barbie,
wow. thats alot of information in a short space.
1) Will or can this procedure damage my mitral valve more than it already is?
generally not.
2) Can this process stop where it is with the aortic valve? I doubt it will stop where it is with the mitral valve but is that possible also?
It is impossible to tell without several points in time and the exact mechanisms of your leaking valves. Serial echocardiography is generally how to tell if it will progress.
3) Also could my mitral valve be causing the mild leakage of the aortic valve?
Most likely not.
4) Also after the ablation say these spots are found what are the odds of other cells saying ok its my turn to try and be pacemaker?
There is always a chance that PVCs can recur after an ablation.
5) Is it possible for this drug to cause pvcs to be worse?
Effexor to my knowlege is not associated with PVCs but could certainly effect how you deal with them
good luck
I was put to sleep, but not with anesthesia. I was on the table for over 7 hours, and had lots of work done for afib, atrial flutter, and pac's, plus they checked for PVC's. Didn't know a thing was happening except at the earliest which was very uncomfortable.
When I woke up I recovered quickly, although my back was killing me. So they gave me some pain meds. Was out of hospital the next day, but was pretty sore.
The doctor told me that being asleep was not a problem, but being under anesthesia was, since that would hinder finding the foci. I could tell immediately when they increased my heart rate at the beginning.
God's speed. Since you have been through this before it can be trying. But the second time around usually produces good results.
Thanks much
My situation is a little different because I have WPWS. But my comment is that when I had the ablation, I was awake.
The process took about 6 hours, and those of you who have had one know it is not a comfortable position. They said they would give me mild sedation, which they did, but I was awake through all of the procedure. I do however think that it would have been better for me to be put out. For starters, I was very agitated after the first two hours. My arms were cramping from the position I was in, and it looked to me like the doctors and nurses were just sitting around talking. I think the meds altered my mood some. I begged the nurses to massage my shoulders and begged them to take the catheters out, that I was done. This is not my true personality at all.
I feel that if I had been asleep I wouldn't have been as much trouble to them, and I wouldn't remember the pain.
I need to have another one but I have been putting it off considering the pain I had with the last one and the recovery.
I had three holes in one leg and four in the other and they had a hard time getting one to clot. Even after sutures. Maybe I am a pain wussy but having them press on the sores hurt badly.
The next problem came when one artery started to bleed after I left the hospital. I had a hematoma from my knee to my stomach. I went to the ER with severe abdominal pain and bloating. The did a cat scan and found that I had blood in my abdominal cavity and that was the cause for the pain. I think maybe the thrashing I did in recovery (due to the pain from the pressure they were applying) may have caused the extra bleeding.
I guess my point is, maybe I would have had a better experience if I had been sedated.
So sorry to hear of your ablation experience. I can't help but wonder if all that discomfort was really necessary. I'm just wondering if more could have been done to ensure a more positive experience :(
I had 2 ablations last year and I have very little recollection of any of the EPS' or actual procedures. Each time, I was given a combination of Versed and Fentynl prior to going to the EP lab. Perhaps it was because I had enough ectopics for them to study even under mild sedation...not sure. Also, everyone was VERY well aware of my anxiety :) (that may have played a significant role)
The first procdure took about 7 hours and I had a few entry points in my right groin. After the procedure the doctor applied firm pressure to prevent bleeding. There was some pain associated with the pressure, and I would have to say that was the worst part. But, they applied pressure for about 20-25 minutes, and I only remember feeling uncomfortable for a few minutes. Stayed flat for 6 hours with a 10# sandbag on my groin to prevent bleeding.
Second time was also about 7 hours and I had 3 venous punctures and 1 arterial (femoral) and they used a St. Jude's "plug" to close off the artery. I definitely felt that, but again, it was relatively short-lived. Despite the plug, I still laid flat and used the sandbag -- figured I might as well give myself a little added insurance :)
For those of you facing ablations, ask your doctors about what to expect. Prior to my procedures, I read and asked a ton of questions!! My doctors were wonderful and provided all the information I needed to be informed and comfortable. I am the BIGGEST chicken in the world and I'm hear to tell you -- I would do it again in a heartbeat if it became necessary. It is not an easy decision, so it is best to make it with as much information and medical support as possible. Good luck everyone!
connie
The doctor gave me the same combination of medicine they gave you, but it must not have been as much. I still remember everything very well.
I am hoping next time, they might sedate me a little more. I will know a little more about the procedure so I will be able to ask questions.
I think because I am only 22, the doctor put everything in "electrical" terms when he explained the situation to me. I didn't know enough about the eps to look it up on the internet. I just knew that I was possibly going to have an ablation.
I am not blaming my doctor for my ignorance, he probably thought I would understand it more in laymans terms, but I could have researched it more if I knew the actual terms for what was going on. I wasn't actually told the term for my condition until I asked at the last appointment. I just thought they didn't know what was wrong, so I asked and he said "Oh honey, you have Wolfe-Parkinson's-White syndrome." "We have known that from the start." But like I said all I was told is that I had a piece of electrical tissue that was short circuiting my heart. I guess my point to that is, if you type that into google, you never know what you'll come up with.
This forum has been a blessing. I like to know stories like yours of how people have had really positive experiences in the same situations as I.
Thank you again.
I Pray that God will give the surgeon the skill he needs to make your August ablation a successful one.
Love, Carolena