SVT/PACs/PVCs
Hey there!
I'd like to share a little background to try to help whoever may take the time to read this to understand what is happening with my situation.
I am 24 years old, I am a female. Back in 2020, I got Covid-19 for the first time. I wasn't extremely ill (thankfully) but I was tired, I ran fevers, and I lost my taste and smell. I never had any issues with my lungs or my oxygen intake, I recovered quickly.. probably within a week and I was back to doing my normal activities. About a month later, I was at my father-in-law's house and I was helping him with some housework because he is not in good health. I bent over to pick up the dog's food bowl off of the ground and I felt my heart skip. When I stood back up, it felt like my heart rate skyrocketed to 300bpm. At the time, I had no idea what was going on. I laid down in my father-in-law's room, and tried not to panic (although I felt like I was dying) and we discussed whether or not we needed to call emergency services. Eventually my heart calmed down and went back into rhythm on its own.
The next day, I was cleaning the kitchen at home and it happened again. I immediately felt faint and sat down to avoid hitting the ground if I passed out. This episode only lasted for about a minute or so and wasn't as severe as the one prior, but it was still scary. After this, I made an appointment to see a cardiologist because I realized that something wasn't right.
They performed a series of tests on me. I wore a Holter monitor, and I completed a stress test. I was cleared of any issues, so I went on my way. A couple of years passed, and throughout this time I suffered through minor palpitations but I had no pain in my chest, no shortness of breath, and no accompanying symptoms. I still decided to get a second opinion. I visited with a different cardiologist, and performed all of the same tests. This cardiologist even performed an echocardiogram. All came back normal except for a few PVCs and PACs from my Holter monitor report.. my cardiologist reassured me that there was nothing to worry about, so I carried on.
Fast forward to a month ago when I had another round of SVT. My heart rate spiked to 226bpm and it lasted for several minutes. I tried everything that I could think of to break it. Vagal maneuvers.. coughing, bearing down. Nothing would make my heart rate lower.. so I called 911. Emergency services arrived and took me to the emergency room but by the time I got there, my heart rate was normal. They took bloodwork, and couldn't find a thing wrong with me. They checked all of my cardiac markers and electrolytes.. but nothing was wrong. They told me that I probably had a run of SVT but there was no way for them to be able to tell without seeing it happen in action. I understand that they can't just diagnose or treat me for something I may or may not have.. but this is just so aggravating.
Before Covid, I could do anything I wanted. I could drink alcohol, I could smoke, I could have a cup of coffee or a piece of chocolate without my heart rate jumping all over the place.. but after Covid, it's just been completely different. I can't walk up a hill without feeling like my heart is going to either explode or just give out on me. I've read some articles online about a link between Covid and ventricular arrhythmias.. but who's to say that it's true.
I was just reaching out to see if anyone may be suffering from something similar, or if anyone has any advice on what to do. I've tried everything that I can think of to help myself. Staying hydrated.. taking magnesium to help with the palpitations.. but to no avail. I am desperate for answers. I just want my life back.
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Thank you so so much. I will look into seeing an electrophysiologist!
Thank you so much. I know that stress doesn’t help my health, and I am under it a lot of the time. I’ve been diagnosed with a panic disorder, and I’ve had it for many years and I am taking medication for it which has helped. I wouldn’t pin everything completely on my anxiety though due to the fact that I know what panic feels like.. I know how my heart feels when I panic. I know how powerful my mind is. I suffered from panic attacks before my heart symptoms began to occur. Thank you though so much. I hope you and your wife are doing super good now!
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2 ReactionsThank you all so much for your helpful comments and kind words. It’s truly appreciated!
I think it's a good idea and I do hope it helps!!
Good luck and let us know if it works for you.
Your story sounds very similar to mine, I feel like my cardiac issues started after having covid for the first time. As you mentioned I had no issues cardiovascular wise prior to having covid, and could take on any task that required my heart rate to increase or to increase my respirations. I am have dealt with "heart palpitations for several years until this week when I ended up in the ER due to experiencing one hour of 180-200 bpm and no end in sight. I did finally convert back to sinus rhythm just before I was going to be shocked to stop the what we now know was SVT. A angiogram determined I do not have any arteries blocked and will see a electrophysiologist for an ablation. Overwhelmed to say the least.
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1 ReactionI have experienced this since my twenties and am 70 now. Ask your cardiologist/electrophysiologist to implant a loop recorder. It’s a tiny device that continually records.
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1 ReactionWow! I just came across this post when researching what is triggering my newly diagnosed SVT suddenly. Started very mildly in Jan 26. Wore holter monitor for week and caught some irregularities. Took couple months to see cardiologist at end of April. During this time episodes very infrequent and didn’t last long. Then cardiologist switched my blood pressure medication around same time I had viral infection and pcp put me on steroids. I ended up in ER five days later on May 27. Heart racing non-stop for hours, sky high BP and anxiety like crazy. ER doctor said my heart was ok and that steroids triggered and very bad for SVT. Said should feel better once steroids out of my system. Few days later I started to feel better. Still had episodes but not all time and not bad until this five days ago. Started picking up again and got really bad that I could sleep. Been like this for days. I’m mostly good during day while at work but in evening and when lie down it cranks up. I’m sure the stress and anxiety cause by it doesn’t make it better. I also realized that some other medications i recently started might trigger. It is so frustrating and my cardiologist isn’t very responsive (only saw him the first time in end April) so I might be looking for new one. After reading your post I realized that I too had Covid in Dec 25 and this started about a month later. My heart just feels like it is going to beat out of my chest and my chest is sore and it can last for hours. Last night for several hours before finally fell asleep but only slept about four hours then up again. Does anyone notice it happened more while lying down or at night? Thank you every who commented. Does make me feel like I’m not alone even when my family doesn’t understand. Prayers!
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1 ReactionYes, your instincts are correct. Find a new doctor, an electrophysiologist who specializes in irregular heart rhythm. If your cardiologist is already an EP, still switch. Sounds like yours has checked out.
It has been noted by my EP that most patients feel the heartbeats while trying to sleep. We are focused on it and there are no other distractions. There is no reason to think that your arrhythmia begins at night in bed other than the stress you feel. It can become a habit. Trying falling asleep while reading or watching TV as a distraction from coding on your heart. Good luck.
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1 Reaction@tlaun44
I was told by my primary care doctor that when you lie down on back, or either side your organs move and your heart beat is felt more.
It means that your PVCs, PACs, and VTAC will be felt more than when you are standing up.
For a while when mine was so bad I slept in a propped up seating position on my bed until heart calmed down. I did not feel the PACs, PVCs, and tachycardia and thus was able to get some sleep even though not much.
To add to all of this you say at work you don't feel it as much. What I am told by my doctors is that your mind is not on heart focus when working, exercising, hobbies, etc. thus you are not going to feel the arrythmia like you do when trying to go to sleep or at rest.
Then at rest you are in heart focus which causes more anxiety and stress and thus the fight or flight reaction body has which will create more PVCs and PACs.
I am on some great medications and as I type this (knocking on wood) my PVCs, and PACs, and VTAC have dramatically been reduced. And I am trying to not be heart focused.
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