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The National Institute for Health and Care Excellence issued draft guidance on polyendocrine metabolic ovarian syndrome.
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The guidance recommends that women with irregular periods be investigated for polyendocrine metabolic ovarian syndrome.
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Up to 4 million women in the UK are estimated to have polyendocrine metabolic ovarian syndrome.
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Polyendocrine metabolic ovarian syndrome was previously known as polycystic ovarian syndrome.
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The World Health Organization estimates that polyendocrine metabolic ovarian syndrome affects up to 13% of reproductive-age women.
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Symptoms of polyendocrine metabolic ovarian syndrome include irregular, very short, long, or absent periods.
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Symptoms of polyendocrine metabolic ovarian syndrome include excess levels of testosterone.
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Symptoms of polyendocrine metabolic ovarian syndrome include ovaries with multiple small follicles.
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Symptoms of polyendocrine metabolic ovarian syndrome include excessive hair growth.
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Symptoms of polyendocrine metabolic ovarian syndrome include weight gain.
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Polyendocrine metabolic ovarian syndrome is associated with a greater risk of developing type 2 diabetes.
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Polyendocrine metabolic ovarian syndrome is associated with a greater risk of developing cardiovascular disease.
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Polyendocrine metabolic ovarian syndrome is associated with a greater risk of developing sleep apnoea.
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Polyendocrine metabolic ovarian syndrome is associated with a greater risk of developing fatty liver disease.
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Polyendocrine metabolic ovarian syndrome is associated with a greater risk of mental health issues.
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Polyendocrine metabolic ovarian syndrome is associated with a greater risk of complications in pregnancy.
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Depression and anxiety are common in people with polyendocrine metabolic ovarian syndrome.
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Polyendocrine metabolic ovarian syndrome is a major cause of female infertility.
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The National Institute for Health and Care Excellence states that polyendocrine metabolic ovarian syndrome is frequently underdiagnosed and inconsistently managed.
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The draft guidance covers girls aged over 10.
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The draft guidance covers adult women.
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The draft guidance covers trans men who are not receiving gender reassignment therapy or surgery.
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The draft guidance covers non-binary people who are not receiving gender reassignment therapy or surgery.
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Patients with suspected polyendocrine metabolic ovarian syndrome should be offered blood tests including male and female hormone levels.
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Patients with suspected polyendocrine metabolic ovarian syndrome should be offered ultrasounds in some cases.
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Polyendocrine metabolic ovarian syndrome should not be discounted in women who have been through menopause.
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Polyendocrine metabolic ovarian syndrome should not be discounted in those with eating disorders.
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Eating disorders disproportionately affect people with polyendocrine metabolic ovarian syndrome.
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Polyendocrine metabolic ovarian syndrome can be more prevalent among black, Asian, and mixed ethnicity women.
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Healthcare professionals should consider ethnicity when assessing symptoms for polyendocrine metabolic ovarian syndrome.
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Those diagnosed with polyendocrine metabolic ovarian syndrome should have an annual review.
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The annual review should monitor symptoms such as menstrual irregularities and excess hair growth.
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The annual review should discuss cardiovascular health.
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The annual review should discuss diabetes.
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The annual review should discuss obesity.
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The annual review should discuss mental health care.
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For those planning a pregnancy, advice on weight, diet, nutrition, exercise, sleep, and mental health is recommended.
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In vitro fertilisation should be offered for women with polyendocrine metabolic ovarian syndrome who meet the standard National Institute for Health and Care Excellence criteria.
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Patients with polyendocrine metabolic ovarian syndrome should not be offered laser hair removal for excess hair growth.
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Patients with polyendocrine metabolic ovarian syndrome should not be offered light therapies for excess hair growth.
National Institute for Health and Care Excellence
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The National Institute for Health and Care Excellence stated that analysis suggests laser hair removal and light therapies are not cost-effective ways of improving overall health and wellbeing for these patients.
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The National Institute for Health and Care Excellence estimates it would cost the NHS up to £100m a year in England to offer laser or light therapies to polyendocrine metabolic ovarian syndrome patients.
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The draft guidance is based on the international evidence-based guideline produced by Monash University.
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The Monash University guideline is used by more than 100 countries.
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Marieanne Ledingham is a consultant clinical advisor for women’s and reproductive health at the National Institute for Health and Care Excellence.
Marieanne Ledingham, consultant clinical advisor
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"PMOS is a common but often overlooked condition that can have a major impact on health and wellbeing. Recommending a simple annual review is an important step towards ensuring people get the ongoing care and monitoring they need. This new guideline will help improve consistency of care, increase awareness of the condition, and support earlier diagnosis and management."
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Consultation on the draft guidelines is open until 11 August 2026.
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Final guidelines are due in December 2026.
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The draft guideline is open for consultation from 1 July to 11 August 2026.
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Dr Rachel Reid-McCann is a researcher at Oxford University.
Rachel Reid-McCann, researcher
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"Not only can irregular periods be burdensome in the short term, but they have also been associated with longer-term chronic health and reproductive outcomes, making prompt investigation important. A PMOS diagnosis in those with irregular periods can open up access to treatment, support and advice that can help improve symptoms and may also reduce longer-term health risks. The key challenge will be ensuring NHS services have the resources needed to implement these recommendations and doing so consistently across the UK."
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Janet Lindsay is the chief executive of Wellbeing of Women.
Janet Lindsay, chief executive
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"For too long, women with [PMOS] have faced delays in diagnosis and inconsistent care. Too often, symptoms such as irregular periods, fertility difficulties or concerns about weight have been dismissed as something they must simply live with. Wellbeing of Women welcomes these draft Nice guidelines, recognising [PMOS] as a complex, lifelong condition that can affect reproductive health, mental wellbeing and long-term health outcomes. The recommendation for regular review is an important step towards ensuring women receive the ongoing support, monitoring and information they need throughout their lives. It is particularly encouraging to see the guideline acknowledge the inequalities that persist in diagnosis and care. Women from black, Asian and other minoritised communities can face additional barriers to investigation and diagnosis, and tackling these disparities is essential if everyone is to receive timely, evidence-based care."
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Sharon Manship has polyendocrine metabolic ovarian syndrome.
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Sharon Manship was part of the committee that produced the new guidelines.
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Sharon Manship lived with the condition for 30 years.
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Sharon Manship sought support for her symptoms in her early 20s.
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Sharon Manship was diagnosed with polyendocrine metabolic ovarian syndrome in her mid-30s.
Sharon Manship
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"It was so disheartening to be told, until I was finally diagnosed in my mid-30s, that my symptoms were just part of being a woman. My hope is that with this new guideline, people with PMOS will be taken seriously, diagnosed earlier and provided with evidence-based support and care from healthcare professionals from the outset, rather than having to go what I went through."
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There is no cure for polyendocrine metabolic ovarian syndrome.
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The NHS offers treatments to manage the symptoms of polyendocrine metabolic ovarian syndrome, including hormone support and fertility drugs.
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