Endocrine profiles and luteal function during GnRH-analogue/HMG therapy
We have found a significant improvement of pregnancy rates after pretreatment with an agonist of gonadotrophin releasing hormone (GnRH-a). The pregnancy rate in patients treated with HMG/HCG was 17% per patient and 5.5% per cycle, in patients treated with buserelin, 25% per patient and 15% per cycle...
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Veröffentlicht in: | Human reproduction (Oxford) 1989-11, Vol.4 (8 Suppl), p.121-126 |
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creator | Braendle, W Lindner, C Lichtenberg, V Goepel, E Bettendorf, G |
description | We have found a significant improvement of pregnancy rates after pretreatment with an agonist of gonadotrophin releasing hormone (GnRH-a). The pregnancy rate in patients treated with HMG/HCG was 17% per patient and 5.5% per cycle, in patients treated with buserelin, 25% per patient and 15% per cycle and in the triptorelin group 25% per patient and 22% per cycle. From 740 HMG/HCG cycles without GnRH-a only 66% were sufficient according to the analytical data. In 16% we found a premature LH discharge and in 18% an irregular LH fluctuation during stimulation. It is clear that gonadotrophin stimulation during pituitary suppression provokes a more intense ovarian reaction with respect to the number of follicles, as well as the endocrine activity. There are also some important practical advantages: ovarian stimulation can be started without any respect to a definite time of menstruation or of the cycle. Of further importance is the much greater flexibility in the timing of HCG administration. Finally, it will be favourable for all patients who need ovulation induction, especially for oocyte retrieval for IVF or GIFT, because no cycle has to be cancelled. |
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The pregnancy rate in patients treated with HMG/HCG was 17% per patient and 5.5% per cycle, in patients treated with buserelin, 25% per patient and 15% per cycle and in the triptorelin group 25% per patient and 22% per cycle. From 740 HMG/HCG cycles without GnRH-a only 66% were sufficient according to the analytical data. In 16% we found a premature LH discharge and in 18% an irregular LH fluctuation during stimulation. It is clear that gonadotrophin stimulation during pituitary suppression provokes a more intense ovarian reaction with respect to the number of follicles, as well as the endocrine activity. There are also some important practical advantages: ovarian stimulation can be started without any respect to a definite time of menstruation or of the cycle. Of further importance is the much greater flexibility in the timing of HCG administration. Finally, it will be favourable for all patients who need ovulation induction, especially for oocyte retrieval for IVF or GIFT, because no cycle has to be cancelled.</description><identifier>ISSN: 0268-1161</identifier><identifier>PMID: 2533217</identifier><language>eng</language><publisher>England</publisher><subject>Anovulation - blood ; Anovulation - drug therapy ; Anovulation - physiopathology ; Buserelin - therapeutic use ; Chorionic Gonadotropin - therapeutic use ; Estradiol - blood ; Female ; Follicle Stimulating Hormone - blood ; Gonadotropin-Releasing Hormone - analogs & derivatives ; Gonadotropin-Releasing Hormone - therapeutic use ; Humans ; Luteal Phase - physiology ; Luteinizing Hormone - blood ; Luteolytic Agents - therapeutic use ; Menotropins - therapeutic use ; Ovulation Induction ; Progesterone - blood ; Testosterone - blood ; Triptorelin Pamoate</subject><ispartof>Human reproduction (Oxford), 1989-11, Vol.4 (8 Suppl), p.121-126</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2533217$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Braendle, W</creatorcontrib><creatorcontrib>Lindner, C</creatorcontrib><creatorcontrib>Lichtenberg, V</creatorcontrib><creatorcontrib>Goepel, E</creatorcontrib><creatorcontrib>Bettendorf, G</creatorcontrib><title>Endocrine profiles and luteal function during GnRH-analogue/HMG therapy</title><title>Human reproduction (Oxford)</title><addtitle>Hum Reprod</addtitle><description>We have found a significant improvement of pregnancy rates after pretreatment with an agonist of gonadotrophin releasing hormone (GnRH-a). The pregnancy rate in patients treated with HMG/HCG was 17% per patient and 5.5% per cycle, in patients treated with buserelin, 25% per patient and 15% per cycle and in the triptorelin group 25% per patient and 22% per cycle. From 740 HMG/HCG cycles without GnRH-a only 66% were sufficient according to the analytical data. In 16% we found a premature LH discharge and in 18% an irregular LH fluctuation during stimulation. It is clear that gonadotrophin stimulation during pituitary suppression provokes a more intense ovarian reaction with respect to the number of follicles, as well as the endocrine activity. There are also some important practical advantages: ovarian stimulation can be started without any respect to a definite time of menstruation or of the cycle. Of further importance is the much greater flexibility in the timing of HCG administration. Finally, it will be favourable for all patients who need ovulation induction, especially for oocyte retrieval for IVF or GIFT, because no cycle has to be cancelled.</description><subject>Anovulation - blood</subject><subject>Anovulation - drug therapy</subject><subject>Anovulation - physiopathology</subject><subject>Buserelin - therapeutic use</subject><subject>Chorionic Gonadotropin - therapeutic use</subject><subject>Estradiol - blood</subject><subject>Female</subject><subject>Follicle Stimulating Hormone - blood</subject><subject>Gonadotropin-Releasing Hormone - analogs & derivatives</subject><subject>Gonadotropin-Releasing Hormone - therapeutic use</subject><subject>Humans</subject><subject>Luteal Phase - physiology</subject><subject>Luteinizing Hormone - blood</subject><subject>Luteolytic Agents - therapeutic use</subject><subject>Menotropins - therapeutic use</subject><subject>Ovulation Induction</subject><subject>Progesterone - blood</subject><subject>Testosterone - blood</subject><subject>Triptorelin Pamoate</subject><issn>0268-1161</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNotj8FKxDAURbNQxnH0E4Ss3BXzkjRpljKMHWFEEF2XtHkdK2lam2Yxf2_Bru5ZHC73XpEt46rIABTckNsYfxhbsFAbsuG5EBz0lpSH4IZm6gLScRrazmOkNjjq04zW0zaFZu6GQF1anDMtw8cxs8H64Zzw6fhW0vkbJzte7sh1a33E-zV35Ovl8Lk_Zqf38nX_fMpG4DBntXUFR87Bga61qEFrw2rV8FwqIYTF3BV53i7EAQzjaGSrkEkwDXAjtNiRx__eZe1vwjhXfRcb9N4GHFKstJFCclks4sMqprpHV41T19vpUq3PxR8IjVIv</recordid><startdate>198911</startdate><enddate>198911</enddate><creator>Braendle, W</creator><creator>Lindner, C</creator><creator>Lichtenberg, V</creator><creator>Goepel, E</creator><creator>Bettendorf, G</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>198911</creationdate><title>Endocrine profiles and luteal function during GnRH-analogue/HMG therapy</title><author>Braendle, W ; Lindner, C ; Lichtenberg, V ; Goepel, E ; Bettendorf, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p121t-bad82e221d17b73b17790b6c2546333ae5d855f33a211902e94f6e0419c129373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Anovulation - blood</topic><topic>Anovulation - drug therapy</topic><topic>Anovulation - physiopathology</topic><topic>Buserelin - therapeutic use</topic><topic>Chorionic Gonadotropin - therapeutic use</topic><topic>Estradiol - blood</topic><topic>Female</topic><topic>Follicle Stimulating Hormone - blood</topic><topic>Gonadotropin-Releasing Hormone - analogs & derivatives</topic><topic>Gonadotropin-Releasing Hormone - therapeutic use</topic><topic>Humans</topic><topic>Luteal Phase - physiology</topic><topic>Luteinizing Hormone - blood</topic><topic>Luteolytic Agents - therapeutic use</topic><topic>Menotropins - therapeutic use</topic><topic>Ovulation Induction</topic><topic>Progesterone - blood</topic><topic>Testosterone - blood</topic><topic>Triptorelin Pamoate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Braendle, W</creatorcontrib><creatorcontrib>Lindner, C</creatorcontrib><creatorcontrib>Lichtenberg, V</creatorcontrib><creatorcontrib>Goepel, E</creatorcontrib><creatorcontrib>Bettendorf, G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Human reproduction (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Braendle, W</au><au>Lindner, C</au><au>Lichtenberg, V</au><au>Goepel, E</au><au>Bettendorf, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endocrine profiles and luteal function during GnRH-analogue/HMG therapy</atitle><jtitle>Human reproduction (Oxford)</jtitle><addtitle>Hum Reprod</addtitle><date>1989-11</date><risdate>1989</risdate><volume>4</volume><issue>8 Suppl</issue><spage>121</spage><epage>126</epage><pages>121-126</pages><issn>0268-1161</issn><abstract>We have found a significant improvement of pregnancy rates after pretreatment with an agonist of gonadotrophin releasing hormone (GnRH-a). The pregnancy rate in patients treated with HMG/HCG was 17% per patient and 5.5% per cycle, in patients treated with buserelin, 25% per patient and 15% per cycle and in the triptorelin group 25% per patient and 22% per cycle. From 740 HMG/HCG cycles without GnRH-a only 66% were sufficient according to the analytical data. In 16% we found a premature LH discharge and in 18% an irregular LH fluctuation during stimulation. It is clear that gonadotrophin stimulation during pituitary suppression provokes a more intense ovarian reaction with respect to the number of follicles, as well as the endocrine activity. There are also some important practical advantages: ovarian stimulation can be started without any respect to a definite time of menstruation or of the cycle. Of further importance is the much greater flexibility in the timing of HCG administration. Finally, it will be favourable for all patients who need ovulation induction, especially for oocyte retrieval for IVF or GIFT, because no cycle has to be cancelled.</abstract><cop>England</cop><pmid>2533217</pmid><tpages>6</tpages></addata></record> |
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subjects | Anovulation - blood Anovulation - drug therapy Anovulation - physiopathology Buserelin - therapeutic use Chorionic Gonadotropin - therapeutic use Estradiol - blood Female Follicle Stimulating Hormone - blood Gonadotropin-Releasing Hormone - analogs & derivatives Gonadotropin-Releasing Hormone - therapeutic use Humans Luteal Phase - physiology Luteinizing Hormone - blood Luteolytic Agents - therapeutic use Menotropins - therapeutic use Ovulation Induction Progesterone - blood Testosterone - blood Triptorelin Pamoate |
title | Endocrine profiles and luteal function during GnRH-analogue/HMG therapy |
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