HRT Benefits And Risks W3 Flashcards
How long should HRT be taken for
For vasomotor symptoms, HRT usually used for 2-3 years (initial review at 3 months to assess efficacy & tolerability)
Annual review recommended because of increased risk of side effects shown in trials
side effects shown in trials
Stroke
Breast cancer
Endometrial cancer
Venous thromboembolism
HRT in women over 60
Prescribed before 60 Has a favourable benefit/risk profile in healthy women
Lower doses must be started n preferably with a trqansdermal route of estradiol administration
Oestrogen side effects of HRT
Nausea and vomiting
Abdominal cramps and bloating
Weight changes (gain)
Breast tenderness and enlargement
Premenstrual-like syndrome
Sodium and fluid retention
Progesterone side effects of HRT
More androgenic drugs (norethisterone, levonorgestrol):
Cause greasy skin + hair
Tend to off-set some of the protective effect of oestrogens on lipid profile
Less androgenic drugs (dydrogesterone, medroxyprogesterone) cause progesterone-like side effects:
Abdominal bloating
Mood changes such as irritability, depression
Breast tenderness
Why do women stop taking HRT
Non-compliance with HRT is most commonly due to:
- Side effects of the progestogen
- Regular monthly bleed induced by combination therapy when periods had been in the process of stopping
- Weight gain §
Short term benefits of HRT
Control symptoms of the peri/post meno including hot sweats, headaches, mood changes, loss of libido and thinning of hair
Long term benefits of HRT
Decreased risk of osteoporosis
Oestrogen rebalances bone re-sorption and formation thus stopping bone loss
Possibly some bone gain during the initial 18-24 months of HRT treatment
Bone-protective effect is probably dosage-related
Protection lasts only as long as HRT is taken
Continuous lifelong use would be required for HRT to be an effective method of preventing hip fractures
Consider change to e.g. bisphosphonates when HRT not appropriate
Risks of HRT
- VTE risk increased with combined or oestrogen only HRT especially in first year of use
- women with predisposing risk factors
- VTE risk is greater with oral than transdermal
Risks of breast cancer
All systemic HRT increases risk after 1 year of use
Combined oestrogen-progesterone (particularly continuous) higher risk than oestrogen only
No increased risk for local vaginal oestrogen
Risk reduces after stopping but excess risk remains for over 10 years compared to women who have never used HRT
Risks of endometrial cancer
Associated with oestrogen – only HRT
Women with uterus => addition of progestogen (minimum of 10 days per 28 day cycle) reduces risk
Risk eliminated if progestogen used continuously
Risks of ovarian cancer
Small increased risk with both combined and oestrogen only HRT
Excess risk disappears within few years of stopping
Risks of stroke
Risk of stroke increases with age
Older women have greater absolute risk of stroke
Combined and oestrogen-only HRT slightly increases this risk of stroke
Coronary heart disease and HRT
Not conclusive!!
Before the menopause, the incidence of CHD in women is lower than in men
After the menopause, the incidence of CHD in men and women becomes similar
CHD is the leading cause of death in post- menopausal women
Oestrogen alone ► no, or reduced, risk of CHD
Oestrogen + progesterone ►little or no increase in risk of
CHD
Tibolone
2.5mg od
Gonadomimetic
Synthetic steroid derivative of norethisterone
Mixed oestrogenic, progestogenic and androgenic activity
Licensed for short-term treatment of symptoms and osteoporosis prophylaxis (2nd line)
Same cautions/ contraindications as Oestrogen HRT
Clonidine
50mcg bd increased if required to 75mcg bd after 2 weeks
Vasomotor symptoms especially hot flushes
Centrally acting ꭤ-adrenergic agonist => possibly reduces noradrenergic activity in blood vessels
What else could women use for
menopausal symptoms?
Anecdotal evidence for:
St John’s Wort
Products containing phytoestrogens
Black cohosh
Red clover
Little efficacy or safety data
Some risks
St John’s Wort – interactions
Liver impairment with black cohosh
Red clover contains coumarins, interacts with warfarin
Possible increased risk from oestrogenic effects e.g. VTE