Anyone experience occasional palpitations or premature ventricular contractions?

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I had PVC's before heart surgery in 2011. In 2008 I was doing a stress test and they stopped it after 5 minutes because they were coming in strings of 3. I still had them after surgery and grew used to them. In around 2015 my doc put me on small doses of Losartan and Amlodipine to bring my blood pressure down a bit. I noticed at a point that I had a lot less PVC's and still today have very few compared to before taking the new meds. Not sure if worth talking to doc about the meds to reduce PVC's if they bother you enough.
 
Hi guys -

So I’m 3.5 years postop, and the dang PVCs / PACs are back. (Posted here 6 months ago about them)

It’s Day 16 of them.

Six months ago I went to my PCP, the ER AND two different cardiologists. No one took me seriously. (They didn’t even tell me how to use their Holter monitor correctly, so when I went in for the results they just brushed me off, saying, ‘They’re not really that frequent, and you only self-noted one episode, so...’ (The nurse had told me NOT to ever push the button, but I did anyway.. once)).

The thing is, I’m aware of them all the dang time, because it feels very differently from usual.

They’re double and triple beats, that happen every 3 - 6 beats or so; but even the ‘normal’ beats are pounding much harder than usual and feel unstable, not a smooth rhythm; my heart feels weak and like something bad is happening in there, lol - not sure how else to describe it.

I’ve tried deep breathing, even Buteyko breathing, meditation, but it is not an anxiety or stress thing, and unfortunately I don’t notice any change no matter what I do. (Taking supplements or not, drinking more water or not, exercising vs resting)

It’s just relentless and exhausting and I’m sometimes short of breath from them - I wouldn’t say severely short of breath for long periods of time... but it is still scary and I wanted to ask if anyone has any ideas.

It’s not sustained tachycardia, so I don’t think going back on Metoprolol is in order; my BP isn’t high.

If you have any idea at all or similar experiences, please let me know! (I need sleep.) Thank you!
 
Have you seen or talked to cardiology about this 16 day episode? I know you feel like they blew you off last time but this might be a different issue?

Another thing you might look into could be a Kardia. This was helpful for me because the cardiac nurses and cardiologists both said “well those are pretty accurate” and it helped them believe my afib reporting. Whereas when they asked “how do you know you are having afib?” and I said “I can easily feel it just taking my pulse that it’s irregularly irregular and 150+ BPM and I become short of breath” wasn’t as reliable. They liked the Kardia. I also have a pulse oximeter that “beeps” with each beat and was able to play that over the phone so they could hear how fast and irregular it was. That is how I got recommended for ER visit the first time I had afib with RVR.

Not sleeping is no good so I guess you need to try to get someone’s attention again. It’s very frustrating but hopefully you can get either a definitive treatment or something to at least help you sleep.
 
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I'm 3 years post op and I'm currently going through the same. I seem to go through a cycle of a few weeks where they ramp up and eventually subside away again for 9 or 10 months and pop back up again. I hate them too. I had this happen last year at this exact same time.
 
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I've had some PVCs off and on for the past years, and also have had hours/days of Afib. Even had an ER visit because I was worried it was something more. .... But after going on 25mg ER Metoprolol Succ (daily) for the past 2 years, the Afib and PVCs are under control finally.
 
Another thing you might look into could be a Kardia.
Looking into this, it seems it might only be good for afib sufferers. People say it doesn’t register HRs below 50 bpm, and that it doesn’t catch bigeminy or trigeminy.

Also - - Is it true with the 6-lead version you absolutely have to sign up for their monthly service? Is it true you can’t take a screenshot, or get the report sent to you as a pdf?
 
I'm 3 years post op and I'm currently going through the same. I seem to go through a cycle of a few weeks where they ramp up and eventually subside away again for 9 or 10 months and pop back up again. I hate them too. I had this happen last year at this exact same time.
Have you noticed any correlation between supplements you take and the arrhythmias? Like maybe remembering to take magnesium setting them off?

I keep trying to figure out what causes this... so far I can only guess caffeine from eating a snack that was covered in chocolate (after not having caffeine or chocolate in a year or so) or overdoing it mowing and raking. Or maybe a supplement (magnesium, D, E, or coq10?) I don’t know what to do other than stop all supplements for a while, and rest.... except resting makes the arrhythmia worse, while exercise makes it better. The problem is that at some point I have to stop to sleep, lol.
 
Have you noticed any correlation between supplements you take and the arrhythmias? Like maybe remembering to take magnesium setting them off?

I keep trying to figure out what causes this... so far I can only guess caffeine from eating a snack that was covered in chocolate (after not having caffeine or chocolate in a year or so) or overdoing it mowing and raking. Or maybe a supplement (magnesium, D, E, or coq10?) I don’t know what to do other than stop all supplements for a while, and rest.... except resting makes the arrhythmia worse, while exercise makes it better. The problem is that at some point I have to stop to sleep, lol.
I my case, I wasn't on any supplements to start with. I just take 75mg aspirin.

I think I noticed mine start up about an hour or so after strenuous running last week where I pushed myself to my limit. I don't notice them under normal exercise though. Could just be that I noticed them and then tuned in.....

The last time I suffered from a bout was this time last year and I started gobbling magnesium and also coenzyme Q10 but they actually seemed to get worse until I threw the whole lot of them away to see what would happen. They resolved in a few days after that.

My cardiologist said that I will likely always have them come and go but that they are not any harm. I hate them.
 
Looking into this, it seems it might only be good for afib sufferers. People say it doesn’t register HRs below 50 bpm, and that it doesn’t catch bigeminy or trigeminy.

Also - - Is it true with the 6-lead version you absolutely have to sign up for their monthly service? Is it true you can’t take a screenshot, or get the report sent to you as a pdf?
A Kardiamobile 6L monitor has helped me study my PVC problem. I am also working on with my electrophysiologist and cardiologist on this issue.

I've been using a Kardiamobile 6L monitor for the last year. The advanced features such as detecting PVCs requires a yearly fee. Note: There are cheaper Kardia monitors that do not have these features, so look carefully at the monitor you are buying.

When I use my monitor it shows some information immediately on my phone app. However, to see the PVC count I need to download an EKG pdf file to my phone; this pdf has more information, including the PVC count for the 30 second reading I just took. I can then save these pdf files, and I also can email these pdf files to someone.

If during a 30 second recording I have several PVCs in a row, it does record all of them.

There are some limitations. I need to sit quietly while I operate the monitor, so I must wait a few minutes after exercising to avoid an EKG that is just useless noise.

I'm happy to further discuss PVCs if you have more questions.
 
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