A subscription to JoVE is required to view this content. Sign in or start your free trial.
Here, we present an optimized method for promptly removing a portion of cumulus-oocyte complexes following egg retrieval to expedite the IVF observation process, reducing the time required for granulosa cell removal, minimizing oocyte exposure to external elements, and does not hinder embryo development, ultimately improving the efficiency of IVF laboratory procedures.
Despite the rapid advancements in clinical and laboratory technologies for in vitro fertilization (IVF), a significant proportion (10%-15%) of patients continue to experience fertilization disorders, leading to low fertilization rates and the production of nonviable embryos. Short-term fertilization involves the early removal of granulosa cells to observe the extrusion of the second polar body, enabling the assessment of fertilization and early remedial measures to address low fertilization rates and complete fertilization failure. However, the observation of short-term fertilization in IVF is impeded by challenges such as excessively large unprocessed clusters of cumulus-oocyte complexes and adhesion between eggs, necessitating complex external procedures for granulosa cell removal, and prolonged observation duration. To tackle this issue, this study proposes a method of immediate partial removal of granulosa cells post egg retrieval. This approach streamlines subsequent stages of short-term fertilization and traditional fertilization monitoring, reduces the time needed for oocyte extrusion, minimizes the likelihood of external environmental impacts on the oocytes, and decreases the risk of missing the critical fertilization observation window. Consequently, the study yields novel clinical evidence aimed at enhancing the operational efficiency of embryonic laboratories in IVF.
In the field of in vitro fertilization-embryo transfer (IVF-ET), the typical fertilization rate falls within the range of 60% to 80%1. However, approximately 4% to 16% of cases encounter either complete fertilization failure or low fertilization rates, presenting challenges in prediction2,3. To improve clinical pregnancy outcomes and decrease the occurrences of complete non-fertilization and low fertilization, the utilization of short-term fertilization in IVF procedures is on the rise4. This approach entails the prompt removal of granulosa cells to monitor the e....
All procedures were conducted in accordance with the standard operating procedures of the Department of Reproductive Medicine at Meizhou People's Hospital and were subject to review by the Ethics Committee of the same department. Written informed consent was obtained from each participating couple.The study included participants undergoing their first IVF cycle with cleavage or blastocyst stage embryo transfer, as well as females between 20 and 45 years of age. Exclusion criteria included the use of donor eggs/sperm .......
In the group undergoing short co-incubation procedures, patients who received rescue were excluded. Out of 47 patients receiving short-term insemination, no significant differences were observed in terms of patients' age and the number of retrieved oocytes (Table 1). The immediate partial removal of OCCC resulted in a loosening of the remaining OCCC around the oocytes (Figure 3), facilitating the detection of a second polar body. The average procedure time was significan.......
The immediate partial removal of granulosa cells can accelerate the early disintegration process of short-term fertilization, reduce the observation time for the second polar body in both short-term fertilization and conventional IVF and do not compromise subsequent embryo development. Currently, laboratories globally employ various strategies to mitigate fertilization disorders and low success rates. The preferred method involves removing granulosa cells for observing the second polar body 4-6 h post short-term fertiliz.......
The authors express their gratitude to the Department of Reproductive Medicine staff at Meizhou People's Hospital in Guangdong, China, for their active participation in this study.
....Name | Company | Catalog Number | Comments |
G-IVFT PLUS | Vitrolife | 10136 | |
OVOIL | Vitrolife | 10029 | |
G-MOPS PLUS | Vitrolife | 10130 | |
Falcon 3003 dish | Corning | 353003 | |
Falcon 3001 dish | Corning | 353001 | |
Falcon 2001 tube | Corning | 352001 | |
Falcon 4013 cup | Corning | 354013 | |
Falcon 3037 dish | Corning | 351058 | |
Pasteur pipette | Darwin | D1150-5P |
Explore More Articles
This article has been published
Video Coming Soon
ABOUT JoVE
Copyright © 2024 MyJoVE Corporation. All rights reserved