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Inside UK’s “gynaecology care crisis”: RCOG calls for ring-fenced funding, innovation and research

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Three quarters of a million (755,046) women across the UK are now waiting for gynaecology treatment.

The Royal College of Obstetricians and Gynaecologists has called for urgent government funding for women’s health and care in the UK, as research shows gynaecology waiting lists have doubled since 2020. 

A new report, published this week by the Royal College of Obstetricians and Gynaecologists (RCOG) finds that three quarters of a million (755,046) women across the UK are now waiting for gynaecology treatment— enough to fill Wembley stadium eight times over.

Waiting lists have increased by a third since 2022 and additional BBC research shows they are now almost double that of 2020. Just before the pandemic 360,400 women were waiting for treatment.

But this is only the tip of the iceberg, according to the RCOG, which believes thousands more are waiting for other forms of care, including diagnostic tests to confirm their condition. 

In order to track the state of gynaecological care in the UK, the RCOG collaborated with LCP Health Analytics, to develop an Elective Recovery Tracker tool, bringing together publicly available datasets in one place for the first time. It also surveyed over 2,000 affected women and over 300 healthcare professionals. 

A quarter of women reported that they had attended A&E as a result of their symptoms, with more than 1 in 10 of those going on to have emergency interventions. 

Over three quarters (76 per cent) of women waiting for care reported worsening mental health and over two thirds (69 per cent) reported being unable to take part in daily activities including work.

Healthcare professionals also reported being deeply concerned for their patients and the majority of primary (65 per cent) and secondary care clinicians (69 per cent) surveyed reported their own health and wellbeing has been affected by managing pressure in their clinics. 

Additionally, over 90 per cent of primary care professionals reported a severe impact on general practice due to longer waits for hospital gynaecology services. 

“No part of life left untouched”

Kerry Briggs, a patient in her early 50s from near Manchester, has been waiting for treatment for fibroids since January 2023. 

“During this time, I’ve experienced severe bleeding, back pain, hip pain and had to manage challenging symptoms of anaemia as a result of my blood loss,” she says.

“The anxiety I’ve felt whilst waiting has been all encompassing. I can’t book anything in advance and I feel completely stuck in the house. If you don’t have cancer, your condition is given less urgency and importance but there is no part of my life left untouched by this. It has to be taken more seriously.” 

Meanwhile, India Weir, 27 from near Edinburgh has also been on and off waiting lists since being diagnosed with endometriosis in 2017. She is currently waiting for surgery to manage my deep infiltrating endometriosis and ovarian cysts.

“Physically, being in pain every single day takes a huge toll on me whilst I have to get on with day-to-day life. Also, living with the uncertainty of when I’ll undergo surgery makes it hard to plan ahead,” India says. 

“It impacts every part of my life and my quality of life. My relationships, friendships, social life, career and mental health are all affected – and my condition is getting worse without treatment and relevant care.”

A way forward?

The RCOG’s Waiting for a way forward report, funded by Theramex, sets out recommendations for the government to support patients and healthcare professionals now, while improving the future of women’s health and care. 

This includes increasing the amount of funding for health services, considering targeted funding to expedite the longest waits, and providing resources to protect gynaecology services against operational pressures.

The government is also urged to consider building on existing digital initiatives, such as the Elective Recovery Tracker, expanding data collection and to commit to ring-fenced funding to enable research, patient participation, innovation and pilots to improve understanding and experiences of gynaecology.

The Elective Recovery Tracker provides regular updates on the backlog in gynaecology elective care and provides visualisations of the size, scale and nature of waits in gynaecology services across the UK.

According to Rebecca Sloan, Women’s health lead at LCP Health Analytics: “The analysis should help healthcare professionals and policymakers to identify where additional resources and focus is likely to have the greatest impact on patient outcomes and health inequalities.”

Last week the Women and Equalities Select Committee continued an inquiry on Women’s Reproductive Health Conditions, which looked at how the NHS can leverage femtech to improve treatment and care. 

Dr Sue Mann, the first National Clinical Director for Women’s Health at NHS England and a consultant and lead for women’s health in City and Hackney, North East London, highlighted the importance of “keeping pace” with innovation in women’s health, but said the NHS must “get better” at producing its own digital information too. 

Innovative pathways for gynaecology 

However, the NHS can also tap into existing “innovative pathways” such as telemedicine to reduce waiting lists, according to some experts, who say many of the needs of those waiting could be met outside of acute hospital care. 

Kat James, director of new projects at the telemedicine company, Consultant Connect, told Femtech World: “There is a history of women’s health being ignored and 750,000 patients waiting for hospital treatment is worrying. The truth is that a large majority of these women do not need hospital-based care, if only the right virtual and community-based alternatives were available.

“Face-to-face hospital-based care is the right place for those that need acute care, but for many conditions, often in the context of menopause related symptoms, community care is the faster way to help women. And this includes innovative pathways like telemedicine, where a patient can be given an immediate treatment plan without having to set foot into a physical healthcare setting.”

Consultant Connect runs a network of NHS consultants who review gynaecology referrals remotely, virtually triaging thousands for NHS trusts around the country. Its data shows that around one third to half of gynaecological referrals don’t need to be on hospital waiting lists. 

“On average 30-40 per cent of patients receive treatment plans written up by ‘virtual’ NHS gynaecologists that their GPs can enact immediately, and another large cohort is directed to community-based care like women’s’ hubs if available in their area,” explains James.

“Not only does this deliver faster care, but also reduces stress, anxiety and unnecessary time of work, childcare and travel that comes with months long waits and hospital appointments.”

Long-term funding and investment

Commenting on the latest figures, leaders from the RCOG, as well as the Royal College of GPs have called on the government to act “urgently” to tackle the UK’s “gynaecology care crisis” with “long-term sustained funding”.

Dr Ranee Thakar, president of the RCOG, said: “A way forward is urgently needed to tackle the UK gynaecology crisis. Our new report shows too many women are waiting too long with serious conditions that can devastate their lives. NHS staff are also deeply concerned and distressed that they do not have the necessary resources to deliver good care, affecting their own wellbeing.

“UK governments must act now. The RCOG is calling on them to commit to long-term, sustained funding to address the systemic issues driving waiting lists, alongside delivering an urgent support package for those currently on waiting lists.

“This investment will not only benefit thousands of individual women but the wider economy too, because the evidence shows that healthy women are the cornerstone of healthy societies. Get it right for women and everyone benefits.”

 

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UK reviews surrogacy firm over rejected insurance claims

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The UK government is reviewing a surrogacy firm after complaints that medical insurance claims involving surrogates in Mexico were rejected.

The Department of Health and Social Care (DHSC) is considering whether UK-based provider My Surrogacy Journey should remain listed on gov.uk as one of four domestic surrogacy agencies available to intended parents.

The review follows allegations concerning its Mexican sister company, where surrogates are based.

Health minister Diana Johnson said: “The department is looking into the allegations about My Surrogacy Journey.

“As part of that assessment, the department will consider whether it is appropriate for that company to remain on the gov.uk list of agencies.”

Emails sent by My Surrogacy Journey chief executive Michael Johnson-Ellis and seen by the Guardian suggest multiple surrogate women in Mexico had their insurance claims rejected.

The emails also suggest 300 couples using the company were moved to a new insurance provider because of the increased risk of claims being rejected.

Commercial surrogacy is banned in the UK, where only altruistic arrangements are permitted.

My Surrogacy Journey operates a not-for-profit UK branch alongside for-profit sister companies in Mexico and the US. All three companies have the same owners and chief executives.

The reported insurance issues relate to surrogacy arrangements in Mexico.

One couple told the Guardian they paid tens of thousands of pounds to cover medical costs after their surrogate had a hysterectomy during childbirth and an insurance claim was refused.

The Guardian said it understood that at least five sets of parents said they had to cover medical costs after insurance claims were rejected.

In an email to the couple whose surrogate underwent a hysterectomy, Johnson-Ellis wrote: “We have already told you that the insurance companies have been declining some of the claims and we are actively working with the broker to get this issue resolved but you should also consider that they may not be paid out and there is nothing we are able to do to change this …

“We appreciate this is not an insignificant sum but this genuinely is out of our control.”

Johnson-Ellis also said the company had switched insurance providers, writing: “We’re also managing this for 300 other journeys, which is a complex position to be in.”

Lawyers acting for My Surrogacy Journey said the company did not comment on individual cases, but that existing insurance policies were in place and claims continued to be accepted and processed.

They said the company understood that a small number of claims had been rejected and was supporting people seeking to resolve those claims with an insurer.

Under the surrogacy arrangements, intended parents are understood to be contractually required to cover medical costs not paid by an insurer.

The couple said they had been recommended the company’s Mexico option. Its website advertises that intended parents using the route can have a baby in “under 18 months”.

They said they were told the UK route could take up to five years and that the US option was much more expensive.

Lawyers for My Surrogacy Journey said prospective parents are given information about typical timelines, costs, legal frameworks and practical considerations, and that the 18-month timeframe is indicative only.

The couple said their surrogate developed placenta accreta, a serious condition in which the placenta attaches to the wall of the uterus.

Emails from Johnson-Ellis acknowledged that the insurance provider investigated the birth after the surrogate experienced health complications.

The parents are considering legal action, while the Guardian said it understood at least four other couples were reviewing their options.

Phil Brickell, MP for Bolton West, raised concerns in parliament about a separate couple who had used My Surrogacy Journey.

He said: “Two of my constituents recently travelled to Mexico, where their children were born by surrogacy.

“Those births were facilitated by a company called My Surrogacy Journey, which is listed on gov.uk.

“While in Mexico, they had repeated traumatic experiences with the company relating to issues including insurance for their children, accusations of bullying towards staff and repeated efforts to silence any constructive criticism.

“I understand that other members of this house have received similar complaints.”

Brickell called for My Surrogacy Journey to be removed from gov.uk pending a review by the Human Fertilisation and Embryology Authority.

Lawyers acting for My Surrogacy Journey said the company was communicating with DHSC and was confident any issues could be resolved.

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‘Limited scientific evidence’ for most menopause supplements, expert says

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Many menopause supplements contain ingredients with limited evidence for symptom relief, while formulations and prices vary widely, a study has found.

Researchers analysed 201 products sold by nine major UK retailers, comparing their ingredients, doses and monthly costs.

Prices ranged from £1.50 to £95 a month, while no single ingredient or category of ingredient was common across all products.

The study, carried out by University College London, found that 80 per cent of products contained herbs, 77 per cent contained vitamins and 74 per cent contained phytoestrogens, naturally occurring plant compounds found in foods including soy and flaxseed.

Vitamin B6 was the most common vitamin, while red clover and sage were the most frequently identified plant ingredients.

Researchers said more evidence was needed on the effectiveness and safety of supplements marketed for menopause symptoms.

Professor Joyce Harper, senior author of the study and professor of reproductive science at University College London, said: “The menopause supplement market is growing rapidly, despite limited scientific evidence that many of these products improve menopause symptoms.

“Some social media influencers promote these products as effective solutions, despite many claims not being supported by scientific evidence.

“This can contribute to the spread of misinformation and help drive a rapidly growing menopause supplement market, leading some women to spend substantial amounts of money on supplements in the hope of improving their symptoms and overall wellbeing.”

Half of the supplements did not contain vitamin D, while less than 24 per cent contained calcium.

The British Menopause Society and International Menopause Society have highlighted vitamin D and calcium as important for maintaining bone health and preventing osteoporosis after menopause.

Researchers also identified botanical ingredients that may carry risks, including black cohosh.

Poppy Sullivan, first author of the study, said: “Certain botanical ingredients in some menopause supplements may also have risks.

“Black cohosh, in particular, is known to carry a potential risk of liver toxicity.”

The amounts of vitamins and minerals included in different products also varied widely.

Sullivan said: “Some nutrients can have adverse effects when consumed in excess over time.

“For example, excessive vitamin D intake can theoretically lead to high calcium levels, which could cause adverse effects such as vomiting and confusion.”

The study found little empirical evidence supporting the effectiveness of even the most expensive products.

Researchers called for more high-quality research, including clinical trials, to determine whether menopause supplement ingredients are effective and safe.

They said the findings could also help healthcare professionals understand the wide variation in supplement formulations.

The researchers acknowledged that the analysis may not have included every menopause supplement available in the UK.

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Ultrasound Direct extends Trice Imaging partnership

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Ultrasound Direct has extended its Trice Imaging partnership for three years, adding a reporting tool across its 70-clinic UK network.

The private ultrasound provider will continue using the Tricefy platform for secure image storage and patient engagement, alongside TriceIQ for efficiency and productivity analytics.

It will also introduce Trice Workspace Reporting across its network. The companies say the tool will help standardise ultrasound reporting templates and workflows and reduce variation between clinics.

Ultrasound Direct carries out an estimated 120,000 patient scans each year across services including pregnancy, fertility, women’s health, men’s health and other diagnostic pathways.

Its network uses a large pool of sonographers working across different ultrasound systems and serves referral routes including self-referring patients, GPs and commercial partners.

Mike Steward, founding director at Ultrasound Direct, said: “Having worked with Trice Imaging since 2018, we first partnered to replace manual methods of providing scan images to expectant parents with Trice’s secure electronic image-sharing platform. Today, every study performed across the Ultrasound Direct Network is recorded and stored on Tricefy, while our clinical services have expanded considerably beyond pregnancy into fertility, women’s health, men’s health and other diagnostic pathways.”

He added: “To continue futureproofing our image management strategy across a network of 70 clinics, a large team of sonographers, varying ultrasound systems and a growing number of referral partners with different needs, we decided to extend with Trice Imaging. This includes the introduction of the new Trice Workspace Reporting module to help us scale and standardise our ultrasound reporting templates and workflow, reducing variability between clinics.”

The partnership began in 2018, initially focusing on replacing manual methods of sharing pregnancy scan images with expectant parents.

Johanna Wollert Melin, founder and chief executive of Trice Imaging Europe, said: “Ultrasound Direct has been a valued partner in the UK for 8 years.”

She added: “At the heart of the relationship is a willingness to explore new ideas, test new tools and the spirit to solve real challenges across a large and complex clinical network.”

Mark A. Samii, chief revenue officer at Trice Imaging, said: “We are delighted to retain and extend our relationship with Ultrasound Direct.”

He added: “The addition of Trice Workspace Reporting addresses a challenge we hear from multi-site providers globally – keeping reporting quality consistent across many users, systems, referral or payer relationships.”

Steward said Ultrasound Direct continues to see growing demand for private diagnostics alongside NHS care from self-referring patients and an increasingly diverse range of professional and commercial referral partners.

He added: “As that development continues, scalable digital infrastructure becomes increasingly important. Our focus is on ensuring that a growing national network can support consistent clinical workflows, different referral pathways and the technology requirements of the future, while continuing to provide patients with accessible diagnostic services.”

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