Sigh. PVC’s have me desperate. How to cope?
First off, thank you for reading. I know from reading posts that people have it worse than I do and I offer my utmost respect for those of you who do.
Briefly-
39 yo/m
Reasonably healthy. Non smoker. Stressful job.
So, a few years ago I started to have an occasional (painful) pvc that always got my attention. Once it hit 3-4 a day, I did like everyone else, and sound of the alarm and got the full gamut of testing.
Benign. Low dose Metoprolol.
Ok great.
Fast forward to these last two months, and the amount of PVCs I am having has increased 100 fold. They are all day. I went from a few a month to one a minute.
Panic. Doctor. Here we go again.
Once again, they are telling me that they are unifocal and harmless. These. Don’t. Feel. Harmless.
They absolutely stop me mid sentence every time. Each one is like a jump scare. My stomach drops like a roller coaster and I have a brief adrenaline shot. Like you’re scaring the heck out of me over and over. Just a Deep painful fear each time.
The doctors don’t seem very concerned. They recommended a magnesium supplement, which I am taking religiously.
No caffeine. No smoking. No alcohols.
Nothing.
This has destroyed my quality of live almost overnight. I wake up in anticipation. I go to sleep in fear.
Does it get better? Is this my life now? Even as I type this, I’m having one about every 30 seconds. I don’t want to go anywhere. I don’t want to do anything. I’m just petrified.
Wonder if switching from a beta to a calcium channel would work? Is this my life now?
The sad thing is… I “know” it’s supposed to be fine but why doesn’t it feel fine? Every shot of adrenaline warns me that I won’t be around much longer.
Just terrible.
Any input is appreciated.
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Great advice and I think I passed on same to mookie7. I had not heard though about potassium. I know both potassium and magnesium are important and take magnesium.
Good advice on electrophysiolgist as that is really going to give him the advice he needs. Stress causing stress and just like you said, when you get PVCs stress goes up then causing additional PVCs so double edge sword. Thus address the stress and see what you can to reduce it.
I found walking, bike riding, swimming great exercises and stress reducers. But find something you like to do and do it. That in itself will help with stress and dealing with this. My electrophysiologist stated clearly that even with ablation you will NOT stop PVCs as they are a normal part of heart beating as long as not excessive.
How much magnesium do you take and what kind.
713, I take 400 mg once a day. When it was recommended to me by my Mayo Electrophysiolgist he did not specify a specific type.
I take a Puritan Pride product called, "Triple Magnesium Complex." The ingredients are, Magnesium Oxide, Magnesium Aspartrate, Magnesium Citrate. I believe on line I read, but was not told this by my electrophysiologist, citrate is the best.
When I told my Electrophsiologist was already taking it he recommended Mexiletine 150 mg and started with lowest dose. I was advised this is a quick metabolizing medication and has to be taken every 8 hours. Told within a day or two if not taken is gone from body. This is different from other rhythm medications that can be highly toxic and in body for long periods of time.
It did improve the PVCs but still there. I was warned that gaining weight will cause PVCs to go up especially atrial. I did gain weight during treatments for prostrate cancer but have been working on getting it down. Stress is also a trigger for PVCs.
Do you have high blood pressure? Stressful job, maybe change doctors.
I have a good friend who has afib, her doctor never mentioned to stop caffeine, I told her to stop caffeine, and other foods that have caffeine like chocolate. She did and the irregular heartbeat stopped. She also takes low dose medicine..
You may of irritated the vagus nerve. It’s a long nerve that can play a roll with afib and pvcs. I’ve heard of people having problems like yours after they eat.
Good luck.
That Vagus nerve you mentioned is very important. My wife is diabetic 1 just diagnosed 2 years ago. No explanation why other than 3 surgeries to stomach could have damaged Vagus nerve. It sends information to/from brain on insulin.
Caffeine I am told can contribute to PVCs if you over do it. I take the pill form on green tea but decaffeinated. I also drink decaffeinated coffee. But those darn PVCs still there coming from 3 different areas of left ventricle.
I take 300 mg of magnesium glycinate. Starting to eat raisins for potassium.
Hi Samantha:
I am sorry you are going through this, as I know it is not fun at all. You do not mention whether or not you've been thoroughly checked out by a Cardiologist or Electrophysiologist, but I will assume you have and that's good.
I have not noticed any particular foods to cause PVCs, but I am not surprised by your observation that foods high in tyramine can trigger them for you. Tyramine, I think is an amino acid, and it can also trigger migraine headaches, so it obviously has a neuro "toxic" effect for some people. It's great you've identified this!
What I do notice is more of a "mechanical" and a "timing" issue in terms of triggering irregular beats. For example, if I over-eat and have abdominal bloating, I can notice more irregular beats, including PVCs. Some foods cause me to bloat at this menopausal stage of life, so I avoid dairy, greasy foods and foods high in sugar. And, speaking of sugar, I can also identify periods of more irregular heartbeats after ingesting larger than usual amounts of carbohydrates, especially on an empty stomach! Think bread before dinner or a bad-for-you treat in the middle of the afternoon. Not only will the resultant rise in blood sugar cause PVCs for me, but then I will be bloated later as well, and the PVCs can continue for several hours. So this is all manageable, for the most part. I just make sure to eat some kind of protein with any carb that I might eat (save the dinner roll or cornbread to eat with dinner, not before dinner), eat less of it (like, treat myself to half or a smaller portion) and never eat a cookie or scone or something carb and high in sugar on an empty stomach.
Now, when this happens, my trick is to go for a walk. In the summer, when it's hot, if I have to, I'll go run an errands to a large department store or Costco or grocery store and move, move, move to make my digestion speed up. And that leads me to the last point and that is, if you are medially cleared to do so, the best thing you can do is to get some exercise every, single day or at least 5 days a week that causes your heart rate to increase. It does not have to be an all out, high intensity workout, but steady and regular. I find that when I back off from this for weeks at a time, my PVCs can creep up again. Hope this is helpful to you and I would love to know how the extra potassium works out for you! Good luck.
All I can say about this is, the first time I was diagnosed with PVCs I was taken to hospital by ambulance and doubled my dose of Metoprolol(now 200 mgs.). They told me if they started anytime ever and they did not go away, I must call ambulance and head to hospital. Now many years later, I was having issues with my PVC's. I had MULTIPLE tests. Nothing has changed much on my meds. My statin was changed to a more aggressive type. I still have another test coming up. All I know so far is the blood pumping into heart is starting to get plugged by cholesterol. Which I had been taking a statin for years beforehand.