Adverse Effects
Adverse effects of
variable severity have been reported with the therapeutic use of estrogens.
Many other effects reported in con-junction with hormonal contraceptives may be
related to their estrogen content. These are discussed below.
Estrogen therapy is a
major cause of postmenopausal uterine bleeding. Unfortunately, vaginal bleeding
at this time of life may also be due to carcinoma of the endometrium. To avoid
confusion, patients should be treated with the smallest amount of estrogen
possible. It should be given cyclically so that bleeding, if it occurs, will be
more likely to occur during the withdrawal period. As noted above, endometrial
hyperplasia can be prevented by admin-istration of a progestational agent with
estrogen in each cycle.
The
relation of estrogen therapy to cancer continues to be the sub-ject of active
investigation. Although no adverse effect of short-term estrogen therapy on the
incidence of breast cancer has been dem-onstrated, a small increase in the
incidence of this tumor may occur with prolonged therapy. Although the risk
factor is small (1.25), the impact may be great since this tumor occurs in 10%
of women, and addition of progesterone does not confer a protective effect.
Studies indicate that following unilateral excision of breast cancer, women
receiving tamoxifen (an estrogen partial agonist, ) show a 35% decrease in
contralateral breast cancer compared with con-trols. These studies also
demonstrate that tamoxifen is well toler-ated by most patients, produces
estrogen-like alterations in plasma lipid levels, and stabilizes bone mineral
loss. Studies bearing on the possible efficacy of tamoxifen in postmenopausal
women at high risk for breast cancer are under way. A recent study shows that
postmenopausal hormone replacement therapy with estrogens plus progestins was
associated with greater breast epithelial cell prolif-eration and breast
epithelial cell density than estrogens alone or no replacement therapy.
Furthermore, with estrogens plus progestins, breast proliferation was localized
to the terminal duct-lobular unit of the breast, which is the main site of
development of breast can-cer. Thus, further studies are needed to conclusively
assess the pos-sible association between progestins and breast cancer risk.
Many studies show an
increased risk of endometrial carcinoma in patients taking estrogens alone. The
risk seems to vary with the dose and duration of treatment: 15 times greater in
patients taking large doses of estrogen for 5 or more years, in contrast with
two to four times greater in patients receiving lower doses for short peri-ods.
However, as noted above, the concomitant use of a progestin prevents this
increased risk and may in fact reduce the incidence of endometrial cancer to
less than that in the general population.
There have been a
number of reports of adenocarcinoma of the vagina in young women whose mothers
were treated with large doses of diethylstilbestrol early in pregnancy. These
cancers are most common in young women (ages 14–44). The incidence is less than
1 per 1000 women exposed—too low to establish a cause-and-effect relationship
with certainty. However, the risks for infer-tility, ectopic pregnancy, and
premature delivery are also increased. It is now recognized that there is no
indication for the use of dieth-ylstilbestrol during pregnancy, and it should
be avoided. It is not known whether other estrogens have a similar effect or
whether the observed phenomena are peculiar to diethylstilbestrol. This agent
should be used only in the treatment of cancer (eg, of the prostate) or as a
“morning after” contraceptive .
Nausea
and breast tenderness are common and can be minimized by using the smallest
effective dose of estrogen. Hyperpigmentation also occurs. Estrogen therapy is
associated with an increase in frequency of migraine headaches as well as
cholestasis, gallbladder disease, and hypertension.
Estrogens should not
be used in patients with estrogen-dependent neoplasms such as carcinoma of the
endometrium or in those with—or at high risk for—carcinoma of the breast. They
should be avoided in patients with undiagnosed genital bleeding, liver disease,
or a history of thromboembolic disorder. In addition, the use of estrogens
should be avoided by heavy smokers.
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