Archive for December, 2009
Criminals win again. Got to love the courts!
Thursday - December 31st, 2009 at 3:12 pm
In a case that could set the first broad judicial standards for the use of Tasers, a federal appeals court in California has ruled that the police can be held liable for using one of the devices against an unarmed person during a traffic stop.
The United States Court of Appeals for the Ninth Circuit, based in San Francisco, said the electrically disabling device constituted excessive force when used against an unarmed man who did not pose a threat, and it refused to allow a police officer immunity for its use.
In a vividly worded opinion issued by the court this week, Judge Kim McLane Wardlaw described a “bad morning” for Carl Bryan, a 21-year-old Californian who drove over large stretches of Southern California to retrieve car keys mistakenly taken by a friend and ended up being Tasered by a Coronado, Calif., policeman and breaking four teeth when he fell to the ground.
Mr. Bryan was stopped twice on his driving odyssey, once for speeding and again for not wearing his seat belt. After the second stop, Mr. Bryan was “agitated, standing outside his car, yelling gibberish and hitting his thighs, clad only in his boxer shorts and tennis shoes,” the court said.
The judge noted, however, Mr. Bryan did not threaten the officer, Brian McPherson, and was not attempting to flee — all elements of a three-part test that the United States Supreme Court has used to determine when significant force is justified. As for the third factor in the Supreme Court test, the severity of the offense at issue, the Ninth Circuit judges observed that “traffic violations generally will not support the use of a significant level of force.”
The court found the policeman’s use of force so exceeded the threat posed by Mr. Bryan that they denied his request for immunity for his actions and for a quick dismissal of the case against him. Instead, the judges will allow the case to go forward.
Eugene G. Iredale, a lawyer for Mr. Bryan, hailed what he called the “landmark decision.”
A lawyer for Officer McPherson, Steven E. Boehmer, did not return calls seeking comment.
Orin S. Kerr, a former federal prosecutor and a professor at George Washington University Law School, called it “an important case” that was unusual in the way it set a broad rule without giving deference to the use of force by the police.
“This decision is trying to create rules to govern cops and is trying to limit the use of Tasering,” he said. “It has a very big real-world impact.”
The court’s rulings affect much of the western United States: Alaska, Arizona, California, Hawaii, Idaho, Montana, Nevada, Oregon, and Washington, along with two territories.
Geoffrey P. Alpert, a professor of criminal justice at the University of South Carolina who recently completed a four-year study of the devices for the Department of Justice, said Tasers and other “conducted electrical devices” were used by more than 17,000 law enforcement agencies and that some departments had already upgraded their rules to allow the devices to be used only in the case of an “active or immediate threat.” If it is not overturned, he said, the Bryan case “is going to impact a lot of departments that have not changed their standards.”
Something’s Very Wrong Here
Thursday - December 31st, 2009 at 3:01 pm
I know Iowa is in a bowl game, but when the State Government gets involved because people are mad they can’t watch the game, the line is crossed. The State government has no right wasting tax payer’s money for bullshit like this. Get satellite or use the internet! How much money is wasted on this? All it is, is a leverage tool for the provider to get the money they want and they are manipulating the government to do it. Do you all honestly believe it is a co-incidence that this is happening now, just when Iowa is in a bowl game? Come on wake up. I predicted this outcome a week ago, it is so predictable. Pure Bullshit!
Here is the story from Radio Iowa. (p.s. Mom, I told you this would happen.)
by Dar Danielson on December 31, 2009
There’s word today that an agreement could allow thousands of Iowa cable customers to see the University of Iowa play in the Orange Bowl next week. An agreement between the Mediacom Cable company and Sinclair broadcasting expires at midnight tonight, and if action isn’t taken, Sinclair stations KDSM in Des Moines, KFXA in Cedar Rapids, and KGAN in Cedar Rapids will stop being transmitted to Mediacom cable customers.
In a letter to Congress today, Mediacom chairman and chief executive officer Rocco Commisso says he’s received a tentative indication that Sinclair may consider a very short-term extension of their agreement. The case involves some 250,000 cable subscribers in Iowa.
Iowa Attorney General Tom Miller has asked the Federal Communion Commission to mandate interim carriage rights for Mediacom until a new contract is negotiated.
Diabetes Cases in Iowa Up
Thursday - December 31st, 2009 at 6:45 am
by Radio Iowa Contributor on December 24, 2009
State health officials say the number of Iowans with diabetes is climbing. Lorene Hinderks is coordinator for the Iowa Diabetes Prevention and Control Program for the Iowa Department of Public Health. Hinderks says the latest rise in cases is startling.
She says there are about 160,000 adults in Iowa with diabetes, of both types one and two. That’s more than 5% of the state’s population. Potential risk factors include being overweight and having a family history of diabetes, while ethnicity and age also play a role.
Hinderks says Iowans who may be at risk need to be educated about diabetes and the other dangers it can bring. “There’s a lot of things associated with diabetes, such as heart disease, stroke, kidney disease, blindness and amputation,” she says. “It’s very serious but there are ways to manage the disease and we like to create awareness of that, too.”
Hinderks gives some examples of how Iowans who have diabetes are dealing with it. “There’s healthy eating habits, physical activity that’s appropriate, there’s medications, there’s self-management education.”
Hinderks says there’s plenty of information about diabetes at the website: www.diabetes.org
Thanks to Pat Powers, KQWC, Webster City
4 Day work week for State Agencies
Thursday - December 31st, 2009 at 6:43 am
by O. Kay Henderson on December 25, 2009
in Business & Economy, Legislature, Politics & Government
Iowa’s governor is pushing the idea of a permanent, four-day work week for most workers in the executive branch of state government.
The State of Utah implemented a four-day work week last year. After just six months, Utah had saved $200,000 on custodial services alone. They’re saving twice as much on utility bills as nearly all state offices in Utah are closed on Friday. Today, about 17,000 Utah state employees work 10 hours a day, four days a week. They get a three-day weekend.
Iowa Governor Chet Culver says while the Department of Corrections can’t shut down on Fridays — prisoners have to be guarded 24 hours a day, most state agencies could shift to a four-day work week.
“I like the idea,” Culver says. “I like the concept.”
Complaints in Utah about its four-day work week have declined and, in some cases, the change has improved operations. The lines at Utah drivers license stations have eased because the offices are open later Monday through Thurday. Utah officials recently announced, however, that one, centrally-located drivers license office will be open on Fridays. starting in February.
“Overall, the Utah experience has been a positive one,” Culver says. “There are certainly drawbacks, but not only have states like Utah moved to it, but a lot of city and local governments around the country have experimented with it, too.”
A consulting firm Culver hired recommended a four-day work week as a budget-cutting move, but it will require legislative approval and changes in the contracts with state employee unions.
“Just the energy savings alone by shutting down buildings and not having to heat or cool them to the extent that you would if people were there — you can realize some real savings, but we want to balance that with the delivery of services,” Culver says. “But I think it’s likely that that idea will get a lot of support.”
So far this fall, Hawaii and the State of Washington have tried a limited four-day week for many state offices. Officials in Virginia and West Virginia are considering the four-day work week, too.
The State of Utah commissioned a poll which found 60 percent of Utah residents believe the four-day work week is a good idea. Nearly 80 percent of the people who were surveyed in Utah said the closure of state government offices on Fridays had no impact on them or their families.
Utah implemented the four-day work week in August of 2008 and the state’s governor at the time estimated the state would save $3 million a year in energy costs. After a year, Utah had saved about half a million dollars on energy, but aides of the current governor say there are related savings. Most of Utah’s vehicle fleet has been idled on Fridays, for example, and the estimated savings in gasoline and related costs amounts to $4.8 million.
Utah’s governor has said he may support moving back to a five-day work week, but a spokesperson for the state employees union says workers have made adjustments in their personal lives to accommodate their 10-hour workdays and it’d be difficult to adjust child care and other arrangements that were just changed in August of 2008.
Revised Diabetes Guidelines
Thursday - December 31st, 2009 at 6:07 am
#diabetes American Diabetes Association Revises Diabetes Guidelines
Dec 31, 2009
This press release is an announcement submitted by Medscape Medical News, and was not written by Diabetes Health.
December 29, 2009 - The American Diabetes Association (ADA) revised clinical practice recommendations for diabetes diagnosis promote hemoglobin A1c (A1c) as a faster, easier diagnostic test that could help reduce the number of undiagnosed patients and better identify patients with prediabetes. The new recommendations are published December 29 in the January supplement of Diabetes Care.
“We believe that use of the A1c, because it doesn’t require fasting, will encourage more people to get tested for type 2 diabetes and help further reduce the number of people who are undiagnosed but living with this chronic and potentially life-threatening disease,” Richard M. Bergenstal, MD, ADA president-elect of medicine & science, said in a news release. “Additionally, early detection can make an enormous difference in a person’s quality of life. Unlike many chronic diseases, type 2 diabetes actually can be prevented, as long as lifestyle changes are made while blood glucose levels are still in the pre-diabetes range.”
The A1c test, which measures average blood glucose levels for a period of up to 3 months, was previously used only to evaluate diabetic control with time. An A1c level of approximately 5% indicates the absence of diabetes, and according to the revised evidence-based guidelines, an A1c score of 5.7% to 6.4% indicates prediabetes, and an A1c level of 6.5% or higher indicates the presence of diabetes.
For optimal diabetic control, the recommended ADA target for most people with diabetes is an A1c level no greater than 7%. It is hoped that achieving this target would help prevent serious diabetes-related complications including nephropathy, neuropathy, retinopathy, and gum disease.
Unlike fasting plasma glucose testing and the oral glucose tolerance test, A1c testing does not require overnight fasting. Compliance with screening may therefore be improved through use of the A1c test, which can be determined from a single nonfasting blood sample.
Recommendation Changes for 2010
Specific changes in the 2010 Clinical Practice Recommendations are as follows:
- A section on diabetes related to cystic fibrosis has been added to “Standards of Medical Care in Diabetes.” New evidence has shown that early diagnosis of cystic fibrosis-related diabetes and aggressive treatment with insulin have narrowed the gap in mortality between patients with cystic fibrosis with and without diabetes and have eliminated the sex difference in mortality rates. New recommendations for the clinical management of cystic fibrosis-related diabetes, based on a 2009 consensus conference, will be published in 2010 in a consensus report.
- Revision of the section “Diagnosis of Diabetes” now includes the use of the A1c level for diabetes diagnosis, with a cutoff point of 6.5%.
- The section formerly named “Diagnosis of Pre-diabetes” is now named “Categories of Increased Risk for Diabetes.” Categories suggesting an increased risk for future diabetes now include an A1c range of 5.7% to 6.4%, as well as impaired fasting glucose and impaired glucose tolerance levels.
- Revisions to the section “Detection and Diagnosis of GDM [Gestational Diabetes Mellitus]” now include a discussion of possible future changes in this diagnosis, according to international consensus. Screening recommendations for gestational diabetes are to use risk factor analysis and an oral glucose tolerance test, if appropriate. Women diagnosed with gestational diabetes should be screened for diabetes 6 to 12 weeks postpartum and should have subsequent screening for the development of diabetes or prediabetes.
- Extensive revisions to the section “Diabetes Self-Management Education” are based on new evidence. Goals of diabetes self-management education are to improve adherence to standard of care, to educate patients regarding appropriate glycemic targets, and to increase the percentage of patients achieving target A1c levels.
- Extensive revisions to the section “Antiplatelet Agents” now reflect evidence from recent trials suggesting that in moderate- or low-risk patients, aspirin is of questionable benefit for primary prevention of cardiovascular disease. The revised recommendation is to consider aspirin treatment as a primary prevention strategy in patients with diabetes who are at increased cardiovascular risk, defined as a 10-year risk greater than 10%. Patients at increased cardiovascular risk include men older than 50 years or women older than 60 years with at least 1 additional major risk factor.
- Fundus photography is now recommended as a screening strategy for retinopathy, as described in the section “Retinopathy Screening and Treatment.”
- Extensive revisions to the section “Diabetes Care in the Hospital” now question the benefit of very tight glycemic control goals in critically ill patients, based on new evidence.
- Extensive revisions to the section “Strategies for Improving Diabetes Care” are based on newer evidence. Successful strategies to improve diabetes care, which have resulted in improved process measures such as measurement of A1c levels, lipid levels, and blood pressure, include the following:
- Delivery of diabetes self-management education.
- Adoption of practice guidelines developed with participation of healthcare professionals and having them readily accessible at the point of service.
- Use of checklists mirroring guidelines, which help improve adherence to standards of care.
- Systems changes, including providing automated reminders to healthcare professionals and patients and audit and feedback of process and outcome data to providers.
- Quality improvement programs, in which continuous quality improvement or other cycles of analysis and intervention are combined with provider performance data.
- Practice changes, which may include access to point-of-care A1c testing, scheduling planned diabetes visits, and clustering dedicated diabetes visits into specific times.
- Tracking systems with either an electronic medical record or patient registry to improve adherence to standards of care.
- Availability of case or (preferably) care management services using nurses, pharmacists, and other nonphysician healthcare professionals following detailed algorithms under physician supervision.
“The most successful practices have an institutional priority for quality of care, involve all of the staff in their initiatives, redesign their delivery system, activate and educate their patients, and use electronic health record tools,” the guidelines authors conclude. “It is clear that optimal diabetes management requires an organized, systematic approach and involvement of a coordinated team of dedicated health care professionals working in an environment where quality care is a priority.”
Diabetes Care. December 29, 2009; January 2010 Supplement.
Story how Merck created demand for a drug
Wednesday - December 30th, 2009 at 10:34 pm
Story from NPR by Alix Spiegel
Katie Benghauser had no concept of all the forces that combined to bring the box of pills to the bottom shelf of her medicine cabinet. All she knew was that three years ago she went in for a routine checkup and her doctor told her it was time for her to take a test.
Not that there was anything in particular about Benghauser that suggested sickness. At 54 she exercised every day and could outrun most 20-year-olds. She was a model of health.
Still, because Benghauser was thin, white, female, in her 50s and had a sister who had some bone problems, she says the doctor told her that she was concerned. “She felt like because my frame is slight and I’m female, that I was at risk for developing osteoporosis.”
Osteoporosis is a disease that causes bones to become thinner, more porous and break more easily. It mostly affects elderly women, who can be devastated by a fall that breaks their hip. One in five elderly women who break a hip will die within a year. Still, just to make sure, Benghauser went in for a test that measured the density of her bones. Two weeks later a letter came in the mail with an unsettling message: Benghauser had a condition called osteopenia, and her doctor recommended medication.
Osteopenia Vs. Osteoporosis
Osteopenia is different from osteoporosis. In fact, though Benghauser is extremely health conscious, she wasn’t familiar with it. “I’d heard of osteoporosis before, but I’d never heard of osteopenia,” she says.
Osteopenia, it turns out, is a slight thinning of the bones that occurs naturally as women get older and typically doesn’t result in disabling bone breaks. Still, Benghauser’s doctor recommended that she go on treatment. As Benghauser asked around, it turned out that many of her peers were taking the pills. For example, she works in an office in Richmond, Va., with seven other women.
“Half the staff is younger, in their 20s and 30s, and then there are four of us that are over 50,” she said. “Three of those four are on some kind of medication for osteopenia.”
The Biography Of A Medication
This is the story of how pills for osteopenia ended up in Benghauser’s medicine cabinet, and in the medicine cabinets of millions of women like her all over the United States. But more broadly, it’s the story of how the definition of what constitutes a disease evolves, and the role that drug companies can play in that evolution.
Osteopenia is a condition that only recently started to be thought of as a problem that required treatment. Until the early 1990s, only a handful of people had even heard the word. And to understand how osteopenia was transformed from a rarely heard word into a problem that millions of women swallow pills to treat, you need to go back to the beginning, to a place very far away from Benghauser’s suburban Virginia home.
A Meeting, A Decision, A Disease
The meeting took place in Rome, in a small hotel at the top of the Spanish Steps. There in 1992, a group of osteoporosis experts gathered under the auspices of the World Health Organization. The meeting had been organized because professional opinion about how to diagnose and measure osteoporosis was all over the map. Doctors and researchers didn’t even have a shared view of how osteoporosis should be defined.
For a long time doctors and researchers were only able to diagnose osteoporosis after a woman experienced a bone fracture. But by the early ’90s technology had evolved, and bone scanners made it possible to determine whether the bones were weak before any fractures occurred.
The question before the experts in Rome then was this: Since after the age of 30 all bones lose density, how much bone loss was normal? And, how much put women at risk and therefore should be considered a disease?
Anna Tosteson is a professor of medicine at the Dartmouth Institute for Health Policy and Clinical Practice and Dartmouth Medical School who attended the meeting. She says that over a two- or three-day period the experts in the room went back and forth and back and forth, looking at research and trying to decide precisely where on a graph of diminishing bone density to draw a line.
“Ultimately it was just a matter of, ‘Well … it has to be drawn somewhere,’ ” Tosteson says. “And as I recall, it was very hot in the meeting room, and people were in shirt sleeves and, you know, it was time to kind of move on, if you will. And, I can’t quite frankly remember who it was who stood up and drew the picture and said, ‘Well, let’s just do this.’ “
So there in the hotel room someone literally stood up, drew a line through a graph depicting diminishing bone density and decreed: Every woman on one side of this line has a disease.
Then a new question arose: How do you categorize the women who are just on the other side of that line?
To address this issue, Tosteson says, the experts — more or less off the cuff — decided to use the term osteopenia. Tosteson says they created the category mostly because they thought it might be useful for public health researchers who like clear categories for their studies. They never imagined, she says, that people would come to think of osteopenia as a disease in itself to be treated. The chairman of the meeting, John Kanis, of the WHO Collaborating Centre for Metabolic Bone Diseases, says the same thing.
Nevertheless, 17 years later Banghauser, of Richmond, Va., a woman whose bone density is just a hair away from that of the average healthy 30-year old, is not only medicated for osteopenia but literally spends her days worried about breaking a bone.
“I used to run marathons, and I would fall and trip on broken sidewalks,” she told me. “And you know initially before I had this diagnosis I didn’t think anything of it. But now every time I fall I get up and think, ‘Oh, good, I haven’t broken anything.’ “
“I’m much more aware of making sure I lift my feet up and I don’t trip on the sidewalks, but you know, if I didn’t know that I had osteopenia, maybe I wouldn’t be so cautious.”
So how did osteopenia change from a category for public health researchers into a condition that millions of women swallow pills to treat?
The answer to that question starts with a man named Jeremy Allen, who lives in a sprawling home in Pennsylvania.
The Man Who Measured Bone
Allen was born in the United Kingdom and came to the United States in 1982, a young man with energy to spare, looking to make a name for himself in the pharmaceutical industry.
After working briefly for the drug company Smith, Kline and French, Allen eventually ended up running North American operations for a massive pharmaceutical research company called IMS Health. He retired from that company in 1991 and set up a consulting business.
“Fosamax was the first [nonhormonal] drug that could credibly make a claim to stop the progress of osteoporosis,” he says.
Until drugs like Fosamax began to emerge, the standard treatments were calcium, vitamin D, weight-bearing exercise and hormonal treatments, though ultimately hormonal treatments proved problematic.
Since osteoporosis is a serious problem that affects millions of women, the potential market for Fosamax was enormous. Fosamax could become a blockbuster drug, one that made over $1 billion a year.
The problem, Allen says, was that after its release, “Merck wasn’t selling its drug.”
Allen had known the president of Merck America, a man named David Anstice, for years; they’d worked together at IMS Health. Allen says Anstice came to him with a proposition: Figure out this problem and then fix it.
“My job description read: ‘Provide some out of the box thinking,’ ” Allen said.
So Allen set to work. He talked to researchers, doctors, and soon the issue with Fosamax sales became clear: To get large numbers of women on Fosamax, large numbers of women needed to get their bones scanned and be diagnosed with osteoporosis. But in America in 1995, there was simply no way to do that. Allen says the machines that actually measured bone density were exceedingly rare.
“The only diagnostic procedure was an expensive machine called a tabletop bone densitometer that was costing the patient between $200, $250, $300 per test,” Allen says. “And there were only a couple hundred testing centers in the United States, which meant that almost everybody had a day’s ride, or had to go from the suburbs to downtown to get the test. It was expensive and it was inaccessible, so lo and behold nobody did it.”
To sell Fosamax, then, Merck and Allen needed to do two things: place machines that could measure bone density in doctors’ offices all across America and bring down the price of the tests.
But Allen says for him this wasn’t just a matter of selling drugs; he considered osteoporosis a public health crisis. He points out that 1 in 5 elderly women with a hip fracture dies within a year. “Clearly that’s not very good,” he says.
And so armed with the firm conviction that he was about to do good in the world, and coincidentally sell a ton of drugs for Merck, Allen set out to completely rework the way the American health care system measured bone.
To do this, Allen figured, the first thing he needed was an institution, an entity whose mission was not just to sell drugs, but to serve the public good.
So he decided to create one. In 1995 he persuaded Merck to establish a nonprofit called the Bone Measurement Institute. On its board were six of the most respected osteoporosis researchers in the country. But the institute itself had a rather slim staff: Allen was the only employee.
“There was no payroll, there was no building, there was no office with the name ‘Bone Measurement Institute,’ ” Allen says. Essentially Allen’s desk at Merck was the only physical space the Bone Measurement Institute actually inhabited. “I was it,” he says.
Boosting Bone Scan Machine Sales
Once the Bone Measurement Institute was established, Allen set out to determine if there was some alternative to the standard way that bone measurement in America was practiced.
Again, in 1995, the usual way to measure bone was to have a women lie on top of a huge, and hugely expensive, table-sized machine that provided detailed images of hip and spine. The machines were effective but because of their high price, the average doctor would never be able to afford them. Allen needed smaller, cheaper options, and soon he found them.
“I figured out you could use what were called peripheral machines,” Allen says.
Peripheral machines were small, often portable units that measured bone density in the forearm, heel, wrist or finger rather than the hip and spine. At the time, few bone measurement companies manufactured the machines, because they didn’t measure the hip and spine.
Still, from Allen’s perspective, they were the perfect solution: They wouldn’t take up much office space and they cost only a fraction of the big machines, which meant that doctors would be able to afford them.
And so Allen started a campaign to ensure that peripherals were both manufactured and promoted. “We went very strongly to the six or seven manufacturers who were either in this business or wanted to get into this business and said, ‘We will fund your development of these other machines.’ “
But, according to Allen, several of the machine manufacturers were less than enthusiastic. In fact, Allen says, two of the dominant players were downright hostile.
“Because it wasn’t as profitable,” he says. “I was a threat to their business model. Their business model was to sell just a few machines at a very, very high price. And I wanted them to sell a lot of machines at a much lower price.”
But Richard Mazess, founder of the Lunar Corp., one of the largest manufacturers of bone density machines, has a very different view of Allen’s attempt to promote peripherals.
Mazess says Lunar’s resistance to embracing the peripheral machines had nothing to do with money or business models. Lunar opposed peripherals, he says, on the merits. “It was diametrically opposed to what the academics thought was best for diagnosis,” Mazess argues, “and would just lead to bad medicine.”
The problem with the smaller peripheral machines, according to Mazess, is that taking a measurement of someone’s heel or forearm isn’t going to tell you what you need to know about the bones in the parts of the body that, if fractured, increase a woman’s risk of death — the hip and spine.
“We were not about to go ahead and tell physicians to use inadequate diagnostic equipment simply because Merck wanted that,” Mazess says. And Mazess says because Lunar refused to cooperate, his company was threatened. He says Merck told him, ” ‘You’re not going to get support from Merck. And we will support your competitors, and we will tell people working with Merck not to use Lunar machines.’ “
“Basically they were going to make sure that we paid the price,” Mazess says.
Lunar wasn’t the only company put on notice that Merck was serious about investing in the smaller peripheral machines to drive down the price of bone density exams. Allen says that to encourage companies to take Merck’s goals seriously, Merck itself purchased a bone measurement business.
“We bought one of the companies, and showed how low the price could become, purely to get everyone’s attention. And we got everyone’s attention,” Allen says. “And subsequently when everyone else moved, we let it go and the company closed. We cheered its demise.”
Merck’s Perspective
Paul Strain is a lawyer who represents Merck’s corporate office. Though Strain wasn’t able to comment on many of the particulars of Allen’s story, he did confirm the broad outline: Merck set up a nonprofit called the Bone Measurement Institute, which worked to spread the number of machines and bring down the price of bone exams.
But from Merck’s perspective, helping to foster and develop diagnostic tests is simply part of the process of putting out many drugs. Strain was quick to point out that doing something about the lack of machines was important because Fosamax was a drug with genuine lifesaving potential.
“Merck had an effective medicine, the first effective nonhormonal medicine for dealing with osteoporosis. And naturally physicians were interested in that,” Strain says. “But there were significant barriers to doctors’ getting these machines because they were very expensive.”
Strain rejects the idea that the peripheral machines were inferior, that a scan of the wrist or forearm doesn’t provide good information about the risk of hip and spine fracture. “There’s a clear correlation, and there are many, many studies that have shown that,” Strain says.
But others disagree. Sanford Baim, a former president of the International Society for Clinical Densitometry, argues that peripheral machines should only rarely be used to diagnose osteoporosis. During menopause bone is lost at different rates at different sites on the skeleton, so the way to best predict hip and spine fracture, Baim says, is to measure the hip and spine directly.
“The risks of spine and hip fracture are more reliably estimated by the central [big] machines, rather than the peripheral [smaller] devices,” agrees Donald Bachman, a radiologist at the Metrowest Medical Center in Natick, Mass.
Nevertheless, Merck did work hard to get the smaller machines into doctors’ offices.
Allen says Merck helped get peripherals through the FDA process by funding trials and assisting with submissions. He says doctors were educated about the availability of these new inexpensive machines and pamphlets from each company were sent out with the Fosamax sales force. Merck also created a leasing program so that doctors could finance the purchase of a machine, large or small.
A Tipping Point For Osteopenia
Merck’s work to restructure the market didn’t stop there. Merck worked to change the very economics of measuring bone by getting bone scans reimbursed by Medicare.
Allen actually left the Bone Measurement Institute before much of this work took place, but in 1997 the institute and several other interested organizations successfully lobbied to pass the Bone Mass Measurement Act, a piece of legislation that changed Medicare reimbursement rules to cover bone scans. Several of those other organizations that lobbied for the bill also got funding from Merck.
It is impossible to overemphasize just how important this legislation was, says Steve Cummings, the director of clinical research at the California Pacific Medical Center Research Institute. Cummings has done bone research and followed these issues for years.
“Up to that point patients needed to pay for bone densitometry out of their own pocket, but once it’s reimbursed [then] clinicians can be reimbursed if they buy the machines. [Clinicians] can be reimbursed if they license the machines. They get paid for making measurements of bone density.”
Thus in the late ’90s and into the early 2000s, Cummings says, measuring bone density became a profitable thing to do.
And something else critical to this story happened in 1997. Cummings points out that that was also the year Merck got clearance from the FDA for a new version of its drug.
“Merck developed a dose of Fosamax, a 5-milligram — a lower dose that was intended for use by women with osteopenia,” Cummings says. Women like Katie Benghauser.
Cummings says to understand how so many women today are treated for osteopenia, look more closely at all the machines — both large and small — that Merck helped place in doctors’ offices.
“I think the critical event in turning ostoepenia into a condition that people believe needs treatment is the report that comes from the bone density machines,” Cummings says.
Discovering She Has Osteopenia
NPR’s Gisele Grayson had her bones scanned on the tabletop densitometer machine. Though only 38, her bone density indicated that she has osteopenia, or a slight thinning of bone.
Most of the machines that ended up in doctors’ offices in the wake of the 1997 legislation would scan the bone and then spit out a report with three distinct colors: green, yellow and red. Green meant normal. Red meant osteoporosis. Yellow meant osteopenia.
The very existence of the word “osteopenia” on a medical report, along with the clear green-yellow-red graph, had a profound effect, says Cummings.
“When millions of women are getting the word ‘osteopenia’ from the bone density test that they are getting in their 50s and 60s, they get worried,” Cummings says. “When a clinician sees the word ‘osteopenia’ on a report, they think that it’s a disease. They want to know: What should I do?”
Additionally, Merck, and eventually other companies, run commercials advertising drugs to prevent osteoporosis. Those commercials don’t feature humped grannies but young-looking women. And Cummings says at a certain stage it simply reaches a tipping point.
“Bone densitometry becomes increasingly available. And women start wanting it, and they hear their friends have had a measurement of bone density, and their friend was told that they have osteopenia, and they want to know if they have that condition. And then their friend starts getting treated with Fosamax or some other drug, and they want to know if they should be treated,” Cummings trails off. “It’s almost viral.”
In fact, Medicare claims for screening exams increased from 77,000 in 1994 to more than 1.5 million annually by 1999. The sale of peripheral machines went up more than 500 percent over the same period of time. And through this process of testing and advertising eventually a cultural consensus took hold. Osteopenia simply became a condition that was seriously considered for treatment. A diagnosis was born.
The Potential Problems With Treating Osteopenia
Now for many people, particularly Allen, what’s described above is all for the good. No one has lost. Everyone has won.
“Fosamax became a successful drug. [Other drugs] that subsequently have been developed have been successful, and there are a lot less women dying of hip fractures or stooped over than there were a generation ago,” Allen says.
Well, maybe.
There is a scientific consensus that it’s beneficial to give Fosamax to women with osteoporosis, especially older women and any woman who has already had a fracture.
And Strain, the lawyer from Merck, argues that Fosamax also is good for women with osteopenia. He says Fosamax and drugs like it build bones and therefore prevent fractures in women with osteopenia.
“It’s well established that there is a clear correlation between bone mineral density and fracture risk,” Strain says. “And by preserving and maintaining bone mineral density Fosamax lowers the risk of fracture.”
But, increasingly, bone scientists like Cummings say Fosamax — and drugs like it — are not a necessarily a win for most women with osteopenia.
Studies in women with osteopenia show that while Fosamax and similar drugs reduce spinal fractures, the drugs may not reduce other types of bone fractures that are more common in women who have osteopenia, say Cummings and Susan Ott, an associate professor in the department of medicine at the University of Washington.
“There was no difference in the number of [nonspine] fractures you had, whether you took the medicine or a placebo,” says Ott. “It does make your bone density go up higher, but the number of fractures is what really matters, and that didn’t really change”
And what about the long term?
There are no long-term studies that look at what happens to women with osteopenia who start Fosamax in their 50s and continue treatment long-term in the hopes of preventing old-age fractures. And none are planned.
So Cummings says treatment should start only when fracture risk is significant, bone density is low, or someone already has a spine fracture.
He says the WHO is promoting a new tool called the FRAX, which looks at a variety of factors that influence the risk of fracture. This allows women and their physicians to more accurately estimate their risk of experiencing a disabling bone break.
Ott agrees. And, she also worries that taking these medications long-term — over 10 years or more — might actually make bones brittle.
Ott points to a very small number of case reports about spontaneous breaks in the upper leg, which — though very rare — could be important, she says, given what’s at stake.
“Instead of preventing fractures you might get fractures,” she says. “But it doesn’t happen right away. It certainly doesn’t happen in the first five years [of treatment].”
The Paradox Of Our Health Care System
There’s still controversy among specialists about when women with osteopenia should get this medication. But what is clear now is that getting that box of pills into Banghauser’s medicine cabinet wasn’t a simple matter. Allen says it took a huge amount of work. Work he loved.
“I get a great sense of satisfaction that I was able to rejigger the marketplace so that women could be treated for osteoporosis before it got them,” Allen says. “That was a good episode of my life.”
From Allen’s perspective, by making a treatment for osteoporosis widely available, he helped save millions of lives.
But Mazess, from the Lunar Corp., doesn’t see it that way. “He was complicit in a plot to misdiagnose American women,” Mazess says of Allen.
From Mazess’ perspective, millions of women with osteopenia are now needlessly exposed to the risks of a medication that may not ultimately help them.
The paradox of our health care system is that both of these men are probably right. That is, drug companies produce incredible drugs that can greatly relieve suffering. But one way they profit from those drugs is to extend their use to as many people as possible, which frequently means that medications are used in populations with milder and milder versions of a disease, so that the risks of medicating can come to outweigh the benefits.
This has been a story about osteoporosis and osteopenia. But there are versions of this story about a lot of diseases. Caleb Alexander, a pharmaco-epidemiologist at the University of Chicago, says the dynamic is well understood:
“There’s a powerful economic incentive for pharmaceutical firms to expand the boundaries of the use of different therapies. So whether you consider treatments for osteoporosis or treatments for depression or treatments for high cholesterol — in all of these settings — pharmaceutical firms stand to benefit if the therapies for these diseases are broadly used,” Alexander says. “Even if they’re used among people who have very mild forms of these diseases.”
So tonight before bed open your medicine cabinet. There you will see a shelf of pillboxes, many with complicated biographies.
The radio story was produced by Gisele Grayson.
Switching back to IE 8
Wednesday - December 30th, 2009 at 9:08 pm
I’m switching back to IE 8 for a while. It seems I have been running across a lot of sites lately that are not working right in Firefox or Chrome. So I will bu using IE 8 as default until I get pissed and switch back to either FF or Chrome.
For those who want to switch back for any reason, to make IE your default browser, open IE 8, got to TOOLS . INTERNET OPTIONS > PROGRAMS tab then click MAKE DEFAULT.
To import any bookmarks from FF (Firefox) into IE 8, Open IE 8 goto FILE > IMPORT & EXPORT > Select Import from another browser, then select FF and wait a few seconds and after green check marks show up, you are done.
It is a real shame that when the World Wide Web was started that Microsoft didn’t opt to follow the standards, because of Microsoft’s failings we now have so many web pages that do not follow the standards of coding and only operate correctly in the Internet Explorer browser. I sure hope Microsft get’s it right with IE 9. I get so tired of switching from one browser to the next for this function or that. Such a pain in the ass. /- Mike
An American in the UK: Diabetes
Wednesday - December 30th, 2009 at 3:21 pm
An American in the UK: Healthcare for Type 1 #diabetes
Dec 29, 2009
As an American living abroad, I tried to follow the debate over healthcare reform in the US, but I had to drop it for my own sanity. How could so many of my fellow Americans say that people like me, with chronic diseases we never asked for, should pay more for healthcare because they don’t want to participate in the risk pool? How could people like me, who live in fear of losing health insurance, be blind to how badly Americans with type 1 diabetes can get ripped off? I had to remind myself, “It’s okay. I don’t live there anymore.”
In October 2007, after living for a few years in the UK under the NHS, then spending several months uninsured in the US, and finally working in California with health insurance for two years, I emigrated to Britain. Beyond my appreciation for the culture, I feel that as a person with type 1 diabetes, I am better off here.
Top 3 reasons I am better off in the UK than the US:
1. Lobbying doctors, health authorities, and elected officials can really make a difference. I first moved to England for grad school in September of 2001 and stayed until April 2004. As a full-time student, I was covered by the National Health Service. On January 1, 2002, my US health insurance expired. My doctors agreed that I should keep using my pump, but I had to lobby local health service administrators to get my pump supplies covered. The battle I faced was similar to the ones my parents fought on my behalf in Virginia when I started using a pump in 1995. I was surprised that the UK was so far behind the US in terms of pump use. I joined a grassroots, patient-led organization to increase access to pumps. I still meet with members of Parliament on a regular basis to discuss diabetes care in the UK. In mid-2003, the NHS decided to fund pump therapy for type 1s who are likely to benefit from a pump. With my doctors’ support, I was the first person in Oxford to get funding under that decision. Today, about 7 percent of UK type 1s have a pump, and we’re getting closer to the European average of 15 percent.
2. No co-pays or deductibles for diabetes care and supplies. I had to pay for my pump supplies until September 2003, but I was grateful not to have to pay for doctors’ appointments and prescriptions. In the UK, only tourists pay for medical care, at the point of service. All type 1s and type 2s taking at least one diabetes drug do not pay the usual £7.10 per item prescription charge. For reference, the national minimum wage is £5.80. Even insulin pumps and supplies are covered at 100 percent. There are no out-of-pocket costs for blood tests either.
3. Economic independence. When I decided to change jobs a few months ago, I didn’t have to think about whether I would get insurance, whether the insurance would be good enough, or whether I would be able to meet the deductible. My access to healthcare is guaranteed, no matter what job I hold. I need to t least £20,000 per year to keep my visa, but that’s less than I can afford to live on anyway. When I worked in California, I couldn’t quit my job when I was beyond ready to leave because I couldn’t afford the $350 per month (plus co-pays) for COBRA that I’d have to pay if I walked out and took the first thing that came up. I became depressed. Keeping my health insurance had to take precedence over my mental health and my professional goals, which I deeply resented.
On balance, the NHS works well for me. It’s not perfect, but I haven’t heard of a healthcare system that is. There are no “death panels” – in fact, the UK’s National Institute of Health and Clinical Excellence (NICE) does cost-benefit analyses using almost all the same criteria as US health insurance companies… Except for the profitability ratios.
Categories: Health Care, International, Type 1 Issues
Big Dogs stores in Iowa? Not anytime soon.
Monday - December 28th, 2009 at 10:31 pm
We use to have a Big Dogs store here in Iowa at the Tanger Outlet Mall in Williamsburg, Iowa. But it has disappeared, so I got to wondering why. Here is what I found out.
Big Dogs was owned and operated as Big Dogs holdings. They also owned The Walking Company. back in 2004, Big Dogs operated 189 Big Dog Stores and 73 The Walking company stores across the country according the their Oct 1, 2004 info release.
According to the November 2007 release, Big Dog Stores were down to 138, but The Walking Company stores were up to 173 nationwide and they were buying up other companies.
Then in the May 2008 release it was announced the Big Dogs was going to change the name of the company from Big Dogs to The Walking Company. At this time there were 100 Big Dog stores and 199 The Walking Company stores.
By their November 2008 release it was official the name of the company was changed to The Walking Company. By this time the Big Dog stores were down to 71 from their 189 four years earlier and The Walking Company Stores were up to 207 from the 73 in 2004. By now it was evident that Big Dogs was starting to become a sideline business.
Now today if you got to www.bigdogs.com and click on the Store Finder at the bottom of the page, there is only 8 stores listed, A far cry from what once was. If you click on the about, it clearly shows Big Dogs is now owned and operated as The Walking Company.
And to the demise of the overall company, according to CNN Money the company has filed bankruptcy.
The Walking Company Holdings, Inc. (PINKSHEETS: WALK) www.thewalkingcompany.com; www.bigdogs.com) today filed for voluntary Chapter 11 Bankruptcy Protection in Santa Barbara, CA. The Walking Company is seeking to shed its unprofitable stores and emerge from Chapter 11 in early 2010.
Early in 2009, The Walking Company implemented a major restructuring in order to try to survive the difficult retail environment. As a result of rapidly expanding its store chain between 2005 and 2008, the vast majority of the lease rents for The Walking Company’s stores are now, in the current weak economic environment, at or above the market rates for malls across the United States. While the restructuring was successful on most fronts, The Walking Company was largely unsuccessful getting its landlords to adjust the occupancy costs under its leases. Filing for Chapter 11 will allow the Company to shed its unprofitable stores and emerge financially strong and able to weather this tough retail cycle. The Walking Company plans to file its plan of reorganization within the next few weeks.
“This action is an unfortunate but necessary and responsible step to preserve The Walking Company’s value for its secured creditors, vendors, landlords, additional creditors and employees in light of the ongoing challenging retail environment,” said Andrew Feshbach, CEO of The Walking Company. Feshbach stated further, “We believe our business model is sustainable in today’s world, despite declining consumer spending and mall traffic at present. However, the unfortunate timing of our rapid expansion caused us to enter into lease commitments at what now appears to be the high water mark for retail space. The chapter process will allow us to shed our unprofitable stores and go forward as a financially viable retailer.”
The company’s Chapter 11 counsel is Arent Fox LLP and the Company’s financial advisor is Clear Thinking Group LLC.
ABOUT THE WALKING COMPANY HOLDINGS, INC.
The Walking Company Holdings, Inc. (the “Company”) consists of its The Walking Company and Big Dogs subsidiaries. The Walking Company is a leading independent specialty retailer of high-quality, technically designed comfort footwear and accessories that features premium brands such as ECCO, Dansko, UGG Australia, MBT and Aetrex, among many others. These products have particular appeal to one of the largest and most rapidly growing demographics in the nation. The Walking Company operates over 210 stores in premium malls across the nation. Big Dogs develops, markets and retails a branded, lifestyle collection of unique, high-quality, popular-priced consumer products, including active wear, casual sportswear, accessories and gifts.
Safe Harbor Statement Under the Private Securities Litigation Reform Act of 1995- With the exception of historical information, the matters discussed in this press release are forward looking statements that involve a number of risks and uncertainties. The actual future sales and other results of the Company could differ significantly from those statements.
CONTACT: Alexis Dilg Investor Information (805) 963-8727, ext. 1303 alexisd@bigdogs.com The Walking Company Holdings, Inc. 121 Gray Avenue Santa Barbara, California 93101 www.thewalkingcompany.com www.bigdogs.com
So who knows what is in store for my beloved Big Dogs clothing stores. To me it does not look like they will return to Iowa any time soon. But as of this posting you can still order online at WWW.BIGDOGS.COM , so get them while you can. /Mike





