Treatment Options and Outcomes in Patients with Idiopathic Inflammatory Myopathies

被引:0
|
作者
Unger, Leonore [1 ]
机构
[1] Stadt Klinikum Dresden, Med Klin 1, Dresden, Germany
关键词
inflammatory idiopathic myositis; standard of care; treatment-refractory disease; INCLUSION-BODY MYOSITIS; INTERSTITIAL LUNG-DISEASE; JUVENILE DERMATOMYOSITIS; REFRACTORY POLYMYOSITIS; DOUBLE-BLIND; AMYOPATHIC DERMATOMYOSITIS; CYCLOSPORINE-A; PILOT TRIAL; ADULT; RITUXIMAB;
D O I
10.1055/a-1423-7579
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Idiopathic inflammatory myopathies (IIM) are a very heterogeneous group of conditions, which can now be increasingly differentiated. This paves the way for targeted treatment. Therapies aim to change pathogenic mechanisms and are focused on reducing disease activity, encouraging muscle development, preventing organ damage, and improving quality of life. The following review summarises existing data on the treatments currently used and provides an overview of future alternatives. Glucocorticoids continue to be an indispensable component of the treatment of polymyositis (PM) and dermatomyositis (DM). A combination of drugs including conventional DMARDs has long been established. The ProDERM study provides a solid basis for the use of immunoglobulins in the clinical setting. In severe forms of the disease, rituximab is increasingly replacing cyclophosphamide. Promising early results obtained with abatacept, janus kinase- inhibitors, apremilast, sifalimumab and lenabasum must be corroborated by further studies. The treatment of extramuscular involvement is a challenging issue. The future value of nintedanib in the treatment of interstitial lung disease associated with myositis (IIM-ILD) is of significant interest. The management of inclusion body myositis (IBM) continues to be a major challenge. A number of studies conducted thus far have yielded no convincing evidence of any improvement in the prognosis of the disease. When a patient shows signs of treatment-refractory disease, it is high time for a clinician to consider cancer-associated myositis. In some cases, a hereditary myopathy may be hidden behind myositis triggered by infection or overexertion. Complications in the course of disease, such as dysphagia, infection or myocardial involvement, are not rare at all. Multimorbidity is quite common. Interdisciplinary cooperation is an absolute prerequisite for supporting and accompanying a patient successfully. A competent interdisciplinary team must include an experienced physiotherapist, an occupational therapist and a psychotherapist.
引用
收藏
页码:388 / 399
页数:12
相关论文
共 50 条
  • [31] LEVEL OF SATISFACTION IN PATIENTS WITH IDIOPATHIC INFLAMMATORY MYOPATHIES
    Loghin-Oprea, N.
    Vetrila, S.
    Mazur-Nicorici, L.
    Cebanu, M.
    Salaru, V.
    Mazur, M.
    ANNALS OF THE RHEUMATIC DISEASES, 2017, 76 : 1284 - 1285
  • [32] Opportunistic infections in patients with idiopathic inflammatory myopathies
    Redondo-Benito, Ada
    Curran, Adrian
    Villar-Gomez, Ana
    Trallero-Araguas, Ernesto
    Fernandez-Codina, Andreu
    Pinal-Fernandez, Iago
    Angel Rodrigo-Pendas, Jose
    Selva-O'Callaghan, Albert
    INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES, 2018, 21 (02) : 487 - 496
  • [33] CAPILLAROSCOPIC ALTERATIONS IN PATIENTS WITH IDIOPATHIC INFLAMMATORY MYOPATHIES
    Kachkovska, V.
    Kovchun, A.
    Prystupa, E.
    Prystupa, L.
    ANNALS OF THE RHEUMATIC DISEASES, 2020, 79 : 500 - 500
  • [34] Familial autoimmunity in patients with idiopathic inflammatory myopathies
    Che, Weng Ian
    Westerlind, Helga
    Lundberg, Ingrid E.
    Hellgren, Karin
    Kuja-Halkola, Ralf
    Holmqvist, Marie E.
    JOURNAL OF INTERNAL MEDICINE, 2023, 293 (02) : 200 - 211
  • [35] Lung Nodules in Patients with Idiopathic Inflammatory Myopathies
    Cappelli, Laura C.
    Mammen, Andrew L.
    Danoff, Sonye K.
    Louie, Grant H.
    Lloyd, Thomas E.
    Christopher-Stine, Lisa
    ARTHRITIS AND RHEUMATISM, 2012, 64 (10): : S95 - S95
  • [36] RELAPSES OF 129 PATIENTS WITH IDIOPATHIC INFLAMMATORY MYOPATHIES
    Choi, J.
    Kim, J.
    Ghang, B.
    Yoo, B.
    ANNALS OF THE RHEUMATIC DISEASES, 2023, 82 : 1650 - 1650
  • [37] Infection is not rare in patients with idiopathic inflammatory myopathies
    Ge, Y. P.
    Shu, X. M.
    He, L. R.
    Wang, G. C.
    Lu, X.
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2022, 40 (02) : 254 - 259
  • [38] Outcome predictors in patients with idiopathic inflammatory myopathies
    Salvador, F. B.
    Isenberg, D. A.
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2012, 30 (06) : 980 - 980
  • [39] MUSCLE OUTCOME IN PATIENTS WITH IDIOPATHIC INFLAMMATORY MYOPATHIES
    Salvador, Fernando B.
    Huertas, Carolina
    Isenberg, David
    RHEUMATOLOGY, 2012, 51 : 94 - 94
  • [40] Diaphragmatic dysfunction in patients with idiopathic inflammatory myopathies
    Teixeira, A
    Cherin, P
    Demoule, A
    Levy-Soussan, M
    Straus, C
    Verin, E
    Zelter, M
    Derenne, JP
    Herson, S
    Similowski, T
    NEUROMUSCULAR DISORDERS, 2005, 15 (01) : 32 - 39