Menopause

Overview

Premature ovarian insufficiency (POI) = loss of normal ovarian function before age 40, affecting ~1 in 100 women
Hormonal signature: FSH >40 IU/L on two occasions at least 4-6 weeks apart + oestradiol <100 pmol/L
Always exclude: pregnancy, hypothyroidism (TSH), hyperprolactinaemia (prolactin) in secondary amenorrhoea
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Menopause over 45 is a clinical diagnosis - bloods not routinely needed. Investigate when symptoms occur under 45 or diagnosis is unclear.

Presentation

Vasomotor - hot flushes, night sweats, palpitations, sleep disturbance
Genitourinary - vaginal dryness, dyspareunia, urinary frequency, recurrent UTIs
Psychological - low mood, anxiety, poor concentration, reduced libido
Menstrual - irregular periods progressing to amenorrhoea

Management

HRT formulation choice
SituationHRT choiceRationale
Uterus intactCombined HRT (oestrogen + progestogen)Progestogen prevents endometrial hyperplasia/cancer from unopposed oestrogen
Post-hysterectomyOestrogen-only HRTNo uterus = no endometrial cancer risk
GSM onlyTopical (vaginal) oestrogenLow systemic absorption; safe even in many with breast cancer history
POI with uterusCombined HRT until age ~51Must continue to age of natural menopause to prevent osteoporosis, cardiovascular and cognitive risk
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POI with an intact uterus: combined HRT (not oestrogen alone) continued until approximately age 51 - this is not optional. Treating for only 5 years is insufficient to protect bone mineral density. The combined oral contraceptive pill is an acceptable alternative.
Sequential (cyclical) HRT - oestrogen daily + progestogen for 12-14 days per cycle; used in perimenopausal women (still having periods); produces regular withdrawal bleed
Continuous combined HRT - both hormones daily; used in post-menopausal women (>1 year since last period); aims for amenorrhoea
Transdermal route (patches, gels) preferred in women with elevated VTE risk - bypasses hepatic first-pass metabolism, avoiding increased clotting factor production seen with oral HRT

Complications

Breast cancer - small increased risk with combined HRT; oestrogen-only carries less risk than combined
VTE - oral HRT doubles baseline risk; transdermal HRT does not carry this risk
Endometrial cancer - risk eliminated by adequate progestogen opposition in women with a uterus
Untreated POI - osteoporosis, cardiovascular disease, cognitive impairment, premature mortality

Alternatives when HRT is contraindicated

Venlafaxine or SSRIs (e.g. fluoxetine, paroxetine) - vasomotor symptoms; unlicensed, effect often short-lived
Clonidine - licensed for hot flushes; allow 2-4 week trial; side effects include dry mouth and drowsiness
CBT - evidence-based for vasomotor and psychological symptoms
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NICE advises against routinely offering SSRIs, SNRIs, or clonidine as first-line for vasomotor symptoms - reserve for when HRT cannot be used.