USA
                [7 ]Department of Ophthalmology, Copenhagen University Hospital Glostrup/Rigshospitalet, Copenhagen, Denmark
                [8 ]ISNI 0000000090126352, GRID grid.7692.a, UMC Utrecht, ; Utrecht, Netherlands
                [9 ]ISNI 0000 0001 2180 3484, GRID grid.13648.38, Universitätsklinikum Hamburg-Eppendorf, ; Hamburg, Germany
                [10 ]ISNI 0000 0001 0663 8628, GRID grid.411160.3, Pediatric Rheumatology Department, , Hospital Sant Joan de Déu, ; Barcelona, Spain
                [11 ]ISNI 0000 0001 0942 9821, GRID grid.11804.3c, 2nd Department of Pediatrics, , Semmelweis University, ; Budapest, Hungary
                [12 ]ISNI 0000 0004 1757 8562, GRID grid.413181.e, AOU Meyer, ; Florence, Italy
                [13 ]ISNI 0000 0004 1757 2822, GRID grid.4708.b, Università di Milano - Istituto Gaetano Pini, ; Milan, Italy
                [14 ]ISNI 0000 0001 1503 7226, GRID grid.5808.5, Pediatric Rheumatology Unit, , Centro Hospitalar Universitário do Porto, ; Porto, Portugal
                [15 ]GRID grid.416655.5, St. Franziskus-Hospital Münster, ; Muenster, Germany
                [16 ]ISNI 0000 0000 9950 5666, GRID grid.15485.3d, Department of Ophthalmology, , Helsinki University Hospital, ; Helsinki, Finland
                [17 ]Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Rheumatology and Clinical Immunology, Berlin, Germany
                [18 ]ISNI 0000 0001 1503 7226, GRID grid.5808.5, Pediatric Ophthalmologist at the Centro Hospitalar Universitario do Porto, , Teaching Unit of the Abel Salazar Institute of Biomedical Sciences, ; Largo do Prof. Abel Salazar, 4099-001 Porto, Portugal
                [19 ]ISNI 0000000417581884, GRID grid.18887.3e, Ocular Immunology and Uveitis Service, Department of Ophthalmology, , San Raffaele Scientific Institute, ; Via Olgettina 60, 20122 Milan, Italy
                [20 ]ISNI 0000 0004 0583 4098, GRID grid.419974.6, Emory Clinic, ; Atlanta, USA
                [21 ]Institut de Recerca Sant Joan de Déu, Barcelona, Spain
                [22 ]ISNI 0000 0004 1937 0247, GRID grid.5841.8, Department of Surgery and Surgery Specializations. Universitat de Barcelona, ; Barcelona, Spain
                [23 ]ISNI 0000 0004 1768 8905, GRID grid.413396.a, Ophtalmology Department, Hospital Sant Pau, ; Barcelona, Spain
                [24 ]ISNI 0000 0001 0663 8628, GRID grid.411160.3, Ophtalmology Department, Hospital Sant Joan de Déu, ; Barcelona, Spain
                Article
                345
                10.1186/s12969-019-0345-2
                6774210
                31575380
                1aa9b90c-3435-4360-808a-eff05754a2b3
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 29 January 2019
                : 3 July 2019
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2019

                Pediatrics
                anterior uveitis,uveitis,juvenile idiopathic arthritis,response,damage,inactive disease,outcome measures

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