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Heart Disease  (Expert Forum)
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Ablation
This forum is for questions and support regarding heart issues such as: Angina, Angioplasty, Arrhythmia, Bypass Surgery, Cardiomyopathy, Coronary Artery Disease, Defibrillator, Heart Attack, Heart Disease, High Blood Pressure, Mitral Valve, Pacemaker, PAD, Stenosis, Stress Tests

Ablation

by dquenzer, Feb 01, 2004 12:00AM
Heading to Mayo for possible ablation Feb. 20.



I have paroxymal afib.



Doctor said success rate is about 70% cure, 30% aren't cured but do get better--less afib.



Do you find these stats warranted?



How long does the "cure" last?  Any research on this?



What are the most common side effects after an ablation?



Thanks



Doug



by CCF-M.D.-RCJ, Feb 01, 2004 12:00AM
Doug,



Thanks for the post.



Q1:"Do you find these stats warranted?"



By "warranted" do you mean acceptable?  We quote an 80% cure rate -- but the folks at Mayo would say that our cure rate is higher because our patient population is different.   Each center right now is trying to establish themselves as one of the dominant centers, so some friendly competition is often found.  The bottom line is that Mayo has some of the best electrophysiologists in the world, although we certainly believe that we do the afib ablation procedure as well (or better) than anyone.



Q2:"How long does the "cure" last? Any research on this?"



The procedure is only about 4-5 years old.  The research done thus far indicates that late recurrences (after 6 months) are very uncommon.  No one can give you stats past 5 years.  Furthermore, each center has different stats due to the relative "newness" of the procedure and the experience of the physicians performing it.



Q3:"What are the most common side effects after an ablation?"



The most common "side effect" after the afib ablation is an increased frequency in the afib episodes during the first 3 months, presumably from the inflammation caused by the ablation/burning.



The major complications of the procedure primarily involve (1) stroke, (2) major bleeding, and (3) pulmonary vein stenosis.  You'll need to discuss the frequency of these complications with the Mayo physicians, as each center quotes different rates.



If you would like to read more, feel free to check out:

http://atrialfibrillation.org/



Best of luck with your procedure.



Member Comments (22)

by Kristin391, Feb 01, 2004 12:00AM
To: dquenzer
What approach are they proposing for your atrial fibrillation?  There are many with varying outcomes.  I have worked closely with some of the best electrophysiologists and I have learned that nothing is for sure and if one area is treated, another one can crop up which is what happened to me.  I get cardioverted periodically and am waiting for better data, better catheters and improved techniques and technologies which, I believe, is soon to come.

by NHS, Feb 01, 2004 12:00AM
To: the doctors
RE: Q3"What are the most common side effects after an ablation?"



The reply was : "The most common 'side effect' after the afib ablation is an increased frequency in the afib episodes during the first 3 months, presumably from the inflammation caused by the ablation/burning."



If you don't mind doing so, could you please say --



1)Which ablation procedure(s)is/are employed at the Cleveland Clinic



2)Which (if any) of these procedure(s)are more likely to cause increased a-fib episodes, and



(3)What percentage of the Clinic's ablation patients experience them.



Thank you, in anticipation of your prompt and positive response.



NHS

by dquenzer, Feb 01, 2004 12:00AM
To: Kristin
I'm not sure what you mean by "approaches".  



The Mayo EP specialist stated the "approach" he is going to use is a catheter ablation of specific hot spots.



These hot spots can come from a number of areas.  He suspects that the hot areas could be pulmonary in origin.  I have been a long distance runner running up to 70 miles a week into my late 30's.  I also ran college track.  He believes that I may have what many athletes have and that is stretched pulmonary veins that become irritated.  So there is a high probability that they will ablate right at the edge of the pulmonary veins and the atrium.  They don't ablate in the pulmonary veins due to the possibility of scarring causing a narrowing.



He also said they will look for "trigger" hot spots.  These are hot spots that get the AFIB going.  They don't try to get all the hot spots, but just the "triggers."



Then he said there could also be veins in the atrium that shouldn't be there.  As I understand these are veins that should have gone away after birth, but didn't.  They found these can become irritated.



It isn't the maze approach.  I have a friend who had a maze done during open heart valve replacement.



I'm sure ablation doesn't work for everyone.  There is that 20 to 30% category.  I have paroxymal AFIB.  I don't have it all the time.  But I want to get this taken care of so I can get off the meds, which eventually don't work and also which can cause numerous other side effects.

by CCF-M.D.-RCJ, Feb 02, 2004 12:00AM
To: NHS
NHS,



Q1:"Which ablation procedure(s)is/are employed at the Cleveland Clinic"



Our approach to afib ablation is called a Pulmonary Vein Isolation, whereby the pulmonary veins are electrically isolated by use of a catheter ablation procedure.



Q2:"Which (if any) of these procedure(s)are more likely to cause increased a-fib episodes"



We just use the one approach.



Q3:"What percentage of the Clinic's ablation patients experience them"



I have to admit I haven't seen any numbers on this.  Perhaps one third or so.



by Lill, Feb 02, 2004 12:00AM
I hope you don't mind me using this thread for related questions.  My 15 year old son is scheduled to go to University of Michigan for consult after 2 EP studies failed to adequately identify the source of his PSVT.  During the last study this past thursday, the cardiologist felt he had a retrograde re-entry pathway adjacent to the AV node.  During mapping of the left side of the heart, he thought his resting heart rate originated in the av node then conducted through the left atrium first.  During both studies, my son had NO episodes of SVT though in everyday life he has many such episodes on a daily basis.  Without antiarrythmics, the event monitor picked up rates of 200 to 240 beats per minute during these episodes.  On flecainide, the rates were 150 to 170 with events lasting seconds to an hour or so.  He is now on rythmol and complains of SOB, dizziness and palpitations (day 3 on rythmol).



Questions:

1. Is U of M a good center to go to?  This will be attempt # 3 at ablation in a 15 year old.  



2. How long should we expect it to take rythmol to become effective?  He started the medication on Friday (150mg Q 8 hours).



3.  Could the increase in events since Sunday,(palpitations,SOB, chest pain and dizziness) be related to the rythmol?  Are there different drugs that may help him?  Flecainide did help at low doses (50mg Q 12) but he developed tremors from it.



4.  Can retrograde re-entry pathways close to the AV node be successfully ablated given the skill of the EP specialist?  We don't want him to end up with a pacemaker at the age of 15, especially since we have not yet exhausted the array of antiarrythmic agents he could try.



Lots of questions, I know.  I would appreciate any help you can give me.



Lill

by Cindy2004, Feb 02, 2004 12:00AM
I had 2 abalations for WPW syndrome in 1998. It had to be repeated in 3 months due to a reoccurence of 250 bpm heart rate.   I have been symptom free since!  I do not need beta blockers any more, and I have not had any problems. I exercise and do all things I used to do (with the exception of drink caffeine - personal thing I guess). Anyway -

I'm really glad this procedure was available and would recommend it to anyone with similar problems.  (I was given a sedative and do not remember a thing about the procedure itself, but I understand they went through my groin and jugular. Recovery was a couple of days of taking it easy.)

by Cathy7, Feb 02, 2004 12:00AM
Has anyone heard of (or, probly not) had a "transthoracic Maze procedure"?



My cardiac surgeon says this is the way to go since it is done on the outside of the heart and there is "practically zero" risk of clots/stroke.  They use small incisions thru the ribs on either side of the chest wall, insert the instruments, including the 'scope, and manipulate the instruments to "burn" around the pulmonary vessels and other hot spots from the outside of the heart.  Each lung is deflated in turn as they work on that side of the heart.  He quoted a "70-90% success rate, but this procedure has only been done in the last year, so there is no long term data yet.



Any comments?  I'm scheduled for one in two weeks.



by arthur, Feb 02, 2004 12:00AM
To: dquenzer
I had PAF and was cured by an rf ablation procedure at the Univ of PA (Philadelphia) about 3.5 years ago.  It was a PV isolation procedure and it took about 6 hours (I was sedated).  The going success rate then is what it sounds like now, about 60% on the first try and about 80% counting a second ablation as warranted.  I was and continue be an athlete...I work out very strenuously at least three times a week (with an average of about 20 mi run per week).  Although I am now 56, my level of training permits me to play competitive soccer in the over 40 age group (aka over-the-hill group).  I mention this as I figure that there's a lot of folks with PAF symptoms that wonder if they'll ever get their lives back.  The answer is yes.



by dquenzer, Feb 02, 2004 12:00AM
To: arthur
Thanks for the encouragement.



I'm hoping I have as good of results as you had.



I'm just looking forward to being more active again.



Doug

by NHS, Feb 02, 2004 12:00AM
To: CCF-M.D.-RCJ
Thank you so much for your prompt reply.





NHS

by jobob52 ford, Feb 06, 2004 12:00AM
To: Cathy7