I'm in the USA, just had my second ablation (a more complicated PVI Cryoballoon Cath) and not knowing ahead of time that I was getting a different kind of ablation, was shocked to find that I am not supposed to lift over 10 lbs. or do anything that might strain my chest muscles for 8 weeks. OMG.
All that aside, I had complications with the first one, one complication being bradycardia quite soon after going home. No one told me to expect that, but I texted back and forth with the electrophysiologist til I got my meds adjusted and got back to a normal heart rate (it had gone to 37 hr at one point and I didn't realize then that this was so dangerous).
This ablation, it seemed I had dodged that bullet for the first week post surgery, then it happened again. Bradycardia in the 40's and 50's . Was not getting an answer from the electrophysiologist, so I went to my primary and she cut my Amiodarone in half. Got a text back from electrophysiologist later that day (2 day lag). Next morning, bradycardia again - when it hit 38, called the regular heart doc's office and they sent me to the ER. Went in to see the NP at the heart doctor's office and she left the Amiodarone at half and replaced the metoprolol with Carvedilol - w/ instructions to not take them if my hr was below 60, and with a 48 hour heart monitor. But she stressed that if my heart rate was above 60 at bedtime, I should take the Amiodarone. Again next morning - bradycardia, although in 50's, not so bad. Today, I decided not to take the Carvedilol again and see if things were all right with the half Amiodarone I took before bedtime the night before. Did fine for a couple of hours this morning, then dipped below 60 again.
I had asked the NP specifically why they didn't anticipate this problem and adjust meds right away, and she told me it wasn't a normal reaction, that most people stay on the same meds at the same rate as before the ablation with no problem (to keep the af from coming back during the recovery period).
Haven't found any other info on this online, so just wondered if anyone else had had this problem and what the solution is? Sorry for the long post, didn't know how else to explain the situation, and now that I understand more about the bradycardia, I'm worried about which is more dangerous between the two (tachy or brady) and about keeping my meds regulated.