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Pain Management In Palliative Care

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Recommended: 3. Literature review palliative care

Pain is a subjective and unique experience that varies from person to person. It also varies according to cause and circumstance. Pain can stem from damage to skin, muscles, organs and bones; it can have emotional and psychological triggers. It is reasonable to anticipate that because pain can have a wide array of origins and interpretations, the treatment of pain needs to be as distinct as the experience of the patient. This is especially significant during end of life care. Providing palliative care, “care designed to give the patient as pain-free a condition as possible, from textbook” has innumerable benefits for the dying patient and their loved ones. It is important to acknowledge the benefits of pain management during palliative care, as well as the potential barriers to providing sufficient pain relief, in order for healthcare providers to provide the best and most personalized care for their patients. The World Health Organization (WHO) identifies the following as a few of the aspects of palliative care: it supports dying as a normal process, provides patients a way to …show more content…

The majority of patients receiving palliative care have some level of moderate to severe pain that needs to be addressed in order for comfort to be achieved. Pain causes distress and anxiety for patients, family members and other caregivers, making it a vital aspect of care. In order for health care professionals to offer comprehensive pain relief, they must accurately assess a patient’s pain, provide pharmacologic and non-pharmacologic measures to combat pain, educate patients on any medication concerns, and perform a self-assessment regarding their own pain-related beliefs. It is through these actions that nurses will bring their patients reprieve from immense discomfort and pain, help to ease anxiety and fear, help to bring about acceptance of the disease process, and promote the ideal nurse patient

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SDLA 4: Activity 1 Palliative care continues to evolve in providing better end-of-life care and so does nursing care. Thus, nursing practice is enhanced to satisfy the demand of the palliative care. A nurse provides complex care and fulfils the needs of the patients. Nursing involves in caring work, which focus on patient experiencing agony in palliative and haematological cancer care. Nurses worked in a taxing environment, that can be highly stressful, and often they experience physical, psychological and spiritual exhaustion.

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642 Words | 3 Pages

The ethical principle of autonomy provides for respect for the patient’s autonomy to make decisions and choices concerning their life and death. Respecting the patient’s autonomy goes against the principles of beneficence and non-maleficence. There also exists the issue of religious beliefs the patient, family, or the caretaker holds, with which the caretaker has to grapple. The caretaker thus faces issues of fidelity to patient welfare by not abandoning the patient or their family, compassionate provision of pain relief methods, and the moral precept to neither hasten death nor prolong life.

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279 Words | 2 Pages

Palliative care is a form of care for people with serious illnesses that is primarily focused on giving relief to ill patients and to improve quality of life and well-being. Hospice care is similar to palliative care because it helps patients to improve their quality of life through caring for them, not curing them. In contrast, palliative care can be implemented at any point after a patient is diagnosed with an illness, however hospice care has specific qualifications and is used when a patient only has 6 months to live. Palliative and hospice care location can both be administered at a patient’s home. Although palliative care is usually taken place in a hospital or facility of care and hospice care usually doesn’t narrow down to a specific

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258 Words | 2 Pages

However, we do recognize patient’s rights to refuse medications and other life-saving or prolonging treatments. So it is very important that we, as nurse, understand our legal rights on ethical issues such as the difference between assisted suicide and palliative care. Palliative care focuses on providing patients with relief from the symptoms and stress of their illness

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978 Words | 4 Pages

Using Lewin’s Framework for Change Model, in the change framework, an EOL caregiver survey was created to establish comfort before and after a patient’s death. This survey incorporated “I” statements with a scoring of zero to four (not at all-very much). Two parts of this study involve both comfort levels with pharmacological and non-pharmacological methods of treating pain as well as advanced care planning (Corcoran, 2016). These statements incorporate the NHPCO standards of quality in palliative care. As a nurse working within this program, I would utilize this survey for students to use in examining their feelings and doubts regarding end of life issues.

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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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Although it may seem easier to the family to push the analgesia for the patient, they must be reminded that the patient is the only one who can truly determine the type and feeling of pain they are experiencing and then have the authority to decide if they need additional medication or

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541 Words | 3 Pages

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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1013 Words | 5 Pages

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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' 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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The World Health Organisation (WHO, 2017) revealed that palliative care is an approach for improving the quality of life of patients experiencing LTCs and life-threatening illness and provide holistic care. In the light of other definitions, palliative care might also be considered as an approach for preventing and suppressing suffering by early identification, appropriate assessment, and treatment of pain and other symptoms (Baldwin & Woodhouse, 2011). Welsh Government (WG, 2013) acknowledges that palliative care covers diversified aspects of palliative care and end of life care. This plan includes the expert palliative care services which are delivered by the National Health Services (NHS).

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1139 Words | 5 Pages

Taken from a denotative point of view, pain is the experience when someone is uncomfortable and in grief, the physical discomfort might be caused due to external pressure, which is an injurious act or a malfunction in their physiological body mechanism. The meaning of this term can accordingly be taken in three alternate perspectives which could either suggest enduring, distress or torment in the ideal setting. However, in a subjective viewpoint, the term can be interpreted emotionally to imply a situation where someone is psychologically affected by their physical state. Although the use of the word pain generally finds its relevance to the physical act of uneasiness, it could also be used to involve someone being in an oppressed condition

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1731 Words | 7 Pages

Introduction With reference to the question posed, it has been suggested that euthanasia may be defined as “the act of intentionally causing the painless death of a sick person”. In other words, it bears the meaning of a “painless, happy or good death” as derived from the ancient Greek language – “eu”, meaning good; and “thanatos”, meaning death. Due to the rapid advancements in medical treatments, patients are capable of being kept “alive” for indefinite periods of time. Hence, in order to distinguish the ancient concept of allowing a patient to die and neglecting them treatment, the medical community has encompassed the idea of drawing a line between active euthanasia and passive euthanasia .

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1149 Words | 5 Pages

Palliative care Palliative care is care given to improve the quality of life of patients who have a serious or life-threatening disease, such as cancer. The goal of palliative care is to prevent or treat, as early as possible, the symptoms and side effects of the disease and its treatment, in addition to the related psychological, social, and spiritual problems. The goal is not to cure. Palliative care is also called comfort care, supportive care, and symptom management. Palliative care used in cancer Palliative care is given throughout a patient’s experience with cancer.

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