Saturday, 12 October 2019

What are the Cochrane date base Review results on Routine trigger in CC/HMG cycles??


What are the Cochrane date base Review results on Routine trigger in CC/HMG cycles??

Dr Pal do you have any evidence about the fact that “there is an apparent lack of effect of hCG as an ovulation trigger in clomiphene-induced cycles in anovulatory women” ? What do U say, Dear  Dr Pal?? .
Anovulation is a common cause of infertility. Drugs used to treat anovulation include 1) selective oestrogen receptor modulators, 2) aromatase inhibitors and 3) gonadotrophins. Ovulation triggers are used with these drugs, as a surrogate for the hormonal surge seen in spontaneous menstrual cycles, to control the timing of ovulation and the timing of sexual intercourse.

Sadly, ovulation triggers given without reliable evidence of oocyte maturity could be inappropriately timed; they increase costs, and the need to time intercourse precisely after the ovulation trigger is given adds to psychological stress. An update of a Cochrane review first published in Issue 3, 2008, of the Cochrane Database of Systematic Reviews.
To determine the benefits and harms of administering an ovulation trigger to anovulatory women receiving treatment with ovulation-inducing agents in comparison with spontaneous ovulation following ovulation induction.
That compared urinary human chorionic gonadotrophin (hCG) versus no treatment in anovulatory women receiving clomiphene citrate. Urinary hCG did not result in an increase in live birth rate over no hCG I(2) = 16%; low-quality evidence), but very serious imprecision around the effect estimate reduces our confidence in the apparent lack of effect of hCG as an ovulation trigger in clomiphene-induced cycles in anovulatory women.
Among this review's secondary outcomes, urinary hCG may not increase ovulation rate (low-quality evidence), clinical pregnancy rate (low-quality evidence) or miscarriage rate in pregnant women (low-quality evidence). Multiple pregnancies and preterm deliveries were uncommon, and ovarian hyperstimulation syndrome, adverse events and deaths were not reported as outcomes in either trial. We found no trials evaluating other ovulation triggers.
CONCLUSIONS:
Evidence is inadequate to recommend or refute the use of urinary hCG as an ovulation trigger in anovulatory women treated with clomiphene citrate. We found no trials evaluating the use of ovulation triggers in anovulatory women treated with other ovulation-inducing agents. .
T



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