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Title
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Insertion experience of women and health care professionals in the Kyleena((R)) Satisfaction Study
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Author
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Abstract
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| Purpose: The Kyleena (R) Satisfaction Study (KYSS) is a prospective, observational study conducted to assess satisfaction with LNG-IUS 12 (Kyleena (R)) in clinical practice and aims to provide adequate information for counselling women on what to expect regarding insertion and satisfaction. Materials and methods: Women deciding to use LNG-IUS 12 during routine counselling were informed of the study and provided informed consent. A baseline analysis was conducted to evaluate demographics, ease of insertion assessed by investigators, pain at insertion rated by women, additional interventions for insertion, and adverse events. Results: 1,110 women (536 parous, 574 nulliparous) had an insertion attempt and were included. Insertion was rated as easy in 494 (92.2%) parous and 516 (89.9%) nulliparous women. Pain was assessed as none or mild by 475 (88.6%) parous and 387 (67.4%) nulliparous women. Additional interventions were not required for most insertions (705; 63.6%). Overall 111 (10.0%) women reported adverse events at the time of baseline analysis. Conclusions: This analysis demonstrates that LNG-IUS 12 insertion is easy and associated with no or mild pain in most women. Additional interventions for insertion are not required in most cases. After 3 months, the number of adverse events is low. Implications: The present baseline analysis of the Kyleena (R) Satisfaction Study (KYSS) demonstrates that most women rate insertion pain of LNG-IUS 12 as none or mild and clinicians consider insertion easy in the majority of cases. |
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Language
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English
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Source (journal)
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European journal of contraception and reproductive health care
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Publication
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Abingdon
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Taylor & francis ltd
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2020
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ISSN
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1362-5187
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DOI
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10.1080/13625187.2020.1736547
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Volume/pages
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p. 1-8
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ISI
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000537938000001
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Pubmed ID
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32223466
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Full text (Publisher's DOI)
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Full text (open access)
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