How frequent and how long are your SVTs?
Anyhow, the symptoms can lessen, or they may worsen, it all depends. Usually people can get adjusted to a beta blocker. You can check your BP at any pharmacy, Wal Mart, Walgreens, Kmart...and it's not a bad idea to do so.
Hang in there. Some SVTs respond really well to beta blockers. I hope you can tolerate your dosing.
My svt's have been being about 1 or 2x/week lately, I used to go alot longer without having them. They usually last several hours, went back to the dr and he ran an ekg and said I needed to go back on meds for sure. I don't know why but once my heart gets into that rhythm it doesn't want to break for several hrs.
Feeling alot better on the toprol today, more awake anyway! Yeah I should check my bp in Walmart-was in there tonight and didn't even think to do it, will next time though. Go back mid Dec for a checkup so will see what dr thinks then. Hope you are doing well, take care, em
Thanks for the post last week regarding my post ablation problems. Things are really no better at this point. I saw my EP on Tues. He is absolutely devistated with my current status. As usual I get my B/P taken, EKG etc. before I see him. The nurse asked me if I normally have high B/P...I told her that I usually run around 90/50 so when she ever said that my B/P was 160/100 I nearly fell off the table. She then proceeded to tell me that my pulse, which was rapid, was irregular. After having the EKG I waited to see the doc. So in he comes to see me to go over the findings of the EKG. He said that it showed a junctional escape rhythm. So in English, it means that the SA node and the AV node are competing against eachother to set the pace. I about lost it! When I told him how easily I become fatigued and the pain I am having in my chest, he is now concerned that I may have heart failure on top of everything else. I am going on Tues for the nuclear stess tolerance test and I am sending readings from the event monitor every 2 hours or if I feel any activity in the mean time. He thinks that the AV node may have been affected or damaged in my last ablation...of course that is a risk with the procedure.
After the testing I will see him to discuss the next step, which he thinks may be a pacemaker. He has promised to "get me there" He hopes that getting me there will be his Christmas gift to me. I hope that it is!
I am so very sorry to hear that. That is devastating you are having so many problems after the ablation. I'm really pulling for you and hope your ep can get things on the right track and soon. I have heard somewhere of pacemakers being used, maybe that will be the option that finally gets things straightened out for you. Please keep us posted on how you are doing, I hope that your doctors are able to help and you are feeling much better very soon. Take care, em
HI, just wanted to know if you are tolerating the beta blocker any better now? I'm in a similar position to what you were in when you started this thread. Is the beta blocker controlling the svt now? thanks sb