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dc.contributor.authorKuan, Kevin
dc.contributor.authorOmoseni, Sean
dc.contributor.authorTello, Javier Ananda
dc.date.accessioned2023-07-05T11:30:02Z
dc.date.available2023-07-05T11:30:02Z
dc.date.issued2023-12-01
dc.identifier284384441
dc.identifierd3d5ade2-9d2a-4f03-b969-4c4942282e59
dc.identifier85164584171
dc.identifier.citationKuan , K , Omoseni , S & Tello , J A 2023 , ' Comparing ART outcomes in women with endometriosis after GnRH agonist versus GnRH antagonist ovarian stimulation : a systematic review ' , Therapeutic Advances in Endocrinology and Metabolism , vol. 14 . https://doi.org/10.1177/20420188231173325en
dc.identifier.issn2042-0188
dc.identifier.otherORCID: /0000-0001-6637-2155/work/138326684
dc.identifier.urihttps://hdl.handle.net/10023/27894
dc.descriptionFunding: School of Medicine Research Investment Fund.en
dc.description.abstractBackground : Endometriosis is an oestrogen-dependent disease that can cause subfertility in women who may require assisted reproductive technology (ART) to achieve their pregnancy goals. Objectives : The aim of this study was to compare ART outcomes in women with endometriosis following the long GnRH-agonist controlled ovarian stimulation (COS) protocol with those taking the GnRH-antagonist COS protocol. Data sources and methods : MEDLINE, Embase and Web of Science were systematically searched in June 2022. Randomized controlled trials (RCTs) and observational studies comparing the long GnRH-agonist COS protocol and the GnRH-antagonist COS protocol in women with all stages/subtypes of endometriosis were included. Data were synthesized into comprehensive tables for systematic review. The Scottish Intercollegiate Guidelines Network (SIGN) checklists were used for the risk of bias assessment of non-randomized studies and randomized studies, and all the included studies were deemed to have acceptable quality. Main results : Eight studies (one RCT and seven observational) with 2695 patients (2761 cycles) were included. Most studies generally reported non-significant differences in clinical pregnancy or live birth rates regardless of the COS protocol used. However, the GnRH-agonist protocol may yield a higher total number of oocytes retrieved, especially mature oocytes. Conversely, the GnRH-antagonist protocol required a shorter COS duration and lower gonadotrophin dose. Adverse outcomes, such as rates of cycle cancellation and miscarriage, were similar between both COS protocols. Conclusion : Both the long GnRH-agonist and GnRH-antagonist COS protocols generally yield similar pregnancy outcomes. However, the long GnRH-agonist protocol may be associated with a higher cumulative pregnancy rate due to the higher number of retrieved oocytes available for cryopreservation. The underlying mechanisms of the two COS protocols on the female reproductive tract remain unclear. Clinicians should consider treatment costs, stage/subtype of endometriosis and pregnancy goals of their patients when selecting a GnRH analogue for COS. A well-powered RCT is needed to minimize the risk of bias and compare the risk for ovarian hyperstimulation syndrome. Registration : This review was prospectively registered at PROSPERO under Registration No. CRD42022327604.
dc.format.extent19
dc.format.extent312695
dc.language.isoeng
dc.relation.ispartofTherapeutic Advances in Endocrinology and Metabolismen
dc.subjectAssisted reproductive technologyen
dc.subjectEndometriosisen
dc.subjectGnRH agonisten
dc.subjectGnRH antagonisten
dc.subjectInfertilityen
dc.subjectOvarian stimulationen
dc.subjectRC Internal medicineen
dc.subjectRG Gynecology and obstetricsen
dc.subjectDASen
dc.subjectMCCen
dc.subject.lccRCen
dc.subject.lccRGen
dc.titleComparing ART outcomes in women with endometriosis after GnRH agonist versus GnRH antagonist ovarian stimulation : a systematic reviewen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. Centre for Biophotonicsen
dc.contributor.institutionUniversity of St Andrews. Cellular Medicine Divisionen
dc.contributor.institutionUniversity of St Andrews. Institute of Behavioural and Neural Sciencesen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.identifier.doihttps://doi.org/10.1177/20420188231173325
dc.description.statusPeer revieweden


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