Louisville Medicine Volume 67, Issue 4 | Page 29

UNDERSTANDING INFERTILITY their chromosomes aligned by a spindle apparatus along the equatorial plate. During traditional (“slow freeze”) cryopreservation techniques, intracellular ice crystals form that may damage the meiotic spindle and compromise the viability of the oocyte. More recently, an alternative cryopreservation technique called vitrification has allowed us to freeze and thaw oocytes with much greater reliability. Vitrification is performed with high concentrations of cryoprotectants that dehydrate the oocytes, followed by rapid cooling in liquid nitrogen that allows the cells to be solidified into a glass-like state without the formation of ice crystals. Oocyte survival rates with vitrification vary by female age but are typically reported around 70-80%. As embryology laboratories gained comfort with vitrification and increasing experience with oncofertility patients, the American Society for Reproductive Medicine elected to remove the experimental label from OC in 2012, and according to the CDC, over 98% of fertility practices in the United States now offer this service to their patients. In 2017, there were nearly 11,000 OC cycles performed across the country. At Kentucky Fertility Institute, we usually see several consultations per week for patients interested in these services, roughly evenly split between those referred for oncofertility and those desiring planned OC. As these technologies are still relatively new, the process of informed consent is especially important, which must include the disclosure that long term outcome data for children born from cryopreserved oocytes is not yet available. However, short term outcomes relating to pregnancy rates and subsequent neonatal outcomes have been reassuring and appear comparable to those for patients using fresh oocytes in traditional IVF treatment. Current prediction models suggest that for at least a 75% probability of future live birth, women up to age 36 should consider cryopreserving at least 15 to 20 mature oocytes. Due to the higher incidence of oocyte aneuploidy in women in their late 30s, women ages 37 to 39 are typically advised to cryopreserve at least 20-30 to achieve similar outcomes. Depending on individual variables and preferences, some patients may require more than one OC cycle to achieve these clinical targets. Interestingly, the cultural reception of planned OC has been mixed. It has been applauded for enhancing women’s reproductive autonomy and providing an option for the dissociation of fertility from conflicting priorities relating to education, professional commitments or other social circumstances. Several high-profile An unfertilized oocyte (photo courtesy Dr. Greg Christensen, PhD, HCLD) tech companies (including Apple and Facebook) quickly added it to their list of employee health benefits as an incentive for attracting and retaining more competitive female employees. However, over the past few years, a number of startup companies have launched with the goal of marketing OC to millennials in their 20s, which has understandably generated a fair amount of criticism. Most women in this younger age group are unlikely to benefit from OC, and surveys have shown a high incidence of regret in young women who pursue it. At Kentucky Fertility Institute, we generally advise that otherwise healthy women in their 20s be managed with education, counseling and serial assessments of ovarian reserve metrics. To optimize the value of OC, careful patient selection and counseling are key. Our typical patients pursuing planned OC are in their mid-30s, and we have observed that most either have highly-demanding jobs (e.g. physicians and executives), or are newly single after ending a long-term relationship. Female aging remains one of the most difficult barriers to fertility for us to overcome in a clinical setting, and despite its limitations, planned OC is among the most effective preventive interventions we have available at the current time, particularly for women who prioritize the use of autologous oocytes in their family-building goals. From its origins in oncofertility to its rapidly-expanding contemporary applications in family planning, OC will undoubtedly have a valuable role in modern reproductive care for the foreseeable future. Dr. Hunter is the Practice Director of the Kentucky Fertility Institute. SEPTEMBER 2019 27