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Worried about my ablation for SVT
Hi everyone. I'm 18.yrs old, I'm having SVT for 10 yrs now. My RFA is scheduled on 22. july Procedure will be done in St.Bartholomews Hospital (London,UK). I'm having about 0-5 SVT episodes per year. I'm a bit nervous now, but I know that I will be so nervous and anxious when the date will come up.. In Pre-Assessement doctor said, that I would be under a light sedation, so, that means I will feel all the catheters going up through my vein? How will they force my heart to start race? With adrenaline or by making an extra heartbeat or what ? I'm worried that I will be able to feel how the palpitations will start and I will be able to feel how they will burn the extra pathway or damaged cells. As Luvyalab mentioned about urinary catheter.. does it hurts when they are applying it?
Many thanks for your replies in advance! Arthur
Many thanks for your replies in advance! Arthur
Best Answer
Sorry Donna, I haven't checked in, in a couple of days!
I had my procedure done at St. Luke's in Houston. Dr. Seger was my EP. He was really an awesome doctor. I go back for my check up on August the 24th. I seem to be getting better every day. Slowly but surely, and that's ok with me . . .
Thank you too, to Tom_h . . . :) I am glad I had the procedure done. I just hope and pray I don't have to have it done again. I really am a big chicken!!!
I had my procedure done at St. Luke's in Houston. Dr. Seger was my EP. He was really an awesome doctor. I go back for my check up on August the 24th. I seem to be getting better every day. Slowly but surely, and that's ok with me . . .
Thank you too, to Tom_h . . . :) I am glad I had the procedure done. I just hope and pray I don't have to have it done again. I really am a big chicken!!!
Hope you continue to do well.I too will be going in to have a cryoablation in august. Im nervous,but also looking forward to resolving my svt issues.Where did you have yours done? It is nice to have all these wonderful people on this site that can relate to each others issues. keep us updated on how your doing.
That's really great to hear your experience and I hope you recover quickly and get this behind you!
Also congrats to noonie7319. The achiness may last for a couple weeks, and the flutters and skips may last for months.
Also congrats to noonie7319. The achiness may last for a couple weeks, and the flutters and skips may last for months.
I had my ablation done on 7-14-11. I was scared to death. I think for the most part the whole procedure went well. I did feel some sensations a few times during it that were uncomfortable, but they would give me something immediately to sedate me! I'm kinda a chicken when it comes to surgery/procedures! I'm still recovering, and hoping and praying that I recover quickly. My chest still feels tight at times and achy. I am having flutters/skips/ racing too. It makes me nervous, but since finding this site I am feeling much better. I know there are people who can relate to what I'm going through. My husband is supportive and so are my girls, but I don't think they really inderstand it much . . . Thanks again to all who have shared their experience with SVT and their ablation procedure.
Congrats for taking the leap w. the ablation. And yep its normal to get these random feelings for up to six months after the procedure but they become less and less and less until you no longer feel your heart in your chest which is a great thing trust me. Sounds like you breezed thru the procedure so thats great....good luck with this and i am sure if it was done for SVT those days are over for you........welcome back to life without the SVT!
previous evening I had many extra beats and missed heart beats though. But I assume it is normal experience.
Congrats on your successful ablation! I'm glad you had a good medical team and a good ablation experience. You must be so relieved! And now you can begin to live a normal life. I wish you all the best. Please keep us posted on your recovery. And take it easy.....don't try to do too much too soon.
Aren't you glad you're on this end of it now and can help others in this forum. Everyone has a little bit of a different story. Just take it easy for awhile and let the heart heal. I tried to do to much too soon and was short of breath, tired, and my chest hurt which are quiet normal. You're young and I'm sure you'll bounce right back. Thanks for sharing your experience here.
Glad to hear it went well. I too will be having a cryoablation done on august 19th in boston,mass.Just keep us updated how your doing. ☺
so, basically, I went in hospital at 7.30 am, at once a nurse said me to wore a gown, which I did. That was in angio day unit (whatever that means), my mother was allowed to come in with me in ward. Then, I guess that was some kind of doctor (male), he explained me everything, and what will be happening. Then I was supposed to sign a consent form. After that, that male doctor/nurse put a catheter on the other side of my palm. Then a waited till 8.30, when nurses came after me. Then we went downstairs bla bla, then there was some more paperwork. Then I met the doctor, and then my mother went back to my ward, and doctor and his assistants took me to the cath lab. I knew how does cath lab looks a like, so there was no surprises about that special room. Then they asked if I had underwear on, and told me wore it off. Then I sat on the procedure table, they started to apply many wires.. There were many people, each of them were responsible for something, I had feeling that I am in good hands, that calmed me a little down. So then, were again safety questions if I have any allergies etc. Then they applied sedation, but I didn't calm down, I was still anxious, and they told, that they would apply more of it.. The I was sleepy and presumably past out. Then I awoke during procedure many times, I felt how they triggered palpitations by making extra beats, and I felt how they burned them. (There very many burns as doctor stated afterwards) When they could not trigger no more palpitations they did cardioversion, which I remember I made sound ( aaahh aaa), that was not painful but very unpleasant... they tried to trigger palpitations by that. Then they were making so many extra beats and tried to trigger palpitations but they coul not any more, pretty much I was awoke for the last 30 minutes of procedure, and I asked doctor for more sedation. I don't know if they gave me, because I was still awake. Then very unpleasant feeling was, when they took catheters out from the groin. That was it, then they unconnected me of the many wires, they they drove me to some after procedure ward, when I rested for 5mins, then they took me up to the angio day ward where were my family. Then I was supposed to lie flat for and hour after they took out catheters. Then they offered me a meal, which was sandwiches, juice,tea or coffee and yoghurt. Bu they said, that at first I have to try a little amount of water, because I could throw up. So, my mother gave me a little of water, and I felt sick. So, I didn't eat anything for another hour. Then I tried again, an the same, I felt sick again. Very weird was that I had and still have like hot waves coming in my body, then I'm starting to sweat, that lasts for max 2 minutess ,that's all. The nurse said that sedation is the thing that causes sickness and sweating. About 3 pm nurse allowed me to try walk, I walked to WC, there was uncomfortable feeling in my groin, but nothing serious. Pretty much that was it.
Arturs Tiesnesis, RFA for SVT 22. July 2011., United Kingdom , London, St.Bartholomew's Hospital
Arturs Tiesnesis, RFA for SVT 22. July 2011., United Kingdom , London, St.Bartholomew's Hospital
Excellent! Glad it went well. Now relax forq few days. Don't be alarmed if you feel any strange beats; it's normal. Give us a rundown of you procedure when you're up to it.
hi! before 4,5 hours doctor took catheters out of my vein in groin, and I am already home! I want to thank you all for your posts, it helped me so much! Before RFA i was diagnosed with SVT, but after ablation the diagnosis is/was AVNRT. Ablation was successful though!
Thanks for your post. I like the lion senerio, I think it started out as a lion cub and now has grown into that roaring lion. Will be glad to have the lion tamed.
I started having SVT before I'd ever had any surgeries. At first they were quite frequent and I was put on meds. Actually, I was first diagnosed with Atrial fribrillation so I don't know even now if that was a misdiagnosis or if I had SVT then because it feels the same. I hated the med so I went off and discovered vagal maneuvers that I used for years to convert back to normal rythm. Some years I had no episodes, and other years more often. I've tried to figure out triggers througout the years and tried to avoid certain things, always stressful trying to figure it out! Toward the end of last year I started having more attacks but could still convert them back. Early this year I had a few attacks that I couldn't vagal right out of and that really scared me. So back to the doctor and was finally correctly diagnosed and had the ablation.
SVT from my understanding is something we are born with, an extra pathway somewhere in the heart. Some people can have the extra pathway all of their lives and never experience SVT. Others like the ones in this thread are the lucky ones who get to experience the extra pathway through SVT. In our sense of trying to understand this, it is only natural to try to figure out what causes this. I felt like stress, caffeine, krill oil, I even wondered about shrimp for a while, etc: For you, you're wondering if it was the surgeries. They possibly helped SVT show its ugly head. I read in another post a wonderful description of living with SVT that compared it to a lion in the basement just waiting for someone to open the door so it could come roaring out. That hit home with me and that's exactly what SVT is!!!! The ablation gets rid of the lion. I still worry about triggers because I've programmed myself for so long to do so. I still have PAC's that led to the SVT and I do try and avoid things that cause those, but it is such a relief to know that they won't lead to SVT.
Good luck with your procedure and glad to hear you're in good hands. That makes all the difference in the world.
SVT from my understanding is something we are born with, an extra pathway somewhere in the heart. Some people can have the extra pathway all of their lives and never experience SVT. Others like the ones in this thread are the lucky ones who get to experience the extra pathway through SVT. In our sense of trying to understand this, it is only natural to try to figure out what causes this. I felt like stress, caffeine, krill oil, I even wondered about shrimp for a while, etc: For you, you're wondering if it was the surgeries. They possibly helped SVT show its ugly head. I read in another post a wonderful description of living with SVT that compared it to a lion in the basement just waiting for someone to open the door so it could come roaring out. That hit home with me and that's exactly what SVT is!!!! The ablation gets rid of the lion. I still worry about triggers because I've programmed myself for so long to do so. I still have PAC's that led to the SVT and I do try and avoid things that cause those, but it is such a relief to know that they won't lead to SVT.
Good luck with your procedure and glad to hear you're in good hands. That makes all the difference in the world.
Yes, physicians that looked at my EKG would usually say that it was a pretty typical waveform. My cardiologist though he saw a telltale delta wave that's indicitive of WPW. My EP looked at me and thought it was the same thing. So going into the cath lab, the team knew where to look first. They were going after an AVRT and were pretty sure it was WPW. But after mapping it, what was though to be WPW was actually CMT, Circus Movement Tachycardia, a concealed AVRT that's in the same family as WPW. So don't be afraid to ask questions. I think my EP was delighted to see a patient that had a rudementary idea of what was wrong with their heart and what he was going to do to fix it.
"As I understand, that AV node is the 'real' pathway, so, how come you can burn the extra pathway which is located within that 'real' pathway, without damaging the 'real' pathway? And if they do so (damage the 'real' pathway), that will result in a having pacemaker? "
I’ve researched and researched and came across this article about the dual pathways. I’m assuming the real pathway as your ep said is the fast pathway. Notice in the diagram where the burn is done on the outside of the AV node near the slow pathway or bad pathway. My ep drew a diagram of how my ablation was done and this is exactly how it was done. The site is posted at the bottom,
I was also very concerned about needing a pacemaker if the fast pathway was affected so I decided to tell my ep that if the burn was too close to the av node to forget it. But the morning of the ablation I decided to trust my ep. I’ll echo what others have said about getting an experienced ep. My ep offered to tell me he’d done between 2,500 and 3,000 ablations and taught other doctors how to do this at the University of Utah. He said he wouldn’t trust just any ep to do an ablation. I asked him if he thought he could do it successfully and he said there was less than a 1% chance I would. Then I asked him if he felt confident in his ability to do the ablation so I wouldn’t end up with a pacemaker and he said he did. That was all I needed to hear. So, don’t be afraid to ask those hard questions. You get what you need to have a successful story.
Another thought, My ep also told me before we went in that he thought he knew exactly what the problem was but wouldn’t know until they mapped the heart during the tachycardia. He also gave me different scenarios about going to the left side and what they would have to do. I think for the most part they know what hey have to do before going in, but to be on the safe side they have to tell you all of the possible scenarios. Go to Tom’s journal for a view of how they thought his was WPW and ended up being something else.
http://medtees.com/avnodalreentry.html
I’ve researched and researched and came across this article about the dual pathways. I’m assuming the real pathway as your ep said is the fast pathway. Notice in the diagram where the burn is done on the outside of the AV node near the slow pathway or bad pathway. My ep drew a diagram of how my ablation was done and this is exactly how it was done. The site is posted at the bottom,
I was also very concerned about needing a pacemaker if the fast pathway was affected so I decided to tell my ep that if the burn was too close to the av node to forget it. But the morning of the ablation I decided to trust my ep. I’ll echo what others have said about getting an experienced ep. My ep offered to tell me he’d done between 2,500 and 3,000 ablations and taught other doctors how to do this at the University of Utah. He said he wouldn’t trust just any ep to do an ablation. I asked him if he thought he could do it successfully and he said there was less than a 1% chance I would. Then I asked him if he felt confident in his ability to do the ablation so I wouldn’t end up with a pacemaker and he said he did. That was all I needed to hear. So, don’t be afraid to ask those hard questions. You get what you need to have a successful story.
Another thought, My ep also told me before we went in that he thought he knew exactly what the problem was but wouldn’t know until they mapped the heart during the tachycardia. He also gave me different scenarios about going to the left side and what they would have to do. I think for the most part they know what hey have to do before going in, but to be on the safe side they have to tell you all of the possible scenarios. Go to Tom’s journal for a view of how they thought his was WPW and ended up being something else.
http://medtees.com/avnodalreentry.html
I had an ablation one year ago for AVNRT which was successful. I can honestly say that the procedure, which should never be undertaken lightly, is very easy, much easier than some dental procedures I've had ...
I had no sedation and was completely awake (my EP's preference) which scared me. However, on reflection I can see that he did me a favor, that it was easy to trigger an SVT event and I got the result I could only hope for. The insertion of the catheters and the pacing of the heart during the procedure were painless.
You are so lucky that medicine has found a cure for this debilitating condition and that you will not have to live the best years of your life like a lot of us have, living in fear of another trip to the ER for an Adenosine fix etc. I had been afraid of flying for so long because of SVT; it was after I had an event at 35,000 feet, 45 minutes out of Heathrow that I decided I had enough of living with this so called benign condition. It put a 'damper' on 30 years of my life and stopped me souring to great heights, personally and professionally ...
Go for it young man - have faith in your doctors and most of all God.
I had no sedation and was completely awake (my EP's preference) which scared me. However, on reflection I can see that he did me a favor, that it was easy to trigger an SVT event and I got the result I could only hope for. The insertion of the catheters and the pacing of the heart during the procedure were painless.
You are so lucky that medicine has found a cure for this debilitating condition and that you will not have to live the best years of your life like a lot of us have, living in fear of another trip to the ER for an Adenosine fix etc. I had been afraid of flying for so long because of SVT; it was after I had an event at 35,000 feet, 45 minutes out of Heathrow that I decided I had enough of living with this so called benign condition. It put a 'damper' on 30 years of my life and stopped me souring to great heights, personally and professionally ...
Go for it young man - have faith in your doctors and most of all God.
My ablation went very smoothly, no complications, and my EP was wonderful. If anyone is interested in the details of the actual ablation, you may view it on my MedHelp journal (check the early April 2011 timeframe). Perhaps it will give you a better idea of what to expect before, during, and after ablation. I've been documenting my progress in the journals from March 2011 onward. Click on my MedHelp name Jannie411 to bring you to my page.
Thanks for the youtube link I was wondering if there would be anything there. Lots of great info very much appreciated.
Thanks, I didn't really think it would, but I was curious. I have heard good things about my EP and the fact that he is head of the department makes me feel very confident about my ablation. The hospital and nursing staff we have already dealt with on several occasions and have always had very good experiences. Would not want to say I am looking forward to the ablation but I think I am ready. Thanks again to all
I've had numerous surgeries over the years for everything from a toncillectomy at 26 to a separated AC joint with a broken clavicle, and a couple of hernias, but I never went into SVT during any of them. I always made sure though that they knew about it before hand so they were carefully monitoring me. The thing I worry about most now is I have severe Obstructive Sleep Apnea, and either have to be intubated, or put on positive airway pressure to splint my throat open. They had my CPAP ready during my ablation, and as I was coming to, I could feel difficulting breathing, but I woke up quickly and didn't need it. Yes, mine was a very positive experience from the hospital and EP to the nursing staff, and I wouldn't hesitate to do it over again. My hospital, UMass has a pretty smooth running operation for catheterization and electrophysiology, so the ride was really smooth throughout the process. Good luck with yours. I hope you feel as good as I do now!
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I'm 59 and have had SVT (AVNRT)since my mid 30's. I just had an ablation a month ago while under light sedation. I thought it was all very interesting. I wanted to be an observer rather than the one on the table. To answer your question about feeling the catheter go up you veins...I didn't feel a thing. The only thing I felt was the shot to deaden the catheter site and that was more like a sting that hurt for a very short time. That was the only pain during the entire procedure.
They do something called pacing your heart to create the SVT. I've read that they use adrenaline but I don't know for sure how they did mine. I felt and heard my heart on the monitors starting to get harder and faster and irregular. I heard the doctor talking about inducing PVCs. They asked if exercise was a trigger and I told them no, but stress was biggest trigger and too much caffeine caused it. I was partly awake when I felt the tachycardia and I was so relieved because I was afraid they wouldn't get the SVT to know where to burn. It was a weak one compared to the ones I had so it didn't scare me at all. Afterwards, I found out it was 180 bpm. Mine were always 240-250.
As far as feeling the burn, I did feel that. I only had one burn on the slow pathway in the AV node. It didn't hurt, just felt like a warming sensation. I let them know I felt it and they must have given me more sedation because I don't remember much after that. They will sedate you as needed so you are very relaxed through the whole thing or asleep.
I didn't have a urinary catheter and I wish I had. You have to lay flat for 4 hours afterward so if your procedure is very long and then you add 4 hours afterward, it'll be worth not having the pain from a full bladder like I had.
I've been to the dentist with a lot more pain and stress than this procedure. When you think how invasive it is, it really is amazing that it all goes so smoothly. I was told the average time for the procedure is 4 hours. Mine was only 2 1/2 hours and felt like only 1/2 hour. I was really surprised at how easy it was.
I found a youtube that was interesting on the procedure for SVT. It is:
http://www.youtube.com/watch?v=nQ4qTSAOvbc&feature=related
Good luck! You'll be so glad when its over and you don't have to worry about those anymore.
Keep us posted.