Psychometric Evaluation of the National Institutes of Health Patient‐Reported Outcomes Measurement Information System in a Multiracial, Multiethnic Systemic Lupus Erythematosus Cohort-Reference-Cited by-同舟云学术

Psychometric Evaluation of the National Institutes of Health Patient‐Reported Outcomes Measurement Information System in a Multiracial, Multiethnic Systemic Lupus Erythematosus Cohort

Published:2019-11-05 Issue:12 Volume:71 Page:1630-1639
ISSN:2151-464X
Container-title:Arthritis Care & Research
language:en
Short-container-title:Arthritis Care Res

Author:

Katz Patricia¹,Yazdany Jinoos¹,Trupin Laura¹,Rush Stephanie¹,Helmick Charles G.²,Murphy Louise B.²^ORCID,Lanata Cristina¹^ORCID,Criswell Lindsey A.¹,Dall'Era Maria¹

Affiliation:

1. University of California San Francisco

2. Centers for Disease Control and Prevention Atlanta Georgia

Funder

Centers for Disease Control and Prevention

Publisher

Wiley

Subject

Rheumatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/acr.23797

Reference25 articles.

2. Clinical trials in systemic lupus erythematosus (SLE): lessons from the past as we proceed to the future – the EULAR recommendations for the management of SLE and the use of end-points in clinical trials

3. US Department of Health and Human Services.Guidance for industry. Systemic lupus erythematosus: developing medical products for treatment. June 2010. URL:https://www.fda.gov/media/71150/download.

4. The Promise of Patient-Reported Outcomes Measurement Information System—Turning Theory into Reality

5. Concepts important to persons with systemic lupus erythematosus and their coverage by standard measures of disease activity and health status

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