“Commissioning social care”
The next item is the committee’s continuing consideration of the Audit Scotland section 23 report entitled “Commissioning social care”, with evidence from a panel of Scottish Government witnesses. I welcome to the meeting Derek Feeley, who is director general for health and social care and chief executive of the national health service in Scotland; Geoff Huggins, who is head of the reshaping care and mental health division; and Brian Slater, who is policy manager in integration and service development. I thank you for attending.
Thank you for the opportunity, convener, but the letter that we sent to the committee in advance of the meeting says more or less what we would say in an opening statement. We are happy to proceed to questions.
I appreciate that.
That is a big question to begin with. First, I agree with Robert Black’s assessment of the issue’s importance. How we will deal with it is one of the nation’s biggest challenges.
There have been previous initiatives with the same or similar purposes—you mentioned joint futures, which goes back more than 10 years. We have a commitment again from the Government to move forward. Why will it be different this time?
A number of factors in the new arrangements will help us to accelerate the integration agenda. We are helped by the fact that there is a broad consensus on the need to do something in this territory. There is political consensus in the manifestos that preceded the 2011 Scottish Parliament elections, but there is also a consensus among the broad range of stakeholders that enough is enough and that we need to move the agenda forward.
We pressed COSLA and representatives from local councils quite hard on why so few of our councils have managed to produce a commissioning strategy. I want to be careful about paraphrasing what they said, but they implied that local authorities had always found it extremely difficult to create joint funding for joint projects. In other words, they found it quite difficult to get the NHS to commit resources to such projects.
It will be different because we will build on some of the early successes of the change fund, which has helped us to move the agenda forward. It is early days, but we are starting to see some promise from the change fund initiatives, which the health boards, their local authority partners and third sector organisations are coming together to agree. Emergency bed days for people aged 75 and over, which had been rising steadily over a number of years, first began to plateau and are now coming down.
The reablement projects are examples of partnership projects being funded by the change fund. Is the change fund funding institutional change in how we deliver services or is it simply an alternative pot of money to fund joint projects?
No. The change fund is about change; it is about redesign, shifting the balance of care and—to use the jargon—bending the spend.
We heard some evidence—it was one of Audit Scotland’s key recommendations—on the role of Social Care and Social Work Improvement Scotland in ensuring that real progress is made and that commissioning strategies are effective and consistent across the country. In your written evidence, you essentially accept the recommendation that the care inspectorate should have such a role. Do you envisage a new and expanded role for the care inspectorate to ensure that what we want—you said that you are optimistic about this—will be delivered? Is that a correct reading of your written evidence?
Geoff Huggins might want to add something, but I think that there are three things we want the care inspectorate to do. First, it should have in its scrutiny programme a commissioning theme. Secondly, it should work with local authorities and health boards to help them to deliver the duty in section 100 of the Public Services Reform (Scotland) Act 2010 to learn from the care inspectorate’s reports and to do more closing of the loop, if you like, from scrutiny through to action taken. Thirdly, it should work outwith the scrutiny process—there are already some encouraging signs in this regard—with partnerships to advise them on how they can improve their commissioning strategies and how they can evaluate their success. Those are the three things on which we would like to see the care inspectorate step up to the plate. The early signs are that it recognises the need to do that and that it wants to be involved.
I do not have much to add, other than that the care inspectorate identified that one of the priorities for 2012-13 will be to work, as part of the strategic work, with local government on better commissioning. The inspectorate has acknowledged that need because of the interaction between the strategic functions and the delivery of individual and local services. It is clearly on the agenda for 2012-13.
Will the care inspectorate have the capacity to do that? There has been significant debate over recent months about its capacity to deliver on things that it has already been doing, and it will have important new responsibilities.
In order for the cabinet secretary to be able to decide last summer on the size and structure of the care inspectorate, we went through a process to ensure that it would be capable of regulating the quality of individual care services and that it continued to deliver on the strategic functions. The budget has been maintained at a level that will enable it to do that, and will grow slightly over the next two years.
The care inspectorate will identify areas in which there should be improvements.
By that time, we will be in the territory of health and social care integration. It is intended that an accountable officer will be appointed jointly by the local authority and the health board. That person will be accountable directly to the chief executives of the local authority and the health board and will have responsibility for spending the integrated budget. They will also have responsibility for ensuring that there is joint and integrated commissioning. The consultation paper is pretty clear on what we require every health and social care partnership to do. Paragraph 5.19—which I say for the benefit of the Official Report staff is on page 32—says:
There will not be a single line of accountability for delivery of the services. When you say that there will be accountability to the chief executive of the health board and to the NHS, that means that one of the core problems that you have identified as being the reason for lack of progress will continue into the changed system.
No it will not, because the joint accountable officer is the person who is accountable.
That joint accountable officer is accountable to two people: the chief executive of the council, who is not accountable to ministers or Parliament, and the chief executive of the health board, who is. That means that the split in accountability will remain.
There will be the joint commissioning strategy, an integrated budget, responsibility through the joint accountable officer, a partnership agreement that sets out exactly what both parties have agreed to, and significantly enhanced transparency around all that. That represents a significant step forward.
We are supposed to have joint commissioning strategies now. Audit Scotland can identify only 11 from 32 authorities, and it is not clear who is accountable for that failure. It seems to me that you are describing a system in which that will continue to be the case. If there is no single line of accountability, who will be responsible for ensuring that we have commissioning strategies throughout Scotland, instead of in less than half the country?
If the consultation paper becomes law, as we hope it will, the newly established health and social care partnerships will be responsible for the joint commissioning strategy, the integrated budget, delivery on the national outcomes, greater transparency, joint and shared accountability and so on.
The Auditor General, who has been in post for a significant time, presented us with the section 23 report, “Commissioning social care”, which he described as
We are investing in prevention—the change fund is designed to do that and to get people to redesign care in a way that shifts the balance towards care at home. Outwith the change fund, we are in the health service and in local government doing a range of things more generally on prevention that are about the shift towards care at home and away from institutional care.
You have had 13 years to understand the issue. Why is the situation getting worse rather than better? Why is it going in the opposite direction from that which the health secretary and all the rest of us seek?
What might be happening is that a different kind of care is being delivered to the group of people concerned. At the same time as the shift to which you refer has happened—on the other side of the balance sheet, if you like—a big growth has occurred in telecare, which I know Mary Scanlon has strongly advocated. We now have 111,000 people with telecare support. We need to understand the position a bit better because it is possible that some home care has been replaced by telecare. I suggest that if that is so, it is good, because it helps people to live independently.
Do you think that the Auditor General got it wrong and that you are concentrating on preventive care rather than tending to provide intensive support after hospital admissions? Was he, perhaps, unaware of befriending services and telecare?
I am not saying that the Auditor General “got it wrong”. He reported a reduction in the amount of home care, which I do not dispute. All I am saying is that I would like to understand better exactly what is going on and what the relationships are between decisions that are made about where to place the bar for access to services.
Do befriending services and telecare account for the 41 per cent reduction in home care? Do you not think that that reduction is significant and that you should be concerned about it? Does it not go in the opposite direction from what was intended?
I am not saying that we should not be concerned about the reduction or that we should not look at exactly what is happening. All I am saying is that there are positive initiatives on the other side of the coin that may be contributing to that reduction.
They may be, but you do not know.
At this time of the year, we visit each health board and their local authority partners to talk about their work, particularly around mental health. This year, a key focus is on older people’s mental health, and one of the really interesting phenomena that we have seen in our visits so far—particularly to Shetland and Grampian—has been the range of additional and new third sector and community services that are appearing as a consequence of the change fund. Those services are to do with older people’s engagement, activity and participation.
I would like to think that people with mental health issues will one day be treated with the respect and dignity that they deserve. There is a long way to go on that.
I am sure that my colleagues will want to add to what I say. We need to be sure that we are comparing like with like.
Did not the Auditor General say that in his report?
I suspect that Fife is reflecting housing-related support, for example, which may not be reflected in the Angus numbers. I am not denying that there will still be a variation; I am simply saying that the variation might not be as extreme as Mary Scanlon might think. Some of the variation will be down to issues that we talked about earlier. Partnerships are at different places in their redesign programmes and in the shift in balance to the care-at-home sector. There may be a range of other issues.
I will let Geoff Huggins cover the eligibility question. On the question of the disparity, as Derek Feeley has said, we might not be counting like for like. Fife Council and Angus Council both submitted written evidence to the committee, and Fife Council tried to explain some of the disparity by saying that it was not counting like for like with Angus Council. I read that correspondence as saying that, if Fife Council were counting in the same way as Angus Council, the figure of 21 hours that is cited in the report would come down to nearer 10 hours, which is around the Scottish average.
The disparity is still significant.
It is still significant, but I think that Mary Scanlon said that the figure in Fife was nine times higher. The disparity is not quite at the level that she suggested. I am not saying that the report is wrong; I am just saying that the councils may not be counting like for like. Our analytical services people are looking at that to ensure that, when the information is collected in the following year, we will count like for like.
The truth is that, as things stand, we cannot adequately explain that discrepancy.
We can only say that it is probably not as great as the discrepancy that you suggested.
It is puzzling that, in the correspondence to which you have referred, Angus Council begins by saying,
There has clearly been a difference in interpretation of the data that has been requested. As I said, our analytical services people are looking at that and seeking to clarify it in the guidance that will be issued for the following year’s collection.
I have raised the subject of funding before. Paragraph 12 of the report refers to the fact that local authorities’ spending on social care has increased by 46 per cent in real terms over the past eight years. The final bullet point in paragraph 23, on page 14, states:
That, at least in part, is what our health and social care integration proposals are designed to assist with. Geoff Huggins may want to talk about the reshaping care for older people work that he has been involved in. Having done that work, the one thing that we can say with absolute certainty is that doing more of the same is not the answer. That is why the work that is being done through the change funds is so important. It is about the redesign of the services that will be necessary for that group of people in the future. The health and social care integration work is important because it provides a more effective way of planning and commissioning those services and delivering against an agreed set of outcomes, which I described earlier.
Again, you talk about using strategies to get us through the next few years. How long can that continue with a budget that, certainly for councils, is unlikely to increase and which might well decrease, as the report suggests? How will you cope with that?
It is hard to be certain about budgets beyond the period of the spending review. We will be able to make significant progress over the spending review period given the resources that we have. Given the additional resource that has gone into the change funds and the fact that the health budget has been protected, we will be able to make significant progress in the next three years. However, we recognise that that will need to prepare the ground for the medium and long term. We cannot use all the resources that we have in the next three years just to stand still; we must use them to rethink and redesign.
The member has outlined a genuine challenge. Historically, modelling on the subject has been done on the presumption that we would continue to offer care home places and care at home to the same proportion of people. However, that will clearly not be the case. We are beginning to see change in the structure of how care is delivered. As Derek Feeley said, there is also increasing participation among older people in providing care and support. Our work on the dementia strategy has indicated that a broad group of people are looking to offer support to one another as well as to receive support from statutory services. We are beginning to see a change in how systems work and in people’s expectations within the systems.
You have highlighted some positive aspects but, if we look back at what happened previously, we find that there was a 46 per cent real-terms increase in council social work budgets. A proportion of the budget cuts must inevitably fall on local councils, which will create strains at that level. Under the present thinking at least, the NHS budget has a degree of ring fencing and a bit of security. How will one partner cope when another partner is struggling? You are counting on the fact that you will be able to make all the changes through partnership working to deal with the situation that is coming, but if some of the partners do not have the money, how will you do that?
That will work out differently in different localities. One area that we are focusing on in our work on the in-patient estate is beds for old-age psychiatry. Across the country, the pattern of provision varies, with some areas having considerably more beds than others, and some having almost no beds. That reflects the degree to which some areas have already gone through a change process, reprovisioned and engaged in different relations with their local authority on services for older people with dementia, cognitive impairment or other illnesses. We will see more such change take place over the next two, three or four years as services across the piece are restructured. That is teaching us that looking simply at NHS mental health services, for example, does not work, because they are of a piece with local government services. There is probably not a national answer to your question, but there are probably 14 times 32 local answers. That takes us back to the discussion about integration and making provision work in a joined-up way locally.
I take you back to the change fund, which we first started to think about prior to the last spending review, when we first saw the projections and anticipated that the health budget from Westminster would be protected and that social budgets would be cut. In England, they tried to cater for the smaller budget in social care by moving money out of health and over to the social work budget in local government. That was just plugging the budget gap and we did not do that in Scotland. We introduced the change fund, which had to be used on a partnership basis and had to be used to redesign services. There was an insistence that we had to do it differently. It was not about just moving a budget from the NHS to local government; it was about ensuring that the plans were signed off jointly and would redesign how we do things in the future.
Good morning. I will continue on the same theme. The convener spoke about the strategic approach to commissioning and how services might look in the future. At our previous meeting, Councillor Douglas Yates told us that, in the next 20 years, there could be a £3.5 billion funding gap and that no amount of commissioning or fancy footwork would fix that.
We need to put commissioning in the broader context. Commissioning will help us to get to that better place, because it will help people to be clearer about what we want in terms of the needs of the population and the outcomes that we seek.
Sorry to interrupt you, but are you referring to the national learning framework?
The national learning framework is part of what the national steering group will try to develop. We are aware that that approach will require a set of capacities and skills that are probably not as well developed as they should be. People will have to understand how to do that work better.
How soon will we know whether we are being successful? We are acutely aware of what the Auditor General said. When will we get an indication of whether the current direction of travel is successful from the point of view of the public purse and affordability?
We are already starting to get an indication that we are making progress and moving in the right direction. I mentioned to the convener the reduction in the number of emergency admissions of over-75s, which had risen inexorably for 20 years. It is the first time that we have managed to reverse that trend.
You said that we will have to use the assets that an ageing population will bring. What does that mean?
It means doing some of the stuff that I mentioned earlier. We often overlook the fact that older people make up a large group of the people who provide care. Some of what we need to do is relatively simple stuff, such as giving people access to the information and support that they need so that they can do what they want to do, which is make a contribution.
In my last question, I will shift to the issue of children in residential care. From my experience in local government, I know that it can be hugely expensive to provide residential accommodation for children in care, and it can have unpredictable impacts on a local authority. There could be a sudden requirement for £1 million in a year out of a local authority’s budget. As part of the new approach to commissioning care generally, are we looking to try to manage that aspect better, in order to provide better outcomes for children in residential care, while smoothing its impact on local authority budgets year on year? A local authority can be taken by surprise by the cost of residential care for children. That is a huge challenge and I hope that the Scottish Government pays attention to assisting local authorities in managing that process better.
I fully recognise what Willie Coffey says; it is an important issue. Our focus on joint commissioning and integration has been on older people, but that is only our initial focus. We recognise that we need to look wider, and some of the partnerships are already making progress on that. Highland has its lead commissioning model, which gives the local authority responsibility for all children’s services. That is a novel approach that we will look at and learn lessons from. The issue is on our agenda and we recognise the need to make progress in that territory.
Around here, Willie Coffey and I are the assets that ageing brings. The same cannot be said for Humza Yousaf, who is next.
Thank you, convener, but I should say that Mark Griffin is even younger than I am so he has a future. I feel like an oldie when I sit next to him.
The money is largely for building capacity in third sector organisations and beyond. It is also for providing information about what is available. I suspect that you are right that there almost requires to be a cultural change if we are to make a broader success of self-directed support, not just direct payments, which are a relatively narrow bit of self-directed support.
Or is it simply passing the buck?
It is certainly not that. I am not sure whether you explored these issues with Ian Welsh when you took evidence from him, but I am reasonably confident that he, his chair and the board members of the alliance will not say that they feel that the buck has been passed to them. They will feel that they have been given some resources and autonomy to do the right thing for their members. They are closer to their members’ needs than we are, so it is absolutely the right thing to do—it is a win-win. We get better outcomes for the people who get supported self-management and give that group a stronger voice.
I do not know whether you saw the reports but, yesterday, various media channels were reporting carers’ reservations about self-directed support. Why are people feeling hindered? Why are they being so hesitant in getting involved in the personalisation agenda?
I suspect that it is because self-directed support is not for everyone. The opportunity could be offered much more widely—indeed, it should be—but there will always be a proportion of the population who will say, “Thank you very much. I’ve had a look at that and it’s not for me. I need a different kind of support.”
You said that resources were being provided to make self-directed support more available and that much of that was going towards capacity building in the third sector and providers. However, in your written evidence, you refer to £23 million of “direct funding to ... councils”. Will that money be ring fenced for this purpose?
The intention is that local authorities will use the money for the purposes that I have described.
Lying behind Humza Yousaf’s question was the concern that councils might see this change as a way of pulling back. What is the guarantee that that £23 million will not be used to plug a gap that councils perceive is there—and, in fact, might really be there—rather than to make the system work for those with anxieties about the shift to self-directed support?
Local authorities will not be able to deliver the change that they need to make in self-directed support if they take such actions.
In its evidence, the City of Edinburgh Council mentioned the provision of web-based information on care alternatives to enable people to make choices. Will that allay the concerns of those who are anxious about self-directed support or will it put many of them off because they will feel that it is not for them? My elderly parents are at the stage of beginning to access care. I have to be honest and say that, if I told them that they had to navigate the web in order to find out what was possible, they would not be able to do that.
I think that there are a number of people in that situation. Web-based solutions have a role to play, but we should not rely entirely on that medium as the sole way in which to get information to people.
You talked about signposting to services through ALISS. Is that a web-based system?
It is web based, but it operates in a different way, because people become members of that community. Members of the public and organisations have ALISS accounts and they undertake to share the information. At some point, information will be posted on ALISS, but you will also find folk in community groups sharing the information. They will say, “I got this from ALISS—you will want to know about it.” It will be on library notice boards and all over the place. All that ALISS does is to provide a community of interest. People who want to share the information come together on ALISS, but they share it in a range of different ways.
I have a question about something that I raised earlier. Given that more than £3 billion is spent on social care and that, according to the Auditor General’s report, it is not sustainable to continue in the current way, I ask you to respond to what we were told by two previous witnesses. The first is Annie Gunner Logan from the Coalition of Care and Support Providers in Scotland, who told us:
Where to start?
Mary Scanlon offered quotes from Ranald Mair and Annie Gunner Logan, but a different view has been expressed on the relative costs and value of council provision versus independent and private provision.
Annie Gunner Logan said that her evidence was based on a report by what was then the Scottish Commission for the Regulation of Care that, generally speaking, showed a disparity of about 20 points in quality of service. I think that the report was from 2011. According to the Coalition of Care and Support Providers in Scotland, the evidence exists.
Brian Slater may be about to attempt to answer it.
I will try. I simply wanted to say that that is why we are trying to improve commissioning skills.
I thank Brian Slater for that explanation of the difference between procurement and commissioning. We got into a bit of a fankle at the previous meeting about the difference between the two, but he has explained it quite well.
As you know, we have been working quite hard on that over the past 12 months. We had quite a busy year last year with the failure of Southern Cross, which required us to work closely with COSLA and individual local authorities to develop contingency plans to ensure that, were adverse events such as the closure of homes to take place, we would be able to make appropriate provision for the secure and safe care of older people.
I will go back to some of the things that the convener raised about how Mr Feeley views future services and particularly the accountable officer. In my time as a councillor, I brought up the point that access to services was extremely difficult for some individuals. When they went to a local elected member about that, it was just as difficult to go through the health board to get the individuals access to services.
The proposals are out for consultation just now, so my comments should be viewed in that context. However, the accountable officer arrangement should help considerably.
We must get that part right because that is where the process falls down at present. The $64,000 question is how we get that right—that is extremely important. We must ensure that there is a directly democratic process as well because the public just want the service to be provided.
That is what the ALISS search engine is—it is a web-based directory—but it is how people use ALISS that is different. Where are we with it? It is growing locally. It is not the kind of thing that we would impose on people; rather, we bring it to people’s attention and invite them to use it in a way that suits them. Although it is a web-based search engine—to non-experts like me, it is a bit like Google—it is what it enables members of ALISS to do that is important.
I am very supportive of ALISS, but we talked about what we were going to do with it two or three years ago. We had an open day involving the third sector and the local authority, and everybody came up with ideas about how we could promote ALISS and ensure that people knew about it. It is a good idea, but the only place that I have heard ALISS mentioned since that seminar is here. That is why I ask where we are with it at the moment.
It is spreading gradually. I could provide the committee with information about where it is being actively used if that would be of value to you.
That would be helpful.
You talked about working with the Long Term Conditions Alliance Scotland. Last week, it was multiple sclerosis week and I was involved in a members’ business debate on the subject. We are constantly told that there is a problem with fluctuating care throughout Scotland, especially for people with multiple sclerosis. One of the biggest issues is direct payments. The problem is not so much that people will not or cannot apply for direct payments; it is in getting access to direct payments. As you said, one of the benefits of carers is the fact that they are normally family members. However, a lot of local authorities cannot make direct payments to family members—I think that that is statutory. We need to look at that situation because it makes life difficult for families that are dealing with long-term conditions.
I confess that I do not know the legal position.
Scottish Government guidance allows such payments, but some local authorities are reluctant to provide them. It also depends on whether the family member lives with the person who receives the care.
I am happy to write to the committee to clarify the point—unless either of my colleagues knows about it—because I am not sure exactly what the supporting rules are.
My concern is that we are talking about the strategic level, but the issue affects people day to day. To get things right, we must think about the people who are behind all the situations that we deal with. It is important to have the answers at all levels.
If you would rather write to us, that would be helpful.
I am happy to do that.
The report that we are discussing refers to a watershed to which the committee has paid no attention yet—that is our fault—and to which Geoff Huggins referred obliquely. I do not think that anybody would be surprised that exhibit 1 says that
There are a number of reasons why that change is likely to happen. Care is becoming significantly more complex and is being provided in a broader range of ways. One of those ways, which we have discussed, is the use of technology—through the web, telehealth, telephone support or devices such as motion sensors. Greater individualisation of care is taking place. That suggests that, over time, we will have a larger number of smaller services rather than a smaller number of larger services. That is also the story behind self-directed support and direct payments. There are natural effects within that.
So Government policy has no preference for how care is delivered.
I do not believe that we have stated a preference.
I appreciate that.