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Clinical outcomes of intrauterine device insertions by newly trained providers : the ECHO trial experience

dc.contributor.authorYacobson, Irina
dc.contributor.authorWanga, Valentine
dc.contributor.authorAhmed, Khatija
dc.contributor.authorChipato, Tsungai
dc.contributor.authorGichangi, Peter
dc.contributor.authorKiarie, James
dc.contributor.authorLouw, Cheryl
dc.contributor.authorMorrison, Susan
dc.contributor.authorMoss, Margaret
dc.contributor.authorMugo, Nelly R.
dc.contributor.authorPalanee-Phillips, Thesla
dc.contributor.authorPleaner, Melanie
dc.contributor.authorScoville, Caitlin W.
dc.contributor.authorThomas, Katherine K.
dc.contributor.authorNanda, Kavita
dc.contributor.authorfor the Evidence for Contraceptive Options and HIV Outcomes (ECHO) Trial Consortium
dc.date.accessioned2024-05-14T05:31:31Z
dc.date.available2024-05-14T05:31:31Z
dc.date.issued2023
dc.descriptionACKNOWLEDGEMENTS : We thank the women who participated in this study for their motivation and dedication and the communities that supported this work. We also want to thank Sister Modiege Didi Maria Mojapelo (Refilwe Bophelo Clinic/NGO, Lanseria, South Africa), who served as one of the ECHO clinical trainers and certified ECHO clinicians in nine South African sites. The ECHO Trial is dedicated to the memory of Ward Cates.en_US
dc.description.abstractOBJECTIVES : To assess the rates of failed insertion, expulsion, and perforation when intrauterine device (IUD) insertions were done by newly trained clinicians, and to examine factors that may affect these outcomes. STUDY DESIGN : We evaluated skill-based outcomes following IUD insertion at 12 African sites in a secondary analysis of the Evidence for Contraceptive Options and HIV Outcomes (ECHO) randomized trial. Before trial initiation, we provided competency-based IUD training to clinicians and offered ongoing clinical support. We used Cox proportional hazards regression to examine factors associated with expulsion. RESULTS : Among 2582 IUD acceptors who underwent first attempted IUD insertion, 141 experienced insertion failure (5.46%) and seven had uterine perforation (0.27%). Perforation was more common among breastfeeding women within three months postpartum (0.65%) compared with non-breastfeeding women (0.22%). We recorded 493 expulsions (15.5 per 100 person-years, 95% confidence interval [CI] 14.1─16.9): 383 partial and 110 complete. The risk of IUD expulsion was lower among women older than 24 years (aHR 0.63, 95% CI 0.50─0.78) and may be higher among nulliparous women. (aHR 1.65, 95% CI 0.97─2.82). Breastfeeding (aHR 0.94, 95% CI 0.72─1.22) had no significant effect on expulsion. IUD expulsion rate was highest during the first three months of the trial. CONCLUSIONS : IUD insertion failure and uterine perforation rates in our study were comparable to those reported in the literature. These results suggest that training, ongoing support, and opportunities to apply new skills were effective in ensuring good clinical outcomes for women receiving IUD insertion by newly trained providers. IMPLICATIONS : Data from this study support recommendations to program managers, policymakers, and clinicians that IUDs can be inserted safely in resource-constrained settings when providers receive appropriate training and support.en_US
dc.description.departmentFamily Medicineen_US
dc.description.departmentMedical Microbiologyen_US
dc.description.librarianam2024en_US
dc.description.sdgSDG-03:Good heatlh and well-beingen_US
dc.description.sponsorshipThe Bill & Melinda Gates Foundation, the American people through the United States Agency for International Development, the Swedish International Development Cooperation Agency, the South Africa Medical Research Council, and the United Nations Population Fund. Contraceptive supplies were donated by the Government of South Africa and US Agency for International Development.en_US
dc.description.urihttps://www.sciencedirect.com/journal/contraception-xen_US
dc.identifier.citationYacobson, I., Wanga, V., Ahmed, K. et al. 2023, 'Clinical outcomes of intrauterine device insertions by newly trained providers : the ECHO trial experience', Contraception: X, vol. 5, art. 100092, pp. 1-8. https://DOI.org/10.1016/j.conx.2023.100092.en_US
dc.identifier.issn2590-1516
dc.identifier.other10.1016/j.conx.2023.100092
dc.identifier.urihttp://hdl.handle.net/2263/95937
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rights© 2023 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY license.en_US
dc.subjectCopper intrauterine deviceen_US
dc.subjectExpulsionen_US
dc.subjectInsertionen_US
dc.subjectProvider trainingen_US
dc.subjectUterine perforationen_US
dc.subjectIntrauterine device (IUD)en_US
dc.subjectEvidence for contraceptive options and HIV outcomes (ECHO)en_US
dc.subject.otherHealth sciences articles SDG-03
dc.subject.otherSDG-03: Good health and well-being
dc.titleClinical outcomes of intrauterine device insertions by newly trained providers : the ECHO trial experienceen_US
dc.typeArticleen_US

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