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Desert Valley Radiology Now Providing the Latest Advanced Body Composition™ Assessment

By , June 21, 2011 6:58 pm

Desert Valley Radiology has expanded its health and wellness services available to men and women with the addition of body composition analysis with their Discovery™ QDR bone densitometry system from Hologic. Notably, DXA is the most common method used in clinical trials investigating bone and body composition outcomes and has numerous advantages over other body composition techniques. This service is offered at Desert Valley Radiology and can be ordered through a DEXA study with emphasis of a body composition assessment. For any questions or additional help needed for ordering this study please call us at 602-867-0404.

The prevalence of obesity has reached pandemic proportions. Globally, 1.8 billion people were obese or overweight in 2007, and the number of obese and overweight people now exceeds the underfed1. In the United States, two thirds of American adults or 72 million people are overweight or obese. Unfortunately, children are not immune to this disease. More than one third of school age children are either overweight or obese according to the latest NHANES data2.

When associated with high waist circumference and high BMI, obesity is an independent risk factor for many cardiovascular diseases and conditions including type 2 diabetes, hypertension, heart disease, stroke as well as some cancers. In 2004 the financial impact both directly and indirectly amounted to $122 billion or 9.4% of total medical care costs3, making obesity a serious public health problem.

About Desert Valley Radiology

Desert Valley Radiology is a physician owned outpatient imaging practice that has been providing excellence in patient care and services for over twenty years in Phoenix. Our primary mission is to offer high quality outpatient imaging services in a caring and compassionate manner to all people who live in, work in, or visit Phoenix, AZ and its surrounding areas. Desert Valley Radiology provides a comprehensive scope of imaging services addressing the needs of our clients. Each and every patient receives personalized care designed to meet his or her individual needs. Our staff is committed to providing exceptional care to the people in our community.
For further information, please call 602-867-0404 or visit their web site www.dvrphx.com

http://www.free-press-release.com/news-desert-valley-radiology-now-providing-the-latest-advanced-body-composition-assessment-1294430955.html

 

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Special Report: An end to AIDS?

By , June 16, 2011 6:16 pm

By Kate Kelland

For his doctors, Timothy Ray Brown was a shot in the dark. An HIV-positive American who was cured by a unique type of bone marrow transplant, the man known as “the Berlin patient” has become an icon of what scientists hope could be the next phase of the AIDS pandemic: its end.

Dramatic scientific advances since HIV was first discovered 30 years ago this week mean the virus is no longer a death sentence. Thanks to tests that detect HIV early, new antiretroviral AIDS drugs that can control the virus for decades, and a range of ways to stop it being spread, 33.3 million people around the world are learning to live with HIV.

People like Vuyiseka Dubula, an HIV-positive AIDS activist and mother in Cape Town, South Africa, can expect relatively normal, full lives. “I’m not thinking about death at all,” she says. “I’m taking my treatment and I’m living my life.”

Nonetheless, on the 30th birthday of HIV, the global scientific community is setting out with renewed vigor to try to kill it. The drive is partly about science, and partly about money. Treating HIV patients with lifelong courses of sophisticated drugs is becoming unaffordable.

Caring for HIV patients in developing countries alone already costs around $13 billion a year and that could treble over the next 20 years.

In tough economic times, the need to find a cure has become even more urgent, says Francoise Barre Sinoussi, who won a Nobel prize for her work in identifying Human Immunodeficiency Virus (HIV). “We have to think about the long term, including a strategy to find a cure,” she says. “We have to keep on searching until we find one.”

The Berlin patient is proof they could. His case has injected new energy into a field where people for years believed talk of a cure was irresponsible.

THE CURE THAT WORKED

Timothy Ray Brown was living in Berlin when besides being HIV-positive, he had a relapse of leukemia. He was dying. In 2007, his doctor, Gero Huetter, made a radical suggestion: a bone marrow transplant using cells from a donor with a rare genetic mutation, known as CCR5 delta 32. Scientists had known for a few years that people with this gene mutation had proved resistant to HIV.

“We really didn’t know when we started this project what would happen,” Huetter, an oncologist and hematologist who now works at the University of Heidelberg in southern Germany, told Reuters. The treatment could well have finished Brown off. Instead he remains the only human ever to be cured of AIDS. “He has no replicating virus and he isn’t taking any medication. And he will now probably never have any problems with HIV,” says Huetter. Brown has since moved to San Francisco.

Most experts say it is inconceivable Brown’s treatment could be a way of curing all patients. The procedure was expensive, complex and risky. To do this in others, exact match donors would have to be found in the tiny proportion of people — most of them of northern European descent — who have the mutation that makes them resistant to the virus.

Dr Robert Gallo, of the Institute of Virology at the University of Maryland, puts it bluntly. “It’s not practical and it can kill people,” he said last year.

Sinoussi is more expansive. “It’s clearly unrealistic to think that this medically heavy, extremely costly, barely reproducible approach could be replicated and scaled-up … but from a scientist’s point of view, it has shown at least that a cure is possible,” she says.

The International AIDS Society will this month formally add the aim of finding a cure to its HIV strategy of prevention, treatment and care.

A group of scientist-activists is also launching a global working group to draw up a scientific plan of attack and persuade governments and research institutions to commit more funds. Money is starting to flow. The U.S. National Institutes of Health is asking for proposals for an $8.5 million collaborative research grant to search for a cure, and the Foundation for AIDS Research, or amfAR, has just announced its first round of four grants to research groups “to develop strategies for eradicating HIV infection.”

THE COST OF TREATMENT

Until recently, people in HIV and AIDS circles feared that to direct funds toward the search for a cure risked detracting from the fight to get HIV-positive people treated. Even today, only just over five million of the 12 million or so people who need the drugs actually get them.

HIV first surfaced in 1981, when scientists at the U.S. Centers for Disease Control and Prevention discovered it was the cause of acquired immunodeficiency syndrome (AIDS). An article in the CDC’s Morbidity and Mortality Weekly Report of that June referred to “five young men, all active homosexuals” from Los Angeles as the first documented cases. “That was the summer of ’81. For the world it was the beginning of the era of HIV/AIDS, even though we didn’t know it was HIV then,” says Anthony Fauci, director of the U.S. National Institute of Allergy and Infectious Diseases, who has made AIDS research his life’s work.

In the subsequent three decades, the disease ignorantly branded “the gay plague” has become one of the most vicious pandemics in human history. Transmitted in semen, blood and breast milk, HIV has devastated poorer regions, particularly sub-Saharan Africa, where the vast majority of HIV-positive people live. As more tests and treatment have become available, the number of new infections has been falling. But for every two with HIV who get a chance to start on AIDS drugs, five more join the “newly infected” list. United Nations data show that despite an array of potential prevention measures — from male circumcision to sophisticated vaginal or anal microbicide gels — more than 7,100 new people catch the virus every day.

Treatment costs per patient can range from around $150 a year in poor countries, where drugs are available as cheap generics, to more than $20,000 a year in the United States.

The overall sums are huge. A recent study as part of a non-governmental campaign called AIDS2031 suggests that low and middle-income countries will need $35 billion a year to properly address the pandemic by 2031. That’s almost three times the current level of around $13 billion a year. Add in the costs of treatment in rich countries and experts estimate the costs of HIV 20 years from now will reach $50 to $60 billion a year.

“It’s clear that we have to look at another possible way of managing of the epidemic beyond just treating everyone forever,” says Sharon Lewin, a leading HIV doctor and researcher from Monash University in Melbourne, Australia.

In some ways, we have been here before. Early AIDS drugs such as AZT came to market in the late 1980s, but within a decade they were overtaken by powerful cocktail treatments known as HAART, or highly active antiretroviral treatment. HAART had a dramatic effect — rapidly driving the virus out of patients’ blood and prompting some to say a cure was just around the corner.

But then scientists discovered HIV could lie low in pools or reservoirs of latent infection that even powerful drugs could not reach. Talk of a cure all but died out.

“Scientifically we had no means to say we were on the way to finding a cure,” says Bertrand Audoin, executive director of the Geneva-based International AIDS Society. “Scientists … don’t want to make any more false promises. They didn’t want to talk about a cure again because it really wasn’t anywhere on the horizon.”

GENE THERAPY

The ultimate goal would allow patients to stop taking AIDS drugs, knocking a hole in a $12 billion-a-year market dominated by Californian drugmaker Gilead and the likes of Pfizer, GlaxoSmithKline and Merck.

It’s unlikely to happen anytime soon, but Brown’s case has opened the door to new ideas. “What it proved was that if you make someone’s cells resistant to HIV…then all the last bits of HIV, that hang around for a long time in patients on treatment, did in fact decay and disappear,” says Lewin.

Now scientists working on mimicking the effect of the Berlin patient’s transplant have had some success. One experimental technique uses gene therapy to take out certain cells, make them resistant to HIV and then put them back into patients in the hope they will survive and spread.

At an HIV conference in Boston earlier this year, American researchers presented data on six patients who had large numbers of white blood cells known as CD4 cells removed, manipulated to knock out the existing CCR5 gene, and then replaced.

“It works like scissors and cuts a piece of genetic information out of the DNA, and then closes the gap,” says Huetter. “Then every cell arising from this mother cell has this same mutation.”

Early results showed the mutated cells managed to survive inside the bodies of the patients at low levels, remaining present for more than three months in five. “This was a proof of concept,” says Lewin. Another potential avenue is a small group of patients known as “elite controllers”, who despite being infected with HIV are able to keep it under control simply with their own immune systems. Researchers hope these patients could one day be the clue to developing a successful HIV/AIDS vaccine or functional cure.

Scientists are also exploring ways to “wake up” HIV cells and kill them. As discovered in the late 1990s, HIV has a way of getting deep into the immune system itself — into what are known as resting memory T-cells — and going to sleep there. Hidden away, it effectively avoids drugs and the body’s own immune response.

“Once it goes to sleep in a cell it can stay there forever, which is really the main reason why we can’t cure HIV with current drugs,” says Lewin. Her team in Melbourne and another group in the United States are about to start the first human trials using a drug called SAHA or vorinostat, made by Merck and currently used in cancer treatment, which has shown promise in being able to wake up dormant HIV.

WHAT ABOUT PREVENTION?

As scientists begin to talk up a cure, the old question of whether that’s the right goal has re-emerged. Seth Berkley, a medical epidemiologist and head of the U.S.-based International AIDS Vaccine Initiative (IAVI) is concerned.

“From a science point of view, it’s a fabulous thing to do. It’s a great target and a lot of science will be learned. But from a public health point of view, the primary thing you need to do is stop the flow of new infections,” says Berkley. “We need a prevention revolution. That is absolutely critical.”

Vuyiseka Dubula agrees. The South African activist finds talk of a cure for HIV distracting, almost disconcerting. “This research might not yield results soon, and even when it does, access to that cure is still going to be a big issue,” she says. “So in the meantime, while we don’t have the answer on whether HIV can be cured or not, we need to save lives.”

Read more http://www.newsdaily.com/stories/tre75030i-us-aids/

 

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Glowing ‘Cornell Dots’: Potential Cancer Diagnostic Tool Set for Human Trials

By , June 14, 2011 7:51 pm

ScienceDaily (June 13, 2011) — The U.S. Food and Drug Administration (FDA) has approved the first clinical trial in humans of a new technology: Cornell Dots, brightly glowing nanoparticles that can light up cancer cells in PET-optical imaging.

A paper describing this new medical technology is published online in the Journal of Clinical Investigation (July 2011). This is a collaboration between Memorial Sloan-Kettering Cancer Center (MSKCC), Cornell University, and Hybrid Silica Technologies, a Cornell business start-up.

For the first time, scientists report a uniquely advanced and comprehensive characterization of Cornell Dots — an ultra small, cancer-targeted, multimodal silica nanoparticle — which has recently been approved as an “investigational new drug” (IND) by the FDA for a first-in-human clinical trial, says Michelle S. Bradbury, M.D., of the Memorial Sloan-Kettering Cancer Center and an assistant professor of radiology at Weill Cornell Medical College.

Cornell Dots are silica spheres less than 8 nanometers in diameter that enclose several dye molecules. (A nanometer is one-billionth of a meter, about the length of three atoms in a row.) The silica shell, essentially glass, is chemically inert and small enough to pass through the body and out in the urine. For clinical applications, the dots are coated with polyethylene glycol (PEG) so the body will not recognize them as foreign substances.

A guiding light within the body: To make the dots stick to tumor cells, organic molecules that bind to tumor surfaces or even specific locations within tumors can be attached to the PEG shell. When exposed to near-infrared light, the dots fluoresce much brighter than dye to serve as a beacon to identify the target cells. The technology, the researchers say, enables visualization during surgical treatment, showing invasive or metastatic spread to lymph nodes and distant organs, and can show the extent of treatment response.

Hooisweng Ow, a coauthor of the paper and once a graduate student working with Ulrich Wiesner, Cornell Professor of Materials Science and Engineering, developed first-generation Cornell dots in 2005. Together, Wiesner, Ow and Kenneth Wang, have co-founded the company Hybrid Silica Technologies (HST) to commercialize the invention. The combined team of MSKCC, Cornell and HST researchers is now in the process of forming a new commercial entity in New York City that will help transition the research into commercial products that will benefit cancer patient care.

“This is the first FDA IND approved inorganic particle platform of its class and properties that can be used for multiple clinical indications, two of which are explored: cancer targeting for diagnostics and future therapeutic diagnostics, as well as cancer disease staging and tumor burden assessment via lymph node mapping,” says Bradbury.

The Cornell Dots were optimized for efficient renal clearance, allowing the body to pass them through the kidneys.

In addition, the scientists were able to perform real-time imaging of lymphatic drainage patterns and particle clearance rates, as well as sensitively detect nodal metastases. Nodal mapping is now being pursued under a new award of a BioAccelerate NYC Prize from the Partnership for New York City and the New York City Economic Development Corporation, which is expected to lead to another clinical trial in humans.

The lead authors of the paper are Miriam Benezra and Oula Penate-Medina, who are researchers at MSKCC. Bradbury and Wiesner are the senior authors.

Read more http://www.sciencedaily.com/releases/2011/06/110613121952.htm

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BrainStorm to start adult stem cell trial for ALS

By , June 13, 2011 6:44 pm

By Tova Cohen

BrainStorm Cell Therapeutics Inc received approval from Israel’s Health Ministry for a clinical trial of its adult stem cell therapy for people with amyotrophic lateral sclerosis (ALS).

“The trial represents a significant step forward in our goal of using stem cells with neuro restoration capabilities to treat ALS,” Adrian Harel, acting CEO of BrainStorm, said on Tuesday.

BrainStorm expects to begin treating patients in the coming weeks and will work with Jerusalem’s Hadassah Medical Center.

The U.S. Food and Drug Administration in February granted orphan drug designation to the company’s NurOwn adult stem cell product for the treatment of ALS, also known as Lou Gehrig’s Disease.

The initial phase of the study is designed to establish the safety of NurOwn and will later be expanded to assess efficacy.

Patients will be transplanted with stem cells derived from their own bone marrow and treated with the NurOwn stem cell technology. The trial will include 24 patients, 12 in an advanced stage of the disease and 12 in an early stage.

The patients will be examined at regular intervals and followed for six months post transplantation.

ALS is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord. According to the ALS Association, 5,600 people in the United States are diagnosed with ALS each year and it is estimated that as many as 30,000 Americans may have the disease at any given time.

Read more http://www.newsdaily.com/stories/tre74g320-us-brainstorm-trial/

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Scientists show heart can repair itself, with help

By , June 9, 2011 7:02 pm

By Kate Kelland

British scientists have managed to transform a type of stem-like cell in adult mouse hearts into functioning heart muscle in research proving that the heart has dormant repair cells that can be reactivated.

Although the research has yet to be translated into humans and is in its very early stages, the results suggest that in the future, a drug could be developed to prompt and prime hearts damaged by cardiac arrest into repairing themselves.

“I could envisage a patient known to be at risk of a heart attack taking an oral tablet…which would prime their heart so that if they had a heart attack the damage could be repaired,” said Paul Riley of University College London, who led the study.

Major advances in medical science in recent years have helped cut the number of people who die from heart attacks, but the damage an attack causes — when heart cells die as they become starved of oxygen — is currently permanent.

If enough dead tissue forms, patients can develop heart failure, a debilitating condition in which the heart is not able to pump enough blood around the body.

Scientists around the world are investigating various ways to regenerate heart tissue, but for now people with severe heart failure must use mechanical devices or hope for a transplant.

Riley’s team, whose study was published in the journal Nature Wednesday, targeted particular cells found in the outer layer of the heart, called the epicardium.

PROGENITOR CELLS

These cells, referred to as epicardium-derived progenitor cells (EPDCs), are known to be able to transform into a number of specialist cells, including heart muscle, in developing embryos.

Scientists had previously thought EPDCs’ ability to transform was lost in adulthood, but in this study Riley’s team found that by treating the healthy hearts of adult mice with a molecule called thymosin beta 4, they were able to “prime” the heart to repair itself after damage.

After causing heart attacks in the primed mice, the researchers also gave them a booster dose of thymosin beta 4 and this prompted the EPDCs to transform into cardiomycytes, and integrate with existing muscle.

“These cardiomycytes can link into the existing muscle of the heart and they home to the area of injury,” Riley told reporters at a briefing in London. “And they are also both structurally and functionally coupled to the heart, and therefore represent a bona fide source of new heart muscle.”

He said that in this study the priming and boosting technique was able to improve the function of the damaged mouse hearts by up to 25 percent — an improvement which would make a dramatic difference to patients with heart failure if it could be translated into humans.

In previous studies, thymosin beta 4 has been shown to encourage regrowth of blood vessels and improve heart function after injury in mice, but this is the first time researchers have used it to regenerate functioning heart muscle.

Riley said his team was looking closely at this chemical and would be screening thousands of other potential drug candidates to see if they might have a similar effect on EPDCs.

Read more http://www.newsdaily.com/stories/tre7574r5-us-heart-cells-repair/

 

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Electricity from microbes a step closer: study

By , June 7, 2011 6:33 pm

By Alister Doyle

Microbes may be harnessed more easily to generate energy after a finding about how they naturally let off tiny electrical charges, scientists said on Monday.

The bacteria, found to have microscopic “wires” sticking through their cell walls, might also be used to clean up oil spills or uranium pollution, according to the report in the U.S. journal Proceedings of the National Academy of Sciences.

The discovery about the exact structure of the bacteria and their atom-sized wires would permit researchers to design electrodes with better contacts to pick up the charges, let off by the microbes to avoid a build-up of electricity.

“We should be able to use this finding to harvest more electricity from the bacteria,” lead author Tom Clarke of the University of East Anglia in England told Reuters by telephone.

“Until now it’s been a bit like trying to build a radio when you don’t know what type or size of battery you are going to put into it,” he said.

“Now we have a blueprint of what the battery looks like,” he said of the study, also involving scientists at the U.S. Pacific Northwest National Laboratory.

“All living things generate electricity, it’s not the stuff of science fiction,” he added. Humans, for instance, use electricity to keep their hearts pumping and brains thinking.

And the bacteria use their wires to discharge excess electricity. “If they get a build-up of charge then everything else stops,” from feeding to respiration, he said.

LIGHTS, PHONES

Still, it could take perhaps a decade to develop use of the bacteria, a type called Shewanella oneidensis that live in oxygen-free environments, as an attractive power source for everything from lights to mobile phone chargers.

Before that, existing uses of such bacteria needed to become 100 or 1,000 times more efficient, he said.

The findings could also help speed development of microbe-based agents to clean up oil or uranium pollution, as well as use of fuel cells powered by sewage or compost.

“These bacteria don’t need energy-rich fuels. They can take in oil slicks, waste oil … degrade it and at the same time produce energy,” he said of the research, funded by the British Biotechnology Council and the U.S. Department of Energy.

Or in stricken nuclear plants, bacteria could separate uranium from waste water, he said. Microbes might in future be enlisted to clean up any accidents such as Japan’s Fukushima Daiichi disaster in March.

Read more http://www.newsdaily.com/stories/tre74m5i9-us-energy/

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Analysis: Fighting E.coli war with smart machines and soap

By , June 6, 2011 7:16 pm

By Ben Hirschler and Kate Kelland

LONDON, June 3, 2011 (Reuters) — Superfast machines helped Chinese and German scientists decode the genes of Europe’s deadly E.coli strain with astonishing speed — but on the front line in the war with bacteria, old-fashioned detective work is what counts.

Finding the source of the infection that has killed 17 people will require laborious on-the-ground investigations by food safety and public health officials.

Armed only with fear, soap and water, consumers must watch and wait. And in the end, the answer may never be found.

Despite recent scientific breakthroughs, there is no sign we are anywhere near conquering the threat from bacteria like E.coli. In fact, some experts reckon just the opposite.

“Infectious diseases are very much this century’s problem and they are going to become more and more so,” said Stephen Smith, lecturer in clinical microbiology at Trinity College Dublin.

It’s not that doctors and scientists are complacent about the risk posed by bacterial, viral and fungal infections. It’s that our modern way of life — global food trade, widespread travel and the growth of mega-cities — gives new opportunities for bugs to evolve and thrive.

“We provide them with new niches, day after day … they will always evolve and we can’t stop that,” Smith said.

As if to drive the point home, British scientists said on Friday they had found a new strain of the “superbug” MRSA in milk from cows and in swab samples from humans, raising concerns about infection across species.

Antibiotics are little use in the current E.coli outbreak, but the spread of antibiotic resistance and the lack of new drugs to fight novel strains is a growing concern.

“New bacteria and infections are just around the corner and we are far from winning the fight against infectious diseases in Europe,” said Giuseppe Cornaglia, president of the European Society of Clinical Microbiology and Infectious Diseases.

This week the world marked the 30th anniversary of the first reported cases of HIV/AIDS, a disease that probably lay undetected for 80 years before being turbo-charged by global travel.

WHAT DID YOU EAT?

Modern gene sequencing machines, like those from Life Technologies Corp that were put to work this week in China and Germany, mean researchers can now unravel the genetic secrets of bacteria in record time.

Five years ago, the three-day job by the Beijing Genomics Institute would have taken months, according to Paul Hunter, a professor of public health at the University of East Anglia.

Such breakneck speed research provides valuable clues, since the E.coli type identified is known to stick to the surface of plant material, pointing strongly to vegetables or salad as the culprit. But this only gets investigators to first base.

“Despite all of the superb and valuable molecular stuff, the bottom line comes down to whether or not an environmental health officer can actually work out where someone got their lettuce from,” Hunter said.

The forensic work on the ground in Germany will be lengthy and will only work if it is done properly.

“The trace-back should be comprehensive, from paddock to plate,” said Robert Hall, senior research fellow at Monash University in Australia and an expert on communicable diseases.

First, investigators need to interview patients and work out what they have eaten in the two weeks or so before they got ill — not an easy task, since many people struggle to remember with any accuracy what they ate two days ago.

Then the hunt will be on to find a common food type, a process that lies at the heart of disease detective work. Once there is a shortlist, microbiological testing should, in theory, nail the culprit.

“As time goes by it’s quite plausible that the contamination event will just naturally die out anyway, and then it will get increasingly difficult to prove where it came from. I suspect we will end up with a situation where we will not be able to prove which farm or even which country was the cause,” Hunter said.

Read more http://www.newsdaily.com/stories/tre7524al-us-ecoli-detection/

 

 

 

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WHO says cell phone use “possibly carcinogenic”

By , June 2, 2011 7:52 pm

By Kate Kelland

Using a mobile phone might increase the risk of developing certain types of brain tumors and consumers should consider ways of reducing their exposure, World Health Organization (WHO) cancer experts said on Tuesday.

A working group of 31 scientists from 14 countries meeting at the WHO’s International Agency for Research on Cancer (IARC) said a review of all the available scientific evidence suggested cell phone use should be classified as “possibly carcinogenic.”

The classification, which puts mobile phone use in the same broad IARC cancer risk category as lead, chloroform and coffee, could spur the United Nations health body to look again at its guidelines on mobile phones, the scientists said.

But more lengthy and detailed research is needed before a more definitive answer on any link can be given.

The WHO had previously said there was no established evidence for a link between cell phone use and cancer.

“After reviewing essentially all the evidence that is relevant … the working group classified radiofrequency electromagnetic fields as possibly carcinogenic to humans,” Jonathan Samet, chair of the IARC group, said in a telebriefing.

He said some evidence suggested a link between an increased risk for glioma, a type of brain cancer, and mobile phone use.

Cellphone use has risen hugely since they were introduced in the early 1980s, with 5 billion in use today. And since phones have become such an key part of daily life — used by many for Web surfing as well as talking — industry experts say a health threat will not stop people using them.

Instead, concerned consumers might opt to buy more accessories such as headsets to reduce the risks, Avian Securities analyst Matthew Thornton said.

“It’s going to take some compelling argument to change behavior,” he said.

The WHO’s position has been keenly awaited by mobile phone companies and by campaign groups who have raised concerns about whether cell phones might be harmful to health.

Industry groups immediately sought to play down the decision, stressing the “possibly carcinogenic” category also includes substances such as pickled vegetables and coffee.

“This IARC classification does not mean that cell phones cause cancer,” said John Walls, vice president of public affairs for the United States-based wireless association CTIA.

He noted the IARC working group did not conduct any new research, but reviewed published studies, and said other regulatory bodies such as the U.S. Food and Drug Administration have stated that “the weight of scientific evidence has not linked cell phones with any health problems.”

John Cooke, executive director of the British-based Mobile Operators Association, said IARC had only found the possibility of a hazard.

“Whether or not this represents a risk requires further scientific investigation,” he said in a statement.

PREVIOUS STUDIES INCONCLUSIVE

The IARC remarks follow a study published last year that looked at almost 13,000 cell phone users over 10 years and found no clear answer on whether the mobile devices cause brain tumors.

Many previous studies have also failed to establish any clear cancer link, but a U.S. study in February found that using a mobile phone can change brain cell activity.

IARC director Christopher Wild said it was important that more research be conducted, particularly into long-term and heavy use of mobile phones.

“Pending the availability of such information, it is important to take pragmatic measures to reduce exposure such as hands-free devices or texting,” he said.

Malcolm Sperrin, director of medical physics and clinical engineering at Britain’s Royal Berkshire Hospital, said he thought the IARC move was appropriate because it reflected the “anecdotal evidence that cancers may be associated with phone usage.” But he added: “It is vitally important to fully understand that there is no definitive correlation.”

Read more http://www.newsdaily.com/stories/tre74u4r9-us-cancer-cellphones/

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Top Medical Software and Applications for Palm PDA

By , May 31, 2011 7:11 pm

by  Lashan Clarke

There are numerous programs available for the medical professional that can be used on the Palm personal digital assistant to improve the medical professional’s tasks. When looking for free medical software for the Palm PDA consider these free applications below.

Free Medical Software and Apps

Anyone within the medical field and owning a PDA should consider the wide range of free medical software. While there are some medical professionals who are aware of what is available, there are others who are not aware of the various medical programs available. However, the best thing about these programs is that they are free. There might be medical PDA software that needs to be purchased from large companies, but there is plenty of medium to small size companies that have released free apps. A medical professional can use free software to see critical information about disease symptoms, diagnosis and treatment. Therefore, one should consider medical software for Palm available free of charge:

Epocrates Rx

This is an extensive application that contains a vast amount of information on common medical conditions. It includes information on laboratory results and treatment drug interactions. The software can also show an image of what the medication looks like, along with the side effects of medicines.

One of the strongest features of this software is the ability to punch in the patient’s medication and have the software reveal any adverse effects or drug interactions with the medicine being taken. Medical professionals who need to complete CME can use this PDA application. The one drawback about the free Epocrates Rx software is that the information contained in the free version is not as extensive as compared to the Epocrates Essentials version, a paid app that contains comprehensive information about drug side-effects and other details.

TheraDoc Antibiotic Assistant LE

TheraDoc can be used to give medical professionals valuable patient diagnosis information right at his or her fingertips. It can be used to collate information on disease and infection treatment at the touch of a button. The TheraDoc Antibiotic Assistant medical software includes a guide to infection control and patient safety, along with other information to improve the patient’s quality of care. One of the great things about the program is that the software can be used to give medical professionals a generated list of antibiotics for a specific disease. This program is completely free, and provides a comprehensive list of some of the most common diseases.

MedWatch

This software can be downloaded from Skyscape. MedWatch is quite useful and includes information about any adverse effect or dangerous equipment. It presents safety issues related to patient care in areas such as diagnostic equipment, medication and other devices. The software also offers an extensive drug database, enabling treatment information to be accessed quickly. MedWatch does require at least the Palm 3.5 operating system to function.

PalmEKG

This is another completely free medical software program for the Palm PDA. It can be downloaded at Emedic. It offers a guide to information on at least twenty-five arrhythmias. Not only does it presents it in an easy-to-read format, but also explains how the various parts of the ECG/EKG will look. PalmEKG is a very popular choice to download and use as free medical software.

Read more: http://www.brighthub.com/health/technology/articles/96582.aspx#ixzz1NxVlt8Mo

 

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PET Scans Predict Effectiveness of Treatment for Multidrug-Resistant Tuberculosis in HIV Patients

By , May 27, 2011 3:33 am

With the deficiencies in knowledge of tuberculosis — as well as in the practices, programs and strategies used to combat the disease and co-infection with human immunodeficiency virus (HIV) — the spread of multidrug-resistant (MDR) tuberculosis poses a major problem for the health care community. Research in the June issue of The Journal of Nuclear Medicine, however, shows that the use of 18F-FDG positron emission tomography (PET) scans can help to determine earlier if treatment for tuberculosis is working or if the disease is MDR.

Tuberculosis and HIV have been linked since the AIDS epidemic began. Approximately 33.2 million people across the world are living with HIV, and an estimated one-third of them are co-infected with tuberculosis. In 2008, the number of MDR tuberculosis cases reached between 390,000-510,000, or 3.6 percent of all incident tuberculosis cases. MDR tuberculosis is very difficult to treat and is often fatal.

“Early detection of drug resistance of tuberculosis allows the initiation of an appropriate treatment, which may significantly affect patient survival. Currently, more than two-thirds of patients with MDR tuberculosis die,” said Mike Sathekge, MD, PhD, lead author of the new study.

In the prospective pilot study, 24 patients with tuberculosis underwent 18F-FDG PET scans prior to receiving tuberculosis treatment — the standard triad: isoniazid, rifampicin and ethambutol. After four months of treatment, the patients received another 18F-FDG scan to measure averaged maximum standardized uptake value (SUVmax) — which measures glucose metabolic activity — derived from early and delayed imaging, percentage change in SUVmax and number of involved lymph node basins.

The researchers found that SUVmax of involved lymph nodes, number of involved lymph node basins and C-reactive protein levels assessed by the PET scan were significantly higher in nonresponders than responders. It was determined that a cutoff of five or more lymph node basins allowed for a separation of treatment responders and nonresponders.

Continue reading: http://www.sciencedaily.com/releases/2011/05/110524111420.htm

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