Commissioning - Health Committee Contents


Written evidence from the Specialised Healthcare Alliance (COM 07)

  1.  The Specialised Healthcare Alliance (SHCA) is a coalition of 54 patient organisations supported by eight corporate members, which campaigns on behalf of people with rare and complex medical conditions for whom key services cannot be sensibly planned, procured and delivered at a local level. It is chaired by Baroness Pitkeathley.

  2.  The Alliance submitted written and oral evidence to the Health Select Committee's inquiry into commissioning before the General Election in May 2010. Our written evidence included a brief history of developments in specialised commissioning leading up to and following the Carter Report of 2006. This submission concentrates on the continuing weaknesses we identified and whether the coalition government's White Paper addresses them effectively in the context of some of the questions posed by the new Committee.

EXECUTIVE SUMMARY

  3.  The White Paper holds out the prospect of addressing the major weaknesses in regional specialised commissioning identified in the Health Select Committee's last report. Crucial detail, however, remains to be elaborated.

  4.  The scope of the NHS Commissioning Board's remit for specialised services needs to be clearly defined. In the Alliance's view, the only credible basis for doing so is the current edition of the Specialised Services National Definitions Set. This should be in its entirety, though subject to regular revision.

  5.  Similarly, the Board's regional structure needs to be clarified and sufficiently extensive to sustain effective engagement with the NHS at local level, eg to ensure that referrals management is consistent with more timely diagnosis of rare and complex conditions. The Alliance recommends a minimum of eight offices. This would also make it easier to retain the best of the important expertise in the current Specialised Commissioning Groups (SCGs).

  6.  Urgent priority should be attached to costing patient pathways covered by the National Definitions Set to inform the budget required by the Board for specialised commissioning purposes from April 2012. A buffer fund may be required to accommodate likely inaccuracies in the sums retained by the Board or devolved to GP commissioning consortia, especially in the first years of the new arrangements.

  7.  In the meantime, PCTs are likely to become increasingly distracted by the move towards GP commissioning consortia. The NHS Commissioning Board should therefore assume early oversight of specialised services from April 2011, initially working through the existing SCGs.

  8.  The accountability of the Board for commissioning specialised services needs to be clearly defined with recourse for individuals and groups who feel they have been poorly served. These patients must also be enabled to play a role in the new Healthwatch arrangements.

CURRENT POSITION

  9.  Historically, specialised commissioning has often been overlooked in the initial development of policy despite accounting for an estimated 10% of NHS expenditure, affecting large numbers of highly vulnerable people. The attention given to it by the Health Select Committee and in the White Paper is therefore most welcome.

  10.  Our previous evidence expressed concern about stalled progress in implementing the fundamentally sound Carter reforms of specialised commissioning, stemming from the reluctance of Primary Care Trusts to pool sovereignty and resources. We suggested that this reluctance might grow as PCTs sought to protect local services in the downturn, to the detriment of clinically and cost effective specialised care. We also highlighted that as a pooled responsibility between PCTs, specialised commissioning sat in a limbo, where it was not properly regulated or performance managed.

  11.  In order to address these weaknesses, we suggested that regional Specialised Commissioning Groups should be re-located within SHAs and funded directly. We also proposed that nationally commissioned services should no longer be funded by top-slicing PCTs but directly, with performance management conducted by the DH. These suggestions found support from the previous Health Select Committee, while observing that there was some risk that they could lead to a lack of coordination and disruption in services more locally.

  12.  In its response to the last report on commissioning, the coalition government broadly accepted the deficiencies in current arrangements, pointing out that under the White Paper, all national and regional specialised services encompassed by the National Definitions Set would be the responsibility of the NHS Commissioning Board. The response expressed the view that this should "ensure that patients with rare conditions can be sure of high-quality and cost effective treatment and are treated equitably with people who have more common conditions. It will also help ensure more effective implementation of Sir David Carter's 2007 (sic) review."

  13.  At the national level, important changes have been introduced since the General Election, with a single Advisory Group on National Specialised Services providing advice to the Secretary of State on which services, products and technologies—usually for patient populations below 500—should be commissioned nationally. This advice will be developed on the basis of an ethical decision-making framework which, in the Alliance's view, could act as the starting point for a more consistent, value-based approach to funding decisions in the wider NHS.

  14.  At the regional level, the current PCT-based arrangements remain in place with a significant risk of deterioration during the transition to the structures outlined in the White Paper.

THE WHITE PAPER AND SPECIALISED SERVICES

  15.  The Specialised Healthcare Alliance agrees with the government that the White Paper's proposal to place specialised commissioning with the NHS Commissioning Board has the potential to address the shortcomings identified in the Health Select Committee's last report. Much important detail, however, remains to be agreed. In particular, early clarification is required in the following areas:

    (a) The number of regional offices and their role will be important in maintaining effective links between the NHS Commissioning Board and the wider NHS, especially if GP commissioning consortia are local in character. From a specialised commissioning perspective, we would see it as desirable to have no fewer than eight regional offices to reflect patient flows and the character and culture of different health economies. These offices should facilitate liaison to ensure the engagement and input of GP consortia and effective provision of those primary and community care services best commissioned at local level for people with specialised conditions;

    (b) While it makes sense for the NHS Commissioning Board to assume responsibility for assessing commissioning from the CQC where GP consortia are concerned, a third party needs to assess the Board's performance for those services which it commissions. The DH would seem best suited to fulfil this role or, alternatively, it could remain with the CQC for those services commissioned by the Board;

    (c) As PCTs focus on supporting the establishment of GP consortia, the danger is that their already inadequate commitment to specialised commissioning will wane with potentially damaging results for patients. We would therefore advocate an early transfer of oversight to the NHS Commissioning Board, initially working through the existing regional Specialised Commissioning Groups and their constituent PCTs;

    (d) During this period a high priority should also be attached to costing the services covered by the National Definitions Set to enable accurate budgets to be set in 2012-13. The survey conducted by the SHCA in late 2009 for the Committee's last inquiry found that the extent to which SCGs were commissioning the National Definitions Set was highly variable and in no case complete. The SCGs' current levels of expenditure do not therefore represent the aggregate funds the NHS Commissioning Board will require for specialised commissioning purposes.

  These points are relevant to several of the key issues raised by the Committee. Others are covered below.

CLINICAL ENGAGEMENT IN COMMISSIONING

  16.  Clinical engagement in specialised commissioning is generally above average, with clinicians often appreciating the greater degree of knowledge which specialised commissioners possess. This situation should be strengthened as a result of the White Paper with the NHS Commissioning Board also being well placed to address unwarranted variations in clinical practice, providing scope for innovation is not squeezed out in the process.

  17.  The greater problem arguably arises in relation to GPs and referral. Late diagnosis is a major problem with rare conditions and has important ramifications for clinical outcomes. In a recent study, the King's Fund observed that GP commissioners are likely to turn to referral management when they take responsibility for the bulk of the NHS commissioning budget. It will be important for the NHS Commissioning Board to ensure that referral management adopts an even-handed approach between over-, under- and mis-directed referral to protect and promote the interests of people needing speedy specialist assessment and care.

  18.  More generally, a range of approaches will be required to ensure the engagement of GPs and their consortia with specialised commissioning. In addition to the role of the regional offices in facilitating liaison (see above), consideration should be given to an extended range of clinical networks in key therapeutic areas, which might also engage local authorities where public health is a major upstream influence on downstream levels of disease. It is important to ensure that those with rare and complex conditions can access generalist services at the local level which meet their needs.

HOW OPEN WILL THE SYSTEM BE TO NEW ENTRANTS?

  19.  The White Paper gives Monitor the role of promoting competition and guarding against purchasers acting anti-competitively. A key tenet of the Carter Report on specialised commissioning is that specialised commissioners should be able to designate providers of specific specialised services using a robust, transparent process.

  20.  The Alliance supports the Carter Report's view that designation of specialised providers helps to secure an appropriate concentration of clinical expertise and activity to safeguard patient access to high-quality, cost-effective services located to maximise geographical convenience. It is important that Monitor's terms of reference recognise the need for some curtailment of free competition in this area.

ACCOUNTABILITY FOR COMMISSIONING DECISIONS

  21.  The proposed remit of HealthWatch is couched in almost entirely local terms. Specialist providers will usually be delivering services to patients from outside the local area and sometimes right across the country. It is important that HealthWatch makes provision to capture the views of such users to help inform specialised commissioning as well. HealthWatch England may be the most appropriate vehicle for doing so.

  22.  As touched on previously, the Specialised Healthcare Alliance also has concerns about the accountability of the NHS Commissioning Board for its commissioning performance (who will guard the guardians?). This needs to be to the Department and, through the Secretary of State, to Parliament.

HOW WILL THE NEW ARRANGEMENTS STRENGTHEN COMMISSIONERS AGAINST PROVIDER INTERESTS?

  23.  The establishment of a dedicated NHS Commissioning Board should itself help to re-balance the relationship between purchasing and provision, which is vital to the delivery of high-quality care and best value. This needs to include the status of commissioning, which has long trailed that of hospital management. The proposals for specialised commissioning, which concentrate resource and expertise through the Board, should be especially effective in delivering these results.

  24.  Similarly, the new arrangements should improve the position of people with rare and complex conditions who have historically been vulnerable to locally led commissioning. A heavy responsibility will however reside with the NHS Commissioning Board to protect the interests of everyone covered by the National Definitions Set and some form of recourse will be necessary for those who may be let down.

HOW WILL THE SYSTEM FACILITATE SERVICE RECONFIGURATION?

  25.  Specialised services by definition cater for larger populations crossing local and regional boundaries, sometimes up to national level. The configuration of services is important in ensuring sufficient patient volumes to support clinical standards and safety on the one hand, while offering the best possible access on the other.

  26.  Current overview and scrutiny arrangements mean that proposals to re-configure national services need to be referred to local committees right across England, generating considerable cost and delay. The Alliance sees merit in the NHS Commissioning Board being able to consult on such proposals with the Secretary of State acting as final arbiter.

October 2010




 
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