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Published in: Reproductive Biology and Endocrinology 1/2005

Open Access 01-12-2005 | Research

Clinical benefit of metaphase I oocytes

Authors: Leen Vanhoutte, Petra De Sutter, Josiane Van der Elst, Marc Dhont

Published in: Reproductive Biology and Endocrinology | Issue 1/2005

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Abstract

Background

We studied the benefit of using in vitro matured metaphase I (MI) oocytes for ICSI in patients with a maximum of 6 mature metaphase II (MII) oocytes at retrieval.

Methods

In 2004, 187 ICSI cycles were selected in which maximum 6 MII oocytes and at least one MI oocyte were retrieved. MI oocytes were put in culture to mature until the moment of ICSI, which was performed between 2 to 11 hours after oocyte retrieval (day 0). In exceptional cases, when the patient did not have any mature oocyte at the scheduled time of ICSI, MI oocytes were left to mature overnight and were injected between 19 to 26 hours after retrieval (day 1). Embryos from MI oocytes were chosen for transfer only when no other good quality embryos from MII oocytes were available. Outcome parameters were time period of in vitro maturation (IVM), IVM and fertilization rates, embryo development, clinical pregnancy rates, implantation rates and total MI oocyte utilization rate.

Results

The overall IVM rate was 43%. IVM oocytes had lower fertilization rates compared to in vivo matured sibling oocytes (52% versus 68%, P < 0.05). The proportion of poor quality embryos was significantly higher in IVM derived oocytes. One pregnancy and live birth was obtained out of 13 transfers of embryos exclusively derived from IVM oocytes. This baby originated from an oocyte that was injected after 22 hrs of IVM.

Conclusion

Fertilization of in vitro matured MI oocytes can result in normal embryos and pregnancy, making IVM worthwhile, particularly when few MII oocytes are obtained at retrieval.
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Metadata
Title
Clinical benefit of metaphase I oocytes
Authors
Leen Vanhoutte
Petra De Sutter
Josiane Van der Elst
Marc Dhont
Publication date
01-12-2005
Publisher
BioMed Central
Published in
Reproductive Biology and Endocrinology / Issue 1/2005
Electronic ISSN: 1477-7827
DOI
https://doi.org/10.1186/1477-7827-3-71

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