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To ask His Majesty's Government what steps they are taking to improve the diagnosis and treatment of atopic dermatitis in primary care.
To ask His Majesty's Government what steps they are taking to improve the diagnosis and treatment of atopic dermatitis in primary care.
Specifically on atopic dermatitis, and the prescribing of appropriate emollients, the relevant doctor or healthcare professional is responsible for working with their patient and deciding on the best course of treatment. Prescribers take account of appropriate national guidance on clinical effectiveness, as well as the local commissioning decisions of their respective integrated care boards when making decisions. The National Institute for Health and Care Excellence (NICE) also publishes a range of guidance on atopic dermatitis and other skin conditions for commissioners and healthcare professionals, with recommendations for diagnosis and referral, which are available at the NICE website.
On dermatology care in general, waiting times, and the proposal for a national service framework, I refer the Noble Baroness to the answer that I provided her on 13 January in response to Question HL13259, which, for ease of reference, is reproduced below:
Modern service frameworks will define an aspirational, long-term outcome goal for a major condition and will then identify the best evidenced interventions and the support for delivery. The Government will consider clinical specialities for future waves of modern service frameworks, including allergy, dermatology, which includes chronic spontaneous urticaria (CSU), and immunology. The criteria for determining other conditions for future modern service frameworks will be based on disease burden, care variation, economic impact, and where there is potential for rapid and significant improvements in the quality of care and productivity.
The Department recognises the potential benefits of virtual clinics in improving access to specialist care for conditions like CSU. A central part of our 10-Year Health Plan is moving care closer to home, and we recognise that we need to do this while retaining access to specialist support. Trusts should provide the infrastructure and resources to facilitate virtual consultations, but this should not replace face-to-face care where it is more appropriate, dependent on clinical need, or preferred by individual patients.
NHS England’s service specification for specialised dermatology services for adults and children is designed to reduce regional disparities in care for CSU by setting consistent national standards for diagnosis, treatment, and follow-up. The specification ensures that all patients, regardless of location, have access to evidence-based interventions and specialist expertise, including advanced therapies where clinically appropriate. The specification addresses historical variations in service provision and supports equitable access across integrated care systems. This approach helps to improve outcomes for patients with CSU and ensures a more uniform level of care throughout England.
Additionally, NHS England’s Getting It Right First Time programme is working to improve capacity and waiting times through its established Further Faster programme. This programme brings together hospital trust clinicians and operational teams with the challenge of collectively going ‘further and faster’ to transform patient pathways, reduce unnecessary follow-up outpatient appointments, and improve access and waiting times for patients.
A Further Faster handbook for dermatology has been produced, to share best practice and support National Health Service dermatology teams to reduce the number of Did Not Attend appointments, reduce unnecessary follow ups and, where appropriate, reduce the number of outpatient appointments by booking patients straight to tests, helping to free up capacity for patients in need of specialist dermatology services.
To ask His Majesty's Government what steps they are taking to support the adoption of artificial intelligence systems that can assist in the early detection of heart disease across the NHS.
To ask His Majesty's Government what steps they are taking to support the adoption of artificial intelligence systems that can assist in the early detection of heart disease across the NHS.
The Government is exploring the role and adoption of artificial intelligence (AI) in the earlier detection and diagnosis in a range of clinical specialties, including cardiovascular disease. This includes the safe and effective adoption of AI tools such as AI-assisted echocardiography, automated electrocardiogram interpretation, and digital stethoscope recordings through robust regulatory and assurance processes.
NHS England’s physiological sciences strategic framework clearly positions AI as a key enabler of community-based diagnostics, supporting faster and more standardised analysis of electrocardiograms and imaging tests.
To ask the Secretary of State for Health and Social Care, with reference to the National Cancer Plan for England, published on 4 February 2026, in which areas is the proactive approach to identifying people at greatest risk of pancreatic cancer currently operating; and whether she plans to expand its...
To ask the Secretary of State for Health and Social Care, with reference to the National Cancer Plan for England, published on 4 February 2026, in which areas is the proactive approach to identifying people at greatest risk of pancreatic cancer currently operating; and whether she plans to expand its...
NHS England is currently operating the pancreatic case finding pilot in selected primary care networks in the following cancer alliances:
- East Midlands;
- East of England;
- Greater Manchester;
- Humber and North Yorkshire;
- North Central London;
- North East London;
- South Yorkshire and Bassetlaw;
- Somerset, Wiltshire, Avon and Gloucestershire;
- Thames Valley;
- Wessex; and
- West Midlands.
NHS England will be undertaking an evaluation of the pilot. This will inform next steps including whether the geographical coverage should be extended.
To ask the Secretary of State for Health and Social Care, what steps her Department is taking to ensure comprehensive support is provided to people with multiple sclerosis at the time of diagnosis.
To ask the Secretary of State for Health and Social Care, what steps her Department is taking to ensure comprehensive support is provided to people with multiple sclerosis at the time of diagnosis.
The Government is committed to improving access to high‑quality care and treatment for people with multiple sclerosis (MS) and other progressive neurological conditions.
Through NHS England’s Neurology Transformation Programme, a new model of integrated care has also been developed to support integrated care boards (ICBs) to deliver the right service, at the right time for all neurology patients. This focuses on providing access equitably across the country, with care as close to home as possible, and early intervention to prevent illness and deterioration in patients with long-term neurological conditions, including MS. A toolkit was developed to support ICBs to understand and implement this new model, which includes components on delivering acute neurology services, improving health equity in neurology, and improving community neurology services.
NHS England has published an updated service specification for specialised neurology services, including MS, which sets out clear expectations for proactive, coordinated care to reduce the risk of avoidable complications and emphasises early identification of clinical risks, personalised care planning, and timely access to multidisciplinary support, including specialist nurses, therapists, and community services.
In addition, the GIRFT Programme for Neurology, the RightCare Progressive Neurological Conditions Toolkit, and the model of integrated neurology care developed through the Neurology Transformation Programme support greater consistency, coordination, and sharing of best practice across local systems and geographical areas. NHS England has developed national neurology dashboards, including an MS data dashboard and an interactive adult neurology dashboard, to support systems in monitoring service delivery, benchmarking performance, and understanding the quality of local neurology services.
The National Institute for Health and Care Excellence (NICE) has issued guidance on the use of disease‑modifying therapies for MS, supporting clinicians to offer clinically- and cost‑effective treatments based on the best available evidence. ICBs are expected to have regard to NICE guidance to ensure patients can access high‑quality care and treatment. NHS England also supports the implementation of treatment algorithms to promote consistent prescribing and reduce unwarranted variation in access to high‑efficacy therapies.
The 10-Year Health Plan will also support improved care and outcomes for people with MS by focusing on earlier diagnosis, more timely access to specialist treatment, and more coordinated, community‑based care. It will prioritise reducing unwarranted variation in services and strengthening multidisciplinary support, helping people with MS to manage their condition more effectively and maintain their quality of life.
Finally, a UK-wide neuro forum has been convened, bringing together the governments, health services, and Neurological Alliances of all four UK nations. The forum will share learnings across the UK, and discuss important neurology services transformation and workforce challenges, as well as best practice examples and potential solutions.
To ask the Secretary of State for Health and Social Care, what steps her department is taking to increase localised preventive care and diagnostic capacity in parliamentary constituencies where UK Health Security Agency profile data indicates Type 2 diabetes prevalence exceeds 12 per cent, such as Leicester East.
To ask the Secretary of State for Health and Social Care, what steps her department is taking to increase localised preventive care and diagnostic capacity in parliamentary constituencies where UK Health Security Agency profile data indicates Type 2 diabetes prevalence exceeds 12 per cent, such as Leicester East.
NHS England commissions the Healthier You NHS Diabetes Prevention Programme available to all integrated care boards (ICBs) in England. For eligible people with recently diagnosed type 2 diabetes, NHS England commissions the NHS Type 2 Diabetes Path to Remission Programme, which is also available to all ICBs in England.
Together, these national programmes complement locally commissioned prevention, weight management and diabetes care services, helping to address the high prevalence of type 2 diabetes by preventing or delaying new cases.
To ask the Secretary of State for Health and Social Care, whether her Department has made an assessment of the adequacy of referral guidance for suspected breast cancer.
To ask the Secretary of State for Health and Social Care, whether her Department has made an assessment of the adequacy of referral guidance for suspected breast cancer.
The Department has made no such assessment. The National Institute for Health and Care Excellence keeps all its guidance under review and its guideline on the recognition and referral of suspected cancer was updated in April 2026. There are no current plans for a further update of the guideline, including a review of the age or family history criteria for urgent investigations.
To ask the Secretary of State for Health and Social Care, if she will review the role of age and family history in urgent referral criteria for patients presenting with possible symptoms of breast cancer.
To ask the Secretary of State for Health and Social Care, if she will review the role of age and family history in urgent referral criteria for patients presenting with possible symptoms of breast cancer.
The Department has made no such assessment. The National Institute for Health and Care Excellence keeps all its guidance under review and its guideline on the recognition and referral of suspected cancer was updated in April 2026. There are no current plans for a further update of the guideline, including a review of the age or family history criteria for urgent investigations.
To ask the Secretary of State for Health and Social Care, whether her Department plans to pilot the provision of NT-proBNP point-of-care testing in community pharmacies for people presenting with symptoms of heart failure.
To ask the Secretary of State for Health and Social Care, whether her Department plans to pilot the provision of NT-proBNP point-of-care testing in community pharmacies for people presenting with symptoms of heart failure.
On the provision of NT-proBNP point-of-care testing, I refer the Hon. Member to the answer provided on 5 June 2025 in response to Question 54244. More broadly, the Cardiovascular Diesease Modern Service Framework sets out the Department's approach to prevention and reduced hospital admissions and is available at the following link:
https://www.gov.uk/government/publications/cardiovascular-disease-modern-service-framework
However, the Department does not hold the specific estimate requested.
To ask the Secretary of State for Health and Social Care, what assessment her department has made of the potential impact of funding for earlier diagnosis and specialist heart failure services on NHS expenditure associated with emergency admissions.
To ask the Secretary of State for Health and Social Care, what assessment her department has made of the potential impact of funding for earlier diagnosis and specialist heart failure services on NHS expenditure associated with emergency admissions.
On the provision of NT-proBNP point-of-care testing, I refer the Hon. Member to the answer provided on 5 June 2025 in response to Question 54244. More broadly, the Cardiovascular Diesease Modern Service Framework sets out the Department's approach to prevention and reduced hospital admissions and is available at the following link:
https://www.gov.uk/government/publications/cardiovascular-disease-modern-service-framework
However, the Department does not hold the specific estimate requested.
To ask the Secretary of State for Health and Social Care, what assessment she has made of the availability and accessibility of NHS services for the diagnosis and treatment of tongue-tie in newborn babies; what the average waiting time is for treatment following referral in each NHS region; and whether...
To ask the Secretary of State for Health and Social Care, what assessment she has made of the availability and accessibility of NHS services for the diagnosis and treatment of tongue-tie in newborn babies; what the average waiting time is for treatment following referral in each NHS region; and whether...
It is for local National Health Service trusts and integrated care boards to determine how their tongue division services are funded and commissioned, as well as the referral criteria. NHS England does not have national guidance, nor monitor waiting times for tongue-tie services.
The National Institute for Health and Care Excellence sets out guidance on tongue-tie, including advising that an assessment for tongue-tie should be considered if there are feeding concerns.
To ask the Secretary of State for Health and Social Care, what mental health care systems in England require a clinical diagnosis prior to treatment; and what assessment she has made of the potential impact of this requirement on (a) young people’s waiting times for mental health treatment and (b)...
To ask the Secretary of State for Health and Social Care, what mental health care systems in England require a clinical diagnosis prior to treatment; and what assessment she has made of the potential impact of this requirement on (a) young people’s waiting times for mental health treatment and (b)...
The interim report of the independent review into mental health conditions, attention deficit hyperactivity disorder, and autism found that access to support is too often slow, fragmented, and heavily dependent on having a diagnosis. Where support depends heavily on a formal diagnosis, demand for assessment can outstrip capacity, contributing to long waits, repeated assessments, and pressure on services. Diagnosis remains essential to inform treatment and enhance understanding, but the review is considering how people can receive appropriate support earlier and according to need. Its final report will make recommendations for the Government, the health system, and wider public services.
To ask the Secretary of State for Education, what steps she is taking to ensure autism in girls does not go unmissed.
To ask the Secretary of State for Education, what steps she is taking to ensure autism in girls does not go unmissed.
Education is a devolved matter, and the response outlines the information for England only.
Effective early identification and support is critical to improving outcomes for all children and young people with special educational needs and disabilities (SEND), including those with autism.
We have proposed the introduction of National Inclusion Standards, which will support education settings to identify and respond to needs earlier and more consistently, drawing on a broad range of evidence and professional expertise, so that all children and young people can receive the support they need to achieve and thrive.
The National Inclusion Standards will be underpinned by a £200 million training package to ensure that all teachers, educators, teaching assistants, support staff and leaders across early years, schools and post-16 settings can be trained to support pupils with SEND, and a new investment of £3.7 billion to drive more inclusive school estates and create additional specialist places.
We will continue to engage closely with young people, parents and professionals as we develop our reforms and how they will work in practice. The department also engages with the devolved governments at ministerial and official level on a range of areas covering education, skills and family policies and will continue to do so.
To ask His Majesty's Government, in the light of the publication of the British Journal of General Practice study Diagnosing in the dark, published on 31 May, what discussions have they had with NHS England and GP organisations to (1) ensure that GPs receive appropriate guidance and training in diagnosing both post-natal post-traumatic...
To ask His Majesty's Government, in the light of the publication of the British Journal of General Practice study Diagnosing in the dark, published on 31 May, what discussions have they had with NHS England and GP organisations to (1) ensure that GPs receive appropriate guidance and training in diagnosing both post-natal post-traumatic...
NHS England has developed eLearning on trauma-informed care and Perinatal Mental Health Birth Trauma to support professionals involved in perinatal care.
The National Maternity and Neonatal Taskforce is developing a National Maternity and Neonatal Action Plan, within which maternal mental health is an area of focus, reflecting Baroness Amos’ recommendation for further consideration.
To ask the Secretary of State for Health and Social Care, what discussions her department has had on improving dementia research, diagnosis and treatment, which haven’t seen significant improvements for nearly 20 years.
To ask the Secretary of State for Health and Social Care, what discussions her department has had on improving dementia research, diagnosis and treatment, which haven’t seen significant improvements for nearly 20 years.
The Government wants a society where every person with dementia receives high-quality, compassionate care from diagnosis through to the end of life.
We will publish the first ever Modern Service framework for Frailty and Dementia to set a clear direction and a long-term blueprint to improve outcomes for people with dementia. It will cover research, diagnosis and treatment. We are engaging with a wide group of partners to understand what should be included to ensure the best outcomes for people living with frailty and dementia.
We will also appoint a Dementia Tsar to bring strong and meaningful national leadership to drive forward the prevention, treatment and care of dementia.
To ask His Majesty's Government what assessment they have made of the extent to which genomic and biomarker testing is routinely embedded at the point of cancer diagnosis across NHS England.
To ask His Majesty's Government what assessment they have made of the extent to which genomic and biomarker testing is routinely embedded at the point of cancer diagnosis across NHS England.
Genomic testing in the National Health Service in England is provided through the NHS Genomic Medicine Service (NHS GMS) and delivered by a national genomic testing network of seven NHS Genomic Laboratory Hubs (GLHs). The NHS GLHs deliver testing as directed by the National Genomic Test Directory, which includes tests for over 200 cancer clinical indications.
From April 2026 NHS England has been embedding a new operating model for delivery of the NHS GMS through seven NHS GMS Lead Providers. Each NHS GMS will deliver a cancer genomics clinical function to bring together multi-profession leadership to embed and drive improvements in end to end cancer genomics pathways and deliver genomic testing in clinically relevant turnaround times. The programme also includes expanding the number of cellular pathology genomic centres to streamline the cancer diagnostic sample pathway and support timely return of genomic test results to inform clinical management and enable cancer patients to access innovative therapies.
In addition, the National Cancer Plan identified diagnostic technologies as a strategic research priority for improving survival rates for those living with or treated for cancer. The Office for Life Sciences has funded a primary care intervention study via the National Institute for Health and Care Research Health Technology Assessment Programme to assess the clinical and cost effectiveness of the use of multi-cancer detection tests in primary care to support future commissioning of diagnostic biomarkers in diagnostic pathways.
To ask the Secretary of State for Health and Social Care, what assessment her Department has made of the adequacy of availability and routine use of Doppler ultrasound and ankle-brachial index testing in primary care for patients presenting with lower-limb symptoms; and whether the Government plans to issue guidance to...
To ask the Secretary of State for Health and Social Care, what assessment her Department has made of the adequacy of availability and routine use of Doppler ultrasound and ankle-brachial index testing in primary care for patients presenting with lower-limb symptoms; and whether the Government plans to issue guidance to...
The Department has published a new cardiovascular disease modern service framework (CVD MSF), which prioritises ambitious, evidence-led, and clinically informed approaches to prevention, treatment, and care, supporting consistent and equitable access across the CVD pathway. This modern service framework can be found at the following link:
https://www.gov.uk/government/publications/cardiovascular-disease-modern-service-framework
We welcome the report of the Vascular and Venous Disease All-Party Parliamentary Group. The Department and NHS England have engaged widely with stakeholders, such as the Stroke Association and Heart UK, to co-produce the CVD MSF and ensure we consider the role of emerging innovations across the CVD pathway.
NHS England has not undertaken a specific national assessment of the availability or routine use of ankle-brachial index testing or Doppler ultrasound in primary care for patients presenting with symptoms suggestive of peripheral arterial disease.
The National Vascular Registry collects information relating to vascular procedures and patient outcomes to support service improvement and quality assurance within vascular services. However, it does not routinely report national data on diagnostic delay, misdiagnosis, or the number of healthcare contacts prior to diagnosis.
To ask the Secretary of State for Health and Social Care, whether the Cardiovascular Disease Modern Service Framework will include standards for the early diagnosis and referral of peripheral arterial disease in primary care, including the routine use of ankle-brachial index and Doppler testing for patients presenting with lower-limb pain.
To ask the Secretary of State for Health and Social Care, whether the Cardiovascular Disease Modern Service Framework will include standards for the early diagnosis and referral of peripheral arterial disease in primary care, including the routine use of ankle-brachial index and Doppler testing for patients presenting with lower-limb pain.
The Department has published a new cardiovascular disease modern service framework (CVD MSF), which prioritises ambitious, evidence-led, and clinically informed approaches to prevention, treatment, and care, supporting consistent and equitable access across the CVD pathway. This modern service framework can be found at the following link:
https://www.gov.uk/government/publications/cardiovascular-disease-modern-service-framework
We welcome the report of the Vascular and Venous Disease All-Party Parliamentary Group. The Department and NHS England have engaged widely with stakeholders, such as the Stroke Association and Heart UK, to co-produce the CVD MSF and ensure we consider the role of emerging innovations across the CVD pathway.
NHS England has not undertaken a specific national assessment of the availability or routine use of ankle-brachial index testing or Doppler ultrasound in primary care for patients presenting with symptoms suggestive of peripheral arterial disease.
The National Vascular Registry collects information relating to vascular procedures and patient outcomes to support service improvement and quality assurance within vascular services. However, it does not routinely report national data on diagnostic delay, misdiagnosis, or the number of healthcare contacts prior to diagnosis.
To ask the Secretary of State for Health and Social Care, what data her Department holds on the rate of misdiagnosis or delayed diagnosis of peripheral arterial disease in England; and what the average number of clinical contacts is that patients undergo before receiving a correct diagnosis.
To ask the Secretary of State for Health and Social Care, what data her Department holds on the rate of misdiagnosis or delayed diagnosis of peripheral arterial disease in England; and what the average number of clinical contacts is that patients undergo before receiving a correct diagnosis.
The Department has published a new cardiovascular disease modern service framework (CVD MSF), which prioritises ambitious, evidence-led, and clinically informed approaches to prevention, treatment, and care, supporting consistent and equitable access across the CVD pathway. This modern service framework can be found at the following link:
https://www.gov.uk/government/publications/cardiovascular-disease-modern-service-framework
We welcome the report of the Vascular and Venous Disease All-Party Parliamentary Group. The Department and NHS England have engaged widely with stakeholders, such as the Stroke Association and Heart UK, to co-produce the CVD MSF and ensure we consider the role of emerging innovations across the CVD pathway.
NHS England has not undertaken a specific national assessment of the availability or routine use of ankle-brachial index testing or Doppler ultrasound in primary care for patients presenting with symptoms suggestive of peripheral arterial disease.
The National Vascular Registry collects information relating to vascular procedures and patient outcomes to support service improvement and quality assurance within vascular services. However, it does not routinely report national data on diagnostic delay, misdiagnosis, or the number of healthcare contacts prior to diagnosis.
To ask the Secretary of State for Health and Social Care, if the Government will adopt a National Foot Attack Pathway to ensure patients presenting with symptoms of peripheral arterial disease receive same-day assessment and referral to specialist vascular services.
To ask the Secretary of State for Health and Social Care, if the Government will adopt a National Foot Attack Pathway to ensure patients presenting with symptoms of peripheral arterial disease receive same-day assessment and referral to specialist vascular services.
The Department has published a new cardiovascular disease modern service framework (CVD MSF), which prioritises ambitious, evidence-led, and clinically informed approaches to prevention, treatment, and care, supporting consistent and equitable access across the CVD pathway. This modern service framework can be found at the following link:
https://www.gov.uk/government/publications/cardiovascular-disease-modern-service-framework
We welcome the report of the Vascular and Venous Disease All-Party Parliamentary Group. The Department and NHS England have engaged widely with stakeholders, such as the Stroke Association and Heart UK, to co-produce the CVD MSF and ensure we consider the role of emerging innovations across the CVD pathway.
NHS England has not undertaken a specific national assessment of the availability or routine use of ankle-brachial index testing or Doppler ultrasound in primary care for patients presenting with symptoms suggestive of peripheral arterial disease.
The National Vascular Registry collects information relating to vascular procedures and patient outcomes to support service improvement and quality assurance within vascular services. However, it does not routinely report national data on diagnostic delay, misdiagnosis, or the number of healthcare contacts prior to diagnosis.
To ask the Secretary of State for Health and Social Care, what plans she has for reducing waiting times (a) in GP practices and (b) for accessing routine diagnostic tests, especially for people with aggressive and/or life-limiting conditions.
To ask the Secretary of State for Health and Social Care, what plans she has for reducing waiting times (a) in GP practices and (b) for accessing routine diagnostic tests, especially for people with aggressive and/or life-limiting conditions.
NHS England’s Medium Term Planning Framework, published in October 2025, sets out a national ambition to improve access to primary care and reduce unwarranted variation. This includes ensuring that 90% of clinically urgent patients, such as those with aggressive and/or life-limiting conditions, are dealt with on the same day.
NHS England is driving the transformation of diagnostics services across the National Health Service. These services will grow their digital capability and become more efficient. They will have new and replacement equipment that will make tests quicker and increase the numbers of patients that get faster access to a test.
NHS England is also expanding community diagnostics centres (CDCs) and other community-based diagnostic services, so more patients can benefit from the increasing numbers of diagnostic services and gain access closer to home and via their general practitioner. CDCs are equipped to provide diagnostic tests for aggressive and/or life-limiting conditions.