Using Magnetic Treatment For Stroke Victims

When people suffer a stroke it is usually experienced on the right half of the brain, but affects the left half of the body. The recovery process for this affliction can include magnetic treatment. This process uses a magnetic coil strapped against the outer scalp. The electric current the coil carries, is designed to reach the inner nerve cells of the brain and stimulate them.

This process was devised as a means to bring balance back to both sides of the brain. What often occurs during a stroke is the disruption of balance, which leaves one side with an overload of activity.

In clinical studies involving the rehabilitation of stroke victims, two groups were formed. One group received the new magnetic treatments, while the other group was given a placebo type of treatment.

At the end of the study, the people in the group who actually received high levels of stimulation showed an initial improvement in brain cell activity of sixteen percent. This number increased to twenty-two percent two weeks later.

The people in the group which did not receive high levels of treatment, showed no improvement. While the brain circuits of the treated group returned to normal, those of the placebo group did not.

Dental Centers Offering Affordable Dental Services

An increased demand for dental care is currently being fueled by the current economic crisis that has led to workers losing their jobs without health benefits including dental benefits. According to Dr. Steven P. Calawa job most of the people in the society cannot afford dental services in private dental offices as they have become very expensive. Most of the children visiting the clinic lack dental insurance programs that can cater for their dental needs according to Dedra Twomey, the clinic’s manager.

Dr Calawa, who is partially retired, recently joined the Greater Nashua Dental Connection which is an affordable option for dental care. He explained that the work in the clinic has been the most gratifying work he has done in his professional career. This is mainly because he is able to assist people who would not have sought him in his private clinic. Since his retirement from full time practice in June he has been working for three days a week in Nashua, Bedford Dental Arts and in Windham respectively. Before retirement he was working in Rockefeller Center in New York for over 30 years.

The Oral Health Coalition, chaired by Kristen Platte, has been setting up dental plans focusing on workforce access to fluoridation and dental care. According to Platte, people in New Hampshire have a vision of improving their oral health as a way of improving their hygiene programs and entire health.

The Families First Health and Support Center has also been witnessing an increase in demand. The Director, Helen Taft, reported that the health center serves about 2000 people. Just like the Great Nashua Dental Connection, the center has been offering its services on a sliding scale to patients without healthcare benefits and who cannot afford to pay fully. It also has a mobile dental van that reaches out to homeless people in Portsmouth, Hampton and Rochester. The center has also been offering payment plans to its patients to cater for denture costs. It has also set up a special fund to help reduce the costs.

According to Terry Miller, a Clinic Hygienist in Nashua, the use of fluoride is the most effective of preventing dental decay. Dr Calawa also pointed out that the inflammatory dental disease is linked to heart disease, diabetes and cancer.

Treatments For MS Under Review After Patient Dies

On Nov. 23, a patient taking Gilenya for treatment of multiple sclerosis has died, according to Novartis AG. Gilenya is one of the latest MS treatments and the first available in pill form to threat this neurological disorder.

It is still unclear what role, if any, Gilyena played in the death. According to Eric Althoff, the official spokesperson for Novartis, it is the first such incident reported within 24 hours of beginning treatment. In excess of 28,000 patients have been treated with the drug.

Sanford C. Bernstein analyst Tim Anderson informed investors it is too early to tell whether this incident will negatively affect the decision to prescribe the drug when considering treatments for MS. Gilenya use carries the possibility that the heart rate will slow after treatment begins. This is why monitoring by a physician is recommended when patients first start taking the drug. With this disease MS drugs often have possible side effects attached to them.

Details of the incident are under review by the Food and Drug Administration in the United State as well as other regulatory entities.

ADHD Heart Health Concerns

The tension surrounding popular medications used to relieve the symptoms ADHD was recently relieved as researchers in the United Stated declared that they do not increase risk of death due to stroke or heart attacks in adults.
Similarly, a study involving teenagers also found that the same risks were also not increased in that group.
The ADHD symptoms include distraction, restlessness and impulsiveness. Although there is no known cure for the condition symptoms can be controlled by combining therapy with stimulant medication.
Because these medications can increase symptoms of heart problems such as heart rate and blood pressure there has been concerns of large issues. Past reports have suggested that there may be increased risk of stroke, cardiac arrest and other conditions.
Because of the large number of patients, including children, involved in the treatment of ADHD health concerns have arisen.
The most recent studies have looked into a large number of patients who display signs of hyperactivity from a number of demographics. The main focus of the study was to compare patients who were taking medications had any higher risk of heart health issues than those patients who did not. Another factor that was considered was any change in health risk factors among medication users when they were actively using the medications or not.
The results of the study concluded that there was no evidence of cardiovascular health risks in users of the medications. The risks appeared to be about the same in those who were currently using the drugs as they were about a year after the use was stopped.
The study does not completely rule out all factor of risk, it is a large step towards peace of mind on the subject matter. Although the the data was analyzed is not completely without imperfection it is not likely that significantly different results will be found.

Healthier Breakfasts For Our Children To Help Prevent Diabietes And Lower Cholestrol

t is a sad fact that the majority of cereals targeted towards children are sub standard when compared against the proposed federal guidelines. This information is gathered from a report put together by the Environmental Working Group (EWG), which is a nonprofit research and advocacy organization.

Only 20 out of the 84 tested cereals met the requirements for sugar, saturated and trans fat, sodium, and whole grain content, which was proposed earlier in the year by the Interagency Working Group of Food Marketed to Children. The new criteria was developed as a direct response to the childhood diabietes and obesity epidemic, of which too much sugar intake is a large part of the problem. Healthier breakfast cereals will also help lower cholesterol, and increase fiber intake, for the better overall health of our children.

Focusing on sugar content, the report discovered that two thirds of the cereals that came under scrutiny contained much more sugar than the proposed recommendations. The new recommendation for sugar content is no more than 13 grams for every 50 to 55 grams of cereal. This is equal to 24% to 26% of the total weight of the contents. Many of the leading brands ranged from 41.4% in Kellog’s Froot Loops, to Kellog’s Honey Smacks having 55.6% of their content made up in sugar.

Overall, the study by the EWG has shown that 67% of cereals have too high a sugar content, 12% contain more sodium than the initial standard recommends, and 85% have too high a sodium content for the final standards. A further 8% contain too high a content of saturated fat, and it is also shown that 31% do not even have an adequate content of whole grains.

In conjunction with cereals that do not meet the standards, there is also an included list of the all the cereals studied that do meet the criteria. A caveat is that the ingredients may still be derived from genetically modified food, or had pesticides involved in their production. Amongst the list were a lot of the Kellog’s Mini Wheats brands, General Mills Cheerios Original, Post Shredded
Wheat, and Quaker Oats.

The food industry is at loggerheads with the new standards, which come into effect in 2016, and have created their own list of requirements that will be implemented in 2014. The food industry standard allows 38% of the food content can be made up of sugar. The EWG has responded that the proposed federal guidelines should be made mandatory, and be more restrictive.

Birth Control Plan B

There has been proposal made to let emergency contraceptives be sold over the counter. If this proposal is passed, Plan b could have been sold to teenagers under the age of 16.

The pill, which is also referred to as Plan B one-step can be obtained without a prescription as long as the patient is over the age of 17. Girls who are under the age of 16 are able to get Plan B with a prescription. Some states allow the pharmacist to write the prescription on the spot. If a woman takes the pill after having unprotected sex, then her chances of getting pregnant are cut in half.

Kathleen Sibelius, who is the secretary for Health and Human services is trying to overrule the proposal made by the Food and Drug Administration. She believes that parents should be involved in their children’s decision to get birth control Dr. Margaret A. Hamburg disagrees. She believes that all young women should have easy access to Plan B.

Sibelius contacted Dr. Hamburg and stated that she did not agree with this proposal. Sibelius is especially concerned about the fact that girls as young as ten or eleven can have access to this pill.

Studies have shown that women do not take emergency contraceptive after having unprotected sex. Many women do not fully understand the risks that come along with having unprotected sex. Forty percent of children today are born outside of wedlock. Half of all pregnancies are unplanned. Additionally, approximately two percent of pregnancies are ended in abortion.

Plan B has about 1.5 milligrams of synthetic progesterone. That is lower than most other contraceptives. The sooner that a woman takes the pill, the more effective it will be. This medication works by preventing ovulation. It may also help prevent the fertilized egg from attaching tot he uterus. Plan B will not work if pregnancy has already occurred.

Plan B first came on the market in 1999. In 2003, a push began to make it available over-the-counter. In 2008, women who were 18 or over could buy this medication over the counter. The following year, the age restriction was lowered to 17.

The Fight Against HIV And Aids

The President of United States, Barack Obama has promoted the fight against AIDS with a new objective of providing treatment to more than six million people around the world by the year 2013. Initially, the goal was set at four million people globally.

As the World AIDS day was marked on Thursday, Obama urged world leaders to step up their efforts to combat AIDS. He also urged China to increase its donations to provide drugs to counter the effects of AIDS.

The immediate former US president Bush spoke to the Washington event by satellite. Bush sought to make HIV and AIDS a priority in his administration when he was in power. The event was sponsored by ONE campaign.

Advocacy groups were happy with the new goals set by the US. The United States is the largest single AIDS donor. The annual funding for AIDS and HIV programs reduced to 15 billion dollars. This is well below the 24 billion dollars UN agencies expected by 2015.

MINORITY GET TREATMENT

New HIV infections fell from 3.1 million in 2001 to 2.7 million in 2010. On the other hand, the number of people who have access to HIV combating drugs rose from 400,000 in 2003 to 6.65 million in 2010.

While these figures might be impressive, the number of people living with AIDS globally is more than 34 million. According to research studies, HIV drugs reduce the spread of the virus to the patient’s partner by up to 96 percent.

Obama also said that as part of the goal to achieve a generation free of AIDS, his government would be providing anti retroviral drugs to 1.5 million expectant mothers who are HIV-positive.

Ocrelizumab – new drug for Multiple Sclerosis (MS)

Ocrelizumab is a new experimental drug that has proven to be effective in a clinical trial that used 220 people with multiple sclerosis. MS is a debilitating autoimmune disease that occurs in a large amount of North Americans. It normally attacks young people and is more likely to be found in women than men.

This study was done by scientists at UCSF Medical Center and included hospitals located in the United States, Europe, and Canada. It was performed on patients with relapsing-remitting MS. This is a form that is known for the accumulation of brain and spinal chord lesions and attacks on the neurological system.

The patients were chosen by random and separated into four groups. Two of these groups got injected with the monoclonal antibody Ocrelizumab at two doses. One group received the standard drug called interferon-beta. The last group received a placebo.

The doctors observed the effectiveness of each treatment through monthly MRI brain scans and counting the marks that were visible that were indicators of inflamed lesions. They also marked the frequency and severity of each neurological attack that led to vision loss, weakness, numbness, or other symptoms.

The trial’s results proved that patients on the drug did well and showed less signs of the disease than those on the placebo or standard medication. In the end, Ocrelizumab reduced brain lesions by 89% and lessened the amount of new attacks over six months. Throughout this short study, interferon did no better than the placebo. Dr Stephan Hauser, leader of the study, claimed “it is a remarkable finding”. he said that the nest step would be to see if the effects would be maintained over time.

Ocrelizumab works differently than other MS drugs. Most of the drugs target a person’s immune system, but in different parts. Multiple Sclerosis involves a person’s immune system attacking the nerve fibers in the brain and spine. This can disrupt the usual flow of the brain’s communication and leads to symptoms like visual impairment, fatigue, weakness and coordination problems, and cognitive difficulties.

While most drugs target the T cells in the immune system, Ocrelizumab targets the CD20 molecule of the B cells, a different part of the immune system. The concluded trial validated the theory that targeting the B cells may end up greatly helping those with Multiple Sclerosis. All of the work was funded by Roche and may someday lead to a better treatment for MS.

Medicare Beneficiaries are Selling Prescription Drugs

Medicare beneficiaries, as many as 170,000 of them, may have been doctor shopping in order to obtain multiple prescriptions of muscle relaxer and non-narcotic painkiller drugs, according to a recent Government Accountability Office audit of the Medicare Part D prescription drugs plan.

Among the commonly used medications sought by the Medicare beneficiaries in question were popular drugs like oxycodone, Adderall (a form of amphetamine and dextroamphetamine), Valium (a brand of diazepam), Xanax (a brand of alprazolam), carisoprodol (sold under the brand Soma), and the non-narcotic painkiller drugs, and brands of tramadol, Ultram and Ultracet .

The audit determined that 170,000 beneficiaries of Medicare had received five or more prescriptions from different doctors for these and other popular medications, all at a cost of approximately $148 million to the Medicare Part D program.

Though Medicare is generally thought of as a program to benefit senior citizens, the overwhelming majority of the suspected doctor shoppers are not on Medicare due to their age. Nearly three-quarters, about 71%, had Part D coverage due to disability. Even more, 72%, benefited from the Medicare Low-Income Cost-Sharing subsidy.

The most sought-after medications were hydrocodone and oxycodone, two of the most prescribed and most abused painkiller drugs in the United States. The findings of the GAO audit have raised heightened concern among government officials and legislators that Medicare benefits are being used to disguise and subsidize addictions. One U.S. Senator, Scott Brown of Massachusetts, referred to the doctor-shopping as “taxpayer-funded drug dealing.”

The GAO audit involved a review of prescriptions filled by beneficiaries of Medicare Part D between May 2010 and October 2011 for a dozen controlled substances, including those listed above. The GAO focused its investigation on specific cases, determining that the doctors who wrote those prescriptions were unaware that their patients had been abusing the drugs, trying to sell them, or visiting other doctors to obtain more.

According to the investigation, one beneficiary received prescriptions for oxycodone from 58 separate doctors, filled at 45 separate pharmacies, totalling 3,655 pills. Another obtained a 994-day supply of hydrocodone from 25 different prescribers.

As a result of these findings, the GAO has recommended imposing limitations on identified doctor shoppers of a single doctor and a single pharmacy. Also recommended is turning over the names of known doctor shoppers to insurance companies that administer Medicare Part D plans.

CMS, the Centers for Medicare and Medicaid Services, has proposed an alternative rule requiring that Part D sponsors include a physician identifier on all prescriptions, allowing insurers to confirm that the prescription was written by an actual doctor. CMS has also proposed new guidelines for detecting and reporting misuse of controlled substances.

What are the “Essential” Health Benefits?

Health insurance reform was a welcomed development for many Americans, but it also raised many questions. One of the most important of these centers on the definition of an “essential health benefit.” The answer to that question is something just about everyone with any sort of a stake in health reform is anxiously waiting for.

The Affordable Care Act defines ten broad categories of essential benefits that all medical insurance providers must cover as essential health benefits. The specifics within those categories are at the discretion of the Department of Health and Human Services. This Friday the Institute of Medicine will make its recommendations, which are expected to have a strong influence on what the HHS ultimately decides are essential benefits.

It would be difficult to overstate how important this will be for the health insurance industry. All plans wanting to sell on the new medical insurance marketplace will be required to offer these benefits. Additionally, the plans will be ranked according to how much of the benefits the insurance company will pay for; 60 percent and the plan is ranked “bronze,” while 90 percent qualifies as “platinum.”

The actual regulations won’t be established by HHS for several more months, but the work is already well underway. Much of it centers on one dilemma that promises to be difficult to resolve: how to make the essential benefits comprehensive enough to be useful, yet also affordable. A sparse benefits package won’t provide the robust coverage envisioned by health reformers. But a package that is too comprehensive will be prohibitively expensive.

Patient groups have tailored their lobbying strategy to match HHS concerns, pragmatically realizing that appeals for policies that include every conceivable coverage option will be wasted energy.

There are also political risks associated with laundry lists of benefits. If a particular benefit is cut from the list, there may not be space to squeeze it back in later. In previous meetings with patient’s rights lobbyists, HHS has suggested allowing plans some flexibility to define their benefits, with affordability being the crucial concern.

The final regulations will likely establish a middle ground, somewhere between the wide-open generality of the ten broad benefit categories and an exhaustively specific list of covered conditions and procedures. Those final rules won’t be ready until May of 2012 at the very earliest, according to sources at HHS. Between now and then, patient groups will have plenty of time to lobby for the best possible outcome in this latest phase of the reform of health insurance.