Literature DB >> 31585377

Measuring racial segregation in health system networks using the dissimilarity index.

Andrea M Austin1, Donald Q Carmichael2, Julie P W Bynum3, Jonathan S Skinner4.   

Abstract

Racial disparities in the end-of-life treatment of patients are a well observed fact of the U.S. healthcare system. Less is known about how the physicians treating patients at the end-of-life influence the care received. Social networks have been widely used to study interactions with the healthcare system using physician patient-sharing networks. In this paper, we propose an extension of the dissimilarity index (DI), classically used to study geographic racial segregation, to study differences in patient care patterns in the healthcare system. Using the proposed measure, we quantify the unevenness of referrals (sharing) by physicians in a given region by their patients' race and how this relates to the treatments they receive at the end-of-life in a cohort of Medicare fee-for-service patients with Alzheimer's disease and related dementias. We apply the measure nationwide to physician patient-sharing networks, and in a sub-study comparing four regions with similar racial distribution, Washington, DC, Greenville, NC, Columbus, GA, and Meridian, MS. We show that among regions with similar racial distribution, a large dissimilarity index in a region (Washington, DC DI = 0.86 vs. Meridian, MS DI = 0.55), which corresponds to more distinct referral networks for black and white patients by the same physician, is correlated with black patients with Alzheimer's disease and related dementias receiving more aggressive care at the end-of-life (including ICU and ventilator use), and less aggressive quality care (early hospice care).
Copyright © 2019 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Alzheimer's disease and related dementias; End-of-life care; Social networks

Year:  2019        PMID: 31585377      PMCID: PMC6810808          DOI: 10.1016/j.socscimed.2019.112570

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


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4.  Does hospice improve quality of care for persons dying from dementia?

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5.  Mapping physician networks with self-reported and administrative data.

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6.  Family evaluation of hospice care: Examining direct and indirect associations with overall satisfaction and caregiver confidence.

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Journal:  Palliat Support Care       Date:  2014-07-03

7.  A proactive approach to improve end-of-life care in a medical intensive care unit for patients with terminal dementia.

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8.  Palliative Care in Dementia.

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9.  Association of Increasing Use of Mechanical Ventilation Among Nursing Home Residents With Advanced Dementia and Intensive Care Unit Beds.

Authors:  Joan M Teno; Pedro Gozalo; Nita Khandelwal; J Randall Curtis; David Meltzer; Ruth Engelberg; Vincent Mor
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Review 10.  Geographical variation in dementia: systematic review with meta-analysis.

Authors:  Tom C Russ; G David Batty; Gena F Hearnshaw; Candida Fenton; John M Starr
Journal:  Int J Epidemiol       Date:  2012-07-13       Impact factor: 7.196

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Review 2.  A Decade of Studying Drivers of Disparities in End-of-Life Care for Black Americans: Using the NIMHD Framework for Health Disparities Research to Map the Path Ahead.

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