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Abstract Number: 327

The Patient Global Assessment and Common Composite Disease Activity Measures Vary Minimally When Patients Reflect on Their Arthritis or Their Global Health: Results from the Canadian Early Arthritis Cohort Study

Vivian P. Bykerk1, Orit Schieir2, Marie-France Valois3, Edward C. Keystone4, Gilles Boire5, Janet E. Pope6, Diane Tin7, Carol Hitchon8, Carter Thorne9, Susan J. Bartlett10 and Boulos Haraoui11, 1Deptartment of Rheumatology, Hospital for Special Surgery, New York, NY, 2McGill University, Montreal, ON, Canada, 3McGill University, Montreal, QC, Canada, 4University of Toronto and Mount Sinai Hospital, Toronto, ON, Canada, 5Rheumatology Division, Centre intégré universitaire de santé et de services sociaux de l'Estrie - Centre Hospitalier Universitaire de Sherbrooke and Universite de Sherbrooke, Sherbrooke, QC, Canada, 6Department of Medicine, University of Western Ontario, London, ON, Canada, 7The Arthritis Program, Southlake Regional Health Centre, Newmarket, ON, Canada, 8University of Manitoba, Winnipeg, MB, Canada, 9University of Toronto, Newmarket, ON, Canada, 10Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 11Institut de Recherche en Rhumatologie de Montréal (IRRM), Montreal, QC, Canada

Meeting: 2018 ACR/ARHP Annual Meeting

Keywords: Disease Activity, measure and rheumatoid arthritis (RA), PRO

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Session Information

Date: Sunday, October 21, 2018

Title: Measures and Measurement of Healthcare Quality Poster I

Session Type: ACR Poster Session A

Session Time: 9:00AM-11:00AM

Background/Purpose: The patient global assessment (PtGA) is a core domain used in RA composite disease activity (CDA) measures for trials and treat-2-target paradigms. The PtGA is asked differently, either referring to the patient’s global health or condition (PtGA-GH), or to their arthritis disease activity (PtGA-AR). Objectives of this study were to assess agreement between PtGA-GH vs. PtGA-AR ratings and between CDA indices calculated using both versions of the PtGA.

Methods: We included patients enrolled in the Canadian Early Inflammatory Arthritis Cohort (CATCH) study between 2011 and 2017 who met 1987 or 2010 ACR/EULAR criteria for RA and simultaneously completed both PtGA-GH and PtGA-AR using a 10 cm VAS (scored 0-10) at baseline, 6- and 12-months of follow-up. Descriptive statistics were used to summarize baseline cohort characteristics, PtGA ratings and CDA indices with differences compared using Wilcoxon-sign rank tests and chi-square tests. Agreement was assessed using intraclass correlation coefficients (ICC) for continuous measures and weighted kappa coefficients for categorical measures. Stratified analyses were also performed by age (older >65) and sex.

Results: Of 571 early RA patients who completed both PtGAs, 71% were female, 83% were white, 17% were current smokers, 17% were erosive, and 60% had completed high-school. Baseline mean(sd) age was 55(15), symptom duration was 5(3) months and comorbid conditions were 2(2). Agreement between PGA ratings, composite CDA measures and classification of remission using both PtGA-GH and PtGA-AR are summarized in Table 1. Mean(sd) PtGA-GH ratings were only marginally higher than PtGA-AR ratings and agreement was high between PtGA ratings at baseline and over the first year follow up (all ICCs > 0.8). Agreement in CDA scores calculated with either PtGA was even higher at baseline and over time (all ICCs > 0.95). There was also high concordance in classification of remission using either PtGA at all time points (all Kappa’s > 0.85). Results of stratified analyses showed that relative to men, women tended to report slightly higher differences in PtGA-GH vs. PtGA-AR (all p’s >0.0001) but overall agreement in PGA ratings, CDA scores and classification of remission was very high and similar in both sexes. Age stratified analyses, which reflects the comorbidies that increase with age, were similar to those in the whole sample.

Conclusion: Results from this large sample of early RA patients followed in a longitudinal study in typical practice settings, showed patients rated their PtGA-GH marginally higher their PtGA-AR, but this difference had minimal impact on composite disease activity indices and classifications of remission commonly used in patient care. These findings suggest common composite measures of RA disease activity can be calculated using either the PtGA-GH or PtGA-AR.

Table 1: Agreement PtGA Indices

Variable

Baseline

6-months

12-months

PtGA – GH

PtGA – AR

PtGA – GH

PtGA – AR

PtGA – GH

PtGA – AR

Patient Global Assessment (0-10)

Mean (SD)

5.7 (2.8)

5.2 (2.8)

3.0 (2.7)

2.8 (2.6)

2.7 (2.6)

2.4 (2.5)

ICC

0.80

0.88

0.88

Composite Disease Activity Indices

DAS28 ESR Mean (SD)

5.0 (1.3)

4.9 (1.3)

2.9 (1.4)

2.9 (1.4)

2.6 (1.4)

2.6 (1.4)

ICC

0.98

0.99

0.99

Remission, Frequency (%)

23 (5%)

23 (5%)

193 (45%)

196 (46%)

243 (56%)

247 (57%)

Kappa (95% CI)

0.93 (0.91, 0.95)

0.97 (0.96, 0.98)

0.98 (0.97, 0.98)

SDAI Mean (SD)

28.7 (14.4)

28.1 (14.4)

10.5 (10.4)

10.2 (10.4)

8.2 (9.8)

7.9 (9.7)

ICC

0.99

0.99

0.99

Remission, Frequency (%)

6 (1%)

6 (1%)

143 (30%)

155 (32%)

192 (41%)

203 (43%)

Kappa (95% CI)

0.95 (0.93, 0.97)

0.95 (0.94, 0.97)

0.95 (0.94, 0.97)

CDAI Mean (SD)

27.1 (13.7)

26.6 (13.7)

9.7 (10.3)

9.5 (10.3)

7.3 (9.2)

7.0 (9.1)

ICC

0.99

0.99

0.99

Remission, Frequency (%)

5 (1%)

6 (1%)

158 (28%)

173 (31%)

210 (38%)

215 (39%)

Kappa (95% CI)

0.93 (0.909, 0.96)

0.92 (0.901, 0.94)

0.92 (0.90, 0.94)

RAPID III Mean (SD)

4.6 (2.4)

4.5 (2.3)

2.5 (2.2)

2.4 (2.2)

2.2 (2.1)

2.1 (2.1)

ICC

0.97

0.98

0.98

Remission, Frequency (%)

52 (9%)

53 (9%)

199 (36%)

206 (37%)

231 (41%)

237 (42%)

Kappa (95% CI)

0.85 (0.81, 0.89)

0.86 (0.83, 0.90)

0.85 (0.815, 0.89)


Disclosure: V. P. Bykerk, Bristol-Myers Squibb, Pfizer Inc, Sanofi, UCB, 5; O. Schieir, Other, 2; M. F. Valois, Other, 2; E. C. Keystone, AbbVie, Amgen, Bristol-Myers Squibb, F. Hoffmann-La Roche Inc, Gilead, Janssen Inc, Lilly Pharmaceuticals, Pfizer Pharmaceuticals, Sanofi-Aventis, 2,AbbVie, Amgen, AstraZeneca Pharma, Biotest, Bristol-Myers Squibb Company, Celltrion, Crescendo Bioscience, F. Hoffmann-La Roche Inc, Genentech Inc, Gilead, Janssen Inc, Lilly Pharmaceuticals, Merck, Pfizer Pharmaceuticals, Sandoz, UCB, 5,Amgen, AbbVie, Bristol-Myers Squibb Canada, F. Hoffmann-La Roche Inc., Janssen Inc., Merck, Pfizer Pharmaceuticals, Sanofi Genzyme, UCB, 8; G. Boire, Merck & Co., 8, 9,BMS, 8, 9,Pfizer, Inc., 8, 9,Amgen Inc., 9,AbbVie Inc., 9,Novartis, 9,Eli Lilly and Co., 9,Janssen, 9; J. E. Pope, None; D. Tin, Multiple, 2; C. Hitchon, Pfizer, Inc., 2; C. Thorne, Amgen Inc., 2, 5, 9,Pfizer, Inc., 2, 5, 9,UCB, Inc., 9,AbbVie Inc., 2, 5, 9,Medexus/Medac, 2, 5, 8,Eli Lilly and Co., 9,Merck & Co., 9,Hospira, 5, 9,Janssen, 9,Sanofi Genzyme, 5, 9,Celgene Corporation, 9,CaREBiodam, 9,Centocor, 5,Novartis, 9; S. J. Bartlett, UCB, Inc., 5,Eli Lilly and Co., 5,Pfizer, Inc., 5; B. Haraoui, AbbVie, Amgen, BMS, Celgene, Eli Lilly, Janssen, Merck, Pfizer, Roche, and UCB, 9,AbbVie, Amgen, BMS, Janssen, Pfizer, Roche, and UCB, 2,Amgen, BMS, Janssen, Pfizer, and UCB, 8.

To cite this abstract in AMA style:

Bykerk VP, Schieir O, Valois MF, Keystone EC, Boire G, Pope JE, Tin D, Hitchon C, Thorne C, Bartlett SJ, Haraoui B. The Patient Global Assessment and Common Composite Disease Activity Measures Vary Minimally When Patients Reflect on Their Arthritis or Their Global Health: Results from the Canadian Early Arthritis Cohort Study [abstract]. Arthritis Rheumatol. 2018; 70 (suppl 9). https://acrabstracts.org/abstract/the-patient-global-assessment-and-common-composite-disease-activity-measures-vary-minimally-when-patients-reflect-on-their-arthritis-or-their-global-health-results-from-the-canadian-early-arthritis-c/. Accessed .
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