Friday, April 11, 2014

Data is at the heart of Somerset's integration masterpiece


South Somerset’s Symphony project constructs morbidity profiles for a range of long term conditions – showing the true cost and the extent of multi-morbidities. Andrew Street, Panos Kasteridis and Jeremy Martin explain
Nurse treating patient
Many people have complex and ongoing care needs and require support from multiple agencies and various professionals
Since the inception of the NHS, an ever-present challenge has been to improve integration of care within the health and social care system.
Many people have complex and ongoing care needs and require support from multiple agencies and various professionals. But care is often fragmented and uncoordinated, with no one agency taking overall responsibility, so it is often left to individuals and their families to negotiate the system as best they can.
‘It is designed to establish greater collaboration between primary, community, mental health, acute and social care, particularly for people with complex conditions’
In South Somerset, the county council, district hospital, community provider and clinical commissioning group have set up the Symphony project to develop a model of integrated care intended to both improve services and boost efficiency. It is designed to establish greater collaboration between primary, community, mental health, acute and social care, particularly for people with complex conditions.

Colloboration at heart

The project is based on the principle of collaborative care, centred on the needs of individual patients, facilitated by integrated financial arrangements and better pathway management. This means that all of the different organisations involved in delivering services will need to work together to deliver a tailored package of care.
Collaborative working is to be incentivised by a shared outcomes framework, with joint responsibility for all organisations to deliver the outcomes and linked financial structures under an “alliance contract”.
To be able to realise these ambitions, arrangements need to be targeted initially at a subset of the population that would be expected to benefit most from integrated care. We developed broad criteria to identify groups most amenable to integrated care:
  • The number in the group needs to form a sufficiently large “risk pool” so that those with high costs are offset by those with low costs.
  • To realise savings, initial focus should be directed toward groups for which current expenditure is relatively high.
  • Those using services across diverse settings are more likely to be benefit from integrated care.
  • There needs should be local consensus that changes to the care pathway are feasible.
We assessed the first three of these criteria by examining patterns of health and social care utilisation and costs for the local population of 114,874 people in 2012. The Symphony project has built a large dataset comprising information about each anonymised individual in the south Somerset population. The dataset has three key features:
  • it links acute, primary care, community, mental health and social care data;
  • costs are assigned to each individual according to the type of care they have received in each setting;
  • demographic characteristics are available for each individual, including age, gender, socio-economic measures, and indicators of morbidity.  
Each individual’s morbidity profile is constructed using United Health’s RISC tool used locally to predict unplanned hospital admissions. We identified 49 chronic conditions to construct the morbidity profile of each individual in the population. Individuals can, of course, have multiple chronic conditions.

Multi-morbidity the norm

The data reveals that for people who have a chronic condition it is unusual to have just a single condition: multi-morbidity is the norm, not the exception. Moreover, while it is well known that multi-morbidity increases with age, our analyses demonstrate that it is multi-morbidity not age that most drives health and social care costs. This insight changed the early focus of the Symphony project away from the frail elderly towards adults with multiple long term conditions.
We are also able to look at the annual costs involved in caring for people with particular conditions, according to the different health and social care settings in which they receive care. For example, figure 1 shows average cost broken down by setting for those with a selection of chronic conditions.
The average annual cost for the 45 people with occupational pulmonary disease (OPD) amounts to £14,142, with inpatient costs accounting for the largest proportion. The annual average cost for the 1,062 people with a diagnosis of dementia is £12,314, with the costs of continuing care and social care being most important.
Drilling down further, we can explore the relationship between costs and the number and type of chronic conditions that people have. The accompanying data video illustrates the analyses undertaken for people with diabetes, this being the fifth most prevalent condition in the South Somerset population (5,625 people, five per cent, with total annual costs amounting to £17m. More than 36 per cent of those with diabetes are treated in three or more settings, with inpatient care accounting for the largest proportion of costs (35 per cent), followed by social care (19 per cent) and prescribing (14 per cent).
Out of this 85 per cent of diabetics suffer from at least one other comorbidity and about 35 per cent have three or more chronic conditions. The average annual cost for someone with diabetes alone amounts to about £1,000, but costs increase progressively the more co-morbidities that a person has. We found that the number of conditions is almost as good at explaining costs as markers for particular conditions.

Cost profiles

We constructed similar morbidity and cost profiles for those with hypertension, asthma, diabetes, fractures, coronary artery disease, cancer, chronic obstructive pulmonary disease (COPD), stroke, dementia, and mental health (other than dementia). These showed multi-morbidity patterns and their relationship with utilisation and costs across health and social care settings. These profiles were shared at a workshop with local health and social care professionals and managers designed to inform the selection of the group.
Following the workshop, further analyses were conducted for those with a diagnosis of diabetes or of dementia. Futher analysis was also conducted for those with a combination of a limited set of comorbidities that local GPs viewed as most significant. These were diabetes, cardiac disease, COPD or OPD, chronic kidney disease or renal failure, depression or anxiety, dementia, stroke and cancer.
In South Somerset 1,458 people have some combination of three or more these conditions. They are older than the rest of the population (78 compared to 51 years), and have higher average annual costs (£8,152 compared to £1,094. Figure 2 shows the prevalence and costs associated with combinations of conditions among this group.
Costs involved for caring for people according to comorbidity
Figure 2: Average costs per Symphony group
The average annual cost of £8,152 is indicated by the red circle. Costs vary from the average according to particular conditions. Most notably, costs are about £14,000 if dementia is among the conditions and £12,000 if CKD/renal is a co-morbidity, but there is little difference to the overall average for the other conditions.
The project board decided that those with three or more conditions should form the initial cohort. The reasons for this included:
  • focusing on multiple conditions avoids Symphony being seen as condition or pathway specific;
  • the group of around 1,500 patients offers a reasonable high level of predictable costs variation, provides a sufficiently large risk pool and a more manageable scale than if the focus were solely on diabetes and/or dementia;
  • the group incurs costs across all settings, thereby offering the prospect of strengthening links across health, mental health and social care;
  • there is an opportunity to reduce inpatient costs, which currently account for 38 per cent of total costs;
  • it was felt possible to develop a service for complex patients, while still operating traditional models for those without diabetes or dementia.

Straightforward calculation

The dataset has made it relatively straightforward to calculate the capitated commissioning budget for this group of complex patients. The aim is to start with this initial cohort to demonstrate feasibility and improved outcomes, through the development of personalised care planning and supported self-management.
‘In many parts of the country health and social care data are not combined into a single individual-level dataset’
The hope is to move quickly to a much larger cohort including all patients with long term conditions, using the complex care team as a catalyst to spread a new culture and ethos across the whole health and social care system in south Somerset.
It is a key part of the foundations on which integrated care is being developed in south Somerset. In many parts of the country health and social care data are not combined into a single individual-level dataset.
In those areas where utilisation data have been joined together, information on costs is lacking. In south Somerset analysis of linked data about the use and costs of health and social care for the local population has made it possible to understand existing patterns of care utilisation and to identify for whom and in what way improvements can be made.
Moreover, by maintaining the dataset year on year, it will be possible to assess whether the efforts made to improve integrated care for the local population succeed in realising their ambition.
Andrew Street is professor of health economics; Panos Kasteridis is research fellow at University of York; Jeremy Martin is programme director at the symphony project

New Dartmouth study offers roadmap for better risk adjustment in Medicare

The methodology Medicare uses to adjust the billions of dollars it pays health plans and hospitals to account for how sick their patients are is flawed and should be replaced, according to a new study by Dartmouth investigators published in the journal BMJ that weighed the performance of Medicare's methodology against alternatives.

The researchers from the Dartmouth Atlas Project compared Medicare's current risk-adjustment methodology, which is based on the diagnoses recorded in patients' claims records, against adjustment indices based on wealth and health. The study found that using indices pegged to a region's poverty rate or the overall health of its population do a better job of explaining the mortality rate of local Medicare populations than the current diagnosis-based adjustment method, raising questions about its efficacy.

The study is the fourth in a series to raise important questions about how the government accounts for differences in the severity of illness in populations so it can make "apples to apples" comparisons that do not to penalize plans or health systems whose patients are sicker than average. This risk adjustment is a critical factor in how Medicare evaluates hospitals' readmission rates, which affects their Medicare payments, and how it pays Medicare Advantage health plans. Diagnosis-based risk adjustment is also used in comparative effectiveness research and in academic research into variations in medical care across America.

Medicare payments to Medicare Advantage plans are projected to surpass $154 billion in 2014, and account for more than a fourth of total Medicare spending, according to the Congressional Budget Office. Medicare Advantage plans use the CMS - Hierarchical Condition Category (HCC) risk adjustment methodology to adjust their payments to health plans. HCC risk adjustment, based on the diagnoses recorded in claims, is so important to Medicare Advantage plans' revenue streams that a cottage industry has sprung up to help plans maximize their risk-adjustment revenue.

"We can and should do better," said David E. Wennberg, M.D., M.P.H. "Our body of work demonstrates that the way we adjust for risk now is biased, and when billions of tax dollars are at stake we need to hit the reset button. This paper gives a very good roadmap of how we can do risk adjustment right."

Three previous studies found significant regional variations in diagnosis patterns. In regions where Medicare patients see doctors more often or get more tests, one study found patients accumulate more diagnoses, even though the increased, accumulated diagnoses did not track with mortality rates, raising questions about the accuracy of a diagnosis-based risk adjustment method. This "observational intensity" suggested diagnosis is not solely an attribute of underlying disease burden, but could also reflect how often patients encounter the health care system.

This new study compared the current Medicare risk-adjustment methodology with three 
alternatives to see which better explain differences in the actual mortality of a population. It drew on the 2007 claims of more than 5 million Medicare beneficiaries in 306 U.S. regions. The first adjusted the current Medicare method to discount diagnoses for the region's observational intensity. The second was based solely on the percentage of a region's 65-plus population below the federal poverty level. The third was a population health index based on five factors: annual rates for hip fractures andstrokesobesity, smoking status and surveys of self-reported illness. Each alternative performed better at predicting regional mortality than the current Medicare diagnosis-based method. The population health index was able to explain over 60% of the variation in regional mortality rates, while the HCC index explained less than 5%.

The article concludes that the federal government should expand its plans for national surveys to assess patients' experience with health care providers to include patient-level population health measures that can be used for risk adjustment as well as outcomes assessment.

Medicare payments to Medicare Advantage plans are projected to surpass $154 billion in 2014, and account for more than a fourth of total Medicare spending, according to the Congressional Budget Office. Risk adjustment is so important to Medicare Advantage plans' revenue streams that a cottage industry has spring up to help plans maximize their risk-adjustment revenue.


Thursday, April 10, 2014

International professors discuss healthcare concerns



By JULIA LISS, Daily Staff Reporter
Published April 9, 2014
Two speakers gave a joint lecture Wednesday on international health policies at the University’s School of Public Health, drawing around 40 graduate students and faculty.
Johan Mackenbach, professor of public health at Erasmus University Medical Center in Rotterdam, the Netherlands, spoke of the recent divergence of life expectancy in Europe and possible explanations for such a trend.
Mackenbach said the trends, which show health disparity based on national income gaps, are the result of a variety of cultural factors. Using charts, graphs and other data to help illustrate his point, Mackenbach showed that periods of democracy had historically higher life expectancies, while periods of more chaotic political climates showed dips in the life expectancies.
Mackenbach outlined 11 specific areas of focus for health policies, including tobacco control, alcohol control, child health and road traffic injury. He said countries that have more preventative health policies — contrary to most U.S. delivery models — showed fewer instances of health problems related to each area of concern.
For example, he said countries with stricter tobacco control regulations and preventative measures to discourage smoking had fewer smokers, lower cigarette sales and fewer smoking-related health issues in the population.
Mackenbach discussed possible reasons for the existing disparities. He found that many countries which could benefit from improved healthcare models often possess the means to do so, but are stymied by the political, social and cultural climate of the country.
John Frank, director of the Scottish Collaboration for Public Health Research & Policy and chair of Public Health Research & Policy at the University of Edinburgh, Scotland, delivered the second address, titled “Influencing Child Health Policies with Scientific Evidence: Lessons from 5 Years in Scotland.”
His lecture aimed to demonstrate the importance of early access to education on an individual’s health and future success. Frank said early education implementation is the single most important indicator for a child’s future.
“You can make people’s chances in life much more equal in only one really cost effective way, and that is giving universal preschool high quality education, half day a week from age two, age one in high risk families,” Frank said.
Frank proposed a plan to combat societal challenges through education, while addressing some of the concerns of implementing potential reforms.
Public Health Prof. George Kaplan acted as the moderator and he introduced both Mackenbach and Frank’s speeches and led a question and answer session after each speaker. The Institute for Healthcare Policy and Innovation, the University’s Robert Johnson Foundation Scholar’s in Health Policy Program and the Center for Social Epidemiology of Population Health sponsored the event.

Wednesday, April 9, 2014

Review of GP services - the patient experience


Hastings and Eastbourne web pictures ENGSUS00120120629112956
Hastings and Eastbourne web pictures ENGSUS00120120629112956
More than half the people interviewed for a review of GP services in Luton said they could not get an appointment when they needed one, while a third had difficulty getting through to the surgery on the phone.

The review was conducted by Healthwatch Luton, supported by volunteers and local organisations.

They completed 962 patient surveys while Healthwatch staff visited and assessed all 39 doctor surgeries in the town.

The results also showed that 26 practices do not have easy access for wheelchair users and 28 do not have a hearing loop system in place.

Only four were judged to have sufficient privacy in the reception area and all but seven kept patients waiting more than 15 minutes after their appointment time.

On the plus side, a significant 88 percent said staff were helpful and understanding and 89 percent had confidence and trust in their doctor.

More than 90 percent said that, overall, they were happy with the quality of care, service and treatment they received although only 80 percent would recommend their surgery to other people.

Healthwatch Luton boss Beth Gregson said: “It shows the importance of identifying and understanding what good patient satisfaction looks like.

“We recognise the increasing pressures and demands on surgeries. However we will continue to struggle to attract quality staff if we cannot narrow the gap between the best rated and the worst.”

Healthwatch Luton manager Nisar Mohammed said: “We have identified a total of 680 recommendations across the board and many of these have already been implemented.

“We hope the results of this review will encourage local people to become actively involved in representing the patient voice within their local surgery.”

The organisation has created individual reports and recommendations for each GP surgery, together with timescales for implementation and a response from the surgery.

> For a copy of individual and overall surgery reports, call 01582 817060 or access them online at http://www.healthwatchluton.co.uk/gp-report

http://www.lutontoday.co.uk/news/health/health-news/review-of-gp-services-the-patient-experience-1-5988384


Medicare provided docs million-dollar paychecks



WASHINGTON
The Medicare program is the source of a small fortune for many U.S. doctors, according to a trove of government records that reveal unprecedented details about physician billing practices around the nation.
The government insurance program for older people paid nearly 4,000 physicians in excess of $1 million each in 2012, according to the new data. Those figures do not include what the doctors billed private insurance companies.
The release of the information gives the public access for the first time to the billing practices of individual doctors nationwide. Consumer groups and news outlets have pressured Medicare to release the data for years. And in doing so today, Medicare officials said they hope the data will expose fraud, inform consumers and lead to improvements in care.
The American Medical Association and other physicians groups have resisted the data release, arguing that the information violates doctor privacy and that the public may misconstrue details about individual doctors.
Among the highest billers were a cardiologist in Ocala, Fla., who took in $18.1 million, mainly putting in stents; a New Jersey pathologist who received $12.6 million performing tissue exams and other tests; and a Michigan vascular surgeon who got $10.1 million.
Some of the highest billing totals may simply reflect a physician who is extremely efficient or who has an unusually large number of Medicare patients.
The highest numbers also may reflect a physician who specializes in procedures that require costly overhead, and in those cases, a large portion of the money may wind up not with the doctor but with pharmaceutical companies or makers of medical devices.
But in some instances, the extremely high billing totals could signal fraudulent doctor behavior, as government inspectors have previously found.
Indeed, three of the top 10 earners already had drawn scrutiny from the federal government, and one of them is awaiting trial on federal fraud charges.
The greatest tallies also may signal that the Medicare payments for some procedures are too high for the amount of work involved or that perverse incentives lead doctors to overuse a procedure.
The specialties most common at the top ranks of the Medicare payments were ophthalmologists, oncologists and pathologists.
This information gives the public "unprecedented access to information about the number and type of health-care services" doctors provided during the year, Jonathan Blum, principal deputy administrator of the Centers for Medicare and Medicaid Services, said in a blog post.
The Medicare program is the nation's largest medical insurer. By virtue of its breadth, the forthcoming billing data are expected to shed light on an array of questions that have arisen about health-care costs as the nation has confronted decades of rising medical bills.
Overall, the information covers $77 billion in billing involving 880,000 practitioners in 2012.
The American Medical Association has warned that the data could contain errors, and in some cases, one doctor's billing number may have been used by multiple support personnel for billing purposes.
In addition, the billing figures reflect what a doctor receives in payment but does not show the actual profit after paying for equipment, support personnel and malpractice insurance. For some procedures, the overhead can reach three-quarters or more of the payment amount.
Many of the highest billers, for example, were in fields with unusually high expenses, and that was likely to limit their personal share of the money. Using the assumptions that Medicare and the American Medical Association make when setting payment rates, only 23 of the 4,000 biggest billers personally earned $1 million or more, according to a Washington Post analysis.
"The AMA is concerned that CMS' broad approach to releasing physician payment data will mislead the public into making inappropriate and potentially harmful treatment decisions and will result in unwarranted bias against physicians that can destroy careers," Ardis Dee Hoven, president of the American Medical Association, said in a statement. "We have witnessed these inaccuracies in the past."
But consumer and public interest groups argued that the information will help consumers make better decisions.
"This data is important because it will make it possible for consumers to identify physicians that will best meet their needs," said Robert Krughoff, president of Consumers' Checkbook, a group that began seeking the release of this information in 2005 and eventually sued for it.
For example, it will allow consumers to know which doctors are most experienced in a given operation. Studies have shown that in several types of surgery, volume matters: Surgeries by doctors who have performed the procedure enough times are less likely to end with the patient's death.
As for the potential that the information might misrepresent a physician's practice, Krughoff said, "the consumer organizations that have pushed for release of this information have a strong obligation to make sure that the information is used properly. But I believe in the marketplace of ideas."
The doctor at the top of the list of largest Medicare billers is Salomon Melgen, an ophthalmologist in West Palm Beach, Fla., who took in $20 million from Medicare in 2012, according to the data released Wednesday.
Most of Melgen's take - about $11.8 million of it - came from injecting patients' eyes with Lucentis, a drug used for macular degeneration, according to the data.
For each shot, Medicare and the patient pay a doctor about $2,000, but the drug is very expensive and the doctor must then pay most of that money to the drug's manufacturer, Genentech.
What may be most interesting about Melgen's practice, however, is that he could have used a much cheaper drug than Lucentis - one called Avastin that many opthalmologists consider an equivalent.
Had he used the cheaper alternative, his bill to Medicare for the shots would have dropped from $11.8 million to less than $500,000.
But physicians have a financial incentive to use more expensive drugs. Medicare pays a doctor more for injecting the more expensive drug - the physician's fee is based on the drug's price - and Genentech offered doctors its own incentive to use the expensive drug: The company gave discounts to those who use high volumes.
Melgen's name appeared in headlines in 2012 as result of his connection to Sen. Robert Menendez, D-N.J., a friend who received campaign contributions from the ophthalmologist.
Melgen's attorney issued a statement before the data release to try to put his client's billing in perspective.
"At all times, Dr. Melgen billed in conformity with Medicare rules," Kirk Ogrosky said.
The use of the more expensive eye drug helps explain why so many of Medicare's top billers are ophthalmologists.
Of the doctors who were paid at least $1 million by Medicare in 2012, 879 were ophthalmologists, who - like Melgen - relied on using the more expensive drug, Lucentis.
Some physicians have suggested that using Lucentis is wasteful because a much cheaper alternative exists.
Melgen, like some other doctors among the top billers, already has drawn scrutiny from Medicare investigators.
Indeed, government inspectors have noted that instances of billing disputes and potential fraud may occur more frequently among the highest Medicare billers.
A December report from Health and Human Services, for example, analyzed the records of 303 physicians who were paid more than $3 million by Medicare in a year.
It found that 13 were responsible for overpayments totaling $34 million, six faced payment reviews, three had their licenses suspended, and two were indicted.
In releasing the data, Medicare officials forbade news outlets from sharing any of the data until 12:01 a.m. today. This provision meant that reporters could not solicit responses from any doctors beforehand.

Tuesday, April 8, 2014

How Is your Organization Administering and Managing Health Risk Assessments?

Launch HRA


Patient Centered Health Risk Assessments are a valuable tool that can be used to identify and capture opportunities for prevention, identify injury risks, reduce modifiable risk factors, and alert providers of an urgent health need.


How are you ensuring that all of your patients complete an annual HRA?


 The Patient Protection and Affordable Care Act of 2010 included several provisions intended to improve the health of Americans and prevent the onset of preventable chronic conditions.

Section 4103 of the ACA, establishes a Medicare Annual Wellness Visit beginning in 2011 that includes a Health Risk Assessment (HRA) without cost to beneficiaries.

Other provisions of Section 4103 include:

·         Establishing standards for interactive, telephonic, or web-based programs used to furnish HRA’s, and

·         Determining ways of using the HRA in the formulation of a personalized prevention plan for beneficiaries.

The law also requires that HRA’s are easily accessible to beneficiaries and that support is provided to those wishing to complete an HRA.

The statute recognizes the critical nature of follow up services by encouraging integration of HRA’s with health information technology (HIT), including electronic medical records (EMR’s), and personal health records (PHR’s) and by leveraging these technologies in developing patient self-management skills and by the management of, and adherence to, provider recommendations, as a means of improving the health of beneficiaries.

In addition to regulatory encouragement, HRA’s offer providers an opportunity to engage with Medicare members in new ways while tackling the benefits of prevention.

Consider the value of administering and managing your HRA’s through a “Learning Health Care System”…


One where personalized assessments, and prevention planning would be available anytime, anywhere, and on any device.

One where experiences are captured, stored, and then used to create individualized learning pathways that promote health literacy, prevention and chronic disease self-management.

Imagine the possibilities!


Click on the image above to launch the new HRA Experience from mHealth Games.

Lawmakers look to expand, regulate telemedicine in Florida, but House Senate bills far apart

MIAMI — The calls may come in the middle of the night and from hospitals more than an hour away. Someone is having a stroke and is en route an emergency room in the Florida Keys, but there aren't any neurologists on call.

Within 15 minutes, a University of Miami neurologist pops onto a computer screen and can order an IV drug that should be given within three hours. It's that sort of potentially life-saving technology that some lawmakers say will drive down health care costs, while also addressing serious doctor shortages around the state.

A Senate bill would increase the use of telemedicine in Florida and establish requirements for health providers who treat patients remotely. A companion bill is also making its way through the House, but that bill doesn't require doctors to have a Florida license — only that they be licensed in their home state and registered in Florida.

"If we didn't have an access problem we wouldn't be here today ... everyone would rather see the doctor face to face, but when your mother is having a stroke in rural Florida and the choice is having a doctor via telehealth versus having no doctor," said Rep. Cary Pigman, an emergency room physician who supports the bill.

The Senate bill requires doctors providing telemedicine services to patients within the state to be licensed in Florida or meet an alternative requirement. For example, an insurer using a doctor that's in-network in another state would also be allowed to treat a Florida patient. The bill recently passed a Senate committee, but has two more stops before it's heard on the floor. Dozens of other states have passed legislation supporting telemedicine.

The Senate bill also would require Medicaid to reimburse for telemedicine services and allow doctors to negotiate payment rates with insurers. The House bill doesn't address payments.

"If you're a patient in Florida and you have a specific heart defect and the guru is a doctor in Philadelphia, you should be able to consult with her," said Republican Sen. Aaron Bean, who is championing the bill.

But critics worry that requirements for doctors in other states could compromise patient care. Some say that doctors practicing telemedicine in Florida should be licensed here.

"It may be the wave of the future, but I still think we need to concentrate on the patients and the bottom line is these (out of state) doctors are not licensed in Florida so they don't have the same accountability," said Sen. Dorothy Hukill, who voted against the bill.

Bean said they will be held accountable through the insurance company or the doctor's network they practice within.

Rep. Gayle Harrell, voted for the bill, but noted it still has problems.
"I also need to know what my recourse action should be should some malpractice incident take place," she said.

She also wants to see a website created where people can find information about the out-of-state doctors who may be treating them. After all, she noted, patients can't walk into the office of an out-of-state doctor and see medical degrees on the wall.

The Florida Chamber and several other groups, including ones representing nurse practitioners, physician assistants, nurses and pharmacists all support the bill.

But the powerful Florida Medical Association is strongly opposed, worrying it doesn't require treatment by a licensed Florida physician or mandate a review of the patient's medical history. The organization said such technology holds great promise, but does not support the bill in its current form.

"This will revert Florida back to the days of the Wild West where anyone with a bottle of whiskey, a pocket knife and Skype can practice medicine. That's what happens to the bill in its current form, said David Custin, a lobbyist for the group.

Several hospitals around the state have had success with telemedicine in recent years, helping patients in rural areas connect to specialists or getting multiple consultations conducted simultaneously for acute emergency cases. University of Miami neurologist Dr. Gustavo Ortiz has done more than 600 consultations since their program's inception in 2009.

Telemedicine saves money by reducing hospital and ER admissions and doesn't require medical transportation, supporters say.

Dr. Kim Landry, an emergency room physician and EMS medical director for four counties in the Panhandle, began a pilot program where 911 responders connect patients remotely to an ER doctor for a quick evaluation.

"Eight out of 10 times, they don't require transport to the hospital, so in a lot of cases, it's made life easier for a lot of sick patients," said Landry, who found those results after testing the program in nursing homes.

During a recent consultation, University of Miami dermatologist Dr. Anne Burdick asked an assistant at a Fort Pierce county health clinic to zoom the camera in on some scaly, white patches on a 10-year-old boy's legs. The boy is often kept indoors and complains of constant itching at night. Burdick, who diagnosed him with eczema, modified his prescriptions and added a monthly bleach bath to reduce bacteria. The boy was one of five pediatric patients seen remotely from her Miami office that day.

Burdick, who estimates 40 percent of her practice includes telemedicine patients, also does medical consultations for two cruise lines, the Indian Health Service and a weekly program for school children.

"For some areas in the state, it's going to be impossible to get specialists to that area and so telemedicine is really the best option, " said Burdick. "The bill will be a really good step forward for Florida."

http://www.dailyjournal.net/view/story/de83d3480a7e46b48960943b1abb6b03/FL--Telemedicine/#.U0PoOPldWSo

Previous Medicaid expansions by states did not erode perceived access to care

Bottom Line: Previous expansions in Medicaid eligibility by states were not associated with an erosion of perceived access to care or an increase in emergency department (ED) use.
Background: In January 2014, the Patient Protection and Affordable Care Act (ACA) expanded Medicaid eligibility so coverage in the public insurance program could be offered to more low-income Americans. However, some have suggested that the demand for medical services created by Medicaid expansion may erode access to care for individuals already enrolled in Medicaid, which can be restrictive.
How the Study Was Conducted: The authors examined previous Medicaid expansions to gauge self-reported perceptions of access to care and the use of ED services by enrollees. The authors examined data from 1,714 adult Medicaid enrollees in 10 states that expanded Medicaid between June 2000 and October 2009, and from 5,097 Medicaid enrollees in 14 bordering states that did not expand Medicaid.
Results: In Medicaid expansion states, the proportion of Medicaid enrollees reporting poor access to care declined from 8.5 percent before the expansion to 7.3 percent after the expansion. In the control states where Medicaid was not expanded, enrollees reporting poor access to care remained constant at 5.3 percent. The proportion of Medicaid enrollees reporting emergency department use decreased from 41.2 percent to 40.1 percent in expansion states and from 37.3 percent to 36.1 percent in states that did not expand Medicaid.
Discussion: "We found no evidence that expanding the number of individuals eligible for Medicaid coverage eroded perceived access to care or increased the use of emergency services among adult Medicaid enrollees."
Authors: Chima D. Ndumele, Ph.D., of the Yale School of Public Health, New Haven, Conn., and the Brown University School of Public Health, Providence, R.I., and colleagues.
JAMA Intern Med. Published online April 7, 2014. doi:10.1001/jamainternmed.2014.588.

Editorial: Health Insurance is Not Health Care

In a related editorial, Mitchell H. Katz, M.D., director of the Los Angeles County Department of Health Services and a deputy editor of JAMA Internal Medicine, writes: "The Congressional Budget Office estimates that by 2022 there will be 12 million new enrollees into Medicaid. Although this is an unprecedented leap forward in providing low-income Americans with health insurance, it is important to remember that health insurance is not health care. Health insurance is a financial mechanism for paying for health care. It is not the care itself, or even a guarantee of care."
"The gap between health insurance and health care can be particularly challenging for many Medicaid recipients to bridge. Studies have shown that a substantial proportion of physicians do not accept new Medicaid patients," he continues.
"Therefore, amid the optimism that millions of previously uninsured persons will gain Medicaid coverage, there is a fear that the newly insured will not be able to find physicians who will care for them, or that the influx of new enrollees will make access harder for those persons who already have Medicaid. In this vein, the results of the study by Ndumele et al in this issue of JAMA Internal Medicine are reassuring," he notes.
JAMA Intern Med. Published online April 7, 2014. doi:10.1001/jamainternmed.2014.598.