Pregnancy

From Rest of What I Know
Revision as of 23:12, 13 November 2024 by Roshan (talk | contribs) (Add gestational diabetes)

Julie and I are expecting for the first time. In keeping with my philosophy of Observation Dharma here is how we are proceeding with things.

This is an IVF pregnancy because Julie and I carry independent mutations in the GJB-2 gene that will cause profound non-syndromic hearing loss in a large percentage of our children.

Raw Material

We have 6 embryos in total of which:

  • 2 are female without any copies of the mutated gene
  • 2 are female with one copy
  • 2 are male with two copies of the mutated gene

Considerations

  1. Children with IVF have higher risk of heart defects[1]
  2. We have United Health Care PPO insurance
  3. We are generally willing to pay out of pocket

Timeline

Pregnancy Appointments and Key Dates
Date Event
2024-09-17 Initial Consultation
2024-09-17 Prenatal Panel Screening
2024-09-17 Myriad genetics test
2024-09-17 Nuchal Translucency Ultrasound
2024-10-14 Second Consultation
2024-10-15 Gestational Diabetes Test - Screening
2024-10-23 Gestational Diabetes Test - Confirmation
2024-11-06 Foetal Echo Ultrasound
2024-11-11 Third Consultation
2024-11-11 MSAFP Test
2024-11-11 Second Trimester Ultrasound
2024-11-11 Pregnancy Delivery Registration
2024-12-03 Second Trimester Ultrasound - Follow Up Face/Heart
2025-03-28 Due Date

Picking the Obstetrician

This is the very first thing to do in this process. In our case, we were recommended a few from Spring Fertility, our IVF clinic. We liked our doctor, Dr. Monica Pasternak, there and trusted her opinion. The two top places we considered were:

Our primary objective was to be near our intended delivery centre and to be near where tests were available, conditional on the service being good.

We had some trouble signing up with GG Ob/Gyn that is likely not their fault (the onboarding calls happened to line up with times that were inconvenient for Julie) and found that our first visit with Dr. Alexandra Neiman was exactly what we were hoping for.

Here's what we were looking for:

  1. Awareness of IVF and genetics
  2. Experienced at delivering children
  3. Personable and easy to ask questions of
  4. Prioritizes delivering her patients' children herself

Some things I was pleasantly surprised by was that Dr. Neiman was very acquainted with pre-implantation genetic testing (PGT), and even whole-genome sequencing (WGS) of the embryo. Perhaps this is normal for obstetricians but I expected familiarity with IVF and carrier screening and maybe PGT but not WGS. That's relatively newer technology.

In any case, it was easy to get setup with her office and we were able to book the meetings we needed so we went with her. One of the advantages of the location was that the CPMC centre we wanted to deliver at was half a block away and the Sutter Health Labs were a block away. In addition, the Stanford Childrens' Hospital branch that does some radiology is located in the same building as Sutter Health Labs. Altogether, this has worked out well.

Initial Screening

Since this was an IVF pregnancy, we had precise dating of the gestational age. To match with traditional dating, the age is advanced (taking into account embryo growth in-vitro etc.). At the time of our initial screening, the foetus had a gestational age of 12 weeks. A lot of things are scheduled around the gestational age of the child so many procedures that follow will involve matching the age.

Blood Panel

Everything starts with an initial blood panel to check a bunch of things. This happened for us at Sutter Health labs. This covers:

  • Haemoglobin A1c
  • MMR immunity
  • HIV presence
  • Herpes immunity
  • Hepatitis C immunity
  • Thyroid Stimulating Hormone with reflex to free Thyroxine: TSH W/RFX to T4F
  • Blood Group

And then there's a composite panel with:

  • WBC Count
  • RBC Count
  • Haemoglobin
  • Haematocrit
  • Corpuscular: Mean Volume (MCV), Mean Haemoglobin (MCH), Mean Haemoglobin Concentration (MCHC)
  • Red Cell Distribution Width
  • Platelet Count
  • Absolute Neutrophil
  • Absolute Lymphocyte
  • Absolute Monocytes
  • Absolute Eosinophil
  • Absolute Basophil
  • Syphilis Presence through Rapid Plasma Reagin
  • Nucleated RBC Auto / 100 WBC

They also do a standard urine test and a test for Chlamydia.

First Trimester Anatomy Scan w/ Nuchal Translucency

This is an early ultrasound scan that tells you:

The Nuchal Translucency was new to me. It's a test that tells you if your foetus is at risk for Down's syndrome. While our whole genome was sequenced and we knew this was already unlikely, it is possible that the blastocyst has different cells.

Myriad Genetics Test

We skipped the carrier screens (OB had Natera pamphlets) because we had our genomes already done for the IVF process. Myriad tests the mother's blood for the foetal DNA and then concludes things based on that. The things they checked were:

  • Trisomies: these affect 13, 18, 21 and the sex chromosomes X and Y
  • Aneuploidy
  • A bunch of other micro-deletions: e.g. 15q11.2 which causes developmental delays[2]

For the most part, we knew all of this from our Orchid PGT-WGS, and there were no surprises here. Absent other information, you can also learn the sex chromosomes here. These results took about a week to arrive.

Second Consultation

About a month later, after we'd traveled to France, Greece, the UK, and back we went to our next appointment. At this appointment, we learned that Julie might be at risk for gestational diabetes. I do not recall how the Dr. Neiman diagnosed this (likely from the blood and urine tests) but nonetheless we had to go through the screens.

Gestational Diabetes - Screening

This is a straightforward test. They give you a glucose drink and then test you an hour later. We did this at our usual Sutter Health Lab.

Gestational Diabetes - Confirmation

If you test positive on the former, they give you this. This is a 3 hr effort so it's important to arrive early enough to do it. We arrived at 11 AM on a Saturday and they could not accommodate us, but were fortunately first in the Wednesday after.

Dealing With Gestational Diabetes

Annoyed by the wait for the confirmation test, I thought I'd do it myself. The test kit I constructed from Amazon was:

  1. A blood glucose monitor: I picked a cheap one, a Metene TD-4116 BG03
  2. The smallest container of Glucose for both of us to test: two pounds of dextrose

This whole exercise ended up being a farce, however, when Julie refused to use my meter or my test and insisted on waiting to be tested by the lab. I enjoyed measuring myself and plugging the data into Apple Health so it wasn't a complete loss in the end. The dextrose remains unused.

Dealing with the actual condition is pretty much like dealing with Type II Diabetes: you manage your diet and exercise and prick yourself after every meal and in the morning to see how your blood glucose fares. This matters because gestational diabetes can lead to extra-large babies which has all sorts of problems. Since our test was done so early, it could be that Julie had Type II diabetes which is sometimes associated with low birth weight if unmanaged. Anyway, all said: you're gonna be pricking yourself every day and measuring.

Devices

The ob/gyn provider set us up with a counselor who set us up with a similar device: the Verio Flex OneTouch. Both these devices are inexpensive, but Julie has the Verio Flex device reporting to her phone.

I just tested both devices simultaneously to compare accuracy and received the following from the same finger: (mg/dL of glucose in blood)[3]

  1. First prick: 88 on Metene, 80 on Verio Flex
  2. Second prick: 101 on Metene (but I dropped the test strip on the floor first accidentally), 88 on Verio Flex
  3. Third prick: 89 on Metene

So these are roughly in the same range for diagnostic reasons when you aren't rubbing them on the floor. After all, if you're close enough to go over all the time, that's just as bad. The Metene comes in a nice bag that's handy to carry around and I find the spring-activated lancet launcher (that pricks your finger) easier to use.

Julie prefers to prick herself manually with the lancet, and prefers using the Verio Flex tools.

Footnotes

  1. Sargisian, Nona; Petzold, Max; Furenäs, Eva; Gissler, Mika; Spangmose, Anne Lærke; Lauesgaard, Sara Malchau; Opdahl, Signe; Pinborg, Anja; Henningsen, Anna-Karina A; Westvik-Johari, Kjersti (26 September 2024). "Congenital heart defects in children born after assisted reproductive technology: a CoNARTaS study". European Heart Journal. doi:10.1093/eurheartj/ehae572.
  2. 15q11.2 Microdeletions (Report). Oxted, Surrey, UK: Unique : Rare Chromosome Disorder Support Group. 2018. Retrieved 2024-11-13.
  3. I did all on the ring finger of my left hand at slightly different spots (which has left it rather sore). For the 1st prick, I first touched to the Metene strip then to the VF strip. For the 2nd the other way around. For the 3rd only the Metene.