New to the forum? Sign Up Here! Already a member? Please login below.
|
|||||
|
||
|
The live birth rate for IVF using testicular sperm is lower than that for using ejaculated sperm. In your age group, you could expect the chances of taking home a baby from IVF of about 20-30% per attempt. The more eggs you produce on the stimulated cycle, the better your chances. I would suggest that you try to culture the embryos to the blastocyst stage prior to transfer because, when testicular sperm are used, embryos may arrest development after the sperm DNA kicks in on Day 3. By waiting until Day 5-6, you can be sure that the embryos transferred are of good developmental potential. |
||
|
||
|
Dr. Smith, |
||
|
||
|
It depends on the presference of the urologist and whether or not mature sperm can be obtained from the epididymus. The use of epididymal sperm is preferable, but the success rate is still lower than fresh, ejaculated sperm. |
||
|
||
|
I am 39 and have failed one icsi trial. We had to do icsi because my husband's sperm do not swim well - he is post chemo. All of my pre icsi trial tests were normal. 1 grade a embryo and one grade b embryo were transferred on Day 3. I am confused as to why it did not implant - as I thought our prognosis was pretty good. What questions should I ask my physicians when we meet with him next week? |
||
|
||
|
There may have been an effect of the chemotherapy on the gentic material of the sperm. When there is a problem with the gentics of the sperm, it shows up after Day 3, not before. So one possible explanation for the failure is due to the sperm genetics. |
||
|
||
|
Dr. Smith |
||
|
||
|
My husband has bilateral undescended testicles. Is there any chance of us being sucessful with ISCI? He is 57 and I am 35. I have never tried to get pregant but assume all is well with me. |
||
|
||
|
It is unlikely that sperm are being produced in the undescended testicles. Your husband should see an infertility-trained urologist to determine whether or not sperm recovery is possible. Otherwise, it using donor sperm would be the only other way. |
||
|
||
|
Reply to cde: |
||
|
||
|
Thank you Dr. Smith for your reply. We met with our physician. |
||
|
||
|
More gonadotropin (FSH) medication does not produce more follicles. The FSH acts to sustain the growth of the number of follicles that have already begun growing for that cycle. It does not act to recruit more follicles into the growing pool. The follicles were on the large side at the time of retrieval and your doctor is right, when they get over 20 mm in diameter it becomes more difficult to retrieve the egg from the follicle. In those cases, docotors can re-expand the drained follicle with culture medium and "flush" the inside and aspirate again. This usually does the trick. If the egg doesn't come out with the initial aspirate, it usually comes out with the "flush". Better yet, don't let the follicles get so big before retrieval (i.e. pay closer attention during the stimulation). |
||
|
||
|
Dr. Smith, |
||
|
||
|
This is a typical reaction to a stimulation that resulted in only a few follicles. However, it rarely makes a significant difference. There is some cycle-to-cylce variation in the number of follicles that are recruited into the growing pool. Sometimes doctors (and patients) think that because they got a couple more follicles growing on a subsequent cycle that it was becasue of a change in brand or dose of gonodotropins. Its simply not true and has no basis in science. If it were as simple as increasing the dose of gonadotropins, then everyone would get lots of eggs on every retrieval and that is simple not the case. Changing the stimulation protocol (i.e. microdose flare) can have a slightly beneficial effect on recruitment, but it won't change the number of growing follicles from, say 5 to 15. Maybe from 5 to 7 would be more realistic. We simple cannot control or the increase the number of follicles that are recruited into the growing pool at the begining of a given cycle with the tools (i.e. medications) we currently have available to us. |
||
|
||
|
Hello, DR Smith! My Hb and I went through IVF In June of 05. I am 25 and my hb is 27 now. The reason for IVF was cause we had never conceived after 5 years of trying! So after 4 failed IUI's Naturally the next step was IVF. So we went through all the steps, they collected 21 eggs from me something happened to 2 of them so it became 19 perfect eggs. They put them in the petrie dish with my hb's perfect sperm to do their job. Well the next morning I get a call from the clinic telling me none of the eggs fertilized. The sperm and the eggs just sat around all night doing nothing!!! Much to my distress they offer me ICSI saying there was still hope..... I excepted not wanting it to be a total failure. So they saved what they could and surprisingly 12 of them became 5 cells. They did the transfer right away at 3 days not wanting to loose anymore time being that they lost that vital time of fertilization. Needless to say it failed I am not pg...and my hb and I are thinking about doing it again only this time with ICSI right away. After hearing my story can you give me any ideas as to what happened? I am really freaked out to do it again my only rock is that doing ICSI first is the answer. Please any advise would be very much appreciated. This was a very weird scenario the first the clinic had ever experienced. I guess I am feel silly for not doing ICSI in the first place. Thank you for listening, I look forward to your response when you get back from your vacation. Merry Christmas!! |
||
|
||
|
Successful fertilization requires a series of steps. First the sperm must bind to the protein coat that surrounds the egg. This binding occurs at the molecular level. If the sperm surface does not have a sufficient number of these binding molecules, the sperm will not bind and fertilization fails. |
||
|
||
|
Dr.Smith, |
||