Evidence map›Paper›PMID 41162665›Full record

ArticleArchives of gynecology and obstetrics2025

GnRH agonist trigger in focus: does protocol choice between PPOS and antagonist strategies affect outcomes?

Yusuf Aytaç Tohma, Fazilet Kübra Boynukalın, Meral Gültomruk, Mustafa Bahçeci, Gürkan Bozdağ

Abstract read
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Article in Archives of gynecology and obstetrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yusuf Aytaç TohmaDepartment of Infertility, Bahceci Ankara IVF Center, Ankara, Turkey.
Fazilet Kübra BoynukalınDepartment of Infertility, Bahceci Fulya IVF Center, Istanbul, Turkey. kboynukalin@bahceci.com.
Meral GültomrukDepartment of Research & Development, Bahceci Fulya IVF Center, Istanbul, Turkey.
Mustafa BahçeciDepartment of Infertility, Bahceci Fulya IVF Center, Istanbul, Turkey.
Gürkan BozdağDepartment of Infertility, Bahceci Fulya IVF Center, Istanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe aim of this study was to assess the effectiveness of the GnRHa trigger in the PPOS and GnRH antagonist protocols when using a GnRH agonist (GnRHa) trigger.

methodsThis retrospective cohort study conducted at Bahçeci Fulya IVF Center (January 2022-January 2024) included 802 patients undergoing ovarian stimulation with a starting dose of 300 IU gonadotropins using either a GnRH antagonist (n = 372) or PPOS protocol (n = 430), followed by a GnRHa trigger. The primary outcome was oocyte yield; secondary outcomes included pregnancy rates following the initial frozen embryo transfer (FET).

resultsBaseline characteristics, including female age, BMI, and infertility duration, were comparable between groups. Although PPOS was associated with a shorter stimulation duration [10 (9-11) vs. 10 (10-11) days, p = 0.002], lower progesterone levels on trigger day [1.3 (0.74-1.48) vs. 1.5 (0.83-1.63) ng/ml, p = 0.002], and higher LH levels [4 (1.89-5.2) vs. 3.3 (1.4-4.1) IU, p < 0.001], oocyte yield and embryological outcomes were similar (p > 0.05 for all). Clinical pregnancy rates [63.6% vs. 63.8%, p = 0.95] and live birth rates [51.7% vs. 52.2%, p = 0.87] were also comparable. Regression analysis identified embryo quality (p = 0.003), but not stimulation protocol (p = 0.766), as a significant predictor of live birth.

conclusionPPOS and GnRH antagonist protocols provide similar oocyte yield and live birth rates following GnRHa trigger. These findings indicate that progestin use in PPOS is not associated with inferior clinical outcomes in the setting of GnRHa trigger; however, the underlying mechanisms and long-term efficacy require further investigations.

Indexed as

Fertility Agents, FemaleGonadotropin-Releasing HormoneOvulation InductionAdultEmbryo TransferFemaleFertilization in VitroHormone AntagonistsHumansPregnancyPregnancy RateProgesteroneRetrospective StudiesFertility Agents, FemaleGonadotropin-Releasing HormoneHormone AntagonistsProgesteroneGnRH agonist triggerGnRH antagonistOocyte yieldProgesterone primed ovarian stimulation

Identifiers

PMID41162665
PMCPMC12705851

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