Asked by: Alex Ballinger (Labour - Halesowen)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what steps his Department is taking to ensure equal access to diagnosis of prostate cancer.
Answered by Ashley Dalton - Parliamentary Under-Secretary (Department of Health and Social Care)
NHS England is taking steps to raise awareness of the symptoms of prostate cancer, where there are opportunities to do so. To address disparities and find ways to better detect prostate cancer, we have invested £16 million in the TRANSFORM trial, aimed at helping to find a way of catching prostate cancer in men, even if they are not displaying any symptoms. This research will ensure that one in ten participants are black men to address identified inequalities.
Asked by: Alex Ballinger (Labour - Halesowen)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what steps he is taking to address the shortages in Pancreatic enzyme replacement medication.
Answered by Karin Smyth - Minister of State (Department of Health and Social Care)
The Department is continuing to engage with all suppliers of pancreatic enzyme replacement therapy (PERT) to boost production to mitigate the supply issue. Increased volumes of PERT are expected for 2025, and specialist importers have sourced unlicensed stock to assist in covering the gap in the market. In December 2024, the Department issued further management advice to healthcare professionals. This includes actions for clinicians to consider unlicensed imports when licensed stock is unavailable and for integrated care boards to ensure local mitigation plans are put in place and implemented. The Department, in collaboration with NHS England, has created a public facing page to include the latest update on PERT availability and easily accessible prescribing advice.
Asked by: Alex Ballinger (Labour - Halesowen)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, whether he has made an assessment of the potential merits of mandatory training for (a) psychiatrists, (b) psychiatric nurses and (c) social workers on legal obligations under section 117 of the Mental Health Act 1983.
Answered by Stephen Kinnock - Minister of State (Department of Health and Social Care)
Section 117 of the Mental Health Act 1983 requires local social services authorities and National Health Service commissioners to provide or arrange for the provision of aftercare to adults or children detained in hospital for treatment under section 3, 37, 45A, or transferred under section 47 or 48 of the Act who then leave hospital. No assessment of patients is required to determine whether they are eligible for s117 aftercare although professionals would of course be expected to work with a patient to understand their individual needs.
There are no plans at present to introduce any such mandatory training or require mandatory recording of the number of people eligible for section 117 who local social services authorities and NHS commissioners have responsibility for.
Asked by: Alex Ballinger (Labour - Halesowen)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, whether his Department has made an assessment of the potential merits of introducing a mandatory and formal way for recording if and when patients have had an assessment for section 117 aftercare.
Answered by Stephen Kinnock - Minister of State (Department of Health and Social Care)
Section 117 of the Mental Health Act 1983 requires local social services authorities and National Health Service commissioners to provide or arrange for the provision of aftercare to adults or children detained in hospital for treatment under section 3, 37, 45A, or transferred under section 47 or 48 of the Act who then leave hospital. No assessment of patients is required to determine whether they are eligible for s117 aftercare although professionals would of course be expected to work with a patient to understand their individual needs.
There are no plans at present to introduce any such mandatory training or require mandatory recording of the number of people eligible for section 117 who local social services authorities and NHS commissioners have responsibility for.
Asked by: Alex Ballinger (Labour - Halesowen)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what steps his Department is taking to tackle medication shortages.
Answered by Karin Smyth - Minister of State (Department of Health and Social Care)
We have inherited ongoing global supply problems that continue to impact medicine availability. We know how frustrating and distressing this can be for patients, and we are working closely with industry, the National Health Service, manufacturers, and other partners in the supply chain to resolve issues as quickly as possible, to make sure patients can access the medicines they need.
Medicine supply chains are complex, global, and highly regulated, and there are a number of reasons why supply can be disrupted, many of which are not specific to the United Kingdom and outside of Government control, including manufacturing difficulties, access to raw materials, sudden demand spikes or distribution issues, and regulatory issues. There are approximately 14,000 licensed medicines and the overwhelming majority are in good supply.
While we can’t always prevent supply issues from occurring, we have a range of well-established processes and tools to manage them when they arise and mitigate risks to patients. These include close and regular engagement with suppliers, use of alternative strengths or forms of a medicine to allow patients to remain on the same product, expediting regulatory procedures, sourcing unlicensed imports from abroad, adding products to the restricted exports and hoarding list, use of Serious Shortage Protocols, and issuing NHS communications to provide management advice and information on the issue to healthcare professionals, including pharmacists, so they can advise and support their patients.
Asked by: Alex Ballinger (Labour - Halesowen)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what steps his Department is taking to reduce medication wastage.
Answered by Karin Smyth - Minister of State (Department of Health and Social Care)
Medicine wastage can be reduced by ensuring that medicines are not overprescribed and those that are prescribed are taken as intended, resulting in the best outcomes for patients.
Overprescribing can be addressed by taking a shared decision-making approach and optimising a person's medicines, ensuring that patients are prescribed the right medicines, at the right time, in the right doses. The National Health Service is driving changes in this area by:
In addition, the New Medicines Service in Community Pharmacy supports patients with newly prescribed medication for long term conditions in understanding how to take the medication effectively, and improves adherence and health gains.
Asked by: Alex Ballinger (Labour - Halesowen)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what steps his Department is taking to improve early detection of breast cancer in women under 50 who do not routinely undergo mammogram screenings.
Answered by Andrew Gwynne
Improving early diagnosis of cancer, including breast cancer, is a priority for NHS England. We will improve cancer survival rates and hit all National Health Service cancer waiting time targets, so that no patient waits longer than they should.
Screening is also crucial to improving early diagnosis, and current United Kingdom guidelines recommend that women with a moderate or high risk of breast cancer because of their family history should start having screening mammograms every year in their forties. The National Institute for Health and Care Excellence’s guidance on the management of people with a family history of breast cancer was introduced in 2004, and has changed over time. The current version of this guidance is available at the following link:
https://www.nice.org.uk/guidance/cg164
We currently do not screen those younger than 50 years old for breast cancer due to the lower risk of women under this age developing breast cancer, and the fact that women below 50 years old tend to have denser breast tissue, which reduces the ability of getting an accurate mammogram. It may also increase the risk of overtreatment and distress for women who do not have breast cancer, but would be subject to invasive and painful medical treatments and diagnostic tests.