Alzheimer’s disease afflicts nearly 12 million people
worldwide, and that number is rapidly increasing. Ruth B. Purtilo, Ph.D.,
director of Creighton University’s Center for Health Policy and Ethics, led
an international dialogue addressing major ethical and scientific concerns
about the diagnosis and prognosis of the disease.
These dialogues resulted in "Ethical Foundations of Palliative Care for
Alzheimer Disease," recently published by Johns Hopkins University Press,
edited by Purtilo the Dr. C.C. and Mabel. L. Criss professor of Ethics, and
and Henk A.M.J. ten Have, M.D., Ph.D., professor of Medical Ethics at the
University Medical Centre Nijmegen, The Netherlands. ten Have is also the
director of the Division of Ethics of Science and Technology, UNESCO, Paris.
"Ethical Foundations of Palliative Care for Alzheimer Disease" is written
for health care workers, ethicists, public policy makers and anyone
interested in the ethical dilemmas facing professionals, caregivers and
society. In the book, leading ethicists and clinicians from the United
States and Europe explore key societal issues surrounding the disease.
People with Alzheimer’s disease are living longer than those who have been
afflicted with the disease in the past. They require interventions for
quality-of-life issues associated with palliative, or long-term, care.
In her foreword, Christine K. Cassel, M.D., president of the American Board
of Internal Medicine, writes that the "palliative care movement in the
United States has reminded modern medicine of human mortality and has shown
us that even though we cannot cure many illnesses, it is not true that
‘there is nothing left to do.’"
Other Creighton contributors to the book, include: Roger A. Brumback, M.D.,
Elizabeth Furlong, R.N., Ph.D., J.D., Amy M. Haddad, R.N., Ph.D., Judith Lee
Kissell, Ph.D., Richard L. O’Brien, M.D., Winifred J. Ellenchild Pinch,
R.N., Ed.D., Patricio F. Reyes, M.D., Linda S. Scheirton, Ph.D., and Jos V.
M. Welie, M.Med.S., J.D., Ph.D. |