When Formularies Attack

When someone other than your doctor decides which drug you take.....

http://goo.gl/Dj3XJT 

Objectives: To collect clinician perceptions on the impact of switching medications for nonmedical (ie, formulary) reasons in long-term care settings under Medicare Part D and to use the qualitative findings to support more robust research into the effects of Part D policies on nursing home patients and providers.

Methods: We collected individual clinician accounts of experiences with and perceptions about Part D plans when medications were switched for nonmedical reasons, including diseases that clinicians believed were most medically risky for switching with nursing home residents and the common health outcomes of switching. Publisher HCPro’s long-term care readership database was used to reach survey participants. Individuals were classified by clinician type and then
e-mailed an invitation to take these electronically disseminated surveys in September 2007.

Results: A total of 569 total case histories representing 555 nursing homes were collected. About three-quarters of the case histories collected showed decreased efficacy after a nonmedical switch for Part D beneficiaries. Switching for those with hypertension, heart disease, diabetes, HIV, and bipolar disorder, among other diseases, was considered most medically risky in this population.

Conclusion: Nurses, physicians, and pharmacists who shared their perceptions regarding the effect of nonmedical switching in long-term care settings reported situations in which switching increased administrative time, increased side effects, and appeared to have increased downstream costs to plans.

Final review of health problems that may be linked to Agent Orange exposure during Vietnam War

http://goo.gl/g5vZ9I

The latest and final in a series of congressionally mandated biennial reviews of the evidence of health problems that may be linked to exposure to Agent Orange and other herbicides used during the Vietnam War changed the categorization of health outcomes for bladder cancerhypothyroidism, and spina bifida and clarified the breadth of the previous finding forParkinson's disease. The committee that carried out the study and wrote this report, Veterans and Agent Orange: Update 2014, reviewed scientific literature published between Oct. 1, 2012, and Sept. 30, 2014.

Bladder cancer and hypothyroidism were moved to the category of "limited or suggestive" evidence of an association from their previous positions in the default "inadequate or insufficient" category. A finding of limited or suggestive evidence of an association means that the epidemiologic evidence indicates there could be a link between exposure to a chemical and increased risk for a particular health effect. A finding of inadequate or insufficient evidence indicates that the available studies are of insufficient quality, consistency, or statistical power to permit a conclusion regarding the presence or absence of such a link. For both bladder cancer and hypothyroidism, new results from a large study of Korean veterans who served in the Vietnam War were compellingly suggestive of an association. In combination with pre-existing supportive epidemiologic findings and substantial biologic plausibility, the new information provided evidence to merit a change in category of association for these two outcomes.


New Procedure Allows Kidney Transplants From Any Donor

http://goo.gl/AXRqoz

In the new study, published Wednesday in The New England Journal of Medicine, doctors successfully altered patients’ immune systems to allow them to accept kidneys from incompatible donors. Significantly more of those patients were still alive after eight years than patients who had remained on waiting lists or received a kidney transplanted from a deceased donor.

The method, known as desensitization, “has the potential to save many lives,” said Dr. Jeffery Berns, a kidney specialist at the University of Pennsylvania’s Perelman School of Medicine and the president of the National Kidney Foundation.

It could slash the wait times for thousands of people and for some, like Clint Smith, a 56-year-old lawyer in New Orleans, mean the difference between receiving a transplant and spending the rest of their lives ondialysis.

The procedure, Mr. Smith said, “changed my life.”


New Health Care Symposium: Health Care Consolidation And Social Justice—Unanswered Questions

http://goo.gl/htHRC9

How will health care consolidation affect health and health care disparities? How will it affect minority and low-income communities? We don’t know, and that’s the problem.

Health care consolidation may offer some promise, and potentially some peril, but we should determine how it impacts those communities with the poorest health and thereby addresses health inequality. After all, those who have the means can already access the greatest medical services, technology, and expertise in the world. Our global rankings in health outcomes do not match our health expenditures because of the disproportionate health burdens suffered by low socioeconomic communities. They are subjected to poor health services, if they receive any at all.

How, then, does consolidation address barriers these vulnerable citizens face, such as geography, cost, and a lack of profitability in addressing many of their health needs? If we are to accept the proposition that consolidation will lead to integrated health care, those who are already receiving the benefits of our current system will inevitably be rewarded. But is there evidence that these benefits will trickle down to those who suffer most?

Moreover, health disparities do not arise only, or even primarily, from health care disparities; heath disparities instead stem largely from social determinants of health that differentially affect minority and low-income communities. The water issues in Flint are an unfortunate reminder that health can no longer be narrowly addressed through improvements in health care services. What good is increased insurance coverage and improved medical technology for those consuming poisoned water from birth?

And this is not just in Flint. As one article rightly pointed out, “America is Flint!” While 4.9 percent of children in Flint have elevated levels of lead, in the most recent data for Iowa 32 percent of tested children had elevated lead levels. The Centers for Disease Control and Prevention (CDC) estimates that 535,000 children between the ages of 1 and 5 suffer from lead poisoning, which research has associated with impaired cognitive development associated with violent and criminal behavior.


A Magic Wand for Home Care

http://goo.gl/Q2AEBX

A magic wand-like device for home care under development through a multi-university project could help doctors monitor their patients between visits from afar.

Goals for the device relate to safety and simplicity.

“Quite frequently in the computer security business, we invent things that are super secure but hard to use, and people don’t understand them,” said Tim Pierson, doctoral student and Wanda’s creator. “We set out to make something that my parents and in-laws could use.”

The wand relies on Wi-Fi to operate, and the prototype currently consists of a ruler with two attached antennas. Plug it into a Wi-Fi router, and it acquires the network name and password. From there, it can be detached and pointed at a medical device to connect the latter to the network, as well.

For example, if a doctor sends a patient home with a Wi-Fi-enabled blood pressure cuff, the patient can simply point the wand at the cuff rather than manually enter a password to establish a Wi-Fi connection. And once the connection is made, blood pressure readings will be transmitted to the doctor’s office.

“One of the good things about this system is that the user doesn’t even have to know that information,” Pierson told the AP. “The wand can get it from your Wi-Fi router and impart it on the device. We talked to a lot of people who have Wi-Fi in their homes and have no idea what their password is.”


Current treatment options for SLE published by Dove Medical Press


http://goo.gl/mCyDhp

ImmunoTargets and Therapy has published the review "Current and emerging treatment options in the management of lupus".

As corresponding author Professor David D'Cruz says "Systemic lupus erythematosus is a complex autoimmune disease that can be life or organ threatening. Conventional immunosuppressive agents are widely used in the management of SLE with recent regimens optimising the use of these agents while minimising potential toxicity. Biologic therapies have advanced the treatment of SLE particularly in patients with refractory disease. The CD20 monoclonal antibody rituximab and the anti-BLyS agent belimumab, are now widely in use in clinical practice. Several other biologic agents are in ongoing clinical trials although the failure of many large scale trials has been disappointing."

Professor David D'Cruz continues "The importance of managing co-morbidities such as cardiovascular risk factors, bone health, and minimising susceptibility to infection should not be neglected. This review article gives a comprehensive but readable overview of treatment approaches for this fascinating but challenging disease."

As Dr Michael R. Shurin, Editor-in-Chief, explains "SLE is an important clinical problem and it will be great to show approved and potential therapeutic approaches to the general public. This is well written review."


Pressure Ulcers: An Underappreciated Public Health Issue

http://goo.gl/Ika5fg

As a geriatric fellow back in the 1980's I became intrigued by the wide prevalence of pressure ulcers and how little literature there was on this disease.  Three decades later, they have not gone away and it amazes me that they are not on the list of recognized public health threats.  

According to the Agency for Healthcare Quality and Research, pressure ulcers affect up to 2.5 million patient per year, and related costs range from $9.1 to $11.6 billion per year in the US. Complications include pain, scarring, infection, prolonged rehabilitation, and permanent disability. They are largely preventable, and 60,000 patients die as a direct result of pressure ulcers each year. They are common across the healthcare continuum, and as many as 42% of patients in ICUs and 28% of hospice patients have pressure sores. According to a recent NPUAP monograph, pressure ulcer prevalence in long-term care ranges from 4.1% to 32.2%.  Pressure ulcers are closely associated with the perception of quality, and have become a risk-management burden for practitioners and facilities caring for patients with this disease. Despite these pressing concerns, pressure ulcers are not on the research funding agenda of the CDC.

The statistics on pressure ulcers are eye-opening when compared to other, more widely recognized public health threats including influenza and gun related deaths. Influenza results in 36,000 deaths per year, and deaths in America from guns number roughly 32,000 per year. Pressure ulcers therefore cause nearly as many deaths per year as influenza and guns combined. The 2016 fiscal year budget for the CDC includes a request for $10 million for gun violence prevention research. There is already $187.5 million allocated for influenza planning and response. But there are no CDC funds allocated or requested for research on prevention and treatment of pressure ulcers. 


CU researchers offer framework to integrate behavioral health and primary care

http://goo.gl/Cg4BRk

"The health care system differentiates physical and behavioral health care, patients don't," said Benjamin Miller, PsyD, director of the Eugene S. Farley, Jr. Health Policy Center and assistant professor of family medicine at the CU School of Medicine. "They seek care in a single setting with providers they trust in clinics that are convenient for them to visit. There should be no 'wrong door' preventing patients from accessing appropriate care."

To improve the quality of care, Miller and the project team make several recommendations. Among them:

  • policymakers and payers should establish payment methodologies that support team, not individual, providers;
  • policymakers and payers should invest in a national technical assistance center focused on how to improve care by revising federal, state and local policy and regulatory barriers;
  • providers should engage communities in service to advancing needs for behavioral health and assure consistency across care delivery;
  • providers should share information on how to operationalize successful strategies, such as telehealth; and
  • businesses and philanthropies could create resources and technical assistance strategies that improve access to data for patients and other providers.


Dementia care at home: Raising knowledge and confidence to improve quality and decrease costs

http://goo.gl/lwfcXo

"The DSM-H program strives to improve the care confidence of HHC clinicians, and in turn, the quality of care delivered to people living with dementia," said Dr. Brody. "We developed the DSM-H primarily for the HHC interprofessional team of RNs, physical therapists, and occupational therapists, as they are the largest provider groups in HHC and provide complimentary but different care to people living with dementia utilizing different bases of knowledge and expertise."

The online interactive education modules were broken up into 45-90 minute blocks (total training time 4.5 hours) for ease of learning and to limit interference with work hours, and they were designed with a mixture of imagery and text with narrative voiceover. Content-specific questions that users had to correctly answer in order to proceed were included to reinforce the learning objectives of the modules.


May Awareness Event for Fibromyalgia and Other Invisible Illnesses-An Interview with a Disability Attorney by Celeste Cooper

http://goo.gl/BE2rNp 

Each year in May I make an effort to do at least one interview to raise awareness for fibromyalgia and other invisible illness. This year I am the interviewer. I picked this topic for two reasons:

  1. I frequently see patient comments regarding denial of application for disability benefits.
  2. Anthony Castelli, Esq., attorney in Cincinnati, Ohio, was willing to give the interview to help patients understand the process.

If you or a family member or friend has significant symptoms or disease that interferes with their ability to work, this is an hour you don’t want to miss.

Attorney Anthony Castelli has more than thirty years experience with:
  • Social Security Disability
  • Personal Injury
  • Worker’s Compensation
  • Wrongful Death
We discuss:
  • The difference between SSI and SSDI
  • Long-Term Disability Insurance and SSA disability
  • When to apply
  • How to apply
  • Turned down, now what? The Appeal Process
  • The benefits of having a disability attorney
  • How the attorney is paid
  • Primary doctor vs. Expert Witness
  • Engaging the primary doctor to write a report
  • The most important thing to remember
  • Resources
You can find the interview by following this link:

*Disclaimer: The time delay on my end is due to my internet connection being from a phone hotspot. I apologize for any inconvenience.