Longterm survival and associated risk factors in patients with adult-onset idiopathic inflammatory myopathies and amyopathic dermatomyositis: experience in a single institute in Japan.

Abstract

Survival of clinically ADM and primary DM was low, mainly due to fatal ILD, compared to primary PM. Establishing therapeutic strategy for ILD may improve the survival in our patient population.

Full Text

• DOI - The Journal of rheumatology (DOI)
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Subjects

• Adult
• Age of Onset
• Aged
• Dermatomyositis
• Diagnosis, Differential
• Female
• Humans
• Japan
• Male
• Middle Aged
• Myositis
• Prognosis
• Retrospective Studies
• Risk Factors
• Severity of Illness Index
• Survival Rate

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Authors

• Yoshioki Yamasaki
• Hidehiro Yamada
• Michiko Ohkubo
• Masaomi Yamasaki
• Kohei Azuma
• Hitoshi Ogawa
• Machiko Mizushima
• Shoichi Ozaki

Publication date

2011-08-02

Journal

Journal topics

• Arthritis
• Rheumatic Diseases

Language

Eng.

Copyright

The Journal of rheumatology

Division of Rheumatology and Allergology, Department of Internal Medicine, St. Marianna University, School of Medicine, Kawasaki, Kanagawa Prefecture, Japan. yams [at] marianna-u.ac.jp

Release reference

J Rheumatol. 2011 Aug;38(8):1636-43

Related books

• Books of Age of Onset
• Books of Arthritis
• Books of Dermatomyositis
• Books of Diagnosis, Differential
• Books of Japan
• Books of Myositis
• Books of Prognosis
• Books of Retrospective Studies
• Books of Rheumatic Diseases
• Books of Risk Factors
• Books of Severity of Illness Index
• Books of Survival Rate