consultation etiketine sahip kayıtlar gösteriliyor. Tüm kayıtları göster
consultation etiketine sahip kayıtlar gösteriliyor. Tüm kayıtları göster

7 Mart 2017 Salı

Funding to two Indigenous sexual health programs cut without consultation

The federal government decided to stop funding two long-running Indigenous sexual health programs without consultation or analysis, and despite a growing sexual health crisis in the Top End, Senate estimates has heard.


Both organisations have accused the government of shortsightedness, and said without their services or any feasible replacement Indigenous LGBTQI people will be less likely to seek medical care.


The Northern Territory Aids and Hepatitis Council’s Aboriginal Sexual Health program, and the Queensland Aids Council’s 2 Spirits program have run for more than 20 years addressing the disproportionately high rate of sexually transmitted infections among Aboriginal and Torres Strait Islander populations.


Both organisations were told last year they should seek alternative funding to continue operating beyond June 2017.


In Senate estimates last week, Department of Health officials said they had done a “desktop review” of programs, which found “really limited evidence that these programs, which we’ve been funding for decades now, have really had any impact”, according to Bobbi Campbell, the first assistant secretary at the department.


Asked if the department had asked the NT and Queensland programs to partner with the department for an evaluation, Campbell said no. “We need to look at this from national perspective.”


The Queensland Aids Council’s executive director, Michael Scott, said his organisation had more than two decades of experience and community rapport, and their annual funding of $ 451,000 was a “drop in the ocean” for the work they did.


“We employ four Indigenous staff and they work from a whole-of-community approach, which means even though we’re funded to work with Indigenous gay men and sistagirls, we do remote outreach to Indigenous remote populations, to the entire community,” he said.


“It is a really important service because we also do training for other organisations, such as Aboriginal medical services, on how to appropriately work with Indigenous gay men and sistagirls.”


During the estimates hearing department officials also pointed to the rising rates of STIs and HIV in Indigenous populations, particularly the remote communities where the two organisations work. While the rate of new cases of HIV among non-Indigenous men and women stabilised in the four years to 2015, the rate among Indigenous men doubled.


Aboriginal and Torres Strait Islander men were twice as likely to have HIV than non-Indigenous men, according to the University of New South Wales Kirby institute for infection and immunity in society, which also reported rates of chlamydia, gonorrhoea and syphilis were, respectively, three, 10, and six times greater than among the non-Indigenous population in 2015. Remote and very remote areas saw even more substantial differences.


Last year the number of syphilis cases in the NT increased to 229 from just 14 in 2012. The high rate is set to continue in 2017, with more cases reported in January than for the whole of 2012.


Scott said his employees had been told people in the community would probably not seek care elsewhere once 2 Spirits closed.


“They forgo health care because they’re not comfortable walking through the door,” he said. “They’ll be living with STIs because they aren’t getting tested. That’s not just a health issue for them but for their communities as well.”


Daniel Alderman, a care and support coordinator for the Northern Territory Aids and Hepatitis Council, said his organisation had heard similar reports.


“This directly affects the most marginalised population we work with, Indigenous clients, [who] as you know suffer significant trauma,” he told Guardian Australia.


“Then we have seen more marginalised communities – sistagirls, brotherboys … they’re shunned from their communities that they live in and suffer significant stigma and discrimination.


“It’s cutting funding to Indigenous employment and one of the common things we hear from our Indigenous clients is they don’t want to access general or Aboriginal medical services because they fear they’ll be discriminated against.”


The Labor MP Warren Snowdon said the government didn’t just fail to perform an evaluation but “ignored the fact that these organisations had been operating for 21 years and providing an important service”.


“It beggars belief they can be canning these programs without any transition to other programs and leaving exposed these people who are involved [to] sexually transmitted infections and Aids,” he told Guardian Australia.


He said the cost of prevention far outweighed the cost of treating someone with HIV, and accused the government of “wiping its hands” of the responsibility.


“You’re prepared to pay for the treatment of HIV … but you’re not prepared to pay upfront for the prevention programs,” he said. “It doesn’t make sense.”


The office of Indigenous health minister, Ken Wyatt, was contacted for comment.



Funding to two Indigenous sexual health programs cut without consultation

10 Şubat 2017 Cuma

How long do you get with your GP? Doctors" consultation times – in data

The doctor will see you now. But for how long? This week the president of the Royal College of General Practitioners, Dr Helen Stokes-Lampard, said GP consultations in the UK are too short for people with complex health needs.


The average consultaton time in the UK is 10.6 minutes. This figure comes from a 2015 survey by the Commonwealth Fund on behalf of the Health Foundation, which surveyed 12,049 doctors in 11 countries. It was the second-lowest: only Germany had shorter consultation periods, at 10.3 minutes. But in Germany 80% of patients get less than 15 minutes with their GP, compared with 92% in the UK.


There is no standard time in the UK: it’s up to GPs to set the duration of appointments. But Stokes-Lampard told the BBC: “We’ve got a crazy situation whereby GPs are ridiculously overworked, there are too few of us and the whole situation is on the brink.”


Methodology: the survey of 12,049 GPs and primary care physicians in 11 countries, including 1,001 GPs in the UK, was carried out between 2 March and 8 June 2015.


GP consultation times – in data

How long do you get with your GP? Doctors" consultation times – in data

27 Şubat 2014 Perşembe

Mitochondrial transfer consultation launched in United kingdom

Mitochondria

Around 1 in 200 kids born in the United kingdom has some form of mitochondrial disorder. The most critical affect the heart, brain, muscles and liver. Illustration: Getty Pictures




The Department of Health has launched a three-month consultation on the draft laws for a radical process that aims to prevent mothers from passing on severe genetic illnesses to their young children.


Mitochondrial transfer has by no means been tried in humans and is presently prohibited in the Uk beneath laws that ban the placing of an egg or embyro into a girl if the DNA has been altered. But scientists doing work on the technique mentioned it provided families fresh hope of preventing lifestyle-threatening diseases for which there are no cures.


The government announced final June that it intends to allow the process, but the laws have to be finalised, debated and accepted by parliament ahead of the Human Fertilisation and Embryology Authority (HFEA) can enable clinics to supply the therapy.


Close to one in 200 young children born in the United kingdom have some form of mitochondrial disorder. The most critical impact the heart, brain, muscle groups and liver. Underneath the process, the nucleus is eliminated from an affected woman’s egg or from a cell in an embryo and transfered to a donor egg or embryo that has healthier mitochondria.


The approach is controversial because it prospects to babies with DNA from 3 men and women: the biological dad and mom and a female donor who gives healthful mitochondria, the small biological batteries that power most cells in the body. The fraction of a cell’s DNA that is in mitochondria is minuscule and impacts only how cells are powered. It does not influence the child’s bodily physical appearance or personality.


One more explanation the process is controversial is that it would be the first to introduce genetic alterations that are passed on not only to the intended little one, but to all subsequent generations. One concern is that any damaging and sudden side-results may then damage the wellness of men and women born extended into the long term.


Launching the consultation, Dame Sally Davies, the chief medical officer, stated: “Making it possible for mitochondrial donation would give girls who carry extreme mitochondrial illness the opportunity to have kids with no passing on devastating genetic issues. It would also maintain the Uk at the forefront of scientific improvement in this spot.”


“I want to inspire contributions to this consultation so that we have as many views as possible before introducing our ultimate rules,” she additional.


Under the draft regulations, donors of mitochondrial DNA would stay anonymous, but could request particulars from the HFEA of the amount and sex of any children born from their material. If someone aged sixteen or in excess of asks the HFEA if they have been born following mitochondrial transfer, the authority will be required to inform them.


Doug Turnbull, a neurologist at Newcastle University and the leader of mitochondrial transfer researcher in the United kingdom, welcomed the draft rules. “This is extremely excellent news for individuals with mitochondrial DNA disease and an critical step in the prevention of transmission of severe mitochondrial disease,” he said.


Final year, the HFEA published results of a nationwide consultation on mitochondrial transfer, which located broad public support for the process. Exams in monkeys recommend that the process is risk-free, but study to best the strategy is ongoing.


Mitochondrial illnesses can affect single or numerous organs and tend to worsen with age. One particular disorder, named Leigh syndrome, generally develops in infants just before the age of two, and brings about progressive degeneration of the brain and nervous system.


Jeremy Farrar, director of the Wellcome Trust, encouraged the government to bring the rules just before parliament as quickly as the consultation period finished in May. “When additional public consultation on the detail of these rules is complete, we urge the government to move swiftly so that parliament can debate the laws at the earliest opportunity and households affected by these devastating disorders can begin to advantage,” he explained.




Mitochondrial transfer consultation launched in United kingdom

24 Şubat 2014 Pazartesi

Lord Saatchi launches the consultation on his medical innovation bill - live

The former marketing guru will claim these days this is the one particular likelihood the public have to set the changes in motion just before the end of this parliament.


Calling on Telegraph readers to support his bill last month, Lord Saatchi said: “There may not have been anything at all to stop Josephine dying, but the horrible considered that haunts me is that her death was a wasted death.


“Indeed, all 165,000 cancer deaths in this country each 12 months are wasted deaths because science advances not one particular centimetre as a outcome of them.


“Nothing new is tried and so absolutely nothing can be learnt that may spare other individuals. Scientific progress is currently being halted by the law and worry of negligence payments.


This culture has to modify.”


Writing in the Telegraph earlier this month Max Pemberton mentioned: “If a treatment method or method has been suggested to be of advantage, why not attempt it, specifically as it might offer new hope to individuals?


“The argument for this is especially powerful in the situation of cancer treatment method.”


People can get portion in the consultation by going to http://saatchibill.tumblr.com the place there is a hyperlink to the Department of Well being consultation.



Lord Saatchi launches the consultation on his medical innovation bill - live