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OESTROGENS FOR HRT
Cautions
-
prolonged exposure to unopposed oestrogens may increase risk of developing endometrial cancer (see
notes above);
-
migraine (or migraine-like headaches);
-
diabetes (increased risk of heart disease);
-
history of breast nodules or fibrocystic disease closely monitor breast status (risk of breast cancer, see
notes above);
-
risk factors for oestrogen-dependent tumours (e.g. breast cancer in first-degree relative);
-
uterine fibroids may increase in size, symptoms of endometriosis may be exacerbated;
-
factors predisposing to thromboembolism (see
notes above);
-
presence of antiphospholipid antibodies (increased risk of thrombotic events); increased risk of gall-bladder disease reported; hypophyseal tumours;
-
porphyria (see
section 9.8.2);
interactions:Appendix 1 (oestrogens)
Other conditionsThe product literature advises caution in other conditions including
Evidence for caution in these conditions is unsatisfactory and many women with these conditions may stand to benefit from HRT.
Contra-indications
-
pregnancy;
-
oestrogen-dependent cancer,
-
history of breast cancer,
-
active thrombophlebitis,
-
active or recent arterial thromboembolic disease (e.g. angina or myocardial infarction),
-
venous thromboembolism, or history of recurrent venous thromboembolism (unless already on anticoagulant treatment),
-
liver disease (where liver function tests have failed to return to normal),
-
Dubin-Johnson and Rotor syndromes (or monitor closely),
-
untreated endometrial hyperplasia,
-
undiagnosed vaginal bleeding,
-
breast-feeding
side effects
-
nausea and vomiting,
-
abdominal cramps and bloating,
-
weight changes,
-
breast enlargement and tenderness,
-
premenstrual-like syndrome,
-
sodium and fluid retention,
-
cholestatic jaundice,
-
glucose intolerance,
-
altered blood lipids?may lead to pancreatitis, rashes and chloasma,
-
changes in libido,
-
depression,
-
mood changes,
-
headache,
-
migraine,
-
dizziness,
-
leg cramps (rule out venous thrombosis),
-
vaginal candidiasis,
-
contact lenses may irritate;
-
transdermal delivery systems may cause contact sensitisation (possible severe hypersensitivity reaction on continued exposure), and headache has been reported on vigorous exercise
Withdrawal bleedingCyclical HRT (where a progestogen is taken for 12?14 days of each 28-day oestrogen treatment cycle) usually results inregular withdrawal bleeding towards the end of the progestogen.
The aim of continuous combined HRT (where a combination of oestrogen and progestogen is taken, usually in a single tablet, throughout each 28-day treatment cycle) is to avoid bleeding, butirregular bleeding may occur during the early treatment stages (if it continues endometrial abnormality should be excluded and consideration given to cyclical HRT instead)
Dose
Counselling on patchesPatch should be removed after 3?4 days (or once a week in case of 7-day patch) and replaced with fresh patch on slightly different site; recommended sites: clean, dry, unbroken areas of skin on trunk below waistline; not to be applied on or near breasts or under waistband. If patch falls off in bath allow skin to cool before applying new patch
Table 28. 5 Se quential HRT preparations (cyclical progestogen tablets).
|
PREPARATION |
OESTROGEN/PROGESTOGEN |
mg |
COMPANY |
|
|
TABLETS |
|
|
|
Nuvelle |
Oestradiol / Levonorgestrel |
2 / 75mcg |
Schering |
|
Climagest 1 mg |
Oestradiol / Norethisterone |
1 / 1 |
Novartis |
|
Climagest 2 mg |
|
2 / 1 |
Novartis |
|
Clinorette |
Oestradiol |
2 / 1 |
|
|
| |