Outcome measures in dermatomyositis: quality of life and the patient perspective
- PMID: 31705532
- DOI: 10.1111/bjd.18600
Outcome measures in dermatomyositis: quality of life and the patient perspective
Comment on
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Evaluating important change in cutaneous disease activity as an efficacy measure for clinical trials in dermatomyositis.Br J Dermatol. 2020 Apr;182(4):949-954. doi: 10.1111/bjd.18223. Epub 2019 Sep 8. Br J Dermatol. 2020. PMID: 31206600 Free PMC article.
References
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- Hundley JL, Carroll CL, Lang W et al. Cutaneous symptoms of dermatomyositis significantly impact patients’ quality of life. J Am Acad Dermatol 2006; 54:217-20.
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- Goreshi R, Chock M, Foering K et al. Quality of life in dermatomyositis. J Am Acad Dermatol 2011; 65:1107-16.
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- Robinson ES, Feng R, Okawa J et al. Improvement in the cutaneous disease activity of patients with dermatomyositis is associated with a better quality of life. Br J Dermatol 2015; 172:169-74.
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- Klein RQ, Bangert CA, Costner M et al. Comparison of the reliability and validity of outcome instruments for cutaneous dermatomyositis. Br J Dermatol 2008; 159:887-94.
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- Brevard JA, Hurtt M, Horobin J et al. Design considerations for clinical trials using the Cutaneous Dermatomyositis Disease Area and Severity Index as a primary endpoint. J Clin Exp Dermatol Res 2017; 8:1-6.
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