Health Systems, Quality of Care, and Outcomes in SLE

SLE 的卫生系统、护理质量和结果

• 批准号: 7926954
• 负责人: EDWARD H YELIN
• 金额: $ 51.37万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-09-05 至 2013-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7926954
• 关键词: Accounting; Adherence; Affect; Autoimmune Diseases; Biological Assay; Caring; Censuses; Characteristics; Communities; Cost Sharing; Data; Data Sources; Disadvantaged; Disease; Distal; Drug toxicity; Environment; Ethnic Origin; Fee-for-Service Plans; Funding; Genetic; Goals; Health; Health Insurance; Health Services Accessibility; Health system; Healthcare; Healthcare Systems; Insurance; Lupus; Managed Care; Marketing; Measures; Medical; Medicare/Medicaid; Monitor; Morbidity - disease rate; Nature; Neighborhoods; Outcome; Outcome Measure; Outcome Study; Participant; Persons; Physicians; Play; Preventive; Progress Reports; Provider; Publications; Quality Indicator; Quality of Care; Race; Research; Research Infrastructure; Research Personnel; Role; Socioeconomic Status; Source; Structure; Surveys; System; Systemic Lupus Erythematosus; Telephone Interviews; Testing; Time; Work; abstracting; adverse outcome; body system; care systems; cohort; cost; design; experience; health care service utilization; low socioeconomic status; meetings; payment; prospective; public health relevance; response; socioeconomics; success

DESCRIPTION (provided by applicant): Prior research has firmly established both that persons of lower socioeconomic status with systemic lupus erythematosus (SLE) experience poorer access to care, actual health care utilization, and outcomes due in part to the nature of their health insurance. The proposed project will assess the role that differences in quality of care play in explaining why persons with SLE from disadvantaged backgrounds have less access to care and poorer health outcomes. The project will draw upon the data from the Lupus Outcomes Study (LOS) to assess the effect of quality of care on SLE outcomes. The LOS currently includes 1,026 persons with SLE from a wide range of environments across the nation, most of whom have been followed for five years. The principal data in the LOS are data from medical charts and annual structured telephone interviews, supplemented by contextual data about the neighborhoods and medical markets of LOS participants from the Census and other publicly available data sources, matched to the survey responses by geocoding. The specific goals of the project are to: 1) describe the extent to which care for SLE adheres to measures of quality cross-sectionally and over time; 2) establish the relationship between quality of care and kind and extent of health care utilization; 3) document differences in quality of care by socioeconomic status, race/ethnicity, local communities, and the nature of medical markets; 4) establish the relationship among such features of the health care system as type of insurance (Medicaid, Medicare, or private), form of insurance (managed care or fee-for-service), and extent of cost sharing and quality of care, after taking personal SES and extent of health care infrastructure into account; and, 5) describe the role that differences in quality of care play in explaining outcome differences by SES, including traditional measures of outcome as well as costs. The project may help reduce disparities in access and outcomes by showing that adherence to standards for quality of care can redound to the disadvantaged with SLE either by assisting their physicians to provide such care or by spurring referral to high quality providers. PUBLIC HEALTH RELEVANCE: Systemic lupus erythematosus (SLE) is a severe autoimmune disease with a potential for significant morbidity due to impacts on many organ systems. Prior research has established that persons with SLE from lower socioeconomic backgrounds have poorer access to care and long-term outcomes. The proposed project will use a cohort of over 1,000 persons with SLE followed for up to ten years to determine the extent to which the poorer outcomes of those of low socioeconomic status is because they are less likely to receive health care that meets minimal criteria for quality. The project could help persons with SLE from low socioeconomic backgrounds by showing that referral to physicians providing high quality care will reduce disparities in outcomes.

描述（由申请人提供）：先前的研究已经确定，社会经济地位较低的系统性红斑狼疮（SLE）患者获得护理的机会、实际医疗保健利用率和结局较差，部分原因是其健康保险的性质。拟议的项目将评估护理质量差异在解释为什么来自弱势背景的SLE患者获得护理的机会较少和健康状况较差方面所发挥的作用。该项目将利用狼疮结局研究（LOS）的数据来评估护理质量对SLE结局的影响。LOS目前包括来自全国范围内各种环境的1，026名SLE患者，其中大多数人已随访5年。LOS中的主要数据来自医疗图表和年度结构化电话访谈，辅以来自人口普查和其他公开数据源的LOS参与者的社区和医疗市场的背景数据，通过地理编码与调查响应相匹配。该项目的具体目标是：1）描述SLE护理在跨部门和随时间推移遵守质量指标的程度; 2）建立护理质量与医疗保健利用的种类和程度之间的关系; 3）记录社会经济地位、种族/民族、当地社区和医疗市场性质的护理质量差异; 4）确定保险类型等卫生保健系统特征之间的关系（医疗补助，医疗保险或私人），保险形式（管理式护理或收费服务），以及在考虑到个人社会经济地位和卫生保健基础设施的范围后，费用分摊的程度和护理质量; 5）描述护理质量的差异在解释SES结果差异中所起的作用，包括传统的结果和成本测量。该项目可能有助于减少获得和结果的差异，表明坚持护理质量标准可以通过帮助他们的医生提供此类护理或促进转诊给高质量的提供者来帮助SLE患者。公共卫生相关性：系统性红斑狼疮（SLE）是一种严重的自身免疫性疾病，由于对许多器官系统的影响，具有显著发病率的潜力。先前的研究已经确定，社会经济背景较低的SLE患者获得护理和长期结局的机会较差。拟议的项目将使用超过1，000名SLE患者的队列，随访长达10年，以确定社会经济地位低的患者的不良结局在多大程度上是因为他们不太可能获得符合最低质量标准的医疗保健。该项目可以帮助来自低社会经济背景的SLE患者，通过向提供高质量护理的医生转诊将减少结果的差异。