Hi WMAC,
I understand your concerns. To some people, PVCs and NSVT has significant impacts in quality of life.
The standard of care for PVCs and NSVT with a structrually normal heart is reassurance that this is not a life threatening rhythm and beta blockers to reduce symptoms. Beta blockers work for some people and not others.
The next step for symptomatic PVC/NSVT in a structurally normal heart is usually a class Ic medication like flecainide. Flecainide may help to reduce your symptoms and is worth trying. Some physicians do not even hospitalize patients for drug loading of flecainide.
If you continue to have significant symptoms and understand the risks of the procedure AND your PVCs/NSVT have on predominant morphology (location in the heart), an ablation is a reasonable options. Important questions are what triggers the rhythm (stress, exercise, caffeine, change in menstrual cycle).
The morphology can be tricky to catch -- it is most helpful to see it on a 12 lead EKG and that is sometimes hard to get.
As far as who to see....that is tricky question because they are all very good. Patrick Tchou and Robert Schweikert two physicians that may be helpful.
If you decide to come, bring records with you. They sometimes don't make it from your doctors office. Any 12 lead EKG with the PVC, echo report, previous EP studies, etc.....
I hope this helps. Thanks for posting.
I would also LOVE to get to the Cleveland clinic but I live in Canada so I don't think it is an option. I would be interested what the docs respond to you and how much the cost would be with no US health care to have an ablation at the clinic.
wmac
If you do and you can live with it then your a heck of alot better person than I and if you dont have it then you have NO idea what it is like! I have read alot of your post and you sound like your a doctor or a med student are you? You seem to have alot advice for everyone.
wmac
My Ep says that if your heart is structuarally normal then even vt wouldn't cuase any major damage unless it was very very fast and lasted for a long time.
Wmac, i wasnt trying to upset you... I was just confused by your post because you kept mentioning vt, i didnt know if you where suffering from that as well.. I definatly know what nsvt is like wmac...Its incredibly terrifying! After my ablation for svt, i was in bigeminy and had runs of nsvt for over a month,, talk about scary!! I totally sympathise with you.. At the end of the day, you're going to have the make the choice for yourself whether or not to try another ablation, leave it alone, or try flecinide, i dont blame you for being scared, i would be to!! I definatly had medication anxiety as well (about taking beta and calcium channel blockers).. Its a scary choice isnt it? Take the risk (even if its small) and take the meds, or try and learn how to cope and do nothing.. I wish there was something i could tell that would make the decision easier, but im sure you know, theres nothing.. I just hope you find a middle road :) Even if you do opt for the meds, i know how scary the "what Ifs" can be... Im quite some time post ablation, havent had another run of svt, with only occasional palps and nsvt and it took me a LONG time to let the what ifs go. I hope theres something that can be done for you that you havent tried yet that helps you cope with that, as well as the nsvt! God bless :)
Sounds as though you're still battling with the ectopics, sorry ; (
I don't know if this will help, but I was on flecainide for a few months and it significantly reduced the pvcs and nsvt episodes I was having.
Hope you find the answers you are looking for, maybe in Cleveland....
sb786: No, VT is not necessarily determined by the number of ectopics...."Technically" a 30 beat run or more is VT, but still not dangerous in a healty heart.
Take care everyone.
connie
Hi sb :) how are you doing? Have you decided whether or not to opt for the ablation yet? I know one of your concerns is your svt leading to vt, and trying to understand the dynamics of your situation, i found a website i thought you might like to read, that might better explain what VT is to you
http://en.wikipedia.org/wiki/Ventricular_tachycardia
I would just shoot myself on the spot. I just hope I get a cure someday soon weather it be meds (which i doubt ill do again) or another eps and ablation or it just stops haahha.....im just so tired of this controling my life and I know its my choice on that part but I cant help it. It does control me everyday and everytime I have an episode I freak and wait for the next one. I dont do alot things because of this. I need my life BACK!!!
It is my understanding that nsvt is basically treated no differently than simple PVCs and the prognosis is basically the same with a normal heart, even normal heart VT pose very "little" risk and the "risk of SCD" is probably on par with the general population than dont have it.
They know alot more about arrhythmias these days than they did 20-30 years ago through long term studies, monitoring & EP studies. Though terrible and annoying to those who feel them they are merely a nuisance and rarely pose a threat to a otherwise normal healthy heart. This is my understanding only I'm not an MD.
To wmac if you are definitely having hard time coping, then maybe a consult with CCF would put your fears to rest. Good luck.
Carrie I would like to hear more of your story about your nsvt!
wmac
Hi WMAC,
I understand your concerns. To some people, PVCs and NSVT has significant impacts in quality of life.
The standard of care for PVCs and NSVT with a structrually normal heart is reassurance that this is not a life threatening rhythm and beta blockers to reduce symptoms. Beta blockers work for some people and not others.
The next step for symptomatic PVC/NSVT in a structurally normal heart is usually a class Ic medication like flecainide. Flecainide may help to reduce your symptoms and is worth trying. Some physicians do not even hospitalize patients for drug loading of flecainide.
If you continue to have significant symptoms and understand the risks of the procedure AND your PVCs/NSVT have on predominant morphology (location in the heart), an ablation is a reasonable options. Important questions are what triggers the rhythm (stress, exercise, caffeine, change in menstrual cycle).
The morphology can be tricky to catch -- it is most helpful to see it on a 12 lead EKG and that is sometimes hard to get.
As far as who to see....that is tricky question because they are all very good. Patrick Tchou and Robert Schweikert two physicians that may be helpful.
If you decide to come, bring records with you. They sometimes don't make it from your doctors office. Any 12 lead EKG with the PVC, echo report, previous EP studies, etc.....
I hope this helps. Thanks for posting.
Anyway, I just wanted to give you an option if you ever wanted to get a second opinion at some time in the future...
Here's some info on him if your ever interested...
http://www.utahheartclinic.com/physician.php?Pid=15&PHPSESSID=b8419545aaae982ac3d04a00729044ed
Im actually from McCall!! I see Dr.Marks
Celest, I went to Dr. Freeman, Dr. Wall did the first eps and Dr. Klein did the second one.
wmac
wmac
thanks for your post
Isn't it your pacemaker already had and ICD? If I'm not wrong, why your pacemaker didn't kick in? I think yours pacemaker is same as mine. Would your cardio turn it down to too low? or your Pacer had some reason FAILED! Don't scare me!
While in the Mountain Home Hospital,they done a Angiogram to see if a blockage caused it.Results had shown no.They sent me to Little Rock Hospital to have a Electrophsiology Study done.Test results had shown I needed the ICD.
use was for preventing my pulse from going low.With this ICD,it slows my pulse down from racing high.I have a Pacer and a Defibrillater (ICD)
http://www.medhelp.org/forums/cardio/messages/34886.html
Wmac, why I have the PCD? It is a very long story. At first they told me put the pacemaker in then I don't have to take medicine. But it wasn't true and it only lasted for 3 days. They gave me a bag of med to take home and enjoy when discharged. After that, each pacemaker replacement, they upgraded.
Now my left wall movement is impaired. My left side beating can't catch up with the right side pacing! Errrrr, hard to understand? Hard to believe too! I've wpw.
http://heart.health.ivillage.com/community/index.cfm
Then it'll show you to login. After login and will bring you right to the front page again. Then you paste the path (website that I given here). You can start to post.
It didn't have the community section at the front page anymore.
Please try again.