Tuesday, January 21, 2014

“When it comes to health, your zip code matters more than your genetic code.”



REALLY? ON THE SOCIAL DETERMINANTS OF HEALTH

One of my daily blog destinations is The Incidental Economist. A while back I ran across this:
Sometimes health policy can’t be about about health care
A paper in this month’s edition of Health Affairs (gated) provides a stark reminder that many determinants of health lay well outside the boundaries of insurance and health care delivery. Hilary Seligman and her coauthors examined temporal trends in the incidence of hypoglycemia (dangerously low blood sugar, usually associated with diabetes), stratified by income*. They posit a plausible story about the “pay cycle” that develops in households, which is well established in the literature, particularly among low-income individuals . Toward the end of the month, a household’s resources—income, SNAP, Social Security, and/or other benefits—can become exhausted, ostensibly changing food consumption patterns...
Policy wonks have a terrible habit of focusing on insurance and health system design (and here I count myself, because health care financing is the research I find most interesting, so it’s what I write about). This gives short shrift to the “social determinants” of health—upstream factors related to lifestyle, environment, and socioeconomic status—that cannot be corrected by medical interventions. We’re fond of highlighting how much more the United States spends on health services, but an idiosyncrasy that receives less attention is how much less we spend on other social services. For a fuller discussion of that than I can provide, you should see this interview with Lauren Anne Taylor and Elizabeth Bradley, authors of The American Health Care Paradox.

These findings also illustrate the difficulty in finding policy solutions to address health disparities. The authors note that food pantries and soup kitchens already ramp up staffing and resources toward the end of the month. We could explore different ways to distribute existing benefits, but that may have other negative impacts (ie: making it harder to pay rent or bills at the beginning of the month).

Of course, in the political arena, the discussion isn’t framed as “expanded coverage or expanded social policy”. Instead, we’re stuck with polemics about “expanded coverage… or not.”  As complicated as insurance is, we default to it in health policy because it seems the most facile way to confront medical problems. That doesn’t make it the most effective way—but it’s hard to be optimistic about changing the terms of the debate.

*Here, “low-income” is defined as residing within a ZIP code where average income is in the lowest decile of admitted patients in a given year. Everyone not matching this criterion is “high income”.
"...focusing on insurance and health system design." Indeed. PPACA, ACOs, HIX, Health IT, Big Data, Quality Measures, "interoperability," organizational leadership, workflow redesign, etc. All the topics nominally the broad focus of this blog.

But, apropos,

Health policy was once thought to be about little more than the provision and funding of medical care: the social determinants of health were discussed only among academics. This is now changing. While medical care can prolong survival and improve prognosis after some serious diseases, more important for the health of the population as a whole are the social and economic conditions that make people ill and in need of medical care in the first place. Nevertheless, universal access to medical care is clearly one of the social determinants of health.

Why also, in a new publication on the determinants of health, is there nothing about genes? The new discoveries on the human genome are exciting in the promise they hold for advances in the understanding and treatment of specific diseases. But however important individual genetic susceptibilities to disease may be, the common causes of the ill health that affects populations are environmental: they come and go far more quickly than the slow pace of genetic change because they reflect the changes in the way we live. This is why life expectancy has improved so dramatically over recent generations; it is also why some European countries have improved their health while others have not, and it is why health differences between different social groups have widened or narrowed as social and economic conditions have changed.
PDF link here.

Recall my coverage of the stirring Keynote of outgoing Kaiser head George Halvorson back in November at NYeC 2013. George has made the mitigation of health care disparities his next focus of action.


This kind of stuff takes us uncomfortably but unavoidably into socioeconomic theory and the heated partisan politics it generates.

to wit:


LIFE ON THE NEW PASTURES
Two issues dominated Barack Obama’s first presidential term: healthcare and the economy. Both reflect the tension between the individualism of the Northern herders and the collectivism of the Southern herders. The Patient Protection and Affordable Care Act, also known as Obamacare, established national health insurance in the United States. Liberals praised it, not as a perfect system but as a historic step in the right direction. The United States had finally joined the rest of the modern world in providing basic healthcare to all its citizens. Conservatives— many of them— despise Obamacare, which they regard as a step toward ruinous socialism. The recent healthcare debate has been awash in misinformation,* but amid the lies and half-truths there can be found an honest philosophical disagreement.

At its core, this disagreement, like so many others, is about the tension between individual rights and the (real or alleged) greater good. Universal health insurance requires everyone to buy in, either through an individual purchase of health insurance or through taxes. Conservatives mounted a  legal challenge to Obamacare, culminating in a landmark Supreme Court decision. The Supreme Court upheld Obamacare on the grounds that it’s funded through a combination of voluntary purchases and taxes (which are both constitutional) rather than by the government’s forcing people to buy something (which is arguably not constitutional). But the tax-versus-forced-purchase distinction is really just a legal technicality. The people who hate Obamacare don’t hate it because they believe that it’s funded by forced purchases rather than forced taxes; what they hate is the forcing. Obamacare might not be socialism, but it’s certainly more collectivist than some people care for, restricting individual freedom in the name of the greater good.

During one of the primary debates, journalist Wolf Blitzer had the following exchange with Texas congressman Ron Paul.
BLITZER: A healthy 30-year-old young man has a good job, makes a good living, but decides, you know what? I’m not going to spend $ 200 or $ 300 a month for health insurance because I’m healthy, I don’t need it. But something terrible happens, all of a sudden he needs it. Who’s going to pay if he goes into a coma, for example? Who pays for that?
PAUL: Well, in a society that you accept welfarism and socialism, he expects the government to take care of him.
BLITZER: Well, what do you want?
PAUL: But what he should do is whatever he wants to do, and assume responsibility for himself. My advice to him would have a major medical policy, but not be forced—
BLITZER: But he doesn’t have that. He doesn’t have it, and he needs intensive care for six months. Who pays?
PAUL: That’s what freedom is all about, taking your own risks. This whole idea that you have to prepare and take care of everybody— [applause]
BLITZER: But Congressman, are you saying that society should just let him die?
As Paul prepared his hesitant answer, a chorus of voices from the crowd shouted, “Yeah! Let him die!” These are the Northern herders. Paul couldn’t quite bring himself to agree— or disagree. He said that neighbors, friends, and churches should take care of such a man, implying, but not explicitly stating, that the government should let him die if no one else is willing or able to pay. As you might expect the more Southerly herders disagree.

(Note: In the Parable of the New Pastures, the Southern herders are extreme collectivists, communists, and are thus far to the left of contemporary mainstream liberals, despite frequent accusations to the contrary. Thus, as we discuss contemporary politics, I refer to contemporary liberals as “more Southerly” rather than “Southern.” Contemporary U.S. conservatives, in contrast, resemble more closely their fictional Northern counterparts.)

Along with healthcare, the miserable state of the U.S. economy took center stage during President Obama’s first term. When Obama took office in 2009, the economy was in free fall, thanks to a housing bubble that burst after a decade of inflated growth and a financial sector that placed enormous bets on housing prices. The government did several things in an attempt to stave off complete financial disaster. First, in late 2008, while President Bush was still in office, the federal government bailed out  several of the investment banks at the heart of the crisis.* Later, the Obama administration bailed out the auto industry and extended aid to homeowners facing foreclosure. These measures were opposed, to varying degrees, by Northern herders who argued that the banks, the automakers, and the desperate homeowners should, like Ron Paul’s hypothetical patient, be allowed to “die.” Why, they asked, should American taxpayers have to pay for these people’s poor judgment? The more Southerly herders didn’t especially relish the thought of bailing out irresponsible decision makers, but they argued that these measures were necessary for the greater good, lest their bad choices sink the whole economy. During Obama’s first year, congressional Democrats passed his $ 787 billion stimulus bill, the American Recovery and Reinvestment Act of 2009. This, too, was opposed by Northern herders who favored less government spending and more tax cuts. Better, they said, to put money into the pockets of individuals who can decide for themselves how to spend it.

Related to both healthcare and the economy is the broader issue of economic inequality, which came to the fore in 2011 with the Occupy Wall Street protests. From 1979 to 2007, the incomes of the wealthiest U.S. households skyrocketed, with the top 1 percent enjoying income gains of 275 percent, while the bulk of Americans gained around 40 percent. (The gains at the tippy top, the top 0.1 percent, were even larger, around 400 percent.) These trends inspired the Occupy slogan “We are the 99%,” calling for economic reforms to restore a more egalitarian distribution of wealth and power.

The story of rising income inequality comes in two versions. According to the individualist Northern herders, the winners earned their winnings fair and square, and the losers have no right to complain. “Occupy a Desk!” read the sign of a Wall Street counterprotester. Presidential hopeful Herman Cain called the protesters “un-American,” and the eventual Republican nominee, Mitt Romney, accused them of waging “class warfare.” In September 2012, the liberal magazine Mother Jones dropped one of the biggest bombshells in U.S. electoral history. They posted online a secret recording of Romney in which he described roughly half of the American population as willful government dependents who will never “take personal responsibility and care for their lives.” According to Romney’s infamous speech, the “47 percent” of the population that earns too little to pay income taxes (on top of payroll taxes) deserve no better than what they’ve got.

The more Southerly herders tell a different story. They say that the wealthy have rigged the system in their favor, noting that rich people like Mitt Romney pay taxes at a lower rate than many middle-class workers, thanks to lower tax rates on investment income, myriad tax loopholes, and overseas tax havens. And now, thanks to the Supreme Court’s decision in Citizens United v. Federal Election Commission, which legalized unlimited campaign contributions to “independent” political groups, the rich can use their money to buy elections like never before. These more Southerly herders say that even in the absence of nefarious system rigging, maintaining a just society requires active redistribution of wealth. Otherwise the rich use their advantages to get richer and richer, passing on their advantages to their children, who then begin life with a big head start. Without redistribution of wealth, they say, our society will bifurcate into permanent classes of haves and have-nots...
Thanks to Science Based Medicine for the tip on this book. See Tribalism and Medical Ethics. Economic disparities are sharply in the rise in the U.S., -- increasingly so. 

e.g., consider the maps below regarding two of our major cities, New York and San Francisco.



Darkest shaded areas depict highest income earners. This is a hot topic of late in my Bay Area -- the new Techie Billionaires pricing everyone else out of the city. Resentment has been building; Google private employee commuter buses have been attacked. Twitter headquarters in downtown SF is the site of protests.

Just in (Jan 22):
The tech protests get personal — and ugly
Breaking the rules of a civil society: Activists target a Google engineer at his Berkeley home


On Tuesday, an activist group styling itself the “Counterforce” took the San Francisco Bay Area “protests” against tech-boom-driven gentrification to a new, absurd and potentially dangerous level. They rallied in front of the Berkeley home of Google engineer Anthony Levandowski, ringing his doorbell at 7 a.m. and passing out fliers in his neighborhood that claimed he “develops war robots for the military and builds surveillance infrastructure.”...

From Counterforce’s manifesto:

After previous actions against the Google buses, many critics insisted that the individual Google employees are not to blame. Taking this deeply to heart, we chose to block Anthony Levandowski’s personal commute. We also respectfully disagree with this criticism: We don’t see one action as better than the other. All of Google’s employees should be prevented from getting to work. All surveillance infrastructure should be destroyed. No luxury condos should be built. No one should be displaced…
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Below, Park Avenue: money, power and the American dream.



Well worth your time. They use the "Monopoly" game analogy, that exemplar of cutthroat winner-take-all capitialism. Moreover, this PBS documentary asks us to consider what it's like playing the Monopoly game wherein those who acquire the most assets get to repeatedly change the rules while playing, in ways that inure to their benefit.

Is that the state of our nation? One Dollar, One Vote? Is this inexorable? Are we headed for a new Feudalism? 

What will be the upshot for health care? Will our socioeconomic trends neuter the progress resulting from our clinical science and information technology advances?
“When it comes to health, your zip code matters more than your genetic code.”
From Oxfam:



Bringing up such issues invariably begets you the epithets "moocher," "taker," "bleeding heart liberal," "socialist," "commie," etc. -- the tried and true ad hominem strategy for shutting down debate. It has been fashionable of late among "conservatives" to sarcastically cite former President Reagan's jibe that "we fought a war on poverty, and poverty won." Fashionable to demonize the halt, lame, and poor.

See "Richistan"
Nonetheless, the problems wrought by extreme economic disparity are real and will not simply be denied away in pursuit of Wishful Thinking fallacy convenience.

Specifically back to the health care implications:

Veronica’s headache
It was an unseasonably warm spring day in South Central Los Angeles in 2011. I had joined this community clinic three years before and had set about implementing an upstreamist approach. Veronica, a 33-year-old woman, sat in my exam room, her head in her hands. Her otherwise tall and formidable figure was slouched over in pain. This was not the first time she had felt this way. For more than a year, her headaches had come and gone. And each time, the pain would ripple through her life, disrupting her family and work. This episode was no different. She had missed about seven days of work as an office manager at an auto parts dealer in the past month. Veronica’s employer, who was understanding, would see her in pain and insist that she leave early and seek help. But the headaches kept coming, straining her relationships at work. Her home life started to suffer, too. It was hard for her to sleep. She often had to call on her aging mother to care for her two sons when Veronica needed to visit the doctor or simply to rest. At school events and her sons’ after-school activities, Veronica was often unable to focus. Usually a stoic woman, she considered herself unflappable in the face of adversity. But these days, she admitted, she was fatigued and often irritable.

Three weeks earlier, Veronica had gone to a local emergency room to seek relief. After a battery of tests, a doctor prescribed her some pain medications. Then she gave Veronica instructions to return to the emergency room if the pain worsened or persisted. The medicines helped for a short while, but they often left her drowsy and unfocused. The pain persisted. So, following instructions, she returned twice more to a local emergency room. All told, she underwent at least a dozen blood tests, two CT scans, and a spinal tap — a procedure in which a needle is placed in the lower back to collect and test a sample of spinal fluid. But for Veronica, each visit to the emergency room ended the same way: She was told her test results were “normal,” sent home with more pain medication, and advised to seek a primary care physician.

Veronica had already tried that approach. When she had visited primary care clinics for headache flare-ups, her experiences hadn’t inspired much confidence. The doctors and nurses seemed rushed. She heard a lot of talk about tests and short-term medications. One doctor wondered if Veronica was exaggerating her pain simply to get narcotics. Despite multiple visits, she didn’t feel much better. In fact, she told me, that’s why she went to the emergency room in the first place.

When I met Veronica, she was exasperated. A $ 1,200 bill for her first hospital visit had arrived at her home. At work, her boss was growing concerned. Veronica was concerned about losing her job. Without a steady income, she worried about paying the rent, roughly $850 per month. She fought back tears as she described the toll this was taking on her family. 

And she grimaced often. On top of everything else, Veronica was still in pain.

Veronica’s story is far too typical in our health care system. Her experience has become commonplace, not just in low-income neighborhoods but in middle-class and more affluent communities as well. Access to quality care is a problem. And even when care is available, it is often poorly coordinated, expensive, and stressful.

When Veronica came to our clinic, though, we did things slightly differently.

The clerk checked Veronica in. The medical assistant recorded vital signs and collected standard information about her health. This is a typical process for many clinics. But then the medical assistant ran down a simple checklist, asking Veronica a few routine, evidence-based questions about her housing. Veronica indicated that her apartment had some problems with mold, water leaks, and roaches. These answers went into her chart, along with other important data. I briefly reviewed the chart and opened the door to greet her. 

Knowing where Veronica lived made a world of difference. I asked her to tell me more about her home and her headaches. She lived with her sons in a two-bedroom, ground-floor apartment in South Los Angeles, not far from the clinic. Veronica insisted that she kept her home as clean as possible, but persistent leaks had led to chronically damp, moldy conditions and the roach infestation. Her landlord hadn’t helped, and she couldn’t afford to move. As she talked, I followed up with more questions and began a targeted physical exam. Within 15 minutes, I felt pretty confident in my diagnosis: Veronica had migraines related to chronic nasal allergies and sinus congestion. These conditions are often caused or made worse by dampness, mold, roaches, and other markers of substandard housing. I asked about her sons’ health. Her eldest was under a pediatrician’s care for severe asthma, another health problem often related to bad housing. I explained my concerns and prescribed her medicines to help with the symptoms. Then I referred her to a program run by our clinic in partnership with two local organizations to help make her housing healthier. One of the partners was a tenants’ rights advocacy group long active in South Los Angeles. The other was a community development agency that created affordable housing and trained residents to become community health workers.

Within a few days, a community health worker from our clinic visited Veronica. She taught her new techniques for controlling dampness in her home. Then, with the help of our partners, she helped Veronica contact the landlord, this time with a doctor’s note and information about local housing codes that the landlord was obligated to meet.

Veronica came back to the clinic a few months later for a routine follow-up visit. She hadn’t been to the emergency room. Her home was healthier. Her allergies lingered but had improved, and her headaches were gone. Her son’s asthma was less active. Veronica and her family had gotten better.

The current standard of care
To improve Veronica’s headache, the health care system had to address where she lived. Why did Veronica go so long before she got that type of care? Did she have to suffer as long as she did? The great irony is that many of the health care professionals who had cared for her provided what is generally considered adequate care. On each occasion, doctors and nurses initiated a diagnostic workup involving expensive machines and procedures. They prescribed medications to help relieve her pain and instructed her to seek further evaluation if required. Based on what we know about Veronica’s experience, most people, including myself, would not find these clinicians at fault for negligence. In fact, on an individual basis, each clinician’s approach was probably well within the bounds of what we consider the current standard of care.

The problem, of course, is that the current standard of care isn’t working. Instead of addressing the cause of disease, health care in the U.S. has long focused on just treating its symptoms. We fixate on the headache and ignore the home. Once upon a time, interacting with patients in their homes and communities seemed like an obvious, integral part of doctoring. But in the last century or so, the culture of medicine has largely been shaped by an exuberant overemphasis on the biologic and molecular phenomena of disease. Improving the social conditions that shape health has become an afterthought.


And that’s the irony. When clinicians ignore the home — or any of the other factors that shape our health — their treatments often are less effective. In clinics and hospitals across the nation, we repeatedly miss precious opportunities to understand and improve people’s health in the context of their social and physical environments. These opportunities are often obscured by the transactions of pills and bills that have come to define the health care experience for many patients and providers. For patients like Veronica, the medical system fails to reduce suffering because it simply doesn’t collect the right data or equip providers with the right tools to address the factors that shape our health where it begins.


This disconnect is striking, especially when one considers the forces that determine how healthy we are as a society. As the New England Journal of Medicine   reported   in 2007, medical care accounts for only about 10 percent of the variation we see in health outcomes. Consider that statistic from another perspective. Let’s say someone asks you to review all the accumulated science about what determines a society’s health. Next, they give you a menu of interventions and $ 100 in small bills. Based on what you learned from your review of the evidence, you’re given the task to spend that $ 100 in whatever way you want with one purpose in mind: Create the greatest health you can for your population. You’d be wise to spend only about $ 10 of your budget on medical care and spend more on improving social and environmental factors such as substandard housing, job stress, poverty, discrimination, and dangerous neighborhoods — what experts often call the “social determinants of health.”

When we think about what really shapes our health, medical care is just one relatively minor force. Experts often think of five general health-defining forces: genes and biology, behavior, medical services, social environment (the ways in which we relate to each another), and physical environment. The latter two, often referred to together as the social determinants of health, are significantly more powerful drivers of wellness than is medical care. The social determinants are shaped by the power and resources that people have, all of which are influenced by the policy choices we make as a society. These policies, in turn, influence the behaviors and choices you and I make every day. For instance, a growing body of research indicates that how close people live to affordable, healthy food outlets or safe, green parks plays a role in their choices to eat healthily or to exercise.

Where we live and work clearly impacts our health behaviors. And these social and environmental forces are also capable of changing our DNA, literally. Epigenetics, an emerging field of science, examines the link between environmental exposures and the regulation of our genes, especially as they pass from one generation to the next. New discoveries in epigenetics reveal that exposure to toxins, such as chemical pollution or even severe emotional stress, can significantly affect the health and development of individuals and their children. For instance, a   study   reported in the Economist in 2011 showed that children born to mothers who experienced stress and psychological abuse during pregnancy were significantly more likely to have DNA changes that reflected a higher sensitivity to stress hormones compared with children of women who did not suffer abuse.   Stress and abuse, in turn, are most often linked with poverty and other socioeconomic factors.

The nature vs. nurture debate can no longer be viewed as a battle between equals. The impact of nurture — in the form of the social and environmental settings that surround us — is far more powerful than we’ve ever imagined. These are the forces that shape or distort our genes, our behaviors, and the landscape of opportunity in our communities.

The current standard of care often ignores these forces. This lack of attention leads to missed opportunities to effectively alleviate suffering and can sometimes even contribute to more suffering. Think of the costs for Veronica. While bouncing in and out of the health care system, Veronica stacked up major opportunity costs. Instead of spending time at work or with her family, she spent days in a hospital or clinic looking for help. The direct economic costs were just as bad. Just one of her three emergency room visits resulted in a bill roughly equivalent to one month’s rent.
Then, ironically, this experience with the health care system took its own toll on her health. Each time a hospital or a clinic discharged her with nothing more than pain medicine, the system unwittingly sent Veronica — without adequate warning, protection, or tools — back to her home, the place where her illness first started...
Manchanda, Rishi (2013-06-06). The Upstream Doctors: Medical Innovators Track Sickness to Its Source (Kindle Single) (TED Books). TED Conferences. Kindle Edition.
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JANUARY 22ND NEWS HEADLINE


So, what about it? Is this OK? Should society simply permit people to acquire all the material wealth they are capable of amassing? Objectively, is there any such thing as an economically just and sustainable society? He Who Dies With The Most Toys Wins? e.g., Venture Capitalist (and Liberal Kristallnacht Victim of late) Tom Perkins.

He Who Dies With The Most Toys Dies, actually. But...


Below, a common blogosphere sentiment.



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FEB 4th UPDATE

Michael Lind of The New America Foundation has written an interesting, nuanced (if somewhat depressing) article just posted at Salon.com, "The 1 percent wins again: The system’s so fixed that a global class war is only a dream"
[P]urported measures of the global 1 percent that conflate different species of the rich in radically different societies — self-made entrepreneurs, bankers dependent on government bailouts, crony capitalists in autocratic regimes, and members of the political elite in petrostates — are not worth the press releases that tout them. Chinese Communist Party princelings, who owe their manufacturing-based wealth to family connections and corruption, have little or nothing in common with Saudi aristocrats — who in turn came by their wealth by methods different from those used by generals in some military dictatorships who are paid by dictators out of the loot derived from plundering the population. And the minority of the global rich who more or less earned their wealth — by founding a business that provides a good or service that people want to pay for — belong in a separate category altogether from aristocrats who inherited their wealth or kleptocrats who manipulated government connections.

In other words, “inequality” is not a single disease; it is a label for a variety of quite different maladies in different societies, some worse than others.  From this it follows that different kinds of harmful inequality, in different countries, must be subject to different remedies. For example, if you want to combat inequality in China, you should want to abolish the monopoly of political power and much economic wealth by Communist Party officials, who use their control of government and of state-owned enterprises to illicitly enrich themselves and their offspring. In contrast, inequality in the U.S. is driven largely by policies like financial sector bailouts that socialize the costs while privatizing the risks of high-income individuals who work in the FIRE (Finance, Insurance and Real Estate) sector. An appropriate policy agenda for reducing U.S. inequality would bear little resemblance to the anti-inequality agenda in China...
Interesting. Read all of it.

I have a bit of FIRE Sector experience, btw. See my posts "Tranche Warfare" and "The Dukes of Moral Hazard." And, I have long followed the Sisyphean‎ writings of the iconoclastic Bill Black of UMKC's New Economic Perspectives.

Another great read: Graeber's "To have is to owe," precursor to to his excellent book "Debt: the first 5,000 years." I was blessed to read that book before I knew who he is. It is a fine piece of social anthropology scholarship.

Mr. Lind notes that
The idea that cross-national class allegiances will trump cross-class national allegiances has appealed to many on the radical left ever since Marx and Engels called on the workers of the world to unite. It didn’t happen in the 19th century, and it didn’t happen in the 20th century. A global class war won’t happen in the 21st or 22nd or 23rd centuries, either. 
To that point I would just add that the efficacy of technologies for suppression of effective dissent are progressing at least as rapidly as the disparities of income and wealth, if not moreso.

FEB 6TH UPDATE
Billionaire Sam Zell Defends Tom Perkins: 'The 1 Percent Work Harder'
 

When the going gets tough, the rich dudes stick together. Or at least rich dude Sam Zell did in an interview with Bloomberg TV Wednesday.

The billionaire chairman of Equity Group Investments backed up fellow rich guy Tom Perkins, who set off a firestorm when he recently compared the "progressive war on the 1 percent" to Nazi anti-Semitism in a letter to the Wall Street Journal. (He later apologized for using the word "Kristallnacht" but defended the overall "message.")

"I guess my feeling is that he’s right," Zell said when asked by Bloomberg's Betty Liu how he felt about Perkins' stance. "The 1 percent are being pummeled because it’s politically convenient to do so."

Zell then said the problem is that all non-rich are just jealous that they don't have the same work ethic that the country's wealthiest do.

"The problem is that the world and this country should not talk about envy of the 1 percent. It should talk about emulating the 1 percent," he said. "The 1 percent work harder. The 1 percent are much bigger factors in all forms of our society."

Liu countered that the ever-widening gulf between the richest and poorest Americans must make it harder for those living under the poverty line to get ahead, no?

Nah, said Zell.
"Lots of people have come from nowhere and become part of the 1 percent," he said.
FEB 7TH UPDATE
5 libertarian oligarchs who made fortunes off the government they want to destroy
RICHARD ESKOW, ALTERNET

The cult of the libertarian-minded ultra-weatlhy would make an intriguing anthropological case study. But it would be a case study with a twist: its research subjects increasingly control our economy, our politics, and even our personal lives.

We’re dealing with a cohort of highly fortunate, highly privileged and highly unaware individuals who have been inappropriately lionized by society. That lionization has led them to believe that their wealth and accomplishments are their own doing, rather than the fruits of collaborative effort – effort which in many cases was only made possible through government support.

But instead of thanking the government and the taxpayers for their good fortune, they’ve allowed their own good press to go to their heads. And they’re biting the hand that feeds them, attempting to shut down the system of taxpayer support and government action which created their world.

Our money-obsessed society gives them far more praise and then they deserve. Our corrupted political system gives them far more influence than we deserve. And, slowly but surely, they are now turning their considerable resources to dismantling government’s role in society...
FEB 14TH UPDATE

Tom Perkins doubles down...

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IN OTHER NEWS

ReportingonHealth.org Launches Health Care Reform Implementation Blog
ReportingonHealth.org has kicked off a new project to track how well the Affordable Care Act is fulfilling its goal of getting Americans insured.

Remaking Health Insurance: The Affordable Care Blog will focus on California, the state with the largest number of uninsured, and move beyond  politics to explore how care is being accessed and how effectively that care is being delivered. Check out our introductory post discussing the scope of the blog.
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JANUARY 23RD UPDATE


Just finished listening to Dr. DeSalvo's DC ONC Conference opening keynote via live streaming. I was to have been there, but the blizzard bumped me off my flights.

She will get no shortage of advice and criticism. e.g., from one of THCB resident trolls:



HHS Secretary Sebelius speaks at 10 a.m. EST.

Update...


FIRST PANEL UPDATE

Best audience question of the day thus far was about  EHR (non) readiness to accomodate "football field size" patient genomic data. The entreprenurial / venture capital panel agreed that they are not ready.

Such readiness is likely a long way off. Beyond database and I/O capacity, we are woefully short of people qualified to counsel patients on the upshot of genetic findings. See AJMC Panel: Genetic Testing Should Come With Counseling: American Cancer Society CMO, Supreme Court Plaintiff Warn of Consumer Risks.
Driving down costs makes [genetic] testing more accessible, but the amount of information can overwhelm patients and primary care physicians if experienced genetic counselors are not part of the process, the panelists agreed.
Link (pdf)
What GAO Found
GAO’s fictitious consumers received test results that are misleading and of little or no practical use. For example, GAO’s donors often received disease risk predictions that varied across the four companies, indicating that identical DNA samples yield contradictory results. As shown below, one donor was told that he was at below-average, average, and above-average risk for prostate cancer and hypertension.


GAO’s donors also received DNA-based disease predictions that conflicted with their actual medical conditions—one donor who had a pacemaker implanted 13 years ago to treat an irregular heartbeat was told that he was at decreased risk for developing such a condition. Also, none of the companies could provide GAO’s fictitious African American and Asian donors with complete test results, but did not explicitly disclose this limitation prior to purchase. Further, follow-up consultations offered by three of the companies failed to provide the expert advice that the companies promised. In post-test interviews with GAO, each of the companies claimed that its results were more accurate than the others’. Although the experts GAO spoke with believe that these tests show promise for the future, they agreed that consumers should not rely on any of the results at this time. As one expert said, “the fact that different companies, using the same samples, predict different directions of risk is telling and is important. It shows that we are nowhere near really being able to interpret [such tests].”...
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UPDATE: ONC TOWN HALL SESSION


Lot of empty seats. Weather must have impacted attendance. I was scheduled to go, but lost my flights owing to JetBlue overbooking caused by the blizzard.

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More to come...

Friday, January 17, 2014

Meaningful Use Stage 2 is off to a bumpy start

As reported on MedPage Today
Few Docs Ready for Stage 2 'Meaningful Use'
Jan 17, 2014, David Pittman, Washington Correspondent, MedPage Today

WASHINGTON -- Roughly one physician in eight has an electronic health record (EHR) system capable of supporting most requirements for Stage 2 of the "meaningful use" program, a government survey found.

Only 13% of office-based physicians reported an intention to participate in the EHR incentive program and had a system meeting 14 of the 17 Stage 2 core objectives, according to a report released this week from the CDC's National Center for Health Statistics (NCHS).

About 56% of all physicians intended to participate in the EHR incentive program but didn't meet the core objectives the NCHS asked about.

"Meaningful use" refers to provisions in the 2009 Health Information Technology for Economic and Clinical Health (HITECH) Act, which authorized incentive payments through Medicare and Medicaid to clinicians and hospitals that use electronic health records in a meaningful way that significantly improves clinical care...

Over on THCB, Incoming ONC head Dr. Karen DeSalvo tried to put a positive spin on the state of health IT in her recent piece Survey Says: EHR Incentive Program Is on Track. Be interesting to hear what she has to say next week at the ONC Annual Conference in DC.

Below, the typical invective hurled by the anti-HIT trolls, this one from Dr. DeSalvo's post.


NEVADA HIE UPDATE

Sources tell me that the ONC funded Nevada State HIE (run out of DHHS, not HealtHIEnevada.org) may be about to fail. It won't be the first one, but it will sure be another multi-million dollar waste of taxpayer money.

Speaking of wasting money:

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MONDAY MORNING UPDATE (JAN 20TH)
Do providers have the EHRs for Stage 2 Meaningful Use?
Jennifer Bresnick, January 20, 2014


Providers may be lacking one big, basic ingredient for a successful Stage 2 attestation: a certified EHR capable of meeting the Meaningful Use objectives.  The National Center for Health Statistics (NCHS) has released a new data brief that highlights the relatively small number of providers operating on an updated EHR as the industry enters the second stage of the EHR Incentive Programs.

While 69% of office-based physicians reported that they intended to participate in meaningful use during a survey in 2013, only 13% of those providers also had an EHR system capable of supporting 14 of the Stage 2 core and menu objectives.  While this number seems exceedingly low, one should note that the survey was conducted between February and June of 2013, long before the majority of EHR vendors had even finished developing their 2014 ONC certified technology.

However, it is no secret that it’s been an achingly slow process to get the new technology through the testing and verification process.  Tight deadlines and major upgrades are slowing the adoption process for providers who have already spent big bucks on their 2011 systems...

Were I a Medicare EP who began attestation in 2011, I'd have by now collected $38k of the full $44k incentive reimbursement potential (not counting the sequester deduction now applied to the payments), ~86% of the total available. It sure looks to me that the combination of costs for Stage 2 upgrades -- certified software update, workflow alterations, administrative expenses -- may well eclipse any remaining potential reimbursements.

A doc I know responds:


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And the hits just keep on coming...
Why specialists don’t like their EHRs

The list of reasons why specialists don’t like their EHRs could go on for pages, but what it really comes down to is this: most EHRs try to satisfy everyone’s needs, an impossible feat in a world with hundreds of medical specialties. Hospitals and primary care practices can sometimes make a one-size-fits-all EHR work, but specialists have a much harder time adjusting to having an EHR as part of their workflow.

A recent Black Book Rankings survey found that specialists are much less happy with their current EHR than family physicians are. However, most physicians place the blame on themselves. The top three reasons for considering a vendor switch all have to do with picking the right EHR:

  1. Solution does not meet the individual needs of the practice, including workflow (80 percent)
  2. The practice did not adequately assess its needs before selecting the original EHR (79 percent)
  3. Design of EHR is not suited for the practice specialty (77 percent)
Moving forward, specialists are taking a lot more care in picking their next EHR, focusing on more than just qualifying for government incentives. According to Black Book, here are the top five “must haves” for a replacement EHR vendor:
  1. Vendor viability (84 percent)
  2. Provider data integration and network data sharing (83 percent)
  3. Demonstrable return on investment (78 percent)
  4. Adoption of mobile devices (75 percent)
  5. HIE support and interoperability
With the EHR market in a constant state of shuffling out the unpopular EHRs, practices are most concerned with an EHR’s past success and future prospects. Practices want proof now, not just promises...
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More to come...

Monday, January 13, 2014

Next up...


Register here. An important two days via which to get a sense of just where the federal Health IT effort is headed and what progress might be expected. Incoming ONC head Dr. Karen DeSalvo certainly has her work cut out for her.

Then, in February,




Register here.

Former President Bill Clinton keynoted last year at HIMSS13 in NOLA. It was fabulous.
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A DOCTOR DEFENDS HIS EMR

I spend a lot of time online defending health IT from the large contingent of irascible Perfectionism Fallacy naysayers. I get called a "troll," a "EHR Vendor shill," and told I have no right to even opine because I'm not a physician.

Well, this man is a physician:
...Modify my note with today’s findings and conclusions.  Write, in the computer, any new orders.  The orders are instantly checked for allergies, compatibility, dose, availability, redundancy and communicated to the proper department.  Complete.  Legible. Efficient. Accessible and transmittable (via encrypted form).  Even fun.

The quality of medical care because of clarity, accuracy, speed and the quality of communication is multiplied, probably exponentially. Problems are not forgotten. Errors are quickly identified. The valuable efforts of patient and professional are not wasted.  The time needed to create extraordinary medical records is cut at least in half.  The medical record is not just another device, like a pencil, tape measure or paper chart. It is a tool to guarantee, amplify and create quality.


Is the future here?  Are present day EMRs the Holy Grail?  Not yet. They still have major problems in data input, across system compatibility and universal access. However, they a stunning technology that saves cost not only by saving time, but by improving the quality of the record and therefore the quality of care.  In the future, not to far away, EMRs will interface with medical information and research databases and work with each doctor with each patient on each day to assure the most accurate diagnoses, the best treatment and the best chance of cure.  Even now, they are revolutionary...
From The Health Care Blog.
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TUESDAY, JANUARY 14TH, MY "EPIC" DAY

Had my initial visit with my new Primary, in the brand-new John Muir Medical Group facility in Walnut Creek. They provide a pretty nice patient portal. I was able to go in ahead of time and start populating some data.



I got there at 7:30 a.m. Everyone was all spiffed out, cherubic, effusively solicitous. This was opening day for the new complex at 1450 Treat Blvd. The place is beautiful. Registration was a breeze, both in the expansive downstairs foyer and up at outpatient internal med in suite 250.

Free patient Wi-Fi. I'd brought my Mac Air, just in case I had any extended wait time. Nice.

Muir uses EPIC. There were bugs. The M.A. doing my vitals and CC, etc. Had trouble logging into the large wall-mounted terminal in the exam room. Had to make a tech support call. I don't like the wall terminal thing. That is so yesterday.

My new doc came in, sporting a laptop. Along with him came an IT dude.

EPIC support. It was needed. I bit weird, being worked up and examined by my new doctor with this IT guy in the room.

Nonetheless, we hit it off. Young doc, a D.O. (I'd weighed the relative merits of going with someone closed to my age). I told them I did Health IT journalism and gave them each my card. The doc kept anxiously apologizing for any glitches in this initial encounter. It'll be big-time shakeout cruise this week for them, I'm sure.

No problem. I'd used the portal internal email a head of time to send him a PDF of my last complete progress note dump from Dr. Gong's Encounter Pro EHR in Vegas (my prior Primary).

He'd not yet seen it.

He told me they'd immediately eRx my two maintenance meds renewals to Walgreens close to the house where I've been getting my scrips, and he wrote me a lab order for fasting bloodwork.

Later in the day I got a call from Dr. Gong's office, telling my they'd gotten a renewal request they couldn't fill because I was overdue for my latest f/up visit.

"Look, I called you in December advising that I'd moved to the Bay Area and was looking for a new Primary, and would like Robert to give me any referrals he could."

Never heard back.

So, now I gotta get in someone's face at Walgreens here to straighten out the eRx mistake.

An "EPIC" day. I really like this new doc. We'll see how my experience with Muir goes.

A COUPLE OF MILESTONES


+200k blog hits, +1,000 Twitter followers. Just keep plugging away.
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MEANINGFUL USE INCENTIVES PAYMENTS UPDATE
Meaningful Use Incentive Payments Reach Nearly $18 Billion, CMS Says
January 15, 2014, Alex Ruoff 

Jan. 14 --The Centers for Medicare & Medicaid Services has issued nearly $18 billion in Medicare and Medicaid incentive payments through its meaningful use program, a CMS official said Jan. 14.

As of November 2013, the CMS had paid 334,081 hospitals and health-care providers more than $17.77 billion in incentive payments to adopt electronic health record systems, Robert Anthony, an eHealth specialist for the CMS, said at a meeting of the Health IT Policy Committee.

Although registration with the meaningful use program slowed slightly in November and December, Anthony said, it remains a widely popular program.

More than 93 percent of all hospitals eligible to receive an incentive payment through the meaningful use program had registered for a payment by November. More than 80 percent of all health-care providers eligible to receive an incentive payment through the meaningful use program had registered for payment by November, he said.

Registration Slowing

Provider registration for the Medicare meaningful use program hit a four-month low in November, according to CMS data. Just 3,081 health-care providers and 30 hospitals registered in November to participate in the Medicare program, the lowest since July.

Registration for the Medicaid meaningful use program by health-care providers hit a four-month low in November, according to the CMS. Just 2,175 health-care providers registered in November to participate in the Medicaid meaningful use program, the lowest since August...


Data source. The relatively easy money has been paid. Going forward it will be significantly more difficult, in pursuit of significantly fewer incentive payment dollars.

apropos, "medical bridges to nowhere"?
Is Meaningful Use based on a 'flawed mindset' of healthcare?
January 15, 2014 | By Ashley Gold


According to Patrick Soon-Shiong, M.D., billionaire and chief executive officer of healthcare IT company NantHealth, the Meaningful Use incentive program was born out of a flawed view of the healthcare industry.

Speaking at the Clinton Foundation's 2014 Health Matters conference in La Quinta, Calif. on Tuesday, Soon-Shiong said the creation of Meaningful Use has built "medical bridges to nowhere," Healthcare IT News reported.

"We've funded systems that don't talk to each other," he said. "Nobody has looked at healthcare as a systems approach."
At the J.P. Morgan 32nd Annual Healthcare Conference in San Francisco a day earlier, Soon-Shiong officially launched NantHealth, a "transformational healthcare IT company converging science and technology through a single integrated clinical platform, to provide actionable health information at the point of care, in the time of need," according to an announcement. The company, it would appear, is Soon-Shiong's answer the HITECH Act.

For instance, according to the announcement, its interoperable Clinical Operating System (iCOS), which can talk to any software, is currently installed in 150 practices, integrating 50 individual systems, managing 3.3 million patient records across 22 electronic medical records.

"Nobody has looked at healthcare as a systems approach," Soon-Shiong said.

Members of Congress are using the continued debate over the Medicare sustainable growth rate as an opportunity to require more interoperability among electronic health records in the Meaningful Use program.

Sens. John Thune (R-S.D.) and Mike Enzi (R-Wyo.) recommended an amendment to the SGR fix that would require interoperability by 2017 in order for a provider to be a meaningful user of EHRs. Sen. John Cornyn (R-Texas) suggested a slightly different amendment that would require the U.S. Department of Health & Human Services to adopt standards to ensure that EHRs were interoperable by 2017. The House SGR bill also called for interoperability by 2017.

Stage 3 of the Meaningful Use program is slated to begin in 2017.

REMINDER


Per CMS:
"Medicare EPs Must Attest by February 28 at 11:59 pm ET to Receive 2013 Incentive.

If you are an eligible professional (EP), the last day you can register and attest to demonstrating meaningful use for the 2013 Medicare EHR Incentive Program is February 28, 2014. You must successfully attest by 11:59 p.m. Eastern Standard Time on February 28 to receive an incentive payment for your 2013 participation.

You must attest to demonstrating meaningful use every year to receive an incentive and avoid a payment adjustment.
"
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More to come...

Wednesday, January 8, 2014

The Society for Science Based Medicine

I just joined this organization.

Overview
What is the Society for Science-Based Medicine?
  • A Society for a community of like-minded individuals, both in and out of health care, who support Science-Based Medicine.
  • People should not suffer, die and lose hope, time and money due to pseudo-medicine. 
The mission of the Society for Science-Based Medicine includes, but is not limited to,
  • Educating consumers, professionals, business people, legislators, law enforcement personnel, organizations and agencies about Science-Based Medicine.
  •  Providing resources and information for information concerning all aspects of Science-Based Medicine. Providing a central resource for communication between individuals and organizations concerned about Science-Based Medicine.
  • Supporting sound consumer health laws for the practice of Science-Based Medicine and opposing legislation that undermines Science-Based Medicine.
  • Encouraging and aiding legal actions in support of the practice of Science-Based Medicine.
Goals of the Society include, but are not limited to
  • Community
  • Education
  • SSBM blog
  • SSBM conference
  • SSBM podcast
  • SSBM wiki
  • Medical school core curriculum 
  • SSBM journal
  • ebooks
  • Legal and legislative advocacy 
This website has three levels of access:

As I've noted repeatedly, ScienceBasedMedicine.org has long been one of my priority daily web stops. I urge everyone involved with health care to join and contribute to SSBM. I will want to see them address some of the controversies generated by Health IT specifically. Accurate, timely, and necessary information is fundamental to doing good science. The anti-HIT ankle biters are legion and loud, but many of their concerns need to be taken seriously and addressed forthrightly.

I recently finished deep study of Mario Bunge's excellent "Medical Philosophy: Conceptual Issues in Medicine." I was alerted to it on SBM back in December.



See my December 4th post Philosophia sana in ars medica sana. I will soon begin connecting some dots between it and another of my serious favs, the Weeds' profound "Medicine in Denial."


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NEWLY FOLLOWING ON TWITTER



Well, apropos of "science based medicine," I'm looking into this author's book after running across her on Twitter. I've reached out to her. We'll see whether she responds.



Scientific "proof"? We shall see.
Introduction
What if I told you that caring for your body is the least important part of your health . . . that for you to be truly vital, other factors are more important? What if the key to health isn’t just eating a nutritious diet, exercising daily, maintaining a healthy weight, getting eight hours of sleep, taking your vitamins, balancing your hormones, or seeing your doctor for regular checkups?
Certainly, these are all important, even critical, factors to optimizing your health. But what if something else is even more important?
What if you have the power to heal your body just by changing how your mind thinks and feels?
I know it sounds radical, especially coming from a doctor. Trust me, I was just as skeptical when I first discovered the scientific research suggesting that this might be true. Surely, I thought, the health of the human body isn’t as simple as thinking ourselves well or worrying ourselves sick.
Or is it?
A few years ago, after 12 years of conventional medical education and 8 years of clinical practice, I had been thoroughly indoctrinated into the dogmatic principles of evidence-based medicine, which I worshipped like the Bible. I refused to trust anything I couldn’t prove with a randomized, controlled clinical trial. Plus, having been raised by my father, a very conventional physician who made fun of anything New Age, I was as hard-nosed, closed-minded, and cynical as they come.
The medicine I had been trained to practice didn’t support the idea that you can think yourself well or make yourself sick with the power of your thoughts and emotions. Sure, my medical school professors diagnosed some illnesses that lacked biochemical explanations as “all in the patient’s head,” but those patients were promptly and quietly referred to psychiatrists, while eyes were rolled and heads were shaken.
It’s no wonder the notion that the mind might have the power to heal the body would be threatening to many mainstream doctors. After all, we spend a decade learning the tools that supposedly give us mastery over other people’s bodies. We want to believe that the time, money, and energy we’ve put into becoming doctors isn’t wasted. We’re professionally and emotionally invested in the idea that if something breaks down physically, you must seek our expertise. As doctors, we like to believe we know your body better than you do. The whole medical establishment is based on such a notion.
Most people are happy to function within this paradigm. The alternative—that you have more power to heal your own body than you’ve ever imagined—lobs the responsibility for health back into your court, and many people feel like that’s just too much responsibility. It’s much easier to hand over your power and hope someone smarter, wiser, and more experienced can “fix” you.
But what if we’ve got it all wrong? What if, by denying the fact that the body is naturally wired to heal itself and the mind operates this self healing system, we’re actually sabotaging ourselves?
As physicians, things inevitably happen on our watch that science simply can’t explain. Even the most closed-minded doctors witness patients who get well when, by every scientific rationale, they shouldn’t. When we witness such things, we can’t help questioning everything we hold dear in modern medicine. We start to wonder if there is something more mystical at play...
Again, we shall see. The foregoing is from the free sample chapter. A few early yellow flags have popped up, but I don't want to be summarily dismissive.

First place I go any more is to the comments on Amazon. I first look at those with low rankings of any book in question. The "one stars" reviews in this case:
Here is the summary of what this book is trying to state:
1. Have a perfect life. If you don't have a perfect life, seek to make it perfect such as leave a difficult marriage, quit a stressful job, find the perfect partner, and so on.
2. If you don't have a perfect life and have stress you can't get away from then meditate as meditation can neutralise the effects of chronic stress. If you can't meditate, be mindful.
The book is well presented but to me that was all there was to it.
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I value Lissa's experience AND her work sounds very much like Andrew Weil's and Louise Hay's. If you are familiar with their works, you will find this to be more of the same. There is nothing original here in my opinion.
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Miserable...is how I felt the entire time I was reading this lousy book - but, I kept soldiering on, waiting for the good part, i.e. Lissa's blinding revelations on how to heal all the dysfunction that is so slavishly laid before us in the first 3/4 of the book. When I got there, all I could do is skim, muttering "Seriously? this is all you've got?"...
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Then I am sure you will think it is OK... or heck for the real naive in this arena even great as so many seem to have posted.
But the truth is... this is a 'copy-cat' book... in my estimation a very poor knock off... of everything that many others have said many years prior! i.e. Dr. Bernard Siegal - Louise Hay - Dr. Weil - Carolyn Myss - and the list could go on ad infinitum!
If you have ever taken a marketing class one of the first things you learn is... Hey Copy Cat works ... if it worked for someone else... copy it!!!
Then she throws in a bit on her own alleged minimal life disruption... which most of us wish we only had her troubles... She came from an incredibly supportive family... married to quote... the love of her life... and as she also admits has more money than she knows what do with... hard to feel sorry for the disruption she claims she overcame and that all of us should learn something from...
The book was a huge waste of my time and money... a total 'copy-cat' work.
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The only thing this book proves is that credulous people can be easily conned out of $20 by disingenuous hoaxsters like this fool. No peer-reviewed science, no tested claims, no cogent theories-- just "feel-good" nonsense that provides no real information of value. Save your money. Think twice about believing things that are too good to be true; usually, and in this case for sure, you're being lied to.
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If you want to read a book loaded with clichés, that all has been written about before, give this a try. But Dr. Lisa just keeps on selling - don't rely on doctors - you can heal yourself, I have the answers - blah, blah, blah. But what about the people who have a genuine positive outlook but unfortunately still die? Did they just not try hard enough? What a message. And, she can't write. But you go, girl - make all your money before being found out to be the vacant yo-yo you are. Am I mad - yep, because I think she is dangerous - really dangerous to people seeking answers. She is no authority - just an old-fashioned shaman.
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A lot of pseudo-scientific claims with NO peer-reviewed evidence. Real scientists don't use words like "proof". Where's the theory? What variables are being tested? What or who is the control? What journal was this published in? Seriously, anyone who buys this feel-good pseudo-intellectual garbage deserves to be ripped off.

Ouch. The two- and three star comments aren't much more forgiving. When I read too many negative comments / rankings, it's usually a show-stopper for me, given that there are so many books to buy and study.

IN OTHER NEWS

EXECUTIVE SUMMARY: CMS AND ITS CONTRACTORS HAVE ADOPTED FEW PROGRAM INTEGRITY PRACTICES TO ADDRESS VULNERABILITIES IN EHRS OEI-01-11-00571
WHY WE DID THIS STUDY
Electronic health records (EHRs) replace traditional paper medical records with computerized recordkeeping to document and store patient health information. Experts in health information technology caution that EHR technology can make it easier to commit fraud. For example, certain EHR technology features may be used to mask true authorship of the medical record and distort information to inflate health care claims. The transition from paper records to EHRs may present new vulnerabilities and require the Centers for Medicare & Medicaid Services (CMS) and its contractors to adjust their techniques for identifying improper payments and investigating fraud.
HOW WE DID THIS STUDY
We sent an online questionnaire to CMS administrative and program integrity contractors that use EHRs to pay claims, identify improper Medicare payments, and investigate fraud. We also reviewed guidance documents and policies on EHRs and fraud vulnerabilities that CMS and its contractors released for health care providers. Lastly, we reviewed documents on EHRs and Medicare claims that CMS provided to its contractors.
WHAT WE FOUND
CMS and its contractors had adopted few program integrity practices specific to EHRs. Specifically, few contractors were reviewing EHRs differently from paper medical records. In addition, not all contractors reported being able to determine whether a provider had copied language or overdocumented in a medical record. Finally, CMS had provided limited guidance to Medicare contractors on EHR fraud vulnerabilities.
WHAT WE RECOMMEND
Although EHR technology may make it easier to perpetrate fraud, CMS and its contractors have not adjusted their practices for identifying and investigating fraud in EHRs. Our report made two recommendations. First, CMS should provide guidance to its contractors on detecting fraud associated with EHRs. CMS could work with contractors to identify best practices and develop guidance and tools for detecting fraud associated with EHRs. Second, CMS should direct its contractors to use providers’ audit logs. Audit log data distinguish EHRs from paper medical records and could be valuable to CMS’s contractors when reviewing medical records. CMS concurred with our first recommendation and partially concurred with our second recommendation.
PDF link to the full report here. Chart "cloning" and "upcoding" have long been issues. We were aware of such potential all the way back in the DOQ-IT days, 2005-2007.
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KATRINACARE.GOV UPDATE
Accenture new lead contractor on Obamacare website
By Roberta Rampton and Eric Beech, Reuters
Accenture has been chosen to replace CGI Federal as the lead contractor on the Obamacare enrollment website, which failed to work when it launched in October for millions of Americans shopping for insurance, the U.S. Centers for Medicare and Medicaid Services said on Saturday.
CGI Federal, a subsidiary of CGI Group, built the website, HealthCare.gov, which struggled with error messages and slow speeds for weeks after its launch. The glitches created a political crisis for President Barack Obama, threatening the roll-out of his signature healthcare law and emboldening its foes among Republican lawmakers to call for its repeal.
"As CMS moves forward in our efforts to help consumers access quality, affordable health coverage, we have selected Accenture to become the lead contractor for the HealthCare.gov portal and to prepare for next year's open enrollment period," the agency said in a statement.
CGI Federal said on Friday that its contract, which was originally awarded in 2011 and is scheduled to end February 28, would not be renewed...
Good riddance to these people. I hope they're forced to return the federal money they've wasted.
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More to come...

Saturday, January 4, 2014

Meaningful Use Stage 2 now fully underway

Well, here we go. Lock and load. If you've spent two or more years in Stage 1, you will now commence with Stage 2 for two years. It shouldn't be all that difficult for you. 

Stage 3 has been pushed back one year, btw.



Click here for the full CMS Stage 2 Guide (pdf).
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Saw this over at iHealthBeat.org while on holiday vacation.
Concern Grows About Doctor Offices Opting Out of Meaningful Use
Monday, December 23, 2013


Health IT experts say they are concerned that more physician offices will opt out of the meaningful use program, despite the federal government's planned changes to the program's timeline, Modern Healthcare reports (Conn, Modern Healthcare, 12/21)...

According to Modern Healthcare, the penalties for failing to meet Stage 2 requirements of the meaningful use program are minimal, while most of the incentive payments linked to achieving Stage 1 of the program already have been doled out. As a result, there are not significant financial benefits from continuing to participate in the program, according to Modern Healthcare.

Meanwhile, more physicians say they believe that meeting meaningful use program criteria will not result in patient benefits that offset the costs and efforts to achieve such requirements.


Jason Mitchell, director of the American Academy of Family Physicians' Center for Health IT, said that for an average family physician who receives about $100,000 annually in Medicare reimbursements, failing to meet Stage 2 of the meaningful use program in 2014 would cost only about $1,000 in penalties in 2015. The penalties increase to 2% of Medicare reimbursements in 2016 and 3% in 2017, bringing the average family physician's combined three-year penalty to just $6,000.


Mitchell said, "We saw a 17% drop off of meaningful users that engaged in 2011 but didn't in 2012," adding, "I think it's going to be more for 2013" (Modern Healthcare, 12/21).
Probably take a good bit of practice-specific Excel sheet work to model out just where the net wash will be for any one organization -- the cost of upgrades, the workflow revisions, consulting assistance, the very real administrative costs of compliance. Moreover, if you're just getting started in 2014 (Stage 1), your total incentive money potential is significantly reduced.

The relatively easy money has been doled out. And, RECs are essentially going away (a totally stupid idea IMO, even though I'm no longer REC and this blog will soon change its name to The KHIT Blog), so assistance will come at market prices.

Interesting article here, btw, courtesy of my blogger friend John Lynn: One EHR Vendor’s Experience with Meaningful Use Stage 2 Certification.

JANUARY 6TH UPDATE

The latest ONC 2014 Meaningful Use certified EHRs, complete ambulatory systems as of this morning.


47 discrete products, culling the obvious dupes from the paltry 76 presented in the search (e.g., minor upgrade releases to the same basic product). Pretty small cohort relative to the thousands of 2011 certs. Industry shake-out at hand?

Well, there's always Clinic Monkey.


NEWS JUST IN
Senators press for EHR interoperability
House and Senate bills also revisit the HITECH Act
With Congress working on a long-term Medicare “SGR fix” in the recent short-term budget deal, lawmakers laid down seeds for addressing issues such as value-based reimbursement and EHR interoperability.
The House and Senate bills also revisit the HITECH Act. Senators John Thune and Mike Enzi, Republicans from South Dakota and Wyoming, added an amendment requiring “interoperability to be achieved by 2017 to be meaningful user under the Electronic Health Record Meaningful Use program,” with rules established via federal committee under the direction of the HHS Office of the National Coordinator.
John Cornyn, a Republican from Texas, added a more specific and different amendment, directing HHS to adopt a common interoperability standard by 2017, as part of the rules for Meaningful Use Stage 3...
Yeah, the hardy perennial "interoperability" illusion. I've been barking about that for a long time.
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The year ahead in health IT policy
January 07, 2014 | Anthony Brino
In a new year with a new ONC chief, the federal health IT policy committee is taking comments from the public and its many expert workgroups, and then crafting recommendations for the third phase of the meaningful use program.
With an open public comment period ending January 14, the health IT policy committee and its subcommittees and workgroups covering meaningful use, privacy and security, standards, ACOs and more are scheduled to convene dozens of times now through the end of the year, brainstorming, discussing and then rehashing recommendations on key areas of EHR functions and information exchange.
The first and last health IT policy meetings on the ONC calendar for 2014 are both being held by the Meaningful Use Workgroup, chaired by Paul Tang, MD, chief innovation and technology officer at Sutter Health’s Palo Alto Medical Foundation.
The workgroup is meeting throughout January and February, and on February 4th making a set of recommendations on the issue of meaningful use stage 3 objectives to the full Health IT Policy Committee, which will be chaired by incoming national coordinator Karen DeSalvo, MD..
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More to come...

Wednesday, January 1, 2014

Happy New Year to everyone in Health IT

Safely back home from eleven days down on the farm in northern Alabama. Long, tiring travel day yesterday, BNA -->  LAS --> OAK. Packed planes ("completely full," as they redundantly say), flight delays at both departures.

Wishing everyone a healthy, happy, and productive 2014. Let's paint the healthcare world a brighter color.
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More to come...