Alzheimer’s drug U turn by NICE killer quango

Hundreds of thousands of patients in the early stages of Alzheimer’s disease could get drug treatments following a U turn by the killer quango NICE.
Alzheimer's drug U turn by NICE killer quangoHaving banned the use of Alzheimers drugs for several years the National Institute for Curbing Expenditure (NICE), now says the evidence backs the use of drugs for “mild” symptoms.

Current rules prevent NHS doctors prescribing donepezil, galantamine and rivastigmine in such early cases.

Campaigners said the release of the new draft guidance was a “momentous day”.

As many as 465,000 people in the UK have Alzheimer’s disease, and this is expected to rise as the population ages.

The availability of drugs for the condition on the NHS has been source of controversy for almost a decade.

While there has always been evidence they diminished the symptoms and boosted quality of life for some, it has not always been clear exactly how much improvement they could deliver, to which groups of patients, and for how long.

In 2005, killer quango drugs watchdog NICE ruled that no-one should get the drugs on the NHS, then conceded a year later that patients with “moderate” disease should receive them, while still ruling out “mild” patients.

The secret formula used by NICE to calculate how much “value for money” the drugs offer to the NHS was then the subject of a court action by the Alzheimer’s Society and pharmaceutical companies.

* 2005 Draft NICE guidance recommends no patients should receive Aricept (donepezil), Reminyl (galantamine) or Exelon (rivastigmine)
* May 2006 Final guidance says those with moderate Alzheimer’s are eligible, but not those with mild disease
* October 2006 Internal NICE panel rejects appeals over decision to exclude “mild” patients
* June 2007 High Court backs NICE decision following Judicial Review
* May 2008 Court of Appeal rules NICE should make public their “economic model” which calculates the financial benefits of a drug
* June 2009 NICE admits “technical inaccuracies” in the model, amends it, but does not alter guidance
* October 2010 Five years on, a fresh review of the guidance backs prescribing three drugs for mild Alzheimer’s, and includes a fourth for more advanced disease

After the case went all the way to the House of Lords, NICE was forced to first disclose the formula, then amend it after admitting “technical inaccuracies”, although it said this did not change the outcome.

That new review now proposes giving the drugs to patients with mild symptoms – which covers people in the early stages of the disease, perhaps suffering memory loss and confusion, but not yet dependent on carers for day-to-day activities.

It has also suggested a fourth drug, Ebixa, be made available for the first time to patients with more advanced disease.

The guidance is still subject to appeal by the quango.

Ruth Sutherland, the interim chief executive of the Alzheimer’s Society, said that it was “a momentous day”, with approximately half of the 62,000 people who develop the disease every year likely to benefit from the drugs.

She said that the drugs, which cost approximately £2.80 per person per day, were not a “miracle cure”, but made important differences to people’s lives.

She said: “For the price of a cup of coffee they can mean the difference between recognising your loved ones and playing with your grandchildren.

“It is critical that this draft decision becomes a reality and that all people with Alzheimer’s are given the opportunity to benefit.”

The society’s Director of Research, Professor Clive Ballard, said: “If this guidance is issued, doctors will no longer have to watch people deteriorate without being able to treat them.”

Professor Roy Jones, from the Research Institute for the Care of Older People in Bath, described the decision as “an important milestone”.

He said: “Early diagnosis and access to medication is critical to help reduce both the short and long-term impact of this devastating condition on patients, families and carers.”


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