Managing and Living With PACs and PVCs
Hello all. I have posted in this forum before and I thank you for your advice. I appreciate more support please.
I am about to turn 56 and I have dealt with PACs and PVCs for the past 20 years. The come and go and now they seem to be getting worse. My cardio, regular doc, and electrophysiologist all say that I am fine and that I have too much stress and anxiety (which I do..I suffer from GAD and depression.) They all say that PACs are benign and that most PVCs are benign.
I had an exercise stress echo in 2019 (all normal). Several EKGs this year...all normal. Another Zio Patch Heart Monitor that I wore for a week. Normal sinus rhythm with PACs. My PAC/PVC burden hovers between 1.5 to 1.8 percent. I have had a recent chest xray and plenty of blood work. All normal. I am borderline type 2 diabetic and my cholesterol and triglycerides are all normal. I do take blood pressure meds and it is well controlled. I try to be active almost every day and I do practice CBT for my anxiety. My resting heart rate is about 55 and my cardio says that is normal.
What else can I do to reduce the PACs and PVCs or manage them? Some days they are fast and furious and some days they simply come and ago. But they are ruining my daily life and causing more depression and fear. They are awful in the morning, reduce a bit in the afternoon, and reduce a bit more in the evening.
My cardio again states that they are fine and to not worry.
I have tried a beta blocker (made my heart rate too low and I was too tired) and a pill called Diltiazem. Really had no effect and made me too tired. I don't qualify for any procedure and the one pill they are still offering me is Flecianide but that one has WAY too many side effects and I have had at least two cardiologists warn me from taking it.
What are you experiences, advice, etc?
Thank you!
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I am in Nashville. I work with an EP at St. Thomas. I like him a lot, although I haven’t had much relief from my pvcs. He is open to doing an ablation but it seems that it’s rarely a long term fix. So I probably won’t go that route until I can’t take it anymore. There are several really good EPs here though. Good luck in your search for a new Dr.
@713j
I take Magnesium Citrate (400 mg).
I got so many diferent opinions on which form was better from MCC I asked my EP (Director of Electrology at Mayo Clinic Jacksonville) which form was best and how much. He answered that there is a lot of research out there about which forms are better than others but recommends taking Citrate form and 400 mg.
It did work. My PVCs did go down. Some individuals have a side affect of the citrate of digestive issues (going to bathroom) but I had none. There are many forms and all have specific targets they provide. My EP likes the Citrate as very easily absorb. If you don't take citrate look at the absorability of the other forms and also what that form is targeting.
You can always go on sites like WEB MD, Mayo Clinic, etc. and put in different forms of magnesium and then make your own decison on what is best for you.
@burke5500
There are a lot of different outcomes on ablations. I can't speak for others success or not success. However I had an ablation on my RV and it stopped the PVCs coming from that area immediately.
That was about 10 years ago and I do not have PVCs anymore from RV only LV. My EP (Mayo Jacksonviille who is Director of Electrophysiology) said we could consider (recenlty) doing ablation on LV side but wanted to try medication first as LV was much harder to do. He did several holter monitor tests and PVCs were coming from several areas of LV.
The medication is working very well. Time to time still (PVCs) flare up.
Yeah I've been taking triple magnesium for quite a while. I also take q10 because I think it's the BP meds, not sure but I know it's something I'm taking, depletes your body of q10. I had the PVC's so bad once they felt like a machine gun. That was scary.
I had SVT and had the cardiac ablation surgery for that. Since the surgery, I have what I guess is PAC and PVC on and off every day, with occasional bad episodes. I have tried 5 different medications. They all send me into migraine hell and do not seem to do anything to calm my heart. Sometimes I feel like the Doctors don't believe me and it is nice to know others are experiencing some of the same things.
I tried Wenxin Keli for about 5-6 weeks back in August-Sept.
It worked - pretty much eliminated my PVC's.
Then after stopping WK, the PVC's remained low for a month or so, but they eventually came back.
I am going to try it again, and see if I can find the lowest "dose" possible (and frequency) that works for me.
There are no studies that have evaluated long term use. I might be the test dummy.
Appreciate any one else's experiences.
FYI I am a 63 y/o male - have had PVC's for ~6 years. Frequency bounces around. have good days and bad days. Interestingly, The highest frequency occurs when I sleep (laying down on my side).
@carol1024
Reference the Co-Q-10. My cardiologists at Mayo Clinic advised me that statin drugs lower your co-q-10. It can cause muscle aches, etc. I have been taking co-q-10 for many years now as I am on a statin drug.
There is a lot of information out there on ubiquinol being better as it is absorbed better.
Has your EP or cardiologist mentioned OTC magnesium for the PVCs? My EP at Mayo has me on 400 mg of magnesium citrate. Check though with your cardiologist or EP as they should be the ones recommended something to you especially OTC and any supplements.
Where can you purchase? Send picture of the packaging? Thank you
I went to chinesemedicine.store/wenxin-keli
It ships from China so takes 8-10 days - think it was around $110 for 6 week supply.
Unable to post an image or a link to the URL.
I do take magnesium and Coq 10. I have for quite some time.