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End Of Life Care Essay

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Recommended: Benefits and disadvantages of palliative care

Palliative care is an approach that focuses on providing relief and improving the quality of life of individuals with serious illnesses (Center to Advance Palliative Care, n.d.). It aims to relieve pain, manage symptoms, and provide emotional and spiritual support to patients and their families. When it comes to end-of-life care, palliative care can help patients and their loved ones navigate the difficult and often overwhelming experience of a terminal illness. It can provide comfort and dignity to patients, reduce stress for family members, and improve the overall quality of end-of-life care. According to the article by Ellen Rand “cancer patients who were randomly assigned to receive early palliative care versus standard medical care reported …show more content…

Hospice care is a type of palliative care that specifically focuses on providing care and support to individuals in the final stages of life. By coordinating the care with the family and a hospice program, terminally ill patients can achieve relief of pain and other unwanted symptoms, leading to a good quality of life during their remaining days (Lee 2002). Hospice care is often delivered in the patient's home, but can also be provided in a hospice facility or hospital. Hospice care is interdisciplinary, meaning that it involves a team of healthcare professionals, including doctors, nurses, social workers, and chaplains, who work together to provide holistic care to patients and their families. This approach emphasizes comfort and quality of life, rather than aggressive medical treatment, and can be a valuable option for individuals facing terminal …show more content…

However, as more people are living longer with chronic illnesses, the need for effective palliative care has become increasingly clear. Palliative care is an approach that focuses on improving the quality of life for patients with serious illnesses, by addressing their physical, emotional, and spiritual needs. According to a report by the World Health Organization (WHO), palliative care should be considered an essential component of healthcare for all patients with serious illnesses, not just those who are nearing the end of life (WHO,

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Recommendation-hospice to evaluate. Palliative care will continue to

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The time of life we call dying is an extremely difficult part of the life cycle, but a normal part," says palliative-care physician Ira Byock, author of Dying Well. "The nature of it isn't medical, it's experiential. " My grandfather had stage 4 lung cancer with metastatic to liver . Only palliative care advised by doctors. He was an strong personality .He loved all his grand kids too much.

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The services provided by Hospice are emotional support, medical services and spiritual resources for people who are in their last stage of a serious illness. Family members are not forgotten as services are provided to them for managing practical details and emotional challenges of caring for someone who is dying. The loved one that comes to Hospice is usually within the life expectancy of 6 months. BBH uses a team approach to provide professional services to provide individualized care to the client. The health care team includes attending physician, the registered nurse, hospice aides, social workers, the hospice chaplain, music therapist, trained volunteers and

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They areinvolved in providing palliative care,into a system of medical care that emphasizes palliation and psychosocial support of patients diagnosed with a life-limiting illness, through professional nursing or other therapeutic services, such as physical therapy, home health aides, nurse assistants, medical social work, nutritionist services, or personal care

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Training and Education: Policymakers should prioritize education and training programs for healthcare professionals and hospice care providers. These programs should focus on ensuring a clear understanding of policy updates, eligibility criteria, and the importance of regular reassessment of patients' prognoses. Improved knowledge and training will facilitate better decision-making and support for patients and their families (Stacey et al., 2020). V. Stakeholder Engagement: Policymakers should actively engage stakeholders, including healthcare professionals, patient advocacy groups, and hospice providers, in the policy review and revision process. Their expertise and perspectives are crucial in developing a policy that is responsive to the needs of patients and promotes high-quality end-of-life care.

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440 Words | 2 Pages

Hospice Isn’t Just for the Sick HospiceDirectory goes on to promote hospice’s commitment to improving overall quality of life, not only for terminally ill patients, but for everyone who surrounds them. Every quality hospice care facility knows that the involvement of friends and family members is an absolutely essential component of effective treatment and care. That’s why, in addition to looking after terminally ill patients directly, hospice serves caregivers http://auburncrest.com/services/what-is-hospice/ by training them in basic support functions and educating them about the intricacies of terminal care. Friends and family members can also access counseling to prepare them for the many losses they will face as illness progresses and bereavement care to help them cope with postmortem grief.

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1106 Words | 5 Pages

Hospice is the care for a person who is terminally ill, meaning without or maybe even with medical interventions they are facing their last months or even weeks of life. Hospice care means instead of trying to diagnose and cure the patient, we try to relieve pain and provide comfort. The definition of hospice is very holistic because it takes into consideration the emotional or spiritual aspects of our patients and not only their disease, it focuses on helping people die with dignity and respect. What's the difference between palliative care and hospice? Yeah, people confuse those often.

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When a patient is at the end of life it is very important to value the patients self dignity and their decisions at the mere end of their lives. The end of life care is to relieve the weight of the patient 's shoulders physically and mentally. I approve of end of life caring. Basic end of life care is summarized by improving the care of quality of life and dignity of the ill person. The important themes to good ethics of end of life care is a combination of human rights,respect,dignified care,and privacy.

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Our team works tirelessly to come up with a plan of care that will make a patient’s passing pain free. Hospice is not created to cure a disease, but to manage the symptoms of an illness and make life more pleasant for those approaching the end of their life and those who love them. As such, hospice is comfort-focused. It is created to address not only physical pain, but also focuses on the mental, emotional, spiritual needs of the patient and their loved ones. In essence, a hospice team is a group of professionals that walk alongside someone as they face death, or a patient’s loved ones as the patient approaches the end of their

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Hospice and palliative care can be easily intertwined; they are both concerned with promoting comfort and relieving patient pain. Hospice and palliative care, however, are different in some aspects. Patients who receive hospice care are nearing the end of their lives and there is no effort to cure their disease; the goal is to provide pain relief, a sense of belonging from family and friends if desired, support through the dying stages, and to assure that the person is able to die with dignity. Palliative care is also focused on reducing discomfort; however, the patient receiving care can be at any stage in their disease. Additionally, palliative care can also be administered during a time when a patient is receiving treatment to cure their illness.

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In all my experiences as a nurse, I’ve realized the importance of communication, providing holistic care to an individual and empowering them with the knowledge to manage their health. When an illness strikes a person, it affects not just his body, but also his mind and spirit. The art of communication is invaluable to patient interaction and establishing a therapeutic nurse-patient relationship, that facilitate coping mechanisms for patients, moreover it prepared myself as a nurse to meet their individual needs. Furthermore, there is at the moment an insurmountable demand for survivorship care as a result of the advancement in technology and medicine, which made living beyond life expectancy possible for increasingly more people. Living after cancer treatment is not free of complications as there are acute and chronic side effects of treatment that requires constant monitoring and attention, and this information spurred me to shift my focus from palliative to survivorship care.

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- The palliative care services should fully identify and support the cultural, linguistic and spiritual needs of care recipients and their families, including rituals and practices around death and dying. - Make sure the cultural and religious acceptability of certain treatments and medications. - Different people will have different views of the concept of quality of life, and that these may be culturally and religiously viewed - Clearly establish the role of family members in decision-making about care and treatment. - Resolve any conflicts around palliative care between staff and care recipients and/or family members by highlighting culturally aware concepts that are acceptable to all included - Give information about palliative care and support services in the preferred language of the patients and their families. - Ensure patients and their families have access to culturally appropriate emotional support and spiritual

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951 Words | 4 Pages

' Practitioner can play a role in improving the quality of life of a terminally-ill patient in both pharmacological aspects and non-pharmacological aspects. After all, what remains in a patient 's mind is the care and love given by practitioner, not the medical information. Something as simple as a warm-hearted pat on the shoulder or a word of assurance can enlighten their day. If we can treat every patient wholeheartedly, as if he/ she is our friend, it makes significant difference in patient life. Conclusion Hepler & Strand define pharmaceutical care as the responsible provision of medicine therapy for the purpose of improving a patient

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During the palliative stage of illness, pursuing full comfort measures is of greatest importance while providing care

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(2008) Preliminary report of a palliative care and case management project in an emergency department for chronically ill elderly patients. Journal of Urban Health, 85 (3), 443-51. Montefiore Medical Center created a program in their Emergency Department that identified chronically ill, elderly patients. They found that these patients were more likely to need palliative or home care, and later on hospice care. This preliminary report and case management pilot project made connecting patients to such services and ultimately allowing patients far more accessible options to these types of care.

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