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. 1992;8(1-2):71-3.

Vaginal rings for contraception: endocrine parameters

  • PMID: 12285565

Vaginal rings for contraception: endocrine parameters

S E Olsson. Adv Contracept Deliv Syst. 1992.

Abstract

PIP: Most of this review of the development of steroid-containing vaginal rings for contraception consists of a table listing drug dose, effect of the ring on bleeding and ovulation, and citation. The advantage of formulating a medicated vaginal ring is that the first-pass effect of an oral route of administration is avoided. Blood levels of the steroid are constant throughout the day. Low-dose progestin rings generally result in menstrual bleeding anomalies. Bleeding patterns improve when the progestin dose is raised and estradiol is added. A levonorgestrel ring developed by WHO has been fairly acceptable, with normal bleeding patterns in 50% of users, 365 ovulatory cycles, and pregnancy rates of 9.8% in women weighing 80 kg, and 1.7% in women 40 kg. Another approach is to combine progestin and estrogen. A ring releasing 120 or 150 mcg 3 keto-desogestrel and 15 mcg ethinyl estradiol daily has prevented ovulation and left bleeding patterns intact. The rings are used for 21 days, and removed for 7, and last 3 months. Generally about 70% of women find vaginal rings acceptable.

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