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Comparison of congenital malformations among babies born after administration of letrozole or clomiphene citrate for infertility treatment in a Korean cohort.

DC Field Value Language
dc.contributor.author서석교-
dc.contributor.author원영빈-
dc.contributor.author윤보현-
dc.contributor.author윤지선-
dc.contributor.author이병석-
dc.contributor.author이인하-
dc.contributor.author이재훈-
dc.contributor.author조시현-
dc.contributor.author최영식-
dc.date.accessioned2018-11-16T17:00:24Z-
dc.date.available2018-11-16T17:00:24Z-
dc.date.issued2018-
dc.identifier.issn0890-6238-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/165568-
dc.description.abstractThis retrospective study investigated and compared the incidence of congenital foetal anomalies after letrozole versus clomiphene citrate (CC) administration for infertility treatment. Data from 142 newborns were included: letrozole group, n = 83; CC group, n = 61. Congenital anomalies were found in 7.2% (6/83) patients in the letrozole group and 18.0% (11/61) patients in the CC group, with no significant between-group difference (p = .066). Major congenital anomaly rate was 2.4% (2/83) in the letrozole group and 3.3% (2/61) in the CC group, with no significant between-group difference (p > 0.999). There was no significant difference in major and minor congenital anomalies between the groups after excluding premature infants (birth at a gestational age of <37 weeks), low birth weight, and very low birth weight. The results of this study demonstrate the stability of letrozole compared to that of CC for infertility treatment in pregnant women.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherPergamon In Cooperation With The Reproductive Toxicology Center-
dc.relation.isPartOfREPRODUCTIVE TOXICOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleComparison of congenital malformations among babies born after administration of letrozole or clomiphene citrate for infertility treatment in a Korean cohort.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Obstetrics and Gynecology (산부인과학교실)-
dc.contributor.googleauthorJisun Yun-
dc.contributor.googleauthorYoung Sik Choi-
dc.contributor.googleauthorInha Lee-
dc.contributor.googleauthorYoung Bin Won-
dc.contributor.googleauthorJae Hoon Lee-
dc.contributor.googleauthorSeok Kyo Seo-
dc.contributor.googleauthorSiHyun Cho-
dc.contributor.googleauthorByung Seok Lee-
dc.contributor.googleauthorBo Hyon Yun-
dc.identifier.doi10.1016/j.reprotox.2018.10.006-
dc.contributor.localIdA01888-
dc.contributor.localIdA05484-
dc.contributor.localIdA02555-
dc.contributor.localIdA04986-
dc.contributor.localIdA02795-
dc.contributor.localIdA05497-
dc.contributor.localIdA04636-
dc.contributor.localIdA03846-
dc.contributor.localIdA04114-
dc.relation.journalcodeJ03520-
dc.identifier.eissn1873-1708-
dc.identifier.pmid30339890-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0890623818300467-
dc.contributor.alternativeNameSeo, Seok Kyo-
dc.contributor.alternativeNameWon, Young Bin-
dc.contributor.alternativeNameYun, Bo Hyon-
dc.contributor.alternativeNameYun, Jisun-
dc.contributor.alternativeNameLee, Byung Seok-
dc.contributor.alternativeNameLee, Inha-
dc.contributor.alternativeNameLee, Jae Hoon-
dc.contributor.alternativeNameCho, Si Hyun-
dc.contributor.alternativeNameChoi, Young Sik-
dc.contributor.affiliatedAuthor서석교-
dc.contributor.affiliatedAuthor원영빈-
dc.contributor.affiliatedAuthor윤보현-
dc.contributor.affiliatedAuthor윤지선-
dc.contributor.affiliatedAuthor이병석-
dc.contributor.affiliatedAuthor이인하-
dc.contributor.affiliatedAuthor이재훈-
dc.contributor.affiliatedAuthor조시현-
dc.contributor.affiliatedAuthor최영식-
dc.citation.volume82-
dc.citation.startPage88-
dc.citation.endPage93-
dc.identifier.bibliographicCitationREPRODUCTIVE TOXICOLOGY, Vol.82 : 88-93, 2018-
dc.identifier.rimsid59202-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Obstetrics and Gynecology (산부인과학교실) > 1. Journal Papers

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