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社会人口学因素对皮肤型红斑狼疮患者的影响。

Influence of Socio-Demographic Factors in Patients With Cutaneous Lupus Erythematosus.

作者信息

Walker Amanda M, Lu Grace, Clifton Shari C, Ogunsanya Motolani E, Chong Benjamin F

机构信息

Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, United States.

Health Sciences Library and Information Management, The University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States.

出版信息

Front Med (Lausanne). 2022 Jul 11;9:916134. doi: 10.3389/fmed.2022.916134. eCollection 2022.

Abstract

Cutaneous lupus erythematosus (CLE) is a chronic autoimmune skin disease with potential for systemic involvement, disfigurement, and significant disease burden. The relationships of demographics and socioeconomic status with patients with CLE are emerging topics with important clinical implications. The primary objective of our study is to perform a literature review of studies that have investigated demographic and socioeconomic factors amongst patients with CLE and determine whether these factors influence diagnosis frequency, disease severity and outcomes or health related quality of life. We searched multiple databases to identify literature addressing CLE and concepts such as race, ethnicity, gender, income, education level and geographic location. Information regarding primary research objective was extracted from all full text articles, and a summary of findings was prepared. We found that race and ethnicity can influence CLE diagnosis frequency and disease outcomes. Chronic cutaneous lupus (CCLE) occurs more frequently in Black patients, often with higher overall disease damage. Differences between genders exist in CLE in terms of health-related quality of life, as female gender was a risk factor for worse quality of life in several studies. Lower income, low educational attainment, and lack of health insurance all contribute to poorer overall outcomes in CLE patients. This review will help inform physicians about populations at risk for potentially worse outcomes to guide treatment decisions for patients with CLE and provide important information to design interventions that address modifiable social determinants of health in this population.

摘要

皮肤红斑狼疮(CLE)是一种慢性自身免疫性皮肤病,有可能累及全身、导致容貌受损并带来重大疾病负担。人口统计学特征和社会经济状况与CLE患者之间的关系是具有重要临床意义的新兴话题。我们研究的主要目的是对调查CLE患者的人口统计学和社会经济因素的研究进行文献综述,并确定这些因素是否会影响诊断频率、疾病严重程度和预后或健康相关生活质量。我们检索了多个数据库,以识别涉及CLE以及种族、民族、性别、收入、教育水平和地理位置等概念的文献。从所有全文文章中提取有关主要研究目的的信息,并编写了研究结果摘要。我们发现种族和民族会影响CLE的诊断频率和疾病预后。慢性皮肤型红斑狼疮(CCLE)在黑人患者中更为常见,通常总体疾病损害程度更高。在CLE中,性别在健康相关生活质量方面存在差异,因为在多项研究中女性是生活质量较差的一个风险因素。低收入、低教育程度和缺乏医疗保险都会导致CLE患者的总体预后较差。这篇综述将有助于医生了解可能预后较差的人群,以指导CLE患者的治疗决策,并为设计针对该人群可改变的健康社会决定因素的干预措施提供重要信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5203/9311297/e9b9353d4476/fmed-09-916134-g0001.jpg

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