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Patient-reported outcome measures in a population of medically indigent patients with systemic lupus erythematosus in Puerto Rico
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. METH...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036258/ https://www.ncbi.nlm.nih.gov/pubmed/27721978 http://dx.doi.org/10.1177/2050312116670927 |
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author | Rodríguez-Rivera, Diana V Rodríguez-Navedo, Yerania Nieves-Plaza, Mariely Vilá, Luis M |
author_facet | Rodríguez-Rivera, Diana V Rodríguez-Navedo, Yerania Nieves-Plaza, Mariely Vilá, Luis M |
author_sort | Rodríguez-Rivera, Diana V |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5036258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-50362582016-10-07 Patient-reported outcome measures in a population of medically indigent patients with systemic lupus erythematosus in Puerto Rico Rodríguez-Rivera, Diana V Rodríguez-Navedo, Yerania Nieves-Plaza, Mariely Vilá, Luis M SAGE Open Med Original Article 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. SAGE Publications 2016-09-23 /pmc/articles/PMC5036258/ /pubmed/27721978 http://dx.doi.org/10.1177/2050312116670927 Text en © The Author(s) 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Rodríguez-Rivera, Diana V Rodríguez-Navedo, Yerania Nieves-Plaza, Mariely Vilá, Luis M Patient-reported outcome measures in a population of medically indigent patients with systemic lupus erythematosus in Puerto Rico |
title | Patient-reported outcome measures in a population of medically indigent patients with systemic lupus erythematosus in Puerto Rico |
title_full | Patient-reported outcome measures in a population of medically indigent patients with systemic lupus erythematosus in Puerto Rico |
title_fullStr | Patient-reported outcome measures in a population of medically indigent patients with systemic lupus erythematosus in Puerto Rico |
title_full_unstemmed | Patient-reported outcome measures in a population of medically indigent patients with systemic lupus erythematosus in Puerto Rico |
title_short | Patient-reported outcome measures in a population of medically indigent patients with systemic lupus erythematosus in Puerto Rico |
title_sort | patient-reported outcome measures in a population of medically indigent patients with systemic lupus erythematosus in puerto rico |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036258/ https://www.ncbi.nlm.nih.gov/pubmed/27721978 http://dx.doi.org/10.1177/2050312116670927 |
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