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Addition of GnRH antagonist in cycles of poor responders undergoing IVF

Concern about the use of gonadotrophin-releasing hormone (GnRH) agonists in ovarian stimulation of poor responder IVF patients has arisen from the claim that GnRH agonists might have a direct deleterious effect through their receptors on the ovary. In this study, we compared two ovarian stimulation...

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Published in:Human reproduction (Oxford) 2000-10, Vol.15 (10), p.2145-2147
Main Authors: Akman, Mehmet A., Erden, Halit F., Tosun, Suleyman B., Bayazit, Numan, Aksoy, Esra, Bahceci, Mustafa
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container_title Human reproduction (Oxford)
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Erden, Halit F.
Tosun, Suleyman B.
Bayazit, Numan
Aksoy, Esra
Bahceci, Mustafa
description Concern about the use of gonadotrophin-releasing hormone (GnRH) agonists in ovarian stimulation of poor responder IVF patients has arisen from the claim that GnRH agonists might have a direct deleterious effect through their receptors on the ovary. In this study, we compared two ovarian stimulation protocols in which no GnRH agonists were used. In all, 40 patients with a poor response in previous treatment cycles were included. They were divided into two groups: group I (n = 20) received ovarian stimulation for 20 cycles, without the addition of either GnRH agonist or antagonist; while group II (n = 20) patients received ovarian stimulation for 20 cycles, including the administration of a GnRH antagonist (Cetrorelix, 0.25 mg daily) during the late follicular phase. There was no statistically significant difference between the groups for mean age, duration of infertility, baseline FSH concentration, cancellation rate, number of ampoules of gonadotrophin used, number of mature oocytes retrieved, oestradiol concentrations on the day of injection of human chorionic gonadotrophin (HCG), fertilization rate and number of embryos transferred. The clinical pregnancy and implantation rates in group II appeared higher than in group I, but were not significantly different (20 and 13.33% compared with 6.25 and 3.44% respectively). The addition of GnRH antagonists to ovarian stimulation protocols might be a new hope for poor responder IVF patients, but this report is preliminary and further controlled randomized prospective studies with larger sample sizes are required.
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In this study, we compared two ovarian stimulation protocols in which no GnRH agonists were used. In all, 40 patients with a poor response in previous treatment cycles were included. They were divided into two groups: group I (n = 20) received ovarian stimulation for 20 cycles, without the addition of either GnRH agonist or antagonist; while group II (n = 20) patients received ovarian stimulation for 20 cycles, including the administration of a GnRH antagonist (Cetrorelix, 0.25 mg daily) during the late follicular phase. There was no statistically significant difference between the groups for mean age, duration of infertility, baseline FSH concentration, cancellation rate, number of ampoules of gonadotrophin used, number of mature oocytes retrieved, oestradiol concentrations on the day of injection of human chorionic gonadotrophin (HCG), fertilization rate and number of embryos transferred. The clinical pregnancy and implantation rates in group II appeared higher than in group I, but were not significantly different (20 and 13.33% compared with 6.25 and 3.44% respectively). The addition of GnRH antagonists to ovarian stimulation protocols might be a new hope for poor responder IVF patients, but this report is preliminary and further controlled randomized prospective studies with larger sample sizes are required.</description><identifier>ISSN: 0268-1161</identifier><identifier>ISSN: 1460-2350</identifier><identifier>EISSN: 1460-2350</identifier><identifier>DOI: 10.1093/humrep/15.10.2145</identifier><identifier>PMID: 11006188</identifier><identifier>CODEN: HUREEE</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adult ; Biological and medical sciences ; Birth control ; Cetrorelix ; Chorionic Gonadotropin - pharmacology ; Embryo Transfer ; Female ; Follicle Stimulating Hormone - blood ; GnRH antagonist ; Gonadotropin-Releasing Hormone - analogs &amp; derivatives ; Gonadotropin-Releasing Hormone - antagonists &amp; inhibitors ; Gonadotropin-Releasing Hormone - pharmacology ; Gynecology. Andrology. Obstetrics ; Hormone Antagonists - pharmacology ; Humans ; IVF ; Luteinizing Hormone - blood ; Medical sciences ; Menotropins - pharmacology ; Ovulation Induction - methods ; poor responders ; Pregnancy ; Pregnancy Outcome ; Sterility. 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There was no statistically significant difference between the groups for mean age, duration of infertility, baseline FSH concentration, cancellation rate, number of ampoules of gonadotrophin used, number of mature oocytes retrieved, oestradiol concentrations on the day of injection of human chorionic gonadotrophin (HCG), fertilization rate and number of embryos transferred. The clinical pregnancy and implantation rates in group II appeared higher than in group I, but were not significantly different (20 and 13.33% compared with 6.25 and 3.44% respectively). The addition of GnRH antagonists to ovarian stimulation protocols might be a new hope for poor responder IVF patients, but this report is preliminary and further controlled randomized prospective studies with larger sample sizes are required.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Birth control</subject><subject>Cetrorelix</subject><subject>Chorionic Gonadotropin - pharmacology</subject><subject>Embryo Transfer</subject><subject>Female</subject><subject>Follicle Stimulating Hormone - blood</subject><subject>GnRH antagonist</subject><subject>Gonadotropin-Releasing Hormone - analogs &amp; derivatives</subject><subject>Gonadotropin-Releasing Hormone - antagonists &amp; inhibitors</subject><subject>Gonadotropin-Releasing Hormone - pharmacology</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Hormone Antagonists - pharmacology</subject><subject>Humans</subject><subject>IVF</subject><subject>Luteinizing Hormone - blood</subject><subject>Medical sciences</subject><subject>Menotropins - pharmacology</subject><subject>Ovulation Induction - methods</subject><subject>poor responders</subject><subject>Pregnancy</subject><subject>Pregnancy Outcome</subject><subject>Sterility. 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Assisted procreation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Akman, Mehmet A.</creatorcontrib><creatorcontrib>Erden, Halit F.</creatorcontrib><creatorcontrib>Tosun, Suleyman B.</creatorcontrib><creatorcontrib>Bayazit, Numan</creatorcontrib><creatorcontrib>Aksoy, Esra</creatorcontrib><creatorcontrib>Bahceci, Mustafa</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Human reproduction (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Akman, Mehmet A.</au><au>Erden, Halit F.</au><au>Tosun, Suleyman B.</au><au>Bayazit, Numan</au><au>Aksoy, Esra</au><au>Bahceci, Mustafa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Addition of GnRH antagonist in cycles of poor responders undergoing IVF</atitle><jtitle>Human reproduction (Oxford)</jtitle><stitle>Hum. Reprod</stitle><addtitle>Hum. Reprod</addtitle><date>2000-10-01</date><risdate>2000</risdate><volume>15</volume><issue>10</issue><spage>2145</spage><epage>2147</epage><pages>2145-2147</pages><issn>0268-1161</issn><issn>1460-2350</issn><eissn>1460-2350</eissn><coden>HUREEE</coden><abstract>Concern about the use of gonadotrophin-releasing hormone (GnRH) agonists in ovarian stimulation of poor responder IVF patients has arisen from the claim that GnRH agonists might have a direct deleterious effect through their receptors on the ovary. In this study, we compared two ovarian stimulation protocols in which no GnRH agonists were used. In all, 40 patients with a poor response in previous treatment cycles were included. They were divided into two groups: group I (n = 20) received ovarian stimulation for 20 cycles, without the addition of either GnRH agonist or antagonist; while group II (n = 20) patients received ovarian stimulation for 20 cycles, including the administration of a GnRH antagonist (Cetrorelix, 0.25 mg daily) during the late follicular phase. There was no statistically significant difference between the groups for mean age, duration of infertility, baseline FSH concentration, cancellation rate, number of ampoules of gonadotrophin used, number of mature oocytes retrieved, oestradiol concentrations on the day of injection of human chorionic gonadotrophin (HCG), fertilization rate and number of embryos transferred. The clinical pregnancy and implantation rates in group II appeared higher than in group I, but were not significantly different (20 and 13.33% compared with 6.25 and 3.44% respectively). 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subjects Adult
Biological and medical sciences
Birth control
Cetrorelix
Chorionic Gonadotropin - pharmacology
Embryo Transfer
Female
Follicle Stimulating Hormone - blood
GnRH antagonist
Gonadotropin-Releasing Hormone - analogs & derivatives
Gonadotropin-Releasing Hormone - antagonists & inhibitors
Gonadotropin-Releasing Hormone - pharmacology
Gynecology. Andrology. Obstetrics
Hormone Antagonists - pharmacology
Humans
IVF
Luteinizing Hormone - blood
Medical sciences
Menotropins - pharmacology
Ovulation Induction - methods
poor responders
Pregnancy
Pregnancy Outcome
Sterility. Assisted procreation
title Addition of GnRH antagonist in cycles of poor responders undergoing IVF
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