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To ask the Secretary of State for Health and Social Care, what steps his Department is taking to help increase the uptake of kidney function tests among at-risk populations in primary care.
To ask the Secretary of State for Health and Social Care, what steps his Department is taking to help increase the uptake of kidney function tests among at-risk populations in primary care.
Early diagnosis of chronic kidney disease (CKD) is supported through widespread access to blood and urine tests across the National Health Service. Phlebotomy is a key part of this pathway. The NHS delivers over one billion blood tests each year, supporting the diagnosis and monitoring of a wide range of conditions, including CKD.
Community diagnostic centres (CDCs) are increasing diagnostic capacity and improving access to testing closer to patients’ homes. Phlebotomy services are currently available in 119 CDCs. CDCs have delivered approximately 1.6 million tests between April 2025 and the end of February 2026. In addition, non-obstetric ultrasound, also used to examine kidneys, is available in 152 CDCs and delivered approximately 1.01 million tests over the same period.
NHS England continues to work with integrated care boards to expand diagnostic capacity and improve referral pathways, helping clinicians access the tests needed to support earlier diagnosis and monitoring of long-term conditions, including CKD.
That this House commends the invaluable and life-saving work being carried out by both Clarissa’s Campaign and Cardiac Risk in the Young; welcomes the major research paper produced by researchers based City St George's, University of London and St George's University Hospitals NHS Foundation Trust; notes their call for repeat electrocardiogram tests in order to identify potentially life-threatening conditions; raises the importance of this report given the statistics that 12 young people die each week due to an undiagnosed heart condition; recognises that researchers report that 40% of those diagnosed with a heart condition during the study went on to receive significant risk-reducing interventions such as heart-transplants with others offered non-clinical treatment pathways to reduce their risk of ill-health; and highlights the importance of this study and campaigns to raise awareness about cardiac risk in the young to save lives.
That this House commends the invaluable and life-saving work being carried out by both Clarissa’s Campaign and Cardiac Risk in the Young; welcomes the major research paper produced by researchers based City St George's, University of London and St George's University Hospitals NHS Foundation Trust; notes their call for repeat...
That this House recognises the life-changing difference early diagnosis and treatment can make for babies with spinal muscular atrophy (SMA); notes that SMA is a rare but serious genetic condition which, if untreated, can cause severe disability or early death; further notes that gene therapies exist which are most effective when given before symptoms appear; acknowledges that SMA is not currently included in the routine newborn bloodspot screening programme (formerly known as heel prick test) in England, Wales or Northern Ireland; also notes that a two-year pilot will begin in Scotland in spring this year and that the National Screening Committee is currently reviewing whether to introduce screening across the UK; and therefore calls on the Government to act urgently with the NHS, devolved health authorities, and the National Screening Committee to introduce SMA screening for all newborns across the UK.
That this House recognises the life-changing difference early diagnosis and treatment can make for babies with spinal muscular atrophy (SMA); notes that SMA is a rare but serious genetic condition which, if untreated, can cause severe disability or early death; further notes that gene therapies exist which are most effective...
To ask the Secretary of State for Health and Social Care, if he will take steps to create a standardised pathway for the genetic testing of people with motor neurone disease.
To ask the Secretary of State for Health and Social Care, if he will take steps to create a standardised pathway for the genetic testing of people with motor neurone disease.
Genomic testing in the National Health Service in England is provided through the NHS Genomic Medicine Service (GMS). Testing is directed by the National Genomic Test Directory, which sets out the eligibility criteria for patients to access testing.
Genomic testing for adult-onset neurodegenerative disorder is included in the Test Directory under specific clinical scenarios including amyotrophic lateral sclerosis, the most common type of motor neurone disease. The Test Directory is routinely reviewed to ensure that genomic testing continues to be available for all patients for whom it would be of clinical benefit, while delivering value for money for the NHS. The directory and associated supporting material are available at the following link:
https://www.england.nhs.uk/publication/national-genomic-test-directory-supporting-material/
The strategic and systematic embedding of genomic medicine in end-to-end clinical pathways and clinical specialities is supported by a network of seven regional NHS GMS Alliances, which play an important role in achieving equitable access to standardised end-to-end pathways of care, including genomic testing, clinical genetics and genetic counselling services.
That this House welcomes the #ProactiveForYourProstate campaign led by Prostate Cancer Research (PCR); congratulates campaigners, such as Teignmouth campaigner Jason Yeo, for their work advocating for prostate-specific antigen (PSA) testing for all men at age 50, and earlier for those in high‑risk categories; calls for the Government to back this campaign; notes with concern that prostate cancer is the second‑leading cause of cancer death among men in the United Kingdom, claiming more than 12,000 lives each year, while survival rates are close to 100 per cent when the disease is detected early; recognises that men of Black heritage, those with a family history of prostate cancer and carriers of certain genetic mutations face up to double the average risk of diagnosis and mortality; is alarmed that the present informed‑choice framework requires men aged 50 and over proactively to request a PSA blood test from their GP, a system that disproportionately fails high‑risk and socio‑economically deprived groups and entrenches health inequalities; applauds PCR and supporters for highlighting the urgent need for an equitable, population‑wide prostate cancer screening programme and for championing greater public awareness; further calls on the Government and the UK National Screening Committee to accelerate the development and roll‑out of a national screening pathway that prioritises high‑risk groups and eliminates postcode or socio‑economic disparities; and urges Ministers to engage with PCR, clinicians, patient representatives and campaigners to introduce interim measures that expand early‑detection access while long‑term protocols are finalised.
That this House welcomes the #ProactiveForYourProstate campaign led by Prostate Cancer Research (PCR); congratulates campaigners, such as Teignmouth campaigner Jason Yeo, for their work advocating for prostate-specific antigen (PSA) testing for all men at age 50, and earlier for those in high‑risk categories; calls for the Government to back this campaign; notes...
That this House recognises the worrying rise in breast cancer cases in younger women; notes with concern that breast cancer accounts for 43% of all cancers diagnosed in women aged 25-49, yet women wait until they are 50 or older to begin routine screening; urges everyone to work together to dispel the misconception that breast cancer only affects older women; commends the medical professionals who provide top class care to patients once diagnosed; and calls on the Government to review the current arrangements for breast cancer screening, including the merits of reducing the minimum age at which women are invited for regular breast cancer screening.
That this House recognises the worrying rise in breast cancer cases in younger women; notes with concern that breast cancer accounts for 43% of all cancers diagnosed in women aged 25-49, yet women wait until they are 50 or older to begin routine screening; urges everyone to work together to...
Much of the content of Lord Darzi’s report has been known for some years. None the less, today’s report is a scathing summary of the complete devastation that the Conservatives have wrought on our health services and on the health of our communities. We Liberal Democrats have long argued that...
Much of the content of Lord Darzi’s report has been known for some years. None the less, today’s report is a scathing summary of the complete devastation that the Conservatives have wrought on our health services and on the health of our communities. We Liberal Democrats have long argued that...
To ask the Secretary of State for Health and Social Care, pursuant to the Answer of 28 April 2021 to Question 185893 on Pregnancy: Screening, on what date the evaluative rollout of non-invasive prenatal testing is expected to be completed.
To ask the Secretary of State for Health and Social Care, pursuant to the Answer of 28 April 2021 to Question 185893 on Pregnancy: Screening, on what date the evaluative rollout of non-invasive prenatal testing is expected to be completed.
A non-invasive pre-natal test (NIPT) was introduced as an evaluative rollout in England on 1 July 2021, as part of the NHS Fetal Anomaly Screening Programme. The UK National Screening Committee (UK NSC) is being kept informed annually on the progress of this rollout.
NHS England has extended the evaluative rollout of the NIPT to March 2026, so that pregnancy outcomes can be included in the final report. The report is expected to go to the UK NSC at the end of 2026.
To ask the Secretary of State for Health and Social Care, with reference to the publication by Kidney Care UK entitled Let’s talk kidneys: opportunities for early intervention in chronic kidney disease, published on 23 December 2023, whether her Department has taken steps to implement annual testing of patients at...
To ask the Secretary of State for Health and Social Care, with reference to the publication by Kidney Care UK entitled Let’s talk kidneys: opportunities for early intervention in chronic kidney disease, published on 23 December 2023, whether her Department has taken steps to implement annual testing of patients at...
The National Institute for Health and Care Excellence’s guidance, Chronic kidney disease: Assessment and management [NG203], updated in November 2021, sets out the best practice for clinicians in the diagnosis and management of chronic kidney disease (CKD). The guidance covers monitoring for those patients at risk as well as pharmacological management and referral, where appropriate, and is available at the following link:
https://www.nice.org.uk/guidance/ng203
In addition to evidence-based guidance to support clinicians in diagnosing problems of the kidney, we are also working to detect people at risk of kidney disease through the NHS Health Check Programme. The programme, which is available for everyone between the ages of 40 and 74 years old who are not already on a chronic disease register, assesses people’s health and risk of developing certain health problems. Using this information, patients are supported in making behavioural changes and accessing treatment which helps to prevent and detect kidney disease earlier.
We are investing in new delivery models for the NHS Health Check, including nearly £17 million for the development and roll-out of an innovative new national and digital NHS Health Check, which will be rolled out this spring, and will give people a choice about where and when to have a check.
The UK National Screening Committee (UK NSC) reviewed CKD and glomerulonephritis in 2011 and concluded that a population-wide screening programme would not be recommended, and has not looked at the evidence for a targeted programme. The UK NSC can be alerted to any new peer-reviewed evidence published which may suggest the case for a new screening programme. Proposals to change or review a topic early can be submitted via the UK NSC’s annual call, which will open in July 2024.
To ask the Secretary of State for Health and Social Care, with reference to the report entitled Let’s talk kidneys: Opportunities for early intervention in chronic kidney disease, published by Kidney Care UK on 13 December 2023, if she will ensure that the Major Conditions Strategy includes (a) increased testing...
To ask the Secretary of State for Health and Social Care, with reference to the report entitled Let’s talk kidneys: Opportunities for early intervention in chronic kidney disease, published by Kidney Care UK on 13 December 2023, if she will ensure that the Major Conditions Strategy includes (a) increased testing...
The National Institute for Health and Care Excellence’s guidance, Chronic kidney disease: Assessment and management [NG203], updated in November 2021, sets out the best practice for clinicians in the diagnosis and management of chronic kidney disease (CKD). The guidance covers monitoring for those patients at risk as well as pharmacological management and referral, where appropriate, and is available at the following link:
https://www.nice.org.uk/guidance/ng203
In addition to evidence-based guidance to support clinicians in diagnosing problems of the kidney, we are also working to detect people at risk of kidney disease through the NHS Health Check Programme. The programme, which is available for everyone between the ages of 40 and 74 years old who are not already on a chronic disease register, assesses people’s health and risk of developing certain health problems. Using this information, patients are supported in making behavioural changes and accessing treatment which helps to prevent and detect kidney disease earlier.
We are investing in new delivery models for the NHS Health Check, including nearly £17 million for the development and roll-out of an innovative new national and digital NHS Health Check, which will be rolled out this spring, and will give people a choice about where and when to have a check.
The UK National Screening Committee (UK NSC) reviewed CKD and glomerulonephritis in 2011 and concluded that a population-wide screening programme would not be recommended, and has not looked at the evidence for a targeted programme. The UK NSC can be alerted to any new peer-reviewed evidence published which may suggest the case for a new screening programme. Proposals to change or review a topic early can be submitted via the UK NSC’s annual call, which will open in July 2024.
To ask the Secretary of State for Health and Social Care, with reference to the report entitled Let’s talk kidneys: Opportunities for early intervention in chronic kidney disease, published by Kidney Care UK on 13 December 2023,, what steps her Department is taking to help ensure patients at risk of...
To ask the Secretary of State for Health and Social Care, with reference to the report entitled Let’s talk kidneys: Opportunities for early intervention in chronic kidney disease, published by Kidney Care UK on 13 December 2023,, what steps her Department is taking to help ensure patients at risk of...
The National Institute for Health and Care Excellence’s guidance, Chronic kidney disease: Assessment and management [NG203], updated in November 2021, sets out the best practice for clinicians in the diagnosis and management of chronic kidney disease (CKD). The guidance covers monitoring for those patients at risk as well as pharmacological management and referral, where appropriate, and is available at the following link:
https://www.nice.org.uk/guidance/ng203
In addition to evidence-based guidance to support clinicians in diagnosing problems of the kidney, we are also working to detect people at risk of kidney disease through the NHS Health Check Programme. The programme, which is available for everyone between the ages of 40 and 74 years old who are not already on a chronic disease register, assesses people’s health and risk of developing certain health problems. Using this information, patients are supported in making behavioural changes and accessing treatment which helps to prevent and detect kidney disease earlier.
We are investing in new delivery models for the NHS Health Check, including nearly £17 million for the development and roll-out of an innovative new national and digital NHS Health Check, which will be rolled out this spring, and will give people a choice about where and when to have a check.
The UK National Screening Committee (UK NSC) reviewed CKD and glomerulonephritis in 2011 and concluded that a population-wide screening programme would not be recommended, and has not looked at the evidence for a targeted programme. The UK NSC can be alerted to any new peer-reviewed evidence published which may suggest the case for a new screening programme. Proposals to change or review a topic early can be submitted via the UK NSC’s annual call, which will open in July 2024.
To ask the Secretary of State for Health and Social Care, pursuant to the Answer of 23 January to Question 10306 on Cervical Cancer: Health Education, if she will make it her policy to provide smear tests for women aged 25 and younger who (a) request one and (b) are...
To ask the Secretary of State for Health and Social Care, pursuant to the Answer of 23 January to Question 10306 on Cervical Cancer: Health Education, if she will make it her policy to provide smear tests for women aged 25 and younger who (a) request one and (b) are...
Cervical screening is not recommended for women below the age of 25 years old, as cervical cancer is rare in under-25s. Screening at a younger age can lead to unnecessary and potentially harmful investigations and treatments.
Women of any age who are experiencing symptoms such as bleeding between periods or after sex, pain or discomfort during sex, or abnormal vaginal discharge should see their general practitioner. They may be offered a pelvic examination and referral to colposcopy or gynaecology if needed.
To ask the Secretary of State for Health and Social Care, how many pharmacies have bought coded stamped lateral flow tests for collection by immunocompromised patients from 17 November.
To ask the Secretary of State for Health and Social Care, how many pharmacies have bought coded stamped lateral flow tests for collection by immunocompromised patients from 17 November.
The NHS Lateral Flow Device (LFD) tests supply service for patients potentially eligible for COVID-19 treatments was launched on 6 November 2023. Information about how many pharmacies have supplied LFD tests will not be available until pharmacies have claimed for the delivery of the service.
To ask the Secretary of State for Health and Social Care, if he will make it his policy to ensure that results from privately purchased rapid lateral flow tests for Covid-19 can be reported on the Gov.uk website.
To ask the Secretary of State for Health and Social Care, if he will make it his policy to ensure that results from privately purchased rapid lateral flow tests for Covid-19 can be reported on the Gov.uk website.
Lateral flow device (LFD) tests which are privately purchased cannot currently be registered on GOV.UK and there is no requirement to report these results to the provider. There are currently no plans to change the policy on reporting private COVID-19 test results.
For citizens that are eligible to order free LFD tests from the UK Health Security Agency, these tests can still be registered on GOV.UK.
To ask the Secretary of State for Health and Social Care, if he will make it his policy to require breast cancer screening invitations to include an appointment time.
To ask the Secretary of State for Health and Social Care, if he will make it his policy to require breast cancer screening invitations to include an appointment time.
During the COVID-19 pandemic, timed appointments were no longer deemed feasible for the recovery of services, based on expert opinion. Services moved to an ‘open appointment’ system where women contacted services to agree a time slot suitable for them.
All services have now recovered, and some have returned to the timed appointments. Several services have retained an open system as they have noted increased uptake and patient satisfaction.
NHS England have commissioned a series of national evaluative projects being led by Professor Stephen Duffy and his team at Queen Mary’s University of London, to provide evidence to inform NHS England on the most appropriate invitation methodology to underpin future pathway changes and improvements in the national screening programme. These are due to report March 2024.
To ask the Secretary of State for Health and Social Care, what assessment he has made of the adequacy of the covid-19 wastewater testing programme in England on monitoring the rate of infection.
To ask the Secretary of State for Health and Social Care, what assessment he has made of the adequacy of the covid-19 wastewater testing programme in England on monitoring the rate of infection.
Wastewater monitoring for COVID-19 and its variants was stood down in April 2022 in response to the Government policy change to Living with COVID-19. Therefore, in England, there has been no wastewater testing for COVID-19 within the last 12 months.
Wastewater sampling, and subsequent analysis, has the benefit of detecting the virus regardless of whether people have symptoms or whether they are tested.
Environmental factors such as rainfall dilution can influence the detection of variants in wastewater. Therefore, low total detections on some days may not be reflective of low community infection levels.
Wastewater monitoring cannot currently estimate the number of cases associated with a detection with a high degree of confidence. For example, in small catchment areas it is possible, but highly unlikely, that a detection is due to a single individual. In larger catchment areas detections are likely to be related to a higher number of cases in the population.
To ask the Secretary of State for Health and Social Care, what representations he has had from (a) medical professionals and (b) patients groups on access to free lateral flow tests for (i) immunocompromised patients and (ii) close contacts of immunocompromised patients after October 2023.
To ask the Secretary of State for Health and Social Care, what representations he has had from (a) medical professionals and (b) patients groups on access to free lateral flow tests for (i) immunocompromised patients and (ii) close contacts of immunocompromised patients after October 2023.
Information on all representations from medical professionals and patients groups about access to free lateral flow tests for immunocompromised patients and close contacts of immunocompromised patients after October 2023, could only be provided at a disproportionate cost.
As set out in the Written Ministerial Statement on 30 March 2023, in 2023/24 the Government will maintain a range of capabilities to protect those at higher risk of severe illness from COVID-19. Given the continued effectiveness of vaccines and improved treatments, for most people there is a much lower risk of severe illness compared to earlier in the pandemic.
Appropriate levels of testing remain to support diagnosis for clinical care and treatment and to protect very high-risk individuals and settings. Those who are clinically extremely vulnerable and immunocompromised are part of the group who are eligible for COVID-19 treatments in the community enabling them easy access to anti-viral treatments.
Testing of symptomatic staff remains in a very limited number of high-risk settings to protect particularly vulnerable people, such as in some hospices and some NHS settings where staff work with profoundly immunocompromised patients. Information on testing in these settings is available at the following link: https://www.gov.uk/guidance/covid-19-testing-during-periods-of-low-prevalence
The leaked WhatsApp messages from the then Health and Social Care Secretary, the right hon. Member for West Suffolk (Matt Hancock), showed that, despite a shortage of covid tests in September 2020, one of the Minister’s advisers sent a test to the home of the right hon. Member for North...
The leaked WhatsApp messages from the then Health and Social Care Secretary, the right hon. Member for West Suffolk (Matt Hancock), showed that, despite a shortage of covid tests in September 2020, one of the Minister’s advisers sent a test to the home of the right hon. Member for North...
To ask the Secretary of State for Health and Social Care, whether his Department plans to take steps to introduce covid-19 testing (a) for people admitted to hospital who are immunocompromised and (b) in other high-risk settings.
To ask the Secretary of State for Health and Social Care, whether his Department plans to take steps to introduce covid-19 testing (a) for people admitted to hospital who are immunocompromised and (b) in other high-risk settings.
As set out in the Living with COVID-19 strategy published last February, we are continuing to offer some COVID-19 testing for those in high-risk settings. Currently, symptomatic or immunocompromised patients who are admitted to hospital for maternity or emergency care receive a Polymerase Chain Reaction test. Residents, patients, or staff in high-risk settings who are symptomatic are also tested and testing can be used to manage an outbreak in these settings.
On 3 November, I tabled a series of written parliamentary questions asking Ministers to publish the protocols for screening, immunisation and prevention in relation to outbreaks of infectious diseases at Manston and other immigration centres, as well as the protocols for sharing information with directors of public health and local...
On 3 November, I tabled a series of written parliamentary questions asking Ministers to publish the protocols for screening, immunisation and prevention in relation to outbreaks of infectious diseases at Manston and other immigration centres, as well as the protocols for sharing information with directors of public health and local...