1-20 of 67 results for subject:Dermatitis
Librarians' tools
- Search time
- 0.231 seconds
- Solr query time
- 0.002 seconds
- Search query
- subject:Dermatitis
- We searched for
- subject_t:Dermatitis OR subject_t:Eczema OR subject_ses:433877
Type
House
Session
Year
Department
Member
More
Primary member
More
Answering member
More
Legislative stage
Legislation
Subject
More
Publisher
To ask His Majesty's Government what steps they are taking to improve awareness and recognition of chronic spontaneous urticaria among primary care professionals to support earlier diagnosis and referral.
To ask His Majesty's Government what steps they are taking to improve awareness and recognition of chronic spontaneous urticaria among primary care professionals to support earlier diagnosis and referral.
To ask His Majesty's Government what steps they are taking to improve awareness and recognition of chronic spontaneous urticaria among patients and people impacted by the condition.
To ask His Majesty's Government what steps they are taking to improve awareness and recognition of chronic spontaneous urticaria among patients and people impacted by the condition.
To ask His Majesty's Government what assessment they have made of the impact of delayed diagnosis and delayed escalation of care for people with atopic dermatitis, particularly on sleep, education, employment and mental health.
To ask His Majesty's Government what assessment they have made of the impact of delayed diagnosis and delayed escalation of care for people with atopic dermatitis, particularly on sleep, education, employment and mental health.
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 assessment they have made of waiting times for people with moderate-to-severe atopic dermatitis to access specialist dermatology care.
To ask His Majesty's Government what assessment they have made of waiting times for people with moderate-to-severe atopic dermatitis to access specialist dermatology 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 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 reduce prescribing restrictions and ensure consistent access to appropriate emollients for patients living with atopic dermatitis.
To ask His Majesty's Government what steps they are taking to reduce prescribing restrictions and ensure consistent access to appropriate emollients for patients living with atopic dermatitis.
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 the Secretary of State for Science, Innovation and Technology, how much funding the Government provided for research into atopic dermatitis in the 2023-24 financial year; and which public bodies provided that funding.
To ask the Secretary of State for Science, Innovation and Technology, how much funding the Government provided for research into atopic dermatitis in the 2023-24 financial year; and which public bodies provided that funding.
The Department of Health and Social Care (DHSC) invests £1.5 billion per year on health research through the National Institute for Health and Care Research (NIHR).
The NIHR supports and delivers research in the following many aspects skin and dermatological conditions including linking genetic research and personalised medicine with common skin diseases such as acne, drug reactions, eczema, and psoriasis and skin cancers including melanoma, squamous cell carcinoma and basal cell carcinoma. It also supports research into skin infections such as herpes simplex, fungal infections, impetigo and cellulitis along with children’s skin disorders and rare skin diseases.
UKRI delivers a substantial portfolio of researcher-led projects and strategic investments. Dermatology research supported by MRC covers the breadth of skin and skin associated diseases including inflammatory skin disease, atopic dermatitis (eczema) and skin cancer research. This includes basic biological mechanisms of disease to early-stage interventions such as diagnostics and treatment development.
In addition to the individual awards stated below, MRC supports other active research grants in the noted areas through strategic awards made to MRC Research Units.
- The Translational skin immunology programme at the MRC Translational Immune Discovery Unit at the University of Oxford investigates the role of T-cells in Inflammatory skin diseases such as psoriasis.
- The Translational Melanoma Research Group from the MRC Human Genetics Unit at the University of Edinburgh is investigating the mechanisms of melanoma development & drug resistance through their programme Targeting developmental cell states in melanoma
Details of UKRI and NIHR funding on specific areas is provided in the table below:
| NIHR | UKRI |
Acne | NIHR allocated £2,148,574.06 for research concerning acne research in 2023-24. | UKRI did not commit any specific funding for acne research in 2023-24. |
Alopecia | NIHR did not allocate any funds for research concerning alopecia research during 2023-24 | UKRI have committed £215,666 for alopecia research for a 3 year period commencing March 2024. |
Psoriasis | NIHR allocated £858,946.12 for research concerning psoriasis research in 2023-24. | UKRI have committed £300, 266 for psoriasis research for a 3 year period commencing February 2024 . |
Pemphigus | NIHR did not allocate any funds for research concerning pemphigus research during 2023-24 | UKRI did not commit any specific funding for pemphigus research in 2023-24. |
Atopic Dermatitis | NIHR allocated £2,045,996 for research concerning atopic dermatitis research in 2023-24. | UKRI have committed £404,880 for atopic dermatitis research for a 3 year period commencing June 2023. |
Epidermolysis Bullosa | NIHR did not allocate any funds for research concerning epidermolysis bullosa research during 2023-24 | UKRI did not commit any specific funding for epidermolysis bullosa research in 2023-24. |
Hidradenitis Suppurativa | NIHR has not allocated any funds for research concerning hidradenitis suppurativa research during 2023-24 | UKRI did not commit any specific funding for hidradenitis suppurativa research in 2023-24. |
Scleroderma | NIHR allocated £155,575 for research concerning scleroderma research in 2023-24. | UKRI did not commit any specific funding for scleroderma research in 2023-24. |
Rosacea | NIHR did not allocate any funds concerning rosacea research during 2023-24 | UKRI did not commit any specific funding for rosacea research in 2023-24. |
Vitiligo | NIHR did not allocate any funds for research concerning vitiligo research during 2023-24 | UKRI did not commit any specific funding for vitiligo research in 2023-24. |
Basal Cell Carcinoma | NIHR did not allocate any funds concerning basal cell carcinoma research during 2023-24 | UKRI did not commit any specific funding for basal cell carcinoma research in 2023-24. |
Squamous Cell Carcinoma | NIHR allocated £1,467,858 for research concerning squamous cell carcinoma research in 2023-24 | UKRI did not commit any specific funding for squamous cell carcinoma research in 2023-24. |
Melanoma | NIHR allocated £1,167,536 for research concerning melanoma research in 2023-24 | UKRI have committed £176,114 for melanoma research between March 24 and August 25. |
Actinic Keratosis | NIHR did not allocate any funds concerning actinic keratosis research during 2023-24 | UKRI did not commit any specific funding for actinic keratosis research in 2023-24. |
To ask the Secretary of State for Defence, how many people were rejected from joining the Armed Forces due to dermatitis in each year since 2010.
To ask the Secretary of State for Defence, how many people were rejected from joining the Armed Forces due to dermatitis in each year since 2010.
This information is not held centrally and could be provided only at disproportionate cost.
To ask the Secretary of State for Health and Social Care, if she will have discussions with NICE on developing (a) national guidelines and (b) quality standards for the management of severe eczema in adults.
To ask the Secretary of State for Health and Social Care, if she will have discussions with NICE on developing (a) national guidelines and (b) quality standards for the management of severe eczema in adults.
The Department regularly holds discussions with colleagues in the National Institute for Health and Care Excellence (NICE) about its guidelines programme. NICE has reviewed its guideline portfolio to identify topics that it thinks will add the most value to the health and care system, considering key factors such as clinical benefit, cost effectiveness, the potential to increase productivity and support workforce issues and the potential to address health inequalities.
Atopic dermatitis (eczema) in young people and adults is one of the topics on which NICE will stop work for the time being to allow them to focus on key priorities. Topics that have been stopped will be reconsidered by NICE’s prioritisation board which is being established in Spring 2024 by its chief medical officer.
To ask the Secretary of State for Health and Social Care, whether he has made an assessment of the implications for his policies of the report by Demos entitled The Costs of Atopic Dermatitis published April 2023.
To ask the Secretary of State for Health and Social Care, whether he has made an assessment of the implications for his policies of the report by Demos entitled The Costs of Atopic Dermatitis published April 2023.
Whilst we have made no specific assessment of Demos’ report, or the economic impact of atopic dermatitis on people living with the condition, or on the National Health Service and the wider economy, we recognise the impact that skin conditions can have on all aspects of life and the importance of ensuring that those affected receive the treatment and support that they need.
To support people with skin conditions, such as atopic dermatitis, the Getting it Right First Time (GIRFT) national report for dermatology makes specific recommendations to ensure early access to diagnosis and treatment across England.
GIRFT is a national programme designed to improve the treatment and care of patients through in-depth review of services, benchmarking and presenting a data-driven evidence base to support change.
A limited range of products, including emollient bath oils, wash creams and moisturising creams and lotions can be prescribed in line with advice from the Advisory Committee on Borderline Substances. It is for the general practitioner and other responsible clinicians to work with their patient and decide on the course of treatment, with the provision of the most clinically appropriate care for the individual always being the primary consideration. Clinicians are accountable for their prescribing decisions, both professionally and to their service commissioners.
To ask the Secretary of State for Health and Social Care, how many eczema cases were diagnosed in 2022.
To ask the Secretary of State for Health and Social Care, how many eczema cases were diagnosed in 2022.
The information is not collected in the format requested.
To ask the Secretary of State for Health and Social Care, what steps his Department is taking to ensure that (a) people with eczema are (i) evaluated and (ii) treated by specialists and (b) patient-initiated follow-ups are adopted across the health system.
To ask the Secretary of State for Health and Social Care, what steps his Department is taking to ensure that (a) people with eczema are (i) evaluated and (ii) treated by specialists and (b) patient-initiated follow-ups are adopted across the health system.
The National Institute for Health and Care Excellence (NICE) publishes a range of guidance on atopic dermatitis, also known as eczema, and other skin conditions for commissioners and healthcare professionals, with recommendations for diagnosis and referral. The guideline for atopic dermatitis in children aged under 12 years is being updated with draft recommendations published in June 2023. NHS England has made a referral to NICE to develop new guidance on atopic dermatitis in adults.
Whilst NICE guidelines are not mandatory, the Government would expect patients presenting with atopic dermatitis symptoms to be managed according to clinical need and in line with all current guidance.
To ask the Secretary of State for Health and Social Care, what steps he is taking with Cabinet colleagues to help support eczema patients with increases in the cost of living.
To ask the Secretary of State for Health and Social Care, what steps he is taking with Cabinet colleagues to help support eczema patients with increases in the cost of living.
No one is excluded from the Government’s cost of living support as a consequence of a health condition or disability such as eczema. Those with needs arising from such a condition may be entitled to the full range of support depending on their circumstances, including access to an extra costs disability benefit such as the Personal Independence Payment.
In addition, for 2023/24, households on eligible means-tested benefits will get up to £900 in Cost-of-Living Payments. This will be split into three payments of around £300 each across the year.
We recognise that people’s mental and physical health are intrinsically linked, and people with long term physical health conditions, such as eczema, may also need emotional and psychological support. We are investing at least £2.3 billion of extra funding a year in expanding and transforming mental health services in England by March 2024. This will enable an extra two million people to be treated by mental health services within the National Health Service by March 2024.
Mental Health is one of the group of conditions included in the Department’s Major Conditions Strategy. The strategy will aim to identify actions in the areas of prevention, treatment, and long-term management of care to improve outcomes for individuals across the six major condition groups.
We have continued to expand NHS talking therapies services for all adults with common mental health problems. These services are accessible to all adults in England. People can be referred by a range of practitioners or refer themselves.
To ask the Secretary of State for Health and Social Care, what steps his Department is taking to provide (a) psychosocial and (b) other mental health support to eczema patients.
To ask the Secretary of State for Health and Social Care, what steps his Department is taking to provide (a) psychosocial and (b) other mental health support to eczema patients.
No one is excluded from the Government’s cost of living support as a consequence of a health condition or disability such as eczema. Those with needs arising from such a condition may be entitled to the full range of support depending on their circumstances, including access to an extra costs disability benefit such as the Personal Independence Payment.
In addition, for 2023/24, households on eligible means-tested benefits will get up to £900 in Cost-of-Living Payments. This will be split into three payments of around £300 each across the year.
We recognise that people’s mental and physical health are intrinsically linked, and people with long term physical health conditions, such as eczema, may also need emotional and psychological support. We are investing at least £2.3 billion of extra funding a year in expanding and transforming mental health services in England by March 2024. This will enable an extra two million people to be treated by mental health services within the National Health Service by March 2024.
Mental Health is one of the group of conditions included in the Department’s Major Conditions Strategy. The strategy will aim to identify actions in the areas of prevention, treatment, and long-term management of care to improve outcomes for individuals across the six major condition groups.
We have continued to expand NHS talking therapies services for all adults with common mental health problems. These services are accessible to all adults in England. People can be referred by a range of practitioners or refer themselves.
To ask the Secretary of State for Health and Social Care, what steps his Department is taking to train community healthcare professionals to (a) support and (b) provide appropriate referrals to specialist care for people with moderate to severe atopic eczema.
To ask the Secretary of State for Health and Social Care, what steps his Department is taking to train community healthcare professionals to (a) support and (b) provide appropriate referrals to specialist care for people with moderate to severe atopic eczema.
Training programmes for healthcare professionals must meet the standards set by the regulatory body for their profession. Whilst not all curricula may necessarily highlight a specific condition, they all nevertheless emphasise the skills and approaches a Health Care Practitioner must develop to ensure accurate and timely diagnoses and treatment plans for their patients.
The standard of training for health care professionals is the responsibility of the independent statutory health care regulatory bodies, which set the outcome standards expected at undergraduate level and approve courses, and higher education institutions which write and teach the curricula content that enables their students to meet the regulators’ outcome standards.
Individual employers are responsible for ensuring their staff are trained and competent to carry out their role, including ensuring staff are aware of care pathways and referral routes for those living with moderate to severe atopic eczema.
To ask the Secretary of State for Health and Social Care, whether his Department has made an assessment of the potential health impacts of Opzelura for patients on the treatment of vitiligo and eczema.
To ask the Secretary of State for Health and Social Care, whether his Department has made an assessment of the potential health impacts of Opzelura for patients on the treatment of vitiligo and eczema.
Opzelura (ruxolitinib), is currently not approved by the Medicines and Healthcare products Regulatory Agency (MHRA). The MHRA has noted that the European Medicines Agency’s Committee for Medicinal Products for Human Use issued a positive opinion for this on the 23 of February 2023 and is currently pending European Commission (EC) approval.
Should an application for Opzelura be received by the MHRA, we have processes in place to review this and, if appropriate, issue a licence in line with an EC decision.
To ask the Secretary of State for Health and Social Care, with reference to the Not Just Skin Deep report by Allergy UK published 22 Nov 2021, what steps his Department is taking to ensure that healthcare professionals have clear guidelines to help diagnose patients with atopic dermatitis.
To ask the Secretary of State for Health and Social Care, with reference to the Not Just Skin Deep report by Allergy UK published 22 Nov 2021, what steps his Department is taking to ensure that healthcare professionals have clear guidelines to help diagnose patients with atopic dermatitis.
Integrated care boards are responsible for working with local communities to understand the needs of the local population and to commission services to meet those needs, including for patients with atopic dermatitis and other skin conditions.
To ask the Secretary of State for Health and Social Care, with reference to Allergy UK's report entitled Not Just Skin Deep: Getting under the skin of eczema, published in November 2022, what steps her Department is taking to improve guidance on diagnosing patients with atopic dermatitis.
To ask the Secretary of State for Health and Social Care, with reference to Allergy UK's report entitled Not Just Skin Deep: Getting under the skin of eczema, published in November 2022, what steps her Department is taking to improve guidance on diagnosing patients with atopic dermatitis.
The National Institute for Health and Care Excellence (NICE) publishes guidance on atopic dermatitis and other skin conditions, which commissioners are expected to take into account. The guideline for atopic dermatitis in those aged under 12 years old is being updated, with draft recommendations to be published in April 2023. A referral has also been made to NICE to develop a new guidance on atopic dermatitis in adults.
Integrated care boards (ICB) are responsible for working with local commissioners and organisations to understand the needs of the local population and commission services to meet those needs, including for patients with atopic dermatitis and other skin conditions. ICBs have a legal duty to have due regard to NICE’s guidelines.
To ask the Secretary of State for Health and Social Care, if she will make an estimate of the potential number of atopic dermatitis patients who are eligible for biologic treatments but are not currently prescribed them.
To ask the Secretary of State for Health and Social Care, if she will make an estimate of the potential number of atopic dermatitis patients who are eligible for biologic treatments but are not currently prescribed them.
No specific estimate has been made as the information requested is not collected.
The National Institute for Health and Care Excellence (NICE) has made recommendations on the use of the biological medicines dupilumab and tralokinumab for the treatment of atopic dermatitis. National Health Service commissioners in England are legally required to make funding available for NICE-recommended treatments to allow clinicians to prescribe to patients, normally within three months of NICE’s guidance.
To ask the Secretary of State for Health and Social Care, how many people have been diagnosed with eczema in the last three years.
To ask the Secretary of State for Health and Social Care, how many people have been diagnosed with eczema in the last three years.
The information is not collected in the format requested.