The UK is losing the ageing medicine battle

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Ageing medicine specialist, Dr Oskar Wenbar, explores the impacts of the UK’s hesitancy to tackle age-related health conditions, and what can be done to stem the flow of ageing medicine PhDs seeking opportunities abroad.


Through my years in academia and now working in tech-enabled healthcare delivery, I’ve noticed a concerning trend – the UK is steadily losing its ageing medicine specialists to opportunities in the US. Most of the PhDs in this field end up going to America – I’ve seen this within my own alumni group – and with universities facing funding cuts and reduced positions, this brain drain will most likely accelerate.

This actually reflects a fundamental difference in how these countries view and treat ageing – and as retirement age increases and our population ages, the corresponding expertise gap will become a critical issue for UK healthcare. When you look at the numbers, each patient properly treated with ageing medicine can save the NHS thousands of pounds annually – but in the UK, we’re losing the very specialists who can properly deliver this care.

Here is my take on what’s happening and what we can do to fix this situation.

A perception chasm

The UK and US have starkly different approaches to ageing medicine. When UK patients visit their GP with age-related symptoms, they’re often told “it’s just a normal part of ageing” with no treatment offered. In contrast, the US healthcare system increasingly views ageing as a condition that can be actively managed and treated. This growing cultural difference profoundly impacts both medical research and patient care. Here’s an example: while the UK readily provides hormone therapy to 2.6 million women for menopause, we have a major blind spot when it comes to men’s ageing. Research shows nearly 40 per cent of men over 45 would benefit from testosterone therapy based on their blood levels, yet less than 1 per cent receive treatment.

This isn’t because the treatment doesn’t work – rather, it stems partly from cultural stigma. While hormone therapy is widely accepted for women, testosterone treatment for ageing men remains taboo in the UK, despite its proven benefits for man age-related health issues such as muscular dysfunction. In the US, by comparison, these treatments are openly discussed and more readily available.

The real cost to patients and the NHS

Alongside the health implications, the UK’s hesitancy around ageing medicine carries significant economic costs. Research in health economics reveals that each patient receiving appropriate testosterone therapy saves the NHS approximately £3,000 annually. These savings derive from multiple health improvements – reduced obesity rates, lower cardiovascular risk, and better mental health outcomes. The benefits extend far beyond what most people associate with testosterone treatment.

The therapy plays a crucial role in maintaining muscle health through specific biological mechanisms. Research shows that testosterone therapy increases the number of satellite cells in muscles – specialised stem cells that are crucial for muscle regeneration and repair. These satellite cells remain present as people age, enabling better muscle maintenance and regeneration well into later life. Without proper hormone levels, many patients develop sarcopenia – age-related muscle degradation that triggers a downward health spiral. Studies show that up to 28 per cent of elderly males and 12 per cent of women will develop clinical sarcopenia. Once people become sedentary due to muscle loss, their overall health tends to decline rapidly, leading to increased cardiovascular risk and overall mortality. By maintaining healthy testosterone levels, we can help people stay mobile and independent well into their 60s, 70s, and 80s.

The prevention gap

The US healthcare system takes a markedly different approach, emphasising prevention rather than just treatment. This is visible in how they handle metabolic health; American doctors often prescribe metformin early on to prevent diabetes and maintain healthy blood sugar levels. In contrast, the UK system typically waits until a disease is fully developed before intervening.

This delayed intervention is particularly problematic because we know testosterone decline begins much earlier than most realise. Research shows levels start decreasing from age 25, with the steepest decline occurring between ages 30-40. By age 35, men typically have only about 76 per cent of the testosterone they had at 25. Yet our system typically waits until symptoms become severe before considering treatment.

This reactive approach can have cascading negative effects on ageing patients. Weight gain illustrates this perfectly: as someone gains weight, they become less mobile and exercise less, which dramatically increases their cardiovascular risk. For men, this creates an additional problematic cycle – excess fat tissue converts testosterone to oestrogen, leading to even lower testosterone levels. This in turn causes further muscle loss and decreased metabolic rate, often culminating in metabolic syndrome. Instead of preventing this cycle, our current system often waits until these issues become serious health problems before taking action.

Why specialists leave

70 per cent of UK PhDs leave academia and many of our ageing medicine PhDs choose to relocate to the United States. The situation in UK universities continues to deteriorate, with ongoing funding cuts leading to fewer academic positions. A recent report from the Office for Students (OfS) warns that 40 per cent of UK universities will be in financial deficit this year.

Additonally, when specialists leave, their workload is simply redistributed among remaining staff rather than new experts being hired. This creates a self-perpetuating problem; without a robust market for ageing medicine in the UK, specialists are naturally drawn to the US, where there’s both stronger economic opportunity and greater cultural acceptance of their work. Why stay in a system that doesn’t fully recognise your expertise when you can practice in one that does?

Reversing the brain drain: what the UK must do now

To address this growing problem, we need to tackle the cultural stigma around ageing medicine in the UK. By increasing funding and training GPs to better recognise age-related conditions, we can create the market needed to retain expertise here.

We also need to embrace technologies that enable regular health monitoring. New capabilities allow patients to track changes over time, enabling early intervention rather than waiting for conditions to worsen. Better utilisation of this data can help develop personalised treatment plans tailored to individual needs.

Of course I’m not talking about advocating unnecessary treatments, but we have to recognise ageing as a manageable condition and give our retirement the necessary support to maintain quality of life as they age. As retirement ages rise and people work longer, often in sedentary jobs, addressing these issues becomes critical for both individual wellbeing and healthcare system sustainability.

Every year we delay, we lose more specialists to markets that better value their expertise, and our growing ageing UK population suffers. The technology and knowledge exist – what’s missing is the cultural shift to implement them effectively. Addressing these issues becomes increasingly important for both individual wellbeing and our healthcare system’s sustainability.


About the author: Dr Oskar Wenbar holds a PhD in Ageing Medicine from the University of East Anglia. His unique background spans clinical pharmacy, academic research, and health technology, giving him firsthand insight into both the research and practical aspects of ageing medicine. His published research on hormone treatments and muscle health in ageing populations has appeared in the Journal of Cachexia, Sarcopenia, and Muscle, and he has observed the brain drain phenomenon both through his academic network and as a healthcare technology leader. He is also the COO and co-founder of Evaro, a digital health platform revolutionising access to healthcare.

 

New national data shows improved respiratory outcomes with digital therapeutics

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Toolkit has driven significant reductions in reliever inhaler usage among asthma and COPD users, with biggest improvements seen in socioeconomically deprived areas.


A respiratory digital therapeutics toolkit is improving outcomes and reducing health inequalities for people with asthma and chronic obstructive pulmonary disease (COPD) in Wales.

The toolkit, which has reached full adoption across 100 per cent of GP practices and hospitals in NHS Wales, is providing a personalised, digital care plan that empowers hundreds of thousands of people to take control of their condition and stay well in the community.

Professor Simon Barry, National Respiratory Clinical Lead at NHS Wales (2016-2024), explained the impact the toolkit is having at a national scale: “Overall, we’re seeing patients showing a significant improvement in wellness scores in as little as three months. The biggest improvement is among patients using the asthma app for four months or more who are seeing their wellness score increase by 41 per cent. Users in socioeconomically deprived areas, and young people are seeing the greatest improvements in their Royal College of Physicians (RCP) 3-questions score.”

In addition, the toolkit has driven significant reductions in the use of reliever inhalers, an important marker of disease control:

  • Asthma app users have a statistically significant improvement in their reliever inhaler usage, with 35 per cent having improved reliever use within one year, and 20 per cent of patients going from some reliever use to no reliever use.
  • COPD app users’ reliever use improved after one year, with the percentage of users making use of relievers decreasing substantially from 67 per cent to 38 per cent.
  • Patients using the app are 42 per cent more likely to be using Dry Powder Inhalers (DPIs) than the general population, accelerating the NHS Wales priority to increase the proportion of low global-warming potential inhalers (DPIs) used vs pressurised Metered Dose Inhalers
  • Improvements are particularly pronounced in socioeconomically deprived areas.

The successful rollout has enabled many more outcome improvements, including reductions in GP visits and A&E admissions to alleviate pressure on overstretched services. The Respiratory Health Improvement Group (RHIG) in Wales will present new national datasets at an upcoming event, showcasing years of progress and population-level improvements.

Chris Davies, Principal and CEO at The Institute of Clinical Science and Technology, said: “Unfortunately, chronic diseases are common and expensive. Right now, £7 in every £10 of UK health and social expenditure goes toward chronic disease management, so it’s time for a new approach. We are delighted to work alongside NHS Wales in transitioning from traditional healthcare delivery to a patient-driven, digital-first model that eases the pressure on the healthcare system and future-proofs the NHS. This approach enables individuals across large populations to have better agency, better empowerment and more confidence when they navigate their health.”

Co-produced with patients, policymakers and clinical experts from within stakeholder groups, including the National Respiratory Audit Programme (NRAP), Asthma and Lung UK (ALUK), NHS Wales and NHS England, the toolkit uses the proven COM-B (Capability, Opportunity, Motivation-Behaviour) model to drive behaviour change. The app provides tailored support, including a personalised care plan and progress tracking, to help individuals manage their health.

The toolkit is expanding to other disease groups, offering a scalable model to meet rising care demand without overburdening healthcare professionals.

Members of the Respiratory Health Improvement Group (RHIG) in Wales will outline how the successful outcomes were achieved across Wales during a webinar on 13 March, chaired by Dr Lia Ali, Clinical Advisor, NHS Transformation Directorate for NHS England. Join the National Transformation of Respiratory Outcomes through Digital Therapeutics event by registering to attend here.

Millions to benefit from expanded Universal Care Plan, improving choice and care

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The expansion of the Universal Care Plan will see new planning sections added for patients with dementia, frailty, learning disabilities and autism, boosting choice and personalised care for patients in the capital.


Millions of patients across London will now receive improved, personalised healthcare as part of a major expansion of the Universal Care Plan (UCP), a shared care planning solution powered by Better. The move marks a major step towards a more holistic, personalised approach to healthcare planning, ensuring patients receive coordinated care that aligns with their individual needs, preferences, and goals.

Enhancing care for more patients

The expansion beyond the UCP’s initial focus on end-of-life and palliative care planning introduces new care planning sections for patients with dementia, frailty, learning disabilities, and autism. It also includes enhanced support for children and young people, as well as contingency planning for carers. This follows an earlier expansion to support people with sickle cell disease.

“This latest expansion moves us beyond disease-specific planning to a truly personalised care and support plan, where what matters to a patient is just as important as what is the matter with them,” said Nick Tigere, Head of the UCP Programme.

Improving patient outcomes and NHS efficiency

The UCP has already demonstrated success in improving outcomes for end-of-life care patients, with 70 per cent achieving their preferred place of death, compared to the national average of 50-55 per cent. Additionally, unplanned hospital admissions are reduced to 30 per cent, significantly lower than the national average of 46 per cent.

By providing a single, integrated care plan, the UCP streamlines care for patients with multiple long-term conditions, ensuring a more coordinated approach across services. This helps to free up NHS resources, reduce hospital admissions, and create capacity for elective procedures, ultimately supporting the NHS’s strategic goal of delivering more care outside of hospital settings.

“Where patients have a UCP, we see fewer unnecessary hospital admissions and a greater likelihood of receiving care in their preferred location. This supports both patient choice and NHS capacity,” said Nick Tigere.

The UCP integrates with social care, care homes, acute care, community hospices, and primary care to ensure seamless information sharing across healthcare providers. It is also connected to the London Care Record, enhancing accessibility for healthcare professionals across different settings, and the National Record Locator, enabling the care plans of Londoners and patients seen in London to be accessed nationwide.

Empowering patients through digital access

As part of the expansion, patients can now view their care plans via the NHS App, with plans to introduce editing functionality in spring 2025. This will allow individuals to update their non-clinical information, such as personal preferences and daily routines, reducing the burden on clinicians while empowering patients to take an active role in their care.

Dr Francesca Leithold, Global Service Delivery Director at Better, highlighted the importance of accessibility in this expansion: “The restructure of the forms is intended to create a clearer interface, structuring information in a better way. Making the care plan editable for patients over the next two quarters will enhance patient engagement and autonomy.”

Additionally, an upcoming GP Connect integration is set to enhance clinical safety by ensuring automatic access to GP medication and allergy records, reducing duplication and administrative workload for healthcare providers.

A future-focused approach to care

The UCP expansion follows a thorough evaluation process assessing digital maturity, readiness, and business case feasibility. The primary aim is to ensure that more Londoners have access to personalised, accessible care plans.

“This expansion marks a significant milestone in the evolution of the Universal Care Plan,” added Dr Leithold. “It demonstrates our commitment to making personalised care plans accessible to more people, providing tailored support that adapts to the needs of every individual. By expanding the scope of the UCP, we are empowering patients, improving outcomes, and supporting a healthcare system that’s more efficient and responsive to the diverse needs of the public.”

News, Population Health

Integrate housing and care budgets to tackle extreme health inequalities, says charity

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Homeless and inclusion health charity publishes solutions to tackle extreme health inequalities, including calling for safe discharge of people facing homelessness, wrap-around care from GPs for people with complex needs, and earlier help for people facing mental health crises.


The Homeless and Health Inclusion charity Pathway UK has published six expert papers setting out practical action plans to address systematic failures in healthcare experienced by people in health inclusion groups, including those experiencing homelessness.

People in inclusion health groups include people experiencing homelessness, Gypsy, Roma and Traveller people, people engaged in sex work, vulnerable migrants and people in contact with the Criminal Justice System.

With their living conditions described as ‘deprivation on stilts’ by Sir Michael Marmot, their health outcomes are typically worse than people living in deprived communities, driving additional pressure on the NHS. People facing homelessness are admitted six times more often to hospital than people who do have homes.

Written by experts in the field of inclusion health, the six papers highlight existing good practice and set out clear policy solutions based on NICE guidelines to tackle major shortcomings in health, housing and social care services which contribute to the poor health outcomes and early mortality experienced by health inclusion groups.

As the government formulates its new homelessness strategy and NHS 10-Year Plan, the charity’s recommendations align with government’s vision which focuses on three transformative shifts: moving care from hospital to community, embracing digital innovation, and prioritising prevention over treatment.

Alex Bax, CEO of Pathway, said: “We are at a turning point in the long and proud history of our National Health Service. These papers show how choices could be made across the NHS to reverse the inverse care law, tilting time and resource towards those who need it most.”

The six authors, Dr Verity Aaminah, Gill Taylor, Dr Chris Sargeant, Dr Jenny Drife, Samantha Dorney-Smith and Gill Leng, set out comprehensive, evidence-based recommendations to achieve this change, which include:

  • Introducing local integrated budgets covering both care and homes to enable improved planning and delivery
  • Establishing a network of specialist hospital teams and a hospital safe discharge programme to prevent discharge from hospital to the street
  • Reforming funding mechanisms for general practice to allow the complex, holistic work that people facing extreme health inequalities require

Dee O’Connell, Pathway’s Director of Programmes, said: “The pressures currently facing our health, housing and care services are huge. But the good news is that our practical policy solutions will tackle the systematic failures that have persisted for so long and which previous policy interventions have failed to solve. It’s now time to stop researching and time to take action.”