Embryo Transfer - Superovulation Protocol Modification

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Peter Elsden

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Variability of Pregnancy Rates from Frozen/Thawed/Transferred Embryos

The problem of low pregnancy rates following the transfer of previously frozen embryos has significantly decreased over the years, but it still does occur as demonstrated in a recent court case. Usually the transfer technician is accused of unacceptable quality work as he/she is the last person to handle the embryo.  However, fault may be due to many other persons in the steps to produce the final product e.g. selection of poor quality embryos to freeze, unacceptable freezing techniques, poor embryo storage practices, recipients too fat or too thin, inaccurate heat detection, inadequate records etc...

As the technician performing the work, or as the donor owner selling the embryos, there is an excellent method to protect oneself: Following embryo and egg collection there are in most cases eggs and degenerate embryos observed. Prepare these normally discarded eggs and embryos for freezing the same as for valuable embryos and place them all in one straw. Around -30°C place the test straw in the liquid nitrogen tank for approximately one minute.  Remove this straw from the tank, thaw and examine the eggs and embryos and record the results. If there is a problem with the freezing method there will be many zona cracks. About 10 to 15 percent of zonae will have one crack even with excellent freezing techniques. Eggs are quite acceptable for this technique.

SUPEROVULATION PROTOCOL MODIFICATION:
Guerra et al recently published a modified superovulation protocol which appears very promising. By extending the 4 day FSH treatment to 7 days, injecting the same amount of FSH, they observed a significant increase in CLs produced. This treatment did not increase the number of follicles recruited but the longer treatment schedule gave the smaller follicles time to mature and be able to ovulate. Extending the superovulation treatment may be useful for those donors producing too few embryos.

May all of your flushes be successful!

Dr. Peter Elsden
www.ETschool.com

References:
Guerra et al  Theriogenology 84 (2015) 467-476
 

beebe

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Apr 29, 2014
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Dr. Elsden
I am about to put a couple of eggs in cows thay will be taken to the technician and then brought home after the eggs are in.  Do you have any advice that would improve the chances of success?  These are rare genetics that can not be replaced.
 

Peter Elsden

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Oct 2, 2011
Messages
36
beebe said:
Dr. Elsden
I am about to put a couple of eggs in cows thay will be taken to the technician and then brought home after the eggs are in.  Do you have any advice that would improve the chances of success?  These are rare genetics that can not be replaced.
Make sure the selected recipients are cycling regularly before synchronisation. Use proven cows as recipients.Vaccinations should be up to date. Recipients should be in good condition,that is not too fat or too thin. When they are fat lutein cysts instead of CLs are frequently present,and if they are too thin the CL often disappears by Day 21.Travelling on the day of transfer will not effect the results providing there is not extreme stress. Naturally employ a proven technician.  Good Luck.
 

beebe

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Apr 29, 2014
Messages
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ETschool.com said:
beebe said:
Dr. Elsden
I am about to put a couple of eggs in cows thay will be taken to the technician and then brought home after the eggs are in.  Do you have any advice that would improve the chances of success?  These are rare genetics that can not be replaced.
Make sure the selected recipients are cycling regularly before synchronisation. Use proven cows as recipients.Vaccinations should be up to date. Recipients should be in good condition,that is not too fat or too thin. When they are fat lutein cysts instead of CLs are frequently present,and if they are too thin the CL often disappears by Day 21.Travelling on the day of transfer will not effect the results providing there is not extreme stress. Naturally employ a proven technician.  Good Luck.
Thank you for your help.  Good luck to you.
 

Peter Elsden

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Oct 2, 2011
Messages
36
Cabanha Santa Isabel - BR said:
Thanks Dr. Elsden.

So, any hormon protocol for fat cows?
Do you have experience with bull natural mating vs. AI on embryos qualityt and quantity?
The superovulation schedule is the same for fat cows. However there is a greater chance of failure to produce embryos as more frequently the fat cow does not ovulate and at the time of recovery you find lutein cysts instead of CLs. Yes, we have data comparing bull mating to AI and there were no differences,providing of course you are using quality semen and the technician is competent. We also compared recipients exibiting normal cycles compare to hormone induced heats and providing a CL is present there are no differences in pregnancy rates.
 

Cabanha Santa Isabel - BR

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Rio Grande - RS - Brazil
ETschool.com said:
Cabanha Santa Isabel - BR said:
Thanks Dr. Elsden.

So, any hormon protocol for fat cows?
Do you have experience with bull natural mating vs. AI on embryos qualityt and quantity?
The superovulation schedule is the same for fat cows. However there is a greater chance of failure to produce embryos as more frequently the fat cow does not ovulate and at the time of recovery you find lutein cysts instead of CLs. Yes, we have data comparing bull mating to AI and there were no differences,providing of course you are using quality semen and the technician is competent. We also compared recipients exibiting normal cycles compare to hormone induced heats and providing a CL is present there are no differences in pregnancy rates.

Thank you Dr. for the answers.
I know that with AI we will inseminate all dnors, showing or not heat. For bull use, ok with showinh heat cows, but the ones that not show heat is my fear!
Thank you again.
 

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