Wednesday, June 06, 2012

Bel's heart check up...



Yesterday we made a family outing up to the Stollery Children's Hospital in Edmonton for Bel's yearly heart check up. For anyone that hasn't read any earlier posts about Bel's special heart, here's a mega-fast re-cap.... She was born with AVSD or Atrioventricular Septal Defect. She had a hole in her Atrial Septum and the muscular portion of her ventricular septum was improperly formed, i.e her AV valve  didn't close and instead of pumping blood just forward into the body and the lungs, it also flows backwards into her atria. The back pressure causes congestion of blood in the left atrium and this in turn causes congestion and pressure in the veins draining the lungs. If left untreated this would cause life threatening pulmonary hypertension.  If she had only ASD (atrial septal defect) they would probably have waited until she was 3 before doing the surgery, it's the risk of Pulmonary Hypertension caused by the defective valve that meant she needed surgery as soon as possible. We didn't find out about her condition until she was 10 months old when our family doctor noticed a heart murmur at her usual baby check up. Within a month we were checking into the Stollery Hospital for her open heart surgery. You can read my first post describing how we found out about Bel's heart here  and about Bel's surgery experience here.
During her surgery they were able to patch up the hole in her atrial septum and carry out a fair repair job on the incomplete valve. As she's so small they could only use her existing tissue for the valve repair, a replacement valve isn't an option as they currently only last 10 to 15 years before requiring replacement. As such, the valve still doesn't close properly, there's still a gap of approximately 3mm causing  a moderate jet of blood back into her atria on every pump. We really don't know quite how the leak will change as she grows. If the gap widens she'll need another open heart surgery to repair it further. Statistically, there's a 30 percent chance she'll need this further surgery so the odds are on
her side.

For now she just has to be monitored every year. On each visit to the Paediatric Cardiology clinic she gets measured and weighed. Kids with this sort of heart defect are commonly small. Isobel was so small on previous visits she was way off the bottom of the growth scale. At her last visit she was on the scale for the first time and measured in the 3rd percentile for weight. At this visit she measured between the 5th and 10th percentile.....hip-hip-horay for a patched up heart! She weighed in at 27 lbs or 12.2 kg. Next she gets an ECG where electrodes are stuck all over her body to make a recording of the electrical activity of her heart as seen below....



This is usually a pretty quick test and swiftly followed by the first in a endless stream of sugar free lollipops dished out by the technicians. Seb usually manages to get in on the lolli action too. 


Next comes the Ecocardigram. This is the one that takes some time. It's basically an ultrasound of the heart and this time took us about 50 minutes. Poor Bel has to stay really still the entire time while the technician makes sure they get all the measurements and pictures the Cardiologist needs. Bel gets to choose a movie which plays on a TV above the bed. Bel did really well but even with a movie on theres only so long a three year old will stay still without getting grouchy. This time we had a particularly un-child-friendly Technician who was a little too abrupt in telling Bel to stay still.


Seb was really good too. He sat and snacked while watching the movie and occasionally feeding Bel a chocolate chip from his trail mix. (it's pretty unheard of for Seb to part with chocolate chips so I was impressed!)  At one point the technician had to turn Bel onto her side, she did it a little roughly and Seb snapped at her "Don't hurt my Isobel!" of course Neil and I loved that!


After all that and a whole lot of waiting around we get to have consultation with our very nice Paediatric Cardiologist Dr Dyck. He's a nice chilled out kind of guy and he seemed pretty happy with Isobel. Her heart is growing at a good rate (not too fast which can be a concern) and the leek is still moderate. He did notice that Bel has a slightly concave chest, a condition known as Pectus Excavatum. He said that this could likely be a result of her surgery and may worsen over time, another thing we'll just have to keep monitoring. In some cases surgery can correct the condition but it's a pretty aggressive surgery with metal plates inserted so I'm really hoping that it doesn't develop to a stage that bothers her enough for surgery. Anyway.....all is well right now. Miss Bel is a highly energetic little monkey and as far as I can tell as healthy as an ox.


After we left the hospital we headed to Whyte Ave for pizza and ice cream. with a quick stop in a back alley for this little photo shoot.......


Miss Bel with an attitude!



Seb was obviously still feeling a bit protective of his little sis, awww!


All in all it was not a bad day  :)

3 comments:

HORNBLOWER RTD. said...

great Blog Sophie! as always. Bel is one brave and calm little girl with her brother keeping an eye on things! He is very PROTECTIVE BIG BROTHER! Very relaxed in the HOSPITAL taking it all in and keeping an eye on Bel too! A good result bet you are relieved! Bel seems to be making good progress which is great. Keep the PICS coming Sophie they get better every time!!!

Neil and Sophie said...

Thanks Hornblower! I've missed your comments :)

Anonymous said...

G'day troops! Glad to hear Bel is doing ok, both monkeys looking very well.

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