Efficacy
of progesterone and progestogens in management of premenstrual syndrome:
systematic review
British Medical Journal v.323, i.7316 6oct01
Katrina Wyatt, lecturer, a Paul Dimmock, research fellow, a Peter Jones, professor of statistics, b Manjit Obhrai, consultant obstetrician and gynaecologist, a Shaughn O'Brien, head of academic obstetrics and gynaecology. a
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@keele.ac.uk
Objective: To evaluate the efficacy of progesterone and progestogens
in the management of premenstrual syndrome.
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.
What is already known on this topic
What this study adds:
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