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The effect of GnRH analogues for pituitary suppression on ovarian response in repeated ovarian stimulation cycles

INTRODUCTION: Ovarian stimulation is employed in assisted reproduction techniques in order to obtain as many oocytes as possible. The early rise in oestradiol levels may lead to the premature end of the respective cycle. In order to avoid such an effect, pituitary suppression has been employed. The...

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Autores principales: Cavagna, Mario, Paes de Almeida Ferreira Braga, Daniela, Biaggioni Lopes, Fabio, de Cássia Savio Figueira, Rita, Iaconelli, Assumpto, Borges, Edson
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3258761/
https://www.ncbi.nlm.nih.gov/pubmed/22295031
http://dx.doi.org/10.5114/aoms.2011.23414
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author Cavagna, Mario
Paes de Almeida Ferreira Braga, Daniela
Biaggioni Lopes, Fabio
de Cássia Savio Figueira, Rita
Iaconelli, Assumpto
Borges, Edson
author_facet Cavagna, Mario
Paes de Almeida Ferreira Braga, Daniela
Biaggioni Lopes, Fabio
de Cássia Savio Figueira, Rita
Iaconelli, Assumpto
Borges, Edson
author_sort Cavagna, Mario
collection PubMed
description INTRODUCTION: Ovarian stimulation is employed in assisted reproduction techniques in order to obtain as many oocytes as possible. The early rise in oestradiol levels may lead to the premature end of the respective cycle. In order to avoid such an effect, pituitary suppression has been employed. The aim of this study was to evaluate whether maintenance or replacement of the type of GnRH analogue (i.e., agonist or antagonist) employed for pituitary suppression in the consecutive intracytoplasmic sperm injection (ICSI) cycle would negatively influence oocyte quality and ICSI outcome. MATERIAL AND METHODS: A retrospective observational study was conducted including 181 women with primary infertility. Patients were divided into four different groups according to the GnRH analogue used for pituitary suppression in the first and consecutive cycle. RESULTS: When a GnRH agonist was employed for pituitary suppression in the first cycle, the consecutive cycle showed comparable outcomes when performed with either a GnRH agonist or a GnRH antagonist. When the first cycle was performed with a GnRH antagonist, the use of the GnRH agonist in the successive cycle led to an increased number of oocytes retrieved (7.5% vs. 10.3%, p = 0.032) and the production of a higher number of embryos (4.5% vs. 6.3%, p = 0.036). CONCLUSIONS: When the first cycle is carried out with a GnRH antagonist, the use of a GnRH agonist in the successive cycle would lead to increased numbers of oocytes collected and embryos produced.
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spelling pubmed-32587612012-01-31 The effect of GnRH analogues for pituitary suppression on ovarian response in repeated ovarian stimulation cycles Cavagna, Mario Paes de Almeida Ferreira Braga, Daniela Biaggioni Lopes, Fabio de Cássia Savio Figueira, Rita Iaconelli, Assumpto Borges, Edson Arch Med Sci Clinical Research INTRODUCTION: Ovarian stimulation is employed in assisted reproduction techniques in order to obtain as many oocytes as possible. The early rise in oestradiol levels may lead to the premature end of the respective cycle. In order to avoid such an effect, pituitary suppression has been employed. The aim of this study was to evaluate whether maintenance or replacement of the type of GnRH analogue (i.e., agonist or antagonist) employed for pituitary suppression in the consecutive intracytoplasmic sperm injection (ICSI) cycle would negatively influence oocyte quality and ICSI outcome. MATERIAL AND METHODS: A retrospective observational study was conducted including 181 women with primary infertility. Patients were divided into four different groups according to the GnRH analogue used for pituitary suppression in the first and consecutive cycle. RESULTS: When a GnRH agonist was employed for pituitary suppression in the first cycle, the consecutive cycle showed comparable outcomes when performed with either a GnRH agonist or a GnRH antagonist. When the first cycle was performed with a GnRH antagonist, the use of the GnRH agonist in the successive cycle led to an increased number of oocytes retrieved (7.5% vs. 10.3%, p = 0.032) and the production of a higher number of embryos (4.5% vs. 6.3%, p = 0.036). CONCLUSIONS: When the first cycle is carried out with a GnRH antagonist, the use of a GnRH agonist in the successive cycle would lead to increased numbers of oocytes collected and embryos produced. Termedia Publishing House 2011-06 2011-07-11 /pmc/articles/PMC3258761/ /pubmed/22295031 http://dx.doi.org/10.5114/aoms.2011.23414 Text en Copyright © 2011 Termedia & Banach http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research
Cavagna, Mario
Paes de Almeida Ferreira Braga, Daniela
Biaggioni Lopes, Fabio
de Cássia Savio Figueira, Rita
Iaconelli, Assumpto
Borges, Edson
The effect of GnRH analogues for pituitary suppression on ovarian response in repeated ovarian stimulation cycles
title The effect of GnRH analogues for pituitary suppression on ovarian response in repeated ovarian stimulation cycles
title_full The effect of GnRH analogues for pituitary suppression on ovarian response in repeated ovarian stimulation cycles
title_fullStr The effect of GnRH analogues for pituitary suppression on ovarian response in repeated ovarian stimulation cycles
title_full_unstemmed The effect of GnRH analogues for pituitary suppression on ovarian response in repeated ovarian stimulation cycles
title_short The effect of GnRH analogues for pituitary suppression on ovarian response in repeated ovarian stimulation cycles
title_sort effect of gnrh analogues for pituitary suppression on ovarian response in repeated ovarian stimulation cycles
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3258761/
https://www.ncbi.nlm.nih.gov/pubmed/22295031
http://dx.doi.org/10.5114/aoms.2011.23414
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