Patient-reported outcome measures in a population of medically indigent patients with systemic lupus erythematosus in Puerto Rico

Author:

Rodríguez-Rivera Diana V1,Rodríguez-Navedo Yerania1,Nieves-Plaza Mariely2,Vilá Luis M1

Affiliation:

1. Division of Rheumatology, Department of Medicine, University of Puerto Rico, Medical Sciences Campus, San Juan, Puerto Rico

2. Graduate Programs, San Juan Bautista School of Medicine, Caguas, Puerto Rico

Abstract

Objective: To determine patient-reported outcomes measures in indigent patients with systemic lupus erythematosus receiving their healthcare through the Puerto Rico government managed care system and compare these measures with non-indigent patients treated in a private fee-for-service setting. Methods: A cross-sectional study was conducted in a cohort of 98 Puerto Ricans with systemic lupus erythematosus. Patients from the public group (n = 40) were treated in a university-based specialized systemic lupus erythematosus clinic and the private group (n = 58) in a community-based rheumatology practice. Demographic and clinical features and patient-reported outcomes measures per LupusPRO instrument were determined. LupusPRO captures quality-of-life measures in 12 domains. Differences among study groups were examined using chi-square, Fisher’s exact, t-tests, and the Wilcoxon signed-rank test. Results: The mean (standard deviation) age of the study population was 44.9 (12.0) years; 94 (95.9%) were women. Patients in the public setting were younger and were more likely to have renal disease and elevated anti-double-stranded DNA antibodies, and being treated with azathioprine and cyclophosphamide. Patients from the public sector were more likely to have better quality-of-life measures in the LupusPRO domains of pain/vitality and coping. No significant differences were observed for the domains of lupus symptoms, physical health, emotional health, body image, cognition, procreation, lupus medications, desires/goals, social support, and satisfaction with medical care. Conclusion: Despite having a lower socioeconomic status and worse clinical status, systemic lupus erythematosus patients from the public sector had equal or better patient-reported outcomes measures than those treated in the private setting. This favorable outcome may be associated with the comprehensive healthcare received by these patients in a specialized lupus clinic.

Publisher

SAGE Publications

Subject

General Medicine

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Self‐concept and body image of people living with lupus: A systematic review;International Journal of Rheumatic Diseases;2021-07-27

2. Socioeconomic and Disability Aspects;Dubois' Lupus Erythematosus and Related Syndromes;2019

3. Socioeconomic consequences of systemic lupus erythematosus;Current Opinion in Rheumatology;2017-09

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