By Kellen Browning July
25, 2017
Frederick Bannon Jr.
was by his mother’s side in intensive care as she fought a rare form of muscle
cancer in late 2014. She was heavily sedated, but he felt confident making
medical decisions for her, thanks to his family’s advance care planning.
Bannon had difficult
end-of-life-care conversations with his parents, both in their
mid-80s, before his mother’s diagnosis. During those discussions, held at
Bannon’s urging, his parents decided how far they wanted doctors to go to keep
them alive should they become too sick to communicate. Bannon then documented
their wishes.
“That helped so much, because you knew at
least one thing was going to be taken care of,” said Bannon, 65, of
San Francisco, whose mother survived and lives with Bannon’s father in
Wethersfield, Conn.
Most Americans avoid end-of-life decisions,
although some people may be more likely to make them if a doctor or social worker starts the
discussion. In California, the state’s attorney general’s office
offers an end-of-life planning checklist on
its website. In the past few years, other websites have encouraged those
conversations, with their own suggestions on how to get started.
Rebecca Sudore, a
geriatrician at the University of California-San Francisco, created prepareforyourcare.org, which provides
step-by-step instructions and video stories to help people navigate the care
they want at the end of their lives. She built the site in 2013 for
families unsure how to broach sensitive questions. In a study published
in JAMA Internal Medicine in
May, she and other researchers found that the website — combined with the use
of an “advance directive” form — prompted participants to plan ahead.
The website is free,
and Sudore makes no money from it. She said she created it as a public service
with the idea of studying its effectiveness.
The site guides
patients in drafting a “summary of wishes” to help families and other
caregivers decide whether their loved ones should undergo life-sustaining
medical interventions such as feeding tubes and ventilators.
For the study, Sudore
approached 414 San Francisco-area military veterans — including Bannon — who
were split into two groups: One received a simplified advance directive, a
legal document allowing a patient to consent to or decline specific medical
procedures well before they occur. The other group was given the directive but also
was pointed to prepareforyourcare.org, which is publicly available in
English and Spanish.
Almost none of the
participants had documented their wishes in the six months before the study.
But nine months after the study began, 35 percent of those who received access
to the website and the directive had updated their medical record, while 25
percent who received just the directive had done so.
Sudore sees stark
contrasts between “deer-in-headlights” families who arrive at the intensive
care unit with outdated directives and no specified plans, and those who have
had ongoing conversations.
Bannon, a Vietnam War
veteran, X-ray technician and colon cancer survivor, praised the site’s
simplicity and accessibility and said it persuaded him and his parents to
document their wishes before his mother’s cancer treatment.
The website appears to
be a useful tool, according to Dr. VJ Periyakoil, associate professor of
medicine and director of Stanford University’s Palliative Care Education and Training Program. (Periyakoil
is friends with the UCSF researchers but was not involved in the study.)
“Clinicians are so
hard-pressed for time, so when the patients get activated by web-based tools, I
think it’s a wonderful thing,” she said.
Seventy percent of Americans
lack an advance care plan, according to the U.S. Centers for Disease Control and Prevention,
and lack of preparation can have undesirable effects, Periyakoil said.
Family members who
have not gone through this process sometimes choose life-sustaining options for
their loved ones that may cause unnecessary suffering, Periyakoil said.
Children “might be
more lured by, ‘I really love Mom. I can’t allow anything bad to happen to her
and I want to keep doing whatever I can to extend her life,’” she said. “And by
doing so, they might end up subjecting Mom or Dad to a lot of measures that are
ineffective and burdensome.”
Periyakoil, who
has studied barriers to
end-of-life care among eight ethnic groups, does not believe there’s a single
solution to encouraging end-of-life conversations, because different groups
have different approaches to discussing death. She suggested the website might
be one of many strategies to consider.
Prepareforyourcare.org
has logged more than 1.7 million page views and 85,000 users in 115 countries
since its 2013 launch.
For Bannon, the site
worked. “Now [my parents are] even more relaxed, because when they do face
their final exit, everything’s in place,” he said.
This story was
produced by Kaiser Health News, which publishes California Healthline, an editorially
independent service of the California Health Care Foundation.
KHN’s coverage related
to aging & improving care of older adults is supported by The
John A. Hartford Foundation, coverage of end-of-life and serious
illness issues is supported by The Gordon and Betty Moore
Foundation, and coverage of aging and long-term care issues is
supported by The SCAN Foundation.
http://khn.org/news/jump-starting-hard-conversations-as-the-end-nears/?utm_campaign=KFF-2017-The-Latest&utm_source=hs_email&utm_medium=email&utm_content=54666700&_hsenc=p2ANqtz-_ct-1PLiM6kPfBiTod2IyDp4iNfS-NgE13JucHqZOWyV3O-us0tn8yTqpVcH1BC7Q1VejEbklfOqT8hszIdYEedNplQA&_hsmi=54666700
No comments:
Post a Comment