Well I've purposely stayed away from this subject till now because I understand how high emotions are running in many parts of the UK over these proposed changes, but about a week ago there was a comment on the DS UK list that prompted me to write something down.
As I understand it there is a huge national review of heart services being undertaken at the moment. I'm sure Penny will give you a better idea of what is happening. I believe it's about improvement, and giving all children an equal chance of survival and a good outcome, no matter where they live.
So as the bulk of it was already written, I figured I might as well post it here on my blog too. Hopefully it may clarify the situation for some people, at least as far as my position on the changes and why I have not accepted invitations to sign up to campaigns to save individuals units. I must stress that these are my personal opinions, but I do not feel it is inappropriate for me as Director of Down's Heart Group to express them here as they are based on a national perspective after over 20 years working and liaising with all of the UK units and not reflective of my own brief personal experiences at one individual unit in 1989. I have met very many of the medical staff who may be affected by these changes and heard firsthand accounts from parents about probably all of them - they are definitely amongst the most gifted and dedicated cardiac teams in the world and we need to take steps to ensure that the UK retains that expertise. (only a few days ago one of our surgeons was mentioned in an Olivier Awards acceptance speech).
And I'd like to thank the surgeon who kept my baby daughter alive: Choreographer tells the harrowing story behind his awards acceptance speech
Getting back to 'Safe and Sustainable', I think I have a pretty good understanding of what this is all about, having been involved in much of the consultation process that has been going on (for far too long now) and attended all the general meetings. What you have to remember is this is not something that happened overnight, originally it all started about 10 years ago and the whole point is not a cost cutting exercise as it has been referred to. It is not actually something that has been government led, it came out of some of the parent groups asking why a few of the recommendations that came out of the 'Bristol Inquiry' had still not been addressed, particularly in relation to ensuring the best clinical outcomes for children undergoing heart surgery.
One of the facts that had been established from research was that there is a correlation between the success rates (both mortality and morbidity) and the number of procedures a surgeon in involved in - basically you need to keep practising to keep up your skills. In some units there is not the capacity for an agreed minimum of operations to take place in a year, so these surgeons are not getting the opportunity to fulfil the criteria and maintain their skill levels.
There were also issues around units with only one surgeon and the problems encountered when they were on holiday or off sick as well as training and progression - with a team of 3 or more surgeons in one unit, it is possible to have one very experienced who mentors other colleagues of varying experience and there is a continual progression as the more senior ones retire. There is a real lack of paediatric cardiac surgeons here in the UK and a few of the really excellent ones have recently retired or will soon do so and if things continue the way they are we will be looking for more and more surgeons from overseas.
The consultants and cardiac teams themselves recognise all of this and whilst naturally none of them wants their own unit to close, they have pretty much all been on-board with the rationale behind 'Safe and Sustainable' since the beginning.
So why has it taken so long? Well one of the reasons was the last General Election when non of the politicians wanted to rock the boat in their own constituencies and since then it is because there has been so much work undertaken in consultation and visiting units etc. to find the best way forward. In an ideal world the Commissioners would agree how many units were needed, what facilities they needed and how to distribute them geographically and we would build 6 or 7 brand new hospitals to meet that need. But of course that's not an option, so a great deal of work has gone into looking at all the possible different options and finally coming up with 4 for further consultation. I attended the meeting about a month ago where there was an hour long presentation explaining the whole process that was gone through and there is a document you can view on-line that details it all (but I'll warn you it's about an inch thick).
So to cut to the chase and clarify - some units will stop providing surgery, but they will continue to do everything else they do and there are also plans to increase knowledge locally with designated paediatricians with cardiac specialist training. In making the suggestions they have, they have taken into consideration many things including:
* number of procedures
* access to other services as many kids have other medical
* retrieval times for sick kids
* national specialist services such as transplantation and ECMO
and whether these could be relocated
* population density
and many more. Whilst we would all like to have a specialist centre on our doorstep and being close to home is desirable during such a traumatic event as your child having heart surgery, there are many parents, who for varying reasons, have travelled the length of the country for their child's operation. Some defects are so rare that only one or two units have experience of repairing them, that some families already have no option - if your child needs a transplant they currently go to the Freeman in Newcastle or Great Ormond Street in London. Cardiac surgery on congenital defects is quite different to that in older patients with acquired issues and then you have to add the size of the heart into the equation and the specialist intensive care required afterwards and it becomes obvious that this is not a procedure that can be done in all local units, so depending on where you live you may already have to travel some distance to a cardiac centre.
I don't doubt that these changes will sadly result in some children dying who might otherwise have survived if their local unit had remained, but I believe that we have to weight against this not only the number of children that will survive who wouldn't without these changes, but also the quality of life of those who survive, because it's a harsh fact that whilst some kids survive as a result of surgery, during the process they sustain neurological damage.
The whole idea of 'Safe and Sustainable' is to build on the fantastic service that we already have, but to look to the future and how we can ensure that the service not only survives for future generations but also improves. We have to take what was learnt from the Bristol and Brompton Inquiries, recent issues surrounding Oxford and do everything that we can to ensure that these mistakes cannot happen again - we cannot be complacent and say "it's working well so leave it alone", we have to be constantly looking to develop and improve in-line with the progress constantly happening in the field of congenital heart disease.
Well that's me off my soapbox - I hope that perhaps it helps explain a little more to some parents. Yes a move will be disruptive I know and you have an affiliation with your unit and it's staff (I fully appreciate that - I feel the same about the cardiologist and surgeon that treated my son), but if you can step back and take a more national perspective, hopefully you will see the rationale behind these changes.
if you want to read more check out
Safe and Sustainable website
Children's Heart Federation website
Central Cardiac Audit Database