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1

Barr, Victoria Jane. "Planning for healthy and equitable communities in British Columbia : a critical analysis of the implementation of an equity lens in Healthy Built Environments initiatives." Thesis, University of British Columbia, 2016. http://hdl.handle.net/2429/59441.

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British Columbia’s communities, as settings in which we work, learn, and play, have a significant role in shaping our health and well-being. Recently, the provincial government has encouraged health authorities to join with local government planners to create local Healthy Built Environment (HBE) teams, so that they can work together for healthier communities. Within our communities, there are significant differences in health status that are unjust or unfair, and are rooted in underlying socio-political processes. International research suggests that we must reduce those inequities if we are to improve health for all. To help address health inequities, researchers have suggested that public health practitioners use an ‘equity lens’ in their day-to-day work. Yet implementing such a lens is challenging. This case study explored the implementation of an equity lens in HBE work in BC. The project examined the work of intersectoral HBE teams at the provincial and local levels, through an in-depth examination of HBE projects within three different BC communities. Data was collected through interviews, participant observation, and the collection of key documents, maps, and photographs. The main research question was: How is an ‘equity lens’ being implemented in association with Healthy Built Environments work in British Columbia? Influenced by the shifting strategic direction of the provincial government, HBE teams reported only limited progress in actively considering equity as integral to their work. The key elements of the implementation of an equity lens included targeting specific, ‘vulnerable’ populations and using community health data to monitor key outcomes. In general, however, the political will to more fully consider equity as integral to HBE work was just not present at either local or provincial levels. There was hope, however, in the form of champions, who worked to re-frame equity issues in more palatable ways, and the desire to explore new tools to better understand equity issues at the local level. There is also evidence of a growing desire within HBE teams to build meaningful, authentic, partnerships, consistent with a broad Healthy Communities approach. The development of those partnerships will be key to collectively building more just, inclusive, and healthier communities.
Applied Science, Faculty of
Community and Regional Planning (SCARP), School of
Graduate
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Garton, Kelly. "Assessing equity in access to healthy diets in Ecuador following the addition of food sovereignty to the constitution." Thesis, University of British Columbia, 2014. http://hdl.handle.net/2429/46388.

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Background: Ecuador shows high and increasing rates of diet-related non-communicable diseases, attributed in part to a nutrition transition toward more animal-based and processed foods. In 2008, Ecuador introduced the right to food sovereignty to its constitution in an effort to improve diets and protect local agricultural production. However, this has not yet translated to evidence of improved nutrition at the community level. Objective: This thesis examines whether the promotion of food sovereignty has contributed to improving access to healthy diets for marginalized populations in Ecuador; if so, it asks how and to what extent, and if not, it explores the barriers to achieving change and opportunities for improvement. This project thus seeks to provide suggestions of entry points for policies and programs to improve access to and consumption of healthy foods. Methods: Complementary qualitative methods were used to examine geographic access, food prices, nutritional knowledge and dietary preferences, and priorities for food policy improvement in three low-income neighbourhoods in the city of Machala, El Oro. Results: Access to affordable healthy foods is still an issue as perceived by the study neighbourhoods. Poor nutritional knowledge, high relative cost of fruits and vegetables, and inequitable geographic access to affordable healthy foods were the main barriers to healthy eating. Price was the primary factor influencing food purchasing and consumption behaviours. Knowledge of the concept of food sovereignty and its inclusion in the constitution was nonexistent, as was the awareness of any new policies or programs implemented to improve access to healthy foods since 2008. Conclusions: As there are no food sovereignty policies in place so far that address price, the affordability of healthy foods could be addressed either by improving the linkages between producers and consumers to reduce intermediaries, or by adopting fiscal policies that subsidize healthy foods and tax unhealthy foods to help make healthy options more affordable and viable. These policy initiatives fall within the potential scope of a commitment to food sovereignty, but greater focus is needed as the government advances in the development of specific policies and programs in order to have an impact on population health.
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Prorock-Ernest, Amy J. "Walking in beauty: Responsive and responsible health and healing among Virginia American Indian people." VCU Scholars Compass, 2017. http://scholarscompass.vcu.edu/etd/4775.

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Little is systematically known about the collective health and well-being of Virginia American Indian people. This study sought to explore the meaning of health and healing among Virginia American Indian people in the context of a reservation-based, non-federally funded health clinic. Using an emergent approach to qualitative research grounded in a constructivist inquiry paradigm and guided by Indigenous research principles, a total of 24 in-depth, semi-structured interviews were conducted with 17 American Indian service-users of the Clinic. Through an inductive thematic analysis of participant stories, a framework for understanding responsive and responsible health and healing was derived. The framework includes seven dimensions: spirituality, physical processes, mental and emotional processes, social relationships, access to resources, contextual factors, and the interconnection among the dimensions. Personal and collective identity was a significant element woven through the dimensions. From the stories told by participants, health seems to be a continuum and healing seems to be a cycle. With constant motion in each of the dimensions, health has to do with sustained engagement in healing processes that continually seek to bring about functional balance in one’s whole health system. Ill health has to do with when a change in any one of the dimensions overtakes one’s ability to bring about a functional balance in the whole health system. The framework is context-dependent, true for the people who participated in the study at the time of the study.
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Richards, Anika Tahirah. "Health Equity Education, Awareness, and Advocacy through the Virginia Department of Health Health Equity Campaign." Diss., Virginia Tech, 2011. http://hdl.handle.net/10919/77312.

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This study showed that health equity must be achieved through education, awareness, and advocacy. A structured program must be put in place to provide accountability towards achieving health equity within organizations, communities, cites, and states. In Virginia, the Health Equity Campaign was a program put in place to provide such accountability to the citizens of Virginia. This study attempted to evaluate the Health Equity Campaign implemented by the Virginia Department of Health Office of Minority Health and Public Health Policy Division of Health Equity in order to get all Virginians to become advocates for health equity in their organizations, communities, neighborhoods. Organizational/group leaders were interviewed in addition to surveying various staff members. This study provides a detailed description of the strength of the Health Equity Campaign's ability to promote education and awareness about health equity and why many participants found it difficult to transition from motivation to advocacy.
Ph. D.
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Napierala, Christoph. "Finance equity in comparison of health systems : discussion of the current overall ranking of health systems by clustering these in their way of financing and equity /." Bühl, 2008. http://www.public-health-edu.ch/new/Abstracts/NC_15.12.08.pdf.

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6

D'Ambruoso, Lucia. "Global health post-2015 : the case for universal health equity." Umeå universitet, Epidemiologi och global hälsa, 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-71419.

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Set in 2000, with a completion date of 2015, the deadline for the Millennium Development Goals is approaching, at which time a new global development infrastructure will become operational. Unsurprisingly, the discussions on goals, topics, priorities and monitoring and evaluation are gaining momentum. But this is a critical juncture. Over a decade of development programming offers a unique opportunity to reflect on its structure, function and purpose in a contemporary global context. This article examines the topic from an analytical health perspective and identifies universal health equity as an operational and analytical priority to encourage attention to the root causes of unnecessary and unfair illness and disease from the perspectives of those for whom the issues have most direct relevance.
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Kimbrough, Jennifer Bennett. "Towards equity in health envisioning authentic health education in schools /." Greensboro, N.C. : University of North Carolina at Greensboro, 2007. http://libres.uncg.edu/edocs/etd/1393/umi-uncg-1393.pdf.

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Thesis (Ph.D.)--University of North Carolina at Greensboro, 2007.
Title from PDF t.p. (viewed Oct. 22, 2007). Directed by H. Svi Shapiro; submitted to the School of Education. Includes bibliographical references (p. 165-169).
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Thorson, Anna. "Equity and equality : case detection of tuberculosis among women and men in Vietnam /." Stockholm, 2003. http://diss.kib.ki.se/2003/91-628-5689-8/.

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9

Akazili, James. "Equity in Health Care Financing in Ghana." Doctoral thesis, University of Cape Town, 2010. http://hdl.handle.net/11427/9390.

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Financial risk protection against the cost of unforeseen ill health has become a global concern as expressed in the 2005 World Health Assembly resolution (WHA58.33), which urges its member states to "plan the transition to universal coverage of their citizens". The study (the first of kind in Ghana) measured the relative progressivity of health care financing mechanisms, the catastrophic and impoverishment effect of direct health care payments, as well as evaluating the factors affecting enrolment in the national health insurance scheme (NHIS), which is the intended means for achieving equitable health financing and universal coverage in Ghana. To achieve the purpose of the study, secondary data from the Ghana Living Standard Survey (GLSS) 2005/2006 were used. This was triangulated with data from the Ministry of Finance and other ministries and departments, and further complemented with primary household data collected in six districts. In addition 44 focus group discussions with different groups of people and communities were conducted. In-depth interviews were also conducted with six managers of District NHI schemes as well as the NHIS headquarters. The study found that generally Ghana's health care financing system is progressive. The progressivity of health financing is driven largely by the overall progressivity of taxes which account for over 50% of health care funding. The national health insurance levy is mildly progressive as indicated by a Kakwani index of 0.045. However, informal sector NHI contributions were found to be regressive. Out-of-pocket payments, which account for 45% of funding, are associated with significant catastrophic and impoverishment effects on households. The results also indicate that high premiums, ineffective exemptions, fragmented funding pools and perceived poor quality of care affect the expansion of the NHIS. For Ghana to attain adequate financial protection and ultimately achieve universal coverage, it needs to extend cover to the informal sector, possibly through funding their contributions entirely from tax, and address other issues affecting the expansion of the NHI. Furthermore, the funding pool for health care needs to grow and this can be achieved by improving the efficiency of tax collection and increasing the budgetary allocation to the health sector.
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Mangalore, Roshni. "Equity in mental health care in Britain." Thesis, London School of Economics and Political Science (University of London), 2007. http://etheses.lse.ac.uk/2702/.

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This thesis explores equity issues in the mental health field in Britain by initially developing a conceptual structure to define equity in mental health and then analysing data from three national psychiatric morbidity surveys to measure inequalities and inequities in both mental health and in the use of services. Standard methods are used for measuring income-related and social class-related inequalities with reference to many indicators of mental health which represent 'normative' or 'felt' needs for services. Inequity in the use of mental health services is also examined by relating use of services to needs. Analyses of income-related inequalities and equity are carried out with reference to the general population using data from the Psychiatric Morbidity Survey 2000 and with reference to the minority ethnic groups in Britain using data from the survey of Ethnic Minority Psychiatric Illness Rates in the Community 2000. Changes in social class-related inequalities and equity for the general population between 1993 and 2000 are examined using data from the Psychiatric Morbidity Surveys for those two years, in order to see if the policy and practice changes that took place since the beginning of the 1990s in the health and social care sectors had exerted any impact on equity in mental health. The three mental health surveys being cross-sectional do not permit the study of causal pathways between income and mental health. Therefore, in order to understand the links between living standards, health and health care utilisation patterns further, data from a longitudinal study, the British Household Panel Survey on general health are examined using robust theoretical and empirical models. The assumption is that many of the factors associated with general health are also associated with mental health and much of the model that links income, health and health care utilisation behaviour is likely to be relevant for mental health as well.
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Whitehead, Margaret. "Bridging the gap : working towards equity in health and health care /." Sundbyberg, 1997. http://diss.kib.ki.se/1997/19970926whit.

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Vitale, Caitlin McManus. "TheRole of the Social Determinants of Health in Rural Health Equity:." Thesis, Boston College, 2020. http://hdl.handle.net/2345/bc-ir:109012.

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Thesis advisor: Karen S. Lyons
Background: Health equity is a complex phenomenon that embodies both the social determinants of health (structural and intermediary) and external factors, such as the health system. As a well-researched phenomenon, it is known that certain populations are more vulnerable than others to experiencing health inequities; specifically, those of low socioeconomic status, racial/ethnic minorities, older adults, and rural residents. However, gaps in knowledge exist in understanding why certain populations remain at higher risk of experiencing health inequities during a time of improved health insurance coverage and technological advances in health care. The purpose of this manuscript dissertation was to identify and address influential factors that serve as road blocks in achieving health equity, guided by the World Health Organization’s Conceptual Framework on the Social Determinants of Health. Methods: First, an integrative review was performed in order to determine current scope of practice restrictions and patient outcomes across the continuum of licensure for advanced practice registered nurses (APRNs), especially certified registered nurse anesthetists (CRNAs). Next, a secondary analysis of large national data set was done to identify the social determinants and risk factors for poor health effect among a national sample at high risk for poor health. And finally, a survey methodology study was completed to determine the roles that satisfaction with health care and physical function have on the perceived health status for rural, older adults in Massachusetts, and to explore the willingness of rural, older adults to use non-physicians for their health care needs. Results: The integrative review revealed the inconsistent use of APRNs at their full licensure. Nationally, APRNs had better geographic distribution in rural areas compared to physicians; yet many states continue to restrict APRN SOP. Second, across the U.S., older adults at the highest risk for poor health live in rural areas, are of lower socioeconomic status, and identify as racial/ethnic minorities. Third, both satisfaction with health care and the physical function of a small sample of older rural adults were significantly associated with physical health. And finally this body of work found that among a small sample of older rural adults, most were willing to use APRNs to meet their health care needs. Conclusions: With the ultimate goal of health equity it is necessary to empower those experiencing health inequities to be both aware of the problems as well as informed enough to push for change. Understanding why the experience of health differs among some individuals more than others helps to target change. The fusion of findings from this body of research has revealed a gap in health care that can be easily filled with simple policy change. APRNs at full SOP can generate means for high quality preventative, cost-saving care, and can better access the most vulnerable populations at a lower cost than physician counterparts
Thesis (PhD) — Boston College, 2020
Submitted to: Boston College. Connell School of Nursing
Discipline: Nursing
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Szende, Agota. "Equity in health and health care in Hungary : health status, finance, and delivery of health care." Thesis, University of York, 2003. http://etheses.whiterose.ac.uk/14056/.

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Bogg, Lennart. "Health care financing in China : equity in transition /." Stockholm, 2002. http://diss.kib.ki.se/2002/91-7349-270-1/.

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McAlister, Seraphina. "Working Within a Public Health Frame: Toward Health Equity Through Cultural Safety." Thèse, Université d'Ottawa / University of Ottawa, 2013. http://hdl.handle.net/10393/24282.

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This study explored how public health nurses (PHNs) work to address health inequities. Cultural safety was used as a theoretical lens. Methods for interpretive description were relied on for data collection and analysis. Data sources included interviews with 14 staff from an urban public health unit and document review of three policies. Two themes emerged: building relationships and working within a frame. Building relationships involved: delivering the message, taking the time, being present, the right nurse and learning from communities. The public health frame influenced the capacity of PHNs to address health inequities through: culture and stereotypes, public health standards, setting priorities, inclusion of priority populations, responding to change and (re)action through reorganization. Discursive formations of priority populations, and partnership and collaboration, were revealed. Findings highlighted downstream public health approaches to addressing health inequities. Importantly, embedding cultural safety as a framework for public health practice can guide upstream action.
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Al-Yaemni, Asmaa Abdullah. "Does universal health care system in Saudi Arabia achieve equity in health and health care?" Thesis, University of Liverpool, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.526777.

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Sims, Anita. "Deprivation and health : social inequality and equity of access to health care services." Thesis, Sheffield Hallam University, 2003. http://shura.shu.ac.uk/20366/.

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The major aims of this research were to investigate and analyse the connections between social deprivation, health inequality and equity of access to health care. Local and national case studies were used to illustrate inequity of access and to explore and assess policies and procedures that attempted to address such inequities at a local level. The available data sources, their limitations and scope were reviewed and described. In depth examinations and critical reviews were made of concepts and tools to measure deprivation and equity. A case study using the (then) new 1991 Census variable, limiting long term illness in a policy context together is described together with validation via a local survey in Shirebrook in North Derbyshire. The use of techniques for operationalising equity as extended to GP allocations is examined in some action research undertaken in North Derbyshire. Social class variations and their influence on place of death amongst cancer patients are examined, quantifying and describing apparent inequity in patterns of access to place of final care for cancer patients in both a local and national context. This work described, analysed and interpreted the connection between social class and access to hospice, home, and hospital deaths.
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Oh, Youngho. "Demand for health services in Korea: Equity in the delivery of health services /." The Ohio State University, 1997. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487945015618772.

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Nyanjom, Eric Othieno. "Equity in health care financing and delivery in Kenya." Thesis, University of Sussex, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.424190.

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Yu, Chai Ping. "Equity in health care financing : the case of Malaysia." Thesis, University of Nottingham, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.479345.

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Jordan, Susan Ann. "Exploring Healthcare Transitions and Health Equity: An Integrative Review." ScholarWorks, 2019. https://scholarworks.waldenu.edu/dissertations/7305.

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Compared to their typically developing peers, adolescents, and emerging adults with special healthcare needs (AEA-SHCN) disproportionately experience healthcare transition (HCT) disparities and poor access to adult care. Theoretical models that describe how access gaps develop and strategies to address unmet HCT needs are not well understood. While HCT researchers describe both system and patient healthcare barriers, a comprehensive approach that discovers how these factors interact and interfere remains misunderstood. An integrative review (IR) was conducted to understand the multiplicity of these factors. An intersectional theory (IT) provided further clarity on how key findings influence patient HCT experiences. Several themes were found to intersect and thus increase the HCT complexity, particularly for patients with social disadvantages. Communication gaps, mismatched goals/expectations, and poorly defined roles were common themes. Poor health equity, disparities in access, and inadequate HCT support intersected with poor patient HCT experiences, while youth with stigma-related diseases were most at-risk for poor provider-relationships. The thematic synthesis provided granularity to these experiences with characterizations as fear, loss, and uncertainty with access change. Social change implications underscore the need to reframe poor patient HCT experiences as potential opportunities for health policy advocates and clinicians to address unmet HCT needs.
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Rho, Yeunsook. "Socioeconomic equity in health care utilization in South Korea." Thesis, University of York, 2013. http://etheses.whiterose.ac.uk/4817/.

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Study Purpose : This study aims to investigate socioeconomic status (SES) related inequity in health care utilisation in Korea, comparing differences between income, wealth and education dimensions of socioeconomic status and inequity changes between 2005 and 2008, before and after implementation of the health insurance benefit expansion policy in 2006. Research Method: Korean Welfare Panel Study (KOWEPS) data on 14,463 individuals in 2005 and 11,909 in 2008 are used to measure income, wealth and education-related inequity for multiple indicators of health care utilisation with varying depth of coverage in the Korean National Health Insurance program, after regression-based indirect standardization for health care need variables (including age, gender, self-assessed health and chronic conditions). Concentration indices are used for statistical tests and extreme group gaps are used to interpret the magnitude of inequity. Results: After allowing for need, considerable pro-advantaged inequality is found for services with relatively shallow coverage, in particular, as medical checkups, total health care expenditure and tertiary hospital use. Conversely, with relatively deep coverage (outpatient visit, inpatient admissions and inpatient days) are utilized equally or favouring the less advantaged across the three socioeconomic dimensions. There was no change in pro-rich or pro-wealth inequality between 2005 and 2008 for any indicator, apart from a small reduction in pro-wealthy inequality for tertiary hospital visits in probability, but on several indicators there was an apparent reduction in pro-educated inequality. Conclusions: There is substantial socioeconomic inequity in health care in Korea for services not fully covered by the National Health Insurance program, with similar patterns of inequity for pro-rich, pro-wealthy and pro-educated dimensions of socioeconomic status. There was no reduction in pro-rich or pro-wealthy inequity in health care between 2005 an 2008. There were signs of a reduction in pro-educated inequality but this may just be a statistical artefact of sample attrition due to confounding between birth cohort and education group. Korea continues to have higher out-of-pocket expenditure and larger socioeconomic inequalities in health care than most other high income OECD countries, despite the health benefit expansion policy of 2006.
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Shakarishvili, George. "Analysing the equity of post-Soviet health care systems : evaluation of 1990s health reforms." Thesis, University of Oxford, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.424683.

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Bernfort, Lars. "Setting priorities in health care - studies on equity and efficiency /." Linköping : Univ, 2001. http://www.bibl.liu.se/liupubl/disp/disp2001/arts244s.pdf.

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Kersten, Ellen Elisabeth. "Spatial Triage| Data, Methods, and Opportunities to Advance Health Equity." Thesis, University of California, Berkeley, 2015. http://pqdtopen.proquest.com/#viewpdf?dispub=3686356.

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This dissertation examines whether spatial measures of health determinants and health outcomes are being used appropriately and effectively to improve the health of marginalized populations in the United States. I concentrate on three spatial measures that have received significant policy and regulatory attention in California and nationally: access to healthful foods, climate change, and housing quality. I find that measures of these health determinants have both significant limitations and unrealized potential for addressing health disparities and promoting health equity.

I define spatial triage as a process of using spatial data to screen or select place-based communities for targeted investments, policy action, and/or regulatory attention. Chapter 1 describes the historical context of spatial triage and how it relates to ongoing health equity research and policy. In Chapter 2, I evaluate spatial measures of community nutrition environments by comparing data from in-person store surveys against data from a commercial database. I find that stores in neighborhoods with higher population density or higher percentage of people of color have lower availability of healthful foods and that inaccuracies in commercial databases may produce biased measures of healthful food availability.

Chapter 3 focuses on spatial measures of climate change vulnerability. I find that currently used spatial measures of "disadvantaged communities" ignore many important factors, such as community assets, region-specific risks, and occupation-based hazards that contribute to place-based vulnerability. I draw from examples of successful actions by community-based environmental justice organizations and reframe "disadvantaged" communities as sites of solutions where innovative programs are being used to simultaneously address climate mitigation, adaptation, and equity goals.

In Chapter 4, I combine electronic health records, public housing locations, and census data to evaluate patterns of healthcare utilization and health outcomes for low-income children in San Francisco. I find that children who live in redeveloped public housing are less likely to have more than one acute care hospital visit within a year than children who live in older, traditional public housing. These results demonstrate how integrating patient-level data across hospitals and with data from other sectors can identify new types of place-based health disparities. Chapter 5 details recommendations for analytic, participatory, and cross-sector approaches to guide the development and implementation of more effective health equity research and policy.

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Green, Colin. "Justice, fairness and equity in health care : exploring the social value of health care interventions." Thesis, University of Southampton, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.484850.

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This thesis is motivated by the need in many health care systems, but especially in the UK NHS, to make difficult choices over the use of limited resources. The starting point forthe thesis is that when making difficult choices over the provision of health care, the overall value of health care interventions to society is a function not only of the total benefits available from health care, but also the distribution of health care resources across different groups in society. The thesis investigates this proposition that 'distribution matters' and presents research to consider the social value of health care interventions. The research in the thesis is undertaken within the analytical framework of health economics, and in the context of health policy decisions over the funding of health care interventions in the UK NHS. The health technology appraisal process is used as an example of an allocation problem, and the thesis uses the UK National Institute for Health and Clinical Excellence (NICE) as an example of the health technology appraisal process. A variety of methods are usedj including an assessment of general theories of justice, a systematic review of the literature on empirical assessment of distributive preferences, an empirical study to investigate issues around the specific social value related to the severity of health condition, a discrete choice experiment (DCE) to explore a range of key social values and the relative weights placed on these social values. The research is drawn together in a policy-relevant analysis of social preferences and NHS decision-making. The thesis makes a contribution to the health economics literature and to the health policy literature. It relates general theories of justice to the process of health technology appraisal. It draws together a broad and complex literature, and characterises the literature according to the general quality of the methods used. The thesis contributes to the empirical evidence base on severity of health as an important social value. It develops a hypothesis that the empirical evidence against the importance of severity of health may be a proxy preference for giving priority to a worst off group of patients in health care priority setting; providing empirical evidence to support this hypothesis. The DCE, in a sample of the general public, finds support for using the social values around level of health improvement, value for money, severity of health, 'and the availability of other treatments, to offer an insight to the societal value of health care interventions. The level of health improvement and value for money had the greatest impact, in the discrete choice analysis, with severity of health condition also shown to have 'an important role in distributive preferences. The research contributes to the empirical evidence on the relative importance of social values in the context of difficult priority setting decisions, and it contributes to the literature on the use of the DCE framework to elicit social preferences. The thesis, extends the current evidence base by using the results from the DCE to derive a measure cif 'strength of preference' across health care interventions described using the experimental design used. The thesis demonstrates how such data may be used in a policy-relevant manner. The research in the thesis provides a greater understanding over what may be meant by equity in the allocation of health care resources, in the framework of health technology. appraisal, through consideration of equity as a balance between competing social values, amidst consideration of opportunity costs.
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Noor, Abdisalan Mohamed. "Developing spatial models of health service access and utilisation to define health equity in Kenya." Thesis, Open University, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.417576.

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Cleary, Susan. "Equity and efficiency in health and health care for HIV-positive adults in South Africa." Doctoral thesis, University of Cape Town, 2007. http://hdl.handle.net/11427/9325.

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Includes bibliographical references (leaves 238-258).
This dissertation presents a framework for assessing equity and efficiency in health and health care for HIV-positive adults in South Africa, which is tested in the extensive analysis of empirical data on the costs and consequences of alternative HIV-treatment strategies in the public health care system. The framework is built through asking three key questions. The first question -- what is the good (value or benefit) of health care -- considers what ought to be in the evaluative space of distributive justice in relation to this dissertation and in health economics more generally. The second question considers the factors that might constitute claims on this good, including personal responsibility, need, the social context as well as the impact of allocations of the good on the health of society and the social fabric. The final question -- how should the good be distributed -- examines alternative social choice rules for distributing the good and develops an approach grounded in procedural justice that legitimizes the choice of one rule over another. To apply this framework, patient and population-level costs and consequences associated with alternative HIV-treatment interventions are analysed in Markov models. These are extensively validated and uncertainty is assessed through probabilistic and multi-way sensitivity analyses. Results of these analyses are key inputs into mathematical programming algorithms that allow an assessment of the implications of choosing one social choice rule over another in terms of gains in the good and the proportion of need that can be met through one or more treatment strategy across a range of budgets. In discussing and concluding, these empirical results are reintegrated into the conceptual framework where the notion of claims on the good and a decision-making approach grounded in procedural justice is further developed. It is argued that the proper implementation of this framework will result in allocations of the good that are fair even if this is at a level of less than universal access to the most effective treatment strategy.
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Dingle, A. "Equity of access to reproductive and maternal health services in Cambodia : equity trends, poverty targeting and demand-side financing." Thesis, London School of Hygiene and Tropical Medicine (University of London), 2016. http://researchonline.lshtm.ac.uk/2572537/.

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Health inequities are a serious public health concern. Achievements in health equity are particularly challenging to attain in reproductive and maternal health in developing countries. Research exploring this issue is of great relevance, given the extent of such disparities, and as pressure builds to include universal health coverage in the post-­‐ 2015 development goals. This thesis examines equity in reproductive and maternal health services in Cambodia, and two health financing interventions aiming to improve health equity, Vouchers for Reproductive Health Services (VRHS) and Health Equity Funds (HEFs). Study objective 1 was to estimate equity in reproductive and maternal health services in Cambodia over the last decade. Analysis was conducted with Demographic and Health Survey data for six health services between 2000 and 2010, revealing that dramatic improvements have been made in reproductive and maternal health equity since 2000, however inequity remains in use of facility-­‐based deliveries and skilled birth attendance. Objective 2 was to qualitatively explore Cambodia’s poverty identification programme, the ID Poor. Semi-­‐structured interviews were conducted with women, service providers and programme implementers. Extensive targeting errors within the programme were found, with implications for the targeting effectiveness of VRHS and HEFs. Objective 3 was to qualitatively explore low uptake of vouchers in the VRHS project, also using interview data. It was found that vouchers were positively received by beneficiaries and had the potential to influence health-­‐seeking behaviour. However several factors were found to improve future voucher performance. Objective 4 assessed the impact of HEFs on financial protection, service utilisation and health outcomes, using difference-­‐in-­‐differences analysis. Evidence of a financially protective effect of HEFs was found; no effect was found for service use or health outcomes. The thesis contributes to knowledge gaps in the health equity, poverty targeting and demand-­‐side financing literature, and provides practical policy implications based on empirical findings.
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Domapielle, Maximillian K. "Extending health services to rural residents in Jirapa District : analyses of national health insurance enrolment and access to health care services." Thesis, University of Bradford, 2015. http://hdl.handle.net/10454/14803.

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This thesis sheds light on differences in health insurance enrolment determinants and uptake barriers between urban and rural areas in the Jirapa district of Ghana. The National Health Insurance Scheme in Ghana has made significant progress in terms of enrolment, which has had a commensurate increase in utilization of health care services. However, there are challenges that pose a threat to the scheme’s transition to universal coverage; enrolment in the scheme has not progressed according to plan, and there are many barriers known to impede uptake of health care. Interestingly, these barriers vary in relation to locality, and rural residents appear to carry a disproportionate portion of the burden. A mixed method approach was employed to collect and analyse the data. On the basis of the primary qualitative and quantitative results, the thesis argues that the costs of enrolling and accessing health care is disproportionately higher for rural residents than it is their urban counterparts. It also highlights that the distribution of service benefits both in terms of the NHIS and health care in the Jirapa district favours urban residents. Lastly, the thesis found that whereas rural residents prefer health care provision to be social in nature, urban residents were more interested in the technical quality aspects of care. These findings suggest that rural residents are not benefitting from, or may not be accessing health services to the extent as their urban counterparts. Affordability, long distance to health facilities, availability and acceptability barriers were found to influence the resultant pro-urban distribution of the overall health care benefit.
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Lightman, Naomi. "Comparative health policy in Canada and the UK: an equity perspective." Thesis, McGill University, 2010. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=86743.

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This thesis compares the health care systems in Canada and the UK with a particular focus on equity of access and equity of outcomes. It explores causal factors such as organization, financing and delivery of care. The paper presents background and historical context on the two health systems, a review of current national and comparative international studies on health equity in each country, and qualitative analysis from four key informant interviews. Overall, the paper finds greater equity in Britain's NHS in terms of access to services and pro-poor allocation of resources than in Canadian Medicare. The Labour government is actively working to redress inequalities in health, while in Canada there are numerous barriers to system reform. Additionally, the current Conservative federal government has not made improving health equity a primary concern in Canada, and creeping privatization of the system is likely leading to further inequity.
Ce mémoire compare les systèmes de santé canadien et britannique en apportant une attention particulière aux questions d'équité d'accès et de soin. On y explore les facteurs causals tels que l'organisation, le financement et l'offre de soins. Une mise en contexte historique, un état de la littérature et une série de quatre entrevues avec des acteurs clés dans les deux pays sont offertes. Ce mémoire conclut à une plus grande équité dans le système public britannique tant en terme d'accès que d'allocation de ressources au profit des plus démunis. En effet, le Parti travailliste britannique s'efforce activement de redresser les iniquités alors que le gouvernement canadien est confronté à de nombreuses difficultés dans ses tentatives de réforme. De plus, le gouvernement Conservateur canadien n'a pas fait de l'amélioration des conditions d'équité une priorité tout en tolérant une privatisation rampante du système qui mènera surement à davantage d'iniquités.
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Pereira, Joao Antonio Catita Garcia. "Equity, health and healthcare : an economic study with reference to Portugal." Thesis, University of York, 1995. http://etheses.whiterose.ac.uk/9765/.

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Meit, Michael, and Kate E. Beatty. "Leveraging Assets to Improve Rural Health and Equity: Challenges and Opportunities." Digital Commons @ East Tennessee State University, 2017. https://dc.etsu.edu/etsu-works/6839.

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34

Chuma, Jane. "Resource allocation in the Kenyan health sector : a question of equity." Master's thesis, University of Cape Town, 2001. http://hdl.handle.net/11427/7714.

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Bibliography: leaves 107-112.
This study examined the current resource allocation decision-making processes, and the distribution of both financial and non-financial resources in the health sector. The study explored how the current resource allocation process has impacted on equity between provinces (equity being defined as equal resources for equal need). It went further to look at possible alternatives that could lead the Kenyan health sector towards geographical equity. The study focused on the public health sector because it is the largest provider of health care services in Kenya. The basic argument underlying the study was that, raising additional funds for health care (e.g. through user fees) might not lead to equity, if the additional resources were to be allocated within the current resource allocation process. Instead, the study argues that the first step towards equity in health care in Kenya is to distribute the current resources in a more equitable manner. This can only be done through the development and implementation of a better resource allocation process.
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Kiracho, Elizabeth Ekirapa. "Equity in the allocation of primary health care resources in Uganda." Master's thesis, University of Cape Town, 2006. http://hdl.handle.net/11427/8915.

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Kirigia, Doris Gatwiri Public Health &amp Community Medicine Faculty of Medicine UNSW. "Beyond needs-based health funding: resource allocation and equity at the state and area health service levels in New South Wales - Australia." Awarded By:University of New South Wales. Public Health & Community Medicine, 2009. http://handle.unsw.edu.au/1959.4/44733.

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Addressing inequities in health both within and between countries has attracted considerable global attention in recent years. In theory, equity remains one of the key policy objectives of health systems and underpins the allocation of health sector resources in many countries. In practice, however, current evidence demonstrates that only limited progress has been made in terms of bridging the health inequity gap and improving the health of the least advantaged. The persistence of inequities in health and health outcomes raises concerns about how governments and health authorities distribute limited health resources to improve the health of the poor and most vulnerable and thereby promote equity. This thesis is about equity and allocation of financial resources in the health system of New South Wales, one of the eight states of Australia. It investigated the extent to which there has been a movement towards equity in resource allocation to Area Health Services under the NSW Health Resource Distribution Formula and whether this has been reflected in equitable resource allocation within Area Health Services. It considered only resources allocated through the NSW Department of Health. The study employed a combination of qualitative and quantitative methods to gather and analyse data. The qualitative component analysed data gathered through semi–structured interviews with policy makers, health executives, managers, and other stakeholders to establish the resource allocation processes and the factors upon which the allocation decisions were based. The quantitative component analysed health expenditure and health needs data to assess the extent to which allocation of resources from the State to Area Health Service levels has been equitable in terms of reflecting the level of health needs. Two indices were constructed and used as proxies for health needs. Principal component analysis was used in the construction of one of the indices, using demographic, socio–economic and health-related data. The other index was developed using a combination of premature mortality and morbidity data. The quantitative study spans the two decades 1989/90 to 2006/07, with a more detailed analysis of material for the years 2003/04 to 2006/07. The findings of the study show a considerable degree of inequity in resource allocation with several Area Health Services (AHSs) receiving less than a fair share of funding for the years analysed, although some movements towards equity were evident. This contradicts the general impression that the introduction of the resource distribution formula in NSW has significantly improved equity in resource allocation. In general, funding allocation at the State level correlated significantly with population size but not with health needs of the eight AHSs in NSW. Similarly, within the AHSs, allocation of funds was based on programs and services and not on health needs. Key issues that emerged from the qualitative data as affecting the equity with which health funds are allocated in the NSW health system include limited use of the resource distribution formula at the state level, lack of an effective resource allocation tool to guide the distribution of funds within AHSs, and insufficient emphasis on equity at the AHS level. It is crucial that these and several other issues identifies in the study are addressed if current inequities in funding and in health outcomes generally are to be effectively reduced.
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Jaramillo, Garcia Alejandra Paula. "Priority Setting: A Method that Incorporates a Health Equity Lens and The Social Determinants of Health." Thèse, Université d'Ottawa / University of Ottawa, 2011. http://hdl.handle.net/10393/19986.

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Research Question: This research adapted, tested, and evaluated a methodology to set priorities for systematic reviews topics within the Cochrane Collaboration that is sustainable and incorporates the social determinants of health and health equity into the analysis. Background: In 2008 a study was conducted to review, evaluate and compare the methods for prioritization used across the Cochrane Collaboration. Two key findings from that study were: 1) the methods were not sustainable and 2) health equity represented a gap in the process. To address these key findings, the objective of this research was to produce and test a method that is sustainable and incorporates the social determinants of health and health equity into the decision making process. As part of this research, the methods were evaluated to determine the level of success. Methodology: With assistance from experts in the field, a comparative analysis of existing priority setting methods was conducted. The Global Evidence Mapping (GEM) method was selected to be adapted to meet our research objectives. The adapted method was tested with assistance of the Cochrane Musculoskeletal Group in identifying priorities for Osteoarthritis. The results of the process and the outcomes were evaluated by applying the “Framework for Successful Priority Setting”. Results: This research found that the priority setting method developed is sustainable. Also, the methods succeeded in incorporating the social determinants of health and health equity into the analysis. A key strength of the study was the ability to incorporate the patients’ perspective in setting priorities for review topics. The lack of involvement of disadvantaged groups of the population was identified as a key limitation. Recommendations were put forward to incorporate the strengths of the study into future priority setting exercises within Cochrane and to address the limitations.
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Alves, Pedro José Fernandes. "Equity Research - Luz Saúde." Master's thesis, Instituto Superior de Economia e Gestão, 2016. http://hdl.handle.net/10400.5/12182.

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Mestrado em Finanças
Luz Saúde, S.A. é uma das maiores empresas da área da saúde em Portugal. Com um serviço diferenciado a empresa tem conseguido um crescimento considerável mesmo em períodos económicos adversos. Com uma estrutura e área de negócio bastante apetecível a investidores estrangeiros, acabou por ser adquirida quase na totalidade em 2014. Este trabalho tem como objetivo determinar o valor intrínseco das ações da Luz Saúde, através de uma análise detalhada do desempenho operacional do grupo e de seu ambiente externo. A avaliação foi baseada no método dos fluxos de caixa descontados, que de acordo com o estabelecido na revisão da literatura constitui a melhor metodologia para avaliar a Luz Saúde. Com esta avaliação, foi possível concluir que o valor da ação da Luz Saúde em 31/12/2014 encontra-se subvalorizada, ou seja, foram cotados abaixo do seu valor intrínseco 3,80 euros, apresentando assim um potencial de valorização de 22,15%, foi dada uma recomendação de compra aos investidores interessados.
Luz Saúde, S.A. is one of the largest companies within the Portuguese health sector. Offering differentiated services, the company achieved considerable growth, in spite of the ongoing economic crisis. Given its structure and desirability to foreign investors, it would eventually be acquired almost entirely in 2014. This study aims to determine the intrinsic value of Luz Saúde, S.A.'s shares, through a detailed analysis of the group's operating performance and external environment. The evaluation was based on the method of discounted cash flows, which according to the literature review, is the best methodology for evaluating Luz Saúde. This evaluation suggests that the company's share price on 12/31/2014 was underestimated, i.e. the share was rated below its intrinsic value of 3.80 euros, thus presenting a potential of appreciation of 22, 15%, resulting in a recommendation to buy for interested investors.
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Price, Juliet. "Socioeconomic position and the National Health Service orthodontic service." Thesis, University of Manchester, 2016. https://www.research.manchester.ac.uk/portal/en/theses/socioeconomic-position-and-the-national-health-service-orthodontic-service(b4b4d25b-826a-4efe-83ae-50c18fafcf6a).html.

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Background: The National Health Service (NHS) aims to achieve maximum health gains with its limited resources, while also ensuring that it provides services according to need, irrespective of factors such as socioeconomic position (SEP). Aim: The aim of this thesis is to explore the relationships between SEP and various aspects of the NHS orthodontic service, including need, demand, supply, and outcomes. Methods: Three main data sources were used: two population-based surveys (the 2003 United Kingdom (UK) Children’s Dental Health Survey (CDHS) and the 2008-2009 NHS Dental Epidemiology Programme for England Oral Health Survey (OHS) in the North West) and an administrative data set (containing 2008-2012 North West NHS orthodontic activity data). The data were used to investigate levels of need and willingness to have orthodontic treatment, treatment utilisation, assessment procedures, and treatment outcomes, and the costs associated with the service. Subsequently, regression analyses were carried out to explore the associations between SEP and the various orthodontic variables. Results: Over a third of 12-year-olds had normative need for orthodontic treatment and over half had patient-defined need. Those in the most deprived groups in the North West tended to have lower levels of treatment compared to those in the least deprived group (despite the fact that normative need was not shown to vary by SEP), and they were more likely to discontinue treatment and have residual post-treatment need (RPTN). There was a great deal of variation among practices/orthodontic clinicians in terms of the percentages of patients with repeated assessments, treatment discontinuations, and RPTN. The major sources of potential inefficiency costs in the NHS orthodontic service in the North West are treatments that result in discontinuations (which cost £2.4 million per year), RPTN (which cost £1.8 million per year), and unreported treatment outcomes (which cost £13.0 million per year). Discussion: The NHS is not delivering orthodontic care equitably between SEP groups in the North West, as those from more deprived groups are more likely to fail to receive treatment, and to have poor outcomes if they do receive treatment. In addition, the wide range of process and outcome indicators between practices/orthodontic clinicians raises issues about quality of the overall service. In particular, treatment outcomes are frequently unreported, which highlights the need to improve the outcome monitoring systems in the NHS orthodontic service.
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40

Gould, Solange M. "Advancing Health Equity and Climate Change Solutions in California Through Integration of Public Health in Regional Planning." Thesis, University of California, Berkeley, 2015. http://pqdtopen.proquest.com/#viewpdf?dispub=3733400.

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Climate change is a significant public health danger, with a disproportionate impact on low-income and communities of color that threatens to increase health inequities. Many important social determinants of health are at stake in California climate change policy-making and planning, and the distribution of these will further impact health inequities. Not only are these communities the most vulnerable to future health impacts due to the cumulative impacts of unequal environmental exposures and social stressors, they are also least likely to be represented in climate change decision-making processes. Therefore, it is imperative that public health and social equity advocates participate in climate change policy-making that protects and enhances the health and well-being of vulnerable communities. Regions have emerged as important policy-making arenas for both climate change and public health in California, because many drivers of climate change are also social determinants of health (e.g. land use, housing, and transportation planning); these play out regionally and are under regional governmental authority. However, the public health sector is not engaged adequately with climate change planning given the magnitude of risks and opportunities inherent for health. Examination of where public health and equity partners have engaged in regional climate change planning and policy-making may offer lessons for how to change the drivers of health inequities and climate change through this work.

This dissertation examines why the public health sector in California is not more engaged with climate change work and regional scale planning given current threats to and opportunities for health, and whether and how public health and social equity stakeholders’ participation in climate change solutions and regional scale planning can improve health and inequities outcomes and decision-making processes. The overarching goal of this research was to inform efforts to increase public health work on climate change and regional-scale planning, strengthen partnerships between public health, social equity, and climate change stakeholders, and formulate strategies that address climate change and health equity.

The first chapter of this dissertation was conducted in conjunction with a study at the Center for Climate Change and Health at the Public Health Institute, where we conducted semi-structured in-depth interviews (n=113) with public health and climate change professionals and advocates. I performed structured coding and conducted inductive-deductive thematic analysis within and across respondent groups. I found that individual-level barriers to public health engagement with climate change include perceptions that climate change is not urgent, immediate, or solvable, and insufficient understanding of public health impacts, connections, and roles. Institutional barriers include a lack of public health capacity, authority, and leadership due to risk aversion and politicization of climate change; a narrow framework for public health practice; and professional compartmentalization. Opportunities include integrating climate change into current public health practice; providing support for climate solutions with health co-benefits; and communicating, engaging and mobilizing impacted communities and public health professionals.

In the second chapter, I conducted two case studies of Sustainable Communities Strategies planning to achieve greenhouse gas reduction targets through integrated regional land use and transportation planning under California Senate Bill 375 (San Francisco Bay Area and Southern California). I used in-depth interviews (n=50) with SCS planning participants, public document review, and participant observation. I analyzed interviews using thematic analysis in an iterative inductive-deductive process. In both regions, climate change planning was a major lever for increasing the language, consideration, funding, and measurement of health impacts into the SCS plans. Public health’s analytic skills and social determinants of health conceptual framework were valuable for both regional planning agencies and equity groups. Political context influenced the priority concerns, framing, and outcomes. Desire to improve public health was influential in both of these environments. In the Bay Area, a health equity frame promoted regional solutions that can improve health, equity, and climate change. In SCAG, a public health frame increased awareness, language, and future funding for active transportation. Public health was a less contested and commonly held value across diverse political jurisdictions that may be an entry point for future discussions of equity and climate change. In both regions, reform of regional governance processes was pursued to sustain institutionalization of health and equity concerns and improve regional democracy. I discuss implications and recommendations for engaging in multi-system integrated regional planning that can simultaneously improve climate change, health, and equity.

In the third chapter, I analyze the same data as a case for understanding regional-scale public health, social equity, and regional planning staff efforts to slow climate change and improve social determinants of health and social equity. In both regions multi-year SCS planning processes, public health and equity stakeholder engagement was instrumental in getting health goals, targets, and indicators into plans. In the Bay Area, advocacy efforts yielded health and equity language in policies and implementation funding guidelines and changes to the basic governance structure. In SCAG, advocacy efforts yielded significant future funding for active transportation and more metrics to monitor the health and equity impacts of planning. Participants in the SCS planning process described their motivations for engaging at the regional level, the barriers to effective regional planning, the achievements of their engagement, and recommendations for improving future efforts. In the interviews, three main themes emerged related to the opportunities and challenges of working at the regional scale: (1) Building regional identity as a foundation for advancing health and equity; (2) The importance of governance structures for health and equity, and the need for regional governance reform; (3) The prospects and barriers of building regional coalitions both within public health networks and with regional equity partners. I discuss implications and recommendations for public health’s engagement with regional planning agencies, creation of coalitions, and reforming of regional governance structures to sustain better consideration of climate change, health, and equity.

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41

Jiménez, Rubio Dolores. "Decentralisation and its impact on health and equity in health : some theoretical considerations and applications to Canada." Thesis, University of York, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.428392.

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42

Carneiro, César Alberto dos Santos. "Essays on Health Economics: Equity and Access to Health Care and Public Hospital Performance under Corporatized Management." Tese, Faculdade de Economia da Universidade do Porto, 2010. http://hdl.handle.net/10216/56320.

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43

Schaff, Katherine Anne. "Local Health Departments Engaging in Policy Change to Achieve Health Equity| An Examination of the Foreclosure Crisis." Thesis, University of California, Berkeley, 2016. http://pqdtopen.proquest.com/#viewpdf?dispub=10086067.

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Early public health efforts in the United States addressed social conditions that contributed to poor health, with public health workers playing a role in large scale societal reforms, such as passing housing and sanitation laws, which led to diminishing deaths from infectious diseases. As chronic diseases became leading causes of death, public health research and practice became more focused on individual behaviors, widely thought to be the primary cause of chronic diseases. However, health inequities along the lines of place, race, class, and other forms or marginalization are still prevalent. A substantial body of research illustrates how social, political, economic, and environmental factors affect multiple health outcomes, including chronic diseases, and contribute to health inequities.

In public health practice, some local health departments (LHDs) and organizations that support their work have called for broader public health interventions that address social policies that contribute to health inequities in addition to providing direct services to individuals. With continued research and support, the approximately 2,800 LHDs nationwide can play a central role in reducing health inequities. However, engaging in this complex work necessitates new approaches, skills, frameworks, and organizational infrastructures for LHDs. The recent foreclosure crisis, which stands to increase racial and health inequities, provides a lens to examine whether and how LHDs can move from a rhetorical commitment to addressing social determinants of health (SDH) into actual public health interventions that reduce health inequities.

Through this dissertation, I examine LHDs’ role in the foreclosure crisis through three related papers. My aim is provide insight into how LHDs responded to the deep and fundamental shifts in access to stable and quality housing and wealth created by the foreclosure crisis that disproportionately impacted African-American, Latino, and some Asian/Pacific Islander communities. Through all three papers, I incorporate a focus on challenges and approaches to addressing the racialized causes and outcomes of the foreclosure crisis. My overall aim is to help advance local public health practice within LHDs to more effectively target the causes of health inequities, including gaining a better understanding of LHD approaches and needs related to addressing SDH through local policy.

In the first paper, A National Survey on Local Health Department Engagement in Addressing the Foreclosure Crisis, I describe the results of a national survey on LHD engagement in the foreclosure crisis, which includes LHD approaches to addressing foreclosure and barriers to engagement. Responses followed a diffusion of innovation pattern, with innovator, early adopter, early majority, late majority, and lagging LHDs. Respondents expressed a high level of interest in adopting innovative approaches to addressing SDH and described a need for models of how other LHDs are preventing or mitigating the impacts of foreclosure, especially through local policies.

In the second paper, Adopting an Innovative Public Health Practice to Address Foreclosure: A Case Study of Alameda County Public Health Department , and the third paper, Policy Entrepreneurs, Agenda-Setting, and Communication: An Exploration of How a Local Health Department Engaged in Addressing the Foreclosure Crisis, I describe findings from qualitative interviews with current and former ACPHD staff and partners. In the second paper, I identify factors that 1) differentiate ACPHD’s innovative approach from traditional LHD activities; and, 2) contributed to ACPHD being an innovator among LHDs.

Finally, in the third paper, I focus on ACPHD’s role as a policy entrepreneur in agenda-setting, including their communication approach. While the second paper focuses on how ACPHD developed into an innovative LHD in the area of local housing policy, the 3rd paper focuses on how in this role, ACPHD interacted in the local policymaking process. This case study also examines how the role of policy entrepreneur can be shared across two organizations (ACPHD and Causa Justa::Just Cause) and provides another way to conceive of entrepreneurism.

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Carneiro, César Alberto dos Santos. "Essays on Health Economics: Equity and Access to Health Care and Public Hospital Performance under Corporatized Management." Doctoral thesis, Faculdade de Economia da Universidade do Porto, 2010. http://hdl.handle.net/10216/56320.

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45

Schneider, Pia Helene. "The contribution of micro-health insurance to equity and sustainability in Rwanda." Thesis, London School of Hygiene and Tropical Medicine (University of London), 2004. http://researchonline.lshtm.ac.uk/682314/.

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Many countries are looking to health insurance to improve access to medical care for low- income groups and to raise additional revenues for a depleted health sector. In Rwanda, concerns about a sharp drop in demand for medical services after the re-introduction of user fees in 1996, motivated the government to design and pilot-test micro-health insurance (MHI) in three districts. This thesis compares the performance of the current Rwandan MHI with the user fee system and against principles of egalitarian equity and sustainability. It draws from the economic and social literature related to health insurance, equity and sustainability; and uses cross-sectional routine and survey data collected on insured and uninsured population groups from health centres, MHI, households, patients and focus groups during the Rwandan pilot phase (7/1998-6/2000). It aims to contribute to the research on equity and sustainability in health financing and utilisation by evaluating and comparing the implications of MHI and of user fees for households and on the health sector. The analysis comprises three main components. First, it examines the demand for health insurance in a binary choice model. Second, following egalitarian equity principles and the minimum standard approach, it evaluates the impact of utilisation and financing of health care on the financial situation of insured and uninsured households. Third, it uses an econometric cost function that allows identification of payer-specific outputs to analyse and compare the cost and efficiency implications of MHI with capitation payment versus user fees in health centres, in order to test the hypothesis that providers adjust the treatment intensity to the expected payment mechanisms. Based on findings, a MHI insurance design is derived to scale up risk-pooling and improve equity and sustainability in the district health system.
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46

Almond, Palo. "A study of equity within health visiting postnatal depression policy and services." Thesis, University of Southampton, 2008. https://eprints.soton.ac.uk/58902/.

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Abstract Postnatal depression (PND) is a psychiatric condition that is estimated to affect 15% of postnatal women. Health visitors (HVs) are the key public health professionals involved in its early detection and treating its mild to moderate forms. It has been suggested that some HVs do not assess women for PND and consequently these women do not get the care they need. Equally other women have clearly been shown to benefit from the advice and treatment they get when HVs have discovered PND. Such inequalities are unfair and unjust since they might be avoidable. Unfair and unjust inequality is known as inequity. This study was designed to examine the factors that promote or hinder equity in health visiting PND services and it was anticipated that in doing so a greater understanding ofthe concept and nature of equity in service provision and access to services would be achieved. A qualitative case study approach was used to study one PCTs health visiting PND service. HVs were observed doing 21 home visits to antenatal and postnatal women. Post-observation interviews were conducted with 16 HVs. Nine Bengali women and 12 English women were interviewed. Additionally 10 interviews were conducted with health visiting managers and other personnel involved in the health visiting PND service. In total, 51 interviews were conducted. Documentary data in the form ofthe PCTs PND Strategy Policy were used in two principal ways. Firstly, they provided contextual information, and secondly they provided a framework for the interviews and sampling the observations. The policy documents underwent a critical analysis and the remaining data were analysed using Ritchie and Spencer's (1994) Framework Analysis method. The findings 'revealed that despite the existence ofa policy to provide 'equal and ' equitable' health visiting PND services, many factors led to inequity in service provision. Whilst PND training had been provided to all HVs, it was inadequate in preparing them to detect and manage PND in Bengali women or understand fully the needs of English women from low socio-economic backgrounds. Problems in the policy process led to a situation where managers and HVs were not always aware that the policy to detect and manage PND in all women was active. Furthermore, ambiguous reference was made in policy documentation implying that groups such as minority ethnic women, were issues for future consideration. Constraints such as the lack of appropriate training, other pressing priorities, and the scarcity ofculturally appropriate resources, made it'difficult to provide an equitable service to all women. The research makes a contribution to knowledge by improving understanding of the nature of equity and equality and PND, particularly from the perspectives of lower socio-economic English women and Bengali women. The findings from the policy analysis process will also facilitate the development of policy and culturally sensitive HV practice and the enhancement ofPND services. Ritchie J, Spencer L. (1994). Qualitative data analysis for applied research In Bryman A, Burgess RG (Eds). Analysing Qualitative Data. Routledge. London
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Mwase, Takondwa Lucious. "Health care financing and expenditure in Malawi : do efficiency and equity matter?" Master's thesis, University of Cape Town, 1998. http://hdl.handle.net/11427/9677.

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Bibliography: leaves 113-118.
The Malawian sector spent about 3.3% of its GNP on health services in 1995/96. The public sector alone spent about 6.2% of its total revenue on health services and this is much high than most other Sub- Saharan African countries (e.g. Zambia, Kenya, Uganda). Despite such high levels of public expenditure, Malawi’s social and health indicators are among the worst in the world. The majority of the Malawian population suffer from a large amount of preventable illness and premature death which could be treated/prevented by simple inexpensive medical interventions. This scenario raises questions with regard to the government stated priority to primary health care and preventive health services. This investigation therefore was undertaken in order to quantify the total health care expenditure in Malawi and its distribution and then evaluate its equity and efficiency implications for the delivery of health services. The analyses focused on the public health sector due to the fact that the public health sector is the largest provider of health services in Malawi and its services are fiee of charge. It was therefore felt that a detailed analysis and evaluation of this sector could go a long way in improving the health status of the majority of Malawians within the resource envelope.
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Benkhalti, Jandu Maria. "Health Impact Assessment and the Inclusion of Migrants." Thesis, Université d'Ottawa / University of Ottawa, 2015. http://hdl.handle.net/10393/32226.

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There is an increasing number of international migrants worldwide and in Canada. The majority of migrants arrive with a health status higher than the average of their host country. This advantage is often lost within ten years of migration due to various reasons, most notably through the social determinants of health. These determinants are the conditions in which individuals live and work and the most relevant to migrant health include racialization, education, employment, housing, social capital, and gender. Health impact assessment (HIA) is a process with the capacity to address changes in health due to the social determinants of health by assessing the intended and unintended impacts on health that a policy, program, or project might have and recommend ways to promote positive and mitigate negative impacts. For this reason, HIA has the potential to address the observed decrease in health experienced by migrants. Various frameworks have been developed to guide the undertaking of HIA including frameworks explicitly aiming at addressing health inequities by considering particular socially disadvantaged population groups. One such example is the Health Equity Impact Assessment (HEIA) tool developed by the Ontario Ministry of Health and Long-Term Care. Although there have been a few studies addressing the inclusion of inequities in HIA in general, there has been no previous assessment of the inclusion of migrants in HIA. This doctoral thesis sought to assess the degree and way in which migrants are included in HIAs globally and across various types of HIAs and contexts. It also sought to assess the degree to which migrants were considered in local initiatives through an examination of the implementation of the Ontario HEIA tool in public health units. A scoping review of the international literature including 117 HIAs and two HIA evaluations found that only 14% of hand-searched HIAs mentioned migrants, 5% analysed migrants and only 2% included them in their recommendations. Although migrant groups were sometimes included in the process, this was seldom the case for citizens. The main reported barriers to considering migrants were a lack of available data and the significant additional resources needed. In order to undertake an evaluation throughout the province, it was first necessary to assess the way in which the Ontario HEIA had been implemented and used by public health units across the province. The scan found that nearly half of public health units had used the HEIA tool either in its original form or modified to the needs of the unit. The use of the tool was found to be influenced by the following factors: the available inputs or resources, the nature of the HIA tool, the actors and stakeholders involved, the decision-making processes within the unit or team involved, the context of the social, economic, and political environments, the nature of the project, program, or policy being assessed, and lastly, the various outputs of completing the HEIA process. Lastly, a Process and Impact evaluation assessed the way in which PHUs with a high proportion of migrants considered these migrants in their HEIAs. This study found that although migrants had been included in HEIAs, this tended to be done when the impact on migrants was anticipated. Additionally, there remains an incoherent terminology accompanied by a confounding of the concepts of migration, racialization, and ethnicity, which are reflected in the type of recommendations developed. These recommendations often focused on translation of documents into various languages and the acquiring of greater information through community partnerships. The process and capacity to include migrants in HEIAs were influenced by the availability of resources and evidence, the prioritisation of recommendations relating to migrants, and the overall impressions the staff had on the HEIA process. Nonetheless, the HEIA process was beneficial in that it strengthened relationships with migrant community organisations. This thesis work also resulted in the development of a HIA-specific theoretical framework based on the literature and empirical findings of this work. This framework is conducive to adopting a tactical approach to HIA by considering the various contextual factors influencing the completion of an HIA and implementation of its recommendations. In conclusion, although migrants are understood to be an important group often facing circumstances of disadvantage, they are only sometimes considered in HIAs. Several procedural and contextual barriers are encountered which influence their consideration. Significant guidance is still required to facilitate their adequate consideration and ensure the development of optimal recommendations. HIA frameworks should explicitly mention migrants as a potentially disadvantaged group and guidance documents could be developed to address the current gaps in understanding migrant issues.
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49

Sörlin, Ann. "Health and the elusive gender equality : Can the impact of gender equality on health be measured?" Doctoral thesis, Umeå universitet, Epidemiologi och global hälsa, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-46298.

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Background: All over the world men and women show different health patterns, and therecan be many and various reasons for these differences. This thesis therefore evaluates theimpact of gender equality on health. To do this, we must be able to measure gender equality.In this thesis, we develop two new measurements of gender equality and evaluate the relationshipbetween gender equality and health. Methods: Two cross-sectional studies, one register-based and one survey study, are used tocompare different measurements of gender equality and different measurements of health,and the relationship between them. Differences between men and women in relation to healthoutcome are also discussed in the thesis. The register study, comprising 1 097 202 individuals,is based on public registers and includes information on workplace, income, sickness absence,full-time/part-time work, level of education, parental leave and temporary parental leave.A gender equality measurement, the Organizational Gender Gap Index or OGGI, was constructedand 123 companies in two sectors were ranked using the index. Employees in 21 of the mostand least gender-equal companies were invited to participate in a survey. A second genderequality index was constructed based on respondents’ own reports regarding gender equalityin their partner relationship. The variables measured were income, full-time/part-time work,educational level, and responsibilities for and sharing of household duties and parental leave.Both indices were evaluated using the single question: How gender equal is your workplace/your relationship with your partner? The four measurements were dichotomized and testedfor a relationship to health. Health was measured by three different measurements: registerbasedsickness absence, self-reported sickness absence in the past year, and self-rated health. Results: The thesis has produced two new measurements of gender equality, described above.On gender equality in the partner relationship, we found a difference between men and women.Men perceive higher gender equality than they report, while women report more gender equalitythan they perceive. When it comes to gender equality at work, we found that employees perceivetheir company to be more gender equal than the OGGI index shows. This thesis confirms thefindings that men have better health than women regardless of measurement. However, inthis study we also found that increased gender equality decreases these differences. If employeesperceive their company to be gender equal, they have higher odds of rating their health asgood, and this is especially so for women. Conclusion: This thesis supports the hypothesis that differences in health between men andwomen can be related to a lack of gender equality. When men and women have differentpossibilities and power to shape society and their own lives, their health will be affected throughembodiment of both biological and sociological determinants in accordance with the eco-socialtheory. Increased gender equality will decrease the differences in health between men andwomen through convergence. The theory of convergence explains why men and women areaffected differently by greater gender equality. Greater gender equality will also decrease thesocial injustice between men and women and improve justice in accordance with the theoryof justice to gender.The differences found between the indices and the single question on perceived genderequality make clear the need for “hard facts” as an complement to people’s own views on gender equality.
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50

McCollum, H. R. "Process, power and politics : setting priorities for community health and equity in the recently devolved Kenyan health system." Thesis, University of Liverpool, 2017. http://livrepository.liverpool.ac.uk/3010963/.

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Devolution in Kenya was politically driven, motivated by the desire to share power and resources across regions, so as to remedy historical inequities. This led to transfer of planning, management and budgeting responsibilities for a range of services, including health, from central government to 47 new sub-national governments (known as counties), starting in 2013. This transition was driven by increasing frustration with inefficiencies and inequities associated with the former centralised government. Objectives for devolution are to strengthen democracy and accountability, increase community participation, improve efficiency and reduce inequities. However, global experiences have shown that transfer of powers does not always lead to achievement of these objectives. Rather, potential risks include that inefficiencies will multiply, inequities will widen and corruption will become more widespread. Health has been the most controversial of all devolved services in Kenya, contributing to recurring health worker strikes. Respondents described that ideally, priorities should be set following a series of consultations between local decision-making actors, guided by local evidence and community-generated priorities, bounded by available resources, using cost-effectiveness and equity principles to identify context-appropriate interventions which advance universal health coverage. This thesis which, to the best of our knowledge, is the first study of its kind, aims to explore priority-setting for community health and equity across counties and multiple health systems levels in Kenya post-devolution. It uses mixed qualitative approaches in ten counties including interviews, focus group discussions and participatory photography research conducted two to three years after devolution took place. It includes respondents from national to community level to analyse county health priority-setting processes, power dynamics and implications for health equity and community health services. This study shows that many respondents across health systems levels identify equity as a guiding principle, with devolution bringing positive ramifications for previously neglected counties, reducing inequities between counties. County decision-makers, who often hold greatest power compared with health workers and community members, perceive building health facilities as the most appropriate way to achieve health equity. Community members who have a more holistic understanding are not yet sufficiently empowered to understand the benefits and limitations of choices available to them or to reflect this within the priorities they identify. There is wide variation between counties, with emerging examples of stronger, more equitable health priority-setting, with inclusion of an illustrative case study. Overwhelmingly the findings from this study relate to power dynamics. We found a lack of clarity surrounding roles for decision-making actors, inadequate information, unclear criteria and processes for guiding priority-setting. Within the confusion created by the limited guidance and capacity, opportunistic actors have seized available power to manipulate priorities to align with personal objectives, such as political re-election. The resulting increase in complexity blurs lines of accountability creating a situation that makes progress beyond a single elected term challenging. This has led to increased focus on tangible curative services, stifling opportunities for strengthening quality and community-based primary health care. Devolution has brought a period of colossal upheaval with changes in roles and power locus within the health system. Clearer guidance, capacity building, stronger community empowerment, involving marginalised groups in priority-setting processes and accountability mechanisms are needed if devolution’s objectives are to be realised.
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