The Hospice e-News

What the Media Said about End-of-Life Care This Week

Week of September 06, 2006

…a service of Florida Hospices and Palliative Care

 


 

STUDY EXPLORES VALUE OF MEDICAL SPENDING

 

A article published in the current NEJM, The Value of Medical Spending in the United States, 1960–2000,” reports on a study that compares the “gains in life expectancy with the increased costs of care from 1960-2000.”  Results show that until age 65, life expectancy rises more sharply than healthcare costs.  But after age 65, the cost of medical care takes a big jump.  The study was financed by federal funds and conducted by researchers at Harvard and the University of Michigan.

 

From 1960 through 2000,” the article abstract says, “the life expectancy for newborns increased by 6.97 years, lifetime medical spending adjusted for inflation increased by approximately $69,000, and the cost per year of life gained was $19,900. The cost increased from $7,400 per year of life gained in the 1970s to $36,300 in the 1990s. The average cost per year of life gained in 1960–2000 was approximately $31,600 at 15 years of age, $53,700 at 45 years of age, and $84,700 at 65 years of age. At 65 years of age, costs rose more rapidly than did life expectancy: the cost per year of life gained was $121,000 between 1980 and 1990 and $145,000 between 1990 and 2000.” 

 

Other figures, also adjusted for inflation, show that annual medical spending was about $700 per person in 1960, compared to more than $6,000 today.  At least half of those costs, however, result from more care being available, not from higher costs of existing care.  Some of the increases in longevity are attributed to a decline in smoking and in fatal accidents, but a Washington Post interview with study author David Cutler says “It is reasonable to attribute at least half of it to more and better health care.”  “On net,” he said, “it's actually been a very good deal.  It's very clear that we don't need to spend every penny we do spend.  What's also clear is that there's a lot of stuff that is worth it.”

 

The Washington Post also spoke with Gerard Anderson, director of the Center for Hospital Finance and Management at Johns Hopkins University’s Bloomberg School of Public Health.  Anderson calls the US “very bad in value for dollar, in terms of the health care dollar.”  In his opinion, the US healthcare system focuses too much on the treatment of illness and not enough on preventive care, with resulting higher costs of care.  “The reason why we're spending so much isn't that we're getting more services,” he said.  “The reason is we're paying much higher prices for the same services that other countries get.”

 

The New York Times article cites Dr. Sidney Wolfe, head of health research at Public Citizen, as agreeing with Anderson.  “The fact that someone is writing this paper shows how desperate the health care system is to justify these out-of-control increases in public spending,” Wolfe says.

 

The authors conclude by saying, “On average, the increases in medical spending since 1960 have provided reasonable value.  However, the spending increases in medical care for the elderly since 1980 are associated with a high cost per year of life gained.  The national focus on the rise in medical spending should be balanced by attention to the health benefits of this increased spending.” 

 

Additionally, the authors say, “We need to continue tracking trends in health care spending and its benefits [with a] focus on specific diseases in order to provide a more detailed picture of the value of health care both within disease categories and across a spectrum of common diseases over time.  Also, the United States should modify its system of tracking the health sector to include a measure of population health in addition to spending, so that policymakers and the public have an informed picture of the benefits obtained for the money spent.”  (NEJM,2006;355:920-7; The New York Times, 8/31; The Washington Post, 8/30; WZZM Website, 8/31)

 

 

WHO DECIDES ON DIALYSIS WHEN THE PATIENT CANNOT?

 

In the 1960’s, a Seattle committee called the “God squad” determined which patients with end-stage kidney disease would get to use the dialysis machines, because there were too few machines to service all the patients.  Today, The New York Times says, that equipment crisis is long over and the current problem is the cost of the service.

 

At an annual cost of $16 billion, more than 300,000 patients a year receive dialysis.  Dr. Tony M. Valeri, director of hemodialysis at Columbia University Dialysis Center, says, “Dialysis is the default choice” as long as the patient is stable enough to undergo it.  But in 2000, a committee of the Renal Physicians Association and the American Society of Nephrology developed guidelines for determining when dialysis should be used.  The committee recommended that dialysis was not appropriate for patients who had “irreversible, profound neurological impairment” and that “it was reasonable to consider withholding dialysis from patients with terminal illnesses unrelated to the kidneys.”

 

The New York Times cites research published in a recent Neurology article as reporting that, at Minnesota’s Hennepin County Medical Center, a random sample of dialysis patients found 73% of them with “either moderate or severe cognitive impairment.”  Only 3% have formal diagnoses of an impaired mental state. 

 

Dr. Alvin Moss, who led the guidelines committee in 2000, refuses to prescribe dialysis when he thinks it inappropriate.  Or, sometimes, the patient is put on dialysis, but removed if there is no improvement.  Moss, who says that he has not yet been sued, says that he has “thoughtful discussions” with families about what dialysis can and cannot do. 

 

Other nephrologists think it safer to provide dialysis to avoid lawsuits, the article says.  Some patients have family members who are unwilling to let their loved one die, Dr. Valeri says.  He’s had family members accuse him of suggesting euthanasia when he has suggested withholding dialysis.  “They think you’re just another Kevorkian,” he says.  (The New York Times, 8/29)

 


PUBLIC POLICY NOTES

 

*  Nebraska’s “humane care” constitutional amendment (see HNN, 8/8) will not appear on the November ballot because it failed to garner enough signatures on the required petitions.  The petition drive was about 4,000 signatures short of the more than 113,000 required.  (The JournalStar, 9/3)

 

*  The origins of the money behind a proposed amendment requiring Nebraska patients to receive food and water, unless they have clearly expressed otherwise in advance directives, are unclear.  But most of the people who were involved in the effort and were spread across nine states, says an article in the Omaha World-Herald, have connections to Americans for Limited Government (ALG).  The ALG president, John Tillman, denies that ALG has any position on the humane care measure.  The article says, “The humane care amendment was created and funded in a way that makes it hard to sort out its backers.”  Deborah Goldberg, director of the Democracy Project at New York University School of Law, says that’s a problem.  “Don’t you have a right to know who’s funding policy initiatives in your state?” she asked.  (Omaha World-Herald, 8/27)

 

*  The provision of the recently-passed immigration bill that makes it easier for foreign nurses to enter the US “represents a Band-Aid approach to the serious nursing shortage facing this country and distracts policymakers from addressing the fundamental problems behind the shortage,” say three Pittsburgh Post-Gazette writers.  “In addition, recruiting nurses from less affluent nations, which are grappling with their own shortage of nurses, does great damage to Third World health-care systems that struggle to provide even basic care to their citizens.”  (Scripps Howard News Service, 8/30)

 

*  In the latter part of 2005, says an article in The Charlotte Observer, 130 new hospices opened in North Carolina “despite projections showing needs won’t support the explosion.”  All managed to beat a deadline before a law requiring a certificate of need went into effect.  A number of the new hospices are being challenged by existing providers “who argue that the state made a mistake when it didn’t require owners to get the certificate.”  Bob Fitzgerald, director of North Carolina’s facility services division, says, “For the most part, there is not the need that supports anywhere near the number of new facilities that we added to our hospice inventory last year.”  (The Charlotte Observer, 8/27)

 

*  If California Governor Arnold Schwarzenegger (R) signs a bill paying for hospice care for children, California will be one of the first states in the country to offer the service.  Public funding of hospice for children is prohibited by federal law, but waivers can be issued, such as the one that Florida has.  Lori Butterworth, of the Children’s Hospice and Palliative Care Coalition, says, “We will have a lot more flexibility about how we care for children who are very sick.  We can care for children who are still getting chemotherapy.  They don’t have to be dying.”   (Santa Cruz Sentinel, 8/27)

 

*  North Carolina’s Wake County senior population is growing faster than any other county in the state, and area experts and care providers have developed the Wake County Aging Plan.  The GOLD Coalition (Growing Older Living With Dignity) has the responsibility of implementing the plan and welcomes participation and review of the plan at www.goldcoalition.com.  (The News and Observer, 8/27)


OTHER NOTES

 

*  A recent study from the National League for Nursing reports “a significant drop” in nursing school admissions.  An NLN research analyst says, “It might just be a blip in the data.  It could mean we’re going to start to see a slowdown.”  Another report, by Staffing Industry Analysts, projects “steady revenue gains for healthcare temporary staffing agencies.”  (Modern Healthcare, 8/28)

 

*  Traditional nursing home business is staying flat or shrinking, while new areas of nursing home service, such as short-term care, hospice, home health care and assisted-living services are growing.  Analysts say that Medicare and Medicaid reimbursement changes “have given nursing home firms a better sense of where their money’s coming from” and that has “stabilized the industry and created opportunities for growth.”  (Investor’s Business Daily, 8/28)

 

*  Karl Bernstein is a retired nuclear engineer who did not make an advance directive or living will.  His wife and son are feuding over the kind of care that Karl, who is an Alzheimer’s and Parkinson’s patient, receives.  Bernstein’s wife signed a DNR order when she placed him in a nursing home, but his son, who is an attorney, filed for, and won, conservatorship shortly after.  The two have been at odds ever since.  Bernstein has not spoken in four years and has an artificial feeding tube.  (The Los Angeles Times, 8/26)

 

*  Dr. Liza Leal, author of Live Well With Chronic Pain, offers pain sufferers four tips.  Make a choice to live well, learn how to live well by becoming an effective pain manager, make plans to live well and take action today, not tomorrow.  (Market Wire, 8/29)

 

*  Art Buchwald aside, says an article in The Miami Herald, not everyone is completely happy to graduate from hospice.  Isabel Capote, who cares for her husband who was discharged from hospice with Alzheimer’s, says “It’s a mixed blessing.”  “You want them to get better,” she says, “but at the same time, you lose out on all the hospice services.”  Capote adds that she’s had a hard time “because of my salary.  If I divorce him, the government pays.  But at home, I pay for it.”  The Miami Herald, 8/29)

 

*  A study funded by NIH and the National Center for Complementary and Alternative Medicine (NCCAM) has found that complementary and alternative medicine “is clinically and economically beneficial.”  The study, which involved a group of warehouse workers with low back pain, found improved quality of life at the end of a three-month treatment period and at a three-month follow up.  The patients received acupuncture, dietary advice and relaxation exercises.  (Managed Care Weekly Digest, 8/28)

 

*  A History of Old Age, edited by Pat Thane, is reviewed in the current JAMA.  “The book is beautifully and lavishly produced, with a plethora of fascinating pictures, photographs, paintings and cartoons,” the reviewer says.  The book examines ambivalence toward aging and “the effects of local culture and economics on the lives of elderly people.”  The reviewer notes several faults with the book, including an “inadequate index” and “no information about the five contributors or their affiliations.”  Still, he says, it “offers an attractive and interesting introduction to the subject and is worth the price for the beautiful illustrations alone.”  (JAMA, 2006;296:1000-1001)

 

Glatfelter Insurance Group is the national sponsor of Hospice News Network for 2006.  Glatfelter Insurance Group provides property and liability insurance for hospices and home healthcare agencies through their Hospice and Community Care Insurance Services division.  Ask your insurance agent to visit their website at www.hccis.com.

 

* There will be no publication of The Hospice e-News on the week of September 12, 2006. *