I had an ablation in 2014 for aFib at Mayo Clinic ( St. Mary’s Hospital). I had many episodes and cardioversion prior to ablation. I took Flecainide and propranolol. That controlled my PVC’s well, but still had AFib episodes. Most would self convert after a few hours. But the Flecainide after taking just 1 dose, I could feel pauses. I would get light headed. After putting up w it for 5 yrs, my Doctor, ordered a 14 day zio patch and discovered what I already knew..pauses lasting 3-4 seconds. That’s called AV Node disfunction..or Sick Sinus Syndrome. It’s kind of the chicken or the egg scenario. Did aFIB cause it or did I have SSS already & meds brought on symptoms. So Mayo’s gave me a pacemaker and got rid of pauses...I feel so much better. Plus, I was switched to Sotalol. Flecainide made me feel bad all the time. My aFib is controlled much better now. I still have an episode a few times a yr, but they self convert. I will never not have aFib because I had mitral valve repair 25 yrs ago, and when you have scar tissue in your heart, aFib can be result. But I have no complaints...lots of energy...I walk on treadmill 35-40 min. a day.
My advise is if you go ahead w ablation, make sure the Doctor does this procedure many times a month...experience matters. If you haven’t tried other meds, you might ask about Sotalol and Ditiazem..that combo really helped me so far. Hope this info help you move forward w your big decision.

I'm 70. Let me start off by saying that for 45 years I've had every type of PVC, palpitation, skipping, jumping, floundering around, fluttering, hesitating, twinging sensations and on and on known to man and then some, and feel every one of them. Some, very scary. I endured them all at work and at play. Doctors always passed them off as semi-normal and never really told me what they were all about or any explanation for them. Over the years my heart would on occasion kick in and race very rapids for 10-15 seconds but would always go back to normal beat. One of these sensations hit me 8 years ago when I was at work. I felt it certainly, but this time it didn't let up. Lasted for 14 hours at a rate of 200-plus bpm. I let it go and told my family doctor about it. He asked me if I wanted to see a cardiologist and I said no, not at this time. Well, the racing started coming on at about a rate of 30-45 days in between episodes. Finally went to see a cardiologist about it. They gave me the standard tests to see how strong my heart was. Ultrasounds, ekg's, holter monitors. They could see all the palpitations but of course no AFIB was evident. To make a long story short I was finally diagnosed with paroxysmal AFIB after having several more episodes. I don't like a lot of medications so I only took a blood thinner and a beta blocker. Didn't take a couple of the other medications they prescribed because of the possible side effects. Anyway, episodes began to be more frequent. Cardiologist advised me that maybe an ablation was in order. I thought about it and researched it. And decided to have it done, especially since my heart would race way up there and no medication was touching it to slow it down. It always would let up on its own, but the feelings and sensations my heart would give me just before and after I went into AFIB were miserable. I had the ablation done in June of 2019, and in fact, I had a severe episode the night before. They took excellent care of me during pre-op and when I reached the operating room arena there were people coming out of the woodwork to wire me up, prep me and make me comfortable. I had no fears. I'm a Vietnam Veterans so I took it in stride. Procedure took a little over 4 hours and I was going home the next day after spending the night. To date I have had no further episodes except for an occasional burst of speed which is scary because I don't want this to come back. However, I am still left with thousands Palpitations every day but I still get through them. Refused any further medications for it. Maybe down the line. They are still scary sometimes but I just live with it. Depending on your situation, how many episodes and how fast your bpm's are during the episode I would seriously consider having it done. Mine was getting REALLY bad and more frequent and would have eventually worn my heart done.

@bikermo Hi and welcome to connect, we are a group of patients that have experienced various health concerns and we share our experiences to help others. I did not have afib but i have had quite a few ablations. My more detailed story is in an earlier post on this thread about may of 2019. But in a nutshell I've had some very successful ones and some that were less successful. My particular issue was a condition called VT for short but basically a really fast heartbeat.
So based on the 2 very successful ones and some not successful ones the doctor i found who knew when medication was best and when an ablation was beast. Thru my experience I've seen two types those that think ablation is always the answer and the ones that use a combination of therapies. The one that for me was the most knowledgeable was when they would weight the advantages of Medicine, pacemaker and ablation and not rely on just one treatment plan. I also will add that within the EP arena there are two types those that specialize on afib and ones that are more for my area of VT. I actually was referred once to one that was experienced with afib and refered me to one who was better quilified in vt.
On the Medicare issue i am on medicare with tricare for life secondary and at least for my situation now which is as a heart transplant recipient is working very well. O was on another insurance plan when i was getting ablations but I do know if your working with Mayo Clinic they do take Medicare and im Sure if you get in contact with the facility that would do it they can probably figure out the out of pocket. Ill also hive one more plug for Mayo. Since getting my transplant here i do like there approach to making sure you are advised as to all options available as to treatment options. They use a team approch which with my prior heart they did do my last ablation and due to what they saw were able to help me decide as to where to go next. Please ask any questions you like.

Have a Blessed Day
Dana

Hi @bikermo. I'm a little older (85) than you. Your AFib situation seems a lot like mine -- no obvious symptoms as long as I'm faithful to my medication regimen. It's been that way for almost all of my 6 years after AFib was diagnosed by my PCP after an EKG during my annual physical. Three close friends in my age group have AFib, and after troubling physical symptoms, they chose ablation. So far as I know, they're fine with it now, several years after their original diagnosis.

With me, ablation is two or three levels removed from my current therapy -- 1) a beta blocker to control BP, soften heart contractions, and stabilize heart rhythm; 2) anticoagulant (Coumadin) to prevent blood clots, and 3) two BP meds (Lisinopril and a diuretic, Amiloride). I chose Coumadin at the outset because an antidote was available for that but not for newer popular anticoagulants. (That's different now -- antidotes are emerging for a few more anticoagulants).

I'm blown away by the extent of competent medical advice available within your family; this may be your other most important advantage (in addition to the asymptomatic arrhythmia). Working only with medical professionals at my HMO, I'm otherwise alone scientifically, so I don't have your challenge of organizing a large consulting group to advise you on the question of ablation. I'd give a lot to have your advantage of such a rich collection of medical expertise to guide me. Martin