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Summary

This comprehensive on-demand teaching session is an in-depth study of various gynaecological disorders including endometriosis, adenomyosis, fibroids, abnormal uterine bleeding, amenorrhoea, anovulation, PCOS, PID, menopause, and HRT. The session is designed for medical professionals who wish to gain further knowledge in these areas, understand potential risk factors and symptoms, familiarise themselves with necessary investigations, and address effective management and treatment options. It also explores the complications associated with these disorders, making it an invaluable resource for those in the field of gynaecology. Be prepared to enhance your skillset and ability to deliver better healthcare.

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Description

In this lecture we will be covering the high yield gynaecological disorders that come up in the UKMLA .

The lecture will cover Aetiology, Pathophysiology, Investigations and management of endometriosis, adenomyosis, fibroids, Dysfunctional uterine bleeding, Amenorrhoea, PCOS and menopause

Learning objectives

  1. By the end of the session, participants should be able to accurately describe and define the listed gynaecological disorders, including their causes, symptoms, and how they affect female reproductive health.

  2. Participants should be able to illustrate the diagnostic process for each of the gynaecological disorders, including the importance and implications of early detection and the various investigative techniques available.

  3. Participants should achieve a solid understanding of the various medical and surgical treatment options available for different gynaecological disorders, understanding the factors that influence the choice of treatment.

  4. Participants should understand the risks and complications that may arise from each gynaecological disorder, including impacts on fertility and general health, and how patients can best manage these.

  5. Participants should be able to evaluate and interpret current research in the field of gynaecology, providing an evidence-based approach to the diagnosis and treatment of these disorders. This will include understanding the principles behind hormone replacement therapy in menopause.

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Gynaecological disordersContent • Endometriosis • Adenomyosis • Fibroids • Abnormal uterine bleeding • Amenorrhoea, Anovulation • PCOS • PID • Menopause • HRTEndometriosis • Endometrial-like tissue, outside of the uterus. • 10% of women of reproductive age • Aetiology - No clear aetiology yet • Retrograde menstruation • Genetics • Lymphatic spread • Coelomic metaplasia • Immune dysfunction • Endometriosis is associated with menstruation. • formation.al changes in the menstrual cycle induce bleeding, chronic inflammation, and scar tissue • Oestrogen dependentEndometriosis • Most commonly • Pelvis • On the ovaries • Peritoneum • Uterosacral ligaments • Pouch of Douglas • Extra-pelvic deposits, are rare: • Bowel • Appendix • Pleural cavity • In the top 50 most painful chronic conditions as per the NHSEndometriosis cont. Risk Factors Signs & Symptoms Investigation • Early menarche • Varies based on severity, location of • Examination usually normal, but may lesions… have posterior fornix / adnexal • Late menopause tenderness, nodules or adnexal • Secondary and Deep Dysmenorrhoea • Nulliparity masses (endometrioma). • Dyspareunia • First degree relative with • The only reliable diagnostic test is endometriosis • Cyclical or Chronic pelvic pain laparoscopy. • Obstruction to vaginal outflow • Subfertility/infertility • Average 7.5 years from onset of symptoms till diagnosis made. • Cyclical rectal bleeding • TVUS excludes endometriomas, but • Painful defecation a negative TVUS doesn’t exclude endometriosis. • Cyclical haematuria • Ca 125 & MRI may be beneficial. • IBS-like symptoms (bloating, diarrhoea, constipation, lower back pain) • Catamenial pneumothorax (rare) • Asymptomatic !Endometriosis Management Management depends on the nature and severity of symptoms and the need for future fertility. 1. Medical • Suppress symptoms (pain), doesn’t reduce recurrence of symptoms once treatment has stopped. Works by inducing pseudo-pregnancy or pseudo- menopause state. • COCP, Medroxyprogesterone acetate , GnRH agonist 2. Mirena IUS • Effective even after three years of use. 3. Surgical – Best if trying to conceive. • Excision of severe and deeply infiltrating lesions, Ovarian cystectomy (for endometriomas), Adhesiolysis, Bilateral oophorectomy with a hysterectomy (if indicated). Complications Infertility (tubal damage), Risk of Ectopic pregnancy, Adhesion formation, bowel obstruction and Increased risk of IBDAdenomyosis • Endometrial-like tissue invading the myometrium, causing inflammation, pain and the formation of adhesions. • S&S - Menorrhagia, Dysmenorrhoea, Chronic Pelvic pain, Dyspareunia, Enlarged boggy uterus and Infertility. • Most common in multiparous, at end of reproductive years • Investigations - TVUS, hysteroscopy or diagnostic laparoscopy, MRI • Tx • Mirena coil • Non hormonal – tranexamic acid, NSAIDs • Hormonal COCP, POP, GnRH agonist • Surgical – hysterectomy, endometrial ablation, uterine artery embolizationFibroids / Leiomyomas • Benign tumours – proliferation of smooth muscle cells and fibroblasts • Age 30- 50 • Most common benign uterine tumour in reproductive age • Regress after menopause typically • Types: Subserosal, intramural or submucosal • Signs and symptoms • Asymptomatic • Menorrhagia, dysmenorrhoea, Abdominal discomfort/bloating • Infertility, pressure symptoms (on bladder or bowel) • Irregularly enlarged uterusFibroids cont. • Investigations – Abdominal and Bimanual pelvic exam, USS (preferably TVUS), hysteroscopy, MRI • Treatment • Asymptomatic – monitor growth, safety net, No action • Mirena useful ( if no distortion of cavity) • Mefenamic and tranexamic acid, NSAIDs • COCP, POP, GnRH agonist (reduce size of fibroids, short term use pre surg.) • Surgery- Myomectomy, Ablation, Uterine artery embolization and Hysterectomy • Complications • Compression of adjacent structures (bladder, bowel) • Subfertility / infertility • Pregnancy complications – Miscarriage, Fibroid vascular infarction (red degeneration) – Acute pain, Foetal malpresentation, Preterm labour, PPH. Usually managed conservatively during pregnancy.Abnormal Uterine Bleeding • Abnormal uterine bleeding, in the absence of pregnancy, genital tract pathology or systemic disease • Heavy menstrual bleeding most common symptom- 50% of women with HMB have no identifiable cause • Rule out all other ddx first ! (bleeding problems, thyroid, fibroids, PID, PCOS, endometriosis/adenomyosis, PREGNANCY…) so blood tests and TVUS as investigations • Tx • Non hormonal – Tranexemic acid, pain relief (paracetamol, NSAIDs (mefenamic acid) • Hormonal – Mirena, COCP , POP, long-acting progestogens (Depo Provera) • Surgical – hysterectomy curativeAbnormal Uterine Bleeding – FIGO classificationPercentage reduction of menstrual blood loss with medical therapies 0 IUS Placebo -25 Prostaglandin Synthetase Inhibitor Combined pill -50 High dose progestogen Tranexamicacid -75 Danazol -100 Amenorrhoea Primary – No menstruation by 15 Secondary – Cessation of y.o with normal secondary sexual menstruation for 3-6 months with characteristics, OR by 13 y o with previously normal menses OR 6- no secondary sexual 12 months with previous characteristics oligomenorrhoea • Gonadal dysgenesis (Turner, • Hypothalamic amenorrhoea 46XO) (stress, excessive exercise) • Congenital adrenal hyperplasia • PCOS • Imperforate hymen! • Premature ovarian failure • Congenital malformations of the • Hypothyroidism, thyrotoxicosis genital tract • Sheehan syndrome • Functional hypothalamic • Asherman’s syndrome amenorrhoea (e.g. anorexia) (intrauterine adhesions) • Exclude pregnancy! Common Causes of Secondary Amenorrhoea Oestradiol FSH LH Prolactin Testosterone Hyperprolactinaemia Low Normal Normal High Normal Low Low PCOS Normal,low, Normal Normal/high Normal Normal/ high Raised LH:FSH Slightly high moderately increased Free androgen index increased Premature ovarian Low High High Normal Normal /Low insufficiency Functional Low Normal/Low Normal/Low Normal/Low Normal/Low hypothalamic (weight loss,Stress,exercise) Data from: [Practice Committee of theAmerican Society for Reproductive Medicine, 2008; Gordon, 2017; Samperi, 2019; BMJ Best Practice, 2022b]Anovulation / Anovulatory Cycle • Menstrual cycle with no release of egg • May still have bleeding, but no progestin secretion from corpus luteum (as no ovulation occurs) → Persistent proliferative endometrium, unstable and prone to irregular & heavy bleeding • Infertility common symptom • Classification • Group I – Hypothalamic pituitary failure (hypothalamic amenorrhoea, or hypogonadotrophic hypogonadism) • Pulsatile GnRH or gonadotrophins + LH • Group II – Hypothalamic - pituitary – ovarian dysfunction (PCOS) – 80%, most common • Group III – Ovarian Failure • Menopausal symptoms, <40 y o • Idiopathic, post chemotherapy/radiotherapy, Post oophorectomy • Raised FSH (>30), Low Oestradiol – Treat as menopauseCauses of Anovulation • Primary ovarian failure • Premature ovarian failure • Genetics (Turner) or autoimmune • Medication - antiepileptics, antipsychotics, chemotherapy • Secondary hormonal disturbance • Contraceptives, Pregnancy • PCOS • Hyperprolactinoma • Kallman’s syndrome (hypogonadotrophic hypogonadism) • Underweight/overweight, stress and significant exercise • HypopituitarismPolycystic Ovary Syndrome • Most common endocrine disorder in women, 80% of all anovulatory subfertility • Hyperinsulinaemia → Reduced Sex Hormone Binding Globulin (SHBG) production in the liver → Increased unbound active testosterone. • Vicious Cycle → Insulin resistance → Weight gain + Excess body fat → Increase insulin secretion → Worsening PCOS • Increased androgen → Stops follicular development → Anovulation and menstrual disturbance • Increased LH pulse amplitude and frequency from pituitary → Increased LH:FSH ratio → Ovaries prefer synthesizing androgen rather than oestrogen • May still have increased oestrogen levels. • The follicular development arrests before maturation of ovulatory follicle. • So, there will be no ovulation, but oestrogen production continues. • As a result to continuous oestrogen exposure, unopposed by progestogen, the endometrium becomes hyperplastic. Polycystic Ovary Syndrome Investigations – Rotterdam Criteria >2 of : Management • Irregular / absent ovulations (irregular menstrual • Weight loss, COCP (co-cyprindiol), cyclical cycle) POP or Mirena– manage symptoms like • Clinical OR Biochemical signs of hirsutism, acne and regulate cycle hyperandrogenism (acne, hirsutism, increased • Metformin as off-label use total testosterone/ low SHBG) • Polycystic ovaries on USS (>12 antral follicles on • If trying to conceive – covered more in an ovary, or ovary volume >10 mL) Infertility • Clomifene +/- metformin, Letrozole, • PCOS can be diagnosed without having Gonadotrophins or pulsatile GnRH polycystic ovaries, and polycystic ovaries alone • Ovarian drilling- damage hormone producing do not diagnose PCOS cells in ovary with diathermy/laser • Assisted reproductionPelvic Inflammatory Disease • Infection of the upper genital tract, almost always due to STI • Causes endometritis, oophoritis, salpingitis, tubo-ovarian abscess, peritonitis • RF – young, early first coitus, multiple sexual partners, history of STI, recent instrumentation of uterus/disruption of cervical barrier • Most common causes: Chlamydia trachomatis, Neisseria gonorrhoeae • In older women, may have descending appendicitis, or Pathogen negative PID • S&S • Fever, dysuria, pelvic / lower abdominal pain, Deep dyspareunia, abnormal vaginal bleeding / discharge. • Fitz Hugh Curtis Syndrome - RUQ pain, as anterior abdominal wall/ diaphragm and anterior liver capsule adhere to each other causing peri-hepatitis • Adnexal tenderness • Infertility, increased risk of ectopic pregnancyPelvic Inflammatory Disease cont. • Investigations • Exclude pregnancy! • Vaginal swabs • FBC, WBC, ESR, CRP • HIV & syphilis • USS – esp if abscess or hydrosalpinx suspected • Gold standard is Diagnostic laparoscopy, but is not routinely done • Treatment • Pain relief • Consider removing any IUD • Consider admission if septic, acutely unwell.. • Start empirical tx until results of swabsPelvic Inflammatory Disease cont. • First line • Ceftriaxone 1g Single IM dose + Oral doxycycline 100 mg BD + Oral metronidazole 400 mg BD for 14 days • Oral ofloxacin (or levofloxacin) + oral metronidazole for 14 days • Mycoplasma +ve – Moxifloxacin, discuss with micro • Alternative to 1 line – Ceftriaxone + Oral azithromycin for 14 days • Advice for adherence and sexual abstinence • If HIV positive – refer to clinic • Abscess may need surgical draining • May need contact tracing • Review in 72 hrs and some may need test of cureMenopause • Permanent loss of menstruation due to loss of ovarian follicular activity. It is diagnosed clinically after 12 months of amenorrhoea (>50 yrs) or after 24 months (<50 yrs) • Mean age 51 yrs • In perimenopause oestrogen levels begin to decline and fluctuate – unpredictable periods, hot flashes, dry skin, night sweats, atrophic vaginitis, osteoporosis, joint pain, decline in sexual function, cognition… • Elevated FSH – should not be used for diagnosis unless atypical presentation • Management • Lifestyle changes – exercise, good sleep hygiene, reduce stress, weight loss, smoking cessation • CVD risk assessment and management, osteoporosis prevention, screening for cervical, breast and bowel cancer • Need for contraception for 2 yrs after LMP (<50) or for 1 yr (>50) until 55 yrs – NOT HRT! but HRT + POP • Non-HRT treatments – CBT, SSRIs/SNRIs, vaginal oestrogen creams to address symptoms • HRT- individualized choice Hormone Replacement Therapy • Transdermal, oral, topical can be used • General Rule: if has uterus add progestogen. If no uterus – oestrogen only can be given • Aim to prescribe the lowest dose for the shortest possible duration. • Vasomotor and mood symptoms : Oral or transdermal preparations • Urogenital symptoms: low-dose vaginal oestrogen first-line and continue treatment for as long as needed to relieve symptoms. Some women on systemic HRT may also benefit from additional low-dose vaginal oestrogen. • Consider transdermal rather than oral HRT for women at increased risk of VTE • Review in 3 months, then annually, unless new symptoms • Sudden change in menstrual pattern, intermenstrual bleeding, postcoital bleeding, or postmenopausal bleeding - 2-week referral if a gynaecological cancer is suspected. • SE : Nausea, breast tenderness, fluid retention, weight gain Hormone Replacement Therapy • Benefits • Decreases vasomotor and urogenital symptoms • Decreases risk of osteoporosis, fragility fractures and colorectal cancer • Risks • Increased risk of Breast & Ovarian cancer (endometrial if oestrogen alone), Increases risk of strokes, VTE and coronary heart disease • CI – Current/past breast Ca, any oestrogen sensitive Ca, undiagnosed vaginal bleed and untreated endometrial hyperplasia • Duration • Cyclical for perimenopausal ( still having menstrual periods) – regular predictable bleeds • Continuous for postmenopausal • Can be continued for 2-5 years, stop gradually! • Monitor any sudden change, new bleedings, treatment efficacy, comorbidities and contraindicationsImpact on risk of breast cancer Comparator + 4 - 4 + 4 + 5 + 3 + 24 - 7The risk lasted >10 years after ceasing MHT 58 studies (92-18)– 108,647 women developed Br Ca at mean age Of 65 years – 51% of those had MHT 5 years of HRT at age of 50 years – Ca incidence 50 to 69 1 in 50 –oestrogen and progestogen daily 1 in 70 – oestrogens and intermittent progestogens 1 in 200 oestrogen only If used for 10 years the risk is twice Lancet Aug 29’th 2019FeedbackResources • Collins, Sally, et al. Oxford Handbook of Obstetrics and Gynaecology. Oxford Oxford University Press -07-01, 2013, oxfordmedicine.com/view/10.1093/med/9780199698400.001.0001/med- 9780199698400. • Dr Colin Tidy. “Endometriosis.” Patient.info, 11 Mar. 2016, patient.info/doctor/endometriosis-pro. • Dr Mary Harding. “Menorrhagia.” Patient.info, 24 Feb. 2016, patient.info/doctor/menorrhagia. • “Fibroids.” NICE, cks.nice.org.uk/topics/fibroids/. • “Fibroids | Doctor.” Patient.info, patient.info/doctor/fibroids-pro. • “Infertility Management.” NICE, cks.nice.org.uk/topics/infertility/management/management/. • “Management of Endometriosis.” NICE CKS, cks.nice.org.uk/topics/endometriosis/management/management-of-endometriosis/. • “Menorrhagia.” NICE, Feb. 2024, cks.nice.org.uk/topics/menorrhagia-heavy-menstrual-bleeding/. • NICE. “Amenorrhoea.” NICE, Feb. 2022, cks.nice.org.uk/topics/amenorrhoea/. • “Dysmenorrhoea.” NICE CKS, cks.nice.org.uk/topics/dysmenorrhoea/. • “Menopause.” NICE, Sept. 2022, cks.nice.org.uk/topics/menopause/. • “Polycystic Ovary Syndrome.” NICE, Sept. 2018, cks.nice.org.uk/topics/polycystic-ovary-syndrome/. • “Scenario: Management of Pelvic Inflammatory Disease.” NICE, cks.nice.org.uk/topics/pelvic-inflammatory-disease/management/management/. • “Scenario: Managing Women with Menopause, Perimenopause, or Premature Ovarian Insufficiency.” NICE CKS, cks.nice.org.uk/topics/menopause/management/management-of-menopause- perimenopause-or-premature-ovarian-insufficiency/.