Session » Quality Measures and Quality of Care - Poster II
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Abstract Number: 1424
Acceptability of a Connected Activity Tracker in 92 Patients with Rheumatoid Arthritis (RA) or Axial Spondyloarthritis (axSpA): A 3-Months Study
- 9:00AM-11:00AM
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Abstract Number: 1414
Access to an Active, Interactive Self-Assessment e-Health Platform Improves Patient-Physician Communication in Rheumatoid Arthritis: Results of a Randomized Controlled Trial Including 320 Patients over 1 Year
- 9:00AM-11:00AM
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Abstract Number: 1430
Adherence to the International Consensus Quality Indicators for Longitudinal Health Maintenance and Preventative Care in a Pediatric Rheumatology Clinic
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Abstract Number: 1411
An Electronic MDHAQ (multidimensional health assessment questionnaire) Beyond an Electronic RAPID (routine assessment of patient index data): 21.3% of Rheumatoid Arthritis Patients Identified As Having Secondary Fibromyalgia Versus 3.5% By Clinicians
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Abstract Number: 1417
Back to Feeling Normal Again: Patients with Rheumatoid Arthritis in Remission
- 9:00AM-11:00AM
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Abstract Number: 1407
Disease Activity Trackers to Support Treat to Target Strategies: A Needs Assessment Survey
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Abstract Number: 1413
Establishing Clinical Severity for Patient Reported Outcomes Measurement Information System Measures in Adult Patients with Rheumatic Diseases
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Abstract Number: 1431
Estimates of Global Status By Physicians and Patients Are More Likely to be Discordant in Osteoarthritis Than in Rheumatoid Arthritis
- 9:00AM-11:00AM
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Abstract Number: 1422
Identifying Generic and Specific Patients’ Perspectives on Disease- and Treatment-Related Issues in Rheumatoid Arthritis, Psoriatic Arthritis, and Psoriasis: A Qualitative Concept Mapping Study
- 9:00AM-11:00AM
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Abstract Number: 1408
Impact of Participation in the Adalimumab (Humira) Patient Support Program on Patient Reported Outcomes Among Patients with Rheumatoid Arthritis: Passion Study
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Abstract Number: 1415
Impact of the Clinical Disease Activity Index to Treat to Target Rheumatoid Arthritis in the Ambulatory Setting
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Abstract Number: 1409
Increase in the Use of Validated Disease Activity Scores in Current Daily Clinical Practice Compared to 2007
- 9:00AM-11:00AM
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Abstract Number: 1410
Is the Self-Assessment of Disease Activity (auto-DAS28) By Patients a Feasible and Acceptable Measure over the Long Term in Rheumatoid Arthritis (RA)? Three-Year Follow-up of a Nurse-Led Program in 771 Patients with Established RA
- 9:00AM-11:00AM
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Abstract Number: 1428
Patient Attitudes Towards Being Prescribed Biosimilars in Inflammatory Autoimmune Diseases in Germany
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Abstract Number: 1429
Patient-Reported Outcomes Measures and Economical Burden of Patients with Ankylosing Spondylitis in a Chinese Prospective Cohort with Smart Management System for Spondyloarthritis
- 9:00AM-11:00AM
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Abstract Number: 1405
Quality Measures in High Priority Rheumatologic Diseases: A Systematic Literature Review and Analysis
- 9:00AM-11:00AM
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Abstract Number: 1421
Responsiveness of Lupus Impact Tracker Among Chinese Patients with Lupus
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Abstract Number: 1418
Rheumatologist: If You Fell Ill with Seropositive Active Rheumatoid Arthritis Yourself, What to Do!
- 9:00AM-11:00AM
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Abstract Number: 1433
Self-Perception Reporting to Healthcare Professionals: Do Individuals with Systemic Sclerosis Report Quality of Life Changes Accurately?
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Abstract Number: 1416
Sustained Improvement in Documentation of Disease Activity Measurement As a Quality Improvement Project at an Academic Rheumatology Clinic
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Abstract Number: 1403
Systematic Appraisal of the American College of Rheumatology Clinical Practice Guidelines
- 9:00AM-11:00AM
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Abstract Number: 1404
Systematic Review and Appraisal of Quality Measures for Inflammatory Arthritis
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Abstract Number: 1432
The EULAR Systemic Sclerosis Impact of Disease Score – a New Patient-Reported Outcome Measure for Patients with Systemic Sclerosis Under Development
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Abstract Number: 1427
The Importance of Outcome Measures in Ankylosing Spondylitis – Validity of the Routine Assessment of Patient Index Data 3 in a Real World Cohort
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Abstract Number: 1406
Towards Harmonized Data Collection in Rheumatoid Arthritis (RA): The EULAR Task Force for Standardizing a Minimum Data Collection for RA Observational Research
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Abstract Number: 1423
Using Self-Reported Patient Experiences to Evaluate Patient Reported Outcomes (PRO) Instruments: Learnings from Digital Patient Communities in Psoriatic Arthritis
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Abstract Number: 1426
Using Self-Reported Patient Experiences to Understand Patient Burden: Learnings from Digital Patient Communities in Ankylosing Spondylitis
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Abstract Number: 1425
Validation of a Patient Reported Experience Measure (PREM) in Patients with Axial Spondyloarthropathies (AxSpA)
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Abstract Number: 1420
Validation of Lupuspro V1.8, Disease Targeted Patient Reported Outcome for Systemic Lupus Erythematosus
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Abstract Number: 1412
Validation of the Danish Version of the Stanford Health Assessment Questionnaire Disability Index and Determination of the Minimal Clinically Important Difference in a Cohort of Rheumatoid Arthritis Patients Using the Rasch Measurement Model
- 9:00AM-11:00AM
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Abstract Number: 1419
Validation of the French Version of Lupus Patient Reported Outcome (LupusPRO), a Disease-Specific Patient Reported Outcome for Lupus Patients