Health Care Reform: Health costs are skyrocketing and the health care system faces numerous pressures and conflicts. What are the major factors driving these growing issues?

Health Care Reform

Health costs are skyrocketing and the health care system faces numerous pressures and conflicts. What are the major factors driving these growing issues?
July 04, 2008

Chances for Reform

CodeBlueNow! explores common ground; cross-sector platforms emerging

Will this be the season of Health Care Reform? With the economy swirling, and the current approach to health care in the U.S. arguably a deeply embedded complication, is it possible to imagine and implement a fundamentally different approach to care that promotes goodness and fairness, quality, access and choice? And can this be done without cues, waiting lines, and "manage-mania"?

Most agree next steps would require cross-sector cooperation, representation, and early agreement on common values and objectives. To this end CodeBlureNow's energetic executive director, Kathleen O'Connor, has pulled together an important  “Town Hall” meeting in Seattle on Sept. 18th from 7 to 8:30 pm with two former Governors Arne Carlson (R-MN) and Richard Lamm (D-CO), followed by an invitational planning meeting of some key thought leaders and organizations the next day to plan for a spring 2009 “Confluence Conference”  with several opinion leaders and organizations working around what Kathleen calls “Deep Reform.”

The Confluence Conference will be dedicated to refining some of the delivery system, management and financing models that various groups are proposing to see if together they can reach concurrence on a core set of values and templates worthy of bipartisan support. The city is behind the effort with supporters including:


Leadership Tomorrow

Executive Alliance

City Club of Seattle

NW Physician Network

These types of efforts are extraordinarily important, and an early bell-weather to indicate whether or not there is true readiness for "Deep Reform."

July 02, 2008

AMA's Virtual Mentor

A valuable resource for both teachers and students

Three things are happening to health education information these days. First, it's going electronic and virtual. Second, it's uniting various audiences, bringing them together, often in new and interactive ways, to inform, educate and bridge. Third, it's changing the power equation, emphasizing that we are all teachers and we are all students.

Case in point: The AMA's "Virtual Mentor"

What is it?

"Virtual Mentor is the American Medical Association's online ethics journal. The journal is open-access and advertisement-free... Founded in 1999, Virtual Mentor (VM) explores the ethical issues and challenges that students, residents, and other physicians are likely to confront in their training and daily practice."

For whom?

"... the journal is a valuable teaching resource for medical educators at all levels as well as for doctors and doctors-to-be. Each monthly issue of VM contains original articles and commentary on a given theme — e.g., access to care; quality-of-life considerations in clinical decision making, public roles of physicians, ethical issues in endocrinology, conflict of values in the clinic."

Who directs it?

"Virtual Mentor is student- and resident-driven. Theme-issue editors are selected in November of each year through a competitive process from among medical students and resident physicians who seek to broaden and deepen their education by taking the time to examine medicine's ever-increasing ethical challenges. The issue editors meet annually with VM editorial staff in Chicago, where we discuss potential topics for the upcoming year. Each editor identifies a theme and month of publication for his or her issue and then solicits articles and case commentary from experienced physicians and other experts in the field who can help VM readers think productively about the topic under discussion. The application process for theme issue editors is announced in VM each September."

I was especially drawn to the June, 2008 issue on Quality of Life for Older Americans exploring "the ethical challenges physicians face in preserving health and well-being in the elderly." Here's the lineup:

Jeanee Lee MD, PGY2 from Duke explores "Autonomy and Quality of Life for Elderly Patients" answering the question:"Why is it that the important problems of older persons are often not the ones that we know how to help?"

Muriel Gillick, MD, a clinical professor of ambulatory care and prevention at Harvard Medical School in Boston who practices palliative care and geriatrics with Harvard Vanguard Medical Associates, comments on  "Family-Centered Decision Making" explaining how "the clinical staff's frustration with their inability to cure and locate a patient's infection can influence how they interpret treatment goals expressed by the patient and patient's family."

Mitchell T. Heflin, MD, MHS, an assistant professor of medicine and geriatrics, and the medical director of the Geriatric Evaluation and Treatment (GET) Clinic at Duke University Center for the Study of Aging and Human Development, explores  "When Home Care Is Not Enough" and the health professional's  "obligation to counsel a family that wants to care for an older relative in the home but may not be able to ensure the appropriate level of care and safety for the relative."

Daniel Callahan, co-founder of the Hastings Center and Senior Lecturer at the Harvard Medical School  and Kenneth Prager, MD, clinical professor of medicine at Columbia College of Physicians and Surgeons in New York City and director of clinical ethics and chairman of the hospital's medical ethics committee sort out "Medical Care for the Elderly: Should Limits Be Set?", taking a close look at the future of Medicare's dwindling resources.

Guest Blog | Michael Millenson | June 16, 2008

Yearning for Universal Coverage Is Not Universal

Many still view universal coverage with apprehension, not anticipation
View bio for Michael MillensonEveryone wants universal health coverage, right? Not quite. As I pointed out in a recent opinion piece for the Washington Post, the yearning for universal health care is far from universal. The reaction to that article – about 160 posted comments or direct emails to me  – confirmed that assessment.  So did the lack of reaction from certain quarters (more on that below).

In the article, I wrote:

Here's a cold truth: Despite much media hand-wringing on the subject, most of us give about as much thought to those who lack health coverage as we do to soybean subsidies. The major obstacle to change? Those of us with insurance simply don't care very much about those without it. It's only when health care costs spike sharply, the economy totters or private employers begin to cut back on benefits that the lack of universal health care comes into focus. Noticing the steadily growing ranks of the uninsured, the broad American public – "us" – begins to worry that we'll soon be joining the ranks of "them."

News media and interest group profiles of uninsured individuals focus disproportionately on middle-class whites, I charged. The reality, however, is this:

Two-thirds of those without health insurance are poor or near poor, according to the Kaiser Family Foundation. And there are clear disparities in how different racial and ethnic groups are affected. Only 13 percent of non-Hispanic white Americans are uninsured, compared with 36 percent of Hispanics, 33 percent of Native Americans, 22 percent of blacks and 17 percent of Asians/Pacific Islanders....

If a lack of health insurance were truly a white middle-class crisis, then conservatives and liberals would long ago have joined together, carved out a compromise and done something.

After criticizing Republicans and Democrats, minority group political leaders and prominent health care foundations, I concluded, in part:

Over the years, our society has gradually provided a medical safety net for the elderly and disabled (Medicare), the poor (Medicaid) and veterans. At one time, these commitments were controversial, and there's no doubt that they're expensive. Yet…[i]t's our willingness to be our brothers' keepers that in part defines who we are as Americans.

OK, I admit it: the truth is more nuanced. Compassion is just one of our traits. The theme of rugged individualism and self-reliance, for example, plays a large role in our national myth. Back in 1949, the New York State Journal of Medicine bemoaned the way advocates of health insurance (versus 100 percent self-pay) ignored the lessons of Darwin:

Any experienced general practitioner will agree that what keeps the great majority of people well is the fact that they can’t afford to be ill. This is a harsh, stern dictum, and we readily admit that under it a certain number of cases of early tuberculosis and cancer, for example, may go undetected. Is it not better that a few such should perish rather than that the majority of the population should be encouraged on every occasion to run sniveling to the doctor?

None of the comments on my article went quite that far, but the gist of many was similar: the uninsured either wouldn’t need insurance if they better managed their own health or would be able to afford it if they better managed their money. So why should I help bail them out?

Others simply invoked the dreaded specter of “socialism.” The canard that universal coverage equates to “socialism” was reportedly instituted by an American Medical Association PR consultant during the Truman administration, but it continues to be wielded cynically today. Pointing out that every other nation in the industrialized world has some form of universal coverage has little impact on an electorate socialized, as it were, to ignore the examples of Germany, Switzerland and a host of other nations.

Of course, there were respondents who called for a Canadian-style system, blamed all evils on insurance company greed or said we needed first to solve the problem of soaring costs. Others were simply grateful that the problem of the uninsured had been highlighted.

But here’s what nobody said: No one addressed the issues of race, class and political and economic self-interest that were at the heart of the article. Indeed, I saw no comments or emails from anyone identifying themselves as black or Hispanic.

Physicians, meanwhile, continue to almost as fragmented as the general public. While a recent survey in the Annals of Internal Medicine found that 59 percent said they support legislation to establish a national health insurance program, while 32 percent opposed it, there were glaring gaps among specialties. For example, psychiatrists were overwhelmingly in favor, while general surgeons were barely so.

Meanwhile, in a less-publicized study by the firm LocumTenens, 63 percent of respondents said they would “continue practicing like they do today,” if universal health care were implemented, 11 percent would change occupations and nine percent said they would retire.

Even if the answers are skewed towards self-selected respondents, a distressing number of physicians continue to react to universal care less like, “I am my brother’s keeper” and more like, “Don’t tread on me.” So do their patients.

June 13, 2008

Homelessness and Healthlessness

Connected at the hip
As the saying goes, one thing leads to another. One of the measurables that has been publicized over the years to help stimulate action in health system reform is the number of uninsured in America. But as the economic downturn expands, and people lose their jobs and their homes, the number of underinsured  may actually provide the tipping point. The number of underinsured has increased 60% between 2003 and 2007, with one in five adults under the age of 65 currently affected.

Back in 1972, Senator Ted Kennedy laid this out in detail in his book, “In Critical Condition: The Crisis in America’s Health Care.”  The facts haven’t changed for the better since then. Roughly one-sixth of the U.S. population more than 5 percent of their disposable income on health care.  Approximately one-fifth at one point or another have been contacted by collection agencies related to their medical bills. And if you or a family member are unlucky enough to contract a terminal illness, there is a four in 10 chance of a severe financial crisis in your future.

An examination of more than 1,700 U.S. debtors  who declared bankruptcy in 2001 shows obvious examples of the gradual, downward, often health-related financial slide they experienced in the two years prior to filing. Out of the debtors with health issues, 38 percent had a lapse in insurance in the two-year lead up. 60 percent avoided a necessary visit to the doctor or dentist, and 47 percent did not fill a prescription they had been given.

Looking at the entire group, 28 percent cited illness or injury as their specific cause of bankruptcy. But nearly half (46%) met at least one of the four criteria for “major medical bankruptcy.” The criteria include illness or injury as a direct cause of insolvency, uncovered medical bills exceeding $1,000, two weeks of work lost to illness or injury, or a history of mortgaging the home to pay medical bills.

For that 28 percent whose illness drove them toward bankruptcy, who was sick in the family? Eight out of 10 times it was the parent. In these cases there was usually a double financial hit – lost wages accounting for 65 percent of the financial loss and unplanned medical bills accounting for 35 percent of the loss. In 13 percent of the cases, a child was ill, and in 8 percent, it was an elderly family member. As for the illnesses that lead to medical bankruptcy in these families, the most common diagnoses include cardiovascular disease, trauma, orthopedic and back problems; and cancer, diabetes, pulmonary disease, psychiatric disorders, and childbirth-related and congenital disorders.

Surprisingly, most of those who eventually slid into medical insolvency were initially insured. More than 75 percent had coverage prior to their illness or injury. In 60 percent of the cases, the coverage was private, with one-third losing the coverage when they stopped working due to illness. Fifty-six percent could no longer afford insurance premiums, and 7 percent couldn’t get new insurance due to preexisting medical conditions. On average for all of the debtors citing medical reasons for bankruptcy, the mean out-of-pocket expenditures from time of illness to bankruptcy was a surprisingly low $11,854.

The truth of the matter is that if you are a working American, low or middle class without significant savings and disability insurance, and you fall prey to a common illness that prevents you from drawing a salary, unpaid medical bills approaching the $10,000 threshold will likely cause you to consider bankruptcy to keep a roof over your family’s head. Such vulnerability, along with our 45+ million citizens who are completely uninsured, fundamentally undermines societal values. The subprime push was justified by the policy goal of creating an "ownership society." The reality is that homelessness and healthlessness are connected at the hip, and that being underinsured places you at nearly the same risk as having no insurance at all.
Guest Blog | Michael Millenson | June 05, 2008

Consumer Reports on Health: Worse Than Average

Good intentions do not good tools make, even if you're Consumers Union
View bio for Michael Millenson

Maybe no one at Consumer Reports has a mother. The first rule of effective consumer information is “tell it to Mom;” that is, explain why something is important in the kind of language you would use if speaking to your mother. Unfortunately, the folks at Consumers Union have now, for the second time, put out purportedly pro-consumer health care information that no one’s mother could love. Their latest offering is at best mildly helpful and at worst seriously misleading. The only explanation I can think of is that the CU folks believe so firmly in their own good intentions that they ignore the impact of what they are actually doing.

And as long as we’re awarding demerits to the self-delusional in the Liberal Do-Gooder category (Conservative Market-Worshippers richly deserving a category of their own), save a sigh of exasperation for the creators of something called the Healthcare Equality Index.

A quick disclosure: I am a subscriber to Consumer Reports online, have known some individuals there for years and did some brief consulting to them some years back. Therefore, let me be clear that my criticisms are based exclusively on public information.

CU’s latest offering is a link to the Dartmouth Atlas of Health Care and its analysis of hospital practice variation. The CU imprimatur suggests this is Major League quality information. The truth is closer to the story of the baseball manager who blurted out about one of his players, “While he can’t hit, neither can he throw.”  In that same vein, while the Dartmouth information is not easy to use, neither is it easy to understand.

The Dartmouth Atlas is a health services research tour de force. It takes an incontrovertible outcome (death from a serious chronic illness) and then applies a complex algorithm to account for all medical resources used during the two years before that outcome. The result is more evidence of practice variation and that “more” care isn’t always “better.” However, expecting this insight alone to prove useful to someone making a decision about their own or a family member’s medical treatment means you’ve spent way too much time in an ivory tower.

How should a CU subscriber interpret the fact that one hospital is “aggressive” and another “conservative” in its resource use? In trying to reassure us that we can choose “conservative” and less costly treatment, CU explains that “aggressive care does not necessarily improve patient outcomes and can sometimes shorten life. But wait: doesn’t that mean aggressive care sometimes does improve patient outcomes and lengthen life? If I listen to CU, there’s no doubt I’ll save money for the federal government (the Atlas uses Medicare data), but if I don’t, I may save my life.

Maybe the folks at CU do have mothers: they just don’t like them very much.

“We’re not at a point yet where we can say which hospitals are bad or good," Dr. John Santa, director of Consumer Reports’ new Health Ratings Center, acknowledged to Chicago Tribune reporter/health blogger Judy Graham.

Whatever happened to, “First, do no harm?”

By the way, the Chicago hospital most aggressive in its use of resources before the patient died was a Catholic one, and the hospital with the lowest score was the public hospital.  However, the Dartmouth Atlas makes no allowances for the impact of religious beliefs in regard to life extension or the impact of patient socio-economic status (or hospital financial status) on intensivity of treatment.

This is the second time CU has been unable to distinguish between information that sets the blood of researchers racing and information real people might reasonably rely upon. Its ConsumerReportsHealth site debuted with “Best Treatments” from the Cochrane Collaboration evidence-based medicine reviews. This carefully constructed tool from the folks at Oxford University gives us epistemological categories such as “treatments that work but whose harms may outweigh benefits.”

Come to think of it, that’s a logical precursor to the Dartmouth University rankings of hospitals where the harms (an adverse event that kills you) may also outweigh the benefits. Unless, of course, they don’t.

The good news is that CU plans to put out genuine cost and quality information on hospitals by the end of 2009. I hope no one tells them that some of those evil for-profit have been doing this since the late 20th century.

Now on to the Healthcare Equality Index.  You might assume this is a clever way to call attention to the disparities in care that we know cause serious harm to African-Americans, Hispanics and other minorities. It is not. Instead, it constitutes the responses to a survey designed to measure “how equitably hospitals in the United States treat their gay, lesbian, bisexual and transgender patients and employees.”

The survey was designed by the Human Rights Campaign Foundation Family Project and the Gay and Lesbian Medical Association. A whopping 88 out of roughly 5,000 U.S. hospitals voluntarily responded and agreed to make their names public. Perhaps some folks have had too little exposure to the ivory tower and the idea of “statistical validity.”

Yes, discrimination against GBLT patients and employees can be a problem, and GBLT individuals’ special health care needs certainly can get short-shrifted by uncomfortable straights. But if you want to talk seriously about health care equality, then get serious. The well-educated, well-insured, solidly upper-middle-class white gay couple is far more likely to get the health care they need than the working-class, dark-skinned, Spanish-speaking couple with no health insurance at all.

Even if they have a subscription to Consumer Reports.

Story of the Week | June 04, 2008

Leveraging Technology to Transform Health Care

A new hope for living to our fullest human potential
In recent years, there has been a lot of discussion about using technology to help manage disease and disability and to help older Americans “age in place.” But starting with the White House Conference on Aging in 2005, a new dialogue began to emerge, one that put an emphasis on the question: “How might technology extend independence, productivity and the quality of life?”

And now, in 2008, a new question is emerging: “How might technology be applied to re-engineer homes for health so aging citizens become a more integrated part of the multigenerational family, the community and a prevention-oriented health delivery system?”  

In other words, is it possible that the technology we have been developing for older Americans might be adapted so that it benefits their children, grandchildren, and great-grandchildren as well?

The answer is yes. In supporting our most senior citizens with the latest technological advances in home design, care-team connectivity, mobility, cognition, entertainment, learning and employment, we can also reorient our support for citizens and their families around a more home-centered approach that reinforces productivity, connectivity and good health. This vision harnesses software and hardware for the home that not only improves individual quality of life, but also advantages family, community and societal goals.  

The re-wiring of the American home for seniors is bringing us amazing innovations – from devices that monitor whether individuals are properly taking their medications to computer programs that help them keep their cognitive abilities sharp. Now we are at a point where a challenge must go out to our technology innovators: Can they come up with new “killer applications” that would apply these ideas more broadly for the health of families? Can we target technologic advances in health to reach our citizens most at risk? Can we, in powering the health technology revolution, broaden our social contract to include universal health coverage? How do we unite the resources of the technology, entertainment, and financial sectors with the traditional health care power players, and incentivize them to work together to create a truly preventive and holistic health delivery system that is equitable, just, efficient, and uniformly reliable? How can each citizen play a role in ongoing research and innovation, and help define lifelong learning and behavioral modification as part of good citizenship?  

The vision for technology must be integrated into a broader and more transformational quality-of-life model, serving all Americans – not just those who are aging. It is not so much about aging as it is about living, and doing so to our fullest human extent. Technology has the power to assist us in healing, providing health and keeping our nation and global family whole. But its capacity to deliver on this promise is dependent on a vision for health that is both broad and inclusive.  

To learn more, watch this week’s video, embedded with this blog, or read the full transcript. Then offer your own insights and comments. Is this idea feasible? Do you feel it is worth pursuing?

Transcript

Read the full transcript of this story.

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