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. 2020 Aug;146(2):e20200016.
doi: 10.1542/peds.2020-0016.

Intrauterine Device Use in Adolescents With Disabilities

Affiliations

Intrauterine Device Use in Adolescents With Disabilities

Beth I Schwartz et al. Pediatrics. 2020 Aug.

Abstract

Background and objectives: Intrauterine devices (IUDs) are increasingly being used in adolescents and nulliparous women for contraception. Levonorgestrel IUDs also have beneficial effects on bleeding and pain. Although they are recommended for menstrual suppression in adolescents with disabilities, there are limited data on their use in this population. Our objective is to describe the characteristics and experiences of levonorgestrel IUD use in nulliparous children, adolescents, and young adults with physical, intellectual, and developmental disabilities.

Methods: A retrospective chart review was conducted for all nulliparous patients ages ≤22 with physical, intellectual, or developmental disabilities who had levonorgestrel IUDs placed between July 1, 2004, and June 30, 2014, at a tertiary-care children's hospital. Descriptive statistical analysis and survival analysis were performed.

Results: In total, 185 levonorgestrel IUDs were placed in 159 patients with disabilities. The mean age was 16.3 (3.3; range of 9-22) years. Only 4% had ever been sexually active; 96% of IUDs were inserted in the operating room. IUD continuation rate at 1 year was 95% (95% confidence interval: 93%-100%) and at 5 years was 73% (95% confidence interval: 66%-83%). The amenorrhea rate was ∼60% throughout the duration of IUD use among those with available follow-up data. Side effects and complications were ≤3%.

Conclusions: In this study, we provide evidence for the therapeutic benefit and safety of levonorgestrel IUD use in adolescents and young adults with physical, intellectual, and developmental disabilities. It should be considered as a menstrual management and contraceptive option for this population.

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Conflict of interest statement

POTENTIAL CONFLICT OF INTEREST: Drs Schwartz and Breech received a Bayer Healthcare Investigator-Initiated Research grant for women’s health (WH-2013-006) to support this study. The sponsor had a minimal role in approving the study design. There was no sponsor involvement in the conduct of the study; collection, analysis, or interpretation of the data; preparation, review, or approval of the article; or decision to submit for publication. Ms Alexander has indicated she has no potential conflicts of interest to disclose.

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