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A case of discrepancy between three ERA tests in a woman with repeated implantation failure complicated by chronic endometritis
Endometrial receptivity array (ERA) is used to determine the timing of embryo transfer (ET) synchronized with the window of implantation (WOI). The effectiveness and evaluation of ERAs in women with recurrent implantation failure remain controversial. We report the case of a patient with recurrent i...
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Published in: | BMC pregnancy and childbirth 2022-12, Vol.22 (1), p.891-891, Article 891 |
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description | Endometrial receptivity array (ERA) is used to determine the timing of embryo transfer (ET) synchronized with the window of implantation (WOI). The effectiveness and evaluation of ERAs in women with recurrent implantation failure remain controversial. We report the case of a patient with recurrent implantation failure that raises the issue of reproducibility of ERA tests.
A 36-year-old Japanese woman with secondary infertility who had previously given birth failed to conceive after three frozen-thawed embryo transfer (FET) cycles. An ERA test was conducted to confirm the WOI. The first ERA test was performed 125 h after progesterone exposure. The laboratory reported that the endometrium was in a non-receptive (post-receptive) phase, and recommended retesting 101 h after progesterone exposure. A simultaneous chronic endometritis (CE) test showed a score of 3. After the antibiotics administration to treat CE, the second ERA test was performed after 101 h of progesterone exposure. The laboratory reported that the endometrium had not reached the WOI and estimated the WOI to be 113 ± 3 h after progesterone exposure. The third ERA test was performed 113 h after progesterone exposure. The laboratory reported that the endometrium was in a non-receptive (pre-receptive) phase and estimated the WOI to be 137 ± 3 h after progesterone exposure. A CE test performed at the same time as the second and third ERA tests showed a score of 1 for the collected endometrium. According to the third ERA test results, the vitrified-warmed blastocyst was transferred at 137 h of progesterone exposure. Pregnancy was achieved and the patient had an uncomplicated vaginal delivery at 39 weeks. One year later, another pregnancy was achieved after FET at 137 h of progesterone exposure, and the patient delivered at 33 weeks due to an unexpected membrane rupture.
Because the results of the ERA test may vary in the presence of CE, CE should be diagnosed simultaneously with or before conducting ERA tests. If CE is diagnosed, ERA testing should be performed after treatment with antimicrobials or other drugs. |
doi_str_mv | 10.1186/s12884-022-05241-6 |
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A 36-year-old Japanese woman with secondary infertility who had previously given birth failed to conceive after three frozen-thawed embryo transfer (FET) cycles. An ERA test was conducted to confirm the WOI. The first ERA test was performed 125 h after progesterone exposure. The laboratory reported that the endometrium was in a non-receptive (post-receptive) phase, and recommended retesting 101 h after progesterone exposure. A simultaneous chronic endometritis (CE) test showed a score of 3. After the antibiotics administration to treat CE, the second ERA test was performed after 101 h of progesterone exposure. The laboratory reported that the endometrium had not reached the WOI and estimated the WOI to be 113 ± 3 h after progesterone exposure. The third ERA test was performed 113 h after progesterone exposure. The laboratory reported that the endometrium was in a non-receptive (pre-receptive) phase and estimated the WOI to be 137 ± 3 h after progesterone exposure. A CE test performed at the same time as the second and third ERA tests showed a score of 1 for the collected endometrium. According to the third ERA test results, the vitrified-warmed blastocyst was transferred at 137 h of progesterone exposure. Pregnancy was achieved and the patient had an uncomplicated vaginal delivery at 39 weeks. One year later, another pregnancy was achieved after FET at 137 h of progesterone exposure, and the patient delivered at 33 weeks due to an unexpected membrane rupture.
Because the results of the ERA test may vary in the presence of CE, CE should be diagnosed simultaneously with or before conducting ERA tests. If CE is diagnosed, ERA testing should be performed after treatment with antimicrobials or other drugs.</description><identifier>ISSN: 1471-2393</identifier><identifier>EISSN: 1471-2393</identifier><identifier>DOI: 10.1186/s12884-022-05241-6</identifier><identifier>PMID: 36456975</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Adult ; Antibiotics ; Case Report ; Case reports ; CD138 ; Chronic Disease ; Chronic endometritis ; Embryo Implantation ; Embryos ; Endometrial receptivity array ; Endometritis - complications ; Endometritis - diagnosis ; Endometrium ; Female ; Humans ; In vitro fertilization ; Infertility ; Laboratories ; Ovaries ; Plasma cell ; Pregnancy ; Progesterone - therapeutic use ; Reproducibility of Results ; Sperm ; Ultrasonic imaging ; Vagina</subject><ispartof>BMC pregnancy and childbirth, 2022-12, Vol.22 (1), p.891-891, Article 891</ispartof><rights>2022. The Author(s).</rights><rights>2022. This work is licensed 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><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c563t-d1b06c866f23e8f1e4b4123f513fd424ea5620b119cb62416e3154fe4729936c3</citedby><cites>FETCH-LOGICAL-c563t-d1b06c866f23e8f1e4b4123f513fd424ea5620b119cb62416e3154fe4729936c3</cites><orcidid>0000-0003-0955-4248</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/PMC9714241/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2755730360?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36456975$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ota, Kuniaki</creatorcontrib><creatorcontrib>Takahashi, Toshifumi</creatorcontrib><creatorcontrib>Mitsui, Junichiro</creatorcontrib><creatorcontrib>Kuroda, Kishio</creatorcontrib><creatorcontrib>Hiraoka, Kenichiro</creatorcontrib><creatorcontrib>Kawai, Kiyotaka</creatorcontrib><title>A case of discrepancy between three ERA tests in a woman with repeated implantation failure complicated by chronic endometritis</title><title>BMC pregnancy and childbirth</title><addtitle>BMC Pregnancy Childbirth</addtitle><description>Endometrial receptivity array (ERA) is used to determine the timing of embryo transfer (ET) synchronized with the window of implantation (WOI). The effectiveness and evaluation of ERAs in women with recurrent implantation failure remain controversial. We report the case of a patient with recurrent implantation failure that raises the issue of reproducibility of ERA tests.
A 36-year-old Japanese woman with secondary infertility who had previously given birth failed to conceive after three frozen-thawed embryo transfer (FET) cycles. An ERA test was conducted to confirm the WOI. The first ERA test was performed 125 h after progesterone exposure. The laboratory reported that the endometrium was in a non-receptive (post-receptive) phase, and recommended retesting 101 h after progesterone exposure. A simultaneous chronic endometritis (CE) test showed a score of 3. After the antibiotics administration to treat CE, the second ERA test was performed after 101 h of progesterone exposure. The laboratory reported that the endometrium had not reached the WOI and estimated the WOI to be 113 ± 3 h after progesterone exposure. The third ERA test was performed 113 h after progesterone exposure. The laboratory reported that the endometrium was in a non-receptive (pre-receptive) phase and estimated the WOI to be 137 ± 3 h after progesterone exposure. A CE test performed at the same time as the second and third ERA tests showed a score of 1 for the collected endometrium. According to the third ERA test results, the vitrified-warmed blastocyst was transferred at 137 h of progesterone exposure. Pregnancy was achieved and the patient had an uncomplicated vaginal delivery at 39 weeks. One year later, another pregnancy was achieved after FET at 137 h of progesterone exposure, and the patient delivered at 33 weeks due to an unexpected membrane rupture.
Because the results of the ERA test may vary in the presence of CE, CE should be diagnosed simultaneously with or before conducting ERA tests. If CE is diagnosed, ERA testing should be performed after treatment with antimicrobials or other drugs.</description><subject>Adult</subject><subject>Antibiotics</subject><subject>Case Report</subject><subject>Case reports</subject><subject>CD138</subject><subject>Chronic Disease</subject><subject>Chronic endometritis</subject><subject>Embryo Implantation</subject><subject>Embryos</subject><subject>Endometrial receptivity array</subject><subject>Endometritis - complications</subject><subject>Endometritis - diagnosis</subject><subject>Endometrium</subject><subject>Female</subject><subject>Humans</subject><subject>In vitro fertilization</subject><subject>Infertility</subject><subject>Laboratories</subject><subject>Ovaries</subject><subject>Plasma cell</subject><subject>Pregnancy</subject><subject>Progesterone - therapeutic use</subject><subject>Reproducibility of Results</subject><subject>Sperm</subject><subject>Ultrasonic imaging</subject><subject>Vagina</subject><issn>1471-2393</issn><issn>1471-2393</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkk-LFDEQxRtR3HX1C3iQgBcvrflb6b4Iw7LqwoIgeg7pdPVOhu5kTDIOc_KrG2fWZddTFZVfPSqP1zSvGX3PWAcfMuNdJ1vKeUsVl6yFJ805k5q1XPTi6YP-rHmR84ZSpjtFnzdnAqSCXqvz5veKOJuRxImMPruEWxvcgQxY9oiBlHVCJFffVqRgLpn4QCzZx8UGsvdlTSqPtuBI_LKdbSi2-BjIZP28S0hcrFPvjsBwIG6dYvCOYBjjgiX54vPL5tlk54yv7upF8-PT1ffLL-3N18_Xl6ub1ikQpR3ZQMF1ABMX2E0M5SAZF5NiYholl2gVcDow1rsBqhWAgik5odS87wU4cdFcn3THaDdmm_xi08FE681xENOtsal4N6OhynW9gw44CCn1YMGCogDWaVCDHqvWx5PWdjcsODoMJdn5kejjl-DX5jb-Mr1m9VZWBd7dCaT4c1eNNUv1HufqIMZdNlxLEF1Pparo2__QTdylUK2qlFJaUAG0UvxEuRRzTjjdH8Oo-ZsVc8qKqVkxx6wYqEtvHn7jfuVfOMQfl6e6rA</recordid><startdate>20221201</startdate><enddate>20221201</enddate><creator>Ota, Kuniaki</creator><creator>Takahashi, Toshifumi</creator><creator>Mitsui, Junichiro</creator><creator>Kuroda, Kishio</creator><creator>Hiraoka, Kenichiro</creator><creator>Kawai, Kiyotaka</creator><general>BioMed Central</general><general>BMC</general><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>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-0955-4248</orcidid></search><sort><creationdate>20221201</creationdate><title>A case of discrepancy between three ERA tests in a woman with repeated implantation failure complicated by chronic endometritis</title><author>Ota, Kuniaki ; Takahashi, Toshifumi ; Mitsui, Junichiro ; Kuroda, Kishio ; Hiraoka, Kenichiro ; Kawai, Kiyotaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c563t-d1b06c866f23e8f1e4b4123f513fd424ea5620b119cb62416e3154fe4729936c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adult</topic><topic>Antibiotics</topic><topic>Case Report</topic><topic>Case reports</topic><topic>CD138</topic><topic>Chronic Disease</topic><topic>Chronic endometritis</topic><topic>Embryo Implantation</topic><topic>Embryos</topic><topic>Endometrial receptivity array</topic><topic>Endometritis - complications</topic><topic>Endometritis - diagnosis</topic><topic>Endometrium</topic><topic>Female</topic><topic>Humans</topic><topic>In vitro fertilization</topic><topic>Infertility</topic><topic>Laboratories</topic><topic>Ovaries</topic><topic>Plasma cell</topic><topic>Pregnancy</topic><topic>Progesterone - therapeutic use</topic><topic>Reproducibility of Results</topic><topic>Sperm</topic><topic>Ultrasonic imaging</topic><topic>Vagina</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ota, Kuniaki</creatorcontrib><creatorcontrib>Takahashi, Toshifumi</creatorcontrib><creatorcontrib>Mitsui, Junichiro</creatorcontrib><creatorcontrib>Kuroda, Kishio</creatorcontrib><creatorcontrib>Hiraoka, Kenichiro</creatorcontrib><creatorcontrib>Kawai, Kiyotaka</creatorcontrib><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>ProQuest Nursing & Allied Health Database</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMC pregnancy and childbirth</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ota, Kuniaki</au><au>Takahashi, Toshifumi</au><au>Mitsui, Junichiro</au><au>Kuroda, Kishio</au><au>Hiraoka, Kenichiro</au><au>Kawai, Kiyotaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A case of discrepancy between three ERA tests in a woman with repeated implantation failure complicated by chronic endometritis</atitle><jtitle>BMC pregnancy and childbirth</jtitle><addtitle>BMC Pregnancy Childbirth</addtitle><date>2022-12-01</date><risdate>2022</risdate><volume>22</volume><issue>1</issue><spage>891</spage><epage>891</epage><pages>891-891</pages><artnum>891</artnum><issn>1471-2393</issn><eissn>1471-2393</eissn><abstract>Endometrial receptivity array (ERA) is used to determine the timing of embryo transfer (ET) synchronized with the window of implantation (WOI). The effectiveness and evaluation of ERAs in women with recurrent implantation failure remain controversial. We report the case of a patient with recurrent implantation failure that raises the issue of reproducibility of ERA tests.
A 36-year-old Japanese woman with secondary infertility who had previously given birth failed to conceive after three frozen-thawed embryo transfer (FET) cycles. An ERA test was conducted to confirm the WOI. The first ERA test was performed 125 h after progesterone exposure. The laboratory reported that the endometrium was in a non-receptive (post-receptive) phase, and recommended retesting 101 h after progesterone exposure. A simultaneous chronic endometritis (CE) test showed a score of 3. After the antibiotics administration to treat CE, the second ERA test was performed after 101 h of progesterone exposure. The laboratory reported that the endometrium had not reached the WOI and estimated the WOI to be 113 ± 3 h after progesterone exposure. The third ERA test was performed 113 h after progesterone exposure. The laboratory reported that the endometrium was in a non-receptive (pre-receptive) phase and estimated the WOI to be 137 ± 3 h after progesterone exposure. A CE test performed at the same time as the second and third ERA tests showed a score of 1 for the collected endometrium. According to the third ERA test results, the vitrified-warmed blastocyst was transferred at 137 h of progesterone exposure. Pregnancy was achieved and the patient had an uncomplicated vaginal delivery at 39 weeks. One year later, another pregnancy was achieved after FET at 137 h of progesterone exposure, and the patient delivered at 33 weeks due to an unexpected membrane rupture.
Because the results of the ERA test may vary in the presence of CE, CE should be diagnosed simultaneously with or before conducting ERA tests. If CE is diagnosed, ERA testing should be performed after treatment with antimicrobials or other drugs.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>36456975</pmid><doi>10.1186/s12884-022-05241-6</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-0955-4248</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Antibiotics Case Report Case reports CD138 Chronic Disease Chronic endometritis Embryo Implantation Embryos Endometrial receptivity array Endometritis - complications Endometritis - diagnosis Endometrium Female Humans In vitro fertilization Infertility Laboratories Ovaries Plasma cell Pregnancy Progesterone - therapeutic use Reproducibility of Results Sperm Ultrasonic imaging Vagina |
title | A case of discrepancy between three ERA tests in a woman with repeated implantation failure complicated by chronic endometritis |
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