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Shah, Ankoor

A5133688439 | I111088046

Mayo Clinic

Boston University

Citations 3

P.306 Comparative analysis of systemic sclerosis in Indian and us cohorts: insights from two national registries

Poster Presentations | June 5, 2026 | Volume: No volume available | Issue: No issue available | Pages: A297.1-A297

10.1136/jsrd-2026-sswc.348

OC.25 Prevalence of organ involvement and baseline predictors of disease progression in patients with limited cutaneous systemic sclerosis: insights from the conquer database

Oral Communications | June 5, 2026 | Volume: No volume available | Issue: No issue available | Pages: A24-A24

10.1136/jsrd-2026-sswc.25

Discordance Between Patient and Physician Global Assessments in Early Systemic Sclerosis

Arthritis Care & Research | April 20, 2026 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.1002/acr.80069 | PMID 42007807

Objective This study aims to identify factors associated with patient global assessment (PtGA) and physician global assessment (PhGA) and discordance between them in systemic sclerosis (SSc). Methods Data from adults with early SSc (<5 years) from the Collaborative National Quality and Efficacy Registry were included. PtGA and PhGA (0–10 scale), clinical evaluations, and patient‐reported outcomes (PROs) were collected every six months. Multivariable mixed‐effects linear regression identified factors associated with PtGA and PhGA using (1) clinical variables and (2) clinical variables plus PROs. Relative weight analysis (RWA) determined the relative importance of each variable. Discordance (≥2 points between PtGA and PhGA) was assessed using multinomial mixed‐effects logistic regression. Results Among 956 patients (83% women, 33% limited disease), mean PtGA and PhGA at enrollment were 4.2 (SD 2.6) and 3.4 (SD 2.0), respectively ( P < 0.001). RWA of clinical variables identified modified Rodnan skin score (mRSS) and New York Heart Association (NYHA) functional class as most influential for both global assessments. After including PROs, PtGA was most influenced by measures of pain, skin symptoms, and physical function. Discordance occurred in 53% of patients (35% PtGA worse, 18% PhGA worse). Worse PtGA was associated with higher overall pain and discomfort. Worse PhGA was associated with higher mRSS, worse NYHA class, higher pain interference, and lower diffusing capacity of the lung. Conclusion Discordance between PtGA and PhGA occurs commonly, highlighting the need for comprehensive symptom management and measurement of disease burden in this complex disease. In SSc, differences in PtGA and PhGA reflect dissimilar weighting of data elements.