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系统性红斑狼疮患者健康的社会决定因素中的种族和民族差异

Racial and Ethnic Disparities Within Social Determinants of Health Amongst Patients With Systemic Lupus Erythematosus.

作者信息

Addanki Sunaina, Patel Krina, Shah Kriya, Patel Lisa, Mauger McHenry, Laloo Anita, Rajput Vijay

机构信息

Medicine, Nova Southeastern University Dr. Kiran C. Patel College of Allopathic Medicine, Fort Lauderdale, USA.

Osteopathic Medicine, Nova Southeastern University Dr. Kiran C. Patel College of Osteopathic Medicine, Fort Lauderdale, USA.

出版信息

Cureus. 2024 Jul 13;16(7):e64453. doi: 10.7759/cureus.64453. eCollection 2024 Jul.

Abstract

Introduction This study aims to identify the influence of social determinants of health (SDoH) on patients with systemic lupus erythematosus (SLE), emphasizing racial and ethnic disparities in healthcare. Methods A cross-sectional study used the National Institute of Health's (NIH) All of Us Research Program (AoU). From 727,000 patients, SLE patients were categorized by race, ethnicity, and responses to the Social Determinants of Health survey from May 2018 until March 2023. Survey questions addressed transportation access, neighborhood safety, provider biases, and food insecurity. JMP Pro 16.0 and R 4.2.2 were used for statistical analysis. Results Significant racial disparities were evident amongst SLE patients for transportation access, neighborhood safety, food security, and respect from healthcare providers (p-value < 0.001). African Americans, Asians, and White participants showed different perceptions regarding neighborhood crime, healthcare provider courtesy, and feeling unheard by providers, with respective p-values of 0.001, 0.010, and 0.023. Hispanic participants perceived higher neighborhood crime rates, felt unsafe during nighttime walks, felt unheard by healthcare providers, and reported worrying about food security compared to non-Hispanic participants, with respective p-values of 0.003, 0.003, 0.009, and <0.001.  Discussion SLE is affected by access to care, treatments, stress, and lifestyle habits. Therefore, identifying SDoH for SLE patients is critical as it impacts disease progression, leading to delays in diagnosis, improper management, and worsening morbidity.  Conclusion Targeted social and community-based interventions may improve access to care, identify implicit biases among providers, and alleviate food insecurity.

摘要

引言 本研究旨在确定健康的社会决定因素(SDoH)对系统性红斑狼疮(SLE)患者的影响,强调医疗保健中的种族和民族差异。方法 一项横断面研究使用了美国国立卫生研究院(NIH)的“我们所有人”研究计划(AoU)。从727,000名患者中,根据种族、民族以及2018年5月至2023年3月期间对健康社会决定因素调查的回答对SLE患者进行分类。调查问题涉及交通便利性、社区安全性、医疗服务提供者的偏见和粮食不安全问题。使用JMP Pro 16.0和R 4.2.2进行统计分析。结果 在SLE患者中,交通便利性、社区安全性、食品安全以及来自医疗服务提供者的尊重方面存在明显的种族差异(p值<0.001)。非裔美国人、亚洲人和白人参与者对社区犯罪、医疗服务提供者的礼貌以及感觉未被提供者倾听的看法不同,各自的p值分别为0.001、0.010和0.023。与非西班牙裔参与者相比,西班牙裔参与者认为社区犯罪率更高,夜间行走时感到不安全,感觉未被医疗服务提供者倾听,并报告担心食品安全,各自的p值分别为0.003、0.003、0.009和<0.001。讨论 SLE受到医疗服务可及性、治疗、压力和生活方式习惯的影响。因此,确定SLE患者的SDoH至关重要,因为它会影响疾病进展,导致诊断延迟、管理不当和发病率恶化。结论 有针对性的社会和基于社区的干预措施可能会改善医疗服务可及性,识别医疗服务提供者中的隐性偏见,并缓解粮食不安全问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b732/11318078/ab21760e64dc/cureus-0016-00000064453-i01.jpg

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