It has been almost three years since I had an ablation to fix my atrial flutter. For those of you unfamiliar with those terms, atrial flutter is a heart condition where the heart beats rapidly because of some rogue cells that throw the electrical circuit out of whack. An ablation is a procedure where a catheter is inserted into the groin and up into the heart to essentially cauterize the area around the cells that are causing that issue. I wrote about my last procedure here, if you'd like to read more about it.
The good news is that I have had no re-occurrence of atrial flutter. The bad news is that in the last year-and-a-half, I have developed atrial fibrillation, or a-fib, which is actually a more common heart ailment. In simple terms, atrial fibrillation is more or less the same as atrial flutter, except that it occurs in a different part of the heart, the left atrium. (Note: I have had several people correct me in saying that the two are not the same. What I actually meant was that they are both arrhythmias and feel similar - IJ)
Having this condition has led me to educate myself as much as possible to understand what it is I'm dealing with and what, if anything, I can do to curtail it. As I mentioned in an earlier post, it used to be that people would simply suffer through"spells" of heart problems and that was about all they could do. How far we have come! I'm lucky to live in an age where my a-fib can be controlled either by medication or by a catheter ablation.
What I learned more recently is that an ablation is not a "cure". For some people, a-fib never returns, for others, it stops the a-fib for a period of time and then they might have to have another one. For a few people, ablation simply does not work. The ablation I had for my atrial flutter three years ago has so far prevented it from returning, which I am grateful for.
When I started to get bouts of a-fib, sometimes lasting 8 or 10 hours, back in December 2017, I made an appointment with my GP to get a referral to my electrophysiologist again. The electrophysiologist is a doctor who specializes in your heart's electrical system and he is the one who performed my last ablation. But getting in to see him wasn't so simple to do. He had left instructions with my GP that if I was to start experiencing a-fib, I was to go on medication first. This started a whole series of events that I really didn't want to have to deal with. The medication he recommended, Sotalol, was not available because there were shortages in Canada. So I had to go on another medication, Bisoprolol, at first. It was initially prescribed as a "pill in the pocket", which meant I only took it when I experienced a-fib. I was only allowed to take so much, but I could add another pill if it wasn't working in an hour or two, and then try another. It never really worked, but I went through weeks of experimenting with that before the Sotalol finally became available.
Whenever you start a new medication, you have to go on a low dose first, and then report back to the doctor in a couple of weeks to increase the dose, and then report back...well, you get the idea. Obviously, you have to introduce it slowly to see what effects, if any, it has on your body. So it was another few months of experimenting with dosages. Sotalol is an anti-arrhythmic drug, which essentially slows the heart down and attempts to control its rhythm. I am probably over-simplifying its description, but that is the gist of it. And it comes with side effects, of course. The main one for me was basically feeling tired and out of breath at any exertion. Your metabolism goes down to about zero. I could barely manage to get up a hill that I included on my daily walks. Eventually, I started using a treadmill instead. Sometimes I'd be fine, other times I felt like I had been hit by a truck. Over time, my body has adjusted to the side effects, but I still have had bouts of a-fib, just not as long and intense. I could take more medication for that, but it's the last thing I want to do! I remember the number of meds my stepmother had to take every day for her heart issues. It was mind numbing.
No. My intention, as soon as I started having a-fib, was to get another ablation. I guess I just had to go through the protocol to get there. My GP finally gave me a referral to the electrophysiologist, but before I could meet him again, I had to have an echo cardiograph and a 24-hour holter monitor.
A holter monitor is basically a portable EKG that you wear for a period of time, to record your heart activity. You have to press a little button any time you feel a palpitation or anything like it. The thing is that every time I've worn a holter monitor, I've had no a-fib! It's terribly frustrating. My mindset was that I had to prove I was having a-fib so that I could get that darn ablation! So I bought myself something called a Kardia, which is a little unit that you put your fingers on every time you have symptoms. It sends the readings to an app on your phone and you can save the readings or print them out. You can even email the readings to your doctor. I saved a whole bunch of readings that I took over months and then printed them out when I was finally off to see the electrophysiologist. He thanked me for doing that and said it was very helpful. Finally things were going my way!
|The Kardia monitor|
It has taken me 15 months to get to the point of getting a date for my procedure. Tomorrow it will finally be done. Yesterday I took my last dose of Sotalol. Today I take my last dose of a blood thinner called Xarelto because, well, you don't want to be bleeding profusely when they make that little cut!
Tomorrow I will check into the hospital at 7am, change into a hospital gown, have an EKG, get a needle inserted attached to a saline solution and lie around in bed until it's my turn for the procedure. They'll knock me out for the three or four hours it takes to do all of the "burns". Then I'll wake up, but have to lie flat on my back for another 3 or 4 hours to make sure the bleeding has stopped. Eventually, they'll let me walk around a bit before I go home. I might have a little bit of a burning sensation around my heart for a couple of days. I'll feel the effects of the tube that was down my throat during the procedure, and I'll probably be a little tired for a day or two. But that's it.
|Catheter ablation procedure|
When you think about it, it's a very small inconvenience for something that will hopefully take away that flopping fish in my chest for awhile. Over the last couple of years, I've "met" many a-fib sufferers online in forums who hesitate to have this procedure done. I understand that anything that involves doing something to your heart can be scary. I'm a little apprehensive, but not scared. I hope that if any of you who are reading this and are suffering from a-fib or atrial flutter, believe me when I say that as intimidating as a catheter ablation sounds, it is a very safe and effective procedure.
I can tell you that when my heart goes into NSR or normal sinus rhythm after a bout of a-fib, it feels something like a calm, glassy, peaceful ocean after a hurricane. I'm looking forward to a lot of that!
Wish me luck!