Patients Want To Die At Home, But Home Hospice Care Can Be Tough On Families

Jan 21, 2020
Originally published on January 23, 2020 2:11 pm

"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."

Copyright 2020 WPLN. To see more, visit WPLN.

RACHEL MARTIN, HOST:

People in this country are thinking differently about death. Fewer Americans are dying in a hospital with the support and care of doctors and nurses. More now choose to spend their final days at home, often getting hospice care. One big reason is because Medicare has allowed more patients to qualify for this benefit. But hospice only goes so far, and the actual burden of 24-hour care falls to the families. Blake Farmer of member station WPLN in Nashville reports.

BLAKE FARMER, BYLINE: Hospice usually means dying at home. And even though surveys show it's what most of us want, it's not all it's cracked up to be, says Joy Johnston.

JOY JOHNSTON: I'm not anti-hospice at all, but I think people aren't prepared for all the effort that it takes to give someone a good death at home.

FARMER: At age 40, Johnston relocated from Atlanta to New Mexico to care for her dying mother. And one intimate task tipped the scales - trying to get her mom's bowels moving. Constipation plagues many dying patients.

JOHNSTON: And it's ironically called the comfort kit that you get with home hospice. They include suppositories. And so I had to do that, and that was the lowest point. And I'm sure it was the lowest point for my mother, as well. And it didn't work.

FARMER: Johnston, like many family caregivers, was surprised that hospice still left most of the work to her. She says the final weeks of her mother's life, she felt more like a nurse than a daughter. Hospice primarily supports from afar, even in the intense final days, when adjusting morphine doses or handling typical symptoms like bleeding and breathing trouble. And that can be scary, says Dr. Joan Teno. She's a leading hospice researcher at Oregon Health and Science University.

JOAN TENO: Imagine if you're the caregiver and that you're in the house, and it's the middle of the night - 2 o'clock in the morning - and all of a sudden, your family member has a grand mal seizure.

FARMER: Teno says that's exactly what happened with her own mother. While it was difficult for me to witness, I knew what to do.

FARMER: Teno's father, who died in the last year, went to a hospice residence with round-the-clock medical attention. Teno called it a godsend. But an inpatient facility is rarely an option. With more people spending more time on hospice, hospice has become the most profitable service sector in health care. For-profit agencies now outnumber the nonprofits. But they aren't building hospice units, mostly because they're not profitable. So it's on families to make do at home, and often that means hiring extra help.

KARRIE VELEZ: You want some yogurt?

JEAN MCCASLAND: (Vocalizing).

VELEZ: Some peach - peach yogurt?

JEAN MCCASLAND: What's that?

FARMER: Hospice patient Jean McCasland is sitting at the kitchen table of her home outside Nashville. Nurse aide Karrie Velez is spooning out yogurt laced with that morning's medication, ground up in a pill crusher.

VELEZ: Because if you don't, she will just spit them out.

FARMER: Like a growing share of hospice patients, McCasland has Alzheimer's. And dementia patients need a service hospice rarely provides - a one-on-one sitter so the family caregiver can get some kind of break each day. John McCasland is Jean's husband of nearly 50 years.

JOHN MCCASLAND: I have said from the beginning that that was my intention - that she would be at home through the duration, as long as I was able.

FARMER: But what hospice provided wasn't enough. He had to drain their retirement accounts to hire a private caregiver out of pocket.

JOHN MCCASLAND: We were told that we would have a nurse visit once a week and more often if we wanted that.

FARMER: Hospice agencies usually bring in a hospital bed, an oxygen machine, a wheelchair - whatever equipment's needed. Prescriptions show up at the house for pain and anxiety. But hands-on help is scarce. Medicare says hospice can include home health aides and homemaker services. But in practice, it's often limited to a couple of baths a week.

JOHN MCCASLAND: I don't know. I guess I've just accepted what's available and not really thought beyond what could be because this is what they say they do.

FARMER: Families rarely consider whether they're getting their money's worth because they're not paying. It's all Medicare. John even keeps his monthly statements in a three-ring binder, but he'd never taken a closer look at what's charged to the government.

JOHN MCCASLAND: That's $200 a day.

FARMER: Nearly $200 every day, whether the hospice agency showed up or not. The daily rate drops a bit after the first two months, but John does the quick math. At that point, after Jean had been on hospice a year, Medicare had paid the agency $60,000.

JOHN MCCASLAND: When you consider the amount of money that's involved, perhaps they would provide somebody round the clock.

FARMER: Far from it. Medicare data reveals that on average, a nurse or aide is only there at the house about half an hour a day. When Jean died in October, the hospice nurse showed up afterward to officially document the death. It was just John and Karrie Velez, the longtime private caregiver, who'd been by her side for several days straight. And that's pretty typical, according to professor Katherine Ornstein.

KATHERINE ORNSTEIN: It does take a toll.

FARMER: Ornstein studies the last year of life at Mount Sinai Hospital in New York. And she finds the increasing burden on loved ones is reaching a breaking point.

ORNSTEIN: You know, our long-term care system in this country is really using families - unpaid family members. That's our situation.

FARMER: For some who've gone through home hospice with a loved one, the experience has changed their own wishes. Coneigh Sea, a social worker from Murfreesboro, Tenn., holds up a portrait of her husband.

CONEIGH SEA: This is probably five years before he died.

FARMER: He died of prostate cancer in their bedroom. Enough time has passed that the fog of managing his medication and bodily fluids - mostly by herself - is cleared. She says it was a burden.

SEA: And for me to say that, there's that guilt. You know? But I know better. It was a burden that I lovingly did.

FARMER: But Sea was scarred. And she recently sat down her grown children to make sure they don't do the same for her.

SEA: I told my family - if there is such a thing, I will come back, and I will haunt you (laughter). Don't you do that.

FARMER: Their options are limited, though. Sidestepping home hospice either means a pricey nursing home or passing away with the often unnecessary chaos and cost of a hospital, which is precisely what hospice was trying to avoid.

For NPR News, I'm Blake Farmer in Nashville.

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