4.7 Article

Obstetric outcome of patients with polycystic ovary syndrome treated by in vitro maturation and in vitro fertilization-embryo transfer

Journal

FERTILITY AND STERILITY
Volume 83, Issue 5, Pages 1461-1465

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.fertnstert.2004.11.044

Keywords

in vitro maturation; IVF-ET; PCOS; obstetric outcome

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Objective: To assess the obstetric outcome of pregnancies resulting from in vitro maturation (IVM) and IVF-ET e of immature oocytes retrieved from women with polycystic ovary syndrome (PCOS). Design: Prospective observational study. Setting: University fertility clinic. Patient(s): One hundred thirty-nine women undergoing 203 IVM treatment cycles. Intervention(s): Immature oocyte recovery from unstimulated ovaries. In vitro oocyte maturation and fertilization. Fresh ET and assessment of obstetric outcomes in the pregnant women. Main Outcome Measure(s): Pregnancy and obstetric outcome. Result(s): Forty-one pregnancies were obtained in 187 ETs, resulting in a pregnancy rate of 21.9%. Except for three patients lost to follow-up in these pregnancies, the abortion and live birth rates were 36.8% (14 of 38) and 63.2% (24 of 38), respectively. The mean (+/- SD) gestational age and birth weight at delivery for singletons were 38.4 +/- 2.0 weeks (range, 33-41.6 weeks) and 3,252 +/- 516 g (1,750-4,100 g), respectively. For twins these were 36.7 +/- 1.9 weeks (34.6-39 weeks) and 2,361 +/- 304 g (1,900-2,990 g), respectively. Pregnancy complications occurred in five patients (13.2%); these included preterm labor (n = 3) and placenta previa (n = 2). Two patients (5.3%) had a major congenital anomaly diagnosed by ultrasonography. Conclusion(s): The abortion rate, gestational age and birth weight at delivery, and obstetric complications of pregnancies conceived by IVM-ET in women with PCOS were comparable with those of other women with PCOS being treated by conventional IVF-ET. In vitro maturation followed by IVF-ET seems to be a useful treatment option for women with PCOS, thus avoiding the risk of ovarian hyperstimulation syndrome. ((c) 2005 by American Society for Reproductive Medicine.)

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