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Ethical and Policy Factors in Care Coordination
Katie L. Cassady
Capella University
NURS-FPX4050: Coordinating Patient Centered Care
Erica Elkins-Little
October 2024
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Ethical and Policy Factors in Care Coordination
According to the American Nurses Association, the Code of Ethics for Nurses with
Interpretive Statements (The Code) was developed as a guide for carrying out nursing tasks in a
manner that conforms to the criteria for nursing care quality and the ethical responsibilities of the
profession. Specifically, for this assessment, the American Cancer Society (ACS) will be
discussed. ACS is a cancer advocacy group that strives to enhance the quality of life for cancer
patients and their loved ones. The ACS has a code of ethics of its own. According to the ACS’s
Code of Ethics, employees and associates should prioritize ethical behavior in all facets of their
work while keeping their mission to fight cancer front and center. This includes acting honorably
and morally, abiding by all society conduct and behavior policies, obeying all federal, state, and
local laws, and upholding core values like integrity, compassion, courage, determination, and
diversity in all actions and decisions.
Government Policies
A government statute called Patient Protection and Affordable Care Act (ACA) seeks to
expand the affordability and accessibility of health insurance for more Americans. In order to
improve patient outcomes and lessen disparities in cancer care, ACS actively advocates for
government policies that guarantee more people have insurance coverage for cancer screenings,
treatments, and follow-up care. These policies, especially those that increase access to
healthcare, like the ACA, has a significant impact on the ACS's ability to coordinate cancer care.
Early diagnosis by assisting individuals in getting screened for cancer sooner, more
age-appropriate therapy, reasonably priced health insurance, coverage for colorectal cancer
screening, and advancements in cancer care are some examples of how the ACA has affected the
ACS. Two significant pieces of legislation that safeguard people and their medical records are
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the ACA and the Health Insurance Portability and Accountability Act (HIPAA): HIPAA offers
patient protections and protects patient health information (PHI). ACA strengthens and expands
upon the privacy protections provided by HIPAA. ACA stipulates that pre-existing conditions
cannot be excluded from coverage or result in higher premiums, and that group health plans are
prohibited from charging different premiums or payments depending on health criteria.
Policy Provisions
Potential ethical conundrums when coordinating cancer care through the ACS can be
brought on by state laws governing insurance coverage for particular treatments, national
policies regarding patient data privacy (HIPAA), and regional differences in access to clinical
trials. These factors can lead to disparities in the way care is delivered and raise issues of equity
and patient autonomy based on geographic location. According to Yabroff et al. (2020), state
policies that promote continuity of health insurance coverage may reduce inequalities. Medicaid
eligibility in certain states, the ACA's increased availability of health insurance coverage options,
the expansion of dependent coverage on parents' private plans for young adults up to age 26, and
the availability of subsidies to reduce premium costs could all help to reduce interruptions and
encourage ongoing health insurance coverage.
According to Edemekong et al. (2024), patient control over medical records and
protection of personal health information are two benefits of the HIPAA national policy. There
may be both civil and criminal sanctions for breaking HIPAA. Almost each medical professional
has the ability to violate HIPAA, making it a dangerous place to work. In the regular course of
work, employees with lower levels of education and comprehension can readily break these
norms. Most criminal infractions are temporary slips that lead to expensive errors. Creating and
maintaining systems that reduce human error is essential, as is HIPAA education and training.
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Disparities in clinical trial access between states can have serious ramifications and
effects, mainly resulting in healthcare access disparities for specific populations, possibly
impeding the creation of treatments that successfully meet the needs of various patient groups,
and aggravating pre-existing health inequities by restricting the applicability of research findings
to larger populations. Research by Bibbins-Domingo and Helman (2022) indicate that improved
representation in clinical trials could lead to even small reductions in health inequities, saving the
American people billions of dollars. Expanding this estimate to include more conditions such as
cancer, lowering the health discrepancy more thoroughly, or calculating over future cohorts
would only raise the potential benefits of improved representation.
Impact of the Code of Ethics
By encouraging open communication, teamwork among healthcare professionals,
patient-centered decision making, and a strong emphasis on advocating for patients' needs across
various healthcare settings, the Code of Ethics for Nurses has a significant impact on care
coordination and continuum, ultimately guaranteeing seamless transitions and consistently
high-quality care throughout the patient journey. According to Haddad and Geiger (2023), all
healthcare workers must sustain ethical principles. Ethical practice acts as a foundation since
nurses deal with ethical dilemmas on a daily basis. When nurses provide patient care, moral
dilemmas come up. These moral issues can occasionally clash with the Code of Ethics or the
personal ethical principles of the nurse. When delivering care, nurses must find a balance in their
role as patient advocates.
For the ACS, a variety of factors influence health, health disparities, and access to
services. These include socioeconomic factors like health insurance status, environmental
disadvantages, cultural factors, migration history, social structures and practices like poverty,
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implicit bias, and discriminatory behavior. Social determinants of health encompass a wide range
of systems and influences that influence day-to-day living. These include development
objectives, political systems, economic systems and policies, social norms, and social policies.
Healthy People (2020) identifies social determinants of health as aspects of the environments in
which individuals are born, live, learn, work, play, worship, and age that affect a range of health,
functional, and quality-of-life outcomes and hazards. According to Healthy People (2020),
important social determinants of health include social and community context, neighborhood and
physical environment, health and healthcare access, education, and financial stability. Certain
factors, such as employment, income, food security, access to high-quality education, housing
quality, community safety, and transportation, have a major impact on overall health outcomes.
Conclusion
In conclusion, the ACS, a community organization which was interested in learning about
ethical and policy concerns pertaining to care coordination, was discussed. This assessment
outlined the ways in which community safety and/or specific health-related government
regulations impacted care coordination. Discussed instances of particular laws, like HIPAA, that
have an impact on the ACS. National, state, and local policy measures that presented ethical
issues for care coordination were discovered by this review. Also mentioned the effects and
ramifications of particular policy clauses. This assessment evaluated how the nursing code of
ethics affected care coordination and continuity. Also discussed the variables that affect health,
access to services, and health inequities. This assessment utilized Healthy People (2020) list of
social determinants of health as a guide while doing this evaluation.
By focusing its work on four key pillars—advocacy, discovery, patient support, and
development—the ACS is enhancing the lives of cancer patients and their families. In essence,
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ethical and policy factors serve as a framework to ensure patients receive the best care while
upholding their autonomy and dignity. They do this by ensuring patient-centered decision
making, protecting patient rights, promoting quality care, and assisting healthcare providers in
navigating complex situations when coordinating care across various healthcare settings while
abiding by legal and moral standards. By offering a clear framework for decision-making,
preventing misconduct, promoting transparency, and ensuring that public officials act in the best
interests of the people rather than their own personal gain, government policies, policy
provisions, and an ACS code of ethics are essential for ensuring ethical governance.
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References
Bibbins-Domingo, K., & Helman, A. (2022, May 17). Why diverse representation in clinical
matters and the current state of representation within the clinical research ecosystem.
Improving Representation in Clinical Trials and Research - NCBI Bookshelf.
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Code of Ethics for Nurses. (2017, October 26). ANA.
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r-nurses/
Edemekong, P. F., Annamaraju, P., & Haydel, M. J. (2024, February 12). Health Insurance
Portability and Accountability Act. StatPearls - NCBI Bookshelf.
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Haddad, L. M., & Geiger, R. A. (2023, August 14). Nursing Ethical Considerations. StatPearls -
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Healthy People. (2020). Healthy People 2020 midcourse review. In Social Determinants of
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