Establishing clinical meaning and defining important differences for Patient-Reported Outcomes Measurement Information System (PROMIS®) measures in juvenile idiopathic arthritis using standard setting with patients, parents, and providers

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

(2016) James P. Witter   RHEUMATIC DISEASE CLINICS OF NORTH AMERICA

Fatigue in patients with juvenile idiopathic arthritis: A systematic review of the literature

(2016) Wineke Armbrust et al.   SEMINARS IN ARTHRITIS AND RHEUMATISM

Long-Term Health-Related Quality of Life in German Patients with Juvenile Idiopathic Arthritis in Comparison to German General Population

(2016) Swaantje Barth et al.   PLoS One

Qualitative Evaluation of Pediatric Pain Behavior, Quality, and Intensity Item Candidates and the PROMIS Pain Domain Framework in Children With Chronic Pain

(2015) C. Jeffrey Jacobson et al.   JOURNAL OF PAIN

The Role of Technical Advances in the Adoption and Integration of Patient-reported Outcomes in Clinical Care

(2015) Roxanne E. Jensen et al.   MEDICAL CARE

Item-level informant discrepancies between children and their parents on the PROMIS® pediatric scales

(2015) James W. Varni et al.   QUALITY OF LIFE RESEARCH

Estimating minimally important difference (MID) in PROMIS pediatric measures using the scale-judgment method

(2015) David Thissen et al.   QUALITY OF LIFE RESEARCH

Coproduction of healthcare service

(2015) Maren Batalden et al.   BMJ Quality & Safety

High prevalence of hand- and wrist-related symptoms, impairments, activity limitations and participation restrictions in children with juvenile idiopathic arthritis

(2014) A Hoeksma et al.   JOURNAL OF REHABILITATION MEDICINE

What Matters Most for Patients, Parents, and Clinicians in the Course of Juvenile Idiopathic Arthritis? A Qualitative Study

(2014) J. Guzman et al.   JOURNAL OF RHEUMATOLOGY

Creating meaningful cut-scores for Neuro-QOL measures of fatigue, physical functioning, and sleep disturbance using standard setting with patients and providers

(2014) Karon F. Cook et al.   QUALITY OF LIFE RESEARCH

Setting standards for severity of common symptoms in oncology using the PROMIS item banks and expert judgment

(2014) David Cella et al.   QUALITY OF LIFE RESEARCH

PROMIS Pediatric Peer Relationships Scale: Development of a peer relationships item bank as part of social health measurement.

(2013) Darren A. DeWalt et al.   HEALTH PSYCHOLOGY

“I'm the One Taking It”: Adolescent Participation in Chronic Disease Treatment Decisions

(2013) Ellen A. Lipstein et al.   JOURNAL OF ADOLESCENT HEALTH

PROMIS® Parent Proxy Report Scales for children ages 5–7 years: an item response theory analysis of differential item functioning across age groups

(2013) James W. Varni et al.   QUALITY OF LIFE RESEARCH

Development and psychometric properties of the PROMIS® pediatric fatigue item banks

(2013) Jin-Shei Lai et al.   QUALITY OF LIFE RESEARCH

Pain Ratings by Patients and Their Providers of Radionucleotide Injection for Breast Cancer Lymphatic Mapping

(2012) Jason S. Radowsky et al.   PAIN MEDICINE

Construction of the eight-item patient-reported outcomes measurement information system pediatric physical function scales: built using item response theory

(2011) Esi Morgan DeWitt et al.   JOURNAL OF CLINICAL EPIDEMIOLOGY

PROMIS Pediatric Anger Scale: an item response theory analysis

(2011) Debra E. Irwin et al.   QUALITY OF LIFE RESEARCH

PROMIS Pediatric Pain Interference Scale: An Item Response Theory Analysis of the Pediatric Pain Item Bank

(2010) James W. Varni et al.   JOURNAL OF PAIN

Agreement between Proxy and Adolescent Assessment of Disability, Pain, and Well-Being in Juvenile Idiopathic Arthritis

(2010) Sham D. Lal et al.   JOURNAL OF PEDIATRICS

Burden of childhood-onset arthritis

(2010) Lakshmi N Moorthy et al.   Pediatric Rheumatology

An item response analysis of the pediatric PROMIS anxiety and depressive symptoms scales

(2010) Debra E. Irwin et al.   QUALITY OF LIFE RESEARCH