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Menopause Professional Tool

Health professional tool

Assessment & management Phases of female Routine screening reproductive cycle Menopausal women are at increased risk of: • Regular cycles , , central adiposity, mood disorders. •  ‘premenopause’ Exclude – thyroid, , iron deficiency, drug side effects • Change in cycle frequency • changes – recent changes in bleeding pattern including heavy bleeding  ‘early perimenopause’ Investigate for iron deficiency and gynaecological pathology • Cycles up to 3-12 months apart • Check last cervical screening test and mammogram •  ‘late perimenopause’ Metabolic syndrome – monitor BP, cholesterol, blood glucose, abdominal girth and weight • Final menstrual period – discuss with patient the need to increase activity and monitor caloric intake •  ‘menopause’ (average age 51 years) density – see bone health section • No menstrual cycles >12 months • Smoking – discuss with patient the need to cease smoking  ‘postmenopause’ Based on symptom report only. Hormonal Key messages screening unreliable due to unpredictable • Hot flushes – dress in layers, natural fibres, reduce weight, reduce alcohol, increase activity, fluctuations. FSH levels may be helpful in reduce caffeine, healthy diet young women. • Dry – local treatments: vaginal oestrogen cream, pessaries and tablets. Encourage patients to select vaginal lubricants and moisturisers most similar (in pH and osmolality) Commonly reported to natural vaginal secretions, as this may make them less likely to cause irritation menopausal symptoms {{There are many vaginal lubricants (for use during intercourse) for urogenital symptoms include: and vaginal dryness. Those listed in pink meet the suggested pH and osmolality composition: Astroglide®, KY® Jelly, pjur® and Yes ®. It is also possible to use natural oils • Hot flushes • eg olive, sweet almond oil • Night sweats • Crawling ® ® {{Vaginal moisturisers (for regular, twice weekly use): Replens , Yes • Muscle/joint pains sensations • ​Emotional health – ask initial screening questions (back page) • Anxiety on skin • Stress management – discuss with patient the need to actively manage stress and mood • Irritability • Overall eg activity, mindfulness, social connectedness • Sleep disturbance diminished • Diet – diet may assist in symptom reduction • Lessened wellbeing concentration • Low Use of natural supplementation • Vaginal dryness There is some evidence of effectiveness for the following supplements: • Painful intercourse Black cohosh (Remifemin® and Femular®) – decrease hot flushes. Monitor for signs of toxicity. HRT/MHT* candidates • Women experiencing menopausal Contraindications for HRT/MHT Alternatives to HRT/MHT symptoms (peri or postmenopause) (consider referral to menopause specialist) Pharmaceutical Dose • Women with early or premature menopause • • (bone sparing and reduces CVD risk) cancer (hormonally sensitive) Escitalopram 10-20mgs daily • • Women with osteoporosis <60 years Thrombophilia/past venous • Venlafaxine 37.5-75mgs daily thrombo-embolic event (VTE) • Women within 5-10 years of last period • Desvenlafaxine 50-100mgs daily • Undiagnosed for vasomotor symptoms • • Active Paroxetine** 7.5-10mgs daily In general use: lowest effective HRT/MHT dose • Uncontrolled • Gabapentin 300-900mgs daily for the short-term relief of menopausal symptoms, • except for early/premature menopause – higher CVD risk or disease • Clonidine 50-150mcg daily dose and long-term therapy. Effectiveness monitored by self-reported symptom control. ** (not to be used with )

Women with a : important to note that HRT/MHT is not a contraceptive Early (<45 years)/ Menopausal transition Postmenopause premature (<40 years) menopause Dosage: lowest effective dose monitored Dosage: lowest effective dose monitored Continue HRT/MHT until 50 years unless by self-reported symptom control by self-reported symptom control contraindicated. Higher doses usually Options: Options: required. 1. Low dose combined contraceptive 1. Continuous oestrogen Options: (if low CVD risk & <50 years) + continuous progestogen 1. Continuous oestrogen 2. Continuous oestrogen (if menopause >1-2 years ago) 2. Continuous oestrogen (high dose oestrogen due to age) + cyclical 10-14 days each month + cyclical progestogen + cyclical or continuous progestogen + contraception (including barrier, sterilisation) (if menopause <1 year ago) 2. Combined contraceptive 3. Continuous oestrogen or IUD 3. + levonorgestrel IUD for progestogen and 3. Tibolone (if menopause is >1-2 years ago) contraception 4. Tissue-selective oestrogen complex (TSEC)

Review: initially 2-6 months then assess benefits/side effects, address concerns, titrate regimen to suit the individual woman – assess need, new development/options, CVD and risk. Then annual review. Special considerations After hysterectomy increase in size – less likely with tibolone or If atrophic endometrium (<4mms on US), Continuous oestrogen or tibolone. transdermal oestrogen and progestogen. reduce progestin/increase oestrogen. Otherwise, increase progestin dose/ deficiency length/type; levonorgestrel IUD. Not OCP or oral oestrogen; Oral oestrogen to increase SHBG: therapy use transdermal oestrogen to lower SHBG; , , consider testosterone if low calculated free or oral as progestogen. Testosterone 1% cream (for women) is testosterone, or tibolone. Can also use . TGA approved for clinically diagnosed hypoactive sexual desire disorder (HSDD) Liver disease, gallstones Breast cancer or low sexual desire with distress, when all Refer to HRT/MHT contraindications. Vaginal Transdermal. other causes are excluded. Free oestriol for vaginal and urinary symptoms. Mastalgia testosterone is measured to exclude a high level. (hypertension, Lower dose, transdermal oestrogen, tibolone, diabetes, hypercholesterolemia) testosterone, evening primrose oil caps. Urogenital symptoms alone Use transdermal if menopausal symptoms Migraine Vaginal oestradiol/oestriol – regular use 2-3 times weekly. bothersome. Transdermal oestrogen and progestogen, Compounded lower dose, avoid oral ; Varicose veins Advise against compounded bioidentical continuous therapy, not cyclic. Transdermal or tibolone preferred routes therapy as not TGA approved. Obesity/morbid obesity of administration. Transdermal. VTE/thrombophilia Tibolone or HRT/MHT (refer to menopause Ovarian cancer Assess baseline risk; high risk if VTE recurrent, spontaneous, with pregnancy/ expert/liaise with oncologist/gynaecologist), No special regimen. Liaise with oncologist/ OCP, family history, smokers; screen for usually only stage 1. gynaecologist, as some cancers are inherited thrombophilia. If normal and hormonally sensitive. low risk, use transdermal or tibolone. OCP, levonorgestrel IUD + oestrogen, Progestogen If high risk or inherited thrombophilia, tibolone, continuous combined HRT/MHT; Change progestogen, tibolone. avoid HRT/MHT unless anticoagulated; with post-surgical menopause need to PV bleeding seek specialist haematological advice consider added progestogen/tibolone. Investigate to determine cause and exclude re use of transdermal HRT/MHT. Fibroids pathology prior to treatment – transvaginal Weight increase No special regimen; theoretically may ultrasound +/– hysteroscopy. Not related to HRT/MHT. Bone health Indications for assessment: • Some chronic eg rheumatoid arthritis, • Family history of osteoporosis chronic liver or disease • Overactive thyroid or parathyroid • use or exposure • Malabsorption eg coeliac disease, inflammatory • Some for breast cancer and epilepsy bowel disease and some Osteoporosis Osteopenia Normal T-score below -2.5 T-score between -1.0 to -2.5 T-score above -1.0

Rx aim: prevent further bone loss and fracture Rx aim: prevent further bone loss Rx aim: prevent further bone loss and fracture

Plain X-ray thoracic lumbar spine to exclude Plain X-ray thoracic-lumbar spine to exclude Regular weight bearing exercise, optimise compression fracture compression fracture intake + vit D levels

Exclude other causes: Regular weight bearing exercise, optimise Monitor bone density at 70 years or earlier • Calcium, phosphate, vit D, PTH, TFT, LFT, calcium intake + vit D levels if requested ESR, serum/ electrophoresis, coeliac antibodies Monitor bone density DXA 2-5 yearly. • Use FRAX risk calculator Use FRAX risk calculator Regular weight bearing exercise, optimise If T-score between -2.0 to -2.5 calcium intake + vit D levels: and they are high fracture risk • HRT/MHT <60 years Refer to specialist for consideration: • Tibolone <60 years • HRT/MHT <60 years • Bisphosphonates • Tibolone <60 years • Raloxifene • Bisphosphonates • Denosumab • • Monitor bone density, DXA 2 yearly • Denosumab and bone markers • Monitor bone density, DXA 2 yearly and bone markers Assessment of emotional wellbeing in menopausal women Women experiencing premature or early menopause are at increased risk of and anxiety. Routine screening is recommended for this patient group.

Initial screening questions Screening tools for depression and anxiety To order copies: 1. During the past month have you often jeanhailes.org.au been bothered by feeling down, • Kessler Psychological Distress Scale 10 (K-10) depressed or hopeless? • Depression Anxiety Stress Scale (DASS-21) 2. During the past month have you often • Patient Health Questionnaire (PHQ9) Public Health & been bothered by having little interest • Generalised Anxiety Disorder Assessment Education or pleasure in doing things? (GAD7) Jean Hailes for Women’s Health 3. During the past month have you been PO Box 3367 bothered by feeling excessively worried East Melbourne VIC 3002 or concerned? Phone: 03 9453 8999 Disclaimer: these are general recommendations which must be modified according to the Email: [email protected] clinical presentation and desires of the individual woman after she has been fully assessed and informed of all available options. Clinics *Change in terminology: Hormone replacement therapy (HRT) is now frequently referred to as Jean Hailes Medical Centre for Women menopausal (MHT). 173 Carinish Road Clayton VIC 3168 Jean Hailes at Epworth Freemasons 412 Victoria Parade East Melbourne VIC 3002 Phone: 03 9562 7555

Jean Hailes for Women’s Health gratefully acknowledges the support of the Australian Government. © Jean Hailes for Women’s Health 2014 Updated June 2021