Thursday, April 13, 2017

Estrogen measurements during an FET

We all know that estrogen can be an issue in fresh cycles because your body is making so many follicles and saturating your body with estrogen.  (Estrogen measurements can be related to the number of mature follicles—lots of follicles equals lots of estrogen.  http://3yearwait.blogspot.com/2015/02/what-do-all-of-those-measurements.html)  Ovarian hyper simulation syndrome can be a risk (http://3yearwait.blogspot.com/2011/05/ivf-side-effects.html), and high estrogen can have a detrimental effect on chances of pregnancy success.  (http://www.ncbi.nlm.nih.gov/pubmed/24757341)

But what about estrogen in a frozen embryo transfer?  Does it even matter?  I mean, they measure it for some reason….

Six days before one of my scheduled FETs, I had an estrogen measurement of 231.  Another time it was 265.  Are those good?  Bad?

Not much appears to be written about this.

In the past, I’ve read e2 should be around 200 per mature follicle.  (That’s why estrogen can be so high on an egg retrieval cycle—lots of follicles.)  Reading non-medical sources, it appears some clinics want at least an e2 measurement of 300 to do a transfer, and prefer 500-1000, with 800 being the ideal.  My clinic looked for anything above 200, although it was not clear to me that they would not do a cycle on less than that.


Here’s more regarding e2 measurements for a retrieval cycle:


Also, here’s something that discusses estrogen:



And estrogen monitoring:


Decrease in e2 after HCG shot is bad:


Info on estrogen:


Friday, April 7, 2017

More links on miscarriages/recurrent pregnancy loss/birth defects

https://www.ncbi.nlm.nih.gov/pubmed/8290380 (“Recurrent pregnancy loss as an indicator for increased risk of birth defects: a population-based case-control study”)

http://www.news-medical.net/health/Multifactorial-And-Polygenic-(Complex)-Genetic-Disorder.aspx(“Multifactorial And Polygenic (Complex) Genetic Disorder”)



http://www.fasebj.org/content/30/1_Supplement/151.6.long?related-urls=yes&legid=fasebj;30/1_Supplement/151.6 (“Maternal plasma folate, vitamin B12 levels and multivitamin supplementation during pregnancy and risk of Autism Spectrum Disorder in the Boston Birth Cohort”)

http://humrep.oxfordjournals.org/content/26/5/1259.full (“SYCP3 mutation may not be associated with recurrent miscarriage caused by aneuploidy”)

http://perspectivesinmedicine.cshlp.org/content/5/3/a023119.full (“Genetic Considerations in Recurrent Pregnancy Loss”)

http://humrep.oxfordjournals.org/content/17/2/446.full.pdf (“Cytogenic analysis of miscarriages from couples with recurrent miscarriage: a case-control study”)



http://spacefem.com/pregnant/mc.php?m=02&d=01&y=16 (“Daily odds of pregnancy miscarriage”)

Thursday, April 6, 2017

Association between family history of hernia and omphalocele?

I think I’ve mentioned in the past I had double-hernia surgery when I was just one month old.  Other women in my family (grandma, cousin) have also had hernias (and repair surgery).  So, for some reason, hernias run in our family.

Well, this article notes a baby with omphalocele and then notes that its dad and paternal grandma both had hernias:


“It will be interesting to know what the male sons of this boy will show from the standpoint of omphalocele and hernia in the future.”

Maybe there’s an association?

Wednesday, April 5, 2017

More links on omphalocele

General information:



Diagnosis:


Stories/outcomes:






http://www.rcst.or.th/ejournal/files/Vol31_No2_48.pdf (“Clinical Outcomes of Omphalocele:
An Analysis of 124 Patients”)

Decisions about termination:




Misc:

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3809310/pdf/pjms-29-866.pdf (“Omphalomesenteric duct cyst in an omphalocele: A rare association”)

http://medicaljournal.in/2014/Volume2/Issue2/AMJI-02-web-case-report-giant-omphalocele-congenital-anomaly-containing-bowel-loops.pdf (A minor omphalocoele occurs when the defect is 4 cm or less (at birth), major or giant omphalocoele has 5 cm or larger defect.  It may include sac may contain small and large bowel, stomach, liver, spleen, urinary bladder, uterus and ovaries.  In some omphoceles, the sac ruptures.)



Tuesday, April 4, 2017

Questions after a diagnosis of omphalocele and treatment options

As previously discussed, after the diagnosis of omphalocele, understanding more about the omphalocele (and potential associated issues) is pretty important to knowing what your prognosis is going to be.  (http://3yearwait.blogspot.com/2016/04/looking-for-sliver-of-hope.html;http://3yearwait.blogspot.com/2016/04/omphalocele-outcomes.html;http://3yearwait.blogspot.com/2016/04/diagnosing-omphalocele.html)  Here is a list of questions I prepared for our follow-up ultrasound and genetic counselor session after our omphalocele diagnosis (which I never got a chance to ask because she had passed away by our follow-up appointment):

Genetic Testing Questions

What does CVS test for that could be the cause/association with omphalocele?
·       Trisomy 13/18/21
·       Trisomy 14, 15, 16, 17?
·       Beckman Weiderman Syndrome (11th Chromosome?)
·       What else?

How accurate is the CVS test?
·       Specifically for Beckman Weiderman Syndrome

When will we have results?

Omphalocele/Spine Questions

How big is the omphalocele?
What organs are in it?
·       Small / large bowel?
·       Stomach?
·       Liver?
·       Spleen?
·       Urinary bladder?
·       Uterus?
·       Ovaries?
Where is it located?
·       Above/below/at the umbilical cord?
Are there any other abnormalities?
·       Brain / head issues that suggest spina bifida?
·       Anything else wrong with the skeleton?  (Short / deformed limbs? Clubfoot?)
·       Heart abnormalities?  (Do we need fetal echocardiogram/other testing?)

Treatment options


This article goes into great detail about all of the treatment options:


(The authors even provide a flow chart! http://medcraveonline.com/JPNC/images/JPNC-01-00024-g001.png)