Post Ablation Recovery – Need Help!!
I had my ablation last Wednesday, March 20th, and was discharged home on the 21st.. Apparently all went well. That day, the 21st, AND the following day, aside from being exhausted and sore, I did not experience a single AFIB episode! You ALL know what a joyous feeling THAT is! I began to foolishly hope that I was going to be one of the very lucky ones I have read about on these sites who say after their ablation, they felt like a million bucks, didn’t have a single issue with their recovery and were back at work in 3 days. Who ARE these amazing people? After 3 days I was still trying to climb out of the fog from the general anesthetic! (Actually, there was a bit of a mishap there. Turned out I was extremely intolerant of this particular anesthetic and had a very nasty and frightening “resurfacing” from it. And please note that it was an INTOLERANCE……NOT AN ALLERGIC REACTION. The difference really CAN be life and death) Sorry, I see I am going into far more detail than I intended, I do apologize. My question, my concern, MY FEAR, is that on Saturday, 3 days post op, I woke up feeling what I can only describe as a sort of “vibrating/buzzing” feeling in my chest. It felt nothing like the pounding, chaotic beats that were MY AFIB experience. This sensation lasted consistently, with a few short pauses, from Saturday to now….Tuesday, the 26th. About 30 minutes ago it just stopped and so far, has not returned. I hope it stays gone as it was becoming not only annoying but frightening. Has anybody out there had this same or similar feeling? Does anybody know what It could have been? I’m trying VERY hard to be logical and think that it’s just part of the healing process…..perhaps nerves calming down? Perhaps the inflammation was pushing on “something?) How’s that for a highly medical term? “SOMETHING” LOL Any stories, experiences, odd sensations would really help me out. I don’t see my EP for another 3 weeks, and while they did give me paperwork about what to expect, for those of us with some anxiety issues, the details are pretty skimpy. I am also trying very hard NOT to call the doctors offices and be one of “those” people. I realize to them, this procedure is basically no big deal, but for me, it has been SO much more than I thought. (Well, my bubble just burst…..I have just had some more episodes of things going on in my chest) Should I expect this to be as bad the entire 3 months before they tell me if the ablation worked or not. Right this minute, I’m feeling like I made a huge mistake having this procedure……maybe I should have tried harder to tolerate the antiarrhythmics? Thanks for listening. Being alone and scared is not fun.
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TMI, keep it simple!
tedkramer…….if your response of "TMI" was directed at my post, why didn't you just skip over it? I realize it was long, but I was very frightened and thought the more information I gave, the easier it would be for someone to address my most salient concerns. I am incredibly grateful to those members who replied and offered support and advice and shared their stories with me. I see, tedkramer, that you have been a member since 2015. Perhaps I should feel honored that in those 3 1/2 years, your one and only post has been to me. Thanks for the advice.
I tried Sotalol, and am now on Amiodorone. Neither stopped my A-fib. I had an ablation last week and knew going into it I would be on a rhythm medication for at least two months post op. Having had 12 cardioversions in a 20 month period, I have no problem taking a medication that may boost the results of the ablation to prevent the persistent A-fib. You should know that those medications are administered in the hospital, for five doses, to prevent any bad outcomes from the drugs. Think of it as a mini vacation and catch up on book reading, correspondence, or whatever you enjoy.
12 cardiofversions in 20 months!!! What a positive attitude you have!
I was also on Amiodorone and after 10 years on a pretty hi dose is what pushed me over to heart transplant. It became toxic to me so be careful with that one. I was also on Mexilatine and i think that was on of the best i was on for controlling arrythmias. But i had to have all 3 at the end which most drs would not do. But for a while they did work.
I have done a lot of reading about the "blanking" period following an AFIB ablation. Much of what I've read has stated that during this time of healing, our AFIB can actually be exacerbated by inflammation and the trauma to the heart and surrounding tissues…..not only by all the poking and prodding, but let's NOT forget the rather massive amount of burns!
Doctors at the Mayo Clinic, the Cleveland Clinic, UC Berkley and several other top notch hospitals have all said this is perfectly normal and to be expected…..as are some other post ablation symptoms that go hand in hand with our hearts healing process. In the month since my ablation, I have had about 4 or 5 episodes of what I believe are AFIB. They feel pretty much the same but are not as strong, only once have they gone over 100 beats and the episodes do not last as long. (I kept a daily journal of my BP/HR and oximeter readings)
Yesterday, at my one month follow up, I saw my EP's PA (the last time I actually saw and talked to my EP was 3 weeks BEFORE the ablation. I "think" I saw him for a minute in the pre-op area the day of the ablation, but I was a bit groggy and don't actually remember. I stayed overnight in the hospital and thought I would see the surgeon before I was discharged, but it was his PA who talked to me and discharged me) At the one month follow up, my EKG showed I was sinus rhythm but the PA thought it would be a good idea for me to wear an event monitor for 7 days. (?) My totally non-medical gut feeling was that it was a bit early in the game to go that route since it was "normal and expected" to still experience AFIB during the first 3 months while the scar tissue was forming. I just wanted him to tell me it was to be expected and unless it really got out of hand, I just had to buck up and get through this blanking period. Instead, I am now scared to death as in his summary report to me he stated "LINDA HAS NOT PREVIOUSLY BEEN ON ANTIARRHYTHMIC MEDICATION BUT WITH CAD AND PRIOR STENTS, WE WILL PROBABLY NEED TO PLACE HER ON SOTALOL OR DOFETILIDE AFTER A THREE-DAY STAY IN THE HOSPITAL IF ANTIARRHYTMIC THERAPY WAS NEEDED. I BELIEVE WE NEED AN OBJECTIVE RECORDING OF HER HEART RHYTHMS TO IDENTIFY AND QUANTIFY HER ARRHYTHMIAS PRIOR TO STARTING ANTIARRHYTHMIC THERAPY. a ZIO PATCH MONITOR WAS STARTED TODAY FOR 7 DAYS." I am ONLY one month post ablation and he's already talking Sotalol? I DO NOT want to be placed on this medication!!!! Why wouldn't he just discuss a second ablation to locate any gaps or possible areas that had "self-healed?" I've read so many posts where people say their second or even third ablation finally did the trick and they are very happy living AFIB free…..some for many, many years. I feel like my recovery is being rushed. I AM a very anxious person, and now I'm concerned that this possible need for Sotalol is only going to trigger more AFIB. Any and all advice would be incredibly welcome. I know this post is already far too long, but could some of you please tell me what some of your symptoms were during the blanking period. You have no idea how reassuring it would be to know. I am a 67 y/o woman with no support and I am very frightened. Thank you so much.
Hi, i will start off by saying most of what your experiencing is normal part of the reason ablations are not done back to back is because of the healing. Now realize i had a much more serious arrythimiths of the lower heart calyed Ventricular Tachacardia. Mine i had to be on meds too one of them was solotol. But my episodes were more dangerous and if an episode could not be paced out i had to be shocked back into sinus rhythm so you are doing excellent so far if your AFib episodes can be controlled with just meds. I had a pacemaker with difibulator. I went thru quit a few ablations more towards the end but in the beginning about 11 years ago i had 1 and it got my heart better but a year later my dr said i was still having more small ones than he liked. So i had a second which worked really well and my third was quite awhile after. I do know they usually don't like doing them any closer than 6 months apart. But everyone the first month or so there would be little ones i could feel but got better after that. Now the fact i had a pacemaker also helped because i was monitored all the time. So that for me gave me confidence that the dr could see how well the ablation took. For you the holter will also give them similar information. So try and relax and see what the holter showes. I was on antiarrhythmic meds for about 10 years and it kept my heart going for quite a while.
Hello — I'm new to this forum. I had my ablation April 25, 2019; it's been a month now. I've since been cardioverted 4 days post-ablation and been put on various strong drugs: Dofetilide (with 3 day hospital stay) and Digoxin, in addition to Metoprolol Succinate daily, with Metroprolol Tartrate when having an attack. Meds obviously aren't working. My attacks are now lasting more than 24 hours, and I'm in a-fib more days than not. My doctor is talking about a stereotaxis ablation (robotic, since some nerves were too close to the esophagus and diaphragm for him to zap completely) or a pacemaker. I'm a 69-year-old female and pretty active. This is zapping my strength, mental attitude and quality of life. I'm aware of a blanking period after an ablation, but this is ridiculous. Any words of wisdom are welcome.
@rubywitch67 Hello.. You haven't posted for a while and I hope that means you are feeling better. I just read your concerns and a few things you mentioned caught my attention. It sounds like you were being cardioverted every few months and I am curious whether it was something you had requested, or prompted by your EP. I just had one done a few days ago and the fellow who did it had a strange reaction when I mentioned my last one was 6 months ago – he acted like it was way too soon. I did ask my EP how often it should be done and he said it was entirely up to me. I've been dealing with afib for more than 20 years and the protocol back then is that they try every drug on you until they stop working — ablation was not option until then. The only one that worked well for me for many years with minimal side effects was propafenone. Sotalol did not work; dofetilide caused problems with the QTc and multaq was especially toxic for my liver. The big bugaboo is actually amiodarone — extremely toxic — and I resisted it as long as I could. It worked very well for about 7 years. But finally they got better at ablations and I was scheduled back in 2017. The first did not work so well so they scheduled another (had to wait a good 3 months) which was cancelled and rescheduled to Sept. Other than the 2 cardiofversions I have been doing well. Would it be possible for you to get a second opinion or even to switch to a different EP? It is odd that he would not discuss all your options with you first instead of sticking it his summary. Having said that , I think it is worth trying a few anti-arrhythmic meds to see if they work for you. It is important to monitor for side effects of course. I did survive the dreaded amiodarone for 7 years…. Unfortunately, my EP is now suggesting going back to it if my atrial flutter persists. Ugh. I am quite happy with a cardioversion if it keeps me in sinus for 6 months. The other option is even worst – AV node ablation and pacemaker. Or another ablation. All of which I will discuss with him in person in a few weeks and get a few other opinions as well. Hope this helps.
I know nothing about ablation, but I do know you should call your doctor. Be one of "THOSE" people, and be safe!!!! My goodness; you just had surgery! Pick up the phone and call…… Best of health. Feel better soon. Lori Renee