Asked by: Sorcha Eastwood (Alliance - Lagan Valley)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what consultation process has been followed with devolved nations in preparation for the Government's response to the Hughes Report, published on 7 February 2024.
Answered by Ashley Dalton - Parliamentary Under-Secretary (Department of Health and Social Care)
The Government is carefully considering the valuable work done by the Patient Safety Commissioner and the resulting Hughes Report, which set out options for redress for those harmed by valproate and pelvic mesh. This is a complex area of work, involving several Government departments, and it is important that we get this right. We will be providing an update to the Patient Safety Commissioner’s report at the earliest opportunity. Although the Hughes Report and its recommendations only cover patients harmed in England, the Government recognises that any response will likely have implications for the whole of the United Kingdom, and is therefore engaging with the devolved administrations on the Hughes Report.
Asked by: Sorcha Eastwood (Alliance - Lagan Valley)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what recent progress his Department has made in preparing Government's response to the Hughes Report, published on 7 February 2024.
Answered by Ashley Dalton - Parliamentary Under-Secretary (Department of Health and Social Care)
The Government is carefully considering the valuable work done by the Patient Safety Commissioner and the resulting Hughes Report, which set out options for redress for those harmed by valproate and pelvic mesh. This is a complex area of work, involving several Government departments, and it is important that we get this right. We will be providing an update to the Patient Safety Commissioner’s report at the earliest opportunity. Although the Hughes Report and its recommendations only cover patients harmed in England, the Government recognises that any response will likely have implications for the whole of the United Kingdom, and is therefore engaging with the devolved administrations on the Hughes Report.
Asked by: Sorcha Eastwood (Alliance - Lagan Valley)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what his planned timeline is for the Government's response to the Hughes Report, published on 7 February 2024.
Answered by Ashley Dalton - Parliamentary Under-Secretary (Department of Health and Social Care)
The Government is carefully considering the valuable work done by the Patient Safety Commissioner and the resulting Hughes Report, which set out options for redress for those harmed by valproate and pelvic mesh. This is a complex area of work, involving several Government departments, and it is important that we get this right. We will be providing an update to the Patient Safety Commissioner’s report at the earliest opportunity. Although the Hughes Report and its recommendations only cover patients harmed in England, the Government recognises that any response will likely have implications for the whole of the United Kingdom, and is therefore engaging with the devolved administrations on the Hughes Report.
Asked by: Sorcha Eastwood (Alliance - Lagan Valley)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what steps he is taking to raise awareness during Teenage and Young Adult Cancer Awareness Month of the signs and symptoms of cancer in April 2025.
Answered by Ashley Dalton - Parliamentary Under-Secretary (Department of Health and Social Care)
NHS England and other National Health Service organisations, nationally and locally, publish information on the signs and symptoms of many different types of cancer, including those that are most common in teenagers and young adults. Further information on cancer signs and symptoms is available on the NHS.UK website.
The Department is committed to improving outcomes for teenagers and young adults with cancer. That’s why we have relaunched the Children and Young People Cancer Taskforce. The taskforce will explore opportunities for improvement in England, including detection and diagnosis, genomic testing and treatment, research and innovation, and patient experience. The taskforce will ensure that the unique needs of children and young people, including teenagers with cancer, are carefully considered as part of the National Cancer Plan for England, due to be published later this year.
As part of this work, the Department is committed to directly engaging with patients and their families to discuss their experiences. We are working with taskforce members to assemble a Patient Experience Panel, made up of young people with lived experience of cancer and their families, which will feed directly into the work of the taskforce.
Asked by: Sorcha Eastwood (Alliance - Lagan Valley)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what plans he has to meet young people with cancer to discuss their experiences during Teenage and Young Adult Cancer Awareness Month in April 2025.
Answered by Ashley Dalton - Parliamentary Under-Secretary (Department of Health and Social Care)
NHS England and other National Health Service organisations, nationally and locally, publish information on the signs and symptoms of many different types of cancer, including those that are most common in teenagers and young adults. Further information on cancer signs and symptoms is available on the NHS.UK website.
The Department is committed to improving outcomes for teenagers and young adults with cancer. That’s why we have relaunched the Children and Young People Cancer Taskforce. The taskforce will explore opportunities for improvement in England, including detection and diagnosis, genomic testing and treatment, research and innovation, and patient experience. The taskforce will ensure that the unique needs of children and young people, including teenagers with cancer, are carefully considered as part of the National Cancer Plan for England, due to be published later this year.
As part of this work, the Department is committed to directly engaging with patients and their families to discuss their experiences. We are working with taskforce members to assemble a Patient Experience Panel, made up of young people with lived experience of cancer and their families, which will feed directly into the work of the taskforce.
Asked by: Sorcha Eastwood (Alliance - Lagan Valley)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, whether he plans to engage with (a) Kidney Care UK and (b) other patient representative organisations ahead of the World Health Assembly's debate on kidney health.
Answered by Ashley Dalton - Parliamentary Under-Secretary (Department of Health and Social Care)
The Department has met with Kidney Care UK and will be arranging further meetings with civil society organisations on the full range of health topics to be discussed in advance of the World Health Assembly in May 2025.
Asked by: Sorcha Eastwood (Alliance - Lagan Valley)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, whether the National Institute for Health and Care Excellence's recommendation of relugolix-estradiol-norethisterone for routine NHS use to treat endometriosis will extend to Northern Ireland.
Answered by Karin Smyth - Minister of State (Department of Health and Social Care)
The National Institute for Health and Care Excellence (NICE) makes recommendations on whether new medicines should be routinely funded by the National Health Service in England. NICE published final draft guidance on 13 March 2025 that recommends relugolix-estadiol-norethisterone as an option for treating symptoms of endometriosis in adults of reproductive age who have had medical or surgical treatment for endometriosis. NICE currently expects to publish final guidance in April 2025. Health is a devolved matter and decisions on the availability of medicines in Northern Ireland are a matter for the Northern Ireland Executive. Further information is available at the following link:
https://www.health-ni.gov.uk/topics/national-institute-health-and-care-excellence-nice
Asked by: Sorcha Eastwood (Alliance - Lagan Valley)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, if he will support the ratification of the World Health Organisation Resolution to include chronic kidney disease in its priority list of non-communicable diseases.
Answered by Ashley Dalton - Parliamentary Under-Secretary (Department of Health and Social Care)
The United Kingdom actively engaged in negotiations on the World Health Organization (WHO) resolution, Reducing the Burden of Non-Communicable Diseases (NCDs) through the Promotion of Kidney Health and Strengthening Prevention and Control of Kidney Disease, in advance of the 156th WHO Executive Board in February 2025. The Executive Board recommended adoption of all resolutions considered to the World Health Assembly, including this one, subject to ongoing budget discussions. If adopted, the resolution will apply to the UK as a Member State of the WHO. We remain committed to tackling NCDs, including kidney disease, domestically and internationally.
Asked by: Sorcha Eastwood (Alliance - Lagan Valley)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what assessment he has made of the adequacy of blood cancer data.
Answered by Karin Smyth - Minister of State (Department of Health and Social Care)
The National Disease Registration Service, through the National Cancer Registration and Analysis Services (NCRAS), collects information on how many people in England are diagnosed with or treated for cancer. Blood cancer is included as a distinct category, labelled haematological neoplasms. This creates a clinically rich data resource that is used to measure diagnosis, treatment, and outcomes for patients diagnosed with cancer. The data held by the NCRAS supports service provision and commissioning in the National Health Service, clinical audits, and public health and epidemiological research, all of which contribute to improved outcomes for those diagnosed with cancer, including those with blood cancer. The information is available at the following link:
https://www.cancerdata.nhs.uk/
National Disease Registration Service analysts attend quarterly meetings with United Kingdom and Ireland Association of Cancer Registries analysts to discuss any differences in the reporting of cancer data and how these can be made analogous. Annual performance indicators, including key performance indicators for haematology, are available at the following link:
Asked by: Sorcha Eastwood (Alliance - Lagan Valley)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what steps he is taking to help reduce inequalities of care for blood cancer patients.
Answered by Andrew Gwynne
I refer the hon. Member to the answer I gave on 8 October 2024 to Question 5808.