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THE HSE SPENT just less than €7.5 million providing injectable beta-interferon to patients suffering from multiple sclerosis (MS) in the first ten months of this year.
The information was revealed by Minister of State Alex White, in response to a question from independent TD Terence Flanagan who also asked about the prescribing guidelines for disease modifying treatments and the extent to which White believed they were being adhered to.
Figures show the number of patients receiving the injection treatments has fallen from 1,103 in 2011 to 866 in 2012. In the first ten months of 2013, 814 patients received the injectable beta-interferon treatment.
Costs from January to October reached €7,480,363 this year, falling from €10.2 million in 2013 and €11.3 in 2011.
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The junior minister said the Medicines Management Programme, which was established by the HSE aims to ensure patients have access to the essential medicines that they need. He said it also” facilitates more cost-effective prescribing with initiatives in relation to high-costs medicines” and ensures value for money in relation to medicines.
White added that another aim of the MMP was enhancing evidence-based prescribing and optimising patient safety thorough a reduction in medication related adverse events.
On the issue of prescribing deadlines, the minister of state said he would refer this to the HSE for a reply.
There have been calls for a cannabis-based drug called Sativec to be approved for the Irish market as it has been identified as suitable for the relief of certain symptoms of MS. The Department of Health has said that it is engaging with experts on how best to make it legally available in Ireland while maintaining existing controls on cannabis.
It is expected that new regulations to allow for this will be introduced early in 2014.
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Public money very well spent. If that’s what it costs, I as a taxpayer have no issue with that. If they can get a get deal, great. Go do that. But don’t stop paying out for MS patients. Their life is hard enough without the worry of affording expensive drugs. I’m sure the State spends (and wastes) other money in far worse ways.
Is this article giving out about the money spent or just letting us all know that a tiny part of the hse budget is spent helping people. It’s not headline news that money is spent on sick people it’s just the way things should be done
The point of the question is that b-inf is not effective for many MS patients, but it’s very expensive. The prescribing guidelines are supposed to ensure that it’s used properly. That’s what Flanagan is asking about.
It’s difficult to understand what this article is about. Very unclear and with no explanations about the beta interferon injections for anyone who doesn’t understand what they do and why they are prescribed. A student of journalism would do better.
Emily
I normally respect your contributions on this website but in this particular case I believe you are overstepping the mark. The treatment of difficult medical conditions such as MS is in the hands of eminently qualified physicians who spend many years in training and in the management of such patients and amateurs should avoid amateurish pontificating on the subject.
Richie, I’d agree that politicians arguing about clinical matters is a bad thing. The thing is that the clinical effectiveness of the ABCR drugs has a wealth of supporting evidence, as does the cost effectiveness. That’s why we have prescribing guidelines. The suspicion is that those guidelines are being ignored. If that’s the case, it means that the drug budget is being misallocated, and someone else is suffering needlessly. It’s legitimate to ask the question.
The answer on its own tells us pretty much nothing, though.
Dermot I completely agree – the article is not at all clear on what it is trying to convey. Also mentioning Sativec in the same context of betaferon is arguably not relevant as they do completely different things for people with MS and are therefore not comparable.
Beta interferon is one of the oldest and first of the modified disease therapies for ms. The reason that figures are now showing a decline is that more effective therapies have been developed in the interim. Savitex is used for pain management in spasms in ms and does not in any way modify the course of the disease.
As one of the 814 thanks! I was diagnosed over 10 years ago & apart from some small relapses am well, working & able to contribute towards the tax bill. Had I not been on interferon I could be costing the state considerably more!
Very Interesting that the Irisg prescribing guidelines are being questioned…..this needs more digging, and comparisons should be drawn between how easy it is to change meds here, versus other countries.
There are 3 alternatives to the injections all of which have a greater efficacy and side effect profile, but they are extremely difficult to get a prescription for, as an MS patient.
I see others changing meds much easier in most other countries; I’m a regular participant on an international message board for MS’ers.
The two major issues are can Sativex be licensed quickly for spasticity and pain?
And can BG12 be licensed as fast as possible – this is an alternative to the injections, has a greater efficacy, and is a tablet.
I am so keen to get BG12. MS doesn’t normally improve over time.
They would be best served appointing an appropriate number of Neurologists as our ratio is a disgrace.
Only then can all MS patients have tailored treatment plans that will minimise prescription costs and minimise relapse rates.
@D Although I agree Ireland is in desperate need of more neurologists, the real problem is HSE prescribing guidelines and funding.
More neuros do not necessarily mean easier access to more choices for those of us with MS.
Is the article not pointing out that spending on MS drug treatment has gone down? Is this because there are less people who need these treatments or because of cuts in funding?
I would imagine Mary, the cost has decreased because MS patients are being offered different medication. I have a family member with it and 6 months ago, he was switched to a daily tablet, while that is also expensive, it isn’t anywhere near the cost of the injections..
Thank you for that Anne. Sorry to hear about your relative. I’m glad that the savings are because there are cheaper medications which are hopefully more effective than older ones.
Is this article intended on causing controversy from begrudging tax payers to promote the wonderful journalism of “the journal” or to highlight that there is fairly adequate funding for a absolute worthy cause?
The main issue raised by the TD & the author is the reduction on actual spend for injectable DMD (disease modifying drugs). Over the past number of years research has been focused on developing oral alternatives to those previously only available via injection. These newer alternatives often cost much more than their injectable counterparts. Many MS patients I know have made the switch. In my case the switch from injections to tablets cost approx €10k more per annum, but the opportunity to switch was grasped with open arms & couldn’t have come quick enough. God bless the HSE.
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