Psychosexual well-being in women using oral contraceptives containing drospirenone

Functional neurology · 2009 · vol. 24(2) , pp. 71–5 · PMID:19775533 · W2060024087
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This study found that oral contraceptives containing drospirenone and estrogen improved water retention, physical health, and psychosexual well-being in women.

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Abstract

Considerable advances have been made in hormonal contraception in recent years, geared at maximizing compliance and minimizing discontinuation. In oral contraceptive (OC) formulations, the estrogenic component, generally ethinyl estradiol (EE), has been reduced significantly and newer progestins like dienogest and drospirenone (DRSP), compounds with different molecular structures, have been introduced; in addition, new regimens (extended, flexible, 24/4 formats instead of the standard 21/7 format) and innovative delivery systems (vaginal rings, transdermal patches, subcutaneous implants and intrauterine devices) are available. The multitude of choices allows hormonal contraception to be tailored to the individual woman in order to obtain non-contraceptive benefits, without significant side effects, and also a favorable risk/benefit profile for her general and reproductive health. Over the past few years, new OC formulations combining DRSP (3 mg), a unique progestin with both antimineralocorticoid and antiandrogenic activities, with estrogen (30 mcg or 20 mcg EE), in two regimens (24/4 and 21/7) of active pills in a 28-day cycle, have shown positive effects on water retention-related weight gain and physical, emotional and psychosexual well-being. It seems likely that the use of a low-dose, well-balanced OC and the shorter 4-day hormone-free interval may minimize the side effects that can impair quality of life and thus increase women's compliance with hormonal contraception therapy.

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MeSH descriptors

Androstenes Contraceptives, Oral Mineralocorticoid Receptor Antagonists Quality of Life Women's Health Androstenes Androstenes Chemistry, Pharmaceutical Contraceptives, Oral Contraceptives, Oral Dose-Response Relationship, Drug Estrogens Estrogens Female Humans Mineralocorticoid Receptor Antagonists Mineralocorticoid Receptor Antagonists Patient Satisfaction Sexual Dysfunctions, Psychological Sexual Dysfunctions, Psychological

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