Publication:
Comparison of a novel flexible progestin primed ovarian stimulation protocol and the flexible gonadotropin-releasing hormone antagonist protocol for assisted reproductive technology

dc.contributor.coauthorAngun, Berk
dc.contributor.coauthorEraslan, Alper
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorAta, Mustafa Barış
dc.contributor.kuauthorTürkgeldi, Engin
dc.contributor.kuauthorUrman, Cumhur Bülent
dc.contributor.kuauthorYıldız, Şule
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T22:59:07Z
dc.date.issued2019
dc.description.abstractObjective: To determine whether a flexible progestin primed ovarian stimulation (fPPOS) protocol is effective for preventing premature ovulation. Design: Retrospective cohort study. Setting: Private assisted reproduction center. Patient(s): Eighty-seven oocyte donors and 191 recipients of fresh oocytes. Intervention(s): Each donor was stimulated with a flexible gonadotropin-releasing hormone (GnRH) antagonist protocol in one cycle and with the new fPPOS protocol in the other, within a period of 6 months. FSH was started on cycle day 2-3, and 0.25 mg/day GnRH antagonist or 10 mg/day medroxyprogesterone acetate (MPA) was started on stimulation day 7 or when the leading follicle reached 14 mm, whichever came first. Main Outcome Measure(s): Duration of stimulation, gonadotropin consumption, duration of GnRH antagonist or MPA administration, number of metaphase II oocytes, and pregnancy rates in fresh oocyte recipients. Results: Duration of stimulation was 11 (10-11) days in both groups. Total gonadotropin consumption was similar. Pituitary suppression was started on day 7 and lasted for 5 days in each group. There were no premature ovulations in any group. The fPPOS yielded a significantly higher number of cumulus oocyte complexes than GnRH antagonist cycles (33 [21-39] vs. 26 [18-36], respectively). Likewise, the fPPOS generated significantly more metaphase II oocytes than GnRH antagonist cycles (24 [17-34] vs. 21 [15-28], respectively). Recipients of fresh oocytes from fPPOS and GnRH antagonist cycles had similar cleavage, blastulation, implantation, and live birth/ongoing pregnancy rates (50% vs. 48.6%). Conclusion(s): FPPOS with MPA seems to be an effective choice for preventing premature ovulation in women undergoing ovarian stimulation without compromising oocyte quality.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue4
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume112
dc.identifier.doi10.1016/j.fertnstert.2019.06.009
dc.identifier.eissn1556-5653
dc.identifier.issn0015-0282
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85069876871
dc.identifier.urihttps://doi.org/10.1016/j.fertnstert.2019.06.009
dc.identifier.urihttps://hdl.handle.net/20.500.14288/7844
dc.identifier.wos487818300018
dc.keywordsProgestin primed ovarian stimulation (PPOS)
dc.keywordsMedroxyprogesterone acetate (MPA)
dc.keywordsProgesterone
dc.keywordsOvarian stimulation
dc.keywordsGnRH antagonist
dc.language.isoeng
dc.publisherElsevier Science Inc
dc.relation.ispartofFertility and Sterility
dc.subjectObstetrics
dc.subjectGynecology
dc.subjectReproduction
dc.subjectBiology
dc.titleComparison of a novel flexible progestin primed ovarian stimulation protocol and the flexible gonadotropin-releasing hormone antagonist protocol for assisted reproductive technology
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorYıldız, Şule
local.contributor.kuauthorTürkgeldi, Engin
local.contributor.kuauthorUrman, Cumhur Bülent
local.contributor.kuauthorAta, Mustafa Barış
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
relation.isOrgUnitOfPublicationd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

Files