107 is of course not life threatening, although I can understand it makes you feel uncomfortable and tired.
It can take more time for things to settle down than the 1 month that has passed now since your ablation.
If you are getting anxiety while measuring your rest heart rate, this can increase it too.
I think you should try to relax, not think about it too much and give it another month at least.
Of course, if your heart rate should go up to real high rates (no need to constantly measure, you will notice if that should happen) you should contact your doctor.
I agree with everything pointed out above. It is way too early to in the healing process for anything to be "normal". You're going to need to give it a lot of time, perhaps up to a year for things to settle down. I get skips and little runs of SVT, and mine was down over 4 years ago. Keep in mind that the conductive circuit remains within your heart. Nothing was removed or taken out. Only a tiny scar tissue barrier was burned across it to prevent conduction.
I am curious as to why your cardiologist would have you on digoxin. It is used today mostly for atrial fibrillation and atrial flutter. It has been surpassed by beta blockers and/or calcium channel blockers as a first line choice. Did you perhaps experience syncope before your ablation? High ventricular rate leads to insufficient diastolic filling time. Digoxin slows down the conduction in the AV node and increases its refractory period, and it can reduce the ventricular rate. The arrhythmia itself is not affected, but the pumping function of the heart improves by improved filling.
The use of digoxin in heart problems during sinus rhythm was once standard. I was on it as a kid in the late 1950's, and it was around way before that Digitalis/Digoxin also have significant side effects. There's a very narrow margin between effectiveness and toxicity. It has a very long half life, so it can build up in your body over time causing an unknowing overdose. I'd be careful with this particular drug by observing the many other side effects it can cause. To the layman that I am, it seems to me that taking Digoxin for your particular heart arrhythmia is like using Malox to treat stomach ulcers when there are numerous and more effective front line medications to treat it.
Well...I just re-read your post and see that your ablation was for atrial flutter. And I as I mentioned, digoxin is used to treat atrial flutter. I was assuming your ablation was for SVT. My apologies for that, but there are still many newer medications to treat A fib and flutter.
I was thinking along other lines. If the dig was for a-flutter and the ablation was done, perhaps weaning off of this particular drug would be warranted. If the ablation worked, the short periods that still may be there will resolve on their own. Dig toxicity is a real problem and the more meds that can mess with the heart, the more chances of strange occurrences....just my opinion.
Thank you all for your responses!
The digoxin was prescribed by my cardiologist who did not like the pill-in pocket method; long story short I was hospitalized, cardioverted and started having sporadic episodes of sinus tachycardia at much higher rates than I had before the cardioversion. The attending physician prescribed 1 metoprolol 50mg for episodes but my cardiologist didn't like that, so he prescribed 100mg Toprol in the morning (that was the only thing I was taking for heart rate after the cardioversion) to that he added the digoxin at noon and Toprol XR 50 mg (half a pill) in the evening. And he also told me to have the ablation to cure the flutter.
My concern is that my rate even on all those meds is much higher than it was when j first had the procedure. It is slowly but surely climbing, from 91bpm yesterday at the ER to now 98bpm. Is that normal? I know-from researching the internet mind you, because I didn't get any post-op instructions or even spoke to the EP after the procedure-that it can take some time to heal. But is it normal to get worse instead of gradually better?
I just don't buy this whole "your potassium is a little low" theory :(
I heard that some patients experience resting heart rate to be "all over the place", shortly after ablation. So that happens sometimes. I don't know if it is exceptional of happening quite often.
So i took the potassium yesterday afternoon; it seemed like it was going to help as I could feel my heart trying to slow down. But now I go from 60 to 99 in a heartbeat. It's jumping all over the place and won't stop-lowest was around 42 highest 101. Is that just the heart getting settled? It's been ongoing for hours and though I'm trying not to worry it's very uncomfortable :(
I just had my 2nd ablation March 23rd for afib. I ended up with tachy-brady syndrome and had to have a pacemaker placed for it. The pacemaker is set not to let my heart go below 80 bpm. I have been in the mid 90's, lately 98 to 100, sometimes a bit over with the exception of 2 days of being in the 80's. No one seems overly concerned with this, under 100 being considered normal. I was told if my resting hr rate stayed at 110 for 48 hours, I should call.My hr seems to come down to the mid 90's as the day goes on. I take Ammiodarone and corgard and will be on them for 3 months. Hope this helps. Good luck to you.
What is tachy-brady syndrome? Now I'm having episodes where it goes as low as 42, but it isn't steady it keeps going up and down all the time; and I mean in like a 10-20 second reading it will go for example from 42-57-72-99. I was doing well after the cardioversion so if I do need something else that would be really sad to me, I was told that this procedure cured a flutter, if it doesn't then it was a complete waste of time; I would've rather let the cardioversion take its course and see what happened :(