Showing posts with label living will. Show all posts
Showing posts with label living will. Show all posts

Tuesday, June 10, 2014

Patients' End-of-Life Wishes Granted/Protected, Study Finds




Wall Street Journal, Monday, June 9, 2014, Page A3, U.S. NEWS:


U.S. NEWS

Patients' End-of-Life Wishes Granted, Study Finds

Filling Out Special Form Results in Desired Treatment in Final Days, According to Research on Oregon Deaths

June 9, 2014 12:11 a.m. ET
Patients who document their end-of-life wishes using a special medical form get the specific care they want in their final days, according to a study published online in the Journal of the American Geriatrics Society.
The study by researchers at Oregon Health & Science University looked at the growing use of the voluntary form, called Physician Orders for Life-Sustaining Treatment, or Polst. The document lets patients request or refuse certain medical treatments such as CPR or intensive care. The study is the largest on the topic so far and the first to look at preferences stated in the form and where people actually die.
Polst programs have been adopted or are in development in 43 states. Proponents say that in addition to giving patients a voice in the face of advanced illness, they can help trim the nation's bill for costly interventions that don't extend life for patients who don't want them. However, the programs remain controversial with some groups in the often-fraught national debate about end-of-life care.
Lead study author Erik Fromme of Oregon Health & Science University reviews a Polst form with patient Helen Hobbs, 96.
The researchers examined death records for 58,000 people who died of natural causes in 2010 and 2011 in Oregon, where the Polst approach was developed in 1991 and which has the most comprehensive data on its use. Nearly 18,000 of the patients, or roughly 30%, had such forms on file at time of death. In comparing the location of death with the medical treatment people requested on their forms, only 6.4% of patients who specified "comfort measures only," or allowing for a natural death while relieving pain and suffering, died in a hospital. Meanwhile, 22.4% of patients who chose "limited additional interventions" died in a hospital and 44.2% of patients who chose "full treatment" died there. Of people with no such form, 34.2% died in a hospital.
"We think almost everyone in our study who wanted to be with family and avoid an unwanted terminal hospitalization, as long as their comfort could be managed, got their wish," said Susan Tolle, senior author of the study and director of the Center for Ethics in Health Care at the university. "There is a remarkable association between where you die and the orders selected on your Polst form."
The forms are meant to be signed by a patient's physician, nurse practitioner or physician assistant after a discussion with the patient. In Oregon, patients can choose to have the form stored in a secure online registry that emergency personnel can access quickly in a crisis.
Some organizations that oppose Polst forms say they pose unacceptable risks to patients' well-being, including Catholic bishops' groups in some states which have said that the forms conflict with church doctrine and ethical values. Wisconsin's Catholic bishops, for example, have published their own guidelines aimed at helping individuals convey their desires regarding health-care decision-making to align with church principles.
Polst forms are revocable at any time. But critics have also raised concerns about whether some patients fully understand their choices and how easily patients can alter the form. Some critics believe only doctors, not other health professionals, should administer the forms.
Unlike an advance directive or living will, which are often recommended for healthy patients to make their end-of-life wishes known to loved ones, and which may designate a surrogate to make decisions, Polst forms are designed for seriously ill or frail patients whose health indicates that such decisions might need to be made in a relatively short time frame. Clinicians are encouraged to offer them to patients if they wouldn't be surprised to see them die within a year, and the forms are revocable at any time.
Research in the same geriatrics journal earlier this year found the increased use of advance directives during the past decade has had little effect on hospitalization and hospital death.
"While there have been many efforts to improve end of life care in the U.S., Polst seems to be the first approach shown to be effective in achieving for patients what they would like in their end of life care, and where that care should be delivered, be it in the hospital or home," said Mark Siegler, director of the MacLean Center for Clinical Medical Ethics at the University of Chicago, who wasn't involved in the study.
Besides providing documents that meet local regulations, Polst programs train health-care providers to discuss end-of-life treatment choices. Once signed by both patient and clinician, the form becomes an enforceable standing medical order in the patient record. States that have adopted the program also have put in place general protections for medical personnel who follow the directives.
Carlos Rivera, 72 years old, survived a heart attack at 50 and was resuscitated by emergency medical personnel. But with advanced heart disease, he said he wouldn't want to repeat the experience and signed a Polst form that includes a do-not-resuscitate order. "It would take the load off my family and relieve them of fighting over what to do," said Mr. Rivera, who retired as a community agent in the Portland school system. "And people have the right to determine their own destiny."
Write to Laura Landro at laura.landro@wsj.com

Thursday, February 27, 2014

Palliative Care: For Terminally Ill Better Care, Lower Costs



JOURNAL REPORTS: HEALTH CARE

Palliative Care Gains Favor as It Lowers Costs

Patients and Families See Another Benefit: Better Care

Updated Feb. 23, 2014 5:03 p.m. ET
Paula Gibson Massey, once an avid hiker, initially resisted signing up for palliative care while fighting lymphoma. Massey Family
Insurers are establishing programs that give the sickest patients the chance to receive extra care for their pain, suffering and emotional needs, in a move that turns out to cut spending substantially.
Such palliative-care programs aim to provide assistance to patients with chronic or terminal illnesses, and go beyond the drug prescriptions and surgeries such patients typically receive. Under the programs, doctors are often called in to prescribe drugs treating pain, anxiety and depression, while home-care aides visit residences to give baths and change sheets. Social workers may try to resolve conflicts between estranged siblings.
The programs have their critics, who say the insurers' real goal is to bolster profits by pushing patients to forgo costly treatments that could prolong their lives. But supporters counter that the lowered costs are simply a fortunate side effect, and that fulfilling patients' wishes and needs is the main goal.
"By improving quality of care for that group, it can also reduce the number of repeat hospitalizations and other emergency interventions, which is extremely expensive for payers," says Emily Warner, a senior policy analyst at the Center to Advance Palliative Care at the Icahn School of Medicine at Mount Sinai.
More to Come
In recent years, insurers including UnitedHealth Group's Optum unit and Highmark Inc. have created such programs—a trend that is likely to continue as the population ages and efforts are made to both cut costs and improve care for patients at the end of their lives.
Studies show that treatment of the most complex patients during their final months accounts for a disproportionate amount of health-care spending. About 25% of Medicare costs cover the last year of patients' lives, while 80% of the government health program's spending during the last month is for hospitalization. A visit to an intensive-care unit alone can cost more than $4,000 a day.
Evidence suggests that the palliative-care programs can make a major dent in those costs. Studies by Kaiser Permanente, for instance, found that such programs can save $5,000 to $7,000 a patient by preventing costly trips to emergency rooms and avoidable readmissions to hospitals. AetnaInc. says it saved $55 million in 2012 among its Medicare Advantage patients.
"If there is an opportunity to impact at the intersection of quality and cost, this is the mother lode," says Randall Krakauer, Aetna's director of medical strategy, who helped establish his company's program.
Typical candidates for palliative care include patients suffering from congestive heart failure, chronic obstructive pulmonary disease and dementia. Many participants have cancer, typically at an advanced stage. Dedicated teams of doctors, nurses, chaplains and social workers step in to interview the patients to assess their needs and develop a plan for their extra care.
Team Effort
Often team members sit in on meetings between patients and their doctors, help explain medical conditions, and help the patients and families reach decisions about the course of treatment. A palliative-care team might also help coordinate a patient's treatment among different doctors.
Many programs offer help drawing up wills and do-not-resuscitate orders. Such orders let doctors and nurses know the patient wants to forgo cardiopulmonary resuscitation, being put on a ventilator and other measures if there is a low chance for recovery. Sometimes, the patients get care in hospices or from visiting hospice nurses for their pain, suffering and emotional needs but give up aggressive medical treatment.
During the 2009-10 health-care-overhaul debate, a proposal to pay doctors for providing counseling about end-of-life services drew fire from some Republicans about "death panels" determining care.
But Thomas Smith, director of the Johns Hopkins Palliative Care Program, points to studies that show patients in such programs do better on quality measures like hospital readmission rates than people who don't elect palliative care. Patient satisfaction levels improve as well. Dr. Smith also cites studies showing members who receive these benefits live as long as or longer than those who aren't participants.
Aetna, which first tried palliative care in 2004, now offers it to anyone with medical coverage in both its commercial and Medicare plans.
In 2012, the company saved an average of $12,600 for each patient who chose to participate, while improving the quality of and satisfaction with their care, Dr. Krakauer says. Aetna bases its data on hospital admissions, survival rates and other data about medical treatment, as well as surveys of patients and their families.
About 90% of eligible members choose to participate, Dr. Krakauer says. And members don't have to give up aggressive treatment in order to participate, though Dr. Krakauer says some ultimately do so. Medicare requires it for patients electing to receive hospice care.
"We will not steer them toward a decision," adds Dr. Krakauer. "If they want the maximum aggressive therapy to the last, we will support them."
To identify members who might be candidates, Aetna uses algorithms to sift through billing and other records. Doctors and nurses also make referrals.
Tough Decisions
Then case managers like Margaret Warnock call the patients. Case managers ask questions to see what the patient's wishes and needs are and whether they might be eligible. They explain what participation would mean.
The decision can be difficult for members like Paula Gibson Massey, an avid hiker and yoga student from Sylvania, Ohio, who died at age 51 after battling cancer.
Mrs. Massey was diagnosed with lymphoma in 2007, and chemotherapy and other treatments progressively lost effectiveness, recalls her husband, Stan Massey. By early 2013, the cancer had spread to Mrs. Massey's spine, causing fractures in her lower back. She was prescribed narcotics for the pain and physical assistance to help her move.
Mrs. Warnock says she spoke with Mrs. Massey about this time, explained the benefits available under her plan and concluded she would be a good candidate for Aetna's palliative-care program. Mrs. Warnock says she explained that Mrs. Massey could receive the program's benefits while continuing with treatment aiming to cure her. But Mrs. Massey didn't want to go on the program.
"She felt it meant admitting she was dying," recalls Mr. Massey, 56, who works in marketing public relations in the Toledo, Ohio, area, including representing hospices and health-care systems.
Mr. Massey says at first he ignored Aetna's calls. The idea appealed to him that his wife could stick with aggressive treatment of her cancer and receive regular visits from hospice nurses who would adjust her medicines, manage her pain and provide other care. Still, he respected his wife's wishes.
Mrs. Warnock stayed in touch. Then, last March, Mrs. Massey's cancer doctor said she probably wouldn't live another 12 months. Later that month, Mrs. Massey signed up for Aetna's program and agreed to start receiving palliative care in her home, Mr. Massey says.
A day later, she suffered a pulmonary embolism. Although she was taken to an emergency room, she had indicated through Aetna's program that she wanted to forgo treatment if her condition was hopeless, and she confirmed her choice with an emergency doctor at the hospital, her husband recalls.
After 90 minutes at the hospital, Mrs. Massey was taken to a hospice center, where she passed away about 36 hours later.
Mr. Rockoff is a staff reporter for The Wall Street Journal in New York. He can be reached at jonathan.rockoff@wsj.com.