I seem to have
benignBenign ear cyst or tumor
Benign positional vertigo pvc's.
HolterHolter monitor (24h) and
ECGEcg
Electrocardiogram (ecg)
Exercise stress test
Post myocardial infarction ecg wave tracings said uniform
ventricularParoxysmal supraventricular tachycardia (psvt)
Ultrasound, ventricular septal defect - heartbeat
Ventricular assist device
Ventricular fibrillation
Ventricular septal defect
Ventricular tachycardia extrasystoles, echo said structurally
normalNormal saline flush heart. I had a lot of PVC's during the echo, but that seemd to be no problem. The cardio told me I could do anything with this. Medication was not prescribed, betablockers made it worse, and other meds could have serious side-effects.
I started exercising again, and wear a polar monitor. I can actuallt see my heart skipping beats. It seems to be worse when my
pulseNeck pulse
Pulse
Pulse - bounding
Pulse - weak or absent
Radial pulse
Takayasu arteritis
Taking your carotid pulse is under 120. I have alot of them while resting and during the day. I am in bigeminy and trigeminy a lot of time, and i have skipped beats as well as two consecutive fast beats.
The cardio sias that i wouldn't be able to feel the skipped beat but only the next fuller beat. But I really do feel the skipped or extra beat, because the sensation in my chest coorsponds with the skipped pulse. When I lay my hand on my chest i feel my heart beat regular, and when it beats extra or skips I do feel an different beat, like its more on the surface of my chest, an extra kick. This keeps frightening me, and although I try exercising I'm still worried about going running or whatever while experiencing the bigeminy. When I feel my pulse during the day I always feel this bigeminy or single skips like every third beat. Sometimes I have a buuterfly feeling in my chest alday and it's like being out of breath.
When should I see a doctro again, or do I really hev to accept this is normal ?
Before august I had a regular pulse, and the cardio got no clue what's causing this. Could this disappear as well
my heart freaks me out!!! Good idea to go out and get your mind off your symptoms I will take your advice. Have a great day.!
Kelly
What I have found that at rest, all the often cited triggers do apply. They are much more frequent after a couple glasses of wine. They are susceptible to anxiety to the point that I can cause the to happen at will by paying attention to my pulse. Since they don't really impact my running in any way I can detect, I have learned to ignore them and go on with life.
Now, I've had over 2 months with no problem. My attitude is that I will have to get used to them coming and going on their own schedule, and that I'm not going to get stressed out about it. I'll enjoy the days when I have no problems, and tough it out when they're bugging me.
In response to your comment about feeling your ectopic beats. I have had PACs and PVCs for 20 years (now 38). I can assure you that there is absolutely no doubt that I, and many others, feel the ectopic beat. I wish I had a dollar for every time a cardiologist has told me I am feeling the compensatory beat. I am not sure why the general belief among doctors is still that you cannot feel the ectopic beat. I experience a whole host of sensations with the ectopic beat - pain, abrupt kick, flip-flop, drawn out contraction, etc. I have actually seen one cardiologist that experienced this himself so I had no trouble convincing him. Having said all that, the fact we can feel these and others cannot does not change the fact that they are just ectopics.
Anyone tried the med Flecanide/tambocor, would appreciate any comments on this drug.
I too suffer from all of the above, woke me up last night couldn't sleep for all the erratic rhythems.
I'm trying very hard to not take pusle and move on with the day. The fresh cool air feels good when feeling bad. There is plenty of that moving about the country.
Everyone stay warm out there
Laura
I was on flecainide for about 4 months for frequent pvcs. The medicine worked very well at reducing the pvcs. I did experience some gastro side effects and the doctor changed the medication to rhythmol. The rhythmol produced less side effects, but I needed to take it 3X/day rather than 2X. For me, that was no big deal, but the doctor said some people prefer 2X/day.
Good luck!
connie
As to how to handle these ectopics may I say there is no easy solution. I also get ectopics from time to time. They are generally due to stress and lack of sleep. I recently got rid of something that was causing me stress and it made a difference in the ectopics I experienced.
Before taking drugs I would surely explore all kinds of other means such as stress reduction and or other lifestyle things that might percipitate them.
I have noticed that not only in my life and in the life of others that these things seem to come and go.
I had this annoying thing since 1997, more or less. In periods, even for years sometimes, i have just ignored them. I have been examinated with holter monitor, eco etc several times. All showed just plain pac:s and som pvc:s (and short runs of pac:s).
Now I have about 15000 to 20000 pvc:s a day, In periods. These periods comes more and more frequent since a became pregmant and stopped taking betablockers.
I still try to ignore them, but it is not easy when they come about 15 a minute. My BP goes down and a feel sick from them. Has anyone of you had an ablation for PVC:s, and if so: did it help?
Your english writing is GREAT!!
I was having 20,000+ per day and had 2 ablations in 2003. Now, I only get occasional pvcs. Pregnancy seems to bring them on in many people. Many of the doctors suspect that hormones play a role in some women.
Has your doctor suggested an ablation? My doctor was not encouraging an ablation until my pvcs started causing problems for me (cardiomyopathy). Prior to my ablations, I took beta blockers on/off for about 12 years. In 2003, I was put on anti-arrythmics because the doctor wanted to eliminate or significantly reduce the number of pvcs I was having. In my case, the frequency led to a cardiomyopathy. Since the procedures, my EF is back to normal and the CM has resolved. Keeping my fingers crossed that it continues.
connie