Blastocyst Transfer: The Preferred Approach!
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The issue of whether it is better to transfer early cleaved embryos rather than blastocysts continues to rage. I have previously written in this blog on this important topic. Here, I once again wish to refocus on the reasons why I personally strongly favor transferring blastocysts.
What we do know for sure (and reported on in 2008) is that cleaved embryos (day 2-4, post-fertilization) that fail to develop into blastocysts are with few exceptions “incompetent” (unable to propagate a viable pregnancy in a “receptive ” uterine environment). So had they been transferred in the “cleaved” state, they almost certainly would not have developed to blastocysts and thus could not propagate a pregnancy anyway.
Simply stated, there is no difference in pregnancy potential by doing an earlier transfer of pre-blastocyst (cleaved) embryos versus forgoing an embryo transfer because none of the embryos developed into blastocysts. There is no validity to the often-stated opinion that an embryo would develop better and have a greater chance of propagating a baby by being inside the uterus earlier, than it would by being allowed to develop into a blastocyst in an incubator.
Don’t get me wrong – I am not saying that there is no place for doing earlier pre-blastocyst transfers! Indeed, if it were possible to determine with confidence, by microscopic grading alone, which embryos would develop into blastocysts by day 5-6 post fertilization (and this is currently not possible), then in terms of outcome, it would not matter whether such embryos were transferred sooner or later. What we now do know for certain (and have reported on) is that if a day-3 embryo is found to have its full quota of 46 chromosomes (i.e. it is “euploid”) as assessed by day-3 metaphase CGH, then, regardless of the age of the egg provider, more than 90% of such embryos will develop into a blastocysts by day 5-6 post fertilization.
By comparison, in the absence of CGH testing, about 40% of embryos derived from the fertilization of eggs extracted from a woman under 35 years, (and +/-10% in women in their mid 40′s) will subsequently develop into blastocysts. Certainly, chromosomal integrity of the embryo is not the sole determinant of “competency” (epigenetic and metabolomic factors also play a role) but, it is by far the most important variable.
So…given the following facts:
- The odds are relatively poor that embryos determined to be of a “High Grade”, microscopically, will turn out to be euploid (chromosomally normal)
- The likelihood of aneuploid (chromosomally abnormal) eggs increases as the age of the egg provider increases.
It is my opinion that there is nothing wrong with transferring up to three (3) such early (day-3), untested embryos to women under 39 years and/or no more than four (4) to women over 40 years, especially if they would agree to pregnancy reduction to twins in the unlikely event of a high order multiple pregnancy (triplets or greater) where the risk to mother and offspring would be greatest.
The strong arguments in favor of blastocyst transfer are:
1) By waiting to day 5-6 many unworthy, aneuploid and “incompetent” embryos can be culled out, thereby providing “relative” confidence that you will not end up with a high order gestation. This allows for the transfer of fewer embryos, minimizing the risk of high order multiple pregnancies.
2) Waiting until day 5-6 post-fertilization affords important diagnostic benefits:
a) Failure of the expected number of cleaved embryos to advance to this stage of development suggests either inherent embryo “incompetence” (which is usually a function of the age of the egg provider…the effect of the ‘biological clock”), and/or may be due to the wrong protocol of ovarian stimulation being applied. (For expansion on this important concept, I urge read the article “An Individualized Approach to Ovarian Stimulation for IVF“)
b) It facilitates the performance of CGH to identify and then selectively transfer only the most “competent” (euploid) blastocysts. In such cases, the transfer of a single blastocyst (SBT) should yield a 60-70% baby rate per embryo transferred to the uterus, provided there is no underlying uterine implantation dysfunction.
Of course, after everything IVF patients go through, it is much easier and far less stressful on the treating physician not have to have to confront patient(s) with the heartbreaking news that they have no surviving embryos to transfer. Undoubtedly, this is one of the main reasons why IVF practitioners still prefer to transfer cleaved embryos rather than blastocysts. But as far as I am concerned, this is not justification to do what ultimately might not be in the in the patents’ best interest. Rather, it is about doing what serves patients best and what they choose after being fully informed regarding associated risks and benefits.
7 Responses to “Blastocyst Transfer: The Preferred Approach!”
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What's confusing to me is how a 5-6 day blastocyst can be aneuploid. Why would they even make it to that stage if they aren't viable?
The fact that babies are born with aneuploiudy-related defects (e.g. Down's syndrome) and miscarriages are often due to aneuploidy, proves that rthis is so.
Geoff Sher
Dr Sher,
i am 36 years old and my wife 35. We tried 3 times IVF (specifically ICSI) but unfortunatelly we had 3 chemical pregnancies. Lately i found out that i suffer from sperm aneuploidy (9% in the four chromosomes which were tested). My questions are:
1. Is there anything to do to decrease the abovemntioned number (achieve less aneuploidy rate)?
2. Is there a way to screen sperms suffering from aneuploidy before ICSI?
Dear Dr.Sher,
I need some more suggestion as I am still struggling to get pregnant and my journey is still going on. My age is 29 and My husband is 31. We are trying to conceive for more than 2 years. I had 2 failed IUI with clomid. With one IUI, I got pregnant but it was diagnosed as ectopic pregnancy. My husband’s morphology is only 1% and so we tried to do 1 fresh IVF cycle with ICSI, which also failed. My doctor has transferred 1 blastocyst embryo on 5th day of grade 3AA. We still have 1 frozen 6 day embryo. I am going to schedule an appointment with my doctor. But I need your opinion about what points I should discuss with my doctor. What could be the reason for failure of my 1st IVF. My doctor also did Saline sonogram and Hystroscopy to see into my uterus and the report was normal. Even I have hsg done which shows my tubes are open. Please suggest me what other test I should do before going to frozen embryo transfer.
As I informed you before, i dont think embryo quality might be a problem for implantation. Does that mean something is wrong in my uterus besides my doctor checked inside the uterus. My lining was also good during embryo transfer as 15mm.
I think that your failure to conceive even with ovarian stimulation and IUI + 1 IVF could have to do with a possible immunologic implantation dysfunction.If you have a lot of pain and heavy bleeding with menstruation and especially if in addition you tend to experience pain with deep penetration during intercourse (deep dyspareunia) or have painful ovulation, then it is possible (not diagnostic) that you have endometriosis as an explanation for this. About 30% of women with endometriosis have autoimmune implantation dysfunction that can thwart an IVF success. I suggest your blood be sent to Reprosource in Boston, MA to have a natural killer(NK) cell activity (NKa) test done because if this exists as A problem you would need specialized treatment (see below).
Please go to the home page of this blog, (www.IVFauthority.com). When you get there look for a “search bar” in the upper right hand column. Then type in the following subjects into the bar, click and this will take you to all the relevant articles I posted there.
1. Endometriosis and IVF”
2. “Immunologic Implantation Dysfunction” (posted on May, 10th and on May 16th respectively.
3. “Embryo Implantation………” (Part-1 and Part- 2—-Posted August 2012)
4. “Traveling for IVF from Out of State/Country– The Process at SIRM-Las Vegas” (posted on March, 21st 2012)
5.“A personalized, stepwise approach to IVF at SIRM”; Parts 1 & 2 (posted March, 2012)
6. “IVF success: Factors that influence outcome”
If interested , consider calling 800-780-7437 or 702-699-7437 to arrange a telephone or Skype consultation (free of charge to those who reside in the United States or Canada) with me so we can discuss your case in detail.. While an audiovisual (Skype) interaction is much more personable and preferable than a discussion by telephone, either will suffice.
Geoff Sher
Hello Dr. Sher,
Just for your info, I never had any pain during intercourse or pain during ovulation. Even my doctor never diagnosed me for endometroisis.
OK…Copy!
Geoff Sher