36 results on '"Daniel Windschall"'
Search Results
2. Patientin mit JIA und Entwicklung von chronischen nichtentzündlichen Gelenkschmerzen – stationäre Schmerztherapie bei chronischen Schmerzen am Bewegungsapparat als Gruppenkonzept
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Arnold Illhardt and Daniel Windschall
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General Medicine - Published
- 2022
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3. Development of Inflammatory Bowel Disease in Children With Juvenile Idiopathic Arthritis Treated With Biologics
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Ilse J, Broekaert, Ariane, Klein, Daniel, Windschall, Betina, Rogalski, Frank, Weller-Heinemann, Prasad, Oommen, Michael, Küster, Ivan, Foeldvari, Kirsten, Minden, Anton, Hospach, Markus, Hufnagel, Thomas, Berger, Til, Geikowski, Jürgen, Quietzsch, and Gerd, Horneff
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Pediatrics, Perinatology and Child Health ,Gastroenterology - Abstract
The aim of our study was to describe the distinct features of inflammatory bowel disease (IBD) in juvenile idiopathic arthritis (JIA) patients and to identify risk factors for its development.Data from the German biologics in paediatric rheumatology registry (Biologika in der Kinderrheumatologie (BiKeR)) collected between 2001 to 2021 were analysed retrospectively.In 5009 JIA patients, 28 developed confirmed IBD before the age of 18 years: 23 (82.1%) with Crohn's disease (CD), 4 (14.3%) with ulcerative colitis (UC) and 1 (3.6%) with IBD-unclassified. The incident rate of IBD during 20 years of observation was 0.56% (0.46% for CD, 0.08% for UC, 0.02% for IBD-U), of whom 20.3% were HLA-B27 positive, 25% had enthesitis-related arthritis and 14.3% psoriatic arthritis. Within 90 days before IBD diagnosis, 82.1% (n=23) received treatment with etanercept (ETA), 39.3% (n=11) NSAID, 17.9% (n=5) systemic corticosteroids, 8 (28.6%) methotrexate (MTX), 14.3% (n=4) sulfasalazine, 10.7% (n=3) leflunomide, and 3.6% (n=1) adalimumab and infliximab, respectively. The incidence of IBD was lower in patients treated with MTX, but higher in patients treated with ETA except if ETA was combined with MTX. Also in patients on leflunomide or sulfasalazine, the IBD incidence was higher.In our JIA cohort, an increased IBD incidence is observed compared to the general population, and the ratio of CD to UC is markedly higher hinting at a distinct phenotype of IBD. Pre-treatment with MTX seems to be protective. Treatment with ETA does not prevent IBD development and JIA patients treated with leflunomide and sulfasalazine may be at an increased risk for IBD development.An infographic is available for this article at: http://links.lww.com/MPG/C985.
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- 2022
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4. Ultraschalldiagnostik in der Kinderrheumatologie
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Daniel Windschall, Clara Malattia, Manuela Krumrey-Langkammerer, and Ralf Trauzeddel
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Rheumatology - Abstract
ZusammenfassungDer Artikel gibt einen Überblick zum aktuellen Stand der Ultraschallbefundung in der Kinderrheumatologie und geht insbesondere auf den praktischen Einsatz und die technischen Aspekte der Gelenksonografie ein. Dabei werden auch die wissenschaftlichen Entwicklungen der letzten Jahre zusammengefasst und berücksichtigt. Neben der Gelenksonografie wird die Ultraschalltechnik in der Kinderrheumatologie zunehmend auch auf weitere Körperregionen und -organe ausgeweitet, die für die kinderrheumatologische Diagnostik relevant sind.
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- 2022
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5. Schmerzen, Bewegungseinschränkungen und entzündliche Veränderungen am Gelenk – immer eine Arthritis?
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Daniel Windschall, Gerd Ganser, Klaus Tenbrock, Hanna Winowski, and Tobias Schwarz
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General Medicine - Abstract
ZusammenfassungSchmerzhafte Bewegungseinschränkungen und Gelenkschwellungen, der Nachweis von entzündlichen Veränderungen in der Sonografie oder Kernspintomografie sowie unauffällige laborchemische Untersuchungen sind typische Befunde der juvenilen idiopathischen Arthritis. Allerdings müssen in der differenzialdiagnostischen Abklärung von Arthropathien auch sehr seltene, nicht entzündliche hereditäre Skelettdysplasien in Betracht gezogen werden. Wir berichten über 3 Patienten aus 2 Familien mit einer multiplen epiphysären Dysplasie Typ 4 (MED4). Zwei der Patienten wurden unter dem Verdacht auf ein primär entzündliches Geschehen zunächst antiinflammatorisch behandelt. Die entzündlichen Veränderungen stellten sich jedoch als sekundär, infolge einer bereits fortgeschrittenen Osteoarthrose, heraus. Exemplarisch werden weitere, primär nicht entzündliche Skelettdysplasien vorgestellt, welche sich im Kindes- und Jugendalter manifestieren und mit einem initial normalen Längenwachstum, unauffälligen Körperproportionen, einer unauffälligen Facies sowie einer normalen kognitiven Entwicklung einhergehen.
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- 2021
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6. Consumer perspective on healthcare services for juvenile idiopathic arthritis: results of a multicentre JIA inception cohort study
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Michaela, Heinrich-Rohr, Kirsten, Moenkemoeller, Martina, Niewerth, Claudia, Sengler, Ina, Liedmann, Tilmann, Kallinich, Gerd, Horneff, Daniel, Windschall, Johannes-Peter, Haas, Frank, Dressler, Ivan, Foeldvari, Frank, Weller-Heinemann, Toni, Hospach, Jasmin, Kuemmerle-Deschner, Dirk, Foell, Jens, Klotsche, and Kirsten, Minden
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Cohort Studies ,Parents ,Rheumatology ,Surveys and Questionnaires ,Immunology ,Quality of Life ,Humans ,Immunology and Allergy ,Child ,Delivery of Health Care ,Arthritis, Juvenile - Abstract
To evaluate healthcare services for patients with juvenile idiopathic arthritis (JIA) from the parent-proxy perspective and to identify factors associated with perceived deficits in care.Patients with JIA from 11 paediatric rheumatology units were enrolled in an inception cohort within the first 12 months after diagnosis. Healthcare services were assessed using The Child Healthcare Questionnaire on satisfaction, utilisation and needs. Factors associated with deficits in care were identified by logistic regression analysis.Data from parents of 835 JIA-patients were included in the analysis. At the assessment (4.7 months after diagnosis), 85% of the patients received drug treatment, and 50% had received multi-professional care. The most frequently used services were physiotherapy (84%), occupational therapy (23%), and telephone counselling (17%). Almost one-third of families reported that they had not received the services that they needed, with health education being the most frequently reported need. Most parents (93%) were satisfied with the overall healthcare provided for their children, especially regarding doctors' behaviour. However, approximately 1 in 3 consumers were dissatisfied with the time to JIA diagnosis and the school services. The lower the child's quality of life, the higher the chance was that the child and the family received multi-professional care, perceived unmet needs, and were dissatisfied with care.According to parents' experience and satisfaction with their child's care, performance at the system level can be further improved by diagnosing JIA earlier, providing additional information at disease onset, and ensuring that the child's social environment is taken into account.
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- 2021
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7. Adherence, helpfulness and barriers to treatment in juvenile idiopathic arthritis : data from a German Inception cohort
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Sabine Kirchner, Jens Klotsche, Ina Liedmann, Martina Niewerth, Debbie Feldman, Frank Dressler, Ivan Foeldvari, Dirk Foell, Johannes-Peter Haas, Gerd Horneff, Anton Hospach, Tilmann Kallinich, J. B. Kuemmerle-Deschner, Kirsten Moenkemoeller, Frank Weller-Heinemann, Daniel Windschall, Kirsten Minden, and Claudia Sengler
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Rheumatology ,Pediatrics, Perinatology and Child Health ,Immunology and Allergy - Abstract
Objectives To develop and evaluate German versions of the Parent Adherence Report Questionnaire (PARQ) and Child Adherence Report Questionnaire (CARQ) and to evaluate adherence in patients with juvenile idiopathic arthritis (JIA). Methods The PARQ and CARQ were translated into German, cross-culturally adapted and administered to patients (age ≥ 8 years) and their parents enrolled in the Inception Cohort Study of newly diagnosed JIA patients (ICON). The psychometric issues were explored by analyzing their test–retest reliability and construct validity. Results Four hundred eighty-one parents and their children with JIA (n = 465) completed the PARQ and CARQ at the 4-year follow-up. Mean age and disease duration of patients were 10.1 ± 3.7 and 4.7 ± 0.8 years, respectively. The rate of missing values for PARQ/CARQ was generally satisfactory, test-retesting showed sufficient reliability. PARQ/CARQ mean child ability total scores (0–100, 100 = best) for medication were 73.1 ± 23.3/76.5 ± 24.2, for exercise: 85.6 ± 16.5/90.3 ± 15.0, for splints: 72.9 ± 24.2/82.9 ± 16.5. Construct validity was supported by PARQ and CARQ scores for medications, exercise and splints showing a fair to good correlation with the Global Adherence Assessment (GAA) and selected PedsQL scales. Adolescents showed poorer adherence than children. About one third of the parents and children reported medication errors. Perceived helpfulness was highest for medication, and adverse effects were reported the greatest barrier to treatment adherence. Conclusions The German versions of the PARQ and CARQ appear to have a good reliability and sufficient construct validity. These questionnaires are valuable tools for measuring treatment adherence, identifying potential barriers and evaluating helpfulness of treatments in patients with JIA.
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- 2023
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8. Efficacy and Safety of Etanercept Biosimilars Compared With the Originator for Treatment of Juvenile Arthritis: A Prospective Observational Study
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Daniel Windschall, A. Hospach, J Michael Ruehlmann, Gerd Horneff, Ariane Klein, S. Mrusek, and Franz Thiele
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musculoskeletal diseases ,medicine.medical_specialty ,business.industry ,Arthritis ,Objective analysis ,Biosimilar ,Original Articles ,Diseases of the musculoskeletal system ,medicine.disease ,Etanercept ,RC925-935 ,Rheumatology ,Internal medicine ,medicine ,Original Article ,In patient ,Observational study ,skin and connective tissue diseases ,Adverse effect ,business ,Paediatric rheumatology ,medicine.drug - Abstract
Objective Analysis of etanercept biosimilars in pediatric patients with juvenile idiopathic arthritis (JIA) in comparison with the etanercept originator in terms of efficacy and safety. Methods Patients diagnosed with JIA who started treatment with either the etanercept originator or a biosimilar after January 1, 2017, were selected from the German BIKER registry (Biologics in Paediatric Rheumatology Registry). Furthermore, patients who started therapy with the originator and switched to a biosimilar during the course of therapy were identified. For both patient groups, disease activity and safety were examined and compared separately. Results After January 1, 2017, 348 patients started treatment with the etanercept originator (n = 293) or a biosimilar (n = 55). Another 57 patients switched to a biosimilar during the course of therapy. A significant decrease or a stable remission of disease activity was observed in both patient groups. The safety profiles were comparable, and frequencies and types of adverse events (AEs) and serious AEs were similar in patients starting therapy with the originator or a biosimilar. Only injection site reactions occurred slightly more frequently under biosimilar therapy, without having an impact on therapy adherence. In patients who switched therapy, the AE rate per 100 patient-years was comparable before (26.4) and after (32.1) the switch. Conclusion In patients with JIA who require treatment with etanercept, the originator is still used much more frequently. However, our study highlights the equivalence of etanercept biosimilars for therapy for JIA. Increased use of these biosimilars in pediatric patients can therefore be recommended without hesitation.
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- 2021
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9. Bericht der Kommission Qualitätssicherung und Versorgung
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Kirsten Minden, Maria Haller, and Daniel Windschall
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General Medicine - Abstract
Auf dem Strategiemeeting im September 2020 wurde vom Vorstand und Beirat der Gesellschaft für Kinder- und Jugendrheumatologie (GKJR) vorgeschlagen, regelmäßig über die Arbeit in den Kommissionen und Arbeitskreisen zu berichten. Im Jahr 2021 erschienen in den Verbandsnachrichten Beiträge der Kommission Sport und Bewegung (Heft 1), der Kommission Pharmakotherapie und Leitlinien (Heft 2) und der Kommission Patientenschulung (Heft 3). Mit dem Bericht der Kommission Qualitätssicherung und Versorgung wird die Reihe nun wieder aufgenommen.
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- 2022
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10. Comparative risk of infections among real-world users of biologics for juvenile idiopathic arthritis: data from the German BIKER registry
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Daniel Windschall, Kirsten Minden, Frank Weller-Heinemann, Franz Thiele, Ivan Foeldvari, Ariane Klein, Gerd Horneff, and A. Hospach
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musculoskeletal diseases ,Male ,medicine.medical_specialty ,Immunology ,Observational Research ,Biologics ,Opportunistic Infections ,Infections ,Receptors, Tumor Necrosis Factor ,Etanercept ,Abatacept ,03 medical and health sciences ,chemistry.chemical_compound ,Biological Factors ,0302 clinical medicine ,Tocilizumab ,Rheumatology ,Internal medicine ,Germany ,Adalimumab ,medicine ,Immunology and Allergy ,Humans ,Immunologic Factors ,030212 general & internal medicine ,Registries ,030203 arthritis & rheumatology ,Anakinra ,Biological Products ,business.industry ,Interleukin-6 ,Tumor Necrosis Factor-alpha ,Incidence ,Odds ratio ,Juvenile idiopathic arthritis ,Infliximab ,Arthritis, Juvenile ,chemistry ,Antirheumatic Agents ,Immunoglobulin G ,Cohort ,Female ,Safety ,business ,medicine.drug ,Interleukin-1 - Abstract
To examine whether treatment with interleukin (IL)-1-, IL-6-, tumour necrosis factor α (TNFα)-inhibitors or Abatacept is associated with an increased risk of common infections, infections requiring hospitalization (SAE) or opportunistic infections among real-world juvenile idiopathic arthritis (JIA) patients. Furthermore, the influence of other patient-related covariates on the occurrence of infections was investigated. Patients diagnosed with JIA and treated with biologics were selected from the German BIKER registry. Incidence rates (IR) of infections per 100 person years were calculated and compared between the different cohorts. Using multivariate logistic regression, odds ratios with 95% confidence intervals (CI) were determined for the influence of patient-related covariates (age, diagnosis, laboratory data, concomitant medication, JIA activity, comorbidities, and premedication) on the occurrence of infections. 3258 patients entered the analysis. A total of 3654 treatment episodes were distributed among TNFα- (Etanercept, Adalimumab, Golimumab, Infliximab, n = 3044), IL-1- (Anakinra, Canakinumab, n = 105), IL-6- (Tocilizumab, n = 400) and T-cell activation inhibitors (Abatacept, n = 105). 813 (22.2%) patients had at least one infection, 103 (2.8%) patients suffered from an SAE infection. Both common and SAE infections were significantly more frequent in IL-1 (IR 17.3, 95% CI 12.5/24 and IR 4.3, 95% CI 2.3/8.3) and IL-6 cohort (IR 16.7, 95% CI 13.9/20 and IR 2.8, 95% CI 1.8/4.4) compared to TNFα-inhibitor cohort (IR 8.7, 95% CI 8.1/9.4 and IR 1, 95% CI 0.8/1.3). When comparing the influencing factors for various infectious diseases, the use of corticosteroids, younger age, cardiac comorbidities and higher JIA-activity are the most striking risk factors. Relative to TNFα inhibitors and Abatacept, IL-1 and IL-6 inhibitors were associated with an increased risk of common and SAE infections. The influencing covariates identified may be helpful for the choice of a suitable biologic to treat JIA.
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- 2021
11. Gelenksonografie im Treat-to-Target-Konzept bei der juvenilen idiopathischen Arthritis
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Daniel Windschall and Faekah Gohar
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030203 arthritis & rheumatology ,0301 basic medicine ,Gynecology ,medicine.medical_specialty ,Routine testing ,business.industry ,Treat to target ,General Medicine ,Musculoskeletal ultrasound ,03 medical and health sciences ,030104 developmental biology ,0302 clinical medicine ,Remission criteria ,Disease remission ,medicine ,Subclinical inflammation ,business ,Paediatric rheumatology - Abstract
In unserem Artikel werden aktuelle Bedeutung und Entwicklung der Gelenksonografie als fester Bestandteil eines „Treat-to-Target“-Konzeptes bei der Behandlung der juvenilen idiopathischen Arthritis (JIA) dargestellt und diskutiert. Dabei nimmt die Gelenksonografie neben der klinischen Untersuchung eine entscheidende Rolle in der fruhen Diagnosestellung einer JIA ein mit dem Ziel, dem Patienten so fruh wie moglich eine effiziente Therapie zukommen zu lassen (Window of Opportunity). Zusatzlich kann die Gelenksonografie, eingebettet in das „Treat-to-Target“-Konzept, eine wichtige Rolle in der Verlaufskontrolle und Evaluation einer subklinischen Entzundungsaktivitat spielen. Bisherige etablierte Diagnose-, Verlaufs- und auch Remissionskriterien einer JIA lassen stringente und objektivierbare bildgebende Kriterien vermissen, obwohl sich Qualitat und Erfahrung bei der Gelenksonografie stetig verbessern. Neben den sonografischen Kriterien haben sich inzwischen auch verschiedene Biomarker zur Beurteilung der Krankheitsaktivitat etabliert. Mit der Entwicklung der Sonografie und sicheren Testung von Biomarkern konnte sich in Zukunft zur fruhen Diagnosestellung und sicheren Remissionseinschatzung eine Kombination aus immunologischen und sonografischen Kriterien etablieren, die das bisherige „Treat-to-Target“-Konzept bei der JIA unterstutzen und verbessern. In this article the current role and development of musculoskeletal ultrasound as a central component of treat-to-target management of JIA is discussed. Musculoskeletal ultrasound alongside clinical examination plays a significant role in the early diagnosis of JIA, with the aim of initiating treatment as soon as possible and within the “window of opportunity”. Including ultrasound in treat-to-target strategies could play an important role in the monitoring and evaluation of clinical as well as subclinical inflammation. However, despite continuous improvements in the quality and experience of ultrasound capabilities, existing diagnostic, prognostic and remission criteria are still lacking objective imaging-specific criteria. Other than ultrasound, immunological biomarkers have also shown utility for the evaluation of clinical activity. The development of ultrasound and routine testing of biomarkers, and potentially both combined, could allow earlier diagnosis and more accurate prediction of disease remission, thereby supporting and improving the ability to treat JIA to target.
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- 2021
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12. Biologics with or without methotrexate in treatment of polyarticular juvenile idiopathic arthritis: effectiveness, safety and drug survival
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Franz Thiele, Ariane Klein, Jens Klotsche, Daniel Windschall, Frank Dressler, Jasmin Kuemmerle-Deschner, Kirsten Minden, Ivan Foeldvari, Dirk Foell, Sonja Mrusek, Prasad Thomas Oommen, and Gerd Horneff
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Rheumatology ,Pharmacology (medical) - Abstract
Objective To investigate the impact of additionally given MTX on biologic treatment of polyarticular JIA in terms of effectiveness, safety and drug survival. Methods Patients suffering from polyarticular JIA and treated with either monotherapy with a first biologic or a combination of a biologic and MTX were selected from the BIKER registry. The TNF-α inhibitors (TNFi) adalimumab, etanercept and golimumab and the IL-6 inhibitor tocilizumab were considered. Upon a non-randomized study design, we adjusted the different cohorts using propensity score matching to improve comparability. Results A total of 2148 patients entered the analysis, who were treated by either combination therapy (n = 1464) or monotherapy (n = 684). Disease activity declined significantly more in patients upon combination therapy than upon biologic monotherapy. Comparison of adjusted cohorts revealed that patients who received TNFi gained more benefit from additionally given MTX than patients treated with tocilizumab. Median survival time of therapy with biologics was significantly longer upon combination therapy (3.1 years) than with monotherapy (2.7 years), as demonstrated by a Kaplan–Meier analysis (log rank test: P = 0.002). The safety profile was moderately affected by additional MTX due to increased incidence of gastrointestinal and hepatic adverse events. Serious adverse events occurred at an equal rate of 3.6 events per 100 patient-years in both cohorts. Conclusion Additionally given MTX improves the effectiveness of biologic treatment in polyarticular JIA without seriously compromising treatment safety. Especially TNFi benefit from combination, while no improvement in outcome has been observed by combining tocilizumab with MTX.
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- 2022
13. Procedures for the content, conduct and format of EULAR/PReS paediatric musculoskeletal ultrasound courses
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Silvia, Magni-Manzoni, Valentina, Muratore, Jelena, Vojinović, Denise, Pires Marafon, Maria Antonietta, D'Agostino, Esperanza, Naredo, Daniel, Windschall, and UAM. Departamento de Medicina
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Settore MED/16 - REUMATOLOGIA ,Consensus ,Outcome Assessment ,Medicina ,Arthritis ,Immunology ,Juvenile ,Ultrasonography/methods ,Arthritis, Juvenile ,Health Care ,Europe ,Rheumatology ,Outcome Assessment, Health Care ,Health services research ,Immunology and Allergy ,Humans ,Rheumatology/education ,Rheumatologists ,Child ,Ultrasonography - Abstract
BackgroundDespite the worldwide increasing request of education on paediatric musculoskeletal ultrasound (PedMSUS), content, conduct and format of PedMSUS courses have never been internationally agreed.ObjectivesTo produce educational procedures for the conduct, content and format of EULAR/PReS PedMSUS courses.MethodsAfter a systemic literature review and expert opinion collection, a panel of items for the development of procedures on PedMSUS courses was identified. Agreement on the items was assessed through Delphi surveys among a taskforce of 24 members, which included 18 experts in PedMSUS (8 rheumatologists, 1 radiologist, 9 paediatric rheumatologists), 1 methodologist and rheumatologist expert in MSUS, 2 patient research partners, 1 health professional in rheumatology and 2 EMEUNET/EMERGE members, from 8 different European countries. Each item was assessed through a 5-point Likert scale (0, full disagreement; 5, full agreement); agreement was reached for >75% of answers rating 4–5. All items with agreement were included in the preliminary core set of educational procedures, which underwent external assessment by a broader Consensus group (Faculty and Tutors of previous EULAR PedMSUS courses and PReS Imaging Working Party members), through Delphi survey.ResultsTwo Delphi surveys produced the preliminary core set of procedures for basic, intermediate, advanced and teach-the-teachers (TTT) PedMSUS courses. A Delphi survey within the Consensus group produced agreement on the proposed procedures.ConclusionsShared EULAR/PReS procedures for the conduct, content and format of basic, intermediate, advanced and TTT PedMSUS courses were identified on international basis.
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- 2022
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14. The new role of musculoskeletal ultrasound in the treat-to-target management of juvenile idiopathic arthritis
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Faekah Gohar and Daniel Windschall
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medicine.medical_specialty ,Arthritis ,Physical examination ,Musculoskeletal ultrasound ,03 medical and health sciences ,0302 clinical medicine ,Rheumatology ,Internal medicine ,medicine ,Humans ,Pharmacology (medical) ,030212 general & internal medicine ,Intensive care medicine ,Musculoskeletal System ,Ultrasonography ,030203 arthritis & rheumatology ,Tenosynovitis ,medicine.diagnostic_test ,business.industry ,Enthesitis ,medicine.disease ,Precision medicine ,Arthritis, Juvenile ,medicine.symptom ,business ,Paediatric rheumatology - Abstract
This article reviews the role of musculoskeletal ultrasound (MSUS) for the diagnosis, monitoring and treat-to-target management of JIA. Technological advancements in MSUS allow more precise evaluation of arthritis, tenosynovitis and enthesitis versus clinical examination alone, which may assist treatment decisions. In adult studies, serum and synovial biomarkers have correlated with MSUS findings. Within paediatric rheumatology, significant developments in the definition of normal and pathology, a necessity for the future integration of MSUS into treat-to-target management, have already been reached or are underway, which in turn could allow tighter control of disease activity and earlier identification of treatment response and failure, bringing the goal of ‘precision medicine’ closer. Additionally, the utility of MSUS for the evaluation of subclinical disease remains an unexamined area of interest. ‘Ultrasound remission’ combined with clinical assessment and immunological markers could therefore potentially improve the treat-to-target management of JIA.
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- 2021
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15. Sonografie in der pädiatrischen Rheumatologie
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Daniel Windschall and Johannes Roth
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- 2022
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16. Re-treatment with etanercept is as effective as the initial firstline treatment in patients with juvenile idiopathic arthritis
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Gerd Horneff, Daniel Windschall, Ivan Foeldvari, Kirsten Minden, Paula Hoff, Johannes-Peter Haas, Ariane Klein, Jens Klotsche, and Martina Niewerth
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medicine.medical_specialty ,Adolescent ,Remission ,Arthritis ,Effectiveness ,Diseases of the musculoskeletal system ,Disease ,Etanercept ,03 medical and health sciences ,Young Adult ,0302 clinical medicine ,Window of opportunity ,Internal medicine ,Disease flare ,medicine ,Humans ,030212 general & internal medicine ,Prospective Studies ,Adverse effect ,Child ,030203 arthritis & rheumatology ,Oligoarthritis ,business.industry ,Hazard ratio ,Inactive disease ,Infant ,Juvenile idiopathic arthritis ,medicine.disease ,Rheumatology ,Arthritis, Juvenile ,Discontinuation ,Methotrexate ,Treatment Outcome ,RC925-935 ,Antirheumatic Agents ,business ,medicine.drug ,Research Article - Abstract
Objectives To determine (i) correlates for etanercept (ETA) discontinuation after achieving an inactive disease and for the subsequent risk of flare and (ii) to analyze the effectiveness of ETA in the re-treatment after a disease flare. Methods Data from two ongoing prospective registries, BiKeR and JuMBO, were used for the analysis. Both registries provide individual trajectories of clinical data and outcomes from childhood to adulthood in juvenile idiopathic arthritis (JIA) patients treated with biologic disease-modifying anti-rheumatic drugs (bDMARDs) and conventional synthetic DMARDs (csDMARDs). Results A total of 1724 patients were treated first with ETA treatment course (338 with second, 54 with third ETA course). Similar rates of discontinuation due to ineffectiveness and adverse events could be observed for the first (19.4%/6.2%), second (18.6%/5.9%), and third (14.8%/5.6%) ETA course. A total of 332 patients (+/−methotrexate, 19.3%) discontinued ETA after achieving remission with the first ETA course. Younger age (hazard ratio (HR) 1.08, p p = 0.004), and shorter duration between JIA onset and ETA start (HR 1.10, p p n = 117 of 161; 72.7%) after the flare. One in five patients (n = 23, 19.7%) discontinued ETA again after achieving an inactive disease and about 70% of the patients achieved an inactive disease 12 months after restarting ETA. Conclusion The study confirms the effectiveness of ETA even for re-treatment of patients with JIA. Our data highlight the association of an early bDMARD treatment with a higher rate of inactive disease indicating a window of opportunity.
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- 2021
17. Experiences with IL-1 blockade in systemic juvenile idiopathic arthritis : Data from the German AID-registry
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Gerd Horneff, Rolf-Michael Küster, Rainer Berendes, Jens Klotsche, Thomas Lutz, Claas Hinze, Christoph Rietschel, Boris Hügle, Elisabeth Weissbarth-Riedel, Dirk Foell, Helmut Wittkowski, Daniel Windschall, Johannes-Peter Haas, Elke Lainka, Prasad T. Oommen, Klaus Tenbrock, Frank Weller-Heinemann, Eggert Lilienthal, N. Fischer, Melanie Baehr, Georg Heubner, Tilmann Kallinich, Tim Niehues, Bernadette Raszka, and Ulrich Neudorf
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0301 basic medicine ,medicine.medical_specialty ,Autoinflammatory disease ,lcsh:Diseases of the musculoskeletal system ,Adolescent ,Canakinumab ,Interleukin-1beta ,Medizin ,Arthritis ,Disease ,Antibodies, Monoclonal, Humanized ,Young Adult ,03 medical and health sciences ,0302 clinical medicine ,Rheumatology ,Systemic juvenile idiopathic arthritis ,Germany ,Internal medicine ,medicine ,Humans ,Immunology and Allergy ,Registries ,Child ,Adverse effect ,Retrospective Studies ,030203 arthritis & rheumatology ,Proinflammatory cytokines ,Anakinra ,business.industry ,lcsh:RJ1-570 ,Infant ,lcsh:Pediatrics ,medicine.disease ,Arthritis, Juvenile ,Blockade ,Interleukin 1 Receptor Antagonist Protein ,030104 developmental biology ,Antirheumatic Agents ,Child, Preschool ,Concomitant ,Pediatrics, Perinatology and Child Health ,lcsh:RC925-935 ,business ,Research Article ,medicine.drug ,Interleukin-1 - Abstract
Pediatric rheumatology 19(1), 38 (2021). doi:10.1186/s12969-021-00510-8, Published by BioMed Central, London
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- 2021
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18. Zunehmende Bedeutung von Gelenkultraschall und MRT
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Daniel Windschall
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Gynecology ,medicine.medical_specialty ,business.industry ,medicine ,business - Abstract
Der Einsatz bildgebender Methoden hat in der Kinderrheumatologie in den vergangenen 15 Jahren deutlich zugenommen. Heute kann man mit sensitiven bildgebenden Methoden erganzend zur physikalischen Untersuchung das Fruhstadium einer kindlich rheumatischen Erkrankung erfassen.
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- 2018
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19. Arthrosonographic Reference Values of the Shoulder Joint in Healthy Children and Adolescents: A Cross-Sectional Multicentre Ultrasound Study
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Hartwig W. Lehmann, Katharina Palm-Beden, Rainer Berendes, Ralf Felix Trauzeddel, Antje Nimtz-Talaska, Maria Haller, Philipp Schoof, Manuela Krumrey-Langkammerer, Daniel Windschall, Ralf Trauzeddel, Christine Nirschl, and Gerd Ganser
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Cartilage, Articular ,Male ,musculoskeletal diseases ,Adolescent ,030204 cardiovascular system & hematology ,03 medical and health sciences ,0302 clinical medicine ,Reference Values ,Joint capsule ,medicine ,Humans ,Child ,Pathological ,Joint (geology) ,Ultrasonography ,030203 arthritis & rheumatology ,Orthodontics ,Ultrasound study ,Shoulder Joint ,business.industry ,Infant ,Capsule ,Anatomy ,Gray scale ultrasound ,Cross-Sectional Studies ,medicine.anatomical_structure ,Child, Preschool ,Reference values ,Pediatrics, Perinatology and Child Health ,Female ,Shoulder joint ,business - Abstract
Background Defining of gray scale ultrasound standard reference values of the shoulder joint in childhood and adolescence during maturation. Patients: We examined 445 healthy girls and boys between 1 year and 18 years of age. Method A cross-sectional multicentre grey-scale ultrasound study was performed to examine the shoulder joint on both sides. The children were divided according to their gender and were further classified into six age groups, which constituted three-year age ranges, to record anatomical development changes. We measured the capsule-bone distance (BCD) as a representation of the intracapsular cavity, as well as the thickness of the joint capsule and joint cartilage. Values were expressed in mean±standard deviation (SD) and minimum-maximum (min-max). The shape of the joint capsule and capsule-bone junction zone was qualitatively analysed. Results The joint cartilage thickness decreased with increasing age in all joints independently from sex and body side. However, the BCD and the capsule thickness increased with age. There was no intraarticular fluid visible. The joint capsule had a predominantly concave form, whereas the capsule-bone junction was mostly sharp. Discussion This study is the first describing age-related normal values of the intracapsular cavity, joint capsule and cartilage thickness as well as their respective shape in a large cohort of healthy children. Conclusion The findings could be helpful to differentiate between physiological and pathological joint conditions and thereby distinguishing age-related variations from alterations caused by inflammation.
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- 2017
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20. Age-related vascularization and ossification of joints in children: an international pilot study to test multi-observer ultrasound reliability
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Esperanza Naredo, Silvia Magni-Manzoni, Paz Collado, Annamaria Iagnocco, George A W Bruyn, Viviana Ravagnani, Juan Carlos Nieto, Maria Antonietta D'Agostino, Nikolay Tzaribachev, Cristina Hernández-Díaz, Jelena Vojinovic, Daniel Windschall, Peter V. Balint, Infection et inflammation (2I), and Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut National de la Santé et de la Recherche Médicale (INSERM)
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Male ,medicine.medical_specialty ,Settore MED/16 - REUMATOLOGIA ,Adolescent ,[SDV]Life Sciences [q-bio] ,Neovascularization, Physiologic ,Pilot Projects ,joint vascularization ,Wrist ,Musculoskeletal ultrasound ,age-related findings ,paediatric cohort ,skeletal maturation ,03 medical and health sciences ,0302 clinical medicine ,Rheumatology ,Osteogenesis ,Reference Values ,medicine ,Humans ,Child ,Grading (tumors) ,030203 arthritis & rheumatology ,business.industry ,Ossification ,Synovial Membrane ,Reproducibility of Results ,Ultrasonography, Doppler ,Metacarpophalangeal joint ,Intra-rater reliability ,3. Good health ,Surgery ,medicine.anatomical_structure ,Epiphysis ,Child, Preschool ,Female ,Joints ,Radiology ,Ankle ,medicine.symptom ,business ,Kappa - Abstract
Objective To determine the intra- and inter-observer reliability of ultrasound (US)-detected age-related joint vascularization and ossification grading in healthy children. Methods Following standardized image acquisition and machine setting protocols, 10 international US experts examined four joints (wrist, second metacarpophalangeal joint, knee, and ankle) in 12 healthy children (divided into four age groups: 2–4, 5–8, 9–12, and 13–16 years). Grey-scale was used to detect the ossification grade, and power Doppler (PD) US was used to detect physiological vascularization. Ossification was graded from grade 0 (no ossification) to grade 3 (complete ossification). A positive PD signal was defined as any PD signal inside the joint. Kappa statistics were applied for intra- and inter-observer reliability. Results According to the specific joint and age, up to four solitary PD signals (mean, 1.5) were detected within each joint area with predominant localization of the physiological vascularization in specific anatomic positions: fat pad, epiphysis, physis, and short bone cartilage. The kappa values for ossification grading were 0.87 (range, 0.85–0.91) and 0.58 for intra- and inter-observer reliability, respectively. The bias-adjusted kappa values for intra- and inter-observer reliability were 0.71 (range, 0.44–1.00) and 0.69, respectively. Conclusion Detection of normal findings (i.e., grading of physiological ossification during skeletal maturation and identification of physiological vessels) can be highly reliable by using clear definitions and a standardized acquisition protocol. These data will permit development of a reliable and standardized US approach for evaluating paediatric joint pathologies. This article is protected by copyright. All rights reserved.
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- 2020
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21. Ultrasound imaging in paediatric rheumatology
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Daniel Windschall and Clara Malattia
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medicine.medical_specialty ,Monitoring ,Normative data ,03 medical and health sciences ,Ultrasound studies ,0302 clinical medicine ,Rheumatology ,Rheumatic Diseases ,Internal medicine ,Synovitis ,medicine ,Humans ,Medical physics ,Pediatric rheumatology ,030212 general & internal medicine ,Ultrasound pathology ,Child ,Ultrasonography ,030203 arthritis & rheumatology ,Tenosynovitis ,Practical aspects ,Ultrasound imaging ,business.industry ,Ultrasound ,Enthesitis ,medicine.disease ,medicine.symptom ,business ,Paediatric rheumatology - Abstract
The role of ultrasound imaging in the diagnosis and monitoring of paediatric rheumatic diseases with special emphasis on recent scientific work regarding the evidence base and standardization of this technique is being reviewed. An overview of the most important practical aspects for the use of musculoskeletal ultrasound in a clinical setting is also provided. Huge scientific efforts and advances in recent years illustrate the increasing importance of musculoskeletal ultrasound in pediatric rheumatology. Several studies focused on setting an evidence-based standard for the ultrasound appearance of healthy and normal joints in children of all age groups. Physiologic vascularization and ossification were two main aspects of these studies. Other publications demonstrate that ultrasound imaging is also an important and useful tool to detect pathology as synovitis, tenosynovitis or enthesitis in children and to monitor pediatric patients with rheumatic conditions. Important practical aspects include training in the use of correct ultrasound techniques, as well as knowledge and experience of normal pediatric sonoanatomy and the appearance of pathological findings on ultrasound.
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- 2020
22. Wrist and Hand
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Daniel Windschall
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medicine.medical_specialty ,Tenosynovitis ,business.industry ,Ossification ,Ultrasound ,Musculoskeletal ultrasound ,Wrist ,medicine.disease ,body regions ,medicine.anatomical_structure ,Synovitis ,Physical therapy ,Medicine ,medicine.symptom ,business ,Paediatric rheumatology - Abstract
Musculoskeletal ultrasound (MSUS) of paediatric wrists and hands can be a challenge due to age-specific physiological development and findings. MSUS of the hands and wrists is an important tool to diagnose inflammatory conditions, and the examiner must be highly knowledgeable about the normal age-related findings in these anatomic regions. This chapter covers the most important standard scans of paediatric wrists and hands and gives an overview of the normal paediatric sonoanatomy. In this chapter, basic pathologic findings are demonstrated by examples from paediatric rheumatology.
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- 2019
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23. US Guided Interventional Procedures in Paediatrics
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Johannes Roth and Daniel Windschall
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musculoskeletal diseases ,medicine.medical_specialty ,business.industry ,Ultrasound ,Arthritis ,medicine.disease ,Joint injections ,Joint aspiration ,Joint injection ,Medicine ,Intraarticular Corticosteroid ,Radiology ,Pediatric rheumatology ,business ,Fluid aspiration - Abstract
Ultrasound imaging guidance of needles introduced for the purpose of joint aspiration or joint injection is becoming increasingly popular. The use of ultrasound increases the safety and efficacy of joint injections in pediatric rheumatology. Needle guidance may be important for diagnostic purposes (fluid aspiration) as well as injections in juvenile idiopathic arthritis (JIA) for short-term relief via intraarticular corticosteroid (CS) injections or longer-term management of limited disease and treatment-resistant multi-joint disease. Ultrasound guidance can also be used to inject steroids into tendon sheaths or around entheses in inflammatory conditions. The following chapter gives an overview of typical indications for ultrasound-guided intraarticular injections in pediatric rheumatology and describes the procedures used for ultrasound guidance of CS injections in specific anatomic regions.
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- 2019
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24. Correction to: Age dependent ultrasound B-mode findings of the elbow joint in healthy children and adolescents
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Daniel Windschall, Maria Haller, Ralf Trauzeddel, Antje Nimtz-Talaska, Hartwig W. Lehmann, Gerd Ganser, Ralf Felix Trauzeddel, Katharina Palm-Beden, Manuela Krumrey-Langkammerer, Philipp Schoof, Christine Nirschl, and Rainer Berendes
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030203 arthritis & rheumatology ,medicine.medical_specialty ,Ultrasound b mode ,business.industry ,Immunology ,Elbow ,Age dependent ,Rheumatology ,03 medical and health sciences ,0302 clinical medicine ,medicine.anatomical_structure ,Physical medicine and rehabilitation ,Internal medicine ,Correct name ,Immunology and Allergy ,Medicine ,030212 general & internal medicine ,business ,Joint (audio engineering) - Abstract
The Second author’s name was incorrectly published in the original article. The correct name is Hartwig Wilhelm Lehmann.
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- 2019
25. Toward Standardized Musculoskeletal Ultrasound in Pediatric Rheumatology: Normal Age-Related Ultrasound Findings
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Annamaria Iagnocco, Jelena Vojinovic, Esperanza Naredo, Daniel Windschall, George A W Bruyn, Maria Antonietta D'Agostino, Paz Collado, Silvia Magni-Manzoni, and Juan Carlos Nieto
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030203 arthritis & rheumatology ,medicine.medical_specialty ,business.industry ,Hyaline cartilage ,Ultrasound ,MEDLINE ,Soft tissue ,Musculoskeletal ultrasound ,030218 nuclear medicine & medical imaging ,03 medical and health sciences ,0302 clinical medicine ,medicine.anatomical_structure ,Rheumatology ,Predictive value of tests ,Medicine ,Radiology ,Pediatric rheumatology ,business ,Prospective cohort study - Abstract
Objective. Musculoskeletal (MS) ultrasound (US) is increasingly being used as an extension of paediatric clinical practice, particularly in the clinical management of children with juvenile idiopathic arthritis (JIA). MSUS is most commonly used in the assessment of effusion and synovial hypertrophy and detection of soft tissue disorders. It can also be used to visualise other structures, such as hyaline cartilage and bone surfaces. Given the unique anatomy of the growing skeleton, many of the difficulties encountered in its use result from misinterpretation of MSUS images. Thus, a detailed knowledge of anatomy in healthy children, both in B-mode and Doppler mode, is mandatory. Additionally, as US is the most operator-dependent imaging modality, the experience and expertise of the examiner will determine the value of the diagnostic information obtained from this technique. Incorrect acquisition and interpretation of images may result in inappropriate disease management. Thus, a systematic scanning method and a standardised evaluation procedure are essential in children.
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- 2016
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26. Development of semiquantitative ultrasound scoring system to assess cartilage in rheumatoid arthritis
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Eugenio de Miguel, David Kane, Artur Bachta, Cristina Hernández-Díaz, Lene Terslev, Nemanja Damjanov, Daniel Windschall, Irina Gessl, Esperanza Naredo, Helen Keen, Juan Carlos Nieto, G. Supp, Marina Backhaus, Wolfgang A. Schmidt, Christian Dejaco, Ana M. Rodríguez, Richard J. Wakefield, Eszter Kővári, Emilio Filippucci, Paul Studenic, Alexander Platzer, Andrea Delle-Sedie, George A W Bruyn, Marwin Gutierrez, David Bong, Marcin Szkudlarek, Uffe Møller-Dohn, Ralf G. Thiele, Annmaria Iagnocco, Paz Collado, Maria Antonietta D'Agostino, Peter Mandl, Hilde Berner Hammer, Christina Duftner, Stephen Kelly, Ingrid Möller, Peter V. Balint, Kei Ikeda, and Carlos Pineda
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Adult ,Male ,rheumatoid arthritis ,medicine.medical_specialty ,Scoring system ,Settore MED/16 - REUMATOLOGIA ,Delphi Technique ,Advisory Committees ,Severity of Illness Index ,cartilage ,ultrasound ,Arthritis, Rheumatoid ,Metacarpophalangeal Joint ,03 medical and health sciences ,0302 clinical medicine ,Rheumatology ,Internal medicine ,Rheumatoid ,medicine ,Humans ,Pharmacology (medical) ,030212 general & internal medicine ,Reliability (statistics) ,Ultrasonography ,030203 arthritis & rheumatology ,Observer Variation ,business.industry ,Cartilage ,Arthritis ,Ultrasound ,Reproducibility of Results ,Metacarpophalangeal joint ,Middle Aged ,medicine.disease ,3. Good health ,medicine.anatomical_structure ,Rheumatoid arthritis ,Female ,Radiology ,business ,Kappa - Abstract
Objectives To develop and test the reliability of a new semiquantitative scoring system for the assessment of cartilage changes by ultrasound in a web-based exercise as well as a patient exercise of patients with RA. Methods A taskforce of the Outcome Measures in Rheumatology Ultrasound Working Group performed a systematic literature review on the US assessment of cartilage in RA, followed by a Delphi survey on cartilage changes and a new semiquantitative US scoring system, and finally a web-based exercise as well as a patient exercise. For the web-based exercise, taskforce members scored a dataset of anonymized static images of MCP joints in RA patients and healthy controls, which also contained duplicate images. Subsequently, 12 taskforce members used the same US to score cartilage in MCP and proximal interphalangeal joints of six patients with RA in in a patient reliability exercise. Percentage agreement and prevalence of lesions were calculated, as intrareader reliability was assessed by weighted kappa and interreader reliability by Light’s kappa. Results The three-grade semiquantitative scoring system demonstrated excellent intrareader reliability (kappa: 0.87 and 0.83) in the web-based exercise and the patient exercise, respectively. Interreader reliability was good in the web-based exercise (kappa: 0.64) and moderate (kappa: 0.48) in the patient exercise. Conclusion Our study demonstrates that ultrasound is a reliable tool for evaluating cartilage changes in the MCP joints of patients with RA and supports further development of a new reliable semiquantitative ultrasound scoring system for evaluating cartilage involvement in RA.
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- 2019
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27. Age dependent ultrasound B-mode findings of the elbow joint in healthy children and adolescents
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Rainer Berendes, Katharina Palm-Beden, Antje Nimtz-Talaska, Daniel Windschall, Hartwig Lehman, Ralf Trauzeddel, Philipp Schoof, Christine Nirschl, Maria Haller, Gerd Ganser, Ralf Felix Trauzeddel, and Manuela Krumrey-Langkammerer
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musculoskeletal diseases ,Male ,medicine.medical_specialty ,Adolescent ,Immunology ,Elbow ,03 medical and health sciences ,0302 clinical medicine ,Child Development ,Rheumatology ,Reference Values ,Internal medicine ,Joint capsule ,Elbow Joint ,medicine ,Immunology and Allergy ,Humans ,030212 general & internal medicine ,Child ,Joint (geology) ,Pathological ,Ultrasonography ,030203 arthritis & rheumatology ,Orthodontics ,business.industry ,Ultrasound ,Age Factors ,Capsule ,Infant ,Adolescent Development ,Healthy Volunteers ,medicine.anatomical_structure ,Child, Preschool ,Female ,business ,Paediatric rheumatology - Abstract
Due to maturation of joints, various changes take place, not only in the field of paediatric rheumatology but also in paediatric orthopaedics musculoskeletal ultrasound plays an important role in both the diagnosis and the follow-up of diseases in this field. To differentiate between physiological and pathological findings, the knowledge of reference values of joint structures is indispensable. The objective was to define B-mode ultrasound age- and sex-related reference values for the elbow joint in healthy children and adolescents during maturation. In a cross-sectional, multicentre ultrasound study we examined both sides of the elbow joints of 437 healthy children and adolescents (194 boys/243 girls) being between one and less than 18 years old. The children were classified into six equal age groups and divided according to their gender. We measured the distance between the outer margin of the joint capsule and the bone surface to define the bone-capsule distance (BCD), the thickness of the joint cartilage as well as the thickness of the joint capsule. The bone–capsule junction zone and the shape of the joint capsule were analysed qualitatively. The bone capsule distance and the capsule thickness increased with age. In contrast, the joint cartilage thickness decreased. In most cases the junction zone was peaked. The joint capsule showed mostly a concave shape. Intra- and interobserver reliabilities were good. We propose B-mode ultrasound age- and sex-related reference values for the elbow joint in a large number of healthy children and adolescents for the first time. By applying these standard values to the ultrasound examination of the elbow joint, it may be possible to achieve greater certainty in the diagnosis of pathological processes.
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- 2018
28. Nachrichten der Gesellschaft für Kinder- und Jugendrheumatologie
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Daniel Windschall
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General Medicine - Published
- 2019
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29. Preliminary Definitions for the Sonographic Features of Synovitis in Children
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Alessandra Bruns, Jelena Vojinovic, Daniel Windschall, Sarah Ohrndorf, Sandrine Jousse-Joulin, Troels Herlin, Cristina Hernandez, Lorenia De la Cruz, Clara Malattia, Maria Antonietta D'Agostino, Severine Guillaume-Czitrom, George A W Bruyn, Juan-Carlos Nieto, Silvia Magni-Manzoni, Patricia Vega-Fernandez, C. Modesto, Peter V. Balint, Anne-Marit Selvaag, Johannes Roth, Tracy V. Ting, Paz Collado, Stefano Lanni, Viviana Ravagnani, Nanno Swen, Esperanza Naredo, Marina Backhaus, Ana M. Rodríguez, Annamaria Iagnocco, Vibke Lilleby, Linda Rossi-Semerano, Nikolay Tzaribachev, Dpt of Pediatrics, Children's hospital of Eastern Ontario Research Institute, University of Ottawa [Ottawa]-Hospital of Eastern Ontario Research Institute, ASST Mantova, Park-Klinik Weissensee, National Institute of Rheumatology and Physiotherapy, Budapest, Centre Hospitalier Universitaire de Sherbrooke, MC Groep Hospitals, Lelystad, Severo Ochoa Hospital, Nuevo Leon, Hôpital Bicêtre, Université Paris-Sud - Paris 11 (UP11)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Bicêtre, Instituto Nacional de Rehabilitacion, Università degli studi di Torino = University of Turin (UNITO), CHRU Brest - Service de Rhumatologie (CHU - BREST - Rhumato), Centre Hospitalier Régional Universitaire de Brest (CHRU Brest), Lymphocytes B, Autoimmunité et Immunothérapies (LBAI), Université de Brest (UBO)-Institut National de la Santé et de la Recherche Médicale (INSERM)-LabEX IGO Immunothérapie Grand Ouest-Institut Brestois Santé Agro Matière (IBSAM), Université de Brest (UBO), Instituto Giannina Gaslini, Genoa, Oslo University Hospital [Oslo], IRCCS Ospedale Pediatrico Bambino Gesù [Roma], Vall d'Hebron Institute of Oncology [Barcelone] (VHIO), Vall d'Hebron University Hospital [Barcelona], Hospital Universitario Ramón y Cajal [Madrid], Universidad de Alcalá - University of Alcalá (UAH), Hospital General Universitario 'Gregorio Marañón' [Madrid], Charité - UniversitätsMedizin = Charité - University Hospital [Berlin], Service de Pédiatrie et Pédiatrie Rhumatologique, Université Paris-Sud - Paris 11 (UP11)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital de Bicêtre, Medisch Centrum Alkmaar, Alkmaar, Cincinnati Children's Hospital Medical Center, Pediatric Rheumatology Research Institute, Bad Bramstedt, Emory University [Atlanta, GA], University Clinical Center, Nis, Asklepios Hospital Weissenfels, Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Infection et inflammation (2I), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut National de la Santé et de la Recherche Médicale (INSERM), Università degli studi di Torino (UNITO), Lymphocyte B et Auto-immunité (LBAI), Université de Brest (UBO)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut Brestois Santé Agro Matière (IBSAM), and Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)
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medicine.medical_specialty ,Settore MED/16 - REUMATOLOGIA ,Consensus ,Ultrasonography ,Pediatric Rheumatology ,Outcome Measures ,Synovitis ,Imaging ,[SDV]Life Sciences [q-bio] ,Delphi method ,MEDLINE ,030218 nuclear medicine & medical imaging ,Likert scale ,03 medical and health sciences ,0302 clinical medicine ,Rheumatology ,Musculoskeletal ultrasonography ,Medicine ,Humans ,Child ,ComputingMilieux_MISCELLANEOUS ,030203 arthritis & rheumatology ,business.industry ,Doppler ,Pediatric age ,Ultrasonography, Doppler ,medicine.disease ,3. Good health ,Synovial hypertrophy ,Clinical Practice ,Physical therapy ,business - Abstract
Objectives Musculoskeletal ultrasonography (US) has the potential to be an important tool in the assessment of disease activity in childhood arthritides. To assess pathology, clear definitions for synovitis need to be developed first. The aim of this study was to develop and validate these definitions through an international consensus process. Methods The decision on which US techniques to use, the components to be included in the definitions as well as the final wording were developed by 31 ultrasound experts in a consensus process. A Likert scale of 1-5 with 1 indicating complete disagreement and 5 complete agreement was used. A minimum of 80% of the experts scoring 4 or 5 was required for final approval. The definitions were then validated on 120 standardized US images of the wrist, MCP and tibiotalar joints displaying various degrees of synovitis at various ages. Results B-Mode and Doppler should be used for assessing synovitis in children. A US definition of the various components (i.e. synovial hypertrophy, effusion and Doppler signal within the synovium) was developed. The definition was validated on still images with a median of 89% (range 80-100) of participants scoring it as 4 or 5 on a Likert scale. Conclusions US definitions of synovitis and its elementary components covering the entire pediatric age range were successfully developed through a Delphi process and validated in a web-based still images exercise. These results provide the basis for the standardized US assessment of synovitis in clinical practice and research. This article is protected by copyright. All rights reserved.
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- 2017
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30. SAT0636 Ultrasonography definitions for synovitis grading in children: the omeract pediatric ultrasound task force
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S Guillaume Czitrom, Troels Herlin, Nikolay Tzaribachev, Annamaria Iagnocco, Gordana Susic, George A W Bruyn, Jelena Vojinovic, M-A D'Agostino, Silvia Magni-Manzoni, Daniel Windschall, Stefano Lanni, Clara Malattia, Paz Collado, Lene Terslev, Viviana Ravagnani, Nemanja Damjanov, C. Hernandez-Diaz, Esperanza Naredo, and JC Nieto Gonzales
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030203 arthritis & rheumatology ,medicine.medical_specialty ,medicine.diagnostic_test ,business.industry ,Physical examination ,Test validity ,Wrist ,medicine.disease ,030218 nuclear medicine & medical imaging ,03 medical and health sciences ,0302 clinical medicine ,medicine.anatomical_structure ,Cohen's kappa ,Synovitis ,medicine ,Content validity ,Physical therapy ,Ankle ,business ,Kappa - Abstract
Background Ultrasound (US) was found to have face and content validity for detecting synovitis in juvenile idiopathic arthritis (JIA) with higher sensitivity than clinical examination. In order to test validity and improve the applicability of US in JIA, the OMERACT US pediatric subtask force recently published preliminary definitions for the sonographic features of synovitis in children. Objectives Aim of this study was to confirm and improve B-mode and color power/Doppler (PD) US definitions for synovial components and grading in children, by using an image and patient based exercise. Methods The definitions were confirmed and modified in a multi-step process. In the 1st step, definitions were developed in multi-round Delphi web based consensus process were ≥80% of participants would need to reach ≥80% of agreement on a Likert scale from 1–5 (1 strongly disagree, 2 disagree, 3 neutral, 4 agree, 5 strongly agree). In the 2nd step, in a face to face meeting, a subgroup of these experts revised the definitions for final wording and performed intra- and inter-observer reliability exercise study in JIA patients as the final 3rd phase of the process. The definitions were tested in four joints (wrist, 2nd MCP, knee and ankle) of JIA patients divided in four age groups following standardized image acquisition and machine setting protocol. Statistics program R (version 3.3.0) was used for the statistical analyses. For intra-rater agreement Cohen kappa and for inter-rater agreement prevalence and bias adjusted kappa (PABAK) were calculated if needed. Results Reliability exercise included 20 JIA patients (distributed in equal numbers by age groups), 14 observers, 4 joints/observer, 3 observers/joint, 360 intra- and 360 inter-observer tests. A 0–3 semi-quantitative B-mode and color power/Doppler US definitions for synovial components and grading, were agreed (presented in Figure 1). Conclusions The proposed synovitis grading for children showed to be reliable why the next step should be to test sensitivity to change in order to possibly be used as an outcome tool in JIA. Disclosure of Interest None declared
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- 2017
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31. OP0288 Reliability of a eular-omeract semiquantitative scoring system for the assessment of cartilage in rheumatoid arthritis
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David Kane, Daniel Windschall, C. Pineda, Lene Terslev, Hilde Berner Hammer, David Bong, Eszter Kővári, Annamaria Iagnocco, Christina Duftner, Peter Mandl, Wolfgang A. Schmidt, C. Hernandez Diaz, Paul Studenic, J-C Nieto, Peter V. Balint, Irina Gessl, M-A D'Agostino, Kei Ikeda, U Moeller-Doehn, Christian Dejaco, A. Rodriguez, Emilio Filippucci, Artur Bachta, A. Delle Sedie, G. Supp, Ralf G. Thiele, George A W Bruyn, E. Naredo, and Helen Keen
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medicine.medical_specialty ,Scoring system ,Hyaline cartilage ,business.industry ,Cartilage ,Normal cartilage ,medicine.disease ,medicine.anatomical_structure ,Rheumatoid arthritis ,Reliability study ,medicine ,Radiology ,business ,Reliability (statistics) ,Kappa - Abstract
Background Joint destruction in rheumatoid arthritis (RA) is comprised of hyaline cartilage and bone damage, with the former more clearly associated with irreversible physical disability than bony damage. Objectives To test the reliability of a semiquantitative scoring system for the assessment of cartilage by musculoskeletal ultrasound (US) in a web-based exercise as well as a patient-based reliability study of patients with RA. Methods Static images of metacarpophalangeal (MCP) joints 2–5 in RA patients and healthy controls were acquired and a dataset of 123 anonymized images including 25 duplicate images was circulated among an international EULAR-OMERACT taskforce of 25 rheumatologist experts in US who independently scored the images using a semiquantitative scoring system. Subsequently 12 taskforce members participated in a patient-based reliability study. During this meeting MCP joints 2–5 of 6 patients with RA were assessed twice on the same day by all experts using US machines (GE) equipped with high-frequency transducers (18–22MHz) with presets calibrated for the appropriate assessment of cartilage. Participants assessed metacarpal cartilage both in the standardized longitudinal midline scan as well as by freehand technique utilizing multiple planes and scored by the semiquantitative scoring system. Intraobserver reliability was assessed by Cohen9s kappa and interobserver reliability by Fleiss9 kappa. Results The three-grade semiquantitative (Grade 0, normal cartilage; Grade 1, minimal change; Grade 2, severe change) scoring system demonstrated excellent (kappa: 0.87) to good (kappa: 0.73) intraobserver reliability in the web-based exercise and the patient-based reliability study respectively. Interobserver reliability was good in the web-based exercise (kappa: 0.64) and moderate (kappa: 0.49) in the patient-based reliability study. The dynamic technique performed slightly better than the longitudinal midline scan alone. Conclusions A semiquantitative scoring system demonstrated good intra- and moderate to good inter-observer reliability in a web-based exercise and patient-based reliability study. Our study demonstrates that US is a reliable tool for evaluating cartilage and supports the use of a new semiquantitative US scoring system for evaluating cartilage change in RA. Acknowledgements The patient-based reliability study was supported by a research grant from UCB. Disclosure of Interest None declared
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- 2017
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32. Proceedings of the 23rd Paediatric Rheumatology European Society Congress: part one
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F. De Benedetti, J. Anton, M. Gattorno, H. Lachmann, I. Kone-Paut, S. Ozen, J. Frenkel, A. Simon, A. Zeft, E. Ben-Chetrit, H. M. Hoffman, Y. Joubert, K. Lheritier, A. Speziale, J. Guido, Roberta Caorsi, Federica Penco, Alice Grossi, Antonella Insalaco, Maria Alessio, Giovanni Conti, Federico Marchetti, Alberto Tommasini, Silvana Martino, Romina Gallizzi, Annalisa Salis, Francesca Schena, Francesco Caroli, Alberto Martini, Gianluca Damonte, Isabella Ceccherini, Marco Gattorno, Marie-Louise Frémond, Carolina Uggenti, Lien Van Eyck, Isabelle Melki, Darragh Duffy, Vincent Bondet, Yoann Rose, Bénédicte Neven, Yanick Crow, Mathieu P. Rodero, Yvonne Kusche, Johannes Roth, Katarzyna Barczyk-Kahlert, Giovanna Ferrara, Annalisa Chiocchetti, Silvio Polizzi, Josef Vuch, Diego Vozzi, Anna Mondino, Erica Valencic, Serena Pastore, Andrea Taddio, Flavio Faletra, Umberto Dianzani, Ugo Ramenghi, Qing Zhou, Xiaomin Yu, Erkan Demirkaya, Natalie Deuitch, Deborah Stone, Wanxia Tsai, Amanda Ombrello, Tina Romeo, Elaine F. Remmers, JaeJin Chae, Massimo Gadina, Steven Welch, Seza Ozen, Rezan Topaloglu, Mario Abinun, Daniel L. Kastner, Ivona Aksentijevich, Donatella Vairo, Rosalba Monica Ferraro, Giulia Zani, Jessica Galli, Micaela De Simone, Marco Cattalini, Elisa Fazzi, Silvia Giliani, Ebun Omoyinmi, Ariane Standing, Dorota Rowczenio, Annette Keylock, Sonia Melo Gomes, Fiona Price-Kuehne, Sira Nanthapisal, Claire Murphy, Thomas Cullup, Lucy Jenkins, Kimberly Gilmour, Despina Eleftheriou, Helen Lachmann, Philip Hawkins, Nigel Klein, Paul Brogan, Anita Dhanrajani, Mercedes Chan, Stephanie Pau, Janet Ellsworth, Jaime Guzman, Florence A. Aeschlimann, Marinka Twilt, Simon W. Eng, Shehla Sheikh, Ronald M. Laxer, Diane Hebert, Damien Noone, Christian Pagnoux, Susanne M. Benseler, Rae S. Yeung, Christoph Kessel, Katrin Lippitz, Toni Weinhage, Claas Hinze, Helmut Wittkowski, Dirk Holzinger, Niklas Grün, Dirk Föll, Pieter Van Dijkhuizen, Federica Del Chierico, Clara Malattia, Alessandra Russo, Denise Pires Marafon, Nienke M. ter Haar, Silvia Magni-Manzoni, Sebastiaan J. Vastert, Bruno Dallapiccola, Berent Prakken, Fabrizio De Benedetti, Lorenza Putignani, Berna Eren Fidanci, Kenan Barut, Serap Arıcı, Dogan Simsek, Mustafa Cakan, Ezgi D. Batu, Sezgin Şahin, Ayşenur Kısaarslan, Ebru Yilmaz, Özge Basaran, Ferhat Demir, Kubra Ozturk, Zübeyde Gunduz, Betül Sozeri, Balahan Makay, Nuray Ayaz, Onder Yavascan, Ozlem Aydog, Yelda Bilginer, Zelal Ekinci, Dilek Yıldız, Faysal Gök, Muferret Erguven, Erbil Unsal, Ozgur Kasapcopur, For the FMF Arthritis Vasculitis and Orphan Disease Research in Paediatric Rheumatology (FAVOR), Hafize E. Sönmez, Betül Sözeri, Yonatan Butbul, Seza Özen, Claudia Bracaglia, Giusi Prencipe, Manuela Pardeo, Geneviève Lapeyre, Emiliano Marasco, Walter Ferlin, Robert Nelson, Cristina de Min, N. Ruperto, H. I. Brunner, P. Quartier, T. Constantin, E. Alexeeva, K. Marzan, N. Wulffraat, R. Schneider, S. Padeh, V. Chasnyk, C. Wouters, J. B. Kuemmerle-Deschner, T. Kallinich, B. Lauwerys, E. Haddad, E. Nasonov, M. Trachana, O. Vougiouka, K. Leon, E. Vritzali, A. Martini, D. Lovell, PRINTO/PRCSG, Stefano Volpi, Claudia Pastorino, Francesca Kalli, Alessia Omenetti, Sabrina Chiesa, Arinna Bertoni, Paolo Picco, Gilberto Filaci, Elisabetta Traggiai, Marie-Louise Fremond, Naoki Kitabayashi, Olivero Sacco, Isabelle Meyts, Marie-Anne Morren, Carine Wouters, Eric Legius, Isabelle Callebaut, Christine Bodemer, Frederic Rieux-Laucat, Mathieu Rodero, Nadia Jeremiah, Alexandre Belot, Eric Jeziorski, Didier Bessis, Guilhem Cros, Gillian I. Rice, Bruno Charbit, Anne Hulin, Nihel Khoudour, Consuelo Modesto Caballero, Monique Fabre, Laureline Berteloot, Muriel Le Bourgeois, Philippe Reix, Thierry Walzer, Despina Moshous, Stéphane Blanche, Alain Fischer, Brigitte Bader-Meunier, Frédéric Rieux-Laucat, K. Annink, N. ter Haar, S. Al-Mayouf, G. Amaryan, K. Barron, S. Benseler, P. Brogan, L. Cantarini, M. Cattalini, A. Cochino, F. Dedeoglu, A. De Jesus, O. Dellacasa, E. Demirkaya, P. Dolezalova, K. Durrant, G. Fabio, R. Gallizzi, R. Goldbach-Mansky, E. Hachulla, V. Hentgen, T. Herlin, M. Hofer, H. Hoffman, A. Insalaco, A. Jansson, I. Koné-Paut, A. Kozlova, J. Kuemmerle-Deschner, R. Laxer, S. Nielsen, I. Nikishina, A. Ombrello, E. Papadopoulou-Alataki, A. Ravelli, D. Rigante, R. Russo, Y. Uziel, Nienke ter Haar, Jerold Jeyaratnam, Anna Simon, Matteo Doglio, Jordi Anton, Consuelo Modesto, Pierre Quartier, Esther Hoppenreijs, Luca Cantarini, Loredana Lepore, Inmaculada Calvo Penades, Christina Boros, Rita Consolini, Donato Rigante, Ricardo Russo, Jana Pachlopnik Schmid, Thirusha Lane, Nicolino Ruperto, Joost Frenkel, Chiara Passarelli, Elisa Pisaneschi, Virginia Messia, Antonio Novelli, Fabrizio Debenedetti, P. A. Brogan, X. Wei, Martina Finetti, Francesca Orlando, Elisabetta Cortis, Angela Miniaci, Nicola Ruperto, Charlotte Eijkelboom, Pavla Dolezalova, Isabelle Koné-Paut, Marija Jelusic-Drazic, Liliana Bezrodnik, Mari Carmen Pinedo, Valda Stanevicha, Marielle van Gijn, Silvia Federici, Hermann Girschick, Gerd Ganser, Susan Nielsen, Troels Herlin, Sulaiman Mohammed Al-Mayouf, Michael Hofer, Jasmin Kuemmerle-Deschner, Susanne Schalm, Annette Jansson, on behalf of PRINTO and Eurofever registry, Marta Marchi, Chiara Marini, Angelo Ravelli, Alberto Garaventa, Sonia Carta, Enrica Balza, Patrizia Castellani, Caterina Pellecchia, Silvia Borghini, Maria Libera Trotta, Anna Rubartelli, Andrew Henrey, Thomas Loughin, Roberta Berard, Natalie Shiff, Roman Jurencak, Susanne Benseler, Lori Tucker, on behalf of ReACCh-Out Investigators, Charalampia Papadopoulou, Ying Hong, Petra Krol, Yiannis Ioannou, Clarissa Pilkington, Hema Chaplin, Stephania Simou, Marietta Charakida, Lucy Wedderburn, Lynn R. Spiegel, Sara Ahola Kohut, Jennifer Stinson, Paula Forgeron, Miriam Kaufman, Nadia Luca, Khush Amaria, Mary Bell, J Swart, F. Boris, E. Castagnola, A. Groll, G. Giancane, G. Horneff, H. I. Huppertz, T. Wolfs, E. Alekseeva, V. Panaviene, F. Uettwiller, V. Stanevicha, L. M. Ailioaie, E. Tsitami, S. Kamphuis, G. Susic, F. Sztajnbok, B. Flato, A. Pistorio, Stephanie J. W. Shoop, Suzanne M. M. Verstappen, Janet E. McDonagh, Wendy Thomson, Kimme L. Hyrich, CAPS, Maarit Tarkiainen, Pirjo Tynjala, Pekka Lahdenne, Janne Martikainen, Acute-JIA Study Group, Meredyth Wilkinson, Christopher Piper, Georg Otto, Claire T. Deakin, Stefanie Dowle, Stefania Simou, Daniel Kelberman, Claudia Mauri, Elizabeth Jury, David Isenberg, Lucy R. Wedderburn, Kiran Nistala, I. Foeldvari, D. J. Lovell, G. Simonini, M. Bereswill, J. Kalabic, Kiem Oen, Brian M. Feldman, Brenden Dufault, Jennifer Lee, Karen Watanabe Duffy, Ciaran Duffy, ReACCh-Out Investigators, N. Tzaribachev, G. Vega-Cornejo, I. Louw, A. Berman, I. Calvo, R. Cuttica, F. Avila-Zapata, R. Cimaz, E. Solau-Gervais, R. Joos, G. Espada, X. Li, M. Nys, R. Wong, S. Banerjee, For Pediatric Rheumatology International Trials Organization (PRINTO)/Pediatric Rheumatology Collaborative Study Group (PRCSG), Rebecca Nicolai, Margherita Verardo, Adele D’Amico, Luisa Bracci-Laudiero, Gian Marco Moneta, Gillian Rice, Anne-Laure Mathieu, Sulliman O. Omarjee, Tracy A. Briggs, James O’Sullivan, Simon Williams, Rolando Cimaz, Eve Smith, Michael W. Beresford, Yanick J. Crow, GENIAL Investigators, UK JSLE Study Group, Madeleine Rooney, Nick Bishop, joyce davidson, Clarissa pilkington, Michael Beresford, Jacqui Clinch, Rangaraj Satyapal, Helen Foster, Janet Gardner Medwin, Janet McDonagh, Sue Wyatt, On Behalf of the British Society for Paediatric and Adolescent Rheumatology, Valentina Litta Modignani, Francesco Baldo, Stefano Lanni, Alessandro Consolaro, Giovanni Filocamo, Helen J. Lachmann, on behalf of Eurofever Registry, Gianmarco Moneta, Camilla Celani, Bilade Cherqaoui, Linda Rossi-Semerano, Perrine Dusser, Véronique Hentgen, Claire Grimwood, Linda Rossi, Isabelle Kone Paut, Veronique Hentgen, Denise Lasigliè, Denise Ferrera, Giulia Amico, Marco Di Duca, Laura Obici, Roberto Ravazzolo, Ryuta Nishikomori, Juan Arostegui, Andrea Petretto, Chiara Lavarello, Elvira Inglese, Federica Vanoni, Michaël Hofer, on behalf of EUROFEVER PROJECT, P. N. Hawkins, T. van der Poll, U. A. Walker, H. H. Tilson, Pascal N. Tyrrell, Raphaela Goldbach-Mansky, Norbert Blank, Hal M. Hoffman, Elisabeth Weissbarth-Riedel, Boris Huegle, Tilmann Kallinich, Ahmet Gul, Marlen Oswald, Fatma Dedeoglu, Aki Hanaya, Takako Miyamae, Manabu Kawamoto, Yumi Tani, Takuma Hara, Yasushi Kawaguchi, Satoru Nagata, Hisashi Yamanaka, Almira Ćosićkić, Fahrija Skokić, Belkisa Čolić, Sanimir Suljendić, Anna Kozlova, Irina Mersiyanova, Mariya Panina, Lily Hachtryan, Vasiliy Burlakov, Elena Raikina, Alexey Maschan, Anna Shcherbina, Banu Acar, Meryem Albayrak, Betul Sozeri, Sezgin Sahin, Amra Adrovic, Nese Inan, Serhan Sevgi, Caroline M. Andreasen, Anne Grethe Jurik, Mia B. Glerup, Christian Høst, Birgitte T. Mahler, Ellen-Margrethe Hauge, Cecilia Lazea, Laura Damian, Calin Lazar, Rodica Manasia, Chloe M. Stephenson, Vimal Prajapati, Paivi M. Miettunen, Dilek Yılmaz, Yavuz Tokgöz, Yasin Bulut, Harun Çakmak, Ferah Sönmez, Elif Comak, Gülşah Kaya Aksoy, Mustafa Koyun, Sema Akman, Yunus Arıkan, Ender Terzioğlu, Osman Nidai Özdeş, İbrahim Keser, Hüseyin Koçak, Ayşen Bingöl, Aygen Yılmaz, Reha Artan, X. Xu, Fatemeh F. Mehregan, Vahid Ziaee, Mohammad H. Moradinejad, Francesco La Torre, Clotilde Alizzi, Pio D’Adamo, G. Junge, J. Gregson, Hasmik Sargsyan, Hulya Zengin, Berna E. Fidanci, Cagla Kaymakamgil, Dilek Konukbay, Dilek Yildiz, Faysal Gok, Iris Stoler, Judith Freytag, Banu Orak, Christine Seib, Lars Esmann, Eva Seipelt, Faekah Gohar, Dirk Foell, Ismail Dursun, Sebahat Tulpar, Sibel Yel, Demet Kartal, Murat Borlu, Funda Bastug, Hakan Poyrazoglu, Zubeyde Gunduz, Kader Kose, Mehmet E. Yuksel, Abdullah Calıskan, Ahmet B. Cekgeloglu, Ruhan Dusunsel, Katerina Bouchalova, Jana Franova, Marcel Schuller, Marie Macku, Katerina Theodoropoulou, Raffaella Carlomagno, Annette von Scheven-Gête, Claudia Poloni, Laura O. Damian, Dan Cosma, Amanda Radulescu, Dan Vasilescu, Liliana Rogojan, Simona Rednic, Mihaela Lupse, Lien De Somer, Pierre Moens, Rocio Galindo Zavala, Laura Martín Pedraz, Esmeralda Núñez Cuadros, Gisela Díaz-Cordovés Rego, Antonio L. Urda Cardona, Ilaria Dal Forno, Sara Pieropan, Ombretta Viapiana, Davide Gatti, Gloria Dallagiacoma, Paola Caramaschi, Domenico Biasi, Daniel Windschall, Ralf Trauzeddel, Hartwig Lehmann, Rainer Berendes, Maria Haller, Manuela Krumrey-Langkammerer, Antje Nimtz-Talaska, Philipp Schoof, Ralf Felix Trauzeddel, Christine Nirschl, Estefania Quesada-Masachs, Carla Aguilar Blancafort, Sara Marsal Barril, Francisca Aguiar, Rita Fonseca, Duarte Alves, Ana Vieira, Alberto Vieira, Jorge A. Dias, Iva Brito, Gordana Susic, Vera Milic, Goran Radunovic, Ivan Boricic, Pauline Marteau, Catherine Adamsbaum, Michel De Bandt, Irène Lemelle, Chantal Deslandre, Tu Anh Tran, Anne Lohse, Elisabeth Solau-Gervais, Pascal Pillet, Julien Wipff, Cécile Gaujoux-Viala, Sylvain Breton, Valérie Devauchelle-Pensec, Sandra Gran, Olesja Fehler, Stefanie Zenker, Michael Schäfers, Thomas Vogl, Severine Guillaume Czitrom, EH Pieter Van Dijkhuizen, Silvia Magni Manzoni, Francesca Magnaguagno, Laura Tanturri de Horatio, Nienke M. Ter Haar, Annemieke S. Littooij, Vitor A. Teixeira, Raquel Campanilho-Marques, Ana F. Mourão, Filipa O. Ramos, Manuela Costa, Wafa A. Madan, Orla G. Killeen, Adriana Rodriguez Vidal, Diana Sueiro Delgado, Maria Isabel Gonzalez Fernandez, Berta Lopez Montesinos, Aleksey Kozhevnikov, Nina Pozdeeva, Mikhail Konev, Evgeniy Melchenko, Vladimir Kenis, Gennadiy Novik, Aysenur Pac Kısaarslan, Butsabong Lerkvaleekul, Suphaneewan Jaovisidha, Witaya Sungkarat, Niyata Chitrapazt, Praman Fuangfa, Thumanoon Ruangchaijatuporn, Soamarat Vilaiyuk, Dan Ø. Pradsgaard, Arne Hørlyck, Anne H. Spannow, Carsten W. Heuck, Talia Diaz, Fernando Garcia, Lorenia De La Cruz, Nadina Rubio, Joanna Świdrowska-Jaros, Elzbieta Smolewska, Mirta Lamot, Lovro Lamot, Mandica Vidovic, Edi Paleka Bosak, Ivana Rados, Miroslav Harjacek, Nikolay Tzaribachev, Polymnia Louka, Romiesa Hagoug, Chiara Trentin, Olga Kubassova, Mark Hinton, Mikael Boesen, Olena A. Oshlianska, Illya A. Chaikovsky, G. Mjasnikov, A. Kazmirchyk, Umberto Garagiola, Irene Borzani, Paolo Cressoni, Fabrizia Corona, Eszter Dzsida, Giampietro Farronato, Antonella Petaccia, Alenka Gagro, Agneza Marija Pasini, Goran Roic, Ozren Vrdoljak, Lucija Lujic, Matija Zutelija-Fattorini, Monika M. Esser, Deepthi R. Abraham, Craig Kinnear, Glenda Durrheim, Mike Urban, Eileen Hoal, Victoria B. Nikolayenko, Kubilay Şahin, Yasar Karaaslan, Adele Civino, Giovanni Alighieri, Sergio Davì, Roberto Rondelli, Andrea Magnolato, Francesca Ricci, Alma Olivieri, Valeria Gerloni, Bianca Lattanzi, Francesca Soscia, Alessandro De Fanti, Stefania Citiso, Lorenzo Quartulli, Maria Cristina Maggio, Manuela Marsili, Maria Antonietta Pelagatti, Valentino Conter, Franca Fagioli, Andrea Pession, Marco Garrone, Mariangela Rinaldi, Jaime De Inocencio, Stella Garay, Daniel J. Lovell, Berit Flato, EPOCA Study Group, Angela Aquilani, Simona Cascioli, Ivan Caiello, Denise Pires-Marafón, Rita Carsetti, Emily Robinson, Salvatore Albani, Wilco de Jager, Sytze de Roock, Trang Duong, Justine Ellis, Kimme Hyrich, Laetitia Jervis, Daniel Lovell, Lucy Marshall, Elizabeth D. Mellins, Kirsten Minden, Jane Munro, Peter A. Nigrovic, Jason Palman, Sunil Sampath, Laura E. Schanberg, Susan D. Thompson, Richard Vesely, Chris Wallace, Chris Williams, Qiong Wu, Nico Wulffraat, Rae S. M. Yeung, M. B. Seyger, D. Arikan, J. K. Anderson, A. Lazar, D. A. Williams, C. Wang, R. Tarzynski-Potempa, J. S. Hymans, Gabriele Simonini, Erika Scoccimarro, Irene Pontikaki, Teresa Giani, Alessandro Ventura, Pier Luigi Meroni, Gaetana Minnone, Marzia Soligo, Luigi Manni, Luisa Bracci Laudiero, Noortje Groot, I. Grein, N. M. Wulffraat, R. Schepp, G. Berbers, C. C. Barbosa Sandoval de Souza, V. Paes Leme Ferriani, G. Pileggi, S. de Roock, Ingrid H. R. Grein, Silvia Scala, Elisa Patrone, Casper Schoemaker, on behalf of Dutch JIA patient organization, Wendy Costello, on behalf of ENCA, Suzanne Parsons, Jean-David Cohen, Damien Bentayou, Marc-Antoine Bernard Brunel, Sonia Trope, Jens Klotsche, Miriam Listing, Martina Niewerth, Gerd Horneff, Angelika Thon, Hans-Iko Huppertz, Kirsten Mönkemöller, Ivan Foeldvari, ICON study group, Achille Marino, Stefano Stagi, Niccolò Carli, Federico Bertini, Adriana S. Díaz-Maldonado, Sally Pino, Pilar Guarnizo, Alfonso Ragnar Torres-Jimenez, Berenice Sanchez-Jara, Eunice Solis-Vallejo, Adriana Ivonne Cespedes-Cruz, Maritza Zeferino-Cruz, Julia Veronica Ramirez-Miramontes, Ankur Kumar, Anju Gupta, Deepti Suri, Amit Rawat, Nandita Kakkar, Surjit Singh, Özge A. Gücenmez, Erbil Ünsal, Bo Magnusson, Karina Mördrup, Anna Vermé, Christina Peterson, Board of the Swedish Pediatric Rheumatology Registry, Caroline Freychet, Jean Louis Stephan, Cathryn E. Harkness, Leanne Foster, Emma Henry, Pauline Taggart, Coskun F. Ozkececi, Esra Kurt, Gokalp Basbozkurt, Daiva Gorczyca, Jacek Postępski, Aleksandra Czajkowska, Bogumiła Szponar, Mariola Paściak, Anna Gruenpeter, Iwona Lachór-Motyka, Daria Augustyniak, Edyta Olesińska, Emediong S. Asuka, Tatyana Golovko, Samuel U. Aliejim, Emilio Inarejos Clemente, Estibaliz Iglesias Jimenez, Joan Calzada Hernandez, Sergi Borlan Fernandez, Clara Gimenez Roca, David Moreno Romo, Natalia Rodriguez Nieva, Juan Manuel Mosquera Angarita, Jordi Anton Lopez, Esmeralda Nuñez-Cuadros, Gisela Diaz-Cordovés, Rocío Galindo-Zavala, Antonio Urda-Cardona, Antonio Fernández-Nebro, Daniel Álvarez de la Sierra, Marina Garcia Prat, Mónica Martínez Gallo, Ricardo Pujol Borrell, Ana M. Marín Sánchez, Etienne Merlin, Sylvie Fraitag, Jean-Louis Stephan, Federico Annoni, Giancarla Di Landro, Sofia Torreggiani, Marta Torcoletti, Georgina Tiller, Jo Buckle, Angela Cox, Peter Gowdie, Roger C. Allen, Jonathan D. Akikusa, Hayde G. Hernández-Huirache, Edel R. Rodea-Montero, William Fahy, Christelle Sordet, Karin B. Berggren, Johanna T. Kembe, Joyce Bos, Wineke Armbrust, Marco van Brussel, Jeanette Cappon, Pieter Dijkstra, Jan Geertzen, Elizabeth Legger, Marion van Rossum, Pieter Sauer, Otto Lelieveld, Levent Buluc, Gur Akansel, Bahar Muezzinoglu, Ljubov Rychkova, Tatyana Knyazeva, Anna Pogodina, Tatyana Belova, Tamara Mandzyak, Ekaterina Kulesh, Alessandro Cafarotti, Cosimo Giannini, Roberta Salvatore, Giuseppe Lapergola, Caterina Di Battista, Maria Loredana Marcovecchio, Raffaella Basilico, Piernicola Pelliccia, Francesco Chiarelli, Luciana Breda, Beverley Almeida, Sarah Tansley, Harsha Gunawardena, Neil McHugh, Juvenile Dermatomyositis Research Group (JDRG), Jessie Aouizerate, Marie De Antonio, Christine Barnerias, Guillaume Bassez, Isabelle Desguerre, Romain Gherardi, Jean-Luc Charuel, François-Jérôme Authier, Cyril Gitiaux, C. H. Spencer, Rabheh Abdul Aziz, Chack-Yung Yu, Brent Adler, Sharon Bout-Tabaku, Katherine Lintner, Melissa Moore-Clingenpeel, Liza McCann, Nicola Ambrose, Mario Cortina-Borja, Juvenile Dermatomyositis Cohort and Biomarker Study (JCDBS), Prasad T. Oommen, Fabian Speth, Johannes-Peter Haas, Working Group 'Juvenile Dermatomyositis' of the German Society for Paediatric and Adolescent Rheumatology (GKJR), Claudio Lavarello, Gabriella Giancane, Angela Pistorio, Lisa Rider, Rohit Aggarwal, Sheila K. Oliveira, Ruben Cuttica, Michel Fischbach, Gary Sterba, Karine Brochard, Frank Dressler, Patrizia Barone, Ruben Burgos-Vargas, Elizabeth Candell Chalom, Marine Desjonqueres, Graciela Espada, Anders Fasth, Stella Maris Garay, Rose-Marie Herbigneaux, Claire Hoyoux, Chantal Job Deslandre, Frederick W. Miller, Jiri Vencovsky, Erdal Sag, Gulsev Kale, Haluk Topaloglu, Beril Talim, Francesco Zulian, Tadej Avcin, Roberto Marini, Anne Pagnier, Michel Rodiere, Christine Soler, Rebecca Ten Cate, Yosef Uziel, Jelena Vojinovic, Ana V. Villarreal, Nydia Acevedo, Yuridiana Ramirez, Enrique Faugier, Rocio Maldonado, Bita Arabshahi, John H. Lee, Ian Leibowitz, Lawrence O. Okong’o, Jo Wilmshurst, Monika Esser, Christiaan Scott, Ezgi Deniz Batu, Nagehan Emiroglu, Hafize Emine Sonmez, Gokcen Dilsa Tugcu, Zehra Serap Arici, Ebru Yalcin, Deniz Dogru, Ugur Ozcelik, Mithat Haliloglu, Nural Kiper, Masato Yashiro, Mutsuko Yamada, Toshihiko Yabuuchi, Tomonobu Kikkawa, Nobuyuki Nosaka, Yosuke Fujii, Yukie Saito, Hirokazu Tsukahara, Sulaiman M. Al-Mayouf, Nora AlMutiari, Mohammed Muzaffer, Rawiah shehata, Adel Al-Wahadneh, Reem Abdwani, Safia Al-Abrawi, Mohammed Abu-shukair, Zeyad El-Habahbeh, Abdullah Alsonbul, Aleksandra Szabat, Monika Chęć, Violetta Opoka-Winiarska, Biman Saikia, Ranjana W. Minz, Christine Arango, Clara Malagon, Maria D. P. Gomez, Angela C. Mosquera, Ricardo Yepez, Tatiana Gonzalez, Camilo Vargas, GRIP study group, Marta Balzarin, Biagio Castaldi, Elena Reffo, Francesca Sperotto, Giorgia Martini, Alessandra Meneghel, Ornella Milanesi, Ozgur Kasapçopur, Maria Teresa Terreri, Ekaterina Alexeeva, Maria Katsicas, Mikhail Kostik, Thomas Lehman, W.-Alberto Sifuentes-Giraldo, Vanessa Smith, Flavio Sztajnbok, Tadey Avcin, Maria Jose Santos, Dana Nemcova, Cristina Battagliotti, Liora Harel, Mahesh Janarthanan, Kathryn Torok, Nicola Helmus, Eileen Baildem, Michael Blakley, Kim Fligelstone, Antonia Kienast, Clare Pain, Amanda Saracino, Gabriele Simoni, Lisa Weibel, Maria K. Osminina, Nathalia A. Geppe, Olga V. Niconorova, Olesya V. Karashtina, Oksana V. Abbyasova, Olga V. Shpitonkova, Sinem Durmus, Hafize Uzun, Angela Mauro, Eleonora Fanti, Fabio Voller, Franca Rusconi, Fernando Garcia-Rodriguez, Ana V. Villarreal-Treviño, Angel J. Flores-Pineda, Paola B. Lara-Herrea, Diego R. Salinas-Encinas, Talia Diaz-Prieto, Maria R. Maldonado-Velazquez, Sarbelio Moreno-Espinosa, Enrique Faugier-Fuentes, Mirella Crapanzano, Ilaria Parissenti, Man S. Parihar, Pandiarajan Vignesh, ManojKumar Rohit, Kavitha Gopalan, Savita V. Attri, Alan Salama, David Jayne, Mark Little, Yulia Kostina, Galina Lyskina, Olga Shpitonkova, Alena Torbyak, Olga Shirinsky, Maria Francesca Gicchino, Maria Cristina Smaldone, Mario Diplomatico, Alma Nunzia Olivieri, C H. Spencer, Richard McClead, Hiren Patel, Chung-Yung Yu, Dita Cebecauerová, Tomáš Dallos, Edita Kabíčková, Martin Kynčl, Daniela Chroustová, Jozef Hoza, Dana Němcová, Vladimír Tesař, Pavla Doležalová, Tuncay Hazirolan, Fatih Ozaltin, Fabiola Almeida, Isabela H. Faria de Paula, Maíra M. Sampaio, Fernando N. Arita, Andressa G. Alves, Maria Carolina Santos, Eunice M. Okuda, Silvana B. Sacchetti, Fernanda Falcini, Marini Francesca, Gemma Lepri, Marco Matucci-Cerinic, Maria Luisa Brandi, Hakan Kisaoglu, Sema Misir, Selim Demir, Yuksel Aliyazicioglu, Mukaddes Kalyoncu, Carlos Eduardo Ramalho, Fabiola D. Almeida, Joan Calzada-Hernández, Rosa Bou, Estíbaliz Iglesias, Judith Sánchez-Manubens, Fredy Hermógenes Prada Martínez, Clara Giménez Roca, Sergi Borlan Fernández, Marek Bohm, Kamran Mahmood, Valentina Leone, Mark Wood, Ken-Ichi Yamaguchi, Satoshi Fujikawa, Working Group of Behçet’s Disease, Pediatric Rheumatology Association of Japan (PRAJ), Kyu Yeun Kim, Do Young Kim, Dong Soo Kim, Maka Ioseliani, Ivane Chkhaidze, Maia Lekishvili, Nana Tskhakaia, Shorena Tvalabeishvili, Aleksandre Kajrishvili, Maiko Takakura, Masaki Shimizu, Natsumi Inoue, Mao Mizuta, Akihiro Yachie, Giovanni Corsello, Maryam Piram, Carla Maldini, Sandra Biscardi, Nathalie Desuremain, Catherine Orzechowski, Emilie Georget, Delphine Regnard, Isabelle Kone-Paut, Alfred Mahr, Mihaela Sparchez, Zeno Sparchez, Nydia Acevedo Silva, Ana V. Villarreal Treviño, Yuridiana Ramirez Loyola, Talia Diaz Prieto, Enrique Faugier Fuentes, Maria D. R. Maldonado Velazquez, Pilar Perez, Sagar Bhattad, Ranjana Minz, Jitendra Shandilya, Pediatric Allergy and Immunology Unit, PGIMER, Chandigarh, Ana Villarreal, Yuridiana Ramírez, Zeynep Birsin Özçakar, Suat Fitoz, Fatos Yalcinkaya, Annacarin Horne, Francesca Minoia, Francesca Bovis, Sergio Davi, Priyankar Pal, Kimo Stein, Sandra Enciso, Michael Jeng, Despoina Maritsi, Randy C. Cron, Anne Thorwarth, Sae Lim von Stuckrad, Angela Rösen-Wolff, Hella Luksch, Patrick Hundsdoerfer, Peter Krawitz, Nuray Aktay Ayaz, Doğan Simsek, Şebnem Sara Kılıc, Emine Sonmez, Aysenur Pac Kisaarslan, Ozge Altug Gucenmez, Z. Serap Arıcı, Fatih Kelesoglu, Zelal Ekinci Ekinci, Maria Miranda-Garcia, Carolin Pretzer, Michael Frosch, F. Gohar, Angela McArdle, Niamh Callan, Belinda Hernandez, Miha Lavric, Oliver FitzGerald, Stephen R. Pennington, Joachim Peitz, Joern Kekow, Ariane Klein, Anna C. Schulz, Frank Weller-Heinemann, Anton Hospach, J-Peter Haas, BIKER collaborative group, Karen Put, Jessica Vandenhaute, Anneleen Avau, Annemarie van Nieuwenhuijze, Ellen Brisse, Tim Dierckx, Omer Rutgeerts, Josselyn E. Garcia-Perez, Jaan Toelen, Mark Waer, Georges Leclercq, An Goris, Johan Van Weyenbergh, Adrian Liston, Patrick Matthys, Carine H. Wouters, Yasuo Nakagishi, Michael J. Ombrello, Victoria Arthur, Anne Hinks, Patricia Woo, International Childhood Arthritis Genetics (INCHARGE) Consortium, Barbara Stanimirovic, Biljana Djurdjevic-Banjac, Olivera Ljuboja, Boris Hugle, MArgarita Onoufriou, Olga Vougiouka, Kenza Bouayed, Sanae El Hani, Imane Hafid, Nabiha Mikou, Nunu Shelia, Mari Laan, Jaanika Ilisson, and Chris Pruunsild
- Subjects
lcsh:Diseases of the musculoskeletal system ,lcsh:RJ1-570 ,lcsh:Pediatrics ,lcsh:RC925-935 ,Meeting Abstracts - Published
- 2017
33. Doppler Sonography of Blood Flow Velocity in the Vertebral Arteries of Preterm and Term Neonates
- Author
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Katrin Hoekstra, Roland Haase, and Daniel Windschall
- Subjects
Male ,medicine.medical_specialty ,Vertebral artery ,Diastole ,030218 nuclear medicine & medical imaging ,03 medical and health sciences ,0302 clinical medicine ,030225 pediatrics ,Internal medicine ,medicine.artery ,medicine ,Basilar artery ,Humans ,Radiology, Nuclear Medicine and imaging ,Prospective Studies ,Prospective cohort study ,Vertebral Artery ,Radiological and Ultrasound Technology ,business.industry ,Infant, Newborn ,Ultrasonography, Doppler ,Blood flow ,Term neonates ,Doppler sonography ,Basilar Artery ,Cardiology ,Female ,Radiology ,business ,Blood Flow Velocity ,Infant, Premature ,Diastolic flow - Abstract
OBJECTIVES This study aimed to evaluate normal blood flow in the vertebral arteries and the basilar artery of preterm and term neonates by Doppler sonography. METHODS Blood flow in both vertebral arteries and the basilar artery was examined in 102 neonates between the biological ages of 28 and 41 weeks. Fifty-one boys and 51 girls underwent Doppler sonography. Measurements were usually undertaken at 6 days old. Systolic and diastolic flow velocities, including the resistive index, were measured and analyzed, taking into consideration biological age, weight, and sex. Anatomic aberrations of the vertebral arteries were recorded. RESULTS Mean blood flow values ± SD in the basilar artery were 35.2 ± 7.4 cm/s (systolic velocity) and 10.9 ± 3.5 cm/s (diastolic velocity). Mean blood flow values in the right vertebral artery were 26.8 ± 9.3 cm/s (systolic velocity) and 8.0 ± 3.7 cm/s (diastolic velocity). Mean blood flow values in the left vertebral artery were 28.6 ± 8.3 cm/s (systolic velocity) and 8.7 ± 3.3 cm/s (diastolic velocity). Systolic and diastolic blood flow in both vertebral arteries was significantly higher from 38 to 41 weeks compared with 28 to 32 and 33 to 37 weeks (P < .05). Regression analysis of systolic and diastolic blood flow velocities in the vertebral arteries versus biological age yielded significant results (P < .05). CONCLUSIONS Sonography is an excellent tool for examining blood flow in the basilar and vertebral arteries of premature and term neonates. Mean systolic and diastolic blood flow velocities in the vertebral arteries increase significantly with age.
- Published
- 2015
34. Ultrasonographic assessment of the skeletal development of the proximal tibia epiphysis, the proximal femur and the distal femur epiphysis in premature and mature newborns
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Daniel Windschall, Michael Pommerenke, Roland Haase, and Theresa Rimsl
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Proximal tibia ,Distal femur ,medicine.anatomical_structure ,Proximal femur ,Epiphysis ,business.industry ,medicine ,General Medicine ,Anatomy ,business - Published
- 2015
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35. Ultrasound Assessment of the Skeletal Development of the Proximal Tibial, Proximal Femoral, and Distal Femoral Epiphyses in Premature and Mature Newborns
- Author
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Roland Haase, Daniel Windschall, and Michael Pommerenke
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Male ,medicine.medical_specialty ,Acoustics and Ultrasonics ,Knee Joint ,Biophysics ,Ossification center ,Sensitivity and Specificity ,030218 nuclear medicine & medical imaging ,03 medical and health sciences ,0302 clinical medicine ,Image Interpretation, Computer-Assisted ,Medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,Femur ,Tibia ,Ultrasonography ,030203 arthritis & rheumatology ,Bone Development ,Radiological and Ultrasound Technology ,business.industry ,Ossification ,Ultrasound ,Infant, Newborn ,Infant ,Reproducibility of Results ,Anatomy ,Cartilage thickness ,Surgery ,medicine.anatomical_structure ,Femoral epiphysis ,Female ,Hip Joint ,medicine.symptom ,business ,Epiphyses ,Infant, Premature - Abstract
We evaluated postnatal skeletal development of the proximal femoral epiphysis, distal femoral epiphysis (DFE) and proximal tibial epiphysis (PTE) in 178 premature and mature newborns, between 25 and 47 wk of biological age, using high-resolution B-mode musculoskeletal ultrasound. Approximate age-related values were determined based on the ossification center size and epiphyseal cartilage thickness. The earliest onsets of visible mineralization were at 30 wk of maturity in the DFE, 31 wk in the PTE and 43 wk in the proximal femoral epiphysis. In preterm and term neonates, significant correlations were observed for transverse and longitudinal length of the DFE and PTE with biological age (R² = 0.35-0.50, p
- Published
- 2015
36. FRI0519 Ultrasound Definition of Cartilage Change in Patients with Rheumatoid Arthritis: A Reliability Study by The Omeract Ultrasonography
- Author
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E. De Miguel, C. Hernandez Diaz, M-A D'Agostino, Marcin Szkudlarek, Daniel Windschall, A. Delle-Sedie, Marina Backhaus, Marwin Gutierrez, U. Moller-Dohn, Paz Collado, Eszter Kővári, C. Pineda, Nemanja Damjanov, Lene Terslev, Emilio Filippucci, Esperanza Naredo, Richard J. Wakefield, Wolfgang A. Schmidt, Christian Dejaco, Peter Mandl, Artur Bachta, A. Rodriguez, Farideh Alasti, Ingrid Möller, Peter V. Balint, Helen Keen, Kei Ikeda, Annamaria Iagnocco, Juan Carlos Nieto, George A W Bruyn, Ralf G. Thiele, David Kane, Hilde Berner Hammer, Christina Duftner, Stephen Kelly, and David Bong
- Subjects
medicine.medical_specialty ,business.industry ,Hyaline cartilage ,Cartilage ,Immunology ,Ultrasound ,medicine.disease ,General Biochemistry, Genetics and Molecular Biology ,030218 nuclear medicine & medical imaging ,3. Good health ,Surgery ,03 medical and health sciences ,0302 clinical medicine ,medicine.anatomical_structure ,Rheumatology ,030220 oncology & carcinogenesis ,Rheumatoid arthritis ,Reliability study ,medicine ,Immunology and Allergy ,In patient ,Radiology ,Ultrasonography ,business ,Kappa - Abstract
Objectives To produce ultrasound (US) consensus-based definitions of cartilage change in rheumatoid arthritis (RA) and assess its intraobserver and interobserver reliability in a web-based exercise. Methods We conducted a Delphi study on US defined cartilage change and a proposed semiquantitative (SQ) US scoring system for cartilage change in RA. A written Delphi questionnaire was developed based on a systematic literature review and expert international consensus and was distributed via consecutive written questionnaires by email to a group 35 rheumatologists from 17 countries with experience in musculoskeletal US. Taskforce members performed US B mode examination of the metacarpal cartilage in metacarpophalangeal joints 2–5 in RA patients and the images were collected in an electronic database. A reference image atlas of cartilage changes was developed for scoring 123 anonymized images including 25 duplicate images. These were sent to the participants who independently scored the images. Intraobserver reliability was assessed by Cohen9s kappa and interobserver reliability by Fleiss9 kappa. Results Group agreement (76–100%) was reached for 6 statements concerning: i) MSUS definition and assessment of normal hyaline cartilage, ii) elementary cartilage lesions in MSUS and iii) grading of elementary cartilage lesions in patients with RA in a two-round Delphi consensus process. A three-grade SQ (0–2) scoring system (grade 0, normal cartilage; grade 1, minimal change: blurring of outer and/or subchondral margin, focal thinning or incomplete loss of homogeneity of echostructure; grade 2, severe: diffuse thinning or complete loss of homogeneity of echostructure) was agreed for scoring cartilage damage in RA. Both intra- and inter-observer reliability were good (κ value of 0.87 and 0.64 respectively). Conclusions This study demonstrates that US is a reliable tool for evaluating cartilage in RA and strongly supports the use of a new reliable semiquantitative MSUS scoring system for cartilage change. Disclosure of Interest None declared
- Published
- 2016
- Full Text
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