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在初级保健中抑郁症治疗的面板数据中检测种族/族裔方面的统计歧视。

Testing for statistical discrimination by race/ethnicity in panel data for depression treatment in primary care.

作者信息

McGuire Thomas G, Ayanian John Z, Ford Daniel E, Henke Rachel E M, Rost Kathryn M, Zaslavsky Alan M

机构信息

Department of Health Care Policy, Harvard Medical School, 180 Longwood Avenue, Boston, MA 02115, USA.

出版信息

Health Serv Res. 2008 Apr;43(2):531-51. doi: 10.1111/j.1475-6773.2007.00770.x.

Abstract

OBJECTIVE

To test for discrimination by race/ethnicity arising from clinical uncertainty in treatment for depression, also known as "statistical discrimination."

DATA SOURCES

We used survey data from 1,321 African-American, Hispanic, and white adults identified with depression in primary care. Surveys were administered every six months for two years in the Quality Improvement for Depression (QID) studies.

STUDY DESIGN

To examine whether and how change in depression severity affects change in treatment intensity by race/ethnicity, we used multivariate cross-sectional and change models that difference out unobserved time-invariant patient characteristics potentially correlated with race/ethnicity.

DATA COLLECTION/EXTRACTION METHODS: Treatment intensity was operationalized as expenditures on drugs, primary care, and specialty services, weighted by national prices from the Medical Expenditure Panel Survey. Patient race/ethnicity was collected at baseline by self-report.

PRINCIPAL FINDINGS

Change in depression severity is less associated with change in treatment intensity in minority patients than in whites, consistent with the hypothesis of statistical discrimination. The differential effect by racial/ethnic group was accounted for by use of mental health specialists.

CONCLUSIONS

Enhanced physician-patient communication and use of standardized depression instruments may reduce statistical discrimination arising from clinical uncertainty and be useful in reducing racial/ethnic inequities in depression treatment.

摘要

目的

检验在抑郁症治疗中因临床不确定性而产生的种族/族裔歧视,即“统计歧视”。

数据来源

我们使用了来自1321名在初级保健中被确诊为抑郁症的非裔美国人、西班牙裔和白人成年人的调查数据。在抑郁症质量改进(QID)研究中,每六个月进行一次为期两年的调查。

研究设计

为了检验抑郁症严重程度的变化是否以及如何按种族/族裔影响治疗强度的变化,我们使用了多元横断面模型和变化模型,这些模型排除了可能与种族/族裔相关的未观察到的时间不变患者特征。

数据收集/提取方法:治疗强度通过药物、初级保健和专科服务的支出进行衡量,并根据医疗支出小组调查的全国价格进行加权。患者的种族/族裔在基线时通过自我报告收集。

主要发现

与白人相比,少数族裔患者抑郁症严重程度的变化与治疗强度变化的相关性较小,这与统计歧视的假设一致。种族/族裔群体的差异效应是由心理健康专家的使用造成的。

结论

加强医患沟通和使用标准化抑郁症评估工具可能会减少因临床不确定性而产生的统计歧视,并有助于减少抑郁症治疗中的种族/族裔不平等。

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