By JoNel Aleccia August
14, 2017
The
90-year-old woman in the San Diego-area nursing home was quite clear, said Dr.
Karl Steinberg. She didn’t want aggressive measures to prolong her life. If her
heart stopped, she didn’t want CPR.
But
when Steinberg, a palliative care physician, relayed those wishes to the
woman’s daughter, the younger woman would have none of it.
“She
said, ‘I don’t agree with that. My mom is confused,’” Steinberg recalled. “I
said, ‘Let’s talk about it.’”
Instead
of arguing, Steinberg used an increasingly popular tool to resolve the impasse
last month. He brought mother and daughter together for an advance-care
planning session, an end-of-life consultation that’s now being paid for by
Medicare.
In
2016, the first year health care providers were allowed to bill for the
service, nearly 575,000 Medicare beneficiaries took part in the conversations,
new federal data obtained by Kaiser Health News show.
Nearly
23,000 providers submitted about $93 million in charges, including more than
$43 million covered by the federal program for seniors and the disabled.
Use
was much higher than expected, nearly double the 300,000 people the American
Medical Association projected would receive the service in the first year.
That’s
good news to proponents of the sessions, which focus on understanding and
documenting treatment preferences for people nearing the end of their lives.
Patients and, often, their families discuss with a doctor or other provider
what kind of care they want if they’re unable to make decisions themselves.
“I
think it’s great that half a million people talked with their doctors last
year. That’s a good thing,” said Paul Malley, president of Aging with Dignity,
a Florida nonprofit that promotes end-of-life discussions. “Physician practices
are learning. My guess is that it will increase each year.”
Still,
only a fraction of eligible Medicare providers — and patients — have used the
benefit, which pays about $86 for the first 30-minute office visit and about
$75 for additional sessions.
Nationwide,
slightly more than 1 percent of the more than 56 million Medicare beneficiaries
enrolled at the end of 2016 received advance-care planning talks, according
to calculations by
health policy analysts at Duke University. But use varied widely among states,
from 0.2 percent of Alaska Medicare recipients to 2.49 percent of those
enrolled in the program in Hawaii.
“There’s
tremendous variation by state. That’s the first thing that jumps out,” said
Donald Taylor Jr., a Duke professor of public policy.
In
part, that’s because many providers, especially primary care doctors, aren’t
aware that the Medicare reimbursement agreement, approved in 2015, has
taken effect.
“Some
physicians don’t know that this is a service,” said Barbie Hays, a Medicare
coding and compliance strategist for the American Academy of Family Physicians.
“They don’t know how to get paid for it. One of the struggles here is we’re
trying to get this message out to our members.”
There
also may be lingering controversy over the sessions, which were famously
decried as “death panels” during the 2009 debate about the Affordable Care Act.
Earlier this year, the issue resurfaced in Congress, where Rep. Steve King
(R-Iowa) introduced the Protecting Life Until Natural Death
Act, which would halt Medicare reimbursement for advance-care
planning appointments.
King
said the move was financially motivated and not in the interest of Americans
“who were promised life-sustaining care in their older years.”
Proponents
like Steinberg, however, contend that informed decisions, not cost savings, are
the point of the new policy.
“It’s
really important to say the reason for this isn’t to save money, although that
may be a side benefit, but it’s really about person-centered care,” he said.
“It’s about taking the time when people are ill or even when they’re not ill to
talk about what their values are. To talk about what constitutes an acceptable
versus an unacceptable quality of life.”
That’s
just the discussion that the San Diego nursing home resident was able to have
with her daughter, Steinberg said. The 90-year-old was able to say why she
didn’t want CPR or to be intubated if she became seriously ill.
“I
believe it brought the two of them closer,” Steinberg said. Even though the
daughter didn’t necessarily hear what she wanted to hear. It was like, ‘You may
not agree with your mom, but she’s your mom, and if she doesn’t want somebody
beating her chest or ramming a tube down her throat, that’s her decision.”
KHN’s
coverage of end-of-life and serious illness issues is supported by The Gordon and Betty Moore Foundation.
http://khn.org/news/end-of-life-advice-more-than-500000-chat-on-medicares-dime/?utm_campaign=KHN%3A%20Topic-based&utm_source=hs_email&utm_medium=email&utm_content=55398653&_hsenc=p2ANqtz-85CRmPTfoeMzJxHx7qli_PT2Dpk8kryvBPxpXkaeWQbvr_jMaUREHTeRjz9A3pFFJFqNRNMcKwEJmQ-PdvTE9eG6mgOQ&_hsmi=55398653
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