Why are some cycles unsuccessful?
Becoming pregnant after IVF depends upon success at every step
of the process. Therefore steps where the process may not succeed
may include:
Unsuccessful stimulation
The following factors can cause a poor response to stimulation:
-
sometimes too few eggs develop meaning that there are insufficient
eggs to give a good result. This is unfortunately common and
is more likely to occur in women over the age of 40;
-
sometimes ovarian cysts develop in response to the hormone
injections. If these cysts are large, treatment in that cycle
is usually discontinued, as it is difficult to monitor the growth
of other follicles. The cysts usually disappear by themselves
in that cycle
If problems crop up at this stage, we normally recommend that you
cancel the cycle (there is no financial cost for doing this) and
start again, possibly with a different treatment plan.
Unsuccessful egg collection
This is uncommon, but can occur when
-
ovulation has occurred earlier than expected;
-
the follicles just do not contain a retrievable egg;
-
hCG was not given approximately 36 hours before the attempted
egg collection;
Unsuccessful fertilisation
This is usually due to a recognised problem with the sperm. However,
occasionally it may occur when the sperm appears to be normal and
sometimes may be the explanation for the couple's failure to conceive
naturally. Fragmented or immature oocytes usually do not become
fertilised. ICSI may be recommended for future treatment cycles
to improve the chance of fertilisation.
Embryo transfer but no pregnancy
Unfortunately, this is still the most common outcome for an IVF
cycle. Usually, we will be unable to tell you why a pregnancy has
not occurred after an apparently straighforward transfer of seemingly
healthy embryos. This the area in which all scientists are hoping
to find the answers. It is currently thought that the major factor
in the failure of the embryo to implant is the quality of embryo
itself. Even though an embryo may look ideal, there are still likely
to be critical defects which limit its ability to implant successfully.
Non-continuing pregnancy
About 75% of those who become pregnant eventually give birth to
a normal baby, however sadly early pregnancy losses are common than
in non-IVF pregnancies. The following things may occur:
-
biochemical pregnancy - a pregnancy lost in the first few days,
where the only sign that the pregnancy has occurred is the biochemical
detection of hormone in blood;
-
ectopic (tubal) pregnancy - this is usually picked up on early
ultrasound. Surgery is usually needed to remove the pregnancy
in this situation;
-
miscarriage - this is where the pregnancy is lost in the early
weeks of pregnancy. Sometimes the fetus itself has not even
formed and only a small sac of fluid is seen on scan (delayed
miscarriage). Sometimes the fetus may be lost even though it
is appears to be healthy on an earlier ultrasound scan.
The risk of miscarriage increases significantly with maternal
age. It is generally accepted that patients under 30 have a
5 - 10% chance of miscarrying. This rises to approximately 15%
in the 30 - 34yrs age group and is approximately 10 -20% for
patients aged 35 - 39. For patients 40 years and older, the
risk of miscarriage is approximately 20 - 40%.
If your treatment cycle is unsuccessful in achieving a pregnancy,
it is suggested that you wait more than one full cycle before starting
again. This is to allow you to wind down and get back to some 'normal'
living again.
Effect of Maternal age on Fetal Abnormalities
|
Crude
Maternal Age-Specific Rates for Fetal Chromosome Abnormalities
(including Trisomy 21 and Downs Syndrome)
|
| |
Maternal
Age
(yrs)
|
Chromosome
Abnormalities
|
|
| |
35 or less
|
1/275
|
|
| |
36
|
1/167
|
|
| |
38
|
1/103
|
|
| |
40
|
1/63
|
|
| |
41
|
1/50
|
|
| |
42
|
1/39
|
|
| |
43
|
1/30
|
|
| |
44
|
1/24
|
|
| |
45
|
1/19
|
|
|
Liveborn
data from Hsu,LYF. Prenatal diagnosis of chromosomal abnormalities
through amniocentesis. In: Genetic Disorders and the Fetus,
4th Ed, Milunsky (ed), The John Hopkins University Press,
Baltimore 1998.
|
|
|