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Dienogest versus norethisterone acetate in management of endometrial hyperplasia without atypia
OBJECTIVES: To compare the effectiveness of dienogest (DIE) and norethisterone acetate (NETA) regimens in the treatment of endometrial hyperplasia (EH) without atypia. METHODS: Participants were premenopausal women with irregular uterine bleeding, and endometrial hyperplasia without atypia on endome...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10348941/ https://www.ncbi.nlm.nih.gov/pubmed/37010614 http://dx.doi.org/10.1007/s00404-023-07015-7 |
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author | Girbash, Ehab F. Sherif, Hala E. Radwan, Ahmed M. Abdeldayem, Hussein M. |
author_facet | Girbash, Ehab F. Sherif, Hala E. Radwan, Ahmed M. Abdeldayem, Hussein M. |
author_sort | Girbash, Ehab F. |
collection | PubMed |
description | OBJECTIVES: To compare the effectiveness of dienogest (DIE) and norethisterone acetate (NETA) regimens in the treatment of endometrial hyperplasia (EH) without atypia. METHODS: Participants were premenopausal women with irregular uterine bleeding, and endometrial hyperplasia without atypia on endometrial biopsy. Enrolled patients were randomly allocated into two groups: group I got DIE 2 mg/day (orally Visanne) for 14 days (10th to the 25th day of cycle) while group II received between the 16th and 25th day of the cycle, norethisterone acetate (NETA) 15 mg/d (orally Primolut Nor) was administered for 10 days. Both groups continued the therapy for six months. RESULTS: The DIE group showed a higher resolution (32.7%) and regression (57.7%) than NETA group (31% & 37.9%, respectively) with significant regression (p = 0.039). No progression in DIE group while four (6.9%) women in NETA group were recorded a progression to complex type without a significance. Also, NETA group showed a significant persistence rate (22.5%) than DIE group (3.8%) (p = 0.005). Also number in NETA group managed by hysterectomy with significant difference (p = 0.042). CONCLUSION: If used as first-line treatment, Dienogest produces a better rate of regression and a lower incidence of hysterectomy than Norethisterone Acetate does when used in EH without atypia. |
format | Online Article Text |
id | pubmed-10348941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-103489412023-07-16 Dienogest versus norethisterone acetate in management of endometrial hyperplasia without atypia Girbash, Ehab F. Sherif, Hala E. Radwan, Ahmed M. Abdeldayem, Hussein M. Arch Gynecol Obstet Gynecologic Oncology OBJECTIVES: To compare the effectiveness of dienogest (DIE) and norethisterone acetate (NETA) regimens in the treatment of endometrial hyperplasia (EH) without atypia. METHODS: Participants were premenopausal women with irregular uterine bleeding, and endometrial hyperplasia without atypia on endometrial biopsy. Enrolled patients were randomly allocated into two groups: group I got DIE 2 mg/day (orally Visanne) for 14 days (10th to the 25th day of cycle) while group II received between the 16th and 25th day of the cycle, norethisterone acetate (NETA) 15 mg/d (orally Primolut Nor) was administered for 10 days. Both groups continued the therapy for six months. RESULTS: The DIE group showed a higher resolution (32.7%) and regression (57.7%) than NETA group (31% & 37.9%, respectively) with significant regression (p = 0.039). No progression in DIE group while four (6.9%) women in NETA group were recorded a progression to complex type without a significance. Also, NETA group showed a significant persistence rate (22.5%) than DIE group (3.8%) (p = 0.005). Also number in NETA group managed by hysterectomy with significant difference (p = 0.042). CONCLUSION: If used as first-line treatment, Dienogest produces a better rate of regression and a lower incidence of hysterectomy than Norethisterone Acetate does when used in EH without atypia. Springer Berlin Heidelberg 2023-04-03 2023 /pmc/articles/PMC10348941/ /pubmed/37010614 http://dx.doi.org/10.1007/s00404-023-07015-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Gynecologic Oncology Girbash, Ehab F. Sherif, Hala E. Radwan, Ahmed M. Abdeldayem, Hussein M. Dienogest versus norethisterone acetate in management of endometrial hyperplasia without atypia |
title | Dienogest versus norethisterone acetate in management of endometrial hyperplasia without atypia |
title_full | Dienogest versus norethisterone acetate in management of endometrial hyperplasia without atypia |
title_fullStr | Dienogest versus norethisterone acetate in management of endometrial hyperplasia without atypia |
title_full_unstemmed | Dienogest versus norethisterone acetate in management of endometrial hyperplasia without atypia |
title_short | Dienogest versus norethisterone acetate in management of endometrial hyperplasia without atypia |
title_sort | dienogest versus norethisterone acetate in management of endometrial hyperplasia without atypia |
topic | Gynecologic Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10348941/ https://www.ncbi.nlm.nih.gov/pubmed/37010614 http://dx.doi.org/10.1007/s00404-023-07015-7 |
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