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Hormonal intrauterine device in women with renal transplantation: a prospective observational study
OBJECTIVE: The main objective of this study is to evaluate the rate of continuity and satisfaction with hormonal intrauterine device in renal transplant recipients. METHODS: This was a prospective observational study. The sample consisted of patients treated at a Family Planning Outpatient Clinic, f...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Médica Brasileira
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511283/ https://www.ncbi.nlm.nih.gov/pubmed/37729224 http://dx.doi.org/10.1590/1806-9282.20230352 |
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author | Amado, Fernanda Costa de Oliveira, Anelisa Pinotti Hamamoto, Tatiana Emy Nishimoto Kawanami Araujo, Edward Guazzelli, Cristina Aparecida Falbo |
author_facet | Amado, Fernanda Costa de Oliveira, Anelisa Pinotti Hamamoto, Tatiana Emy Nishimoto Kawanami Araujo, Edward Guazzelli, Cristina Aparecida Falbo |
author_sort | Amado, Fernanda Costa |
collection | PubMed |
description | OBJECTIVE: The main objective of this study is to evaluate the rate of continuity and satisfaction with hormonal intrauterine device in renal transplant recipients. METHODS: This was a prospective observational study. The sample consisted of patients treated at a Family Planning Outpatient Clinic, from August 2016 to September 2021. Information on each patient’s age, parity, and associated diseases as well as satisfaction with the method were analyzed. Patients were invited to participate through electronic messages, and the questionnaire included questions about acceptance of the contraceptive method. RESULTS: A total of 40 patients were included in the study. The mean age of the renal transplant patients was 32.5 years. The mean duration of hormonal intrauterine device use was 37 months. Acceptance of the method was high, with 97.5% of patients remaining on the method for 1 year and 85% of patients using the hormonal intrauterine device at the time of the study. There were no pregnancies or renal transplant complications in the study. Regarding satisfaction with the method, the majority (77.5%) scored 10. CONCLUSION: Patients were satisfied or very satisfied with the hormonal intrauterine device. Therefore, the continuation rate was high. Furthermore, this contraceptive method proved to be safe and effective in kidney transplant recipients. No complications, graft rejection, or graft failure were observed after intrauterine hormonal device insertion and during follow-up. |
format | Online Article Text |
id | pubmed-10511283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Associação Médica Brasileira |
record_format | MEDLINE/PubMed |
spelling | pubmed-105112832023-09-21 Hormonal intrauterine device in women with renal transplantation: a prospective observational study Amado, Fernanda Costa de Oliveira, Anelisa Pinotti Hamamoto, Tatiana Emy Nishimoto Kawanami Araujo, Edward Guazzelli, Cristina Aparecida Falbo Rev Assoc Med Bras (1992) Original Article OBJECTIVE: The main objective of this study is to evaluate the rate of continuity and satisfaction with hormonal intrauterine device in renal transplant recipients. METHODS: This was a prospective observational study. The sample consisted of patients treated at a Family Planning Outpatient Clinic, from August 2016 to September 2021. Information on each patient’s age, parity, and associated diseases as well as satisfaction with the method were analyzed. Patients were invited to participate through electronic messages, and the questionnaire included questions about acceptance of the contraceptive method. RESULTS: A total of 40 patients were included in the study. The mean age of the renal transplant patients was 32.5 years. The mean duration of hormonal intrauterine device use was 37 months. Acceptance of the method was high, with 97.5% of patients remaining on the method for 1 year and 85% of patients using the hormonal intrauterine device at the time of the study. There were no pregnancies or renal transplant complications in the study. Regarding satisfaction with the method, the majority (77.5%) scored 10. CONCLUSION: Patients were satisfied or very satisfied with the hormonal intrauterine device. Therefore, the continuation rate was high. Furthermore, this contraceptive method proved to be safe and effective in kidney transplant recipients. No complications, graft rejection, or graft failure were observed after intrauterine hormonal device insertion and during follow-up. Associação Médica Brasileira 2023-09-18 /pmc/articles/PMC10511283/ /pubmed/37729224 http://dx.doi.org/10.1590/1806-9282.20230352 Text en https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Amado, Fernanda Costa de Oliveira, Anelisa Pinotti Hamamoto, Tatiana Emy Nishimoto Kawanami Araujo, Edward Guazzelli, Cristina Aparecida Falbo Hormonal intrauterine device in women with renal transplantation: a prospective observational study |
title | Hormonal intrauterine device in women with renal transplantation: a prospective observational study |
title_full | Hormonal intrauterine device in women with renal transplantation: a prospective observational study |
title_fullStr | Hormonal intrauterine device in women with renal transplantation: a prospective observational study |
title_full_unstemmed | Hormonal intrauterine device in women with renal transplantation: a prospective observational study |
title_short | Hormonal intrauterine device in women with renal transplantation: a prospective observational study |
title_sort | hormonal intrauterine device in women with renal transplantation: a prospective observational study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511283/ https://www.ncbi.nlm.nih.gov/pubmed/37729224 http://dx.doi.org/10.1590/1806-9282.20230352 |
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