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Parkinson's drug listed on PBS
19:34 AEST Mon Jun 2 2008
By Melissa Jenkins

The listing of a Parkinson's drug on the Pharmaceutical Benefits Scheme (PBS), which previously cost up to $15,000 a year, has opened a new chapter of treatment for sufferers of the disease.

Pramipexole imitates the natural chemical dopamine, which controls movement and co-ordination and is reduced in Parkinson's sufferers.

The drug retails as Sifrol and has been listed on the PBS for moderate to advanced Parkinson's sufferers for use with another drug, called levodopa.

Its listing means rather than costing up to $15,000 a year, the drug will be available for $30-a-month for non-pensioners and $5 for pensioners.

Neurologist Victor Fung, who sits on the Parkinson's Australia scientific advisory board, said pramipexole was the only drug of its kind listed on the PBS that did not have potential heart-valve complications.

"The concern surrounding heart-valvular disease in patients has created a significant unmet medical need for a well-tolerated and effective treatment," he said.
"The availability of Sifrol is long overdue.

"It will open an exciting new chapter in the treatment of Parkinson's disease in Australia."

Dr Fung warned that 15 per cent of patients taking pramipexole, or other dopamine agonists, can suffer side-effects including compulsive gambling, hyper-sexuality and binge eating.

But, he said, the benefits of the drug outweighed the risks. "On balance, it helps a significant number of people and Australia is really 10 years behind the rest of the world in terms of this drug being available for routine treatment," Dr Fung said.

Parkinson's sufferer John Silk, 72, of St Ives in Sydney, said he was planning to switch his medication to pramipexole in a fortnight. "It will rid me of the fear of stretching the heart too far," he told AAP.

There are an estimated 80,000 Parkinson's sufferers in Australia, with 25 new cases diagnosed daily.

Dr Fung said it was a widely-held view amongst neurologists that the drug should be available on the PBS to early stage Parkinson's suffers.

Global pharmaceutical company Boehringer Ingelheim sells pramipexole.

A Special thank you to ninemsn for this article.
http://news.ninemsn.com.au/health

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Cannabis shrinks brain volume: study
07:07 AEST Wed Jun 4 2008
By Tamara McLean

Heavy marijuana use over many years appears to shrink parts of the brain that control emotion and memory, an Australian study shows.

Brain scans on 15 men who smoked at least five joints a day for more than a decade show for the first time that they have structural brain abnormalities not seen in non-smokers.

The researchers from the University of Melbourne say their findings should settle the historic controversy over the long-term effects of cannabis use with solid proof of the damage it causes.

"These findings challenge the widespread perception of cannabis as having limited or no consequences on the brain," said study leader Dr Murat Yucel, a clinical neuropsychologist at the Melbourne Neuropsychiatry Centre.

"Although modest use may not lead to significant neurotoxic effects, these results suggest that heavy daily use might indeed be toxic to human brain tissue."
The study, published in the US journal Archives of General Psychiatry, showed two important areas of the brain were smaller in long term smokers.

The hippocampus, thought to regulate emotion and memory, was 12 per cent smaller in volume and the amygdala, involved with fear and aggression, was reduced by seven per cent.

The smokers also were more likely to show mild signs of psychiatric disorders, but not enough to be formally diagnosed with one, Dr Yucel said.

The men also performed "significantly worse" in a memory test that involved trying to recall a list of 15 words.

He admitted the findings did not necessarily prove marijuana was responsible for the difference in brain volume but the findings strongly suggest this was the cause.

If this was the case, this indicated everyone was vulnerable to potential changes in the brain, some memory problems and psychiatric symptoms if they used heavily enough and for long enough, the researchers said.

The study involved men who were around the age of 40 and who had not taken other illicit drugs more than 10 times.

Another recent research review from the University of NSW showed that cannabis smokers had a 40 per cent increased risk of developing schizophrenia, and smoking daily drives the risk up two-fold. Other studies have linked the habit to gum disease and lung cancer.

Statistics show a third of Australians have smoked at least once in their life, with about 300,000 using daily.

A Special thank you to ninemsn for this article.http://news.ninemsn.com.au/health

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Blood thinner recalled - Clexane

Batches of a common blood-thinning medicine have been recalled in Australia after testing positive to a dangerous contaminant.

The medicines watchdog, the Therapeutic Goods Administration (TGA), has recalled five batches of Clexane, commonly used in patients undergoing heart and joint surgery, and in patients with kidney failure and other conditions.

Clexane contains heparin, intravenous forms of which have been linked to severe allergic reactions, including dozens of deaths, in the US.

TGA head Dr Rohan Hammett said all intravenous forms of the drug in Australia had been tested and cleared.
"At this stage, the Clexane product, or five batches of it, have tested positive for that contaminant and we are recalling those batches of Clexane," Dr Hammett said on ABC radio.

"It is important to note that to date there have been no reports of adverse events or untoward reactions to Clexane in Australia.

"This is purely precautionary at this stage."
Dr Hammett said there were different theories about how the contamination may have occurred.

"The TGA is actively investigating where the contamination may have occurred along the manufacturing supply chain," he said.

Australian Medical Association president Rosanna Capolingua praised the recall.

"This is a very serious situation, there have been a number of recorded deaths due to anaphylaxis, which is a severe allergic reaction, to heparin products, to Clexane for instance, in the United States," she said.

Dr Capolingua said hospitals should think very carefully about rationing unaffected batches of Clexane.

The US Food and Drug Administration (FDA) has identified a Chinese plant as the source of the contaminated heparin, according to the New York Times newspaper.

The FDA had identified the contaminant as oversulphated chondroitin sulphate, a "cheap fake additive", the newspaper said.

The FDA launched an investigation after a spike in reported deaths of patients given heparin between November and February.

The US FDA yesterday sent a warning letter to Changzhou SPL, the Chinese plant identified as the source of contaminated heparin, the Times said.

The FDA had identified 12 Chinese companies that supplied contaminated heparin to Australia, Canada, China, Denmark, France, Germany, Italy, Japan, the Netherlands, New Zealand and the United States, the report said.

A Chinese official disputed the assertion the blood thinner has caused death, but admitted heparin produced in China contained a contaminant.

"We don't have a strong evidence to show that it is heparin or its contaminant that caused the problem,'' Ning Chen, second secretary of the Chinese embassy, told the Times.

He said the illnesses associated with heparin had occurred only in the US and said Chinese inspectors should be allowed to inspect the US plant where the final stage of the drug's production took place.

23.04.08

 

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New stem cell hub opens in Brisbane
Thursday Apr 3 00:02 AEDT

Australia's second hub for cutting-edge stem cell research will open in Brisbane on Thursday.

The Australian Stem Cell Centres (ASCC) Brisbane laboratories at the University of Queensland will include the first human embryonic stem cell production facility in Queensland, federal Science Minister Kim Carr said.

Scientists in Brisbane will investigate possible treatments of blood-related disease and kidney diseases using cell lines expanded from existing human embryonic stem cell lines, known as MEL1 and MEL2, created in Melbourne, he said.

ASCC chair Vicki Sara said the Brisbane hub linked scientists from four internationally renowned Brisbane-based research institutes.

"This state has everything to offer in terms of outstanding facilities, first class institutes, outstanding scientific talent and a lifestyle that no state can match," Prof Sara said.

The ASCC employs scientists within their own dedicated laboratories on the University of Queensland campus with the ASCC's chief scientist, Prof Melissa Little, also based at the Queensland laboratories.

It also funds six external research groups in Brisbane focusing on blood and the development of a safe, transfusible blood product from various stem cell types, Prof Sara said.

ASCC chief executive officer Stephen Livesey said the Brisbane hub was another step towards developing a product to save and improve the lives of patients with blood-related diseases.

Other projects in Queensland include the application of adult stem cells to kidney disease and heart disease.

There is also research underway into normal tissue repair, comparisons between different stem cell types, investigations into the safety and effectiveness of embryonic stem cells, and the development of processes to boost cell numbers.

The headquarters of the ASCC and the first major cluster of research facilities was established in 2003 in Melbourne.

©AAP 2008

A SPECIAL THANK YOU TO AAP FOR THIS ARTICLE





Tests urged for women on natural HRT
Sunday Apr 6 12:18 AEST

Women who take menopause medication containing the herbal extract black cohosh are being recommended to have liver function tests after a South Australian woman suffered organ failure while taking the remedy.

Thousands of Australian women, and millions worldwide, take over-the-counter remedies with black cohosh for the relief of menopausal symptoms like hot flushes, night sweats and irritability.

The extract, first used for gynaecological conditions by North American Indians, is a key ingredient in more than 200 drugs and is marketed as a natural and safe alternative to controversial hormone replacement therapy (HRT).

But while studies show the extract is well tolerated, there are emerging reports of a rare but severe side effect on the liver.

Seven women have suffered liver failure in the past decade, five requiring liver transplantation, and in a new case, reported in the Medical Journal of Australia on Sunday, an otherwise healthy 51-year-old Adelaide women also had to undergo a transplant.

Her treating physician, Dr Elizabeth Chow from Flinders Medical Centre in Adelaide, said the patient had taken the drug within the recommended dose over three years.
Dr Chow said the latest case was further proof tighter regulations were required to monitor the use and safety of these preparations.

She called for more randomised-controlled trials to test products and said new guidelines were needed recommending women who take black cohosh to have their liver tested.

"We recommend that liver function be checked before and during use of black cohosh," she said.
The public also needed to be better briefed about the risks of using complementary medicines, and in particular black cohosh, a member of the buttercup family.

"There is a widespread belief in the community that 'natural' plant substances are safe, effective and free of side effects," she said.

The Therapeutic Goods Administration updated labels on black cohosh products in 2006 and again in November 2007 in response to adverse drug events reported worldwide.

©AAP 2008

A SPECIAL THANK YOU TO AAP FOR THIS ARTICLE

Dodgy doctors jeopardise Medicare: govt
Thursday Apr 3 19:03 AEDT

Federal Health Minister Nicola Roxon says "dodgy" doctors rorting Medicare are undermining the entire system.

Ms Roxon said that while rorting of the system was not widespread, she vowed to come down hard on those doctors who did the wrong thing.

A total of 27 doctors were referred to the Professional Services Review (PSR) - the agency that investigates doctors suspected of inappropriate use of the Medicare system - last financial year, with indications that figure will grow to at least 60 cases this year.

Of the 27, 16 resulted in doctors either agreeing or being ordered to make repayments to Medicare totalling more than $1.7 million, an increase from the previous year when doctors paid back $1.3 million.

One doctor alone had to repay $400,000.
The doctors faced punishments including reprimands, counselling and disqualification from using Medicare schemes for various periods of time.

"It's really important we send a strong message to those doctors who are doing the wrong thing," Ms Roxon said.
"And I think it's important for other doctors to be doing that too, because it jeopardises the benefits of Medicare for everybody if it's being rorted or if it's more extensively rorted.

"We want to come down hard on these practices, but I'm calling today on the doctors to also assist us in this fight.

"If we don't stop the dodgy practices, then it is compromising for all doctors and for Medicare."

Australian Medical Association (AMA) president Rosanna Capolingua said there was only a very small number of doctors rorting the system, adding that the increase in the number of doctors being investigated was because the efficiency of the PSR system had been improved.
Dr Capolingua said the majority of doctors did the right thing.

"It's a very small number that have been picked up ... the majority of doctors ... are actually very actively thinking about what (patients) need and picking the appropriate investigations for your clinical conditions or concerns at the time," she said.

"Indeed, the AMA believes very firmly that doctors need to practice appropriately," she said.

Dr Capolingua said the AMA supported the PSR.
"We supported its establishment and worked to establish the PSR and have been involved in the recent review of the PSR which has actually enabled the increased reporting that has just become evident in the current report," she said.

"The PSR has been established to monitor any doctors, and there's a very small number of those, a very small percentage of the total scheme of things, that are outside what we believe to be appropriate practice.
"And we support the PSR in taking the appropriate action to investigate and look at the issues around those particular doctors of concern."

Dr Tony Webber, who heads the review body, said examples of misuse of the Medicare scheme included ordering unnecessary patient tests to receive a rebate.
"It would be inappropriate to order a prostate blood test on 25-year-olds, and that has happened," Dr Webber said.

"I've seen on a number of occasions tests that you would normally associate with older age groups being ordered for teenagers.

"Which, in our view, is most inappropriate and most inappropriate use of commonwealth money."

Dr Webber said the rorting was not widespread, but computerisation had made it easier for doctors to over-order pathology tests.

©AAP 2008

©AAP 2008
A SPECIAL THANK YOU TO AAP FOR THIS ARTICLE




 

Call to change cough medicine marketing
9:24a.m. 28 March 2008

Australia should follow the lead of UK authorities and overhaul the marketing of children's cough medicines, a Sydney hospital professor says.

Six cough medicines sold for children under two years old have been removed from sale in the UK and another 90 have been temporarily taken from shelves to upgrade overdose warnings on their packaging.

Asked on the Seven Network if Australia should take similar action, Professor Dominic Fitzgerald from Westmead Children's Hospital said, "absolutely".

"There is no clear benefit from using these medications and there's no justification in my mind for continuing to market them," he said.

Professor Fitzgerald's main concern about the medications was their unproven effectiveness and fears of overdose.
"Studies both in the US and in the UK (and) several other countries around the world have clearly demonstrated there's no benefit for these medications so the first thing to think about is, why give something if there's no real benefit?" he said.

"We're focusing here on the under-two-year-olds ... the real issue is there's a potential mix of up to a dozen different medications. Some are antihistamines which have sedative affects and others are cough suppressants.

"The difficulty you have is cough is such a common symptom, it's non-specific and usually related to ... a simple common cold.
"A cold will last several days and get better by itself so there is no need necessarily to give any medication. Sometimes less is better than more.

"But the potential problem here is when parents understandably give some medication ... and the medication doesn't seem to do anything to help the child ... `maybe I should give more' and so ... inadvertently parents can give excessive doses of these medications."

Professor Fitzgerald said studies had shown that old-fashioned remedies such as honey on a teaspoon or a warm lemon drink were more effective than the proprietary medications in calming coughing children.

©AAP 2008
A SPECIAL THANK YOU TO AAP FOR THIS ARTICLE

 

 

Gluten-free cracker brand recalled
Saturday Jan 12 19:08 AEDT

A popular brand of gluten-free cracker has been voluntarily recalled by its manufacturer due to fears it may contain unsafe levels of what the NSW Food Authority has called a "naturally occurring compound".

The Piranha Vege Crackers have been recalled across the country by Tixana Australia Pty Ltd, after a batch to be exported to Japan was rejected by quarantine officials.

The Japanese authorities detected unusually high levels of an unnamed compound, which could be harmful to consumers, especially children, the Food Authority said.

A spokesman for the NSW Food Authority said it could not yet release the name of the compound, but said it was "naturally occurring".

Consumers have been urged to return or destroy the crackers, which are usually displayed in health food sections of supermarkets and other retailers.

"These crackers may cause adverse reactions if eaten in moderate to large amounts," the authority's chief scientist Dr Lisa Szabo said.

"The authority is working with the manufacturer and conducting further tests to determine whether the problem is isolated to particular batches."

©AAP 2008
A SPECIAL THANK YOU TO AAP FOR THIS ARTICLE

Sleeping tablet Stilnox may be monitored
Friday Jan 11 15:38 AEDT

A popular sleeping tablet that has sparked dangerous and bizarre reactions among Australians could be rescheduled to strictly monitor who is accessing it.

A federal government committee will meet next month to decide whether Stilnox should be changed to schedule 8 status, bringing it into line with addictive drugs like morphine.

If approved, doctors would have to fill out extra paperwork and pharmacists would be required to keep comprehensive records of who they dispense it to.

Stilnox, known generically as zolpidem, hit headlines last February when the Therapeutic Goods Administration's (TGA) adverse events monitoring body alerted prescribers to a number of adverse neurological and psychiatric reactions.

A national drug reactions hotline fielded more than 500 calls from Stilnox users reporting crashing cars, having sex, fighting and binge-eating from the fridge while apparently asleep.

The manufacturer Sanofi-Aventis has said it was difficult to establish whether these behaviours were triggered by the drug, were "spontaneous" or caused by an underlying condition.

But two months ago, the TGA announced that Stilnox would carry extra warnings of possible side-effects "including rage reactions, worsened insomnia, confusion, agitation, hallucinations and other forms of unwanted behaviour".

The drug would also be sold in smaller packs, with a maximum of 14 pills, to limit exposure to these "worrying and potentially dangerous adverse effects", the regulator said.

At its February meeting, the National Drugs and Poisons Schedule Committee will consider the new proposal to reschedule the medication to schedule 8, a listing designed for controlled substances.

©AAP 2008
A SPECIAL THANK YOU TO AAP FOR THIS ARTICLE

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Measles cases surge tenfold in NSW

09:30 AEST Sat Jun 28 2008

Children not even 12 months old have been infected as measles cases surged more than tenfold in NSW this year.

Parents are urged to have their children immunised against the disease, which is highly contagious to people who have not been vaccinated.

Three cases diagnosed this month took the total number this year to 38.

Only three cases were diagnosed in NSW in 2007 and they were all exposed while overseas, NSW Health has reported

The department's director of communicable diseases Jeremy McAnulty said people could not be complacent.
"We are seeing cases in infants less than 12 months of age who are not yet due for immunisation and cases in young adults who have missed out on the MMR (measles mumps and rubella) vaccine," Dr McAnulty said in a statement.

He urged parents to have their children vaccinated when they were 12 months old, with a second dose before they started school - at around four years old.

Adults up to 42 years of age should have two doses of the MMR vaccine unless they have already had the measles.

Initial symptoms include fever, fatigue, runny nose, coughing and sore red eyes.

They are followed by a rash that typically starts on the face and spreads over the body, lasting a few days.
"Measles is one of the most easily spread diseases and just being in the same room as someone with measles can result in infection," Dr McAnulty said.

©AAP 2008
A SPECIAL THANK YOU TO AAP FOR THIS ARTICLE

 

 

New treatment for prostate cancer
17:07 AEST Thu Jun 26 2008
By Rosemary Desmond


A new prostate cancer treatment with fewer side effects may one day help reduce hospital waiting lists and give patients a better quality of life.

The Image Guided Radiation Therapy (IGRT) treatment targets tumours with pinpoint accuracy without damaging the surrounding blood vessels vital for sexual activity or injuring the bladder and rectum.

About 19,000 Australian men are diagnosed with prostate cancer each year and 2,600 die, making it the second most fatal cancer in men.

IGRT, which involves the production of high resolution images of the anatomy surrounding a tumour, is available at five cancer referral centres in Australia, including Brisbane's Princess Alexandra Hospital.

Director of radiation oncology services at the hospital, Professor Bryan Burmeister, said it was hoped a trial soon to be under way will lead to shorter treatment times, a reduction in lengthy hospital waiting lists and a better quality of life for patients.

"Across the world, we are now seeing a trend to try and reduce waiting lists by shortening the overall course of radiation treatment," Prof Burmeister told reporters.

"We are doing this already in breast cancer and we want to do this in prostate cancer as well."

But he said it could only be done if the side effects of the treatment were reduced or maintained at existing levels over the shorter course of the radiation.

Prof Burmeister said the trial would compare the usual seven weeks of conventional radiation treatment to four weeks of more intense radiation therapy using the IGRT.

"If that trial is successful, in other words if the outcomes are the same, patients with prostate cancer will routinely be treated with four weeks of treatment, rather than seven weeks of treatment and that will make a huge impact on waiting lists because prostate cancer is such a common disease," he said.

Evert Klaasen, 65, from the southeast Queensland town of Gayndah, is one of the first men to receive the new treatment.

He has received three weeks of treatment but will still have to undergo the full seven weeks.

"The only side effects that I've got is I have to go to the toilet more often, especially of a night-time," Mr Klaasen said.

If the treatment is successful, the former truckie wants to finish renovating his house and to travel around Australia with his wife

©AAP 2008
A SPECIAL THANK YOU TO AAP FOR THIS ARTICLE




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