Insight
‘Alarming’ rise in HIV diagnosis rates needs attention, gov says

Alarming increases in HIV diagnoses among women require urgent government focus, with new cases rising 33 per cent between 2019 and 2024, MPs have warned.
Sexual health services are “extremely stretched” with funding “pared to the bone”, threatening the UK’s ability to meet the United Nations AIDS 2030 zero transmission target, according to the Women and Equalities Committee report.
While new diagnoses fell among gay and bisexual men, significant disparities emerged in other groups.
New diagnoses in 2024 compared with 2019 were 35 per cent lower in men exposed through sex with men (1,238 to 810), but 26 per cent higher in females exposed through sex with men (596 to 749).
Overall, new diagnoses decreased 14 per cent in men but increased 33 per cent in females.
Black African and Asian populations saw increases of 80 per cent and 40 per cent respectively, while diagnoses among people of white ethnicity decreased 40 per cent.
The report warned the interim target of an 80 per cent reduction by 2025 is unlikely to be met.
Sarah Owen, chair of the Women and Equalities Committee and Labour MP, said: “With sexual health services stretched as they are, the Government will struggle to meet its adopted United Nations AIDS target of zero HIV transmissions by 2030.
“The forthcoming HIV action plan needs to include additional funding to that already earmarked if sexual health services are to be able to tackle HIV transmission effectively.
“Increases in HIV diagnoses among women are alarming and the action plan must include steps to address these concerns.
“Given the high cost to the NHS of late diagnosis, a fully resourced opt-out community testing programme in areas of high prevalence would represent a significant long-term saving.
“It should be introduced as soon as possible.”
MPs recommended expanding emergency department opt-out testing programmes to GP practices, abortion clinics, women’s health hubs, cervical screening centres and sexual health clinics.
Such expansion should include locally tailored campaigns targeting specific groups.
Just two thirds of heterosexual men and women are having their PrEP needs identified at sexual health services, with even fewer having them met.
PrEP is antiretroviral medication given to HIV-negative people to reduce infection risk.
The committee called for national digital access to PrEP to address delays in accessing sexual health services.
PrEP should also be available through community pharmacies and primary care, with increased walk-in appointments.
Ministers should enable nurses and health advisers to initiate PrEP prescriptions and provide targeted training to reduce missed opportunities, particularly in Black African communities.
Additional sexual health funding beyond that already earmarked for the public health grant will be needed to support increased testing.
Given the high NHS costs of late diagnosis, upstream community testing funding would deliver significant long-term savings, the report stated.
The report also highlighted concerning drops in testing among young people alongside decreased contraception use.
MPs called for public awareness campaigns on testing and contraception specifically targeting this age group.
Opt-out testing expansion to further emergency departments should automatically include hepatitis B and C tests.
Metro mayors should consider whether shared postal testing services across combined authorities might improve access and value compared with current individual local authority approaches.
Owen added: “Meeting the 2030 target requires focus on testing and improved access to PrEP, yet we know that people are struggling to access it, particularly if they live outside of major cities.
“As the Committee’s new report on tackling HIV transmission recommends, the Government should roll out digital access to HIV pre-exposure prophylaxis (PrEP) antiretroviral medication nationally to help address unacceptable delays and challenges in accessing sexual health services and prescriptions.”
“The roll out of injectable PrEP has the potential to be a huge step forwards in the battle against HIV.
“We urge it to be made available to vulnerable people, particularly women who may face barriers in accessing daily tablets.”
Insight
Black women want more accessible breast cancer screening info, study finds

Black women in the UK want clearer, more accessible breast cancer screening information, research has found.
The study looked at why Black African and Black Caribbean women are less likely than white women to attend breast screening.
Researchers at the University of Surrey held focus groups and interviews with 47 Black African and Black Caribbean women aged 50 to 71.
Women in this age group are routinely invited for NHS breast screening.
The researchers said only 45 per cent of Black women attend screening, compared with 63 per cent of white women.
Anietie Aliu, lead author, postgraduate researcher at the University of Surrey and registered nurse, said: “Diagnosing breast cancer early can dramatically improve a person’s chance of survival.
“Breast cancer screening plays an important role in this by identifying the cancer and ensuring a person receives speedy treatment.
“Despite the importance of screening, Black women are less likely to attend appointments than white females.
“This puts them at risk of a potential cancer being diagnosed late and spreading to other areas of the body. We need to understand what is preventing Black women from attending these appointments and help identify ways to remove such barriers.”
The study found a need to increase awareness of breast cancer screening, especially among women less familiar with the service.
Some women, particularly those born outside the UK, knew little about breast screening before receiving their first invitation.
Others questioned why they needed screening when they had no symptoms.
The importance of trusted conversations was also identified.
Researchers found that some Black women expected their GPs to speak to them about breast screening, particularly before they reached screening age.
Although NHS breast screening is organised through national screening services, researchers said GPs often have established relationships with patients and may be well placed to offer brief advice on preventive care, including breast screening.
Participants called for stronger links between GP practices, breast screening services and Black community champions.
They said this could help women receive trusted information, ask questions and feel reassured.
Faith and religious beliefs also shaped decisions for some women.
Some Black African Christian women said illness, including cancer, was not permitted by God in their bodies, while others saw screening as a personal choice that did not conflict with Christian faith.
Muslim women highlighted the importance of being able to state their religion on medical appointment forms to help ensure they were seen by a female mammographer.
A mammographer is a healthcare professional trained to carry out breast screening scans.
Aliu added: “Breast screening can save lives, but our findings show that attendance is shaped by multiple factors, not just awareness, although awareness remains important.
“Women need relatable screening information, reassurance, flexible appointments and services that are accessible within their communities.
“Many felt that invitation letters were too formal, and that leaflets and media imagery did not reflect them, making it harder to relate to screening.”
Dr Afrodita Marcu, senior research fellow at the University of Surrey and member of the research team, said: “We need a more collaborative approach, where primary care, screening services and community voices work together to support women before, during and after the invitation.”
The researchers said future breast screening interventions should be designed with Black women, rather than for them.
They said user-friendly and culturally relevant resources, developed with communities, healthcare professionals and screening services, could improve understanding, reduce fear and make breast screening feel more accessible and reassuring.
Dr Robert Kerrison, associate professor of cancer care at the University of Surrey, said: “There is no question that breast screening can be lifesaving, but we need to make it easier for women to understand, access and feel reassured by the programme.
“This means improving communication, addressing practical barriers and making sure healthcare professionals and community partners are supported to provide clear and trusted information.”
The team has also explored healthcare professionals’ perspectives and worked with stakeholders to develop user-friendly materials with Black women.
Researchers said this co-designed approach could help ensure breast screening messages are culturally relevant, practical and shaped by the people they are intended to support.
News
“Women’s voices should be heard and pain should never be ignored,” says Wales’s first Women’s Health Minister

Women’s pain should not simply be endured, Wales’s first women’s health minister has said.
Delyth Jewell said she was determined to tackle the normalisation of pain in women’s healthcare and ensure women’s voices are listened to.
Speaking during a Women’s Health Summit at the Temple of Peace on Thursday, July 16, she said: “For too long, women’s health has been treated as an afterthought. No woman should be afraid to speak up about pain or things that don’t feel right.
“Women should be believed about their bodies, and I am determined to change the culture that has let too many women down.”
She added: “Women’s voices helped create the Women’s Health Plan. Now we’re making sure those voices continue to shape what comes next.”
The summit brought together clinicians, researchers and women with lived experience to tackle the normalisation of pain in healthcare and identify how women’s voices can better shape NHS services.
Lived experience means insight from people who have personally gone through a health issue or used healthcare services.
The event focused on pain linked to clinical procedures and long-term health conditions, drawing on research evidence, clinical expertise and women’s personal experiences.
Following the summit, minimum standards for service user engagement will be drafted to ensure women’s voices continue to influence the delivery and future priorities of the Women’s Health Plan.
Service user engagement means involving people who use health services in decisions about how care is designed, delivered and improved.
Work will also begin to refresh and strengthen the plan, including gathering feedback directly from women across Wales.
The NHS Wales Women’s Health Plan was developed after discovery work in 2022, when women across Wales shared their experiences of healthcare.
Many said they had not felt listened to, had symptoms dismissed or had lived with pain for years before receiving a diagnosis.
Insight
The Healthcare AI Playbook: What it actually takes to build trustworthy AI for care

Hosted by Amanda Ducach, CEO, and Morgan Rose, chief science officer, EmaEQ
Healthcare companies have spent the last two years hearing the same advice: get AI into your product. Few have been told what that actually takes.
Most default to the fastest option. Plug in a general-purpose model, wrap it in a chat window, and call the box checked. It looks like progress on a roadmap slide. It rarely holds up once a real patient is on the other end of it.
We’ve spent years building AI specifically for healthcare, and the lesson that keeps repeating itself is simple: accuracy is not the same thing as trust, and trust isn’t something you bolt on after launch. It has to be part of how the system is built from the first line of code, not a feature added once regulators or users start asking questions.
That distinction is the whole reason clinical accuracy gets treated as a checkbox instead of a discipline. A model can sound confident and still be wrong in ways that matter enormously in a health context.
Knowing the difference, and building for it deliberately, is what separates AI that’s genuinely safe for care from AI that’s simply fast to ship.
On July 20th, we’re hosting a live conversation about exactly this: what companies should be paying attention to before they choose an AI to build with, what clinical accuracy really requires, and the pillars we hold every AI system to before it gets anywhere near a patient’s care.
The Healthcare AI Playbook Webinar: July 20th, 1:30-2pm EST, live on LinkedIn.
Register here: https://www.linkedin.com/events/7482643171823509504?viewAsMember=true
If your team is building anywhere near healthcare, or evaluating what’s already in your product, this is the conversation we think the industry needs right now.
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