Login / Signup

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

Patricia KatzJinoos YazdanyLaura TrupinStephanie RushCharles G HelmickLouise B MurphyCristina M LanataLindsey A CriswellMaria Dall'Era
Published in: Arthritis care & research (2019)
PROMIS measures appear reliable and valid in persons with lupus across racial/ethnic groups.
Keyphrases
  • patient reported outcomes
  • systemic lupus erythematosus
  • disease activity
  • health information
  • public health
  • healthcare
  • mental health
  • quality improvement
  • social media
  • health promotion
  • human health