Nervous about SVT
Posted , 4 users are following.
I'm a 50 year old woman who experienced on March 30th what I was told a SVT. My heart rate had reached 222 beats per minute by the time I got to the ER. I was admitted into ICU and over the course of a 9 day stay o had first an ablation Done to see if it would correct my issue. During the ablation they thought they saw a blockage so the next day I had a catheter done to check. Thank God no blockage and the heart muscles were strong but my rate now would not go past 50 beats per minute and normal is 60. My cardiologist suggested I get a pacemaker to fix the issue so I did. I haven't had it yet a week now. I feel a lot better but still quite nervous since this is all new to me. I was hoping I could get some advise from someone who has experienced this.
0 likes, 7 replies
jenny02938 shirl1228
Posted
shirl1228 jenny02938
Posted
They burned out to of the veins. They weren't allowing my blood to flow thru my heart which made my rate so high. They thought by doing that it would bring my heart rate back to normal but it didnt. Sue to my rate being so high when I arrived it did some minor damage. My heart rate after the ablation wou ldnt go any higher than 52 beats per minute. Normal is 60. Sometimes it would drop into the 40's. They checked for blockage but my arteries were clear so my cardiologist gave me the option of either try and treat with meds or fix it with a pacemaker. I chose the pacemaker. I'm just nervous because it's something new to me. I'm only 50 and having one isn't the norm for someone my age.
jenny02938 shirl1228
Posted
shirl1228 jenny02938
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No meds for me. I actually chose to do the pacemaker. To me it was what was best. Taking a bunch of pills has never been something I would want to do. I know me I would probably forget or not take timely. And after a while your body becomes immune to meds so with the pacemaker you get it checked every 6 months for the first year or so then after that, you go like every 7 years unless you feel something different. It comes with a wireless monitor you keep bedside so your readings are constantly being given to your doctor. If they feel u need to go to the ER they will call u. I'm an active person and want to live life the way I used to and felt this was the closest thing to allowing me to do so. Thank you Jenny for responding. It's nice to know that I can talk to someone who is experiencing the same thing. Appreciate you. 😊
jenny02938 shirl1228
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Hi Shirl - that makes sense. And I appreciate you, too!
I also do not want to take meds. My ECHO today was normal, and now I have the Zpatch on to capture any episodes. I've had 3 episodes in the last 3 weeks. I'm hoping to catch some on the monitor. Depending on the severity, I'll go from there on treatment, but I can't do the beta blockers. They just make me feel awful.
shirl1228 jenny02938
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Keep me posted Jenny on your progress. I don't blame you about
Beta blockers. Hope all works out wonderfully for you and you won't need anything. 🤞🤞
sher6390 shirl1228
Posted
First...hugs! I have heard it takes about 3 months after the ablation to feel "better". I had mine about 5 weeks ago. Have some patience with yourself during the recovery period. I did not need a pacemaker so I am not sure about that.