POSTCOITAL/EMERGENCY CONTRACEPTION
Postcoital
or emergency contraception (ECP) maybe used for women who
experience unprotected sexual intercourse. Making postcoital contraception
widely and easily available is one of the most important steps that can be
taken to reduce the high rates of unintended pregnancy and abortion. It is
estimated that the regular use of postcoital contraception would prevent more
than 1.5 million unintended pregnancies in the United States each year.
Combined oral conceptive regimens
used for emer-gency contraception, known collectively as the Yuzpe method, were
first reported by Albert Yuzpe in 1974. These regimens require taking 2 tablets
within 72 hours of unprotected intercourse, followed by another two tablets in
12 hours. Subsequently, the use of a progestin-only regimen, known as “Plan B,” was approved for behind-the-counter
dispensing to women over 18 years of age without a prescription. Plan B
consists of two tablets of levonorgestrel taken 12 hours apart. This method is
asso-ciated with a lower incidence of nausea and emesis than the Yuzpe method
and with greater effectiveness. Both methods act by preventing ovulation and
fertilization, and will not terminate an existing pregnancy. Emergency
contraception can also be accomplished with a copper-containing IUD.
The failure rate for the Yuzpe
regimen is estimated at 25%; for Plan B, 11%. Multiple unprotected coital
events or an interval greater than 72 hours may be associated with an
increasing failure rate, although some evidence of suc-cess is seen out to 120
hours after unprotected intercourse. If the woman is already pregnant, these
medications have no ill effect on the fetus. The amount of hormone in these
regimens is not associated with alterations in clotting fac-tors or teratogenic
risk.
The copper IUD is another
recommended option for emergency contraception (except in patients with Wilson
disease) and, in limited studies, has a failure rate of approx-imately 0.1%. An
additional advantage of IUD insertion is the contraceptive effect that is
provided for up to 10 years. Before using this method, a pregnancy test is
required be-cause of the risk to an implanted pregnancy.
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