Select Committee on Public Administration Minutes of Evidence


Examination of Witnesses (Questions 364 - 379)

TUESDAY 18 JANUARY 2005

MR PETER HAY, MR GRAHAM URWIN, MS CHRIS FEARNS AND MS DOREEN HARRISON

  Q364  Chairman: We are delighted that you could join us this afternoon. We had an informal discussion this morning about some of the health issues around choice and related mattes, and it would be nice to extend that into the social care field. Can you briefly say what you think the increasing emphasis on choice has come to mean in the social care field, and flag up one or two of the areas where this kicks in?

  Mr Hay: Thank you, Chairman. I have tried to give you in the paper some very practical examples of the range of choices that we are working with at any point. I will leave the paper with you and will not talk you through it. At the end I outline the outcomes that face people who use social care services. It is different from education and the NHS; it is not a universal service and is one designed to provide specific support for people on the edge of communities, to keep them in our communities. Choice, in terms of people with mental illness—we know that only a quarter of them get employment. We know that there are poor outcomes for children that are looked after in educational attainment, and we know of the difficulties about child poverty facing families with disability. Those are the outcome bits where we have to bring choice to bear on some of those outcomes that we are delivering for some of those people. At the opposite end of the spectrum is the importance of choice in people's daily lives and how fundamental that can be. One of the biggest rows as Director of Social Care that I have ever walked into was the one that became known as the "dippy egg" row, with older people in residential care making a very serious stance about the council's stance in catering terms of "dippy egg" and beef. As a Council catering service, we had applied rules which applied to schools, ie, children, who did not have choice in that sense, to old people's establishments. People in their late eighties in frail condition were not being allowed soft eggs and they were not being allowed to eat beef. That raises the big question that sometimes it is the choice in daily routine that is really important, and particularly in the case of residential care, when food is really, really important. One of the big issues we are facing now is the right of older people to run a hot bath at any time of day or night when they are in care, and what that means in terms of regulation. At night it is an issue of staffing levels, which is where the regulator comes in; but there is also people's right to be independent. The whole issue particularly around adults is, "whose risk is it anyway, and who is taking the choice about risk?" We have a community with growing numbers of older people, and clearly growing areas of challenge around that such as dementia, so the issue of risk and how much risk is tolerable to take in making decisions about one's life are critical. That is one that we struggle with on a day-to-day basis, and clearly there are bigger implications around that whole issue, as I have outlined. Choice is linked to the whole concept of trying to empower people to be part of our society and to be part of social inclusion. There is the work we have done with carers, aligning all our expenditure around their wishes and needs and choices about how that money is used, as well as the work we have done with young people in care, where they have designed and run a service about bullying, because they have identified that as a big issue. People's choices in running and designing services are quite critical. I have talked a little bit about choice in the shape and provision of services, with direct payments being obviously a major issue. We have moved significant numbers of people into direct payments this year, which we are very proud of, and we are also very proud of the way in which we have tried to ensure equality of access to that from all communities. It is not just one way of working. Finally, the take on choice for us is how we fit it around new ways of thinking about choice. I know that the adult green paper is still eagerly awaited, and I have put a reference in to a scheme that we are working on at the moment which sees the value of a care package in cost terms being shared with carers, and giving some choice about the services that are deployed. Those are very extensive issues. All of that fits with the tensions between individual choice, and—a bit like schools but slightly different—where individual choice begins and ends, and what that means. If direct payments mean that ten people withdraw from a service aimed for 40, what does that mean for the remaining 30? Does it affect economic viability of running a particular service? Those are the kinds of things we wrestle with in how we plan and shape services. That said, our experience is that people know also the limits of choice. We have been doing some work today with parents of children with disability, and one of the things they are immensely responsive to is if we say, "the limit of the resources we have is X; we can do what we like within X". That works quite well. Sometimes we are frightened to put parameters on the table, but when we do we find how amazingly keen people are to work within those parameters and to help make the choices. That is a different way of working than perhaps traditional approaches in local government and planning.

  Q365  Chairman: In our discussions we have been tossing around an idea as to whether choice is a means or an end; that is to say, is it a value in itself because people should have choice over their lives, or is it just a useful tool to produce improvements in services? Do you see choice as something that is so important to people that they ought to exercise it? We asked this of the PCT this morning, and they said people are that not much fussed about choice; all they want is to know that the services or any other public body provides are good services whether or not choice is an ingredient. Is it a bit of your toolkit that enables you to lever up quality, or do you think it is important in itself so that you have to deliver it, irrespective of the consequences it might have?

  Mr Hay: Experience would suggest that choice is meaningful when it is about levering up quality. A choice between two things of poor quality is not really a choice. It is about how it fits with driving quality. Our general experience is that people are not that fussed on who the provider is. The choice of provider is not as important as the choice of fit to that person.

  Q366  Chairman: We have heard a quite different story, talking about council housing.

  Mr Hay: Absolutely.

  Q367  Chairman: They told us that the reason the council tenants voted to stay with the Council, irrespective of the fact that it was not in their housing interests to do so was because it did matter to them who the provider was, so I am not sure that we are entirely persuaded of that.

  Mr Hay: No, and perhaps it ranges from different sectors, but it is the quality of the service being offered, and particularly in social care where it is not that universal fit. It is something you come into contact with at a particular stage in your life. It is what we provide and what you think about that service as you get it. Clearly for us a big issue is anticipating what choice might be. A big issue in this city is the future of our residential care for older people, where the clear message to us is that that is not a choice people will want to be taking in the kind of numbers that they are now and would want to exercise the choice to live at home for longer. Part of our work is to have a range of services that will enable people to make, or be in line with choices people will make, at the point they get there, because to some extent we are anticipating that now. We will move the shape of services to be in line with a generation of older people that are going to be more consumer orientated than people who are in our care at present.

  Q368  Mr Prentice: I just wonder how many elderly people want to run a bath in the middle of the night.

  Mr Hay: Believe it or not it has come up as an issue with the regulator. It was about somebody who was feeling discomfort and ran a bath for comfort, and it was about their ability to do that and whether they should be allowed to do it.

  Q369  Mr Prentice: I ask the question because in your paper you say "social care is a rationed service" and choice requires spare capacity and additional resources. The fascinating thing you said is that people are prepared to work within parameters. If you tell them the choice will be constrained, amazingly they accept that.

  Mr Hay: I put that in there because essentially we are set up by legislation to accept the criteria for assessment linked to resources. Clearly, we are resource constrained. Ultimately, the Council puts a sum of money aside and that is what we have to work to. There is a level of need in the community, which at some levels you could almost say is infinite, and where you draw the line is a choice element made in local government but increasingly in consultation with local people in a whole range of ways, as well as about the electoral mechanisms. Then, working within those choices where we recognise the resource constraints, we decide how to use it best. For example, in relation to parents with children with disabilities, we have at the moment six units that provide residential care. Perhaps that is the wrong balance of resources; perhaps we could use slightly less and use more in communities. Would that provide a stronger range of support or a weaker range of support?

  Q370  Mr Prentice: To what extent do people engage positively in those kinds of debates? When you tell us people are prepared to work within the parameters, and there are resource constraints, are the parents of a severely disabled young person prepared to go along with what you consider to be the appropriate level of resources?

  Mr Hay: Not always, and clearly they can take that into a political dimension as well. Clarity in discussions about what we have and what we can work within and—

  Q371  Mr Prentice: It is just that there are cynics out there who say choice is only meaningful if it can be exercised, and just to have a discussion about possibilities without anything happening on the ground could leave people feeling cynical.

  Mr Hay: That is absolutely right. In setting up those arrangements, as an authority you have to be clear that you are going to follow that through. That is why I mentioned service design with people because you have to follow through, otherwise it is a talking shop, and that in itself creates frustration and anger.

  Q372  Mr Prentice: What about people who are confused about the choices? You mention in your paper the mentally ill and we heard this morning about that. To what extent is choice meaningful or does it confuse mentally ill people?

  Mr Hay: A clear part of the remit on social care is dealing with people who have no choice, whether that is mental illness or people who have complete mental incapacity and guardianship. The issues in those areas are how you demonstrate what you have done to best effect, and where you have taken choice away and how you have done that. It is also back to being clear on an individual basis what elements of choice you are removing and what elements you are giving back, because we also want people to re-integrate into the community at some point in the future. Clearly, that is an individual tool, but there are significant challenges for us within that and that will pose a whole range of other risks and dimensions alongside that, which are increasingly difficult for us to manage.

  Q373  Mrs Campbell: Can I come back to our friends from the PCT. You call yourselves the "listening PCT", and this Committee is inquiring into choice and voice in public services. Can you tell us the ways in which the health voice networks operate have made a difference to the care you provide?

  Ms Harrison: Do you mean the way we consult with users?

  Q374  Mrs Campbell: No, I mean what practical difference has consultation made to what you provide.

  Ms Harrison: It has made a significant difference, I would say. We consult regularly with service users and the wider public, and that then influences the way we develop our strategic thinking and commissioning of services. In terms of service provision, we do very regular satisfaction surveys, focus groups and patient forums with our service users, and we have made quite a lot of significant improvements in the services as a direct result of people saying "we would like things to be done this way, rather than this way". I feel we could demonstrate quite clearly in many areas where we have had significant change.

  Q375  Mrs Campbell: Do you want to give us one or two practical examples?

  Ms Harrison: In terms of satisfaction surveys, if you think about people, and older people's services, they make choices about times of meals and the kind of meals they want to eat, the times they want to go to bed and get up. As a result of that, we have introduced a protective mealtimes policy so that doctors and other people cannot go in and say "we want to examine you now" in the middle of their dinner. That may seem quite trivial, but that is about exercising choice in your daily life. On things like, "are your spiritual and psychological needs being met?"—"no, we spend long, boring days waiting for the physiotherapist to come". We have set up activity programmes that are meaningful and age-appropriate for those people so that the time passes more quickly. That is a small way we have changed things. Graham has just whispered to me about a programme we are doing. We are looking at different ways in which different groups can be empowered, and one of the areas we are looking at is people with particular conditions being given some—using the expertise they have developed over the years, because if you have a long-term condition you develop expertise on how you handle that. It is about sharing that with other sufferers with the same illness in order that they may be able to manage their disease process better and have a better quality of life. A good example of that which I can give you is the Breathe Easy Group, for people with chronic chest conditions. It is a self-help group. They go through an exercise programme because people with chronic breathing difficulties tend to sit around because they are frightened because they get short of breath on the slightest exertion. If we can gradually increase their level of exercise, that gives a significant improvement to the quality of life. That means that somebody who sat at home and could not do anything can start to go out for a period and do things to improve the quality of life.

  Mr Urwin: I think that reflects on some of our more focused initiatives. We described a process to you this morning where we engage in a whole range of activities, where we invite people to meet with us, which gives us an opportunity to do a number of things. We can ask them their views on very specific subjects but we can also engage with them more generally. At all of those sessions where we have invited people to come and talk to us, we have had a range of other activities going on as well. We have a range of services that puts health back into individuals' hands and gives them choice. The first choice people should have is choice about their lifestyle. All the choices we offer about the way our services are run and delivered become secondary to empowering people in the first instance to make a choice about their lifestyle.

  Q376  Mrs Campbell: Can I ask you about two groups that are often quite difficult to consult, elderly people who are at home who find it difficult to come to consultation meetings, and ethnic minority groups where there might be a language barrier. Do you make any special efforts to reach out to those people?

  Mr Urwin: Every document that we produce inside its cover has a very short statement in all the major languages that we know to be used within Birmingham. We do not produce all of our documents in a number of languages, but effectively we have a message there which invites people to contact us, and we will arrange a document to be produced in an appropriate language or for a specific interpretation service. It is also important to say that four PCTs in Birmingham jointly fund a project called the Birmingham Integrated Language Translation Service, which means that if anybody presents for interaction with the Health Service—and this is at a point when somebody is diagnosed, or they suspect something is wrong—we will arrange for an interpreter to be available within that service so that we can make sure the message is appropriately communicated. In some regards we know that it is not appropriate to have a family member interpret, especially where we have communities of Bangladeshi Muslim women where the translation is done by a child or a male family member, so it is very important that we offer those services in a range of ways. I would be the first to say, though, that when we described to you this morning the public consultation events, these are events where the invitations went out with local free newspapers through the front door of every home within our patch, but we are the first to acknowledge that the people who become engaged with us are those who at that point in time want to become engaged with us. We have to do an awful lot more to engage prospectively with people who we do not engage with at present. Once people start to access the services, we are very, very good at breaking down the barriers for them, to make sure that there are interpreting services and culturally appropriate services. What we sometimes do not do is reach out to those communities in a prospective way, and that is something that will be a big challenge to us over the coming years. When you talked about those hard-to-reach groups and choice, I thought you were going to ask me something different, so I would quite like to answer the question I thought you might have been going to ask! I told you this morning that we provide learning disability services across the city, and we have 1,000 staff working in those areas. We are continually working on the Valuing People Programme that effectively allows them to make more choices about the circumstances they are in. Maybe they do not have a choice about where they live for example, but increasingly we are involving users and carers in the interviews of the staff we employ. Indeed, we do not employ staff now to work in residential care homes, for people with learning disability or nursing homes for learning disability, unless we have engaged the patients or the service users in that process. That enables them to have choices over their lives which may be constrained choices but nevertheless they are being valued as individuals and giving them more say in how their lives are managed and run.

  Q377  Mr Hopkins: Can I return to long-term care and choices in care because I am very dubious about the genuineness of this apparent choice. In my own local authority some seven years ago, the local authority chose to close a care home. I took up this issue with the local councils—against the then Labour council. Some of the local councillors were passionate about keeping this care home open and wanted it to stay as a local authority home and not become a private care home. The arguments the local authority came back with were that people wanted to stay in their own homes. Fine, care in the community and all that—and secondly they wanted if possible to move into sheltered housing. That again is fine, but we are talking about people for whom sheltered housing was not really possible and families who might be uncomfortable about the possibility of looking after an elderly and frail relative. I had a long discussion with the assistant director of social services in private and we went through all the arguments. In the end he said to me, "it is about money". I said: "Ah, so you are restricting choice because of money" and he said: "It is obvious, isn't it? Private care homes are non trade union; they work longer hours, they have shorter holidays and all this saves us money, whereas if we employ properly trained staff in our care homes with proper holidays and pay, with trade union membership, it costs more." I said: "Ah, that is what it is all about!" The officer was moving jobs and left about two weeks later, so you could say that he did not care any more and he was burning his boats locally. What he was doing was restricting choice in   care. That process has continued. Another restriction on care is that the Government refuses to provide free personal care for people in long-term care unless they are extreme cases, and they are provided then with medical care not personal care. Families are having to sell granny's home, lose what little equity there is in the family, to pay for long-term personal care. That means perhaps that these families try their best to keep granny at home as long as possible to avoid having to put them into a home, as they would see it, and losing the equity in the house. It is never said—it is unspoken—but these factors restrict choice. Do you not think that the Government, if it were really serious about choice, should provide local authority homes, if that is what people choose, or free personal care, so that there is no constraint on them living in the residence of their choice, and particularly involving the families? That is a long question, but that is the reality, certainly where I live.

  Mr Hay: I will take that in two halves, the first point being around closure of residential homes. That is an issue that has quite a history here in this city, as we have 29 of our own homes still, and we have spent 13 years in various guises dealing with what we are going to do about them. There is quite a salutary issue in relation to choice about that. It is a matter of public record that some of our 29 are in extremely bad condition and are very close to not meeting regulatory standards. I have taken it upon myself, as part of my duties, to see what it is like at the front end, and we went into one that is particularly poor. The quality of care was fine. The building reflects years of under-investment. What was quite interesting was that the overwhelming voice of the people in the service was, "if you had lived in what I lived in in the 1930s this does not really shake on it." The physical condition of the building was not an issue for them. In 20 years' time, physical conditions for the next generation will be a very different issue, and some of our choice is to keep up the standards and expectations. I thought it was an interesting question back because often we hear that one of the reasons for closures is the quality of the building, and one of the big voices back was that that was not an issue for them. There is of course—and it is an important issue particularly for current generations—a kind of psychological contract about local authorities and standards. There is an issue about trust in private sector care, and we have to be honest and identify that. There is something about the welfare contract, if you like, that is there particularly for older people and for a whole range of vulnerable people. It is an issue as much for the older parents of a young adult with learning disabilities who know they are facing death at some point and want to know who will pick up the care of this young adult as it is for older people. It is an important issue. In the closure debate, not only are there issues about the cost of running homes but there is also obviously the difference in benefit, which means that even without the cost differential it is £100 per week more being a local authority home than a private home, and if you factor in the costs of labour and all the rest of it you can see the difference. So if we are talking about running a rationed service, there are clearly issues of efficiency that affect that, and it has not always been transparent in relation to those issues. The position that we have reached is that we have to honour where we are with current people and build an alternative alongside that. We have moved from the debate that closure is the only option, which has not been deliverable because of that level of protest and concern, to building something up and then moving in to that arrangement. That is how we have handled the care home issue because it is still a live issue for us. It is a complex position to be in, but it is slightly different to the "all or nothing" bust closure.

  Mr Urwin: There seemed to be a presumption in the question that the alternative to local authority provision was for-profit provision, when actually we have a very viable mixed economy here where a number of housing associations, which have roots in their local communities and are in some instances faith-specific, expand their remit; and they offer a range of services where they also offer care homes and staff recruitment. I would not want us to feel that the only alternative to local authority provision is provision by the for-profit sector. There are a number of other statutory not-for-profit providers in this market and we have a very diverse mixed economy in operation.

  Q378  Mr Hopkins: People are fearful of losing that little bit of equity. For working-class families, granny and granddad bought their little terraced house after years of struggle. It is the only bit of equity in the family, and now that is threatened by looking after granny because the government will not provide free long-term care. It is free in Scotland but not in England.

  Mr Hay: Again, that is a policy choice, and we work within policy choices. Those with equity of course increasingly now are extremely well advised and we also find that those for whom that policy has been devised, ie, those with great resources, tend to have taken tax advantages some years ago and that money is untouchable, so it is building in an equity, and it is the whole issue of choice and equity that comes back consistently around that. Equally, it has created a degree of reticence on the part of older people, particularly where money is such an issue as you have referred to, about coming forward at an early stage for preventative type services. There is a fear element that is not always helpful, and it is how you can get over some of those issues and create more care at home. That is partly what is driving the issue about people wanting to stay at home for longer. It also comes down to the choice society makes about where to put the resources. At the moment the cost of care in the community, particularly for older people, is borne by the individuals and the families.

  Q379  Mr Prentice: Chris, you told us earlier today that fortunately there are open lists in South Birmingham, or open practice lists. On the key question of patient choice in relation to the GP, what does that mean in practice? How much choice does the patient have?

  Ms Fearns: Until the new GP contract came in last April, people could go to the door of a GP practice and for no very good reason be turned away on the grounds that that practice could not take anybody else on its list that day, but the next day it might decide differently on the basis of a number of issues. I would like to think that that was not happening wholesale, but there were elements of that. The new contract states that you cannot do that any more. The rules have changed and you have to categorically declare publicly that you are either open or closed, and if you are closed the PCT has to approve that closure, and it has to have approved it for very good reasons, which are detailed in the contract guidance. At the moment we have a small number of practices that are without doubt under pressure for a variety of reasons and will no doubt be coming forward at some point to discuss closure with us, possibly on a temporary basis. We will look at those cases individually. It the main, all are open at the moment, so if a patient applies to a practice and that practice turns them down, they are within their right to come to us and complain, and we will have to follow that up, and we will follow that up immediately on the grounds that that is not legitimate, without good reason. The doctor has to give good reason, and that guidance is detailed in the contract.


 
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