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The effect of early coasting on blastocyst development and outcome following blastocyst transfer in IVF/ICSI programme

OBJECTIVE: Coasting is a well-known strategy to decrease severity of Ovarian Hyperstimulation Syndrome (OHSS). The purpose of this study is to assess the effect of Coasting on blastocyst development and subsequent clinical outcome following exclusive blastocyst transfer. METHODS: We conducted an obs...

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Detalles Bibliográficos
Autores principales: Kailasam, Chandra, Griffith, Heather, Wilson, Paul, Gordon, Uma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Brazilian Society of Assisted Reproduction 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6210612/
https://www.ncbi.nlm.nih.gov/pubmed/30106541
http://dx.doi.org/10.5935/1518-0557.20180053
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author Kailasam, Chandra
Griffith, Heather
Wilson, Paul
Gordon, Uma
author_facet Kailasam, Chandra
Griffith, Heather
Wilson, Paul
Gordon, Uma
author_sort Kailasam, Chandra
collection PubMed
description OBJECTIVE: Coasting is a well-known strategy to decrease severity of Ovarian Hyperstimulation Syndrome (OHSS). The purpose of this study is to assess the effect of Coasting on blastocyst development and subsequent clinical outcome following exclusive blastocyst transfer. METHODS: We conducted an observational cohort study of patients having blastocyst transfer following IVF/ICSI treatment. Patients undergoing IVF/ICSI cycles were included in the study. Patients at risk of OHSS were coasted. Outcome following exclusive blastocyst transfer was compared between coasted and non-coasted groups. The main outcome measures were the rate of blastocyst development and live birth rates in coasted and non-coasted cycles. Within coasted cycles, outcome was further analysed based on coasting duration and serum estradiol (E(2)) drop (difference between peak E(2) and E(2) on day of HCG). RESULTS: A total of 166 coasted cycles and 656 non-coasted cycles had blastocyst transfer. Blastocyst development (45.97% vs. 48.6%) and live birth rates (45.18% vs. 43.44%) were not significantly different between coasted and non-coasted cycles. The overall clinical pregnancy (54.21% vs. 49.08%) and implantation rates (43.95% vs. 39.54%) following blastocyst transfer in coasted cycles were not significantly different from those of non-coasted cycles. CONCLUSION: Coasting duration up to 6 days and drop in serum E(2) levels did not compromise blastocyst development, implantation, clinical pregnancy or live birth rates. We conclude that coasting with subsequent blastocyst transfer can be used as an effective strategy in patients at risk of OHSS with no detrimental effects on blastocyst development or live birth outcome.
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spelling pubmed-62106122018-11-13 The effect of early coasting on blastocyst development and outcome following blastocyst transfer in IVF/ICSI programme Kailasam, Chandra Griffith, Heather Wilson, Paul Gordon, Uma JBRA Assist Reprod Original Article OBJECTIVE: Coasting is a well-known strategy to decrease severity of Ovarian Hyperstimulation Syndrome (OHSS). The purpose of this study is to assess the effect of Coasting on blastocyst development and subsequent clinical outcome following exclusive blastocyst transfer. METHODS: We conducted an observational cohort study of patients having blastocyst transfer following IVF/ICSI treatment. Patients undergoing IVF/ICSI cycles were included in the study. Patients at risk of OHSS were coasted. Outcome following exclusive blastocyst transfer was compared between coasted and non-coasted groups. The main outcome measures were the rate of blastocyst development and live birth rates in coasted and non-coasted cycles. Within coasted cycles, outcome was further analysed based on coasting duration and serum estradiol (E(2)) drop (difference between peak E(2) and E(2) on day of HCG). RESULTS: A total of 166 coasted cycles and 656 non-coasted cycles had blastocyst transfer. Blastocyst development (45.97% vs. 48.6%) and live birth rates (45.18% vs. 43.44%) were not significantly different between coasted and non-coasted cycles. The overall clinical pregnancy (54.21% vs. 49.08%) and implantation rates (43.95% vs. 39.54%) following blastocyst transfer in coasted cycles were not significantly different from those of non-coasted cycles. CONCLUSION: Coasting duration up to 6 days and drop in serum E(2) levels did not compromise blastocyst development, implantation, clinical pregnancy or live birth rates. We conclude that coasting with subsequent blastocyst transfer can be used as an effective strategy in patients at risk of OHSS with no detrimental effects on blastocyst development or live birth outcome. Brazilian Society of Assisted Reproduction 2018 /pmc/articles/PMC6210612/ /pubmed/30106541 http://dx.doi.org/10.5935/1518-0557.20180053 Text en http://creativecommons.org/licenses/by/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
Kailasam, Chandra
Griffith, Heather
Wilson, Paul
Gordon, Uma
The effect of early coasting on blastocyst development and outcome following blastocyst transfer in IVF/ICSI programme
title The effect of early coasting on blastocyst development and outcome following blastocyst transfer in IVF/ICSI programme
title_full The effect of early coasting on blastocyst development and outcome following blastocyst transfer in IVF/ICSI programme
title_fullStr The effect of early coasting on blastocyst development and outcome following blastocyst transfer in IVF/ICSI programme
title_full_unstemmed The effect of early coasting on blastocyst development and outcome following blastocyst transfer in IVF/ICSI programme
title_short The effect of early coasting on blastocyst development and outcome following blastocyst transfer in IVF/ICSI programme
title_sort effect of early coasting on blastocyst development and outcome following blastocyst transfer in ivf/icsi programme
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6210612/
https://www.ncbi.nlm.nih.gov/pubmed/30106541
http://dx.doi.org/10.5935/1518-0557.20180053
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