Wakefield sees an increase in endometriosis hospital admissions

Charity Endometriosis UK said women forced to go to hospital with endometriosis are being "let down" by the NHS as they are not getting the treatment they need elsewhere.

NHS Digital data shows there were around 165 hospital admissions with a main diagnosis of endometriosis in the Wakefield CCG area in 2019-20.

This was up from 150 the year before.

Last year, between one and seven were classed as emergencies.

Endometriosis is a chronic condition – which affects around 10% of women and has no known cure – in which tissue similar to the lining of the womb grows elsewhere in the body, such as around the ovaries. In extremely rare cases it can occur in men.

The tissue sheds in the same way that blood does during the menstrual cycle, but has nowhere to escape to, causing inflammation, pain, and a build-up of scar tissue.

Data from the 195 CCGs in England which provided data shows hospitals admitted 21,900 patients with the condition last year, including a record 2,905 emergency admissions.

Endometriosis Awareness Month, which takes place every March, aims to raise greater recognition for the disease, but Endometriosis UK said the figures show there is still a lack of understanding.

Chief executive Emma Cox said the health service is not providing women with the help they need from non-emergency care and should "face up to the scale" of the problem.

She added: "We’re letting these people down by not providing them with the treatment and management they need to manage their condition – endometriosis is a chronic condition but so few people get offered pain management."

But she said society in general is also responsible for not taking the condition seriously, with many people still too scared to discuss the "taboo" subject of menstrual conditions.

The charity has called on the NHS to implement NICE guidelines – which were adopted in 2017 but have not yet been implemented – to help all healthcare practitioners better recognise the symptoms of endometriosis.

A recent report from a group of MPs found that it takes an average of eight years to receive a diagnosis in England – a figure which has not improved for a decade.

Ms Cox said the coronavirus pandemic has caused "real problems" as women have not been able to access medical support in the same way as before, leaving a backlog of operations.

However, she said working from home has helped some sufferers manage their condition because they are not having to commute to work.

And she added that a new University of Edinburgh study into the effects of a non-hormonal drug on endometriosis treatment is "very exciting", though cautioned it is in the earliest stages.

An NHS spokeswoman said: “NHS staff have made huge efforts to maintain care for those patients who have needed it urgently throughout the pandemic and are increasingly bringing back more services safely.

"Anyone who thinks they are showing signs or symptoms of endometriosis should contact their GP for advice, treatment and referral for tests so they can get any treatment they need as quickly as possible.”

Symptoms of endometriosis

Painful, heavy or irregular periods

Pelvic pain

Painful bowel movements

Pain when urinating

Pain during or after sex

Difficulty getting pregnant

Fatigue