ABSTRACT
This article reviews the two intrauterine devices (IUDs) available in the United States:
the TCu380A, marketed as ParaGard (Duramed Pharmaceuticals, Inc. Pomona, NY), and
the levonorgestrel-releasing intrauterine system (LNG-IUS), marketed as Mirena (Bayer
HealthCare Pharmaceuticals, Inc., Wayne, NJ). The properties of the two devices are
detailed, as well as noncontraceptive indications and appropriate candidates for use.
Studies consistently demonstrate that the devices are safe, effective, and provide
cost savings when compared with other reversible methods. The TCu380A may be used
as postcoital contraception with close to 100% effectiveness. Menstrual blood loss
is likely to increase with the TCu380A and decrease with the LNG-IUS. Reduction in
menstrual blood loss and endometrial suppression make the LNG-IUS an increasingly
popular treatment for menorrhagia, endometriosis, adenomyosis, and as an adjunct to
estrogen therapy. IUDs may be inserted immediately after a first- or second-trimester
abortion, immediately postpartum, and ≥4 weeks postpartum. Candidacy for IUDs has
expanded, and includes nulliparous women, adolescents, and women with immunocompromised
conditions including HIV.
KEYWORDS
Intrauterine device - intrauterine system - LNG-IUS - ParaGard - Mirena
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Noa'a ShimoniM.D.
Columbia University Medical Center, Department of Obstetrics and Gynecology
622 W. 168th St., New York, NY 10032
eMail: ns2476@columbia.edu