Professional Documents
Culture Documents
Equitable Care Theory
Equitable Care Theory
Introduction
Equity is an abstract concept that encompasses philosophical issues such as fairness and
social justice, makes its definition and measurement very complicated. Before John Rawls' A
Theory of Justice (2017), researchers mainly evaluated the justice or fairness in the social
distribution based on the distribution of results. Since then, the concept of has undergone major
changes: Rawls’ "difference principle" seeks to maximize the availability of commodities for
disadvantaged groups; Sen (2019) talks about capabilities from the perspective of the set of
possible functions enjoyed by individuals, And emphasized the distribution of capabilities;
Dworkin (2018) equated justice with the equality of resources, not results; and Roemer (2018)
emphasized equality of opportunity. This evolution of social justice theory in the past 30 years is
about moving away from actual after-event results (such as income) and its impact on personal
well-being, and moving the bet (as ability or opportunities) toward the potential result set.
Equity related to health and medical care can be viewed from three broad perspectives: (i)
Equity in health, (ii) Equity in the provision of health services, and (iii) Equity in health
financing. Although all three are covered in this investigation, the first two constitute the focus
of this investigation. In this context, it is important to discuss the operational definitions of (i)
and (ii).
Health equity is defined as the minimization of avoidable health inequalities and their
determinants, which occur between people with different levels of potential social advantages or
privileges. Inequality exists when there are differences in health and well-being care and its
determinants that are considered avoidable, unfair, and unfair. Therefore, not all inequalities in
health between population groups are considered inequalities. Inequality in health and medical
care specifically refers to the differences between groups of people related to their social status,
and these differences are measured by characteristics such as income or wealth, occupation,
education, geographic location, gender or race. health inequality caused by unavoidable and
inevitable conditions, such as biological and genetic variation, does not constitute.
Theoretical Framework
Measuring the fairness of healthcare is a real challenge, especially because there is no
consensus on how to define and measure this concept. In the literature on the conceptualization
of fairness, can find some common foundations through the understanding of the three fields: 1st,
people with equal needs receive equal care 2nd, people with equal needs equal treatment and 3rd,
The result of equal treatment of people with the same needs is. Although the nature of fairness is
oversimplified, the definition provided by these three domains is a useful framework that
outlines the possible inequalities of in the healthcare sector.
Regarding access to health care, the definition of the concept depends to a large extent
on the context in which is being analyzed. Goddard and Smith defined the opportunity to obtain
medical care as "the ability to ensure that a specific service area has a specific level of quality, is
affected by a specific maximum degree of inconvenience and personal cost, and at the same time
has a specific level of information". Regarding the scope of the services provided, the Equity
Literature extends the aspect of “providing equal services for people with the same needs”. This
refers to the fact that factors such as age, gender, and income should not require people with
similar needs to enter different doors (for example, public providers) or that they are treated
differently. Services provided. Service quality is also an inherent element of the visit, because in
terms of the structure of the, the care provided, or the results, poor quality may affect the visit.
Regarding personal discomfort, cost, and information, there may be considerable differences in
the personal costs of using services (such as user fees and transportation costs) and the
understanding of availability and usability. The effectiveness of the service (for example,
because of language or cultural differences). Although cannot completely match these aspects, in
some aspects, the difference in cost and information distribution will become unacceptable. The
patient-provider interaction plays an important role in the assessment of the fairness of treatment
and treatment outcomes. The changes produced by this interaction depend on the knowledge,
skills, preferences, perceptions, attitudes, and prejudices of the patient and the healthcare
provider. In addition, the broader social determinants of health, such as the social environment in
which people live and work, may lead to unfair treatment and treatment outcomes. For example,
the unequal recovery rate of among different social groups may occur even if there is no
inequality in their access or treatment.
Discussion
In developing the equity standards, the project group identified five main areas that should be
addressed to ensure the delivery of equitable services in healthcare:
The first standard, Equity in Policy Its objective is to promote equity by providing fair
opportunities, reducing health inequalities, and providing sustainable and profitable policies.
This standard aims to ensure that a fair strategy is developed and that the implementation of is
integrated into all relevant organizational plans and quality management systems. Therefore, all
monitoring systems and evaluation processes should reflect and support equity policy measures.
profound institutional changes towards equity, especially regarding the measures taken to raise
WHO to address the barriers that prevent people from accessing and benefiting from health care
services. On the one hand, it is necessary to guarantee physical accessibility and the geographic
distribution of services and facilities, including outreach interventions for the most vulnerable
groups. On the other hand, effective intervention is needed to improve communication and
information. With regard to language barriers, a lot of work has been done and needs to be
consolidated and maintained, but more attention must be paid to the information intervention to
solve health literacy. This standard encourages healthcare organizations to address more difficult
obstacles, such as the power imbalance in communication between patients and doctors, and to
increase trust, respect, openness and empathy in the relationship with patients. Other difficult
obstacles are legal and financial, depending on the rules outside health services, such as the lack
organizations take action where eligibility rules compromise human rights, suggesting that
concrete solutions be provided to ensure that ineligible people receive appropriate information,
The aim of the third standard, Equitable Quality of Care, the organization offers high
quality terms, and always approves the unique personal features and plays these to improve your
health and happiness. Health Suppliers should be able to take into account individual experiences
and opinions in maintenance management of the care process from diagnosis to the hospital.
Therefore, in the case of immigrants, suppliers are taught by customs, and preparing the value of
a specific ethnic minority culture to people can respond to the needs of multiple diversity.
Instead, all levels of health personnel work that act beyond differences and learn to invest in the
relationship with to create other knowledge. This approach helps to understand the intersections
of racial, ethnic, gender, classes, and eliminate the relationship and influence of this intersection
in relation to the experience of current disease. Only patients are only to help.
The fourth standard, Equity in Participation, aims to ensure that service users and
community members have a fair opportunity to participate in the planning, delivery and
evaluation of the service. Promoting active participation does not mean that only establishes
contacts with well-organized community groups, which may not represent the needs of
individuals or the needs of groups that are smaller, less organized, or completely marginalized.
By assuming that “community groups” are always homogenous entities whose members share
interests, values and identities, we may ignore the fact that communities are related to gender,
race, ethnicity, religion, and economic status. The difference, can produce a relationship that
isolates specific individuals, denying them an equal voice or not even being able to participate.
Therefore, the main purpose of this standard is to ensure that individuals and social groups who
fairness activities in other sectors of society. Organizations should actively participate in equity-
related networks, think tanks, and research programs, such as partnerships that provide
innovative services to vulnerable groups and cross-sector cooperation to address broader health
determinants.
Nursing Paradigm
The environment includes the internal and external variables, as well as events and
issues that influence both the nurse and the patient. The external variables provide nurses with
significant opportunities to hone their knowledge, gain relevant experience, and create a unique
relationship with the patient. The internal conditions include variables within the nurse that can
impact the outcome of the care provided to the patient. These variables include the nurse's
knowledge and experiences, sincere interest to care or a caring attitude for the patient, and
receptivity to different forms of knowing. The synergy of these variables in the external and
internal environment affects the nurse by facilitating the development and use of the nurse’s
intuitive skill (as shown by the arrow connecting the environment and the nurse).
Variables in the patient's internal and external environment are all part of the patient's
experience which can bring about either a positive or negative patient situation (as shown by the
arrow connecting the environment and the patient). Favorable events and issues, correct
knowledge, and good experience result in a positive patient situation while unfavorable events
and issues, faulty knowledge, and bad experience result in a negative patient situation. The latter
gives rise to a health need or situation that requires the intervention of the nurse.
To enhance the use of intuition, a deep connection between the nurse and the patient is
crucial. This connection is built through a genuine nurse-patient relationship which enables the
nurse to understand the patient’s situation holistically. Intuition, therefore, is a valid form of
knowing that guides the nurse in performing nursing actions to address the health needs of the
patient (as shown by the arrow connecting the nurse and the patient) and result to positive health
outcomes (as shown by the arrow connecting the patient and the health). It is the ultimate goal of
Lastly, when the patient is able to meet his/her needs through the help of the nurse, a
positive health outcome is achieved. A positive health outcome resulting from nurses’ intuitive
skill serves as a positive feedback and a motivation for nurses to further develop and promote
this form of knowing in their practice (as shown by the arrow connecting the health and the
nurse).
Conclusion
Impact on health policy, quality of care, and equity is applicable to many health care
systems. When evaluating health system reform, the first thing to consider is the degree to which
different groups of people enter the health system. Not only is coverage important, but it is also
important to have a more detailed understanding of differentiated use of services and the barriers
patients encounter in getting the care they need. Therefore, it is important to pay attention to non-
financial barriers such as system transparency, caregiver characteristics, and waiting lists.
Qualitative research presenting the views and experience of care providers and patients can help
explain the mechanisms that led to the observed differences. Second, differentiated goals for
specific patient groups must be taken into account. Without them, equal achievement levels can
give an impression of equity in care when in fact there may be inequality (for example, due to
the different prevalence of hypertension among different races, the rate of blood pressure
measurement of different races may be equal Show that there is inequality in health). Third, it is
important to find indicators that include complexity. In this case, non-disease-specific and
patient-centered indicators (such as functional status and quality of life) may be useful. Fourth, it
is essential to collect information at the patient level and create possibilities to monitor the
trajectory of personal healthcare utilization. Finally, plans in a broader health system impact
criteria. The conceptual framework provided in this article is a guide for developing new
evidence and using existing evidence to assess equity in the health system.
References
Ali, I., and H. H. Son. 2017. “Measuring Inclusive Growth.” Asian Development Review 24(1):
11–31.
Asian Development Bank. 2019. Equity in the Delivery of Health and Education Services in the
Philippines. Background country study prepared for RETA 6461: Equity in the Delivery
ofPublic Services in Selected Developing Member Countries, Manila.
Department of Health. 2018. “Accelerate a Unified Strategy to Save Mothers, Newborns, and
Children.” Health Policy Notes 1(2):1–14
Dworkin, R. 1981. “What is Equality? Part 2: Equality of Resources.” Philosophy and Public
Affairs10(3):185–246.
Gwatkin, D. R. 2020. “Health Inequalities and the Health of the Poor: What do We Know? What
can We Do?” Bulletin of the World Health Organization 78(1):3–18.
Kakwani, N. 2017. “Growth Rate of per Capita Income and Aggregate Welfare: An International
Comparison.” Review of Economics and Statistics 79:201–11.
Kakwani, N., A. Wagstaff, and E. van Doorslaer. 2017. “Socioeconomic Inequalities in Health:
Measurement, Computation, and Statistical Inference.” Journal of Econometrics
77(1):87–103.
Kraft, A. D., S. A. Quimbo, O. Solon, R. Shimkhada, J. Florentino, and J. W. Peabody. 2019.
“TheHealth and Cost Impact of Care Delay and the Experimental Impact of Insurance on
Delays:Evidence from a Developing Country.” The Journal of Pediatrics. Forthcoming.
Kraft, A. D., C. R. Tan, Jr., S. A. Quimbo, J. J. Capuno, E. Yap, N. Juban, and M. Cabaraban.
2016. “Private Provider Study, Volumes I-IV.” Final report submitted to the PhilTIPS.
QuezonCity.
Lakshminarayanan, R. 2018. “Decentralization and its Implications for Reproductive Health:
ThePhilippines Experience.” Reproductive Health Matters 11(21):96–107.
NSO. Various Years. Annual Poverty Indicator Survey. National Statistics Office, Manila.
Various Years. National Demographic and Health Survey. National Statistics Office,
Manila.
Peabody, J., R. Shimkhada, C. Tan, and J. Luck. 2016. “The Burden of Disease, Economic Costs
and Clinical Consequences of TB in the Philippines.” Health Policy and Planning 20(6)