Hi. I had a pacemaker implanted in August of 2008 due to lower heart rate/dizziness. I am now using it less than 1% of the time. I have experienced very seldom PVCs in the past. However, the last two weeks, they have been increasing to having them almost every 30 seconds and last for hours at a time.
I went to my cardio doctor and he put me on a 14 days event monitor. I saw an EP yesterday and was told I am indeed having lots of PVCs based on the event monitor findings, 12-lead EKG and pacemaker check.
He said I could: 1) continue on my present Metoprolol (25 mg. twice a day - isn't helping me), 2) increase the Metoprolol (which would have lots of side effects and make the pacemaker need to be used more; resulting in pacemaker surgery again since I only have one lead now since they couldn't get the second lead in the first time) or 3) ablation.
I never knew of anyone who had ablation and the thought of it was extremely frightening. I go to see him again in two weeks to discuss what I would like to do.
Reading online about this, it seems like people have ablations done multiple times. I'm so unsure about it. I know it's now 100% successful either. I'm guessing I have to decide whether I want a better quality of life without PVCs or risk the ablation being done?
Help ease my mind on what I should do and also any questions I can add to my list to ask my EP the next time I see him. Thanks!!