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A blastocyst is an embryo that has developed for five to
seven days after fertilization. At this point the embryo has
two different cell types and a central cavity. It has just
started to differentiate. The surface cells, called the
trophectoderm, will become the placenta, and the inner
cells, called the inner cell mass, will become the fetus. A
healthy blastocyst should begin hatching from its outer
shell, called the zona pellucida by the end of the sixth
day. Within about 24 hours after hatching, it should begin
to implant into the lining of the mother's uterus.
The ultimate goal of in vitro fertilization (IVF) and
embryo culture is to provide high quality embryos which are
capable of continued normal development and result in live
births. However, under standard IVF culture conditions, only
about 20-40% of human embryos will progress to the
blastocyst stage after 5 days of culture. This low rate of
embryo development is partly due to the result of a less
than optimal culture environment for the embryos. For this
reason, embryos have usually been transferred into the
uterus after only 2-3 days of culture.
One problem with this is that 2 to 3-day-old embryos are
normally found in the fallopian tubes, not in the uterus.
The embryo first moves into the uterus at about 80 hours
after ovulation. The implantation process begins about 3
days later - after blastocyst formation and hatching have
occurred. Therefore, if in vitro culture conditions could be
improved so that blastocysts formed at a higher rate, then
embryos could be placed into the uterus at the blastocyst
stage - at a more "natural" time, and shortly before
implantation should occur.
Transferring blastocysts following IVF also provides
another benefit - reduction of the possibility of multiple
pregnancy. Some 2 or 3-day-old embryos do not have the
capacity to become high quality blastocysts and a viable
pregnancy. However, on day two or three of culture we do not
have reliable methods to determine which embryos will be
viable long-term. By culturing embryos to the blastocyst
stage we have more opportunity to choose the most competent
ones for transfer. We can then transfer fewer embryos and
obtain high pregnancy rates with less risk for high order
(triplets or higher) multiple pregnancy.
In the past, it was very difficult to get good numbers of
high quality blastocysts with in vitro culture systems -
unless "feeder" cells were utilized - coculture. However,
new culture media have recently become available that yield
much higher blastocyst formation rates. This makes
blastocyst transfer a viable option for some couples with
infertility.
With the success our clinic has with day 3 transfers,
only a few select patients have been selected for blastocyst
culture and transfer.
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