HRT Benefits And Risks W3 Flashcards

1
Q

How long should HRT be taken for

A

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

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2
Q

side effects shown in trials

A

 Stroke
 Breast cancer
 Endometrial cancer
 Venous thromboembolism

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3
Q

HRT in women over 60

A

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

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4
Q

Oestrogen side effects of HRT

A

 Nausea and vomiting
 Abdominal cramps and bloating
 Weight changes (gain)
 Breast tenderness and enlargement
 Premenstrual-like syndrome
 Sodium and fluid retention

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5
Q

Progesterone side effects of HRT

A

 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

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6
Q

Why do women stop taking HRT

A

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 §

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7
Q

Short term benefits of HRT

A

Control symptoms of the peri/post meno including hot sweats, headaches, mood changes, loss of libido and thinning of hair

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8
Q

Long term benefits of HRT

A

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

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9
Q

Risks of HRT

A
  • 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
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10
Q

Risks of breast cancer

A

 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

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11
Q

Risks of endometrial cancer

A

 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

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12
Q

Risks of ovarian cancer

A

 Small increased risk with both combined and oestrogen only HRT
 Excess risk disappears within few years of stopping

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13
Q

Risks of stroke

A

 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

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14
Q

Coronary heart disease and HRT

A

 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

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15
Q

Tibolone

A

 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

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16
Q

Clonidine

A

 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

17
Q

What else could women use for
menopausal symptoms?

A

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