A Qualitative Study Essay

This essay’s primary focus is on Anthony Vella a 46-year-old man who was diagnosed with stage 4 pancreatic cancer six months ago. After being diagnosed with cancer, he underwent chemotherapy. However, his oncology team notified him two weeks ago stating that further chemotherapy was unlikely to be effective. Anthony has been married to Luisa for 20 years and decides to spend more time with his wife Luisa. However, after suffering from severe nausea and abdominal pain, Anthony was admitted to the oncology ward and a referral was made to the consultative palliative care team. A care plan was personalized for Anthony which focused on symptom control. Anthony’s symptoms were well managed by the team giving him the chance to return home and to spend

To identify the palliative care needs, the research presented the patients with the Short Form 36 (SF36), using the Hospital and Anxiety and Depression Questionnaire (HADS). The patients and significant others (n=35), were separated for the researcher to conduct an unstructured interview. Following the questionnaire, the multiprofessional clinical team conducted a focus group debate (n=18).

An American sex educator, birth control activist, author, and nurse, that’s who Margaret Sanger was. Sanger “created” the expression "birth control", established the first birth control clinic in the United States, and set up associations that later developed into the Planned Parenthood Federation of America. A fervent women's activist, human rights lobbyist, and supporter of sex-positivity, Sanger was additionally a eugenicist, trusting that anti-conception medication was at any rate as imperative an apparatus for restricting the generation of 'the unfit' as it was for women's freedom. Sanger concurred with numerous driving researchers and progressives of her day in attributing to purported Social Darwinism, a problematic term since it doesn't

Another disparity recognized is the standards of care from one palliative care or hospice care center to another. The varying degrees of care are due to lack of education and standards of care. The Center to Advance Palliative Care has recommendations for hospice and palliative care centers to measure and monitor care standards. These guidelines will help quantify data and allow for process improvement to occur among hospice and palliative care facilities. These improvements essentially allow for better education standards and improved standards of care within the hospice and palliative care centers. The most essential part of the paradigm that is palliative and hospice care is the patient. In the article, Is This Palliative care’s Moment,

It examined 266 patients died from cancer or caused related to cancer, but died for caused related to cancer was excluded. Therefore, there were only 265 patients fit the criteria (Amano et al., 2015). It measured the association between early referrals palliative care which means over three months before death and inpatient hospice utilization. This study also measured the relationship between the timing for referring hospice care toward the aggressive end of life care. In this study, researchers divided participants into two groups. The experimental group was for early referral palliative care and the control grout (Amano et al., 2015). The result of experimental group illustrated that the rate of inpatient hospice utilization was 74 percent which is significantly higher than the control group. Moreover, the statistic data displayed that there were no significant indicators for aggressiveness end-of-life care (Amano et al., 2015). In concluding, the early referrals palliative care would associate with more beneficial on inpatient hospice utilization and less aggressive end-of-life care (Amano et al.,

Proper medical care is needed by all individuals whether they are in good medical condition or not. People should not wait to develop serious medical conditions before visiting the medical centers. Most people live with condition without cure called “terminal illnesses. However, these people have the possibility to prolong their lives through the use of special medication called Palliative. On a Saturday morning, Nancy went to see her doctor because she wasn’t feeling well lately and she had a big lump on her chest, Dr.Sue gave her an assessment. After a few weeks, she received a letter in mail about her recent checkup. “You have a lump on your chest due to the cancer that has been developing”, was written in the letter, She was shocked and she felt horrible. Her daughter wedding is coming up in six months. She wants to spend as much time with her daughter and attend the wedding. However, she doesn’t want aggressive treatment, which would keep her away from home and be hospitalized. She wanted to look happy and healthy at least for her daughter 's wedding. She doesn’t want to go through chemotherapy either, because chemotherapy can have serious effects on her. She learned about palliative care. According to the Palliative Care Organization, Palliative care is a type of care relieves the patient from symptoms, pain and stress related to serious illnesses. According to Meier and McCormick “Palliative care aims to

This critique reviewed a quantitative study based upon palliative care and how it met emotional or spiritual needs of the families of patients with serious illnesses. The critique used eight criteria to analyze the quantitative study. The criteria include the identification of the problem, the determination of the purpose of the study, the review of the literature, the selection of the sample size and the research design, methods for collecting the data, the analysis of the data, study findings as well as the utilization of study findings.

According to the article by DiMartino at el. (2014), Cancer is considered the second leading cause of death in the United States and majority of patients that are diagnosed with cancer will die from these disease without receiving proper care, such as hospice. Some people in the United States and other places all over the world believe in a myth that says hospice speeds up a person’s death. But, without hospice patients may feel like they are a burden to their families and they would want to die sooner. However, through this research and six articles a reader can see that, “hospice provides extra time for the families and the patient to say their goodbyes, to seek out resolutions, and find the closure that the both parties need” (Connor et

The assignment prompt gives the impression that the student has a considerable amount of freedom in choosing the subject of their paper and also how to organize as long as they satisfy the requirements laid out in the prompt. The requirement of a 10-15 page paper implies that good writing in the psychology field (or the other social sciences) cannot just be simple statements but rather more in depth and nuanced analysis. The prompt also asks for hypotheses to be laid out in the paper, which function as the thesis. It also calls for datasets to be used, which means that a good psychology writing will have quantitative data that will be analyzed throughout the paper. The prompt also specifically notes that the APA style of citation should be used, and good writing in any social science subject should follow the commonly used method of referencing in that field or what the class or professor require.

According to the American Cancer Society in 2014 there is an estimated of 585,720 cancer deaths in the United States. Remaining in the second place of the most common cause of death in the country. Being diagnosed with terminal cancer changed any person life. The patient start suffering all kind of physical and psychological problems, related to the imminent death. During this period the doctor, the patient, and the family form an indispensable bond in order to help the terminal ill person to cope with the symptoms and complications the best possible way. However, this bond is usually broken in cases where one of the subjects decide to withhold information from another.

According to Allen et al. (2012), “millions of people with chronic illnesses endure unrelieved pain, uncontrolled physical symptoms and unresolved psychosocial or spiritual problems.” This issue occurs because palliative care is often considered a form of end-of-life care. Palliative care is a treatment that can be used for patients who suffer from chronic illnesses and diseases while receiving curative treatment. (Horowitz, Grambling & Quill, 2014) purposely states the misconceptions of palliative care and advocated for seriously ill patients that education must bring under control the misconceptions. Some patients do not receive appropriate symptom management because the palliative care treatment needed is often confused with end-of-life care. However, end-of-life care attempts to relieve pain and suffering when a disease is no longer responsive to curative treatment. Pain and suffering could ultimately be controlled or even eliminated through the proper utilization of palliative care. Patients who are not referred to palliative care in a timely manner is more likely to have poor quality of life, uncontrolled symptom management and increased amounts of visits to the emergency room during the disease process. Patients with life limiting illnesses bear the burden of increased discomfort and increased suffering. Nurses experience clinical practice issues and difficulties in the clinical setting during the delivery of comfort and symptom management. These issues

During the palliative care intake visit, the patient and family are questioned about advanced directives and life plans, setting the stage for further end of life discussions. Ideally, during the second and subsequent visits, the advanced care-planning process continues where the wishes, hopes, dreams, and desires of the patient begin to unfold. Within the registered nurse patient assessment are questions

“Palliative care is an approach that improves the quality of life of patients and their families facing the problem associated with life-threatening illness, through the prevention and relief of suffering by means of early identification and impeccable assessment and treatment of pain and other problems, physical, psychosocial and spiritual.” (who.int, 2014)

Patients with chronic or life-threatening illnesses may turn to palliative care for its symptom relieving benefits as well as its ability to improve their quality of life. A key factor in quality palliative care is effective communication between medical professionals and the patient as well as the patient’s caretakers. Pain management, continuity of care among caretakers and medical providers, and concentration on the patient’s personal preference are all major aspects of palliative care. Good palliative care should begin with a discussion on advanced care directives, preferably initiated by a physician. (Fine, et al. 595,

For some people, preparing for an unforeseen or eventual serious illness makes just as much sense as preparing for an eventual death event in their life or in the life of a loved one. As such, our article covers one growing trend in health care: palliative care.