4.7 Article

Are good patient and embryo characteristics protective against the negative effect of elevated progesterone level on the day of oocyte maturation?

Journal

FERTILITY AND STERILITY
Volume 103, Issue 6, Pages 1477-U145

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.fertnstert.2015.02.038

Keywords

Elevated progesterone; premature luteinization; implantation; IVF

Funding

  1. Program in Reproductive and Adult Endocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland

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Objective: To evaluate if an elevated progesterone (P) level on the day of human chorionic gonadotropin (hCG) administration is associated with a decrease in live-birth rate in patients with a good prognosis. Design: Retrospective cohort study. Setting: Large, private, assisted reproductive technology (ART) practice. Patient(s): One thousand six hundred twenty fresh autologous ART cycles. Intervention(s): None. Main Outcome Measure(s): Live-birth rate. Result(s): A total of 934 blastocyst and 686 cleavage-stage embryo transfer (ET) cycles were evaluated. Serum P levels were not associated with markers of oocyte or embryo quality, including fertilization, embryo stage at transfer, and embryos available for cryopreservation. Patient age, stage of ET, embryo quality, the number of embryos transferred, and P level on the day of hCG administration were all significantly associated with live birth. Higher P levels were associated with decreased odds of live birth for cleavage- and blastocyst-stage embryos, poor-fair and good-quality embryos, and poor-and high-responder patients. The nonsignificance of interaction tests of P levels with embryo stage, embryo quality, patient age, and ovarian response indicated that the relationship between P level and live birth was similar regardless of these factors. Conclusion(s): An elevated serum P level on the day of hCG administration was negatively associated with live birth, even in ETs with a good prognosis. (C) 2015 by American Society for Reproductive Medicine.

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