Catheter ablation post-op

My ablation procedure was a doddle compared to yours. My usual comment is that it was definitely no worse than just a single SVT episode of the same duration, and I have not had even one SVT episode since (and, apart from trying to encourage others here. have been able to forget about the whole thing). 

I didn't get breathlessness or lightheadiness afterwards. I wonder if this might instead be due to some medication you are taking? I mention this because I was prescribed too high a dose of beta blockers once and that had me almost fainting so I had to go off them. These symptoms do not sound common to me so I'd recommend you speak to your GP or doctor about them again as soon as you can - and keep pestering the medics until you are confident you know what's going on.

wishing you all the best

Not sure if I can help but I'll share my experience with you, Just to reassure you that you are not alone.

I am female and was diagnosed with AVRNT, a form of SVT at age 45 after one of my scary attacks being captured on a ecg.

At the time i was quite heavily into my running and other forms of exercise, I didn't have an svt during exercise but did suffer from bad etopic beats which made me stop during a couple of runs after becoming light headed breathless and a funny heartbeat. My more severe svt came simply from bending down. I was referred to a cardiologist who said I was a good candidate for catheter ablation, medication was not a good option for me as my blood pressure and bpm is quite low due to being fit.

I was them put on the waiting list for the ablation, I reduced my levels of activity as I seemed to be losing my exercise tolerance which could have been due to the svt. I had my ablation in March 2015, like you I had a horrific experience with the procedure being terminated due to the location of my problem being nesr the av node, dangerous territory I believe, risk of pace maker. Unfortunately after 14 burns they only classed my ablation as partially successful. After 4 days of the procedure I felt like I was not picking up in general I felt worse, light headed, funny heart sensations, breathlessness, dizzy and a whole lot more besides that put me in hospital for 11 days. I eventually started to pick up around 5 weeks after, and started to get my life back, I can't say I felt better but felt I had more premature beats etc. Month 5 after the procedure I had a full blown svt attack, I was devastated as it confirmed my worst fears, I was then put on the dreaded medication which gave me horrible side effects, ironic I had the ablation to avoid the medication. I then proceeded to have more svt attacks and I went back to see my cardiologist who confirmed the first ablation was unsuccessful and he felt I required another procedure to see if they could sort me out, as you can imagine after my first procedure I was horrified to think I might have to go through it again. My cardiologist explained I was very technically challenging due to the location of the abnormal area and the 2nd ablation carried slightly more risk. They told me they would put me to sleep for the ablation due to the trauma of the first and would use the freezing technology which was more suitable due to the complexity of where my problem was. After much consideration I decided to go a head with the 2nd ablation, I felt like I had no choice really, the tablets made me feel ill and weren't holding my svt. I spent the next couple of months terrified building myself up to go through with the procedure.

I had my 2nd procedure on March 10th this year, just under a year from the previous one. On the day of the ablation I was very nervous and scared, wondering if I was going to experience the same nightmare as before. I just had to hold on to the belief that the professionals knew best and would look after me. After the procedure I had the expected symtoms of having done a boxing round with a heavy weight, and tried to rest up, After approximately 8 days I felt I was turning a corner, my heart felt more settled, definately different then before, I'm 7 weeks in and have resumed some of my activities, like you I've had feelings where I think I may svt but it doesn't occur, I have premature beats or little flutters which I hope will settle, all in all I'm hopeful that things are looking brighter, it's a very scary thing to go through and the physical effects are horrible, but also the mental torture you go through and the threat day in day out also takes its toll! I truly have my fingers crossed all has worked for you, but if you are unfortunate to be in that 2%, you will get through it, trust me if I can, anyone could. Best of luck at the doctors and for the future, let's hope we're both well on the way to recovery svt free. X

I live in Tucson, Arizona in the USA. I just got newly diagnosed with SVT in July of this year with my first attack and was driven to the ER by my husband. My episode lasted for over an hour and the doctors got it under control with medicine. I went to see my PCP for a follow up and she refered me to my cardiologist. I had to have a 2D ultrasound done on my heart, and had to talk with her. She was very nice and understood my concerns I had. She advised me that I was a great candidate for the procedure and she has done over 300 of them successfully. I set up the date for the procedure which was 8/29/2017. I have had a few minor episodes in the wait time for my ablation, but nothing serious to send me to the hospital. I also had never had any type of surgery or procedures done and was nervous as hell, also thinking about my 10 year old daughter. I asked my cardiologist if I could have deep sedation so I could be asleep during the procedure. She honored my request. I am recuperating well with minor pain in the groin sights. My cardiologist told me she got the whole area carterized off and I shouldn't have any problems in the future. She also advised me on what to expect while I am recuperating. She said as my heart is healing, I should expect little flutter palpitations but not like the full attack. I have felt a little, and I am not winded. Also, if you have been sick with a cold/flu or sinuses have been acting up, you should stay away from certain medicines too. They cause your heart to palpate more like an SVT attack, full on or minor depending on how much and how often. Sudafed, NyQuil, and Benadryl will cause your heart to palpate fast. You can take Tylenol products and Mucinex products. If you're having that much problems with your cardiologist, you can request for another cardiologist and have a second opinion. If they suggest you have to get another ablation procedure done, ask for deep sedation where you can be put under to sleep. It won't be general anesthesia but it will be just under general anesthesia. That's what I had done and I hardly remember anything. All I remember was the doctors talking, and my anesthesiologist asking me if I was okay periodically. I remember them doing slight pressure here and there, but nothing painful. I hope this helps you out, especially hearing about a new person having it done. If you want, I can let you know periodically how I am doing and handling it. My uncle has AFib and takes medicine to control it. I thought I would regret it, but I know I did a wonderful thing for me and for my daughter, and wouldn't change my decision if given the choice.