Care of Patient and Family Flashcards
US Hospice founded?
Connecticut Hospice Florence Wald (former Dean of Yale Nursing School) early 1970s
US Hospice modeled after?
work of Dame Cicely Saunders at the St. Christopher’s hospice in London, England
Hospice developed to
address specific needs of the dying and their families
Hospice: medicare/medicaid benefit began?
1980s
Palliative care model branched off?
from traditional hospice programs in late 1980s in academic teaching hospitals such as Cleveland Clinic and Medical College of Wisconsin
Palliative focus: goal
address problems facing hospice philosophy in addressing long-term, progressive disease paths as well as in allowing patients a choice of hterapies
Palliative focus: effort
made to improve the quality-or-life concerns for those patients whose death was not near yet, a distinct and complicated set of care issues
Palliative: medicare/medicaid
not regulated or funded by Medicare
Common fears of dying patient
pain fear of being a burden fear of loss of control and independence death bodily changes
Fears of dying patient:pain
lingering and uncontrolled suffering relieving discomfort provides improved quality of life
Fears of dying patient: being a burden
family face tasks of dealing with own fears as well as increased responsibility for the patient that can be taxing and unwelcome by either party
Fears of dying patient: loss of control and independence
patients need to maintain a sense of control in decision-making in all areas of their life and care sense of control helps alleviate feelings of guilt, frustration and helplessness
Fears of dying patient: dying alone
ill persons often feel they will be abandoned
Fears of dying patient: death
facing the unknown. leaving loved one or “unfinished business”
Fears of dying patient: bodily changes
loss of body parts and changes to physique can be unnerving and shift the patient’s sense of self
National Consensus Project: 5 goals
Identify definitions, philosophies and principles create clinical ractice guidelines enable clinical practices to grow and improve provide key elements of palliative care promote quality recognition, initiatives, and stability
National Consensus Project: promote
quality recognition initiatives for growth and certification stability for reimbursement and practice measures
National Consensus Project: key elements of palliative care
that may be used in practices where there is an absence of formal care programs
National Consensus Project: enable clinical practices to
grow and improve their resources and performances through structural organization and defined requirements
National Consensus Project: create clinical practice guidelines for
high quality care for both the patient and family
National Consensus Project: identify
definitions philosophies principles concerning palliative care that will be nationally recognized
Palliative care: recognizes and respects
each individual’s uniqueness across the lifespan and in diverse settings
Palliative care:center
patient centered and guided in order to improve the patient’s quality of life through supportive care
Palliative care: is both
scientific humanistic