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Katrina Wyatt a Academic Department of Obstetrics and
Gynaecology, Keele University and North Staffordshire Hospital,
Stoke-on-Trent ST4 6QG, b Department of Mathematics, Keele University, Keele ST5 5BG
Correspondence to: S O'Brien pma06{at}keele.ac.uk
Objective:
To evaluate the efficacy of progesterone
and progestogens in the management of premenstrual syndrome.
What is already known on this topic
What this study adds
Design:
Systematic review of published randomised, placebo controlled trials.
Studies reviewed:
10 trials of progesterone therapy
(531 women) and four trials of progestogen therapy (378 women).
Main outcome measures:
Proportion of women whose
symptoms showed improvement with progesterone preparations
(suppositories and oral micronised). Proportion of women whose symptoms
showed improvement with progestogens. Secondary analysis of efficacy of
progesterone and progestogens in managing physical and behavioural symptoms.
Results:
Overall standardised mean difference for all trials that assessed efficacy of progesterone (by both routes of
administration) was
0.028 (95% confidence interval
0.017 to
0.040). The odds ratio was 1.05 (1.03 to 1.08) in favour of progesterone, indicating no clinically important difference between progesterone and placebo. For progestogens the overall standardised mean was
0.036 (
0.014 to
0.060), which corresponds to an odds ratio of 1.07 (1.03 to 1.11) showing a statistically, but not clinically, significant improvement for women taking progestogens.
Conclusion:
The evidence from these meta-analyses does not support the use of progesterone or progestogens in the management of premenstrual syndrome.
The premenstrual syndrome affects about 1.5 million women in the United
Kingdom
There is no evidence to support the claimed efficacy of progesterone in
the management of premenstrual syndrome
Read all Rapid Responses
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