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Ectopic pregnancy risk factors for ART patients undergoing the GnRH antagonist protocol: a retrospective study

BACKGROUND: In-vitro fertilization is a known risk factor for ectopic pregnancies. We sought to establish the risk factors for ectopic pregnancy in GnRH antagonist cycles examining patient and stimulation parameters with an emphasis on ovulation trigger. METHODS: We conducted a retrospective, cohort...

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Autores principales: Weiss, A., Beck-Fruchter, R., Golan, J., Lavee, M., Geslevich, Y., Shalev, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804527/
https://www.ncbi.nlm.nih.gov/pubmed/27005813
http://dx.doi.org/10.1186/s12958-016-0146-0
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author Weiss, A.
Beck-Fruchter, R.
Golan, J.
Lavee, M.
Geslevich, Y.
Shalev, E.
author_facet Weiss, A.
Beck-Fruchter, R.
Golan, J.
Lavee, M.
Geslevich, Y.
Shalev, E.
author_sort Weiss, A.
collection PubMed
description BACKGROUND: In-vitro fertilization is a known risk factor for ectopic pregnancies. We sought to establish the risk factors for ectopic pregnancy in GnRH antagonist cycles examining patient and stimulation parameters with an emphasis on ovulation trigger. METHODS: We conducted a retrospective, cohort study of 343 patients undergoing 380 assisted reproductive technology (ART) cycles with the GnRH antagonist protocol and achieving a clinical pregnancy from November 2010 through December 2015. RESULTS: Significant risk factors for ectopic pregnancy in the univariate analysis included prior Cesarean section (CS), endometriosis, mechanical factor infertility, longer stimulation, elevated estradiol and progesterone levels, GnRH agonist trigger, higher number of oocytes aspirated, and insemination technique. Independent risk factors for ectopic pregnancy in the multivariate analysis included GnRH agonist trigger, higher number of oocytes aspirated, insemination technique, and prior Cesarean section. CONCLUSION: Excessive ovarian response, IVF (as opposed to ICSI), prior Cesarean section and GnRH agonist trigger were found to be independent risk factors for ectopic pregnancy. Caution should be exercised before incorporating the GnRH agonist trigger for indications other than preventing OHSS. When excessive ovarian response leads to utilization of GnRH agonist trigger, strategies for preventing ectopic pregnancy, such as a freeze all policy or blastocyst transfer, should be considered. Further studies should elucidate whether adjusting the luteal support can reduce the ectopic pregnancy risk.
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spelling pubmed-48045272016-03-23 Ectopic pregnancy risk factors for ART patients undergoing the GnRH antagonist protocol: a retrospective study Weiss, A. Beck-Fruchter, R. Golan, J. Lavee, M. Geslevich, Y. Shalev, E. Reprod Biol Endocrinol Research BACKGROUND: In-vitro fertilization is a known risk factor for ectopic pregnancies. We sought to establish the risk factors for ectopic pregnancy in GnRH antagonist cycles examining patient and stimulation parameters with an emphasis on ovulation trigger. METHODS: We conducted a retrospective, cohort study of 343 patients undergoing 380 assisted reproductive technology (ART) cycles with the GnRH antagonist protocol and achieving a clinical pregnancy from November 2010 through December 2015. RESULTS: Significant risk factors for ectopic pregnancy in the univariate analysis included prior Cesarean section (CS), endometriosis, mechanical factor infertility, longer stimulation, elevated estradiol and progesterone levels, GnRH agonist trigger, higher number of oocytes aspirated, and insemination technique. Independent risk factors for ectopic pregnancy in the multivariate analysis included GnRH agonist trigger, higher number of oocytes aspirated, insemination technique, and prior Cesarean section. CONCLUSION: Excessive ovarian response, IVF (as opposed to ICSI), prior Cesarean section and GnRH agonist trigger were found to be independent risk factors for ectopic pregnancy. Caution should be exercised before incorporating the GnRH agonist trigger for indications other than preventing OHSS. When excessive ovarian response leads to utilization of GnRH agonist trigger, strategies for preventing ectopic pregnancy, such as a freeze all policy or blastocyst transfer, should be considered. Further studies should elucidate whether adjusting the luteal support can reduce the ectopic pregnancy risk. BioMed Central 2016-03-23 /pmc/articles/PMC4804527/ /pubmed/27005813 http://dx.doi.org/10.1186/s12958-016-0146-0 Text en © Weiss et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Weiss, A.
Beck-Fruchter, R.
Golan, J.
Lavee, M.
Geslevich, Y.
Shalev, E.
Ectopic pregnancy risk factors for ART patients undergoing the GnRH antagonist protocol: a retrospective study
title Ectopic pregnancy risk factors for ART patients undergoing the GnRH antagonist protocol: a retrospective study
title_full Ectopic pregnancy risk factors for ART patients undergoing the GnRH antagonist protocol: a retrospective study
title_fullStr Ectopic pregnancy risk factors for ART patients undergoing the GnRH antagonist protocol: a retrospective study
title_full_unstemmed Ectopic pregnancy risk factors for ART patients undergoing the GnRH antagonist protocol: a retrospective study
title_short Ectopic pregnancy risk factors for ART patients undergoing the GnRH antagonist protocol: a retrospective study
title_sort ectopic pregnancy risk factors for art patients undergoing the gnrh antagonist protocol: a retrospective study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804527/
https://www.ncbi.nlm.nih.gov/pubmed/27005813
http://dx.doi.org/10.1186/s12958-016-0146-0
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