1)HOW CC ACTS? CC is a drug of
considerable pharmacologic potency. With careful selection and proper
.Management of the patient, CLOMID has been demonstrated to be a useful therapy
for the .Anovulatory patient desiring pregnancy.
Clomiphene citrate is capable of interacting with
estrogen-receptor-containing tissues, including the hypothalamus, pituitary,
ovary, endometrium, vagina, and cervix. It may compete with estrogen for
estrogen-receptor-binding sites and may delay replenishment of intracellular
estrogen receptors.
Clomiphene citrate initiates a series of endocrine events culminating in a
preovulatory gonadotropin
surge and subsequent follicular rupture. The first endocrine event in
response to a course of
clomiphene therapy is an increase in the release of pituitary
gonadotropins. This
initiates steroidogenesis and folliculogenesis, resulting in growth of the
ovarian follicle and an
increase in the circulating level of estradiol. Following ovulation, plasma
progesterone and estradiol
rise and fall as they would in a normal ovulatory cycle.
Available data suggest
that both the estrogenic and antiestrogenic properties of clomiphene may
participate in the initiation of ovulation. The two clomiphene isomers have
been found to have mixed estrogenic and antiestrogenic effects, which may vary
from one species to another. Some
data suggest that zuclomiphene
has greater estrogenic activity than enclomiphene. Clomiphene
citrate has no apparent progestational, androgenic, or antiandrogenic effects
and
does not appear to
interfere with pituitary-adrenal or pituitary-thyroid function
Why En- clomiphene is better?
En & Zu clomiphene. En is more potent as OI. Half
life is short, But Zu last long in the body as many as 1 month after
stimulation. In obese women higher dose –no benefit.
Q.4. What is
the prevalence of CC resistance case & how do we treat that? About
20-25 % cases do not respond to CC. The options are further investigations
& treat with followings:.
Q.5. Is
there any Carry Over Effect?
Although there is no evidence of a “carryover
effect” of CC , spontaneous ovulatory
menses have been noted in some patients after CLOMID therapy.
1
Q.5. what is the pregnancy rates?
CLINICAL STUDIES
During clinical
investigations, 7578 patients received, CC some
of whom had
impediments to ovulation
other than ovulatory dysfunction (In those clinical trials, successful therapy
characterized by pregnancy
occurred in approximately
30% of these patients.
There were a total of 2635
pregnancies reported during the clinical trial period. Of those
pregnancies, information
on outcome was only available for 2369 of the cases. Table 1
summarizes the outcome of
these cases.
Of the reported
pregnancies, the incidence of multiple
pregnancies was 7.98%: 6.9% twin, 0.5%
triplet, 0.3% quadruplet,
and 0.1% quintuplet. Of the 165 twin pregnancies for which sufficient
information was available;
the ratio of monozygotic to dizygotic twins was about 1:5. Table 1
reports the survival rate
of the live multiple births.
A
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