Erin had her ablation last Monday, June 19th, so I thought I would recap the day for her future reference. We hope this was a one-time thing and will all be a distant memory very soon! It all started back in March 2016 when I took her in for a flu test when she was sick, and the pediatrician noticed her rapid heart rate. They sent us to the ER, but it had self-corrected by the time we got there. Fast-forward to September 2016: repeat performance, except the arrhythmia continued in the ER, so she got two rounds of adenosine, which converted her back to a normal rhythm, followed by a night in the PICU (September post). She was on oral atenolol between September and April at varying doses, and had two rounds of portable monitoring during that time to help tweak the dose, until she had a good checkup in April and was taken off of it. We spoke too soon though, because in May 2017, the SVT returned during a stomach bug, buying her 6 rounds of adenosine, an esmolol drip, another overnight hospital stay, and resuming the daily atenolol at home (May post). We had already decided to have the ablation after the April checkup, but she didn't quite make it to the scheduled date in June before having that one last hurrah in May.
Atenolol, the beta blocker she was on between September and April, basically slowed her heart down and made it less susceptible to being triggered into SVT. It did seem to work, as she had the flu in March and did not have an episode. However, she was on a very low dose and had been doing well, which prompted the cardiologist to discontinue it in April. The cardiologist explained the ablation in detail during that visit, and we decided to go ahead and try it during the summer, since the risks were relatively low and the chance of achieving a permanent fix to the SVT from the procedure was very high.
So, in we went, back to UNC (refer to Anna's story 2-1/2 years ago!), though this time to the Electrophysiology Lab, which is different from a regular cath lab. They still do procedures via catheterization, but it has different equipment. The lab handles adult and child cases. We arrived at 10am for the 11am procedure, got checked and prepped, and finally went back at 12:30pm. Erin handled the waiting and pre-op like a pro. The entire procedure lasted from 12:30-3:30pm, including putting her to sleep with the mask, starting the IV, etc. Dr. Ferns came out at 3:30 saying that she was able to locate and burn the tissue, but it was tricky because Erin was "very sensitive" to the catheter. When she would advance the catheter, even without doing anything, Erin would go into heart block, which is where the electrical signals literally get blocked and the heart rate slows down. It would resolve and she could continue, but the process sounded like it was pretty stop-and-go. The bad spot was very close to the AV node - I'm not sure if that's what made her so sensitive to the catheter or not, but she said this sensitivity only happens to her about once every 2 or so years. However, she was able to burn the site, which is preferred over freezing (freezing is necessary when the spot is too close to heart muscle tissue).
It took Erin a little while to wake up, but she did great once she did wake up. I'd say she started waking up around 4:00 (they gave her extra propofol to keep her sleepy since she had to lay flat for an hour after the procedure) and was nearly back to herself by 6:30 or 7:00. She had 3 tiny pin-prick-type incisions in each side of her groin without any stitches. She had a pressure dressing over each site - the right side had minimal bleeding that afternoon, but the other one didn't have any. We loaded her up and were home eating Chick-Fila by 7:30pm, she was in bed shortly after, slept great, and was back to herself the next day! We were able to remove the dressings Tuesday morning and she was clear to play other than no heavy lifting, running, jumping, baths, or swimming for 5 days. We were told to watch for signs of hematoma, infection, and/or skipped heart beats (that's normal). She also was supposed to keep moving gently when awake to reduce the risk of blood clots (no long car trips for a few days). She healed great, and so far, no signs of any SVT recurrence! She has a follow-up appointment 4 weeks after the procedure, and at that point, they'll be able to tell if there is any regrowth.
I'm not sure how long this link will be active, but here is a short article and video featuring the doctor who did Erin's procedure, where you can get a peek at the EP lab. The equipment can measure down to the tenth of a millimeter! http://news.unchealthcare.org/uncchildrens/news/care-2015/issue-2/heart
We aren't sure if Erin has had this her whole life and we just didn't realize it, or if it started recently. I know she's had rapid heart rate in the past when she's been sick, but I always chalked it up to dehydration. I know better now! I maintain that I have learned so much since having kids, and this is just another example. Modern technology is amazing, and so is Erin! We are so very proud of how she has handled all of this, and again, we hope this is soon to be a distant memory and a fun story to tell!

