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.coauthor | Angun, Berk | |
dc.contributor.coauthor | Eraslan, Alper | |
dc.contributor.department | School of Medicine | |
dc.contributor.kuauthor | Ata, Mustafa Barış | |
dc.contributor.kuauthor | Türkgeldi, Engin | |
dc.contributor.kuauthor | Urman, Cumhur Bülent | |
dc.contributor.kuauthor | Yıldız, Şule | |
dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
dc.date.accessioned | 2024-11-09T22:59:07Z | |
dc.date.issued | 2019 | |
dc.description.abstract | Objective: 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.indexedby | WOS | |
dc.description.indexedby | Scopus | |
dc.description.indexedby | PubMed | |
dc.description.issue | 4 | |
dc.description.openaccess | YES | |
dc.description.publisherscope | International | |
dc.description.sponsoredbyTubitakEu | N/A | |
dc.description.volume | 112 | |
dc.identifier.doi | 10.1016/j.fertnstert.2019.06.009 | |
dc.identifier.eissn | 1556-5653 | |
dc.identifier.issn | 0015-0282 | |
dc.identifier.quartile | Q1 | |
dc.identifier.scopus | 2-s2.0-85069876871 | |
dc.identifier.uri | https://doi.org/10.1016/j.fertnstert.2019.06.009 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/7844 | |
dc.identifier.wos | 487818300018 | |
dc.keywords | Progestin primed ovarian stimulation (PPOS) | |
dc.keywords | Medroxyprogesterone acetate (MPA) | |
dc.keywords | Progesterone | |
dc.keywords | Ovarian stimulation | |
dc.keywords | GnRH antagonist | |
dc.language.iso | eng | |
dc.publisher | Elsevier Science Inc | |
dc.relation.ispartof | Fertility and Sterility | |
dc.subject | Obstetrics | |
dc.subject | Gynecology | |
dc.subject | Reproduction | |
dc.subject | Biology | |
dc.title | Comparison of a novel flexible progestin primed ovarian stimulation protocol and the flexible gonadotropin-releasing hormone antagonist protocol for assisted reproductive technology | |
dc.type | Journal Article | |
dspace.entity.type | Publication | |
local.contributor.kuauthor | Yıldız, Şule | |
local.contributor.kuauthor | Türkgeldi, Engin | |
local.contributor.kuauthor | Urman, Cumhur Bülent | |
local.contributor.kuauthor | Ata, Mustafa Barış | |
local.publication.orgunit1 | SCHOOL OF MEDICINE | |
local.publication.orgunit2 | School of Medicine | |
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relation.isOrgUnitOfPublication.latestForDiscovery | d02929e1-2a70-44f0-ae17-7819f587bedd | |
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