2019
DOI: 10.1093/humrep/dez213
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Perinatal outcomes among young donor oocyte recipients

Abstract: STUDY QUESTION Is the use of donor oocytes in women <35 years of age associated with an increased risk of adverse perinatal outcomes compared to use of autologous oocytes? SUMMARY ANSWER Among fresh assisted reproductive technology (ART) cycles performed in women under age 35, donor oocyte use is associated with a higher risk of preterm birth, low birth weight and stillbirth (when zero embryos were cryopreserved) as compar… Show more

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Cited by 3 publications
(3 citation statements)
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“…Previous studies suggested that donor sperm or oocyte embryo transfer is associated with a risk for preeclampsia in frozen cycles (40,41). Furthermore, donor sperm embryo transfer is associated with an increased risk of SGA, and donor oocyte embryo transfer is associated with a higher risk of preterm births and LBW (41)(42)(43)(44)…”
Section: Discussionmentioning
confidence: 99%
“…Previous studies suggested that donor sperm or oocyte embryo transfer is associated with a risk for preeclampsia in frozen cycles (40,41). Furthermore, donor sperm embryo transfer is associated with an increased risk of SGA, and donor oocyte embryo transfer is associated with a higher risk of preterm births and LBW (41)(42)(43)(44)…”
Section: Discussionmentioning
confidence: 99%
“…The high occurrence of obstetric complications after OD has been associated with advanced maternal age. Yet, also in young women, aged <35 years, the use of donated oocytes compared with autologous oocytes was associated with a higher rate of preterm birth and low birth weight ( 47 ). In the SR by Moreno-Sepulveda et al., there was no difference in the rate of preterm birth and low birth weight when adjusted for pre-eclampsia ( 46 ).…”
Section: Perinatal Outcomementioning
confidence: 99%
“…Abnormalities in the maternal immune response can occur after exposure to novel maternal or paternal antigens, such as donor sperm or donor oocyte. Previous studies that focused on donor oocyte outcomes have found higher rates of hypertensive disorders of pregnancy and fetal growth restriction, supporting this immunologic theory for placental dysfunction [ 35 ]. It is important to note that the gestational parent in the co-IVF cycle will technically have both a non-autologous oocyte and donor sperm, which may negatively potentiate poor perinatal outcomes.…”
Section: Discussionmentioning
confidence: 62%