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Journal of Palliative Medicine
Special series features Promoting Excellence in End-of-Life Care
The Journal of Palliative Medicine continues
a special series of articles describing the experiences and exciting results
of 22 innovative
projects funded by Promoting Excellence in End-of-Life Care. The articles,
edited by Ira Byock, M.D., Promoting Excellence Director, are included
in the Innovations section of the journal.
Authored by team members of the projects featured, the articles present a
broad range of contexts of care, and discuss potential future directions for
their programs. They also reflect on the implications of their projects’ experiences
for similar patient populations and settings elsewhere.
The articles are available by journal subscription by visiting the Journal
of Palliative Medicine Web site. Address reprint requests or correspondence
to the authors (e-mail addresses listed below). |
June 2004: Volume 7, No. 3:
- The Balm of Gilead Project: A Demonstration Project on End-of-Life
Care for Safety-Net Populations describes a comprehensive end-of-life
program for the populations served by the “safety net” public
health system in Alabama’s largest county. The Balm
of Gilead, located at Cooper
Green Hospital in Birmingham, serves terminally
ill persons,
predominantly
of minority ethnic status, who as a group are relatively younger
than the national hospice population and typically lack personal
financial resources.
The demonstration project addressed the holistic needs associated
with terminal illness in each of its stages and each of its treatment
settings.
Authors of the article are Elizabeth A. Kvale, M.D., Beverly R.
Williams, Ph.D., James L. Bolden, M.B.A., Carol G. Padgett, Ph.D.
and F. Amos Bailey.
M.D. (Pages 486-493)
April 2004: Volume 7, No. 3:
- Project ENABLE: A Palliative Care Demonstration Project for
Advanced Cancer Patients in Three Settings describes Project
ENABLE (Educate, Nurture,
Advise Before Life Ends), one of four cancer center/hospice collaborations
in the 22 original Promoting Excellence demonstration projects.
The jointly sponsored Norris Cotton Cancer Center/Hospice of Vermont
and New Hampshire
program provided an integrated approach to the management of life-limiting
cancer. Project ENABLE was aimed at alleviating the symptoms of
disease and treatment, enhancing clinician and patient/family communication,
offering
support for families, friends and other caregivers, addressing
emotional and spiritual needs of dying people and providing conceptual
and administrative
structure to provide end-of-life care consistent with patients’ values
and preferences. Authors of the article are Marie Bakitas, M.S.,
ARNP, Marguerite Stevens, Ph.D., Tim Ahles, Ph.D., Marie Kirn,
M.A., Karen Skalla,
M.S., ARNP, Nancy Kane, M.S., R.N. and E. Robert Greenberg, M.D.
(Pages 363-372)
- The GRACE Project: Guiding End-of-Life Care in Corrections
1998-2001,
by Margaret Ratcliff, M.S.W. and Elizabeth Craig, discusses the GRACE (Guiding Responsive Action
in Corrections at End of Life) Project, a
collaborative
venture between Volunteers of America and several partners that
promotes the development of end-of-life care programs in correctional
settings.
The project established a resource center, developed and published
standards and a handbook, and pioneered demonstration programs
at four sites. (Pages 373-379)
February 2004: Volume 7, No. 1:
- “Integrating Case Management and Palliative Care” discusses
a partnership between Mount
Sinai School of Medicine in New York,
Franklin Health (a care management organization) and South Carolina
Blue Cross Blue Shield. The project developed an enhanced model
of care for seriously ill patients’ complex needs by combining
palliative care with a case management approach. Diane E. Meier,
M.D., William Thar, M.D., Ashby Jordan, M.D., Suzanne L. Goldhirsch,
M.A., Albert Siu, M.D. and R. Sean Morrison, M.D. author the article. (Pages
119-134)
- “Palliative Care in the Pueblo of Zuni,” by
Bruce Finke, M.D., Theresa Bowannie, and Judith Kitzes. M.D., M.P.H.,
presents a New Mexico collaboration between a tribally operated
home health care agency and a federally operated Indian
Health Service hospital, with the support of a palliative care center
within an academic medical center, that brings culturally proficient
palliative care services to the American Indian population. (Pages
135-143)
December 2003: Volume 6, No. 6:
- “The FOOTPRINTS SSM Model of Pediatric Palliative Care,” by
Suzanne Toce, M.D. and Mary Ann Collins, M.H.A., describes an
innovative program of advance care planning and end-of-life care
coordination for
children at SSM Cardinal Glennon Children’s
Hospital in St. Louis. (Pages
989-1000)
- “The PhoenixCare Program” discusses
the three-year demonstration established by the Phoenix-based Hospice
of the Valley that provided patient access to palliative care and supportive
services prior to hospice eligibility – within a managed
care setting. The article is authored by Carol A. Lockhart, Ph.D.,
Barbara E. Volk-Craft, R.N., M.B.A., Gillian Hamilton, M.D., Ph.D.,
Leona S. Aiken, Ph.D. and Frank G. Williams, Ph.D. (Pages 1001-1012)
October 2003: Volume 6, No. 5:
- “Palliative Care Management: A Veterans Administration Demonstration
Project,” (Kenneth Rosenfeld, M.D. and Jennifer Rasmussen,
M.P.H.) describes Pathways of Caring, a three-year Veterans Health Administration
(VA) project in Los Angeles, California, targeting patients with inoperable
lung cancer and advanced heart failure as well as chronic lung disease. Because
of its success, this program will be expanded and its care model extended
institution-wide. (Pages 831-839)
- “Completing a Life: Development of an Interactive Multimedia
CD-ROM for Patient and Family Education in End-of-Life Care” (Karen
Ogle, M.D., Darcy Drew Greene, M.F.A., Brian Winn,
M.S., Dan Mishkin, Leslie G. Bricker, M.D., and Angela K. Lambing,
M.S.N., R.N.C.S.) describes
a comprehensive, interactive, educational CD-ROM that assists people
with terminal
illness in addressing important end-of-life issues. The format and
design of the CD, developed by the Henry
Ford Health System and Michigan State
University in East Lansing, Michigan, generate a sense of empowerment
at a time when patients often express a loss of control. (Pages 841-850)
August 2003: Volume 6, No. 4:
- “Do It Your Way: A Demonstration Project on End-of-Life
Care for Persons with Serious Mental Illness” (Mary Ellen
Foti, M.D.) describes a demonstration project developed and implemented
in a Massachusetts
public mental health system that improves access to advance care planning
and end-of-life care for people with serious mental illness. (Pages 661-669)
- “CHOICES: Promoting Early Access to End-of-Life Care Through
Home-Based Transition Management” (Brad Stuart, M.D., Carol
N. D’Onofrio, Dr.P.H., Susanne Boatman, R.N., GNP, and Glen Feigelman,
LCSW) A
comprehensive home-based care coordination program designed to bridge
the gap between home health and hospice for Medicare + Choice enrollees
with advanced
chronic illness. This article describes the San
Francisco East Bay region's CHOICES program,
which demonstrates that concurrent disease modifying and palliative care
for patients with advanced illness can be based in home settings. Included
are eligibility and discharge criteria examples, as well as with the CHOICES
Program Sutter VNA & Hospice Advanced Directive Intervention List. (Pages
671-683)
- Project Safe Conduct Integrates Palliative Goals into Comprehensive
Cancer Care describes Project
Safe Conduct, a collaborative venture
between a National Cancer Institute comprehensive cancer center -- Ireland
Cancer Center at
Case Western Reserve University and University Hospitals of Cleveland – and
a freestanding, community-based hospice – Hospice of the Western Reserve – to
make palliative care accessible to persons suffering from advanced lung cancer
as they pursued life-prolonging treatments. This innovative project was one
of four winners of the 2002 Circle of Life Award. Authors of the article
are Elizabeth Ford Pitorak, M.S.N., APRN, CHPN, Meri Beckham Armour, M.S.N.,
R.N. and Holly D. Sivec. (Pages 645-655)
June 2003: Volume 6, No. 3:
- “The Comprehensive
Care Team: A Description of a Controlled Trial of Care at the Beginning
of the End of Life” (Michael W. Rabow, M.D., Jane Petersen,
B.A., Karen Schanche, M.S.W, Suzanne L. Dibble, DN.Sc., and Stephen J.
McPhee, M.D.) describes
an outpatient palliative care consultation service for patients with
serious illness who are continuing to receive treatment for their underlying
disease.
The study, conducted at the University of
California, San Francisco,
revealed that the patients, all with cancer, advanced congestive heart
failure or advanced
chronic obstructive pulmonary disease, found the palliative care consultation
and services helpful. The patients reported improved satisfaction with
their family, their primary care physicians and the medical center. However,
barriers to
the implementation of palliative care treatments must still be explored,
as this study revealed that primary care providers did not implement a
significant
number of the consultation team’s recommendations. (Pages 489-498)
- “Establishing a Culturally Sensitive Palliative Care
Program in Rural Alaska Native American Communities” (Christine
A. DeCourtney, M.P.A., Kristina Jones, R.N., M.P.H., Melanie P. Merriman,
Ph.D., Nina Heavener, R.N., B.S.N., and P. Kay Branch, M.A.) describes
the Helping Hands Program, developed by the Bristol Bay Health Corporation
in Dillingham, Alaska. Palliative care programs
that provide an option for patients to die at home are available in most
U.S. communities. However, Alaska Natives living in remote Alaska villages
often
die alone in hospitals and nursing homes hundreds of miles from home. The Helping Hands Program is a village-focused, culturally sensitive, volunteer
and primary
care program combined with a regionally based physician and home health nurse
to deliver multi-disciplinary palliative care and end-of-life services to
remote communities. Since the program was implemented in 1999, the percentage
of home
deaths for selected causes has changed from 33% in 1997 to 77% in 2001. The
program may be expanded throughout Alaska, centralized in Anchorage. (Pages
501-510)
- “Enhancing Communication for End-of-Life Care: An Electronic
Advance Directive Process” (Leslie J. Bricker, M.D., Angela
Lambing, M.S.N. and Carolyn Markey, M.S., R.N.) describes the development
of an electronic advance
directive in the Henry Ford Health System in Detroit, Michigan. With the
integration of an electronic advance directive note within the electronic
medical record,
patients’ treatment wishes can be accessed at any site within the Henry
Ford system. This article describes the development and implementation of
the
integration process, shares the health system’s policy and procedure
on advance directives and reports on the successes of the program. (Pages
511-519)
April 2003: Volume 6, No. 2:
- Expanding the Realm of the Possible, by Ira Byock, M.D.
and Jeanne Sheils Twohig, M.P.A., introduces the 21-article Promoting
Excellence in End-of-Life
Care series that showcases the original
22 demonstration projects funded
by the Promoting Excellence national program office. This article
explains the selection process, the criteria for funding, common programmatic
threads that emerged with the diverse projects, typical services offered
by the projects,
evaluation methods and future implications of project findings. (Pages
331-333)
- Integrating
Palliative Care into Nursing Homes is an interview conducted
by the Journal of Palliative Medicine’s “Innovations” Associate
Editor, Anna L. Romer, Ed.D. with Howard Tuch, M.D. and Pamela Parrish,
R.N., B.A., CHPN, researchers with a collaborative project between Genesis ElderCare
and the University of Pennsylvania School of Nursing. This Promoting
Excellence demonstration project explored and compared two interventions aiming to
integrate palliative care expertise and practice into the nursing home
setting. (Pages 297-309)
- Palliative Excellence in Alzheimer Care Efforts (PEACE): A Program
Description discusses the PEACE
program, a disease management
model for dementia that incorporates advance planning, patient-centered
care, family support and
a palliative care focus with dementia patients from the time of diagnosis
through its terminal stages. The PEACE demonstration project provides an
innovative model for providing quality palliative care for dementia patients
and their caregivers, and is coordinated through the primary care geriatrics
practice of the University of Chicago. Authors of the article are Joseph
W. Shega, M.D., Amy Levin, R.N., B.S.N., Gavin W. Hougham, M.A., Ph.D.,
Deon Cox-Hayley, D.O., Daniel Luchins, M.D., Patricia Hanrahan, Ph.D.,
Carol Stocking,
Ph.D. and Greg A. Sachs, M.D. (Pages 315-320)
- The Renal Palliative Care Initiative, by David M. Poppel,
M.D., Lewis M. Cohen, M.D. and Michael J. Germain, M.D., explains a collaborative
effort
in Massachusetts between a large tertiary care hospital, Baystate
Medical Center, and a large nephrology practice, the Western new England Renal
and
Transplant Associates, to bring the practices of palliative medicine to
eight dialysis clinics in the Connecticut River Valley. The initiative
introduced
an improved approach to symptom assessment and control, advance care planning
and high quality palliative care to dialysis patients, and developed an
annual renal memorial service that is widely attended by center staff and
patient
families. (Pages 321-326)
Journal of Palliative Medicine Web site
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Promoting Excellence in End-of-Life Care was a
national program of the Robert Wood Johnson Foundation dedicated to long-term
changes in health care
institutions to substantially improve care for dying people and their
families.
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