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  • Vicky Foxcroft – 2015 Parliamentary Question to the Department of Health

    Vicky Foxcroft – 2015 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Vicky Foxcroft on 2015-10-20.

    To ask the Secretary of State for Health, pursuant to the Answer of 23 July 2015 to Question 7788, whom his Department has consulted on the matter of compensation packages for people affected by NHS contaminated blood.

    Jane Ellison

    The Department is considering wider reform of the ex-gratia financial assistance and other support for those affected with HIV and/or hepatitis C by infected NHS-supplied blood or blood products. We are doing this within the context of the spending review and in a way that is sustainable for the future.

    In order to help develop the shape and structure of any new scheme, we plan to consult publicly on scheme reform soon. The Department has alrady engaged with representative groups of infected/affected individuals. These individuals were nominated from the Contaminated Blood Campaign, Tainted Blood and The Haemophilia Society. The event was held in a neutral venue and had an independent facilitator. A report from this one off event will be made public soon. Discussions are ongoing with other interested parties.

    While we are working to establish a full and fair resolution, liability has not been established in the majority of cases, so it would not be appropriate to talk about payments in terms of compensation, particularly on the scale that some may envisage.

  • Karin Smyth – 2015 Parliamentary Question to the Department of Health

    Karin Smyth – 2015 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Karin Smyth on 2015-10-20.

    To ask the Secretary of State for Health, what information Health Education England holds on the number and proportion of doctors who completed their foundation training and are (a) not working in the NHS and (b) working abroad in the latest period for which figures are available.

    Ben Gummer

    Health Education England does not hold this information.

  • Sharon Hodgson – 2015 Parliamentary Question to the Department of Health

    Sharon Hodgson – 2015 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Sharon Hodgson on 2015-10-20.

    To ask the Secretary of State for Health, if he will place in the Library an explanation of the organisational structure, including current post-holders, of the senior management of NHS England.

    George Freeman

    An organogram and explanation of the roles of the chief executive and the seven national directors of NHS England is attached.

  • Nicholas Brown – 2015 Parliamentary Question to the Department of Health

    Nicholas Brown – 2015 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Nicholas Brown on 2015-10-20.

    To ask the Secretary of State for Health, what progress he has made in establishing a smaller number of specialist children’s heart units, as recommended by the Safe and sustainable review of children’s congenital heart services, published by the NHS in February 2011.

    Jane Ellison

    On 12 June 2013 my Rt. hon. Friend the Secretary of State announced in Parliament that the Safe and Sustainable review’s proposals for children’s congenital heart services could not go ahead in their current form. In July 2013, after discussions with key stakeholders, NHS England established a new congenital heart disease review, encompassing services for adults as well as children.

    The new review has now been completed and the board of NHS England has agreed its proposals. NHS England is now working on implementation of the proposals and commissioning services against the new requirements. This is being done in collaboration with provider trusts.

  • Steve McCabe – 2015 Parliamentary Question to the Department of Health

    Steve McCabe – 2015 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Steve McCabe on 2015-10-20.

    To ask the Secretary of State for Health, whether his Department has made an assessment of the desirability of including ulcerative colitis and Crohn’s disease on the long-term prescription list.

    George Freeman

    We have not made an assessment of the desirability of including ulcerative colitis and Crohn’s disease on the list of medical exemptions which provide exemption from prescription charges.

    Other exemption arrangements are in place, in England, based on age and income, to support those who cannot afford to pay for their prescriptions. Additionally, for those who need multiple prescriptions and do not qualify for exemption, Prescription Prepayment Certificates (PPC) can be purchased, which allow someone to claim as many prescriptions as needed. A 12 month PPC costs £104 and benefits anyone who needs 13 or more prescriptions a year.

  • Sarah Wollaston – 2015 Parliamentary Question to the Department of Health

    Sarah Wollaston – 2015 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Sarah Wollaston on 2015-10-20.

    To ask the Secretary of State for Health, how he plans for the Public Health Outcomes Framework to continue to give a comprehensive picture of children’s school readiness, when the Early Years Foundation Stage Profile becomes non-compulsory in September 2016; and if he will make a statement.

    Jane Ellison

    The consultation on updating the Public Health Outcomes Framework was published on 3 September and closed on 2 October. We are considering the responses and intend to publish our proposals early next year.

  • Glyn Davies – 2015 Parliamentary Question to the Department of Health

    Glyn Davies – 2015 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Glyn Davies on 2015-10-20.

    To ask the Secretary of State for Health, what steps his Department is taking to improve the quality of care provided for people with incontinence in the UK.

    Jane Ellison

    NHS England has advised that according to a survey conducted in 2008, there are over 14 million adults who have bladder control problems and 6.5 million with bowel control problems in the United Kingdom.

    The Department does not collect information on the number of people living with urinary and faecal incontinence specific to Northern Ireland, Scotland and Wales. This is a matter for devolved administrations.

    The Healthcare Quality and Improvement Partnership (2010) established that in order to achieve the best clinical outcomes, continence services have to be integrated across primary and secondary care and care home settings.

    They also concluded that ‘there is an urgent need for improved and equitable practice for all people with bladder and bowel problems’ through the development of commissioning frameworks, evidence-based training for health professionals and patient empowerment to increase their expectations of cure.

    Improving continence care provision through integrated services brings many benefits including:

    – a better quality of life and more independence through finding solutions appropriate to individual needs;

    – less reliance on pads and products by using alternative treatments;

    – a reduction in admissions to hospitals and care homes;

    – fewer complications, such as urinary tract infections, faecal impaction and skin breakdown; and

    – a reduction in costs.

    NHS England’s Excellence in Continence Care guidance provides a framework that enables commissioners to work in collaboration with providers and others to make a step change to address shortfalls so that safe, dignified, efficient and effective continence care is consistently provided.

    This guidance is aimed at commissioners, providers, health and social care staff and as information for the public and has been produced in partnership with patient and public advocates, clinicians and partners from the third sector. The roles of everyone involved in the care of people with continence needs are made clear in the guidance and publication via a launch is planned for ‘Self Care Week’ beginning 16 November. The launch will both raise awareness and promote understanding.

    In addition the National Institute for Health and Care Excellence has produced a range of guidance for clinicians to support them in the diagnosis, treatment care and support and people with continence problems e.g. Urinary incontinence in women (September 2013), Faecal incontinence in adults (June 2007), Urinary incontinence in neurological disease: assessment and management (August 2012) and Lower urinary tract symptoms in men: management (May 2010).

  • Glyn Davies – 2015 Parliamentary Question to the Department of Health

    Glyn Davies – 2015 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Glyn Davies on 2015-10-20.

    To ask the Secretary of State for Health, what estimate his Department has made of the number of people with (a) urinary incontinence and (b) faecal incontinence in England.

    Jane Ellison

    NHS England has advised that according to a survey conducted in 2008, there are over 14 million adults who have bladder control problems and 6.5 million with bowel control problems in the United Kingdom.

    The Department does not collect information on the number of people living with urinary and faecal incontinence specific to Northern Ireland, Scotland and Wales. This is a matter for devolved administrations.

    The Healthcare Quality and Improvement Partnership (2010) established that in order to achieve the best clinical outcomes, continence services have to be integrated across primary and secondary care and care home settings.

    They also concluded that ‘there is an urgent need for improved and equitable practice for all people with bladder and bowel problems’ through the development of commissioning frameworks, evidence-based training for health professionals and patient empowerment to increase their expectations of cure.

    Improving continence care provision through integrated services brings many benefits including:

    – a better quality of life and more independence through finding solutions appropriate to individual needs;

    – less reliance on pads and products by using alternative treatments;

    – a reduction in admissions to hospitals and care homes;

    – fewer complications, such as urinary tract infections, faecal impaction and skin breakdown; and

    – a reduction in costs.

    NHS England’s Excellence in Continence Care guidance provides a framework that enables commissioners to work in collaboration with providers and others to make a step change to address shortfalls so that safe, dignified, efficient and effective continence care is consistently provided.

    This guidance is aimed at commissioners, providers, health and social care staff and as information for the public and has been produced in partnership with patient and public advocates, clinicians and partners from the third sector. The roles of everyone involved in the care of people with continence needs are made clear in the guidance and publication via a launch is planned for ‘Self Care Week’ beginning 16 November. The launch will both raise awareness and promote understanding.

    In addition the National Institute for Health and Care Excellence has produced a range of guidance for clinicians to support them in the diagnosis, treatment care and support and people with continence problems e.g. Urinary incontinence in women (September 2013), Faecal incontinence in adults (June 2007), Urinary incontinence in neurological disease: assessment and management (August 2012) and Lower urinary tract symptoms in men: management (May 2010).

  • Louise Haigh – 2015 Parliamentary Question to the Department of Health

    Louise Haigh – 2015 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Louise Haigh on 2015-10-20.

    To ask the Secretary of State for Health, what recent representations he has received from (a) universities, (b) healthcare professionals and (c) the Royal Colleges on replacing bursaries for nursing, midwifery and allied healthcare service tuition with student loans.

    Ben Gummer

    The Department has received a number of representations from organisations, including Royal Colleges, professional bodies and representatives of universities, about a number of issues relating to healthcare student education funding in England including a potential move from the current system of funding to student loans.

    No decisions have been taken on any changes to the funding of health care education and training in England. The Department will consider all of its expenditure as part of the Spending Review. The Government will announce the outcome of the Spending Review on 25 November 2015.

  • Jim Fitzpatrick – 2015 Parliamentary Question to the Department of Health

    Jim Fitzpatrick – 2015 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Jim Fitzpatrick on 2015-10-20.

    To ask the Secretary of State for Health, what assessment his Department has made of the recommendations contained in the report from the Ear Foundation entitled Bending the Spend, published in October 2015; and if he will make a statement.

    Alistair Burt

    The Department in conjunction with NHS England jointly published the Action Plan on Hearing Loss in March 2015. The Action Plan sets out the case for action to tackle the rising prevalence and personal, social and economic costs of uncorrected hearing loss and the variation in access and quality of service.

    The areas highlighted within the Bending the Spend report concur with and further strengthen those in the Action Plan. This includes the need to assess strategies for the earlier identification and management of hearing loss and the development of commissioning guidance to underpin the Action Plan, which NHS England will co-produce with stakeholders such as the Ear Foundation.

    A Cross System Oversight Group had its first meeting on 14 October 2015. This will not only review and monitor progress of the implementation of the Action Plan, but will also provide a forum for government departments, arm’s length bodies and stakeholders within the hearing loss community to engage with each other to ensure connections are made and maintained across the system.

    Membership of this group includes the Hearing Loss and Deafness Alliance of which the Ear Foundation is a member.