Commissioning - Health Committee Contents


Written evidence from Neurological Commissioning Support (COM 120)

1.  INTRODUCTION

  1.1 Neurological Commissioning Support (NCS) is a unique consultancy organisation developed by three leading charities; the Multiple Sclerosis (MS) Society, Motor Neurone Disease (MND) Association, and Parkinson's UK. We work alongside all those planning for, and providing, health and social care services: commissioners from Primary Care, Social Services, and GP consortia, in order to improve the way that neurological services are commissioned. This is done through a service user focus on the key elements of commissioning and, in particular, the planning component.

  We liaise with service commissioners on a regular basis and have representation on many Primary Care Trust (PCT) and Local Authority commissioning groups through regional staff and members. Additionally, all of our three founder organisations support a comprehensive branch structure and have contact with thousands of people affected by neurological conditions, which provides a unique perspective on the experiences these people have of their local health and social care services.

2.  EXECUTIVE SUMMARY

  2.1 NCS believes that neurology should be part of specialised commissioning in the future, a view mirrored by the third sector neurology organisations that we represent.

  2.2  Patients and carers have not been given the consideration they deserve in this White paper. They play a huge role in delivering health and social care and need to have a central place in the new system.

  2.2.1  NCS feels that more detail is needed on how patients and carers will be included in GP consortia. Their place in commissioning is an essential part of the new system and should not be tokenistic. NCS would like to see patient and carer representation on the boards of both the GP consortia and the NHS Commissioning Board.

  2.3  Workforce planning is not addressed in the White Paper. As this was previously part of the Strategic Health Authority's role, we recommend that the NHS Commissioning Board takes over this responsibility.

  2.4  NCS believes that the Government should use the term "GP led" rather than "GP commissioning" to reflect the multi-disciplinary nature of general practice today. IT also feels that the whole multidisciplinary team (MDT) should be involved in GP-led commissioning including designated MDT and service user posts on the NHS Commissioning Board and "GP consortia".

  2.5  NCS feels there is a need to pilot "GP consortia commissioning". Given the significant reorganisation proposed, there is a need to build on and transfer existing capacity and knowledge from World Class Commissioning which demonstrated that knowledge and experience of commissioning was developing.

  2.6  Commissioning requires a wide range of skills and it is important that accountability is retained especially when services are decommissioned so that the implications of service loss and risk management in relation to this loss are fully understood.

3.  CLINICAL ENGAGEMENT IN COMMISSIONING

3.1 How will commissioners access the information and clinical expertise required to make high quality decisions about the shape of clinical services?

  3.1.1 GP-led commissioning could bring clinical expertise right to the forefront of commissioning and is to be welcomed. Traditionally, commissioners have focussed on programmes, whereas providers and clinicians' focus has been on systems, but these two developments now need to take place in an integrated way. This has implications for clinicians: for GP's who need to develop commissioning skills but also for hospital clinicians who will need to also have clinical engagement in commissioning for the whole population of patients for which they can make a specialised input and not solely the referred population. The value and skills of the multidisciplinary team in providing this clinical expertise should not be forgotten, and in particular the nursing professional which has been involved in commissioning in recent years. It is essential that this continues, with nurses involved both within GP consortia and on the NHS Commissioning Board.

  3.1.2 Service users have demonstrated their expertise in the development of commissioning strategies and shared decision-making for prioritisation of services and the contribution that these individuals can bring should not be underestimated.

  3.1.3 Clinical networks, care pathways and resources such as Map of Medicine can ensure high quality decisions are made by proving the relevant information is available whilst also keeping the workforce up to date on condition-management issues.

  3.1.4 NCS also feels strongly that clinical services should be equally relevant to the prevention of condition deterioration and the promotion of health; there needs to be greater focus for long term conditions' commissioning on the public health aspect of clinical services.

3.2 How will commissioners address issues of clinical practice variation?

  3.2.1 To prevent health inequality NCS feels there must be a national system in place to monitor and address clinical practice variation. This would be possible, for example, through using standards for general practice accreditation potentially through the Royal College of General Practitioners. Regular audit using a common audit tool would indicate if variations were resulting.

  3.2.2 Monitoring commissioning practice through tools like Neuronavigator, (the Year of Care tool developed by NCS for motor neurone disease, Parkinson's and multiple sclerosis), would also be possible once this tool is rolled out nationally. The process for creating this tool is easily transferrable, and could be replicated in similar tools for other conditions.

3.3 How will GPs engage with their colleagues within a consortium and how will consortia engage with the wider clinical community?

  3.3.1 NCS believes that the Government should use the term "GP led" rather than "GP commissioning" which reflects the multi-disciplinary nature of general practice. Commissioning requires an appropriate range of health and social care professionals and if these are not involved in the commissioning process then new models will fail. Engagement could be undertaken through local clinical networks if these are in place, and if not currently established, they should be encouraged to facilitate communication. It is also vital that the clinical skills of practitioners in secondary care are utilised and there must be ways in which this essential expertise is utilised. Mechanisms to facilitate this need to be developed.

  3.3.2 The third sector and service users have a key role to play in commissioning and engagement with the wider clinical community, and they have a unique perspective on understanding those services which are required. For example NCS has demonstrated in both Gloucestershire and Wandsworth the valuable insight into health and social care service delivery which people affected by neurological conditions have had. This has included contributing to changes that have delivered better value for money, more efficient, and effective services, and a higher quality of care provision. This same way of working can be easily replicated for the services needed by those living with other conditions; the expertise that those living with any given condition have about that same condition should be recognised and utilised accordingly.

3.4 How open will the new system be?

  3.4.1 The proposed reforms are radical. For this reason, NCS feels that there should be an appropriate piloting and phasing programme in place to move to GP consortia commissioning. It would be wise to develop the system in a range of pilot areas before full implementation is undertaken. It would also be advised to ensure that open lines of communication are established between all of the commissioning bodies across the country, particularly between health and social care. It is also highly necessary that strong networks between GP-led consortia be created to allow for the sharing of best practice, the coordination of care across wider areas, and a level of peer support and accountability.

3.5 Will care providers be free to offer new solutions which offer higher clinical quality, better patient experience or better value?

  3.5.1 It is imperative that the move to GP consortia is appropriately managed and moved forward through a pilot phase. NCS is concerned that the timeframe for this change alongside the need to make efficiency savings will not result in better care for service users as consortia may not be in a position to assess which solutions offer best care and value. There is a danger that the inexperience of new GP commissioners combined with a real drive to make efficiency savings could see essential services cut without full understanding of the implications that this will have further down the line of both quality of care and a later detrimental impact on finances. As an example, in one area NCS discovered that two patients had been refused non invasive positive pressure ventilation (NIPPV) because of the cost for this, totalling £12,000. Both patients were subsequently admitted into hospital in respiratory crisis and had to be ventilated which later resulted in a bill of almost £1 million pounds, both patients subsequently having lengthy stays in an intensive care unit.

  The expertise in current commissioning models should also not be lost and there should a way identified that will help to retain the skills of the current commissioners which will assist with this. The third sector could have an increased role in identifying best practice in market provision.

3.6 Will commissioners be free to access new commissioning expertise?

  3.6.1 It is obvious that the new GP consortia will not be able to develop commissioning expertise quickly. The Kings Fund has indicated that commissioners will need to utilise commissioning expertise from commissioning support organisations such as Neurological Commissioning Support. NCS feels that in the near future other third sector organisations could also take on the role of commissioning support for specific conditions. NCS believes that it, and organisations like it, will be able to assist in making the right commissioning decisions whilst helping to develop the expertise within GP consortia.

3.7 What arrangements will be made to encourage the Third Sector both as commissioners and providers?

3.7.1 NCS firmly believes that the third sector should work closely with commissioning consortia staff to explore options for future service improvement and in some cases could take over commissioning for specific areas, such as neurology. The third sector is able to provide the expertise required to develop quality services from a service user perspective and in this tight financial climate can often highlight what would be best value services for a particular client group. Additionally, smaller third sector organisations like NCS provide competition to larger profit-making commissioning support agencies.

4.  ACCOUNTABILITY FOR COMMISSIONING DECISIONS

4.1 How will patients make their voice heard or their choice effective?

  4.1.1  Consortia will need to ensure that full and adequate consultation is undertaken with service users and citizens when making commissioning decisions. The third sector and organisations like NCS can ensure this occurs in a transparent way.

  Methods of consultation will need to be wide ranging to meet the needs of a diverse population. Employing new technology and modern communications will be required to ensure full consultation across the entire demographic, including age and ethnicity. NCS has successfully used artistry, social networking such as Facebook and Twitter, local media, websites, flyering and posters in local community centres and leisure areas, in order to reach as diverse a population as possible. Graphic artistry and social networking specifically, targeted service users with communication difficulties and those of a younger age with good results.

  4.1.2  There will also need to be in place systems to ensure effective monitoring and managing of NHS performance to ensure that the views of patients are recorded and acted upon accordingly.

4.2. What will be the role of the NHS Commissioning Board?

  4.2.1 NCS believes that the role of the NHS Commissioning Board should be to:

    Adopt a coordinating role, sharing examples of best practice and coordinating evidence-based research so that all consortia can learn from its findings and act on these, rather than each commissioning on an individual consortia basis.

    Provide support and encouragement for consortia so that commissioners can feel confident about their new roles. NCS do not feel that the Board should adopt a "policing" model seeking out commissioning "failures" as this will not be constructive to development.

    Make full use of the current expertise and knowledge that PCT and SHA staff have about commissioning.

  4.2.2  A commitment has already been made to provide consortia with resources to fund management costs. Additionally, NCS feels that further resources should be provided to support commissioning education programmes which should help the new commissioners to understand such things as the commissioning cycle; financial management; constitutional and governance issues, and workforce planning.

  4.2.3  Workforce planning should also fall under the remit of the Board as should training and education, to ensure that there is a workforce fit for purpose to meet commissioning need. For example, in its' report: Halfway through: are we halfway there? (NCS 2010), Neurological Commissioning Support has discovered that there are insufficient numbers of health and social care staff with specialist training and understanding in neurology who are competent to manage the needs of the 8 million people living with a neurological condition in England (and 10 million in the UK). The lack of understanding of the needs of these people has led to excessive and costly length of stays in hospital or inappropriate emergency admission where preventative treatment would have been more cost effective as well as enhancing the individual's quality of life.

  4.2.4  NCS also believes the NHS Commissioning Board could take on a role to monitor and correct inequity of service provision. This would then enable a universal approach to assessment, benchmarking, and the monitoring and correction of any significant unequal service provision or patient outcomes.

4.3  What legal framework will be required to underpin commissioning consortia?

  4.3.1 Mechanisms must be in place to detail how the business of consortia will be conducted and how they will engage with, and be accountable to, both their local communities and the tax payer.

4.4. How will commissioning interface with the Public Health Service?

  4.4.1 There needs to be a greater focus on public health for long term conditions, with a recognition of neurology as an area of health which falls within this bracket, but should not be subsumed by it. There needs to be a system in place that will ensure the Public Health Service and the NHS work together seamlessly. People with long term conditions can remain independent for longer if adequate information and health promotion strategies are employed to keep them well, and many more expensive treatments and emergency admissions can be avoided if appropriate preventative treatments are provided in a timely fashion. Commissioning to date has not universally taken this into account and greater emphasis on this important issue needs to be undertaken.

4.5 How will commissioning interface with Health Watch?

  4.5.1 It is important that Health Watch works closely with existing patient participation groups (PPGS). NCS and its third sector partners would like to be further involved in developments with Health Watch as we feel many of our existing networks would be of benefit to this new and important entity.

4.6 Where will the "buck" stop when commissioners face hard choices?

  4.6.1 NCS has experienced the conflicts of interest that can ensue when difficult decisions need to be made about decommissioning services where there is a need to provide clinical care whilst achieving the best outcomes—both financially and for the patient. It is vital that national political accountability is not lost in the new system and thought must be given as to how consortia receive support to make hard choices about service provision. The Government must acknowledge its role in such changes.

  4.6.2  There are challenges relating to unbundling health spend and difficulties in understanding all of the costs associated with care; commissioners in the future need to estimate current costs and spend for services and any quality improvements made. Poor quality services are unfortunately both common and costly.

  4.6.3  There needs to be greater flexibility across the different payment systems and across agencies which could release money (from hospital admissions) in order to fund services. The overall health and social care must be seen as such, rather than individual agencies unnecessarily keeping hold of their "pot" of money to the detriment of health and social care in general, as may be the case at times.

5.  INTEGRATION OF HEALTH AND SOCIAL CARE

5.1 How will any new structures promote the integration of health and social care?

  5.1.1  The key to this will be reform of the social care system. The care needs of people living with a long-term neurological condition span health and social care, but these services are not, on the whole, integrated. Information is key to integrated working but commissioning knowledge about the totality of needs of service users is not known. For example record sharing (which could facilitate integration between social, primary and secondary care) is not commonplace. Issues such as bed blocking are often found with service users needing to stay in expensive hospital beds because of inadequate social care provision. In the same way, it is not uncommon for someone discharged from hospital to be readmitted shortly afterwards due to a lack of social care provision on discharge, leaving the patient vulnerable and with inadequate support. We are also concerned about the complexity of the funding system and care lottery that results in huge inequalities.

  5.1.2  NCS has developed a Year of Care tool (called Neuronavigator) for the health and social care of people with motor neurone disease, Parkinson's disease and multiple sclerosis which can help consortia to understand the totality of need for these conditions and promote integration of thoughts around commissioning.

  Tools such as this should be available to consortia to assist with integration, further supported by the development of integrated care pathways, with each care pathway reflecting the holistic needs of individuals.

5.2 What arrangements are proposed for health and social care budgets?

  5.2.1 Both health and social care are required to make significant cuts to their overall budget. NCS is concerned these cuts, such as in social care, are being made in a service that is already underfunded and this will leave many social care needs unmet. Failure to meet social care needs places greater pressure on health care and deprives the individual of core services.

  5.2.2 The principles of patient empowerment and personal budgets are to be welcomed but NCS feels that these budgets many not be suitable for everyone and the Government should await findings from the piloting of personal health budgets, and apply its learning, before rolling them out. NCS also feels that, whilst the principle of personal choice is entirely correct, there needs to be a readiness of clear and concise information on services, and on people's right to access these services, before this element of choice can be realistically given. The third sector could assist with advocacy and brokerage when personal budgets are used, as well as information provision, if requested.

5.3 What will be the role of local authorities in public health and commissioning decisions?

  5.3.1 The role of Local Authorities in public health and commissioning decisions will be focused on prevention. Insufficient work to date has been done on this important aspect of living with long-term neurological conditions and NCS would expect to see a greater emphasis on the delivery of public health initiatives and promotion in the new structures.

  5.3.2 NCS feels that it would seem sensible to align GP consortia with current Local Authority boundaries (this would, however, have to depend on the size of the individual GP consortium). Local authorities already have significant information about their populations, which they use to inform local public service provision and aligning the two could ensure better service provision.

5.4 How will the new arrangements strengthen commissioners against provider interests?

  5.4.1 The proposals set out in the White Paper increase the scope for competition within healthcare delivery. As yet this is largely untested in the UK health system and may introduce substantial elements of risk to the core operations of NHS funded health and social care. The Government should outline a system to provide effective checks so that there is a level playing field for providers and commissioners, thus preventing fragmentation of healthcare. The system must ensure guaranteed standards of safe, high quality and efficient healthcare for all service users, and carers, across England.

5.5 How will vulnerable groups of patients be provided for under this system?

  5.5.1 NCS feels that there are significant risks in the development of local systems which could exacerbate health inequalities. Strategies must be put into place to ensure this does not arise. Suggestions for addressing this include a sharing of best practice and specialist information by those consortia who have specific specialists amongst their number.

  5.5.2  An additional safeguard that NCS suggest is that there should be an identified accountable officer in each consortia for equity and equality issues, thus ensuring that they underpin all decisions made on service provision.

  5.5.3  It is important that the system provides for effective advocacy for people with severe and enduring mental health illness and other complex health problems.

  5.5.4  All opportunities must be taken to ensure that communication is effective and encourages people to speak up and let their views be known.

  5.5.5 Current good practice must be allowed to continue and where PCT commissioners are making progress, this must be encouraged to continue within the new arrangements. Current work and objectives within PCTs which have strong measurement systems and research behind them should be considered for continued action under the new consortia.

  5.5.6 The Government must be careful to ensure that there are no perverse incentives or disincentives for GP consortia or practitioners to work in particular areas or patient groups.

5.6 How will the proposed system facilitate service reconfiguration?

  5.6.1 Where difficult decision have to be made for example on decommissioning hospitals because of local opinion about services. NCS has experienced this in one of the PCT areas it worked with. Consortia will need support when making unpopular changes and the Government must acknowledge this and offer solutions to provide support.

6.  TRANSITIONAL ARRANGEMENTS

6.1 Will the new arrangements safeguard current examples of good practice?

  6.1.1 All current knowledge and expertise in commissioning should be noted and utilised. The skills required to commission are very different from clinical skills and will take time to acquire. NCS recommends that existing expertise is employed within the new consortia. The value of commissioning support agencies in particular areas of commissioning should also be highlighted by the Government.

6.2 Who will drive innovation during the transitional period?

  6.2.1  There are many models of good practice across the country and these should be highlighted. NHS Innovations holds information on a plethora of outstanding practice initiatives across the country, and as a resource should be called on to inform future plans. The third sector, where it has supported commissioning, has often done so in innovative and unique ways, and this should be noted. Continued partnerships of this nature will spur on innovation under the new systems coming into place.

  In this time of finding efficiency savings it is essential that innovation is not stifled, but given space to flourish even more widely. In times of newness and uncertainty, innovation can help to build and strengthen systems coming into place, However, NCS fears that this may not be the case, and steps should be taken to protect current, and encourage further, innovative working.

6.3 How will transitional costs (redundancy etc) be minimised?

  6.3.1  NCS feels that expertise should be retained wherever possible and there is a danger that a wealth of experience and knowledge will be lost from the health service during this reform. Arrangements should be put in place, where necessary, for the redeployment of staff to minimise the loss of jobs and expertise from the healthcare service. Systems need to be established and implemented to assist staff in moving from the acute sector to working in the community, for example.

7.  RESOURCE ALLOCATION

7.1 How will resources be allocated between commissioners?

  7.1.1 NCS believes that any resource allocation must be representative of need and demography. It should also seek to address health inequalities.

7.2 What arrangements are proposed for risk sharing between commissioners?

  7.2.1 Consortia will have to take part in risk-sharing arrangements but Government needs to ensure mechanisms are in place for its overall financial control in the new structures.

7.3 What arrangements will be made to safeguard patient care if a commissioner gets into difficulty?

  7.3.1 The Government must ensure that mechanisms are in set up and put into place to ensure services are sustainable. NCS believes that the Government also need to demonstrate how it will manage the risks associated with system reform, something which, as yet, does not seem to have had a great deal of though given to it.

8.  SPECIALIST SERVICES

8.1  What arrangements are in place for commissioning of specialist services?

  8.1.1 NCS has concern for neurology services in the move towards GP-led commissioning consortia and this is mirrored by the third sector. We therefore feel that neurology would be better considered under specialist services.

October 2010




 
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