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  • Craig Tracey – 2016 Parliamentary Question to the Department of Health

    Craig Tracey – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Craig Tracey on 2016-04-08.

    To ask the Secretary of State for Health, if he will make it his policy for palliative care funding to provide universal access to bereavement services for bereaved families of children and young people.

    Ben Gummer

    A review of the allocation methodology of the annual children’s hospice grant is being considered to support an equitable, transparent and evidence based formula making use of data from all children’s hospices in 2016/17. The aim is to provide clear advice to hospices on the grant for 2016/17 and a proposed way forward to review the formula and how hospices can contribute to that process.

    Adult hospices, including voluntary sector hospices, receive on average around a third of their funding from the National Health Service and it is for local commissioners to ensure that the services they commission meet the needs of their local populations, including in end of life care.

    Clinical commissioning groups (CCGs) have responsibility for ensuring that they are meeting the needs of those requiring children’s palliative care services, considering the full range of local provision, both statutory and voluntary sectors, and the wishes of children and young people and their families. CCGs will need to make sure that they provide information on the support available locally for children with palliative care needs and their families.

    Many maternity units have specialist bereavement midwives and dedicated bereavement suites to support parents but we know that this support is not available in every unit and we are currently considering the actions that we can take to improve bereavement services further. For families of older children and young people chaplaincy services may be able to provide support.

    It is the responsibility of the professional regulators to set the standards and outcomes for education and training and approve training curricula to ensure newly qualified healthcare professionals are equipped with the knowledge, skills and attitudes to provide high quality patient care. It is the responsibility of employers to ensure staff receive appropriate development to deliver safe and effective healthcare. This includes training in providing care to children and young people with life-shortening conditions.

  • Craig Tracey – 2016 Parliamentary Question to the Department of Health

    Craig Tracey – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Craig Tracey on 2016-04-08.

    To ask the Secretary of State for Health, if he will take steps to require health commissioners to make publicly available information on how they commission palliative care for children and young people across their locality.

    Ben Gummer

    A review of the allocation methodology of the annual children’s hospice grant is being considered to support an equitable, transparent and evidence based formula making use of data from all children’s hospices in 2016/17. The aim is to provide clear advice to hospices on the grant for 2016/17 and a proposed way forward to review the formula and how hospices can contribute to that process.

    Adult hospices, including voluntary sector hospices, receive on average around a third of their funding from the National Health Service and it is for local commissioners to ensure that the services they commission meet the needs of their local populations, including in end of life care.

    Clinical commissioning groups (CCGs) have responsibility for ensuring that they are meeting the needs of those requiring children’s palliative care services, considering the full range of local provision, both statutory and voluntary sectors, and the wishes of children and young people and their families. CCGs will need to make sure that they provide information on the support available locally for children with palliative care needs and their families.

    Many maternity units have specialist bereavement midwives and dedicated bereavement suites to support parents but we know that this support is not available in every unit and we are currently considering the actions that we can take to improve bereavement services further. For families of older children and young people chaplaincy services may be able to provide support.

    It is the responsibility of the professional regulators to set the standards and outcomes for education and training and approve training curricula to ensure newly qualified healthcare professionals are equipped with the knowledge, skills and attitudes to provide high quality patient care. It is the responsibility of employers to ensure staff receive appropriate development to deliver safe and effective healthcare. This includes training in providing care to children and young people with life-shortening conditions.

  • Kate Osamor – 2016 Parliamentary Question to the Department of Health

    Kate Osamor – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Kate Osamor on 2016-04-08.

    To ask the Secretary of State for Health, if his Department will carry out an assessment of the potential (a) health, (b) economic and (c) social effects of its proposals to reduce community pharmacy funding.

    Alistair Burt

    Community pharmacy is a vital part of the National Health Service and can play an even greater role. In the Spending Review, the Government re-affirmed the need for the NHS to deliver £22 billion in efficiency savings by 2020/21 as set out in the NHS’s own plan, the Five Year Forward View. Community pharmacy is a core part of NHS primary care and has an important contribution to make as the NHS rises to these challenges. The Government believes efficiencies can be made without compromising the quality of services or public access to them. Our aim is to ensure that those community pharmacies upon which people depend continue to thrive and so we are consulting on the introduction of a Pharmacy Access Scheme, which will provide more NHS funds to certain pharmacies compared to others, considering factors such as location and the health needs of the local population.

    The Government’s vision is for a more efficient, modern system that will free up pharmacists to spend more time delivering clinical and public health services to the benefit of patients and the public.

    We are consulting the Pharmaceutical Services Negotiating Committee (PSNC) and others, including patient and public representatives, on our proposals for community pharmacy in 2016/17 and beyond. We announced on 16 March 2016 that the consultation period was to be extended to allow more time to develop the proposed changes with the PSNC and others. It will now close on 24 May 2016.

    An impact assessment will be completed to inform final decisions and published in due course.

  • Anne-Marie Trevelyan – 2016 Parliamentary Question to the Department of Health

    Anne-Marie Trevelyan – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Anne-Marie Trevelyan on 2016-04-08.

    To ask the Secretary of State for Health, pursuant to the Answer of 17 March 2016 to Question 30491 on A&E departments: EU nationals, whether he plans to collate or estimate the information requested.

    Alistair Burt

    There are no plans to collect, estimate or publish this information.

  • Craig Tracey – 2016 Parliamentary Question to the Department of Health

    Craig Tracey – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Craig Tracey on 2016-04-08.

    To ask the Secretary of State for Health, if he will ensure provision of sustainable and long-term funding for (a) children’s hospice sector and (b) other voluntary sector end-of-life care services.

    Ben Gummer

    A review of the allocation methodology of the annual children’s hospice grant is being considered to support an equitable, transparent and evidence based formula making use of data from all children’s hospices in 2016/17. The aim is to provide clear advice to hospices on the grant for 2016/17 and a proposed way forward to review the formula and how hospices can contribute to that process.

    Adult hospices, including voluntary sector hospices, receive on average around a third of their funding from the National Health Service and it is for local commissioners to ensure that the services they commission meet the needs of their local populations, including in end of life care.

    Clinical commissioning groups (CCGs) have responsibility for ensuring that they are meeting the needs of those requiring children’s palliative care services, considering the full range of local provision, both statutory and voluntary sectors, and the wishes of children and young people and their families. CCGs will need to make sure that they provide information on the support available locally for children with palliative care needs and their families.

    Many maternity units have specialist bereavement midwives and dedicated bereavement suites to support parents but we know that this support is not available in every unit and we are currently considering the actions that we can take to improve bereavement services further. For families of older children and young people chaplaincy services may be able to provide support.

    It is the responsibility of the professional regulators to set the standards and outcomes for education and training and approve training curricula to ensure newly qualified healthcare professionals are equipped with the knowledge, skills and attitudes to provide high quality patient care. It is the responsibility of employers to ensure staff receive appropriate development to deliver safe and effective healthcare. This includes training in providing care to children and young people with life-shortening conditions.

  • Craig Tracey – 2016 Parliamentary Question to the Department of Health

    Craig Tracey – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Craig Tracey on 2016-04-08.

    To ask the Secretary of State for Health, if he will take steps to ensure that all health and social care staff involved in providing care to children and young people with life-shortening conditions receive specialist training.

    Ben Gummer

    A review of the allocation methodology of the annual children’s hospice grant is being considered to support an equitable, transparent and evidence based formula making use of data from all children’s hospices in 2016/17. The aim is to provide clear advice to hospices on the grant for 2016/17 and a proposed way forward to review the formula and how hospices can contribute to that process.

    Adult hospices, including voluntary sector hospices, receive on average around a third of their funding from the National Health Service and it is for local commissioners to ensure that the services they commission meet the needs of their local populations, including in end of life care.

    Clinical commissioning groups (CCGs) have responsibility for ensuring that they are meeting the needs of those requiring children’s palliative care services, considering the full range of local provision, both statutory and voluntary sectors, and the wishes of children and young people and their families. CCGs will need to make sure that they provide information on the support available locally for children with palliative care needs and their families.

    Many maternity units have specialist bereavement midwives and dedicated bereavement suites to support parents but we know that this support is not available in every unit and we are currently considering the actions that we can take to improve bereavement services further. For families of older children and young people chaplaincy services may be able to provide support.

    It is the responsibility of the professional regulators to set the standards and outcomes for education and training and approve training curricula to ensure newly qualified healthcare professionals are equipped with the knowledge, skills and attitudes to provide high quality patient care. It is the responsibility of employers to ensure staff receive appropriate development to deliver safe and effective healthcare. This includes training in providing care to children and young people with life-shortening conditions.

  • Chris Leslie – 2016 Parliamentary Question to the Department of Health

    Chris Leslie – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Chris Leslie on 2016-04-08.

    To ask the Secretary of State for Health, what analysis his Department or NHS England has undertaken of the potential effect on medical research of dismantling the Corsellis Brain Collection; and if he will place any such analysis in the Library.

    George Freeman

    Started in the early 1950s by Professor Nick Corsellis at Runwell Hospital, in recent years the Corsellis Collection of brain pathology specimens has been managed and maintained by West London Mental Health Trust (WLMHT). The excess costs of maintaining the collection can only be supported by WLMHT from funds received for patient care. Therefore WLMHT has decided to dispose of the collection by seeking expressions of interest in the brain tissue of value for research, mainly sub-collections of the less common pathologies, and to respectfully dispose of that tissue for which no scientific purpose could be envisaged.

    WLMHT has received expressions of interest, but none in taking the complete collection. The original timescale for closure was by the end of March 2016, but WLMHT will support a further three months activity to meet the additional requests for tissue samples. The collection will close by the end of June.

    The Department and NHS England have not made any specific assessment of the contribution of the collection to medical research and health improvement in the United Kingdom, or undertaken any specific analysis of the potential effect on medical research of dismantling the collection.

    The Medical Research Council supports a range of brain tissue banks which have been set-up around specific disorders and diseases generally to collect post-mortem brain tissue from consented donors.

  • Sir Nicholas Soames – 2016 Parliamentary Question to the Department of Health

    Sir Nicholas Soames – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Sir Nicholas Soames on 2016-04-08.

    To ask the Secretary of State for Health, what the structure is of NHS Property Services and to whom they report.

    George Freeman

    NHS Property Services is a limited company, registered at Companies House, and 100% owned by the Secretary of State for Health, to whom it is accountable.

    It is governed by a company Board consisting of a Chair, Chief Executive and an appropriate mix of executive and non-executive directors, including a Departmental ‘shareholder representative’ director.

  • Louise Haigh – 2016 Parliamentary Question to the Department of Health

    Louise Haigh – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Louise Haigh on 2016-04-08.

    To ask the Secretary of State for Health, what the planned timetable is for the scoping exercise for special provisions, including fast tracking for treatment, for people with obstructive sleep apnoea who drive for a living.

    George Freeman

    The National Institute for Health and Care Excellence (NICE) has been asked to develop a clinical guideline and quality standard on sleep disordered breathing (including obstructive sleep apnoea). NICE will develop the scope of the clinical guideline, including the key questions that will be addressed by the guidance, in consultation with stakeholders.

    NICE has advised that there is currently no timetable for developing this guidance.

  • Paul Blomfield – 2016 Parliamentary Question to the Department of Health

    Paul Blomfield – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Paul Blomfield on 2016-04-08.

    To ask the Secretary of State for Health, what assessment has been undertaken of the effect on the earnings of people employed under the Experts by Experience programme of implementing the new Care Quality Commission contracts on 1 February 2016.

    Ben Gummer

    The Care Quality Commission (CQC) is the independent regulator for health and adult social care in England. It is responsible for its own staffing requirements and decisions on contracts around the supplying of Experts by Experience for its inspections of providers. The CQC is not the employer of Experts by Experience and does not set rates of pay. The Experts by Experience service has been an outsourced service since its inception.

    The CQC has advised that contracts were awarded on the basis of a formal procurement that focused on quality and value for money. Whilst negotiating the new Experts by Experience contracts, the CQC worked closely with suppliers to ensure that there was minimum impact on the individual earnings of existing Experts by Experience as well as on the rates for newly appointed Experts by Experience.

    The CQC is aware of concerns amongst some Experts by Experience in relation to moving between organisations, including rates of pay, in order to continue participating in the work. However, the CQC’s decision to award these new contracts focussed on expanding the numbers of Experts by Experience involved in the CQC’s inspections, ensuring that the high quality contribution Experts by Experience have provided to date is maintained and delivering value for money.