Dissertations, Theses, and Capstone Projects
Date of Degree
6-2020
Document Type
Dissertation
Degree Name
Ph.D.
Program
Anthropology
Advisor
Dána-Ain Davis
Committee Members
Murphy Halliburton
Setha Low
Paul Brodwin
Subject Categories
Community Health and Preventive Medicine | Health Policy | Inequality and Stratification | Medicine and Health | Science and Technology Studies | Social and Cultural Anthropology | Work, Economy and Organizations
Keywords
medical anthropology, care work, health policy, United States, homelessness, elder care
Abstract
This dissertation examines the delegation of responsibility for providing health care to particular categories of marginalized populations in the United States in the absence of a uniform and universal health care system. It explores how the U.S. federal government governs patient populations at a distance by mandating that healthcare providers collect, produce, and report on patient data. Drawing from eighteen months of ethnographic research in Massachusetts clinics for the homeless and the frail elderly between 2014-2015, I argue that when marginalized patients are unable to satisfy the neoliberal ideal of self-governance to maintain their health in cost-effective ways, providers are activated to bring them into compliance. Through the lens of political economic, science and technology studies, and critical medical anthropologies, I identified how reimbursement models and government funding requirements redesigned under the 2010 Affordable Care Act obligate health care providers to reframe the care they provide. Providers cultivate what I term the “logic of costs,” a budgetary lens for making care decisions that frames management of costs as essential to care. Data creation and reporting practices require providers to adopt a logic of costs, as such data informs whether their clinics will be deemed effective and the clinics’ funding reauthorized. I trace the incongruities between actual care practices and the metrics that clinics end up recording and submitting to represent their work and their patients. I argue that this work is made possible through the creation of “shadow standards,” unofficial, undocumented, and yet routinized healthcare practices that make the creation and reporting of health data possible, even when providers do not have the resources to comply.
Recommended Citation
Whitten, Margarite J., "Shadow Standards and the Logic of Costs: Care, Stewardship, and Data in U.S. Community Health" (2020). CUNY Academic Works.
https://academicworks.cuny.edu/gc_etds/3718
Included in
Community Health and Preventive Medicine Commons, Health Policy Commons, Inequality and Stratification Commons, Medicine and Health Commons, Science and Technology Studies Commons, Social and Cultural Anthropology Commons, Work, Economy and Organizations Commons