Endometriosis and cumulative live birth rate after fresh and frozen IVF cycles with single embryo transfer in young women: no impact beyond reduced ovarian sensitivity—a case control study
Purpose To investigate the impact of symptomatic and surgically confirmed endometriosis on ovarian sensitivity index (OSI) and cumulative live-birth rates (LBR) using predominantly single embryo transfer (SET). Methods Cross-sectional case-control study in a University-based ART program. Women with...
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Veröffentlicht in: | Journal of assisted reproduction and genetics 2019-08, Vol.36 (8), p.1649-1656 |
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creator | Feichtinger, Michael Nordenhök, Emelie Olofsson, Jan I. Hadziosmanovic, Nermin Rodriguez-Wallberg, Kenny A. |
description | Purpose
To investigate the impact of symptomatic and surgically confirmed endometriosis on ovarian sensitivity index (OSI) and cumulative live-birth rates (LBR) using predominantly single embryo transfer (SET).
Methods
Cross-sectional case-control study in a University-based ART program. Women with symptomatic and surgically confirmed endometriosis (
N
= 172), who underwent IVF/ICSI at Karolinska University Hospital were compared to controls without clinically suspected endometriosis (
N
= 2585). Two thousand seven hundred fifty-seven patients underwent 8236 treatment cycles (4598 fresh and 3638 frozen cycles). Primary outcome measures included Ovarian Sensitivity Index (OSI) estimated as collected oocytes/FSH dose and cumulative LBR/oocyte pickup (OPU). Generalized estimated equation (GEE) model accounting for dependencies between consecutive treatments were applied. Secondary outcomes included number of oocytes, pregnancy rate per OPU and per ET, LBR per ET, and miscarriage rate.
Results
Patients diagnosed with endometriosis had significantly fewer oocytes collected (8.47 vs. 9.54,
p
= 0.015) and lower OSI (
p
= 0.011) than controls. There were no differences in cycle cancelations (
p
= 0.59) or miscarriages (
p
= 0.95) between the two groups. Cumulative LBR/OPU did not differ between women with endometriosis and controls (35.6% vs. 34.7%, respectively,
p
= 0.83). In both groups, more than 60% of women had consecutive FETs after fresh ETs (
p
= 0.49) with SET in > 70% of cases. The results were similar whether ovarian endometrioma was present or not.
Conclusions
Our data support that a diagnosis of endometriosis, with or without present endometrioma, does not negatively affect ART cumulative results. The impact of endometriosis was discernible on OSI but not on clinical relevant outcomes including pregnancy and LBR. |
doi_str_mv | 10.1007/s10815-019-01519-5 |
format | Article |
fullrecord | <record><control><sourceid>proquest_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_swepub_ki_se_478326</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2258485106</sourcerecordid><originalsourceid>FETCH-LOGICAL-c549t-db43adf3f0adf968ae093cc16b72f5522e0dd423a75e02924b0a436dcea9cef13</originalsourceid><addsrcrecordid>eNp9kstu1DAUhiMEoqXwAiyQJTYsCPgS58ICqSotVKrEBrq1HOck45LYgy8zCisegufhYXgSnM5QKBLI8rFlf-c_PtafZY8JfkEwrl56gmvCc0yaNHmK_E52SHjF8ooxfDftMa9zXJT1QfbA-yuMcVNTdj87YCQNTNhh9v3UdHaC4LT12iNpOqTiFEcZ9AbQuIRWu7BCTgZAsg_gUO_Ar67R3tkvYND55RlSsxrBo61OrNdmGAHB1LrZouCk8X3K0wbNNpoBbVNF8woZi_S0liqgFmab5Bx0UUGH7EY6LQ3yYLxOD9Fh_vH1m0RKekDKmuDsiHyI3fwwu9fL0cOj_XqUfTw7_XDyLr94__b85PgiV7xoQt61BZNdz3qcYlPWEnDDlCJlW9Gec0oBd11Bmaw4YNrQosWyYGWnQDYKesKOsnyn67ewjq1YOz1JNwsrtdgffUo7EEVVM1om_vk_-Tf68lhYN4gYBWtYgxf51zs8sROksqlFOd7Kun1j9EoMdiPKCldNtQg82ws4-zmCD2LSXsE4SgM2ekEpbxgveMkT-vQv9MpGZ9LvLVRd1JzgpQG6o5Sz3jvobx5DsFjcJ3buE8l94tp9YpF-8mcbNym_7JYAtv-WdGUGcL9r_0f2J1hl7T8</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2258485106</pqid></control><display><type>article</type><title>Endometriosis and cumulative live birth rate after fresh and frozen IVF cycles with single embryo transfer in young women: no impact beyond reduced ovarian sensitivity—a case control study</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>SWEPUB Freely available online</source><source>SpringerLink Journals - AutoHoldings</source><creator>Feichtinger, Michael ; Nordenhök, Emelie ; Olofsson, Jan I. ; Hadziosmanovic, Nermin ; Rodriguez-Wallberg, Kenny A.</creator><creatorcontrib>Feichtinger, Michael ; Nordenhök, Emelie ; Olofsson, Jan I. ; Hadziosmanovic, Nermin ; Rodriguez-Wallberg, Kenny A.</creatorcontrib><description>Purpose
To investigate the impact of symptomatic and surgically confirmed endometriosis on ovarian sensitivity index (OSI) and cumulative live-birth rates (LBR) using predominantly single embryo transfer (SET).
Methods
Cross-sectional case-control study in a University-based ART program. Women with symptomatic and surgically confirmed endometriosis (
N
= 172), who underwent IVF/ICSI at Karolinska University Hospital were compared to controls without clinically suspected endometriosis (
N
= 2585). Two thousand seven hundred fifty-seven patients underwent 8236 treatment cycles (4598 fresh and 3638 frozen cycles). Primary outcome measures included Ovarian Sensitivity Index (OSI) estimated as collected oocytes/FSH dose and cumulative LBR/oocyte pickup (OPU). Generalized estimated equation (GEE) model accounting for dependencies between consecutive treatments were applied. Secondary outcomes included number of oocytes, pregnancy rate per OPU and per ET, LBR per ET, and miscarriage rate.
Results
Patients diagnosed with endometriosis had significantly fewer oocytes collected (8.47 vs. 9.54,
p
= 0.015) and lower OSI (
p
= 0.011) than controls. There were no differences in cycle cancelations (
p
= 0.59) or miscarriages (
p
= 0.95) between the two groups. Cumulative LBR/OPU did not differ between women with endometriosis and controls (35.6% vs. 34.7%, respectively,
p
= 0.83). In both groups, more than 60% of women had consecutive FETs after fresh ETs (
p
= 0.49) with SET in > 70% of cases. The results were similar whether ovarian endometrioma was present or not.
Conclusions
Our data support that a diagnosis of endometriosis, with or without present endometrioma, does not negatively affect ART cumulative results. The impact of endometriosis was discernible on OSI but not on clinical relevant outcomes including pregnancy and LBR.</description><identifier>ISSN: 1058-0468</identifier><identifier>ISSN: 1573-7330</identifier><identifier>EISSN: 1573-7330</identifier><identifier>DOI: 10.1007/s10815-019-01519-5</identifier><identifier>PMID: 31313013</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adult ; Assisted Reproduction Technologies ; Birth Rate ; Case-Control Studies ; Cross-Sectional Studies ; Cumulative live-birth ; Cumulative pregnancy rate ; Embryo transfer ; Embryo Transfer - methods ; Endometriosis ; Endometriosis - physiopathology ; Female ; Fertilization in Vitro - methods ; Follicle-stimulating hormone ; Frozen-thawed ; Gynecology ; Human Genetics ; Humans ; Medicine ; Medicine & Public Health ; Miscarriage ; Oocyte Retrieval ; Oocytes ; Ovulation Induction - statistics & numerical data ; Patients ; Pregnancy ; Pregnancy Outcome ; Pregnancy Rate ; Reproductive Medicine ; SET ; Sperm Injections, Intracytoplasmic</subject><ispartof>Journal of assisted reproduction and genetics, 2019-08, Vol.36 (8), p.1649-1656</ispartof><rights>The Author(s) 2019</rights><rights>Journal of Assisted Reproduction and Genetics is a copyright of Springer, (2019). All Rights Reserved. © 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c549t-db43adf3f0adf968ae093cc16b72f5522e0dd423a75e02924b0a436dcea9cef13</citedby><cites>FETCH-LOGICAL-c549t-db43adf3f0adf968ae093cc16b72f5522e0dd423a75e02924b0a436dcea9cef13</cites><orcidid>0000-0003-4378-6181</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707971/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707971/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,550,723,776,780,881,27901,27902,41464,42533,51294,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31313013$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-393901$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:141714239$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Feichtinger, Michael</creatorcontrib><creatorcontrib>Nordenhök, Emelie</creatorcontrib><creatorcontrib>Olofsson, Jan I.</creatorcontrib><creatorcontrib>Hadziosmanovic, Nermin</creatorcontrib><creatorcontrib>Rodriguez-Wallberg, Kenny A.</creatorcontrib><title>Endometriosis and cumulative live birth rate after fresh and frozen IVF cycles with single embryo transfer in young women: no impact beyond reduced ovarian sensitivity—a case control study</title><title>Journal of assisted reproduction and genetics</title><addtitle>J Assist Reprod Genet</addtitle><addtitle>J Assist Reprod Genet</addtitle><description>Purpose
To investigate the impact of symptomatic and surgically confirmed endometriosis on ovarian sensitivity index (OSI) and cumulative live-birth rates (LBR) using predominantly single embryo transfer (SET).
Methods
Cross-sectional case-control study in a University-based ART program. Women with symptomatic and surgically confirmed endometriosis (
N
= 172), who underwent IVF/ICSI at Karolinska University Hospital were compared to controls without clinically suspected endometriosis (
N
= 2585). Two thousand seven hundred fifty-seven patients underwent 8236 treatment cycles (4598 fresh and 3638 frozen cycles). Primary outcome measures included Ovarian Sensitivity Index (OSI) estimated as collected oocytes/FSH dose and cumulative LBR/oocyte pickup (OPU). Generalized estimated equation (GEE) model accounting for dependencies between consecutive treatments were applied. Secondary outcomes included number of oocytes, pregnancy rate per OPU and per ET, LBR per ET, and miscarriage rate.
Results
Patients diagnosed with endometriosis had significantly fewer oocytes collected (8.47 vs. 9.54,
p
= 0.015) and lower OSI (
p
= 0.011) than controls. There were no differences in cycle cancelations (
p
= 0.59) or miscarriages (
p
= 0.95) between the two groups. Cumulative LBR/OPU did not differ between women with endometriosis and controls (35.6% vs. 34.7%, respectively,
p
= 0.83). In both groups, more than 60% of women had consecutive FETs after fresh ETs (
p
= 0.49) with SET in > 70% of cases. The results were similar whether ovarian endometrioma was present or not.
Conclusions
Our data support that a diagnosis of endometriosis, with or without present endometrioma, does not negatively affect ART cumulative results. The impact of endometriosis was discernible on OSI but not on clinical relevant outcomes including pregnancy and LBR.</description><subject>Adult</subject><subject>Assisted Reproduction Technologies</subject><subject>Birth Rate</subject><subject>Case-Control Studies</subject><subject>Cross-Sectional Studies</subject><subject>Cumulative live-birth</subject><subject>Cumulative pregnancy rate</subject><subject>Embryo transfer</subject><subject>Embryo Transfer - methods</subject><subject>Endometriosis</subject><subject>Endometriosis - physiopathology</subject><subject>Female</subject><subject>Fertilization in Vitro - methods</subject><subject>Follicle-stimulating hormone</subject><subject>Frozen-thawed</subject><subject>Gynecology</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Miscarriage</subject><subject>Oocyte Retrieval</subject><subject>Oocytes</subject><subject>Ovulation Induction - statistics & numerical data</subject><subject>Patients</subject><subject>Pregnancy</subject><subject>Pregnancy Outcome</subject><subject>Pregnancy Rate</subject><subject>Reproductive Medicine</subject><subject>SET</subject><subject>Sperm Injections, Intracytoplasmic</subject><issn>1058-0468</issn><issn>1573-7330</issn><issn>1573-7330</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>D8T</sourceid><recordid>eNp9kstu1DAUhiMEoqXwAiyQJTYsCPgS58ICqSotVKrEBrq1HOck45LYgy8zCisegufhYXgSnM5QKBLI8rFlf-c_PtafZY8JfkEwrl56gmvCc0yaNHmK_E52SHjF8ooxfDftMa9zXJT1QfbA-yuMcVNTdj87YCQNTNhh9v3UdHaC4LT12iNpOqTiFEcZ9AbQuIRWu7BCTgZAsg_gUO_Ar67R3tkvYND55RlSsxrBo61OrNdmGAHB1LrZouCk8X3K0wbNNpoBbVNF8woZi_S0liqgFmab5Bx0UUGH7EY6LQ3yYLxOD9Fh_vH1m0RKekDKmuDsiHyI3fwwu9fL0cOj_XqUfTw7_XDyLr94__b85PgiV7xoQt61BZNdz3qcYlPWEnDDlCJlW9Gec0oBd11Bmaw4YNrQosWyYGWnQDYKesKOsnyn67ewjq1YOz1JNwsrtdgffUo7EEVVM1om_vk_-Tf68lhYN4gYBWtYgxf51zs8sROksqlFOd7Kun1j9EoMdiPKCldNtQg82ws4-zmCD2LSXsE4SgM2ekEpbxgveMkT-vQv9MpGZ9LvLVRd1JzgpQG6o5Sz3jvobx5DsFjcJ3buE8l94tp9YpF-8mcbNym_7JYAtv-WdGUGcL9r_0f2J1hl7T8</recordid><startdate>20190801</startdate><enddate>20190801</enddate><creator>Feichtinger, Michael</creator><creator>Nordenhök, Emelie</creator><creator>Olofsson, Jan I.</creator><creator>Hadziosmanovic, Nermin</creator><creator>Rodriguez-Wallberg, Kenny A.</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>ACNBI</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>DF2</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0003-4378-6181</orcidid></search><sort><creationdate>20190801</creationdate><title>Endometriosis and cumulative live birth rate after fresh and frozen IVF cycles with single embryo transfer in young women: no impact beyond reduced ovarian sensitivity—a case control study</title><author>Feichtinger, Michael ; Nordenhök, Emelie ; Olofsson, Jan I. ; Hadziosmanovic, Nermin ; Rodriguez-Wallberg, Kenny A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c549t-db43adf3f0adf968ae093cc16b72f5522e0dd423a75e02924b0a436dcea9cef13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Assisted Reproduction Technologies</topic><topic>Birth Rate</topic><topic>Case-Control Studies</topic><topic>Cross-Sectional Studies</topic><topic>Cumulative live-birth</topic><topic>Cumulative pregnancy rate</topic><topic>Embryo transfer</topic><topic>Embryo Transfer - methods</topic><topic>Endometriosis</topic><topic>Endometriosis - physiopathology</topic><topic>Female</topic><topic>Fertilization in Vitro - methods</topic><topic>Follicle-stimulating hormone</topic><topic>Frozen-thawed</topic><topic>Gynecology</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Miscarriage</topic><topic>Oocyte Retrieval</topic><topic>Oocytes</topic><topic>Ovulation Induction - statistics & numerical data</topic><topic>Patients</topic><topic>Pregnancy</topic><topic>Pregnancy Outcome</topic><topic>Pregnancy Rate</topic><topic>Reproductive Medicine</topic><topic>SET</topic><topic>Sperm Injections, Intracytoplasmic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Feichtinger, Michael</creatorcontrib><creatorcontrib>Nordenhök, Emelie</creatorcontrib><creatorcontrib>Olofsson, Jan I.</creatorcontrib><creatorcontrib>Hadziosmanovic, Nermin</creatorcontrib><creatorcontrib>Rodriguez-Wallberg, Kenny A.</creatorcontrib><collection>Springer Nature OA/Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SWEPUB Uppsala universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Uppsala universitet</collection><collection>SwePub Articles full text</collection><jtitle>Journal of assisted reproduction and genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Feichtinger, Michael</au><au>Nordenhök, Emelie</au><au>Olofsson, Jan I.</au><au>Hadziosmanovic, Nermin</au><au>Rodriguez-Wallberg, Kenny A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endometriosis and cumulative live birth rate after fresh and frozen IVF cycles with single embryo transfer in young women: no impact beyond reduced ovarian sensitivity—a case control study</atitle><jtitle>Journal of assisted reproduction and genetics</jtitle><stitle>J Assist Reprod Genet</stitle><addtitle>J Assist Reprod Genet</addtitle><date>2019-08-01</date><risdate>2019</risdate><volume>36</volume><issue>8</issue><spage>1649</spage><epage>1656</epage><pages>1649-1656</pages><issn>1058-0468</issn><issn>1573-7330</issn><eissn>1573-7330</eissn><abstract>Purpose
To investigate the impact of symptomatic and surgically confirmed endometriosis on ovarian sensitivity index (OSI) and cumulative live-birth rates (LBR) using predominantly single embryo transfer (SET).
Methods
Cross-sectional case-control study in a University-based ART program. Women with symptomatic and surgically confirmed endometriosis (
N
= 172), who underwent IVF/ICSI at Karolinska University Hospital were compared to controls without clinically suspected endometriosis (
N
= 2585). Two thousand seven hundred fifty-seven patients underwent 8236 treatment cycles (4598 fresh and 3638 frozen cycles). Primary outcome measures included Ovarian Sensitivity Index (OSI) estimated as collected oocytes/FSH dose and cumulative LBR/oocyte pickup (OPU). Generalized estimated equation (GEE) model accounting for dependencies between consecutive treatments were applied. Secondary outcomes included number of oocytes, pregnancy rate per OPU and per ET, LBR per ET, and miscarriage rate.
Results
Patients diagnosed with endometriosis had significantly fewer oocytes collected (8.47 vs. 9.54,
p
= 0.015) and lower OSI (
p
= 0.011) than controls. There were no differences in cycle cancelations (
p
= 0.59) or miscarriages (
p
= 0.95) between the two groups. Cumulative LBR/OPU did not differ between women with endometriosis and controls (35.6% vs. 34.7%, respectively,
p
= 0.83). In both groups, more than 60% of women had consecutive FETs after fresh ETs (
p
= 0.49) with SET in > 70% of cases. The results were similar whether ovarian endometrioma was present or not.
Conclusions
Our data support that a diagnosis of endometriosis, with or without present endometrioma, does not negatively affect ART cumulative results. The impact of endometriosis was discernible on OSI but not on clinical relevant outcomes including pregnancy and LBR.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>31313013</pmid><doi>10.1007/s10815-019-01519-5</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-4378-6181</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; SWEPUB Freely available online; SpringerLink Journals - AutoHoldings |
subjects | Adult Assisted Reproduction Technologies Birth Rate Case-Control Studies Cross-Sectional Studies Cumulative live-birth Cumulative pregnancy rate Embryo transfer Embryo Transfer - methods Endometriosis Endometriosis - physiopathology Female Fertilization in Vitro - methods Follicle-stimulating hormone Frozen-thawed Gynecology Human Genetics Humans Medicine Medicine & Public Health Miscarriage Oocyte Retrieval Oocytes Ovulation Induction - statistics & numerical data Patients Pregnancy Pregnancy Outcome Pregnancy Rate Reproductive Medicine SET Sperm Injections, Intracytoplasmic |
title | Endometriosis and cumulative live birth rate after fresh and frozen IVF cycles with single embryo transfer in young women: no impact beyond reduced ovarian sensitivity—a case control study |
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