Comorbidity Burden in Psoriasis Patients with Skin of Color.

Q3 Medicine
Hannah Peterson, Margaret Y Huang, Kathryn Lee, Paige Kingston, Danielle Yee, Edwin Korouri, Rosario Agüero, April W Armstrong
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引用次数: 0

Abstract

Background: Psoriasis is a chronic disease with increased risk of numerous comorbidities. Known differences exist regarding treatment outcomes for psoriasis patients with skin of color (SOC). However, factors contributing to these differences are relatively unknown.

Objectives: This study aims to compare the comorbidity burden in SOC psoriasis patients vs. White patients, as measured by the Charlson Comorbidity Index (CCI) score.

Methods: We utilized the National Ambulatory Medical Care Survey (NAMCS) to identify visits for adult psoriasis patients occurring in the years 2002-2016 and 2018. The CCI was used to objectively measure comorbidity burden. Patients were identified by race, and SOC was defined as any reported race besides White Only. A multiple linear regression was run to compare the CCI among adult psoriasis patients based on race and ethnicity, controlling for age, sex, insurance status, and geographic region.

Results: A total of 39,176,928 weighted visits were analyzed. Compared to White patients, patients with SOC did not have statistically significant differences in comorbidity burden, as measured by CCI score (p=0.073 for Black/African American Only vs. White Only, p=0.073 for American Indian/Alaska Native Only vs. White Only, p=0.435 for Asian Only vs. White Only, p=0.403 for Native Hawaiian/Pacific Islander Only vs. White Only, p=0.195 for Other vs. White Only).

Conclusion: Patients with SOC were not found to have differences in comorbidity burden compared to White patients. These results highlight that social factors such as socioeconomic status and access to healthcare may contribute more directly to psoriasis treatment outcomes than patient race.

有色皮肤银屑病患者的共病负担
银屑病是一种慢性疾病,并发多种合并症的风险增加。有色皮肤银屑病患者的治疗结果存在已知差异。造成这些差异的因素相对未知。本研究旨在通过Charlson共病指数(CCI)来比较SOC银屑病患者与白人患者的共病负担。我们利用国家门诊医疗调查(NAMCS)来确定2002-2016年和2018年发生的成年银屑病患者的就诊情况。CCI用于客观测量共病负担。患者按种族进行识别,SOC被定义为除白人以外的任何报告种族。基于种族和民族,在控制年龄、性别、保险状况和地理区域的情况下,运行多元线性回归来比较成年银屑病患者的CCI。共分析了39176928次加权访视。SOC患者与白人患者在共病负担方面没有统计学显著差异,通过CCI测量(仅限黑人/非裔美国人与仅限白人的P=.073,仅限美洲印第安人/阿拉斯加原住民与仅限白色的P=.773,仅限亚洲人与仅限怀特的P=.435,仅限夏威夷原住民/太平洋岛民与仅限白人的P=.403,其他人与仅限White的P=.195)。与白人患者相比,SOC患者的共病负担没有差异。这些结果强调,社会经济地位和获得医疗保健等社会因素可能比患者种族更直接地影响银屑病的治疗结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.30
自引率
0.00%
发文量
19
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