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DOI 10.5935/1518-0557.20240004

Медицинская библиотека · JBRA assisted reproduction · 2024

High ovarian responders have the highest risk of premature progesterone rise.

Cortés-Vazquez Alfredo, Vásquez-Ramírez Greys Thelma, Cortés-Algara Alfredo Leonardo, Moreno-García Jesús-Daniel, Drakopoulos Panagiotis

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Аннотация

OBJECTIVE

Late follicular phase progesterone elevation is a complication that affects approximately 38% of IVF cycles. There is a lack of consensus on the appropriate cut-off levels for progesterone on hCG day. Although premature progesterone rise occurs in all kinds of ovarian responses, there is a knowledge gap regarding the ovarian response with the highest risk of this phenomenon. Our study aims to assess the relative risk of each kind of ovarian response for premature progesterone rise and evaluate the prevalence of premature progesterone rise in each ovarian response.

METHODS

A retrospective, cross-sectional, comparative and analytic study was performed at the Reproductive Endocrinology Department in Centro Médico Nacional 20 de Noviembre in Mexico City. All conventional-antagonist cycles were grouped according to their ovarian response and were evaluated from 2015 to 2020. Pearson's Squared-chi, Cramer's V, cross-table and the relative risk were calculated.

RESULTS

The prevalence of premature progesterone rise oscillated from 20.8 to 67.9% for low and high ovarian responders, respectively. After calculating the relative risk, high ovarian responders had a 1.38 higher risk for premature progesterone rise than other groups.

CONCLUSIONS

High ovarian responders have the highest risk for premature progesterone rise compared to normal and low ovarian responders. High ovarian responders have a 67.9% prevalence of premature progesterone rise.

Для цитирования: Cortés-Vazquez Alfredo, Vásquez-Ramírez Greys Thelma, Cortés-Algara Alfredo Leonardo, Moreno-García Jesús-Daniel, Drakopoulos Panagiotis. High ovarian responders have the highest risk of premature progesterone rise.. JBRA assisted reproduction. 2024. DOI: 10.5935/1518-0557.20240004.

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