End-Of-Life Care Essay

Palliative Care: Helping Patients Live Better Lives and Die Better Deaths Executive Summary People today are living longer than their forebears. By 2030, an estimated 72 million people of the U.S. population will be older than 65 years old and an estimated 9 million people will be older than 85 years old (Heinle, McNulty, & Hebert, 2014). Most adults will live with at least one chronic illness until they die (Heinle et al., 2014). Palliative care (PC) is specialized care that ensures that patients

End of Life Care – Immune Systems as You Age. According to the National Library of Medicine, an individual's immune system slows down with age. Since the purpose of the immune system is to protect the body from harmful substances such as bacteria, viruses, cancer cells, and so forth. When the immune system is compromised, it cannot protect the body the same way it did when it was at full strength. Because the immune system slows down with age, seniors are at higher risk for illness and disease

frequently care for dying patients. Instead of simply providing medication to ease pain during the dying process, I wanted to learn about ways to enhance the comfort of the dying patients and possibly assist their family during a difficult time. This desire led me to examine the conceptual model of comfort. Through my research of the concept of comfort care at end of life, I discovered Katherine Kolcaba’s theory of comfort. I found her theory to be useful in describing the concept of comfort care and decided

HIV Patients and Case Managers during End of Life Experience Jennifer R. Molestina Albizu University April 2015 Abstract As researchers develop more and more treatments for HIV that improve patients ' quality of living and extend their lives, it is necessary to remember the importance of pain control, symptom management, excellent communication, and psychosocial support from time of diagnosis to time of death. Case managers must remember the fact (and prepare themselves accordingly) that

As the role of pharmacists in patient care continues to grow, the ethical challenges they face every day also increases. After the discussion with my preceptor about ethical situations that a pharmacist can experience, we decided to explore further about the controversial topic of end of life care, specifically avoidance of killing. Each of us can agree that killing a person is unethical. The word “killing” itself carries a negative message, it is morally wrong. The ethics principle nonmaleficence

INTERPROFFESIONAL PALLIATIVE CARE OF AN ALS PATIENT 1 INTERPROFESSIONAL PALLIATIVE CARE OF AN ALS PATIENT 6 Interprofessional Palliative Care of An Als Patient Students Name Institution Affiliation Needs and Inter-Professional Plan In its early stages, ALS usually has symptoms of muscle wasting and mild weakness which spread gradually in the body. Tim Simmons diagnosed with ALS 2 years ago, after which he retired to pursue his activities of interest. ALS life expectancy is usually

contribution to the care of an elderly gentleman, nursed in his own home living with his wife who provided him with nursing care between his private carer visits. The gentleman was also receiving care from a private agency and had district nurse involvement, as his condition worsened he had been referred by his doctor to a specialist palliative care team who assessed the patient and put him on the Liverpool Care Pathway (LCP). The LPC is a best-practice model of care, supporting care in the last hours/days

When Mr. David Lawrence died from cancer, his daughter and son were shattered, but his wife was completely devastated. All of the people that he had impacted in his life came to grieve and show their support for the family. The family was extremely close and easy going. His daughter, Hanna, even though she had moved out of the house and become independent, still frequently came over for dinner and spent time with her family. Being very active in groups and clubs, her brother, Anthony was always

no cure. These people tend to be heavy users of health care resources, accounting for at least 50 per cent of all general practitioner (GP) appointments, 64 per cent of outpatient appointments and 70 per cent of all inpatient bed days (Department of Health 2012a). Special analysis of ‘Social Care at the End of Life’ project data indicates that an estimated 18 per cent of people with long-term conditions are in receipt of state-funded social care (T Georghiou,

(Elder, Ayala, Parra-Medina, & Talavera, 2009). Due to these various issues navigating the health care system can prove difficult especially when it comes to the end of life care, it is prevalent in the Mexican culture for the elderly to be taken care of by their younger family members such as their children. However, if they have a major illness or the family simply don’t have the ability to take care of them anymore