Abstract
Abstract
End-of-life care is not just a medical treatment, but can be the turning point in someone’s life to end unnecessary suffering and honor their wishes to have quality over quantity in life. This paper will discuss end-of-life care from the perspectives of patient autonomy, communication, ethical decision making, and system influences. It will explore the impact of honoring patient preference. Not to mention how speaking honestly and compassionately may affect enhancing the quality of life of patients experiencing terminal or life-limiting illnesses.
One of the key aspects of this paper is the significance of communication in end-of-life care. Specifically, in relation to prognosis, treatment options, advance directives, and goals of care from the patient and family perspectives. Patients are more likely to feel respected and that they have the final say, and families experience less emotional distress and conflict. It will also consider how cultural and religious beliefs, along with how family dynamics affect perspectives concerning death and what is considered appropriate care. Along with emphasizing how culturally sensitive and individually based care is necessary to help people with such issues.
Ethical issues are a crucial aspect of this paper. Concerns about withholding or withdrawing life-sustaining treatment, the use of interventions near the end of life, and the disagreement between the patient's own preferences and those of the health care personnel. Such ethical challenges are hard on the heart for both sides, and ethical guidelines and interprofessional collaboration are necessary to shape their decisions of care for the patient.
This paper extends by exploring the effects of end-of-life care on family caregivers and healthcare care providers. Caregiver burden, emotional overload, grief, despair, and moral distress are considered essential, but frequently overlooked, elements of the end-of-life experience for caregivers. It will explore policy issues such as access to hospice and palliative care services, legal considerations surrounding advance directives, and imbalances in end-of-life care.
It will conclude that quality end-of-life care is best achieved with an integrated healthcare approach that extends beyond medical intervention. Integrating emotional, ethical, cultural, and systemic factors. Emphasizing how end-of-life care is geared towards respecting the patient’s autonomy and honoring their wishes. Making their final moments as painless and comfortable as possible.
Year Manuscript Completed
Spring 2026
Senior Project Advisor
George Barton
Degree Awarded
Bachelor of Integrated Studies Degree
Field of Study
Health Care Administration
Document Type
Thesis
Recommended Citation
Courtney, Alexis N., "Patient-Centered End-of-Life Care: Balancing Ethics, Communication, and Quality of Life" (2026). Integrated Studies. 737.
https://digitalcommons.murraystate.edu/bis437/737