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The Hastings Center guidelines for decisions on life-sustaining treatment and care near the end of life /

This new work updates and significantly expands The Hastings Center's 1987 Guidelines on the Termination of Life-Sustaining Treatment and Care of the Dying. Like its predecessor, this second edition will shape the ethical and legal framework for decision-making on treatment and end-of-life care...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Berlinger, Nancy
Autor Corporativo: Hastings Center
Otros Autores: Jennings, Bruce, 1949-, Wolf, Susan M.
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Oxford : Oxford University Press, [2013]
Edición:Revised and expanded second edition.
Temas:
Acceso en línea:Texto completo
Tabla de Contenidos:
  • The Function and Sources of These Ethics Guidelines
  • Legal and Ethical Consensus Informing These Guidelines: Rights, Protections, and Key Philosophical Distinctions.
  • pt. One. Framework and Context. Ethics Goals for Good Care When Patients Face Decisions about Life-Sustaining Treatment or Approach the End of Life
  • Section 2 Ethics Education Competencies for Health Care Professionals Caring for Patients Facing Decisions about Life-Sustaining Treatment or Approaching the End of Life
  • Section 3 Organizational Systems Supporting Good Care and Ethical Practice
  • Section 4 Social, Economic, and Legal Contexts
  • A. Social Context
  • B. Economic Context
  • C. State and Federal Context.
  • pt. Two Guidelines on Care Planning and Decision-Making. Section 1 Guidelines for Advance Care Planning and Advance Directives: Using Patient Preferences to Establish Goals of Care and Develop the Care Plan
  • Section 2 Guidelines for the Decision-Making Process
  • A. Evaluating the Patient
  • B. Determining Decision-Making Capacity
  • C. Identifying the Key Decision-Maker
  • D. Surrogate Decision-Making
  • E. Making the Decision at Hand
  • F. Documenting the Decision
  • G. Implementing the Decision
  • H. Changing Treatment Decisions
  • I. Conflicts and Challenges Related to Treatment Decision-Making.
  • Section 3. Guidelines Concerning Neonates, Infants, Children, and Adolescents. A. General Guidelines for Pediatric Decision-Making Concerning the Use of Life-Sustaining Treatments
  • B. Guidelines for Decision-Making and Care Involving Nonviable Neonates and Neonates at the Threshold of Viability
  • C. Guidelines for Decision-Making about Life-Sustaining Treatment for Viable Neonates
  • D. Guidelines for Decision-Making about Life-Sustaining Treatment for Young Children
  • E. Guidelines for Decision-Making with Older Children
  • F. Guidelines for Decision-Making with Adolescents
  • G. Guidelines for Decision-Making by Mature Minors and Emancipated Minors.
  • Section 4. Guidelines for Care Transitions. A. General Guidelines for Hand-Offs between Professionals and Transfers Across Care Settings
  • B. Guidelines on Care Transitions for Nursing Home Residents
  • C. Guidelines on Portable Medical Orders
  • D. Guidelines on Discharge Planning and Collaboration with Nursing Homes, Home Care, Hospice, and Outpatient Care
  • E. Guidelines on Care Transitions for Patients Who Will Die in the Hospital.
  • Section 5. Guidelines for the Determination of Death. A. Procedural Guidelines for Making a Determination of Death and for Making a Declaration of Death
  • B. The Determination of Death: Continuing Ethical Debates.
  • Section 6 Guidelines for Institutional Policy. A. Guidelines on Ethics Services in Institutions Providing Care for Patients Facing Decisions about Life-Sustaining Treatment on Approaching the End of Life
  • B. Guidelines on Palliative Care Services
  • C. Guidelines Supporting Advance Care Planning
  • D. Guidelines Supporting Portable Medical Orders
  • E. Guidelines Supporting Care Transitions
  • F. Guidelines on the Role of Institutional Legal Counsel and Risk Management in Supporting Good Care
  • G. Guidelines on Conflict Resolution.
  • pt. Three. Communication Supporting Decision-Making and Care. Section 1 Communication with Patients, Surrogates, and Loved Ones
  • A. Conducting a Family Conference When a Patient's Condition Is Deteriorating
  • B. Supporting the Decision-Maker When Loved Ones Disagree
  • C. Discussing Values Concerning Nutrition and Hydration
  • D. Using Electronic and Telephone Communications with Seriously Ill Patients or with Surrogates and Loved Ones.
  • Section 2. Communication and Collaboration with Patients with Disabilities. A. Life-Sustaining Treatments and Accommodation of Stable or Progressive Disabilities
  • B.Communication When a Patient's Disability Affects Speech
  • C.Communication When a Patient's Disability Affects Cognition
  • D.Communication and Collaboration with Recently Disabled Patients Concerning Life-Sustaining Treatments.
  • Section 3. Psychological Dimensions of Decision-Making about Life-Sustaining Treatment and Care Near the End of Life. A. Coping as a Factor in Treatment Decision-Making
  • B. Hope as a Factor in Treatment Decision-Making
  • C. Ambivalence, Denial, and Grief as Factors in Treatment Decision-Making
  • D. Existential Suffering as a Factor in Treatment Decision-Making
  • E. Spirituality and Religion as Factors in Treatment Decision-Making
  • F. Religious Objections During Treatment Decision-Making
  • G. Moral Distress as a Factor in Treatment Decision-Making
  • H. Integrating Bereavement Care for Loved Ones and Professionals into Care Near the End of Life.
  • Section 4. Decision-Making Concerning Specific Treatments and Technologies. A. Forgoing Life-Sustaining Treatments: Ethical and Practical Considerations for Clinicians
  • B. Brain Injuries and Neurological States
  • C. Mechanical Ventilation
  • D. Cardiopulmonary Resuscitation and Cardiac Treatments
  • E. Dialysis
  • F. Nutrition and Hydration
  • G. Chemotherapy and Other Cancer Treatments
  • H. Routine Medications, Antibiotics, and Invasive Procedures
  • I. Blood Transfusion and Blood Products
  • J. Palliative Sedation.
  • Section 5. Institutional Discussion Guide on Resource Allocation and the Cost of Care. A. Developing a Practice of Discussing Resource Allocation and the Cost of Care: Six Strategies
  • B. Discussing Uncompensated Care for Patients Without Insurance.