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Development of practice and consensus-based strategies including a treat-to-target approach for the management of moderate and severe juvenile dermatomyositis in Germany and Austria.
Hinze, Claas H; Oommen, Prasad T; Dressler, Frank; Urban, Andreas; Weller-Heinemann, Frank; Speth, Fabian; Lainka, Elke; Brunner, Jürgen; Fesq, Heike; Foell, Dirk; Müller-Felber, Wolfgang; Neudorf, Ulrich; Rietschel, Christoph; Schwarz, Tobias; Schara, Ulrike; Haas, Johannes-Peter.
Afiliación
  • Hinze CH; Department of Pediatric Rheumatology and Immunology, University Hospital Münster, Albert-Schweitzer-Campus 1, Building D3, 48149, Münster, Germany. claas.hinze@ukmuenster.de.
  • Oommen PT; Department of Pediatric Oncology, Hematology and Clinical Immunology, University Hospital Düsseldorf, Düsseldorf, Germany.
  • Dressler F; Department of Pediatric Pulmonology, Allergy and Neonatology, Hanover Medical School, Hanover, Germany.
  • Urban A; Department of Pediatrics, St. Mary's Hospital, Amberg, Germany.
  • Weller-Heinemann F; Division of Pediatric Rheumatology, Prof. Hess Children's Hospital, Bremen, Germany.
  • Speth F; Division of Pediatric Rheumatology, University Medicine, Rostock, Germany.
  • Lainka E; Division of Immunology, Bone Marrow Transplantation and Rheumatology, University Hospital Ulm, Ulm, Germany.
  • Brunner J; Department of Pediatrics, University Hospital Essen, Essen, Germany.
  • Fesq H; Department of Pediatrics, Medical University Innsbruck, Innsbruck, Austria.
  • Foell D; German Center for Pediatric and Adolescent Rheumatology, Garmisch-Partenkirchen Department of Dermatology, Oberammergau Center for Rheumatic Diseases, Oberammergau, Germany.
  • Müller-Felber W; Department of Pediatric Rheumatology and Immunology, University Hospital Münster, Albert-Schweitzer-Campus 1, Building D3, 48149, Münster, Germany.
  • Neudorf U; Department of Pediatric Neurology, University Hospital Munich, Munich, Germany.
  • Rietschel C; Department of Pediatrics, University Hospital Essen, Essen, Germany.
  • Schwarz T; Department of Pediatrics, Clementine Children's Hospital, Frankfurt, Germany.
  • Schara U; Department of Pediatric Rheumatology, St. Josef Hospital, Sendenhorst, Germany.
  • Haas JP; Department of Pediatric Neurology, University Hospital Essen, Essen, Germany.
Pediatr Rheumatol Online J ; 16(1): 40, 2018 Jun 25.
Article en En | MEDLINE | ID: mdl-29940960
ABSTRACT

BACKGROUND:

Juvenile dermatomyositis (JDM) is the most common inflammatory myopathy in childhood and a major cause of morbidity among children with pediatric rheumatic diseases. The management of JDM is very heterogeneous. The JDM working group of the Society for Pediatric Rheumatology (GKJR) aims to define consensus- and practice-based strategies in order to harmonize diagnosis, treatment and monitoring of JDM.

METHODS:

The JDM working group was established in 2015 consisting of 23 pediatric rheumatologists, pediatric neurologists and dermatologists with expertise in the management of JDM. Current practice patterns of management in JDM had previously been identified via an online survey among pediatric rheumatologists and neurologists. Using a consensus process consisting of online surveys and a face-to-face consensus conference statements were defined regarding the diagnosis, treatment and monitoring of JDM. During the conference consensus was achieved via nominal group technique. Voting took place using an electronic audience response system, and at least 80% consensus was required for individual statements.

RESULTS:

Overall 10 individual statements were developed, finally reaching a consensus of 92 to 100% regarding (1) establishing a diagnosis, (2) case definitions for the application of the strategies (moderate and severe JDM), (3) initial diagnostic testing, (4) monitoring and documentation, (5) treatment targets within the context of a treat-to-target strategy, (6) supportive therapies, (7) explicit definition of a treat-to-target strategy, (8) various glucocorticoid regimens, including intermittent intravenous methylprednisolone pulse and high-dose oral glucocorticoid therapies with tapering, (9) initial glucocorticoid-sparing therapy and (10) management of refractory disease.

CONCLUSION:

Using a consensus process among JDM experts, statements regarding the management of JDM were defined. These statements and the strategies aid in the management of patients with moderate and severe JDM.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Dermatomiositis Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies / Qualitative_research Límite: Child / Humans País/Región como asunto: Europa Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Dermatomiositis Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies / Qualitative_research Límite: Child / Humans País/Región como asunto: Europa Idioma: En Año: 2018 Tipo del documento: Article