This document discusses how Leininger's Theory of Culture Care Diversity and Universality and humor therapy can be combined to improve outcomes for home health patients. It provides an overview of Leininger's theory, which focuses on preserving, accommodating, and restructuring a patient's cultural care based on their beliefs, values, and practices. It also describes humor therapy, its advantages of reducing stress and pain, and the need to ensure humor is culturally appropriate. The document presents a case study of a 72-year-old Irish-American man with leg ulcers who enjoyed British comedy and agreed to have humor therapy added to his wound care. His clinician incorporated humor therapy by playing comedy movies to distract from pain during treatment
This document discusses crisis, crisis intervention, and nursing management of crisis. It defines crisis as a state of disequilibrium caused by an event overwhelming an individual's coping abilities. There are three types of crisis: developmental, situational, and adventitious. Crisis intervention aims to reduce distress, help solve problems, and improve coping. Nursing management includes assessment, short-term counseling, referral to mental health services if needed, and helping the individual stabilize and prevent future crises. Therapeutic techniques focus on support, expression of feelings, and gaining understanding to facilitate recovery.
Crisis intervention aims to help individuals in crisis situations restore equilibrium and minimize long-term psychological trauma. A crisis is a state of disequilibrium caused by an event overwhelming a person's coping abilities. Crises can be developmental, social, or situational. Signs of crisis include stress, anxiety, depression, withdrawal, and substance abuse. Techniques of crisis intervention include catharsis, clarification, suggestion, reinforcement, supporting defenses, raising self-esteem, and exploring solutions. Effective crisis management can promote personal growth.
Lecture 21: Psychological issues at the end of life Dr.Reem AlSabahAHS_student
This document discusses psychological issues at the end of life from a holistic perspective. It addresses the physical, emotional, social, psychological, and spiritual needs and concerns of dying individuals. Regarding physical needs, it discusses pain management, body image, and finding meaning in illness. Emotionally, it explores common fears, loss/grief, and positive emotions. Socially, it addresses concerns for loved ones and communication patterns. Psychologically, it focuses on maintaining control and contributing to others. Spiritually, it examines religion/spirituality, meaning of life/death, and hope. The document also introduces palliative care and its role in improving quality of life compared to hospice care. Finally, it provides an overview
Narrative medicine as a tool to detect the burden of illness: an application to myelofibrosis. Progetto realizzato da ISTUD per Novartis. Presentazione di Maria Giulia Marini.
Hospice aims to treat the whole person rather than the disease and focus on quality of life over length of life. It provides comfort and dignity for patients dealing with terminal illness through physical, spiritual, and emotional support for patients and their families. There are several ethical issues around patient autonomy, access to care, and overcoming barriers for underserved groups. A lack of communication and cultural understanding can negatively impact minority groups' access and experience with hospice care. Additionally, over-reliance on technology risks losing personal interactions that are important for end-of-life care.
Palliative care aims to improve quality of life for patients facing life-limiting illnesses through comprehensive pain and symptom management as well as psychosocial and spiritual support. It can be provided alongside curative treatment or as the main focus of care. The goals are to prevent and relieve suffering through early identification of issues, addressing physical, psychological, social and spiritual needs using a multidisciplinary team approach. Palliative care strives to help patients and their families cope with illness and bereavement.
Dr. Elizabeth Paulk gives an excellent review of palliative care topics including end of life discussions, hospice, pain management, and family counseling.
This document discusses crisis, crisis intervention, and nursing management of crisis. It defines crisis as a state of disequilibrium caused by an event overwhelming an individual's coping abilities. There are three types of crisis: developmental, situational, and adventitious. Crisis intervention aims to reduce distress, help solve problems, and improve coping. Nursing management includes assessment, short-term counseling, referral to mental health services if needed, and helping the individual stabilize and prevent future crises. Therapeutic techniques focus on support, expression of feelings, and gaining understanding to facilitate recovery.
Crisis intervention aims to help individuals in crisis situations restore equilibrium and minimize long-term psychological trauma. A crisis is a state of disequilibrium caused by an event overwhelming a person's coping abilities. Crises can be developmental, social, or situational. Signs of crisis include stress, anxiety, depression, withdrawal, and substance abuse. Techniques of crisis intervention include catharsis, clarification, suggestion, reinforcement, supporting defenses, raising self-esteem, and exploring solutions. Effective crisis management can promote personal growth.
Lecture 21: Psychological issues at the end of life Dr.Reem AlSabahAHS_student
This document discusses psychological issues at the end of life from a holistic perspective. It addresses the physical, emotional, social, psychological, and spiritual needs and concerns of dying individuals. Regarding physical needs, it discusses pain management, body image, and finding meaning in illness. Emotionally, it explores common fears, loss/grief, and positive emotions. Socially, it addresses concerns for loved ones and communication patterns. Psychologically, it focuses on maintaining control and contributing to others. Spiritually, it examines religion/spirituality, meaning of life/death, and hope. The document also introduces palliative care and its role in improving quality of life compared to hospice care. Finally, it provides an overview
Narrative medicine as a tool to detect the burden of illness: an application to myelofibrosis. Progetto realizzato da ISTUD per Novartis. Presentazione di Maria Giulia Marini.
Hospice aims to treat the whole person rather than the disease and focus on quality of life over length of life. It provides comfort and dignity for patients dealing with terminal illness through physical, spiritual, and emotional support for patients and their families. There are several ethical issues around patient autonomy, access to care, and overcoming barriers for underserved groups. A lack of communication and cultural understanding can negatively impact minority groups' access and experience with hospice care. Additionally, over-reliance on technology risks losing personal interactions that are important for end-of-life care.
Palliative care aims to improve quality of life for patients facing life-limiting illnesses through comprehensive pain and symptom management as well as psychosocial and spiritual support. It can be provided alongside curative treatment or as the main focus of care. The goals are to prevent and relieve suffering through early identification of issues, addressing physical, psychological, social and spiritual needs using a multidisciplinary team approach. Palliative care strives to help patients and their families cope with illness and bereavement.
Dr. Elizabeth Paulk gives an excellent review of palliative care topics including end of life discussions, hospice, pain management, and family counseling.
This document discusses the relationship between personality, personality disorders, and responses to illness. It covers how personality is shaped by past experiences and biology, and influences how patients interact with their treatment team and cope with illness. Specific personality types like dependent clingers and entitled demanders are known to stir dislike in physicians due to their demanding behaviors. The document also discusses transference and countertransference between patients and care providers.
This document summarizes an article about using art therapy and in-home therapy to provide mental health support for Native Americans living with HIV/AIDS. Historical and personal trauma from events like genocide, forced relocation, and abuse have left this population distrustful of services and facing mental health issues. The Family & Child Guidance Clinic uses a Bowen family systems approach and integrates art therapy to address trauma, substance abuse, and isolation in a culturally-sensitive manner. In-home therapy was also introduced to engage isolated clients who were not accessing clinic services. The goal is to empower clients and help them manage mental health issues so they adhere to medical treatment for their HIV/AIDS.
This document discusses psychosocial care needs at the end of life. It begins with an introduction to palliative care, defining it as care that aims to relieve suffering for patients and families facing life-threatening illness. It then provides statistics on the aging population in India and discusses cultural factors relevant to end-of-life care in the Indian context. Finally, it examines mental health issues at the end of life and evidence-based psychosocial interventions, as well as the role of social work from an Indian perspective.
This document discusses how trauma experienced by individuals can be transmitted across generations and negatively impact entire communities. It defines trauma and explores theories of its transgenerational transfer. Experiencing or being exposed to unresolved trauma is linked to increased rates of family violence, substance abuse, mental health issues, and criminal behavior in subsequent generations. Government policies are also discussed as exacerbating trauma and community dysfunction in Indigenous communities in Australia. The transmission of historical trauma through cultural and family systems helps explain the phenomenon of "dysfunctional community syndrome" seen in some Indigenous communities with high levels of compounded, unresolved trauma.
The document discusses communication and decision making near the end of life. It provides statistics on hospital deaths and quality of end of life care in Canada. It emphasizes the importance of communication between physicians and patients, and outlines principles for discussions around end of life issues, including assessing understanding and goals, developing care plans, and providing closure.
This document discusses moving the NSW homelessness sector towards trauma-informed care. It notes that homeless populations experience high rates of trauma, especially women. Trauma-informed care focuses on safety, control, strengths and compassionate engagement through listening. Training teaches the impacts of trauma, complex trauma, and uses a neuroscience lens. It emphasizes relationship-building, predictability, stability and right-brain interactions over explicit trauma memory work. The goal is cultural change to better support consumers in a trauma-informed manner.
Crisis intervention is an immediate and short-term psychological care to restore equilibrium. I think this will be useful. This is very important topics in Advanced nursing practice and education too.
The document discusses physician burnout and argues that organizing toward collective action can help address burnout caused by feelings of powerlessness when treating patients facing socioeconomic hardships. It notes that while burnout is usually attributed to work overload and bureaucracy, its origins may also lie in caring for marginalized patients whose health issues stem from deep-rooted social problems beyond a physician's control. Organizing with others around such issues can combat isolation and empower physicians to enact meaningful change, providing a strategic and therapeutic approach to fighting burnout.
This document discusses crisis, its causes, phases, and resolution. It defines crisis as a state of disequilibrium caused by an event overwhelming an individual's coping abilities. Crises can be situational, developmental, trauma-related, or due to psychopathology. The phases of a crisis include increased anxiety, overwhelmed coping mechanisms, increased pressure, and potential psychotic symptoms if unresolved. Nurses play a key role in crisis resolution through assessment, diagnosis, planning, implementation, and evaluation to help clients return to pre-crisis functioning.
Crisis intervention is an immediate and short-term psychological care aimed at assisting individuals in a crisis situation in order to restore equilibrium to their bio-psycho-social functioning and to minimize the potential of long-term psychological trauma.
This document discusses palliative care and end-of-life care. It addresses how palliative care aims to improve quality of life for patients facing life-threatening illnesses through pain management and treatment of physical, psychosocial and spiritual problems. The document also discusses communicating with patients about end-of-life wishes, providing psychological and bereavement support for families, and ensuring patients have a peaceful death. The goal of palliative care is to never stop caring for patients, even when a cure is not possible.
This document discusses various aspects of end-of-life care including communicating bad news, managing symptoms, types of pain, loss and grief, components of a peaceful death, and postmortem care. It emphasizes the nurse's role in ensuring patients have a good death free from avoidable suffering by properly assessing and treating physical and psychological symptoms, respecting patient wishes, and supporting families through the dying process. The document provides guidance on steps to take when pronouncing death and caring for the deceased's body in a gentle, respectful manner.
This document provides information on the care of terminally ill and dying patients. It discusses concepts of loss, grief, and the grieving process. It describes the physical and psychosocial manifestations of approaching death. It outlines nursing care for dying patients, including meeting physical needs, providing spiritual support, and supporting families. Advanced care planning tools like living wills and healthcare proxies are explained. The document also covers post-mortem care including organ donation, medico-legal issues, autopsies, embalming, and physiological changes that occur after death.
‘Loss and Grief’: Emotional Experiences by Terminally Ill PatientsZulfiquer Ahmed Amin
A concept developed by Kubler Ross to identify the emotional responses of the terminally ill patients or their near relatives. Idea, is to adopt appropriate behavior to handle these sensitive situations.
The document summarizes the history of hospice care from its origins in the 11th century to modern developments. It traces the establishment of early hospice homes in the 19th century France, Ireland, and US focused on caring for the dying poor. The modern hospice movement began in the UK and US in the 1960s-70s led by pioneers like Cicely Saunders and Florence Wald who established principles of palliative care, education, and research. The Medicare hospice benefit in 1982 expanded access across the US. The philosophy of hospice is to relieve suffering and bring peace and dignity to the end of life.
The document discusses the nursing role in palliative care. It outlines that nurses coordinate treatment plans, manage symptoms, educate, and conduct research as part of a multidisciplinary team. The nursing role aims to relieve physical and mental suffering, maintain patient independence, and support families. Nurses provide holistic assessments of patients' physical, psychological, social, and spiritual needs and communicate regularly with families. Effective palliative nursing depends on open communication, addressing patient and family needs, and working as part of a collaborative team to improve patients' quality of life until death.
This document discusses crisis, crisis intervention, and the role of nurses. It defines crisis as a sudden event that disturbs one's homeostasis and usual coping mechanisms. Crises are personal, acute, and have potential for growth or deterioration. The document outlines phases of crisis and types according to Baldwin. It discusses balancing factors like perception, support, and coping that determine if a problem is resolved or becomes a crisis. Nursing roles include assessment, defining the event, developing an action plan, and helping individuals understand and cope with feelings to attain mastery over the crisis.
The document outlines 12 general principles of mental health nursing care:
1) Accept patients unconditionally for who they are without judgment.
2) Use self-understanding to better understand patients and avoid increasing their anxiety.
3) Provide consistent behavior to increase patients' emotional security through a quiet, accepting environment.
4) Reassure patients in an acceptable, empathetic manner by truly listening and agreeing with their problems.
The course of death and dying has changed tremendously in the past.docxarnoldmeredith47041
The passage discusses several key aspects of end-of-life care including palliative care, hospice care, communication about death and dying, and spiritual concerns. Palliative care focuses on comprehensive management of physical, psychological and spiritual distress to improve quality of life, while hospice care emphasizes comfort for dying individuals. Effective communication is important but challenging when discussing death, and social workers must address spiritual issues which often arise for patients facing end of life.
The course of death and dying has changed tremendously in the past.docxrtodd643
The course of death and dying has changed tremendously in the past few decades because of social and technological advances. Increases in average life expectancy due to advances in medical science and technology (National Center for Health Statistics, 2010) have influenced our beliefs and attitudes about life and death. The course of illness and dying has changed; at one time, the onset of illness and subsequent death from certain illnesses was sudden and rapid, but now the typical death may be more prolonged. The place where death occurs has moved from the home or community to the hospital, nursing home, or institutional setting. These changes have posed enormous challenges in end-of-life and palliative care.
PALLIATIVE CARE
Palliative care is an interdisciplinary care model that focuses on the comprehensive management of physical, psychological, and existential distress. It is defined as “the active total care of patients whose disease is not responsive to curative treatment.” Control of pain and other symptoms and psychological, social, and spiritual problems is paramount. “The goal of palliative care is the achievement of the best possible quality of life for patients and their families” (World Health Organization [WHO], 1990, p. 7). Palliative care aims to improve the patient's quality of life by identifying physical, psychosocial, and spiritual issues while managing pain and other distressing symptoms. Palliative care “affirms life and regards dying as a normal process; is applicable early in the course of illness, in conjunction with other therapies that are intended to prolong life, such as chemotherapy or radiation therapy, and uses a team approach to address the needs of patients and their families, including bereavement counselling, if indicated” (WHO, 2004, p. 3).
The palliative care model applies throughout the entire course of illness and attempts to address the physical, psychosocial, and spiritual concerns that affect both the quality of life and the quality of dying for patients with life-limiting illnesses at any phase of the disease. It includes interventions that are intended to maintain the quality of life of the patient and family. Although the focus intensifies at the end of life, the priority to provide comfort and attend to the patient's and family's psychosocial concerns remains important throughout the course of the illness. In the model's ideal implementation, patient and family values and decisions are respected, practical needs are addressed, psychosocial and spiritual distress are managed, and comfort care is provided as the individual nears the end of life.
Palliative medicine is the medical specialty dedicated to excellence in palliative care. Palliative care specialists, including social workers, typically work on teams and are involved when patients’ disease is advanced, their life expectancy is limited, and medical and psychosocial concerns become complex and more urgent. In practice, these problems ofte.
The document discusses optimizing palliative care and end of life care. It defines palliative care as an approach that improves quality of life for patients facing life-threatening illness through pain and symptom management and addressing psychosocial and spiritual needs. Palliative care aims to prevent and relieve suffering for the patient and support system. The document outlines the philosophy and principles of palliative care, who provides palliative care as an interdisciplinary team, common palliative interventions and services provided, and barriers to palliative care access.
This document discusses the relationship between personality, personality disorders, and responses to illness. It covers how personality is shaped by past experiences and biology, and influences how patients interact with their treatment team and cope with illness. Specific personality types like dependent clingers and entitled demanders are known to stir dislike in physicians due to their demanding behaviors. The document also discusses transference and countertransference between patients and care providers.
This document summarizes an article about using art therapy and in-home therapy to provide mental health support for Native Americans living with HIV/AIDS. Historical and personal trauma from events like genocide, forced relocation, and abuse have left this population distrustful of services and facing mental health issues. The Family & Child Guidance Clinic uses a Bowen family systems approach and integrates art therapy to address trauma, substance abuse, and isolation in a culturally-sensitive manner. In-home therapy was also introduced to engage isolated clients who were not accessing clinic services. The goal is to empower clients and help them manage mental health issues so they adhere to medical treatment for their HIV/AIDS.
This document discusses psychosocial care needs at the end of life. It begins with an introduction to palliative care, defining it as care that aims to relieve suffering for patients and families facing life-threatening illness. It then provides statistics on the aging population in India and discusses cultural factors relevant to end-of-life care in the Indian context. Finally, it examines mental health issues at the end of life and evidence-based psychosocial interventions, as well as the role of social work from an Indian perspective.
This document discusses how trauma experienced by individuals can be transmitted across generations and negatively impact entire communities. It defines trauma and explores theories of its transgenerational transfer. Experiencing or being exposed to unresolved trauma is linked to increased rates of family violence, substance abuse, mental health issues, and criminal behavior in subsequent generations. Government policies are also discussed as exacerbating trauma and community dysfunction in Indigenous communities in Australia. The transmission of historical trauma through cultural and family systems helps explain the phenomenon of "dysfunctional community syndrome" seen in some Indigenous communities with high levels of compounded, unresolved trauma.
The document discusses communication and decision making near the end of life. It provides statistics on hospital deaths and quality of end of life care in Canada. It emphasizes the importance of communication between physicians and patients, and outlines principles for discussions around end of life issues, including assessing understanding and goals, developing care plans, and providing closure.
This document discusses moving the NSW homelessness sector towards trauma-informed care. It notes that homeless populations experience high rates of trauma, especially women. Trauma-informed care focuses on safety, control, strengths and compassionate engagement through listening. Training teaches the impacts of trauma, complex trauma, and uses a neuroscience lens. It emphasizes relationship-building, predictability, stability and right-brain interactions over explicit trauma memory work. The goal is cultural change to better support consumers in a trauma-informed manner.
Crisis intervention is an immediate and short-term psychological care to restore equilibrium. I think this will be useful. This is very important topics in Advanced nursing practice and education too.
The document discusses physician burnout and argues that organizing toward collective action can help address burnout caused by feelings of powerlessness when treating patients facing socioeconomic hardships. It notes that while burnout is usually attributed to work overload and bureaucracy, its origins may also lie in caring for marginalized patients whose health issues stem from deep-rooted social problems beyond a physician's control. Organizing with others around such issues can combat isolation and empower physicians to enact meaningful change, providing a strategic and therapeutic approach to fighting burnout.
This document discusses crisis, its causes, phases, and resolution. It defines crisis as a state of disequilibrium caused by an event overwhelming an individual's coping abilities. Crises can be situational, developmental, trauma-related, or due to psychopathology. The phases of a crisis include increased anxiety, overwhelmed coping mechanisms, increased pressure, and potential psychotic symptoms if unresolved. Nurses play a key role in crisis resolution through assessment, diagnosis, planning, implementation, and evaluation to help clients return to pre-crisis functioning.
Crisis intervention is an immediate and short-term psychological care aimed at assisting individuals in a crisis situation in order to restore equilibrium to their bio-psycho-social functioning and to minimize the potential of long-term psychological trauma.
This document discusses palliative care and end-of-life care. It addresses how palliative care aims to improve quality of life for patients facing life-threatening illnesses through pain management and treatment of physical, psychosocial and spiritual problems. The document also discusses communicating with patients about end-of-life wishes, providing psychological and bereavement support for families, and ensuring patients have a peaceful death. The goal of palliative care is to never stop caring for patients, even when a cure is not possible.
This document discusses various aspects of end-of-life care including communicating bad news, managing symptoms, types of pain, loss and grief, components of a peaceful death, and postmortem care. It emphasizes the nurse's role in ensuring patients have a good death free from avoidable suffering by properly assessing and treating physical and psychological symptoms, respecting patient wishes, and supporting families through the dying process. The document provides guidance on steps to take when pronouncing death and caring for the deceased's body in a gentle, respectful manner.
This document provides information on the care of terminally ill and dying patients. It discusses concepts of loss, grief, and the grieving process. It describes the physical and psychosocial manifestations of approaching death. It outlines nursing care for dying patients, including meeting physical needs, providing spiritual support, and supporting families. Advanced care planning tools like living wills and healthcare proxies are explained. The document also covers post-mortem care including organ donation, medico-legal issues, autopsies, embalming, and physiological changes that occur after death.
‘Loss and Grief’: Emotional Experiences by Terminally Ill PatientsZulfiquer Ahmed Amin
A concept developed by Kubler Ross to identify the emotional responses of the terminally ill patients or their near relatives. Idea, is to adopt appropriate behavior to handle these sensitive situations.
The document summarizes the history of hospice care from its origins in the 11th century to modern developments. It traces the establishment of early hospice homes in the 19th century France, Ireland, and US focused on caring for the dying poor. The modern hospice movement began in the UK and US in the 1960s-70s led by pioneers like Cicely Saunders and Florence Wald who established principles of palliative care, education, and research. The Medicare hospice benefit in 1982 expanded access across the US. The philosophy of hospice is to relieve suffering and bring peace and dignity to the end of life.
The document discusses the nursing role in palliative care. It outlines that nurses coordinate treatment plans, manage symptoms, educate, and conduct research as part of a multidisciplinary team. The nursing role aims to relieve physical and mental suffering, maintain patient independence, and support families. Nurses provide holistic assessments of patients' physical, psychological, social, and spiritual needs and communicate regularly with families. Effective palliative nursing depends on open communication, addressing patient and family needs, and working as part of a collaborative team to improve patients' quality of life until death.
This document discusses crisis, crisis intervention, and the role of nurses. It defines crisis as a sudden event that disturbs one's homeostasis and usual coping mechanisms. Crises are personal, acute, and have potential for growth or deterioration. The document outlines phases of crisis and types according to Baldwin. It discusses balancing factors like perception, support, and coping that determine if a problem is resolved or becomes a crisis. Nursing roles include assessment, defining the event, developing an action plan, and helping individuals understand and cope with feelings to attain mastery over the crisis.
The document outlines 12 general principles of mental health nursing care:
1) Accept patients unconditionally for who they are without judgment.
2) Use self-understanding to better understand patients and avoid increasing their anxiety.
3) Provide consistent behavior to increase patients' emotional security through a quiet, accepting environment.
4) Reassure patients in an acceptable, empathetic manner by truly listening and agreeing with their problems.
The course of death and dying has changed tremendously in the past.docxarnoldmeredith47041
The passage discusses several key aspects of end-of-life care including palliative care, hospice care, communication about death and dying, and spiritual concerns. Palliative care focuses on comprehensive management of physical, psychological and spiritual distress to improve quality of life, while hospice care emphasizes comfort for dying individuals. Effective communication is important but challenging when discussing death, and social workers must address spiritual issues which often arise for patients facing end of life.
The course of death and dying has changed tremendously in the past.docxrtodd643
The course of death and dying has changed tremendously in the past few decades because of social and technological advances. Increases in average life expectancy due to advances in medical science and technology (National Center for Health Statistics, 2010) have influenced our beliefs and attitudes about life and death. The course of illness and dying has changed; at one time, the onset of illness and subsequent death from certain illnesses was sudden and rapid, but now the typical death may be more prolonged. The place where death occurs has moved from the home or community to the hospital, nursing home, or institutional setting. These changes have posed enormous challenges in end-of-life and palliative care.
PALLIATIVE CARE
Palliative care is an interdisciplinary care model that focuses on the comprehensive management of physical, psychological, and existential distress. It is defined as “the active total care of patients whose disease is not responsive to curative treatment.” Control of pain and other symptoms and psychological, social, and spiritual problems is paramount. “The goal of palliative care is the achievement of the best possible quality of life for patients and their families” (World Health Organization [WHO], 1990, p. 7). Palliative care aims to improve the patient's quality of life by identifying physical, psychosocial, and spiritual issues while managing pain and other distressing symptoms. Palliative care “affirms life and regards dying as a normal process; is applicable early in the course of illness, in conjunction with other therapies that are intended to prolong life, such as chemotherapy or radiation therapy, and uses a team approach to address the needs of patients and their families, including bereavement counselling, if indicated” (WHO, 2004, p. 3).
The palliative care model applies throughout the entire course of illness and attempts to address the physical, psychosocial, and spiritual concerns that affect both the quality of life and the quality of dying for patients with life-limiting illnesses at any phase of the disease. It includes interventions that are intended to maintain the quality of life of the patient and family. Although the focus intensifies at the end of life, the priority to provide comfort and attend to the patient's and family's psychosocial concerns remains important throughout the course of the illness. In the model's ideal implementation, patient and family values and decisions are respected, practical needs are addressed, psychosocial and spiritual distress are managed, and comfort care is provided as the individual nears the end of life.
Palliative medicine is the medical specialty dedicated to excellence in palliative care. Palliative care specialists, including social workers, typically work on teams and are involved when patients’ disease is advanced, their life expectancy is limited, and medical and psychosocial concerns become complex and more urgent. In practice, these problems ofte.
The document discusses optimizing palliative care and end of life care. It defines palliative care as an approach that improves quality of life for patients facing life-threatening illness through pain and symptom management and addressing psychosocial and spiritual needs. Palliative care aims to prevent and relieve suffering for the patient and support system. The document outlines the philosophy and principles of palliative care, who provides palliative care as an interdisciplinary team, common palliative interventions and services provided, and barriers to palliative care access.
Ethical, moral and legal issues in oncologyManali Solanki
The document discusses end of life care and ethics in oncology nursing. It defines end of life care as treating, comforting, and supporting those living with or dying from chronic life-threatening illnesses. It also discusses the importance of communication, education, and addressing spiritual-psychosocial needs of dying patients and their families. The document outlines several ethical issues that may arise in end of life care, such as medical futility, terminal sedation, euthanasia, physician assisted suicide and advocates respecting patient autonomy.
This document provides information on transcultural nursing concepts and models. It discusses Madeleine Leininger's theory of transcultural nursing, which introduced the concepts of cultural care preservation, accommodation, and repatterning. It also describes Joyce Geiger and Ruth Davidhizer's transcultural assessment model, which identifies six cultural phenomena to assess: communication, space, social organization, time, environmental control, and biological variations. Finally, it examines cultural values and care meanings and actions for several cultures including Anglo-American, Mexican American, Haitian American, African American, and North American Indian cultures.
How useful are advance directives in directing end of life care and do people really understand or want to know the true status of their health as the end nears?
This document provides an overview of the history and foundations of psychiatric mental health nursing. It discusses definitions of mental health and mental illness from organizations like the WHO and APA. The Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR) is introduced as the taxonomy used by mental health professionals for diagnosis. The development of institutions and community mental health in response to developments like psychopharmacology is summarized. Current issues like the high prevalence of mental illness and limitations of treatment access are also outlined.
The document provides an overview of the history of mental health nursing and psychiatric care. It discusses how views of mental illness have changed over time from seeing it as demonic possession to the current biopsychosocial understanding. It outlines factors that influence mental health and illness, including individual, interpersonal, and social factors. The principles of psychiatric nursing are described, such as acceptance, understanding, respect, reassurance, and avoiding unnecessary anxiety. The development of the field of psychiatric nursing is also summarized, from the first trained nurses in the 1800s to the establishment of standards of care.
Professional practice level 4 assignment finalDave Manriquez
This document discusses ethical decision making and cultural considerations in healthcare using the case of a Korean patient, Mr. K.S. It notes that in Korean culture, the family does not want the patient to know their diagnosis due to beliefs that it could negatively impact their health. It analyzes this case using the CLPNBC Professional Standards and identifies both issues like lack of informed consent and potential solutions like providing interpreter services to overcome language and cultural barriers in patient care.
This document describes a study that examined differences in distress levels in children undergoing venipuncture when assigned to different treatment groups involving positioning and distraction interventions. It found that children positioned supine without distraction had higher distress scores than other groups based on self-report, physiological measurements, and behavioral observations. Gender, age, and temperament also impacted pain response. The majority of subjects were admitted for outpatient radiological procedures under sedation.
The document provides an introduction to palliative care and a holistic approach. It defines palliative care according to the WHO as improving quality of life for patients facing life-threatening illness through preventing and relieving suffering. Key principles of palliative care discussed include taking a holistic, patient-centered approach and using a multidisciplinary team. Factors affecting provision of palliative care and strategies for improving services are also outlined.
This document discusses the importance of culture in health and healthcare. It begins with an introduction to anthropology and definitions of culture. It then explores how culture shapes views of health, illness, and healers. Various cultural practices that impact health are described, such as hot-cold beliefs, susto, and female genital mutilation. The PEN-3 model for developing culturally-competent health interventions is introduced. Case studies demonstrate how understanding cultural contexts can improve care. The document recommends training healthcare workers in cultural competence and centering culture in approaches to well-being.
This document discusses perspectives on mental health from different cultures and societies. It begins by defining perspective and examining how people can hold multiple, sometimes contradictory beliefs about mental illness. It then explores how perspectives vary between psychiatrists, physicians, and public health specialists based on their disciplines. The document also defines stigma and discrimination related to mental illness, and how cultural and religious teachings can influence beliefs about the causes and nature of mental illness. Finally, it reviews how attitudes toward mental illness differ among individuals, families, ethnicities, cultures and countries.
The document discusses palliative care, which aims to improve quality of life for patients facing life-threatening illness. It defines palliative care according to the WHO as preventing and relieving suffering through early assessment and treatment of pain and other problems. Palliative care is applicable early on and provides relief from symptoms, affirms life, and offers support for patients and their families coping with illness and bereavement. Common symptoms in advanced cancer patients and effective palliative care approaches are described.
Module 4.1 - Discussion
Applying Nursing Theory
Instructions:
Select one (1) of the following scenarios related to a specific nursing. Think about what you would do in the scenario presented and post your ideas.
Post two (2) discussion questions based on the readings along with your answers.
TheoristScenarioFlorence
Nightengale
Using Nightengale’s concepts of
ventilation
,
light
,
noise
, and
cleanliness
, analyze the setting in which you are practicing nursing (working as an employee or student).
Using Nightengale’s theory, evaluate the nursing interventions you have identified for an individual patient in your facility or practice.
OR
Your hospital patient is an 82 year-old woman. She does not have immediate family and has been living alone in her own home. Her hospitalization was unanticipated; it followed a visit to the emergency room for a burn on her lower leg. The patient has been hospitalized for 14 days. She pleads with you to allow her friend to bring her dog, a 16-year-old Scotty Terrier, to the hospital. She tells you that none of the other nurses have listened to her when she asked them about such a visit. Based on Nightingale’s model, and 13 cannon,
what actions would you take for this patient?
Betty Neuman
Martina is a middle-aged Hispanic woman who brings her family to a local free clinic to obtain medical care. She works part time in a restaurant for minimum wage. She lives in a small apartment with her daughter and four preschool children; her daughter speaks only very broken English. Martina’s medical diagnoses are hypertension, arthritis, and depression.
Use the Neuman System Model as a
conceptual framework
to respond to the following:
Describe the family as a system.
How does the dominant Anglo culture impact on the family’s stability as a system?
What stressors (actual and potential) threaten the family?
What additional assessment data are needed related to Martina’s medical diagnoses?
What additional assessment data are needed related to the family’s health status?
How will cultural differences influence planning for prevention as intervention at primary, secondary, and tertiary levels?
OR
Using the Neuman System Model, organize a patient care conference in your workplace to deal with a patient situation that has been difficult to manage. Involve caregivers from nursing and at least one other disicpline to discuss each of the following:
What factors comprise the patient's normal and flexible lines of defense and lines of resistance?
What stressors are causing the problems with this patitent? What is the patient's reaction to the stressor? What is each discipline's perspective on the problem or isssues that are involved?
How is the situation influenced by the patient's family system? By the patient's environment?
What would be the ideal coutocme in this situation from each discipline's perspective? From the patient's perspective?
What goals would be appropariat.
Ethics in Pandemics - Basic Principles and Advanced Planning.pptxMike Aref
The document discusses ethics considerations during pandemics and public health emergencies. It begins with a brief history of pandemics and infectious diseases. It then covers various bioethical frameworks and methods of analysis that can be applied to challenges that arise, including principlism, narrative ethics, and casuistry. The document also discusses the differences between clinical ethics and public health ethics. It uses several case examples to demonstrate how different bioethical approaches could be applied to issues like visitor restrictions, goals of care conversations, changing PPE recommendations, and resource allocation. Throughout, it emphasizes the importance of transparency, inclusion, reasonableness and revisiting decisions as more information becomes available.
Presentation on Health and Medicine (sociology)Koushik Ahmed
This document contains information about 5 employees - Koushik Ahmed, Tusar Modak, Rezwan Ahmed, Shuvajit Banik, and Maftab Ahmed - and their working sections (A, B, C, D, and E). It then provides summaries on various topics related to health, medicine, sociology, healthcare, mental illness, and environmental issues. The sections cover perspectives like functionalist, conflict, interactionist, and labeling approaches as well as concepts such as social epidemiology, social class, race, gender, age, patterns of care, pollution, global warming, and sociological views of the environment.
Presentation on Health and Medicine (sociology)Koushik Ahmed
This document contains information about 5 employees - Koushik Ahmed, Tusar Modak, Rezwan Ahmed, Shuvajit Banik, and Maftab Ahmed - and their working sections (A, B, C, D, and E). It then provides summaries on various topics related to health, medicine, sociology, healthcare, mental illness, and environmental issues. The sections cover perspectives like functionalist, conflict, interactionist, and labeling approaches as well as concepts such as social epidemiology, social class, race, gender, age, patterns of care, pollution, global warming, and sociological views of the environment.
This document provides an overview of palliative care, including its definition, goals, scope, principles, and models. Palliative care aims to relieve suffering and improve quality of life for patients facing serious illnesses. It focuses on addressing physical, psychological, social, and spiritual needs through a holistic, team-based approach. While still limited in availability worldwide, palliative care services are expanding, especially to address needs for chronic disease management in addition to cancer care.
Similar to Laughter, leininger, and home healthcare (20)
Cell Therapy Expansion and Challenges in Autoimmune DiseaseHealth Advances
There is increasing confidence that cell therapies will soon play a role in the treatment of autoimmune disorders, but the extent of this impact remains to be seen. Early readouts on autologous CAR-Ts in lupus are encouraging, but manufacturing and cost limitations are likely to restrict access to highly refractory patients. Allogeneic CAR-Ts have the potential to broaden access to earlier lines of treatment due to their inherent cost benefits, however they will need to demonstrate comparable or improved efficacy to established modalities.
In addition to infrastructure and capacity constraints, CAR-Ts face a very different risk-benefit dynamic in autoimmune compared to oncology, highlighting the need for tolerable therapies with low adverse event risk. CAR-NK and Treg-based therapies are also being developed in certain autoimmune disorders and may demonstrate favorable safety profiles. Several novel non-cell therapies such as bispecific antibodies, nanobodies, and RNAi drugs, may also offer future alternative competitive solutions with variable value propositions.
Widespread adoption of cell therapies will not only require strong efficacy and safety data, but also adapted pricing and access strategies. At oncology-based price points, CAR-Ts are unlikely to achieve broad market access in autoimmune disorders, with eligible patient populations that are potentially orders of magnitude greater than the number of currently addressable cancer patients. Developers have made strides towards reducing cell therapy COGS while improving manufacturing efficiency, but payors will inevitably restrict access until more sustainable pricing is achieved.
Despite these headwinds, industry leaders and investors remain confident that cell therapies are poised to address significant unmet need in patients suffering from autoimmune disorders. However, the extent of this impact on the treatment landscape remains to be seen, as the industry rapidly approaches an inflection point.
Mercurius is named after the roman god mercurius, the god of trade and science. The planet mercurius is named after the same god. Mercurius is sometimes called hydrargyrum, means ‘watery silver’. Its shine and colour are very similar to silver, but mercury is a fluid at room temperatures. The name quick silver is a translation of hydrargyrum, where the word quick describes its tendency to scatter away in all directions.
The droplets have a tendency to conglomerate to one big mass, but on being shaken they fall apart into countless little droplets again. It is used to ignite explosives, like mercury fulminate, the explosive character is one of its general themes.
Travel vaccination in Manchester offers comprehensive immunization services for individuals planning international trips. Expert healthcare providers administer vaccines tailored to your destination, ensuring you stay protected against various diseases. Conveniently located clinics and flexible appointment options make it easy to get the necessary shots before your journey. Stay healthy and travel with confidence by getting vaccinated in Manchester. Visit us: www.nxhealthcare.co.uk
5-hydroxytryptamine or 5-HT or Serotonin is a neurotransmitter that serves a range of roles in the human body. It is sometimes referred to as the happy chemical since it promotes overall well-being and happiness.
It is mostly found in the brain, intestines, and blood platelets.
5-HT is utilised to transport messages between nerve cells, is known to be involved in smooth muscle contraction, and adds to overall well-being and pleasure, among other benefits. 5-HT regulates the body's sleep-wake cycles and internal clock by acting as a precursor to melatonin.
It is hypothesised to regulate hunger, emotions, motor, cognitive, and autonomic processes.
DECLARATION OF HELSINKI - History and principlesanaghabharat01
This SlideShare presentation provides a comprehensive overview of the Declaration of Helsinki, a foundational document outlining ethical guidelines for conducting medical research involving human subjects.
The skin is the largest organ and its health plays a vital role among the other sense organs. The skin concerns like acne breakout, psoriasis, or anything similar along the lines, finding a qualified and experienced dermatologist becomes paramount.
8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptxHolistified Wellness
We’re talking about Vedic Meditation, a form of meditation that has been around for at least 5,000 years. Back then, the people who lived in the Indus Valley, now known as India and Pakistan, practised meditation as a fundamental part of daily life. This knowledge that has given us yoga and Ayurveda, was known as Veda, hence the name Vedic. And though there are some written records, the practice has been passed down verbally from generation to generation.