The Australian Infection Control Association (AICA) has warned the Federal Government against proceeding with the planned swine flu vaccination program, warning that the use of multidose vials poses an unacceptable risk.
The Association, which represents health professionals — mainly nurses — working in infection control, says the use of multidose vials in the current context is “unacceptable practice from an infection prevention risk management perspective”.
Using multidose vials would breach national Infection Control Guidelines, which state: “The Australian Drug Evaluation Committee (ADEC) has advised that injectable products packaged in multidose vials should not be used except where products such as insulin are intended solely for the exclusive use of an individual patient.”
AICA president Claire Boardman told Crikey by email that healthcare facilities are required to comply with these guidelines, and said the use of multidose vials would pose a “significant potential risk to patient safety”, and that numerous adverse events related to their use had been well documented.
“We advise strongly against the use of multidose vials and do not support this mechanism for dissemination of the vaccine,” she said.
Her statements follow similar concerns raised recently by the Australasian Society of Infectious Diseases, but contrast with CSL’s insistence that the multidose vials are safe.
Ms Boardman says there is no justification for using the multidose vials as “the occurrence and distribution of H1N1 in 2009 within Australia does not constitute an emergency”.
She warned that the “high risk of failure” of the pandemic vaccination campaign had the potential to compromise future vaccination campaigns.
There is also the risk that there may be poor uptake of seasonal influenza vaccination next year, if this campaign goes ahead when there is not a public health emergency, she says.
If the vaccine was to be used, the informed consent process should ensure recipients were made aware that the vaccine had not been approved by the Therapeutic Goods Administration, she added.
One reason the AICA comments are significant is that the association has been prepared to make them in public. Many similar concerns are being raised behind closed doors.
In wide circulation are 1970 Medical Journal of Australia articles, describing the deaths of two men in Geelong in 1969 as a result of infection related to multidose syringes in a mass influenza vaccination program.
As well, these are some of the media clips doing the rounds:
- The New York Times: Growing Focus on Reused Medicine Vials (here and here)
- Newsday: Health Commissioner Wants Ban on Multidose Vials (here and here)
- USA Today: CDC Warns of Safety Problems at Clinic (here and here)
- BBC News: Hepatitis C warning for US clinic (here and here)
But many experts are wary of speaking out publicly, because of the political repercussions and also because they fear fanning the campaigns of anti-vaccinationists more broadly.
However, if a report in the latest British Medical Journal (here and here) is anything to go by, it seems that health professionals and the general public may vote with their feet — in choosing not to take up vaccination if it is offered. The report cites surveys conducted in several countries of health care workers and the general public, showing scepticism about the merits of pandemic influenza vaccination.
One issue highlighted by the unfolding debate is that Minister Roxon has repeatedly framed the availability of a vaccine as the answer to the pandemic.
You can understand that she might have wanted to reassure the public for reasons of politics and public health. But the simplicity of the message doesn’t do justice to the complexities involved in weighing up the potential costs and benefits of vaccination in the current context.
It also has the effect of painting the Government into a corner and encouraging a line of media questioning — “when will the vaccination start?”, rather than “what are the pros and cons of starting the vaccination now?”
The Australian Government’s Chief Medical Officer, Professor Jim Bishop, responded to the AICA concerns with this statement:
The use of multi-dose vials was always envisaged during the pandemic planning phase. Their use means that a large vaccination program can be rolled out more quickly, and they are more efficient than single dose vials when used in large vaccination clinics.
Single use syringes and single use needles will be used to draw up and administer the vaccine, so there are no concerns with cross contamination between patients. Training will be delivered to vaccination providers on use of multi-dose vials to maximise infection control and minimise wastage.
MDV will only be used for adults and children from five years of age, and single use syringes will be produced for pandemic influenza vaccine use in children 0-5 years of age.
It is important to note that the expert advisory committees and the chief health officers around the country agreed on the use of multidose vials in agreeing to the pandemic plan.
Other countries such as the USA intend to use multidose vials for the pandemic influenza vaccine rollout.
I’m neither a doctor nor nurse, so pls correct me if I don’t quite get this. Following the MDV protocol, a fresh needle and syringe are loaded from a MDV. A person is then given the injection and that needle and syringe are disposed of. Then a completely new needle and syringe are loaded from the MDV and so it goes on. Where’s the problem? How can cross infection occur? Alex
I think the risk is that from the moment you first open the vial, there is potential for the contents to be contaminated… the level of risk would increase with the amount of time that passes between first opening the vial and taking the last dose from it. If the whole vial is used up within say half an hour as vaccinees roll through a clinic in a mass immunisation programme, it shouldn’t be a problem. In lower-volume situations where you do one immunisation per day or even per week, the risk would be much greater. The concern is not so much contamination with the virus that you are vaccinating against, but with any old bacteria/virus particles that might make their way in.
My mother in law (MIL) took a regular flu shot about nine months ago, was paralysed within 24 hours and couldn’t walk for three months. Doctors said it wasn’t Guillain Barre but admitted it could have been the vaccine. They then proceeded to treat her as if it were Guillain Barre. She is still not back to normal nine months down the track.
So why do we need this again? Is it going to be like the strain of Swine Flu that with the help of the client follower media scared the heebie jeebies out of the US population in 1976. The media event was supported by a multi million dollar governmental campaign to inoculate anything and everything. Well the campaign had to be abandoned after too many people began dying from the vaccine or suffering debilitating sickness just like my mum in law. The dying people (25 admitted), turned out to be a little embarrassing for the authorities because they could only uncover only one person actually dying from the flu itself. A further 5000 suffered Guillain Barre syndrome, a particularly nasty nerve disease; however some writers say the actual figure would have been dramatically higher to force the government to quit such a major program.
The Asia Times reported yesterday that 60% of Hong Kong’s health workers are going to refuse the H1N1 shot and now according to the Guardian newspaper, UK medicos have been warned of the dangers of the untested vaccine by leading authorities (it takes years to test these things properly – not six weeks!). So without adequate testing, reportedly dangerous levels of mercury and squalene in the cocktail and according to some reports, lots of other “nasties, we are supposed to stand idly by while they dose up our youngest and fairest. Does this strike you as a little odd?
And something for the conspiracy buffs, an Austrian investigative journalist who has been tracking Baxter labs for a long while, one Jane Burgemeister has filed bioterrorism charges with the FBI as well as local Austrian authorities against WHO and the UN along with many significant others including the major producer of the H1N1 vaccine Baxter Labs against whom she is alleging “there has been a deliberate act to cause and profit from a pandemic”.
http://www.opednews.com/populum/diarypage.php?did=13611
Baxter is no stranger to complaints. As was reported in the India Times, Baxter was behind some strange synthetic flu virus inadvertently being released into the Czech Republic’s ferret population.
http://timesofindia.indiatimes.com/Health-Science/Science/Virus-mix-up-by-lab-could-have-resulted-in-pandemic/articleshow/4230882.cms.
The article states that:
“It’s emerged that virulent H5N1 bird flu was sent out by accident from an Austrian lab last year and given to ferrets in the Czech Republic before anyone realised. As well as the risk of it escaping into the wild, the H5N1 got mixed with a human strain, which might have spawned a hybrid that could unleash a pandemic”
You won’t find these items reported in the mainstream Western press needless to say.
Pause for thought though wouldn’t you say?
.