Integrating PROMIS in Arthritis Clinical Care: Feasibility, Impact, and Content Validation



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Developing and Implementing a Patient Reported Outcomes Network in Canada: Potential Benefits and Challenges Montreal, QC, Canada Integrating PROMIS in Arthritis Clinical Care: Feasibility, Impact, and Content Validation Clifton O. Bingham III, MD Associate Professor, Johns Hopkins University, Baltimore MD Susan J. Bartlett, PhD Associate Professor, McGill University, Montreal CA 5-6 November 2013

Rheumatoid Arthritis Rheumatoid arthritis (RA) is a chronic, systemic, and frequently disabling disease that affects up to 1% of the population Associated with considerable diseaseand treatment-related morbidities and premature mortality Multiple aspects of physical, emotional, and social health are impacted Current measures used in clinical care to guide treatment decisions have limited inclusion of patientvalued outcomes

Current Outcome Measures Used in RA Clinical Trials and Decision Making RA Core Set: Swollen Joints, Tender Joints, Patient Global Assessment, MD Global Assessment, Patient Assessment of Pain, HAQ-DI, ESR/CRP DAS Swollen Joints, Tender Joints, ESR/CRP, Patient Global Health CDAI Swollen Joints, Tender Joints, Patient Global Assessment of Disease, MD Global Assessment SDAI - CDAI+ CRP

Outcome Measures in Rheumatology Established in 1992 to Develop, Improve, Validate Outcome Measures for Clinical Trials RA Core Set, RA Remission, OA Response, MRI RAMRIS, Psoriatic arthritis Core Set, etc Evolved to encompass spectrum of rheumatic diseases and settings (RCT, LOS, practice) Filter 1.0: Truth, Discrimination, Feasibility Filter 2.0: Framework for developing Core Outcome Sets Patient inclusion in research process since 2002 Resulted in addition of Fatigue to recommended RA Core Set

RA Patients and Providers have Different Perspectives When Rating the Importance of Disease Signs and Symptoms: RA Flare Favoured by Patients Bartlett SJ et al, Ann Rheum Dis 2012; Bingham CO et al, Ann Rheum Dis 2012; Bingham CO et al J Rheumatol 2009, Hewlett SH, et al, Rheumatology 2010; Bingham CO et al, J Rheumatol 2011; Alten R et al, J Rheumatol 2011; Bykerk VB, et al, J Rheumatol 2013 (in press)

Patient-Reported Outcome Measurement Information System (PROMIS ) www.nihpromis.org Developed to improve the precision of evaluating Health Related Quality of Life (HRQoL) across multiple areas of physical, mental, and social health Tested mostly in research settings Limited evaluation in clinical care settings Limited evaluation in specific disease states Domains identified by RA patients are included in PROMIS Evaluation of PROMIS in RA has been limited to assessments of physical function Addresses floor and ceiling effects of HAQ and SF12

PCORI Pilot Project Objectives Hypothesis tested: Integrating PROs into routine care will improve the assessment of patient-valued symptoms and influence medical decision-making Objective: To evaluate the feasibility and impact of integrating PROMIS in RA patients seen in a busy clinical practice setting Acceptability to Patients and Providers Integration within Practice Workflow Patient-Care Team Interactions Shared Decision-Making Validity and Responsiveness of PROMIS measures 7

Research Methods (1) People with RA seen in routine clinical care are eligible Assessment Center programmed with PROMIS instruments and legacy measures In waiting room, patient given an ipad linked to online AC module PROMIS SFs, CATs, and other measures completed

Research Methods (2) Routine clinic visit with provider takes place Review/discussion of PROMIS results Patient and provider rate value of information, and impact on clinical decisionmaking (survey) Interviews and focus groups with patients, providers, clinic and research staff

Mixed Methods Analytic Approach Qualitative (Surveys, Interviews, Focus Groups) Patients Providers Clinic Staff Research Staff Stakeholders Quantitative PROMIS Data Legacy PROs Standard Clinical Outcomes Validation

Selection of Domains Patient Identified Legacy PROMIS SF, Scale or PROMIS Domain Measure Score Item PROMIS CAT Global Assessment VAS Global 1.1 G1, G2 Pain VAS Pain Intensity 3a G7 Pain Interference Physical Function MHAQ Global Physical Score G6, G3 Physical Function Participation None G9r G5 Participation Satisfaction Fatigue VAS Fatigue G8 Fatigue Systemic Features Global VAS G1, G2 Sleep None Sleep Disturbance Sleep Interference Emotional Distress None Global Mental Score G4, G10 Depression Anxiety Anger Other Measures: Patient assessed disease change, Minimal important difference, Patient acceptable symptom state, Flare assessment, Stiffness, Self-management

Multilevel Mixed Methods Approach with Patient Incorporation throughout Research Process Input Outcomes RA Patients OMERACT CPATH/FDA NIH/PROMIS EULAR RA Patients Research Team PCORI Pilot Project: Integrating PROMIS in Arthritis Clinical Care Stakeholders RA Patients Feasibility and Acceptability RA Patients Truth, Relevance, and Content Validity RA Patients Effects on Communication and Decision Making RA Patients Ability to Detect Change/ Discrimination RA Patients Value and Implications of Study Results RA Patients

Preliminary Results PROMIS In Clinic: Feasibility 12 PROMIS Instruments Administered: Global health, Pain (Intensity, Interference), Fatigue, Physical function, Sleep (Disturbance, Interference), Depression, Anxiety, Cognition general concerns, Social roles (Participation, Satisfaction) (n=107) Mean SD Median Min Max Time to Complete (minutes) 12.1 4.5 10.8 5.7 32 Number of Questions 67.8 9.5 65.0 58 98 Time for completion includes clinic interruptions (moving to rooms, vital signs, etc.) Interviews ongoing with patients, providers, and clinic staff to determine effect on clinic flow

Example PROMIS Reports Active RA Mild RA Breakup w/ Sig Other RA in Remission Poor Sleep 2 o Sinus Surgery

Preliminary Observations: Clinical Decision-Making New comorbidities and symptoms have been identified by PROMIS measures that did not surface during the usual clinical encounter E.g., fatigue, sleep, depression, anxiety Some of these resulted in changes in RA therapy to address symptoms, referrals for evaluation of symptoms, and/or treatment of comorbidities

Participant Characteristics (n=107) Variable Value Range Sociodemographic Age (yrs.) 55.5 ± 13.0 22-85 Sex (% female) 53 (77%) Minority race (%) 17 (16%) Completed some college 74% RA Characteristics Disease duration (yrs.) 12.0 ± 9.3 1-41 CDAI 8.8 ± 8.7 0-33.5 MD Global Assessment (VAS) 15.7 ± 17.1 0-75 Patient Reported Outcomes Patient Global (VAS) 29.8 ± 26.6 Pain (VAS) 33.2 ± 28.6 MHAQ (0-3) 0.3 ± 0.4 Values are mean ± SD, unless otherwise indicated Bartlett SJ, Orbai AM, Duncan T, DeLeon E Bingham CO. Validity of PROMIS CATs, Short Forms and Global Health Items in Rheumatoid Arthritis. Qual Life Res 2013; 22(Supp 1) 119: Abstract 3024

Preliminary Results Distribution of Selected PROMIS CAT T-Scores in RA Patients (n=107) Better Worse * *Scores inverted for demonstration

Regression coefficient, effect sizes and mean scores by CDAI disease activity level for legacy and PROMIS measures: Global and General Health Variable Source B Effect Size (β/se) Remission N=29 Low N=45 Moderate N=21 High N=12 Patient Global VAS 17.8 8.4 5.5 + 6.5 a 29.6 + 23.2 b 50.0 + 21.4 c 53.4 + 27.8 c MD Global VAS 13.2 11.1 3.4 + 3.8 a 10.9 + 9.5 b 26.9 + 13.0 c 43.8 + 22.6 d PROMIS Global Physical Score -5.6-7.4 53.8 ± 6.9 a 44.1 ± 8.2 b 39.2 ± 5.6 c 38.4 ± 6.3 c PROMIS Global Mental Score -3.1-3.6 54.7 ± 8.1 a 48.2 ± 8.2 b 48.6 8.2 b 44.1 ± 8.6 b Bartlett SJ, Orbai AM, Duncan T, DeLeon E Bingham CO. Validity of PROMIS CATs, Short Forms and Global Health Items in Rheumatoid Arthritis. Qual Life Res 2013; 22(Supp 1) 119: Abstract 3024

Regression coefficient, effect sizes and mean scores by CDAI disease activity level for legacy and PROMIS measures: Pain, Fatigue, and Physical Function Variable Source B Effect Size (β/se) Remission N=29 Low N=45 Moderate N=21 High N=12 Pain VAS 17.6 7.4 6.2 ± 8.2 a 35.7 ± 25.3 b 54.1 ± 26.8 c 52.4 ± 25.7 c PROMIS Pain Intensity SF 4.1 5.7 38.4 ± 7.3 a 46.3 ± 6.4 b 48.7 ± 6.6 b 50.3 ± 8.4 b PROMIS Pain Interfere CAT 4.9 5.8 46.6 ± 7.9 a 55.4 ± 8.4 b 59.2 ± 4.7 b 60.1 ± 10.7 b Fatigue VAS 16.8 6.2 13.4 ± 18.1 a 45.1± 28.3 b,c 59.0 ± 28.3 c 58.9 ± 25.7 c PROMIS Fatigue SF 4.1 5.1 46.8 ± 7.1 a 54.7 ± 9.1 b 58.0 ± 5.2 b 58.1 ± 8.1 b PROMIS Fatigue CAT 5.6 6.2 46.2 ± 8.8 a 55.3 ± 8.7 b 60.0 ± 6.8 c 62.0 ± 11.3 c mhaq* Scale.2 5.2 0.1 ± 0.4 a 0.3 ± 0.3 a 0.5 ± 0.4 b 0.7 ± 0.6 b PROMIS PF CAT -5.2-6.7 50.4 ± 9.0 a 43.0 ± 7.5 b 38.7 ± 5.6 c 35.2 ± 7.1 c PROMIS Anxiety CAT 2.2 2.6 48.0 ± 7.5 a 52.0 ± 9.1 b 51.9 ± 7.3 a,b 55.6 ± 8.2 b Bartlett SJ, Orbai AM, Duncan T, DeLeon E Bingham CO. Validity of PROMIS CATs, Short Forms and Global Health Items in Rheumatoid Arthritis. Qual Life Res 2013; 22(Supp 1) 119: Abstract 3024

Regression coefficient, effect sizes and mean scores by CDAI disease activity level for PROMIS measures: Emotional and Social Health Variable Source B Effect Size (β/se) Remission N=29 Low N=45 Moderate N=21 High N=12 PROMIS Anxiety CAT 2.2 2.6 48.0 ± 7.5 a 52.0 ± 9.1 b 51.9 ± 7.3 a,b 55.6 ± 8.2 b PROMIS Depression CAT 2.4 2.6 47.1 ± 8.2 a 49.5 ± 9.3 a 51.5 ± 9.1 a 54.4 ± 9.1 b PROMIS Anger CAT 2.0 2.1 45.2 ± 8.4 46.8 ± 9.7 49.5 ± 11.1 51.1 ± 8.9 PROMIS Participation CAT -4.9-5.9 55.9 ± 9.3 a 50.0 ± 8.4 b 46.2 ± 6.3 b 40.7 ± 8.6 b,c PROMIS Satisfaction CAT -5.0-5.2 55.3 ± 10.0 a 47.3 ± 10.1 b 44.6 ± 6.8 b,c 39.8 ± 9.3 c Bartlett SJ, Orbai AM, Duncan T, DeLeon E Bingham CO. Validity of PROMIS CATs, Short Forms and Global Health Items in Rheumatoid Arthritis. Qual Life Res 2013; 22(Supp 1) 119: Abstract 3024

Conclusions Our preliminary data suggest that the integration of PROMIS CATs and short forms is possible within clinical care settings The immediate availability of results allows for evaluation and discussion with patients at the time of the clinic visit Our preliminary assessments indicate that PROMIS measures demonstrate considerable impact of RA across multiple areas of HRQL

Funding We gratefully acknowledge support from: Patient Centered Outcomes Research Institute (PCORI) Pilot Project NIH/NIAMS P30-AR053503 (Rheumatic Diseases Research Core Center) Ira J. Fine Discovery Fund Sibley Hospital Foundation Donald M. and Dorothy L. Stabler Foundation Johns Hopkins Arthritis Center Research Fund OMERACT

Acknowledgements Johns Hopkins Rheumatology Trisha Duncan MD Ana-Maria Orbai MD Uzma Haque MD Grant Louie MD MHS Rebecca Manno MD MHS Thomas Grader-Beck MD Victoria Ruffing RN CCRP Laura Manning RN Marilyn Towns CCRC Michelle Jones Brandy Miles Tony Keyes Wes Linda Penny Athanasiou Joyce Kosmas Bonnie Hebden Johns Hopkins Bloomberg School of Public Health Katherine Clegg-Smith PhD Elaine De Leon MPH Northwestern University Richard Gershon PhD David Cella PhD Monica Prudencio Arredondo Stakeholders/Advisors Kenneth Saag MD MPH Patience White MD James Witter MD PhD Laure Gossec MD PhD Sarah Hewlett RN PhD Enkeleida Nikai Amye Leong MBA Kelly Young Ernest Choy MD PhD