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| Maria Fabrizio for WPLN
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"I'm not anti-hospice at all," says Joy Johnston, a writer from
Atlanta. "But I think people aren't prepared for all the effort that it
takes to give someone a good death at home."
Even though
surveys show it's what most Americans say they want, dying at home is "not all it's cracked up to be,"
says Johnston, who relocated to New Mexico at age 40 to care for her dying mother some years ago. She ended up writing
an essay about her frustrations with the way hospice care often works in the U.S.
Johnston,
like many family caregivers, was surprised that her mother's hospice
provider left most of the physical work to her. She says that during the
final weeks of her mother's life, she felt more like a tired nurse than
a devoted daughter.
According to a
recent Kaiser Family Foundation poll,
seven in 10 Americans say they would prefer to die at home. And that's
the direction the health care system is moving, too, hoping to avoid
unnecessary and expensive treatment at the end of life.
The home hospice movement has been great for patients, says Vanderbilt palliative care physician
Parul Goyal, and many patients are thrilled with the care they get.
"I
do think that when they are at home, they are in a peaceful
environment," Goyal says. "It is comfortable for them. But," she notes,
"it may not be comfortable for family members watching them taking their
last breath."
Still, when it comes to where we die, the U.S. has reached a tipping point. Home is now the most common place of death,
according to new research, and a
majority of Medicare patients
are turning to hospice services to help make that possible. Fewer
Americans these days are dying in a hospital under the close supervision
of doctors and nurses.
Hospice allows a patient deemed to have fewer than six months to live
to change the focus of their medical care — from the goal of curing
disease to a new goal of using treatments and medicines to maintain
comfort and quality of life. It is a form of palliative care, which also
focuses on pain management, but can be provided while a patient
continues to seek a cure or receive treatments to prolong life.
Usually, hospice care is offered in the home, or sometimes in a nursing home.
Since the mid-1990s,
Medicare has allowed the hospice benefit to cover more types of
diagnoses, and therefore more people. As acceptance grows among
physicians and patients, the numbers continue to balloon — from 1.27
million patients in 2012 to 1.49 million in 2017.
According to
the National Hospice and Palliative Care Association, hospice is now a
$19 billion industry, almost entirely funded by taxpayers. But as the
business has grown, so has the burden on families, who are often the
ones providing most of the care.
For example, one intimate task
in particular changed Joy Johnston's view of what hospice really means —
trying to get her mom's bowels moving. Constipation plagues many dying
patients.
"It's ironically called the 'comfort care kit' that
you get with home hospice. They include suppositories, and so I had to
do that," she says. "That was the lowest point. And I'm sure it was the
lowest point for my mother as well. And it didn't work."
Hospice
agencies primarily serve in an advisory role and from a distance, even
in the final, intense days when family caregivers, or home nurses
they've hired, must continually adjust morphine doses or deal with
typical end-of-life symptoms, such as bleeding or breathing trouble.
Those decisive moments can be scary for the family, says
Dr. Joan Teno, a physician and leading hospice researcher at Oregon Health and Science University.
"Imagine if you're the caregiver, and that you're in the house," Teno
says. "It's in the middle of the night, 2 o'clock in the morning, and
all of a sudden, your family member has a grand mal seizure."
That's exactly what happened with Teno's mother.
"While it was difficult for me to witness, I knew what to do," she says.
In
contrast, Teno says, in her father's final hours, he was admitted to a
hospice residence. Such residences often resemble a nursing home, with
private rooms where family and friends can come and go and with
round-the-clock medical attention just down the hall.
Teno
called the residence experience of hospice a "godsend." But an inpatient
facility is rarely an option, she says. Patients have to be in bad
shape for Medicare to pay the higher inpatient rate that hospice
residences charge. And by the time such patients reach their final days,
it's often too much trouble for them and the family to move.
Hospice care is a lucrative business. It is now the
most profitable type of health care service
that Medicare pays for. According to Medicare data, for-profit hospice
agencies now outnumber the nonprofits that pioneered the service in the
1970s. But agencies that need to generate profits for investors aren't
building dedicated hospice units or residences, in general, mostly
because such facilities aren't profitable enough.
Joe Shega,
chief medical officer at for-profit Vitas, the largest hospice company
in the U.S., insists it's the patients' wishes, not a corporate desire
to make more money, that drives his firm's business model. "Our focus is
on what patients want, and 85 to 90 percent want to be at home," Shega
says. "So, our focus is building programs that help them be there."
For many families, making hospice work at home means hiring extra help.
'I guess I've just accepted what's available'
At
the kitchen table of her home outside Nashville, hospice patient Jean
McCasland is refusing, on the day I visit, to eat a spoonful of peach
yogurt. Each morning, nurse's aide Karrie Velez pulverizes McCasland's
medications in a pill crusher and mixes them into her breakfast yogurt.
"If you don't, she will just spit them out," Velez says.
Like a
growing share of hospice patients,
McCasland has dementia. She needs a service that hospice rarely
provides — a one-on-one health attendant for several hours, so the
regular family caregiver can get some kind of break each day.
John McCasland (right) of Goodlettsville, Tenn., hired a
private caregiver to help with his wife, Jean (left), who suffered from
dementia for eight years. Even when hospice took over, he still found
he needed the extra help from Karrie Velez (center). Jean died in
October after 13 months on home hospice. Blake Farmer/WPLN
When Velez is not around, John McCasland — Jean's husband of nearly 50 years — is the person in charge at home.
"I
have said from the beginning that was my intention, that she would be
at home through the duration, as long as I was able," John says.
But
what hospice provided wasn't enough help. So he has had to drain their
retirement accounts to hire Velez, a private caregiver, out-of-pocket.
Hospice
agencies usually bring in a hospital bed, an oxygen machine or a
wheelchair — whatever equipment is needed. Prescriptions show up at the
house for pain and anxiety. But hands-on help is scarce.
Medicare
says hospice benefits can include home health aides and homemaker
services. But in practice, that in-person help is often limited to a
couple of baths a week. Medicare data reveals that, on average, a nurse
or aide is only in the patient's home 30 minutes, or so, per day.
Jean
McCasland's husband hasn't complained. "I guess I've just accepted
what's available and not really thought beyond what could be," John
says. "Because this is what they say they do."
Families rarely
consider whether they're getting their money's worth because they're not
paying for hospice services directly: Medicare gets the bills. John
keeps his monthly statements from Medicare organized in a three-ring
binder, but he had never noticed that his agency charges nearly $200 a
day, whether there is a health provider in the home on that day or not.
That
daily reimbursement also covers equipment rentals and a 24-hour hotline
that lets patients or family members consult a nurse as needed; John
says it gives him peace of mind that help is a phone call away. "There's
a sense of comfort in knowing that they are keeping an eye on her," he
says.
The rate that hospice charges Medicare drops a bit after
the patient's first two months on the benefit. After reviewing his
paperwork, John realizes Medicare paid the hospice agency $60,000 in the
first 12 months Jean was on hospice. Was the care his wife got worth
that?
"When you consider the amount of money that's involved, perhaps they would provide somebody around the clock," he says.
Sue
Riggle is the administrator for the McCaslands' hospice agency and says
she understands how much help patients with dementia need.
"I
think everybody wishes we could provide the sitter-service part of it,"
says Riggle. "But it's not something that is covered by hospices."
Her
company is a small for-profit business called Adoration; she says the
agency can't provide more services than the Medicare benefit pays for.
I
checked in again with John and Velez (Jean's long-time private
caregiver) this winter. The two were by Jean's side — and had been there
for several days straight — when she died in October. The hospice nurse
showed up only afterward, to officially document the death.
This experience of family caregivers is typical, but often unexpected.
'It's a burden I lovingly did'
"It does take a toll" on families, says
Katherine Ornstein, an associate professor of geriatrics and palliative medicine at Mount Sinai Hospital in New York, who
studies what typically happens in the last years of patients' lives.
The increasing burden on loved ones — especially spouses — is reaching a
breaking point for many people, her research shows. This particular
type of stress has even been given a name:
caregiver syndrome.
"Our long-term-care system in this country is really using families — unpaid family members," she says. "That's our situation."
A few high-profile advocates have even
started questioning whether hospice
is right for everybody.
For some who have gone through home hospice with a loved one, the
difficult experience has led them to choose otherwise for themselves.
Social
worker Coneigh Sea has a portrait of her husband that sits in the
entryway of her home in Murfreesboro, Tenn. He died of prostate cancer
in their bedroom in 1993.
Coneigh Sea is a social worker from Murfreesboro, Tenn.,
who cared for her husband as he died on home hospice. Now, she wants to
make sure her children don't do the same for her.
Blake Farmer/WPLN
Enough time has passed since then that the mental fog she
experienced while managing his medication and bodily fluids — mostly by
herself — has cleared, she says. But it was a burden.
"For me to say that — there's that guilt," she says, then adds, "but I know better. It was a burden that I lovingly did."
She
doesn't regret the experience but says it is not one she wishes for her
own grown children. She recently sat them down, she says, to make sure
they handle her death differently.
"I told my family, if there is such a thing, I will come back and I will haunt you," she says with a laugh. "Don't you do that."
Sea's
family may have limited options. Sidestepping home hospice typically
means paying for a pricey nursing home or passing away with the cost and
potential chaos of a hospital — which is precisely what hospice care
was set up to avoid.
As researchers in the field look to the
future, they are calling for more palliative care, not less — even as
they also advocate for more support of the spouses, family members and
friends who are tasked with caring for the patient.
"We really
have to expand — in general — our approach to supporting caregivers,"
Ornstein says, noting that some countries outside the U.S. pay for a
wider range and longer duration of home health services.
"I
think what we really need to do is be broadening the support that
individuals and families can have as they're caring for individuals
throughout the course of serious illness," Ornstein says. "And I think
that probably speaks to the expansion of palliative care in general."
Blake
Farmer's reporting on end-of-life care is part of a reporting
fellowship on health care performance, sponsored by the Association of
Health Care Journalists and supported by the Commonwealth Fund.
Full Article & Source:
Patients Want To Die At Home, But Home Hospice Care Can Be Tough On Families
