Commissioning: further issues - Health Committee Contents


Written evidence from Homeless Link (CFI 16)

Homeless Link, the national membership organisation for agencies working with people who are homeless, is pleased to contribute to the Health Committee's follow-up inquiry. Our particular interest is the way that Commissioning of health services impact on homeless people and the agencies which work with them.

We welcome the Committee's further review of what we see as critical aspects of the proposals to reform commissioning processes and structures. The health needs of homeless people are known to be among the most severe and most costly in our communities. Without action to ensure these needs are addressed in these new commissioning processes, there is a significant risk that the health reforms will overlook vulnerable groups and will fail in its aim to improve "the health of the poorest fastest."

We have focussed our submission below on the points raised in the Commissioning report of most concern and relevant to the client group we support.

SUMMARY OF KEY RECOMMENDATIONS

—  If homeless people are to have the services they need then they must be more visible in the new commissioning system; this means a standard flag in GP systems and a requirement for JSNAs to record the needs of groups with significant levels of health inequalities such as homeless people.

—  Mechanisms which will incentivise joint working need to include a fully integrated outcomes framework to ensure that services join up to meet the needs of homeless people. This should be underpinned by the recognition of the wider services which contribute to health outcomes in addition to those which are clinically driven.

—  In order that homeless people are not left behind there should be a statutory duty for Health and Wellbeing Boards and GP consortia to address the needs of homeless people within their commissioning and planning structures.

—  There needs to be a clear point in the commissioning process where wider agencies than those involved in Health and Wellbeing boards or consortia can provide input into decisions or challenge those which have not taken into account specific patient groups.

1.  CONTEXT FOR OUR SUBMISSION

1.1  The health of homeless people is significantly worse than the general population. High levels of complex need contribute to and are caused by a person's homelessness resulting in high levels of working age mortality, a higher level of long term conditions and greater likelihood that people will have more than one health need.

—  Eight in 10 homeless people have one or more physical health need.

—  Seven in 10 of homeless people have one or more mental health need.

—  Over half use drugs, and one in five drink alcohol problematically.

—  Nearly half of those with a mental health problem self medicate with drugs or alcohol.[49]

1.2  Not only is their poor health significant but the cost to the NHS of homeless people is much higher. A report by the Department of Health last year found that:

—  The total cost of hospital usage is conservatively estimated to be £85 million, four times greater than an equivalent number of non-homeless hospital users.

—  Inpatient costs are eight times higher than comparison population (aged 16-64).

—   Homeless people attend A&E five times as frequently as the non-homeless, this would imply a total of around 53,000 attendances annually by homeless people, costing around £5 million per annum.[50]

1.3  The reason for this enduring ill health is the complexity of individuals and their circumstances. Homeless people often have a range of conditions which services are not equipped to respond to, for example mental health and substance use problems combined with enduring physical health issues. Their ill health is also often caused or made worse by factors outside of health, for example poor housing, and, correspondingly, their ill health often makes their other circumstances worse.

1.4  Homeless people have spent decades being understood only in terms of their housing needs, while their significant health problems are a key and often defining factor in the homelessness. Over the past few years we have significant progress, with improved access into mainstream provision and the development of specialist services in some areas to meet the needs of the most disadvantaged. However, we are concerned that amid the transition to new systems in the NHS, rather than building on what we have learnt from these services they will be lost. We are already seeing evidence of this as spending decisions are being made. While the health reforms do represent an opportunity to get it right, there is a significant risk that these reforms will overlook vulnerable groups and fail to address the health of homeless people.

We would like to make comments on three of the specific points outlined in the Committee's inquiry:

2.  The Committee's intention to review the arrangements proposed for integrating the full range of clinical expertise into the commissioning process [paragraph 91]

2.1  We are pleased that the Committee identifies the need for GPs, in their new role as commissioners, should draw on a wide pool of practitioners in order to make informed decisions which bring the most benefit to patients. This is of heightened concern for people who are homeless, who are often not visible to mainstream services making it hard for some health professionals to have an understanding of their health needs and how to adequately meet them.

2.2  Rightly, organisations like the NHS Confederation have raised concerns about the accountability for commissioning services for people not registered with GPs. Although homeless people who are engaged with homelessness services are often encouraged to register with GPs by services, this does not mean that they are a visible population within the GP population. For example, while many care records systems may have the function to record an individual's housing status there is not a consistent marker in the system. There is little evidence that this information is being audited or aggregated by services to give them a picture of need. Among the GPs we have spoken to who are experts at working with homeless people they believe that this activity is undertaken variably and as such homeless people are unlikely to be flagged in electronic systems.

2.3  They are also less likely to be visible in the practice. Data gathered by St Mungo's and Homeless Link shows that while homeless people are likely to be registered with a GP they do not always maintain contact with their GP particularly if they have more serious health needs. Instead Accident and Emergency is often used to access secondary healthcare. This can mean that they are not a visible presence in their GP practice and may mean that healthcare needs are not always captured on their records:

In St Mungo's 2010 snapshot survey key workers were asked to estimate where their clients most often access health care from. A third stated that their clients most regularly access health care through accident and emergency. This was despite 95% being registered with a GP.

Homeless Link's national Health Audit data found that:

—  85% were registered with a GP and 82% had visited their GP in the previous 6 month period

—  However, despite this, 41% had been to A&E and 31% had been admitted to hospital at least once in the previous six months.

—  There was also evidence of attitudinal and access barriers at a GP level. 9% had been refused access, usually due to behaviour or having no fixed abode status.[51]

2.4  It would seem from this evidence that even where clients are registered, this still results in high access of acute services. While this is due in some cases to the severity of health need among this population, it also indicates that some GP practices and other services are not managing homeless people's health at a primary care level. Evidence that more complex and serious conditions among homeless people are not being supported through their GP also comes from soon to be published joint research between Marie Curie and St Mungo's looking at homeless people dying with advanced liver failure. One of the key findings of the report was the limited involvement of GPs despite clients requiring palliative support.

2.5  Homeless people, for a range of reasons may lack visibility among GPs for the full range of health needs. Similarly, due to the way information about individuals is recorded, homeless people are often not seen as a group for which action could be targeted.

2.6  This lack of visibility and the poor use of primary care services despite high levels of ongoing health needs indicates that existing commissioning processes do not take account of homeless people's needs and that the services available to them are not the right ones. If the visibility of vulnerable groups was made a priority in the new commissioning system this could play an important role in securing the right services for homeless people.

2.7  We suggest to the Committee that if homeless people are to have the services they need then they must be more visible in the new commissioning system; this means a standard flag in GP systems and a requirement for JSNAs to record the needs of groups with significant levels of health inequalities such as homeless people.

2.8  Commissioners must also draw on the expertise of local providers and specialist health professionals who have a more detailed understanding of the needs of complex groups. In many areas, PCTs have developed specialist commissioning teams for vulnerable groups such as homeless people, which has led to the provision of more responsive and targeted services. This expertise must be safeguarded in the new structures.

2.9  GP commissioners must also make clear channels by which housing, social care and voluntary sector providers can input into decisions and service design. Good health should not be seen as an outcome which can be achieved solely through clinically driven solutions: solutions which take into account and work holistically around wider social care, housing and welfare needs are more likely to be sustained and achieve better outcomes. Voluntary sector providers which work with the groups GP commissioners often perceive as "hard to reach" are well placed to provide this expertise. We would urge the NHS commissioning board to place a greater requirement on Consortia to systematically seek and incorporate this into service design.

3.  The Committee's intention to review the effectiveness of the structures proposed in the Bill which are designed to safeguard co-operative arrangements which already exist and promote the development of new ones [paragraph 107]

3.1  The Committee has rightly attached significance to services which work across health and social care boundaries or are otherwise intimately linked. As above, we believe health outcomes are rarely achieved solely through clinically driven health services in isolation, particularly for more complex client groups.

3.2  It is important that the mechanisms used to ensure integration across services and sectors are judged in terms of their ability to meet the needs of those with the most complex conditions and multiple needs. One of the biggest failures in the current system is the disjoint between services which result in homeless people falling through the net and stuck in a cycle of deteriorating health and worsening life circumstances.

3.3  There are many examples of where the failure of services to collaborate currently contributes to the poor health of homeless people, for example:

—  Siloed approaches to people with multiple needs, resulting in services "passing the buck" and requiring individuals to follow, for example, substance use pathways before they can access mental health support regardless of whether this is the right approach for individuals.

—  Gaps between Supporting People services and social care: there is limited access to personal care and support through social services which can undermine vulnerable people's ability to recover from health conditions.

—  Poor and inappropriate housing is a cause of physical and mental health problems; however there are limited health interventions in housing environments or initiatives to tackle how housing contributes to ill health beyond current environmental health measures.

3.4 To achieve better joined-up working in health for the benefit of homeless people it is important that the accountability and foundations of shared and integrated services are built on an understanding of reducing inequalities and tackling multiple conditions. This needs to be underpinned in the new outcomes framework. Health outcomes must be recognised as a shared responsibility across services to enable health and social care commissioners to release resources to flexibly meet local needs in partnership.

3.5 The JSNA presents a key opportunity to identify health inequalities and multiple conditions, and look at how local services can best join up to meet them. However, this needs to be articulated as a specific duty for local authorities as they co-ordinate the JSNA. There needs to be a clear process for review and redress for communities should they feel the JSNA fails in achieving this aim. We ask the Committee to seek greater clarity on how local authorities will facilitate this process.

3.6  In order that consortia and health and wellbeing boards can drive forward more integrated working, there need to be clearer mechanisms for involving the wide range of agencies who meet health outcomes in shaping services in each locality. Providing clear channels for local providers to access to Health and Wellbeing Boards will help identify shared outcomes, and develop opportunities for pooled budgets and joint commissioning.

3.7  Given the important of housing related support to achieving health outcomes for each locality, we believe improved integrated working would also be achieved by including a local director of housing or other delegated authority from housing, in membership of health and wellbeing boards as a minimum requirement.

4.  The Committee's intention to review the arrangements for local accountability proposed in the Bill [paragraph 118]

4.1  We strongly believe there needs to be clearer mechanisms to hold all commissioning decisions to account, not just those at a consortia level.

4.2  There has been great emphasis on decisions been driven by the local partnerships between consortia and health and wellbeing boards, which will be underpinned by the JSNA and other evidence of local need. However, what the current proposals lack, are clear channels for the public and local stakeholders to challenge not only the decisions been taken in response to this evidence, but the needs assessment process itself if they feel some groups have been excluded from this.

4.3  This presents a real risk for "unpopular", hard to work with and expensive groups such as homeless people. If they are protected in the commissioning system by accurate assessment and recording of their needs, it is to be hoped that the services they need will follow. However, if this does not take place there is a strong risk that homeless people will be even further left out in the cold literally as well as metaphorically in many cases. At present there is inadequate detail about how both patients and groups which support them can challenge service design if they feel this is the case, outside of the proposed HealthWatch. As it stands, we do not feel HealthWatch has enough authority within the commissioning process to provide a means to challenge service design and delivery.

4.4  The services which homeless people need are unlikely to be profitable and highly likely to be more expensive than mainstream alternatives. Sophisticated commissioners will need to understand the long term costs and benefits of interventions but this focus may be lost if there is an over emphasis on shorter terms gains on investment.

4.5  Where homeless people do access mainstream support there is a danger that they will be excluded from service provision or written off because of the high cost of working with them. As we have seen in some parts of the last Government's back to work programmes, those who are hardest and most expensive to work with are "parked" by providers while those for whom it is easier to achieve outcomes with are "creamed". In a payments by results model there is a danger that this perverse incentive will transfer to the NHS.

4.6  To an extent there is already anecdotal evidence that this happens in the NHS. The specialist homeless GPs we work with and service providers say that some GPs will not register homeless people or people with no fixed abode (NFA). How the NHS, GP Consortias and providers can be held to account to provide an adequate service for all under the new system is an important question.

4.7  We would like there to be clear opportunities in the commissioning process where agencies not invited to participate in Health and Wellbeing boards or consortia can provide input into decisions or challenge those which have failed to take into account specific patient groups.

4.8  We believe that homeless people and other vulnerable groups need specific protection within the system to ensure their needs are not missed, in particular those who have been or are sleeping rough or at risk of sleeping rough. We would like to see a statutory duty for Health and Wellbeing Boards and GP Consortia to address the needs of homeless people within their commissioning and planning structures.

Homeless Link is the national umbrella organisation for frontline homelessness charities in England. Currently we have more than 470 member organisations. Our members include hostels, day centres, outreach and resettlement agencies, housing advice centres, health projects, drug and alcohol services and faith run voluntary services. As the collaborative hub for information and debate on homelessness, we seek to improve services for homeless people and to advocate for policy change.

Through this work, we aim to end homelessness in England. www.homeless.org.uk

We would like to thank Hazel Cheeseman, Policy and Public Affairs Manager at St Mungos, for her input to this submission.

February 2011


49   Homeless Link's Health Needs Audit, 2010. Data based on over 700 homeless people www.homeless.org.uk Back

50   Healthcare for Single Homeless People, Office of Chief Analyst; Department of Health, 2010 Back

51   Homeless Link's Health Needs Audit, 2010 Back


 
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