Sue,
I remember your history. Your options are pretty well spelled out for you.
Your options are really meds, no meds or an attampt at an ablation. Each carries risks and benefits. I think the main issue needs to be how well you can live with your symptoms as you are now. An ablation may help with both the
SVTParoxysmal supraventricular tachycardia (psvt) and PACs.
Thus it could impact your
palpitationsHeart palpitations.
It is very difficult to balance the risks and benefits of any procedure, especially when you take into account your
familyBirth control and family planning
Choosing a primary care provider
Ewing’s sarcoma
Family troubles - resources. You should focus on how well you can deal with doing nothing and how that will impact your overall sanity and well being. If you are miserable all the time from worry about the
SVTParoxysmal supraventricular tachycardia (psvt) and
palpitationsHeart palpitations, it might make it easier to reason through to undergo an ablation.
You might talk to others on this forum who have undergone an ablation to get some more insight from those that have gone through it.
good luck
Looking forward to hearing from you.
Thanks, Sue
Thanks again, Sue
I understand that chronic afib is much more difficult to cure via ablation than paroxyzmal afib (PAF), because of gradual physiological changes (remodeling) that occur in the cardiac tissue. The possibility of a cure remains, however, it's not as high a success rate as for PAF.
Some EPs insist on a preliminary procedure which establishes the protocol necessary to induce the arrhythmia. In this way, on the day of the actual ablation procedure, the EP has a better chance of inducing the arrhythmia for ablation. Without this preliminary step, you simply take the chance that it won't show up when you're all wired up, which could be disappointing.
-Arthur
Thanks Alice,
Betty Jo
***@****
Take care!
I had an ablation for frequent pvcs in August and it was considered a success. I am scheduled to go back in November so they can try and ablate another foci as I am multi-focal. The doctors are being conservative and that's OK by me!! I have been on beta blockers and more recently Tambacor and Rythmol, but opted for the ablation rather than the medicine. Good luck...
Last year after an annual checkup, my EF had declined enough to indicate cardiomyopathy. That's a very long story, but the bottom line is that the doctors are confident that the CM was a result of the frequency of pvcs. After 3 months on Tambacor this year, EF improved 10%. Although the antiarrythmics appeared to be effective, I did not like the side effects, and knew I would have to take them forever. I also have MVP/MR and there is a possibility that the valve will need repair in the future. With that in mind, it would be ideal to have no CM and good EF.
I am very fortunate because my doctor is extremely conservative and would not recommend the procedure withou very careful consideration. Although the pvcs are annoying, I have pretty much learned to live with them. Absent the CM issue, my doctor probably would designate them as benign. However, my records have been reviewed by MANY doctos and this seems to be the consensus.
It does take time for the heart to heal. In August,the pvc activity was markedly reduced. About week 6, the activity picked up. Event montitor and holter showed significant enough frequency to warrant further treatment. Otherwise, I face the RX again...UGH!!! Thanks for asking.
Last year after an annual checkup, my EF had declined enough to indicate cardiomyopathy. That's a very long story, but the bottom line is that the doctors are confident that the CM was a result of the frequency of pvcs. After 3 months on Tambacor this year, EF improved 10%. Although the antiarrythmics appeared to be effective, I did not like the side effects, and knew I would have to take them forever. I also have MVP/MR and there is a possibility that the valve will need repair in the future. With that in mind, it would be ideal to have no CM and good EF.
I am very fortunate because my doctor is extremely conservative and would not recommend the procedure withou very careful consideration. Although the pvcs are annoying, I have pretty much learned to live with them. Absent the CM issue, my doctor probably would designate them as benign. However, my records have been reviewed by MANY doctos and this seems to be the consensus.
It does take time for the heart to heal. In August,the pvc activity was markedly reduced. About week 6, the activity picked up. Event montitor and holter showed significant enough frequency to warrant further treatment. Otherwise, I face the RX again...UGH!!! Thanks for asking.
Oh, once the first foci was ablated, they did try to identify other foci, but my extra beats settled down. The doctor said the heart settled down immediately after she ablated, what is perceived to be, a major foci....