Prevalence of thrombophilia in women with severe ovarian hyperstimulation syndrome and cost-effectiveness of screening
To determine the prevalence of markers of thrombophilia in patients with severe ovarian hyperstimulation syndrome (OHSS) and to evaluate the cost-effectiveness of screening for factor V Leiden and prothrombin G20210A mutations in women entering an IVF program. Case–control study and cost-effectivene...
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Veröffentlicht in: | Fertility and sterility 2004-04, Vol.81 (4), p.989-995 |
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creator | Fábregues, Francisco Tàssies, Dolors Reverter, Juan C Carmona, Francisco Ordinas, Antonio Balasch, Juan |
description | To determine the prevalence of markers of thrombophilia in patients with severe ovarian hyperstimulation syndrome (OHSS) and to evaluate the cost-effectiveness of screening for factor V Leiden and prothrombin G20210A mutations in women entering an IVF program.
Case–control study and cost-effectiveness analysis.
University teaching hospital.
Women undergoing controlled ovarian hyperstimulation for IVF complicated by severe OHSS (group 1, n = 20), women undergoing controlled ovarian hyperstimulation for IVF without development of severe OHSS (group 2, n = 40), and healthy control subjects (group 3, n = 100).
Investigation of markers of thrombophilia. Estimate of number of IVF patients needed to detect a case of severe OHSS and thrombosis associated with thrombophilia genetic mutation was calculated from the available data.
Blood samples were analyzed for inherited (resistance to activated protein C due to the factor V Leiden mutation; prothrombin G20210A mutation; deficiencies in antithrombin, protein C, and protein S) and acquired (presence of circulating lupus anticoagulants and/or anticardiolipin antibodies; deficiencies of antithrombin and protein S; acquired protein C resistance) markers of thrombophilia. The cost of preventing one thrombotic event in a patient developing severe OHSS after IVF and having factor V Leiden or prothrombin G20210A mutations was calculated.
None of the OHSS patients or controls had antithrombin, protein C, or free protein S deficiencies. All of them tested negative for antiphospholipid antibodies. No patient in group 1 had the factor V Leiden or prothrombin G20210A mutations. The prothrombin G20210A mutation was detected in 1 out of 40 patients (2.5%) in group 2. Both factor V Leiden and prothrombin G20210A mutations were detected in two of the control subjects (2%) (group 3). The estimated cost of preventing one thrombotic event arising as a consequence of screening for factor V Leiden and prothrombin G20210A mutation is a minimum of $418,970 and $2,430,000, respectively.
The prevalence of thrombophilia is not increased in women with severe OHSS. Screening for V Leiden and prothrombin G20210A mutation in an IVF general population is not cost-effective. |
doi_str_mv | 10.1016/j.fertnstert.2003.09.042 |
format | Article |
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Case–control study and cost-effectiveness analysis.
University teaching hospital.
Women undergoing controlled ovarian hyperstimulation for IVF complicated by severe OHSS (group 1, n = 20), women undergoing controlled ovarian hyperstimulation for IVF without development of severe OHSS (group 2, n = 40), and healthy control subjects (group 3, n = 100).
Investigation of markers of thrombophilia. Estimate of number of IVF patients needed to detect a case of severe OHSS and thrombosis associated with thrombophilia genetic mutation was calculated from the available data.
Blood samples were analyzed for inherited (resistance to activated protein C due to the factor V Leiden mutation; prothrombin G20210A mutation; deficiencies in antithrombin, protein C, and protein S) and acquired (presence of circulating lupus anticoagulants and/or anticardiolipin antibodies; deficiencies of antithrombin and protein S; acquired protein C resistance) markers of thrombophilia. The cost of preventing one thrombotic event in a patient developing severe OHSS after IVF and having factor V Leiden or prothrombin G20210A mutations was calculated.
None of the OHSS patients or controls had antithrombin, protein C, or free protein S deficiencies. All of them tested negative for antiphospholipid antibodies. No patient in group 1 had the factor V Leiden or prothrombin G20210A mutations. The prothrombin G20210A mutation was detected in 1 out of 40 patients (2.5%) in group 2. Both factor V Leiden and prothrombin G20210A mutations were detected in two of the control subjects (2%) (group 3). The estimated cost of preventing one thrombotic event arising as a consequence of screening for factor V Leiden and prothrombin G20210A mutation is a minimum of $418,970 and $2,430,000, respectively.
The prevalence of thrombophilia is not increased in women with severe OHSS. Screening for V Leiden and prothrombin G20210A mutation in an IVF general population is not cost-effective.</description><identifier>ISSN: 0015-0282</identifier><identifier>EISSN: 1556-5653</identifier><identifier>DOI: 10.1016/j.fertnstert.2003.09.042</identifier><identifier>PMID: 15066453</identifier><identifier>CODEN: FESTAS</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adult ; Alanine ; Biological and medical sciences ; Case-Control Studies ; Cost-Benefit Analysis ; Embryology: invertebrates and vertebrates. Teratology ; Factor V - genetics ; Factor V Leiden ; Female ; Fundamental and applied biological sciences. Psychology ; Genetic Testing - economics ; Glycine ; Humans ; IVF ; Male ; Mutation ; ovarian hyperstimulation syndrome ; Ovarian Hyperstimulation Syndrome - genetics ; Ovarian Hyperstimulation Syndrome - physiopathology ; Point Mutation ; Prevalence ; Prothrombin - genetics ; prothrombin mutation ; Severity of Illness Index ; thrombophilia ; Thrombophilia - epidemiology ; Thrombophilia - genetics</subject><ispartof>Fertility and sterility, 2004-04, Vol.81 (4), p.989-995</ispartof><rights>2004 American Society for Reproductive Medicine</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c452t-eacd6e2edec35995dae2b0a973dcfc73183fbe3098a019b24a3b8e2d337b1c433</citedby><cites>FETCH-LOGICAL-c452t-eacd6e2edec35995dae2b0a973dcfc73183fbe3098a019b24a3b8e2d337b1c433</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.fertnstert.2003.09.042$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15624491$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15066453$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fábregues, Francisco</creatorcontrib><creatorcontrib>Tàssies, Dolors</creatorcontrib><creatorcontrib>Reverter, Juan C</creatorcontrib><creatorcontrib>Carmona, Francisco</creatorcontrib><creatorcontrib>Ordinas, Antonio</creatorcontrib><creatorcontrib>Balasch, Juan</creatorcontrib><title>Prevalence of thrombophilia in women with severe ovarian hyperstimulation syndrome and cost-effectiveness of screening</title><title>Fertility and sterility</title><addtitle>Fertil Steril</addtitle><description>To determine the prevalence of markers of thrombophilia in patients with severe ovarian hyperstimulation syndrome (OHSS) and to evaluate the cost-effectiveness of screening for factor V Leiden and prothrombin G20210A mutations in women entering an IVF program.
Case–control study and cost-effectiveness analysis.
University teaching hospital.
Women undergoing controlled ovarian hyperstimulation for IVF complicated by severe OHSS (group 1, n = 20), women undergoing controlled ovarian hyperstimulation for IVF without development of severe OHSS (group 2, n = 40), and healthy control subjects (group 3, n = 100).
Investigation of markers of thrombophilia. Estimate of number of IVF patients needed to detect a case of severe OHSS and thrombosis associated with thrombophilia genetic mutation was calculated from the available data.
Blood samples were analyzed for inherited (resistance to activated protein C due to the factor V Leiden mutation; prothrombin G20210A mutation; deficiencies in antithrombin, protein C, and protein S) and acquired (presence of circulating lupus anticoagulants and/or anticardiolipin antibodies; deficiencies of antithrombin and protein S; acquired protein C resistance) markers of thrombophilia. The cost of preventing one thrombotic event in a patient developing severe OHSS after IVF and having factor V Leiden or prothrombin G20210A mutations was calculated.
None of the OHSS patients or controls had antithrombin, protein C, or free protein S deficiencies. All of them tested negative for antiphospholipid antibodies. No patient in group 1 had the factor V Leiden or prothrombin G20210A mutations. The prothrombin G20210A mutation was detected in 1 out of 40 patients (2.5%) in group 2. Both factor V Leiden and prothrombin G20210A mutations were detected in two of the control subjects (2%) (group 3). The estimated cost of preventing one thrombotic event arising as a consequence of screening for factor V Leiden and prothrombin G20210A mutation is a minimum of $418,970 and $2,430,000, respectively.
The prevalence of thrombophilia is not increased in women with severe OHSS. Screening for V Leiden and prothrombin G20210A mutation in an IVF general population is not cost-effective.</description><subject>Adult</subject><subject>Alanine</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Cost-Benefit Analysis</subject><subject>Embryology: invertebrates and vertebrates. Teratology</subject><subject>Factor V - genetics</subject><subject>Factor V Leiden</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic Testing - economics</subject><subject>Glycine</subject><subject>Humans</subject><subject>IVF</subject><subject>Male</subject><subject>Mutation</subject><subject>ovarian hyperstimulation syndrome</subject><subject>Ovarian Hyperstimulation Syndrome - genetics</subject><subject>Ovarian Hyperstimulation Syndrome - physiopathology</subject><subject>Point Mutation</subject><subject>Prevalence</subject><subject>Prothrombin - genetics</subject><subject>prothrombin mutation</subject><subject>Severity of Illness Index</subject><subject>thrombophilia</subject><subject>Thrombophilia - epidemiology</subject><subject>Thrombophilia - genetics</subject><issn>0015-0282</issn><issn>1556-5653</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU2P0zAQhi0EYsvCX0C-wC3dsR3n4wgrPlZaCQ5wthx7Ql0ldvGkQf33uGql5cZlfHned0aPGeMCtgJEc7ffjpiXSEuZWwmgttBvoZbP2EZo3VS60eo52wAIXYHs5A17RbQHgEa08iW7ERqaptZqw9bvGVc7YXTI08iXXU7zkA67MAXLQ-R_0oxlhmXHCVfMhVptDjby3emAmZYwHye7hBQ5naIvaeQ2eu4SLRWOI7olrBiR6FxPLiPGEH-9Zi9GOxG-ub637OfnTz_uv1aP37483H94rFytZSmwzjco0aNTuu-1tygHsH2rvBtdq0SnxgEV9J0F0Q-ytmroUHql2kG4Wqlb9v7Se8jp9xFpMXMgh9NkI6YjmVZ0ICV0BewuoMuJKONoDjnMNp-MAHN2bvbmybk5OzfQm-K8RN9edxyHGf1T8Cq5AO-ugCVnpzHb6AL9wzWyrntRuI8XDouRNWA25ML5Z3zIxaPxKfz_mr-QdKl-</recordid><startdate>20040401</startdate><enddate>20040401</enddate><creator>Fábregues, Francisco</creator><creator>Tàssies, Dolors</creator><creator>Reverter, Juan C</creator><creator>Carmona, Francisco</creator><creator>Ordinas, Antonio</creator><creator>Balasch, Juan</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</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>7X8</scope></search><sort><creationdate>20040401</creationdate><title>Prevalence of thrombophilia in women with severe ovarian hyperstimulation syndrome and cost-effectiveness of screening</title><author>Fábregues, Francisco ; Tàssies, Dolors ; Reverter, Juan C ; Carmona, Francisco ; Ordinas, Antonio ; Balasch, Juan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c452t-eacd6e2edec35995dae2b0a973dcfc73183fbe3098a019b24a3b8e2d337b1c433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>Alanine</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Cost-Benefit Analysis</topic><topic>Embryology: invertebrates and vertebrates. Teratology</topic><topic>Factor V - genetics</topic><topic>Factor V Leiden</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic Testing - economics</topic><topic>Glycine</topic><topic>Humans</topic><topic>IVF</topic><topic>Male</topic><topic>Mutation</topic><topic>ovarian hyperstimulation syndrome</topic><topic>Ovarian Hyperstimulation Syndrome - genetics</topic><topic>Ovarian Hyperstimulation Syndrome - physiopathology</topic><topic>Point Mutation</topic><topic>Prevalence</topic><topic>Prothrombin - genetics</topic><topic>prothrombin mutation</topic><topic>Severity of Illness Index</topic><topic>thrombophilia</topic><topic>Thrombophilia - epidemiology</topic><topic>Thrombophilia - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fábregues, Francisco</creatorcontrib><creatorcontrib>Tàssies, Dolors</creatorcontrib><creatorcontrib>Reverter, Juan C</creatorcontrib><creatorcontrib>Carmona, Francisco</creatorcontrib><creatorcontrib>Ordinas, Antonio</creatorcontrib><creatorcontrib>Balasch, Juan</creatorcontrib><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>Fertility and sterility</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fábregues, Francisco</au><au>Tàssies, Dolors</au><au>Reverter, Juan C</au><au>Carmona, Francisco</au><au>Ordinas, Antonio</au><au>Balasch, Juan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevalence of thrombophilia in women with severe ovarian hyperstimulation syndrome and cost-effectiveness of screening</atitle><jtitle>Fertility and sterility</jtitle><addtitle>Fertil Steril</addtitle><date>2004-04-01</date><risdate>2004</risdate><volume>81</volume><issue>4</issue><spage>989</spage><epage>995</epage><pages>989-995</pages><issn>0015-0282</issn><eissn>1556-5653</eissn><coden>FESTAS</coden><abstract>To determine the prevalence of markers of thrombophilia in patients with severe ovarian hyperstimulation syndrome (OHSS) and to evaluate the cost-effectiveness of screening for factor V Leiden and prothrombin G20210A mutations in women entering an IVF program.
Case–control study and cost-effectiveness analysis.
University teaching hospital.
Women undergoing controlled ovarian hyperstimulation for IVF complicated by severe OHSS (group 1, n = 20), women undergoing controlled ovarian hyperstimulation for IVF without development of severe OHSS (group 2, n = 40), and healthy control subjects (group 3, n = 100).
Investigation of markers of thrombophilia. Estimate of number of IVF patients needed to detect a case of severe OHSS and thrombosis associated with thrombophilia genetic mutation was calculated from the available data.
Blood samples were analyzed for inherited (resistance to activated protein C due to the factor V Leiden mutation; prothrombin G20210A mutation; deficiencies in antithrombin, protein C, and protein S) and acquired (presence of circulating lupus anticoagulants and/or anticardiolipin antibodies; deficiencies of antithrombin and protein S; acquired protein C resistance) markers of thrombophilia. The cost of preventing one thrombotic event in a patient developing severe OHSS after IVF and having factor V Leiden or prothrombin G20210A mutations was calculated.
None of the OHSS patients or controls had antithrombin, protein C, or free protein S deficiencies. All of them tested negative for antiphospholipid antibodies. No patient in group 1 had the factor V Leiden or prothrombin G20210A mutations. The prothrombin G20210A mutation was detected in 1 out of 40 patients (2.5%) in group 2. Both factor V Leiden and prothrombin G20210A mutations were detected in two of the control subjects (2%) (group 3). The estimated cost of preventing one thrombotic event arising as a consequence of screening for factor V Leiden and prothrombin G20210A mutation is a minimum of $418,970 and $2,430,000, respectively.
The prevalence of thrombophilia is not increased in women with severe OHSS. Screening for V Leiden and prothrombin G20210A mutation in an IVF general population is not cost-effective.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>15066453</pmid><doi>10.1016/j.fertnstert.2003.09.042</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Access via ScienceDirect (Elsevier); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Adult Alanine Biological and medical sciences Case-Control Studies Cost-Benefit Analysis Embryology: invertebrates and vertebrates. Teratology Factor V - genetics Factor V Leiden Female Fundamental and applied biological sciences. Psychology Genetic Testing - economics Glycine Humans IVF Male Mutation ovarian hyperstimulation syndrome Ovarian Hyperstimulation Syndrome - genetics Ovarian Hyperstimulation Syndrome - physiopathology Point Mutation Prevalence Prothrombin - genetics prothrombin mutation Severity of Illness Index thrombophilia Thrombophilia - epidemiology Thrombophilia - genetics |
title | Prevalence of thrombophilia in women with severe ovarian hyperstimulation syndrome and cost-effectiveness of screening |
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