Ahh i see about the beta blocker.. thats VERY fast for AVNRT, anything above 300 is ususally considered fib.. I personally suffered from AVNRT, and my rate was sustained at 250 and my ep described it as the worst avnrt he'de seen.. But i step down for you! lol
After my ablation, i had one reocurrance of SVT, and was told this is not out of the realm of normalcy when recovering from an ablation.. You may also have more than one re-entry loop that they didnt find during the first two ep studies.. I understand how devestating that can be..Maybe another ep study is the best course of action, as it doesnt sound like meds are helping you much.. Personally, i can do without ever getting another dose of adensoine for the rest of my life.
I was on 360mg of Diltiazam but was switched the other day to Verapamil. I cannot take betaclockers because of asthma. As far as the hert rate the other day...The cardiologist careully measured the distances and said that it was ireggualy regular not ireggulary irregular. My SVT was classified as AVNRT.
if the rate was that fast it would probably be classified as AFIB... which is a kind of svt.. ask your doc to clarify.. You should probably be on a beta or calcium channel blocker
I was had my procedure at Tufts NE Med Ctr. in Boston by the director of EP. Yes, I am very frustrated and need releif as I have not felt well since Sept. I lead a very healthy lifestyle but lately not able to participate the way I would like to. It has been tough on my family(husband, 2 kids 9&17) My 9yr old has asked santa to make her mom's heart better:(, talk about a tug of the heartstrings. At this point I'd fly to the moon if I had to!
Have you gone to Cleveland Clinic? If not, it's time. I'd get there no matter what it took (plane tickets, long drive, anything). They're the best of the best in heart care. This has got to be frustrating beyond anything I can comprehend. I hope you find relief from this so you can live your life outside of constant arrhythmias and symptoms.