Afternoon Symposium - What Comes After the Big Chill: The Metabolic and Clinical Consequences of Oocyte and Ovarian Tissue Cryopreservation

Date:October 22, 2012

Time:4:15 pm - 6:15 pm

Location:Ballroom 6 - San Diego Convention Center

Presenters

David F. Albertini, Ph.D. (Chair), University of Kansas Medical Center

S. Samuel Kim, M.D., University of Kansas Medical Center

Tommaso Falcone, M.D., Cleveland Clinic

Evelyn Flaherty-Brown, Ph.D., The University of Edinburgh

What Comes After the Big Chill: The Metabolic and Clinical Consequences of Oocyte and Ovarian Tissue Cryopreservation - A Look to the Future

Needs Assessment and Description
As oocyte and ovarian tissue cryopreservation gain widespread usage in the field of human assisted reproductive technology (ART), the need to validate and improve the safety and efficacy of these procedures is paramount to future applications. Few efforts have been made to document the short-term consequences of thawing, transplantation or subsequent culturing of ovarian cortical strips, especially with respect to metabolic properties of follicles. The goal of this live course is to inform clinicians and scientists of recent methodological and outcome measures that are being used to evaluate the integrity and developmental potential of oocytes and tissues subjected to cryopreservation.

Learning Objectives
At the conclusion of this session, participants should be able to: 

  1. Review current protocols adopted for cryopreservation and thawing of human oocytes and ovarian tissues and summarize their utility in human ARTs. 
  2. Discuss the link between sample thawing and the recovery of metabolic function in the context of embryo transfer and tissue transplantation.

ACGME Competency
Medical Knowledge

TEST QUESTION:
Thawing of ovarian tissues with subsequent culture or transplantation is likely to result in which of the following: 

  1. Widespread apoptosis of somatic ovarian cell types 
  2. Widespread apoptosis of oocytes 
  3. Activation of cell survival pathways 
  4. Tissue necrosis

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