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Clinical outcomes of intrauterine device insertions by newly trained providers: The ECHO trial experience.
Yacobson, Irina; Wanga, Valentine; Ahmed, Khatija; Chipato, Tsungai; Gichangi, Peter; Kiarie, James; Louw, Cheryl; Morrison, Susan; Moss, Margaret; Mugo, Nelly R; Palanee-Phillips, Thesla; Pleaner, Melanie; Scoville, Caitlin W; Thomas, Katherine K; Nanda, Kavita.
Afiliación
  • Yacobson I; FHI 360, Durham, NC, United States.
  • Wanga V; Department of Global Health, University of Washington, Seattle, WA, United States.
  • Ahmed K; Setshaba Research Centre, Soshanguve, Gauteng, South Africa.
  • Chipato T; Faculty of Health Sciences, Department of Medical Microbiology, University of Pretoria, Pretoria, Gauteng, South Africa.
  • Gichangi P; University of Zimbabwe, College of Health Sciences, Harare, Zimbabwe.
  • Kiarie J; International Centre for Reproductive Health, Nyali, Mombasa, Kenya.
  • Louw C; University of Nairobi, Nairobi, Kenya.
  • Morrison S; Department of Public Health and Primary Care, Faculty of Medicine and Health Sciences, Ghent University, Ghent, East Flanders, Belgium.
  • Moss M; UNDP-UNFPA-UNICEF-WHO-World Bank Special Programme of Research, Development and Research Training in Human Reproduction, World Health Organization, Geneva, Switzerland.
  • Mugo NR; Madibeng Centre for Research, Brits, North West, South Africa.
  • Palanee-Phillips T; Department of Family Medicine, University of Pretoria, Pretoria, Gauteng, South Africa.
  • Pleaner M; Department of Global Health, University of Washington, Seattle, WA, United States.
  • Scoville CW; Department of O&G, Faculty of Health Sciences, University of Cape Town/Groote Schuur Hospital, Cape Town, Western Cape, South Africa.
  • Thomas KK; Department of Global Health, University of Washington, Seattle, WA, United States.
  • Nanda K; Center for Clinical Research, Kenya Medical Research Institute, Nairobi, Kenya.
Contracept X ; 5: 100092, 2023.
Article en En | MEDLINE | ID: mdl-37188149
Objectives: 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.
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Guideline Idioma: En Revista: Contracept X Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Guideline Idioma: En Revista: Contracept X Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos