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Biomedical subjects

S R Connor

Publications and source records attributed to S R Connor.

6 recordsLinked to original sources

History of the National Hospice Organization.

The National Hospice Organization grew out of efforts by the founders of the earliest hospice programs in the United States to protect their emotional investments in hospice care, to advocate for hospice interests in Congress and other public policy forums, to define standards for the fledgling movement, and to provide education on the nuts and bolts of running hospice programs for others who were interested in starting hospices in communities from coast to coast. Unlike the model of St. Christopher's Hospice in England, which began as a free-standing in-patient facility and later added home care services, most U.S. hospices started as home care-based programs, often largely manned by volunteers. Among the crucial issues that have dominated the work of NHO during its first 21 years were passage and maintenance of the Medicare hospice benefit, ideological battles over the hospice philosophy, and efforts to extend hospice care to other populations, such as people with AIDS.

Foundations↗

New initiatives transforming hospice care.

Hospice care has been successful in serving a large segment of the terminally ill population in the United States. This article addresses a number of significant trends that may impact the future of hospice care. It is proposed that as many as one-third of those who die will not be in a position to make use of any end-stage program of care. Of the remaining, some will have difficulty being served by hospices due to uncertain prognosis and continued efforts at curative treatment. New models of caring for chronically terminally ill persons are being developed and are reviewed. A clearer definition of who ought to be served by hospice programs is encouraged.

Chronic Disease↗

Denial in terminal illness: to intervene or not to intervene.

This research examined effects of psychosocial intervention on denial-related coping ability in terminally ill cancer patients. Most patients considered deniers were seen using interpersonal denial in the service of preserving relationships important to them. Denial use as a result of intrapsychic impoverishment was seen infrequently. Twenty-four patients with various terminal cancers were assigned to either an experimental (n = 13) or a control (n = 11) group. A pretest versus posttest multifactorial analysis of variance model was used. Experimental subjects received a structured psychosocial intervention just before posttest. Results showed that, as predicted, interpersonal deniers in the experimental group had a statistically significant (p < .005) decrease in denial scores at posttest, whereas denial scores increased in the control group. Data indicate that, in the absence of psychological dysfunction, patients using interpersonal denial may respond favorably to sensitive psychosocial intervention. Still others may benefit only after they have had sufficient time to muster adaptive coping strategies. Areas for further research are suggested.

Adaptation, Psychological↗