After a 30 day event monitor for
palpitationsHeart palpitations i was told that i had marked sinus arrythmia. Although no actual palps were caught on the event recorder, the dr told me that my symptoms correltated with the marked sinus arrythmia. I was told that normaly sinus arrtyhmia has no symtpoms but that i had "marked" sinus arrythmia and that the variance between my inhale/exhale was great enough to cause symptoms. Have you(or anyone out there) ever heard of sinus arrythmia causing symptoms? The palps really dont bother me much anymore but i am still interested in recieving a proper diagonses. I use are world famous Veterans hospitals were it is real easy to get pushed to the side. I know that without the
EcgsEcg
Electrocardiogram (ecg)
Exercise stress test
Post myocardial infarction ecg wave tracings you cant say much but does this sound logical to you? If so what is the standard treatment (if any) for marked sinus arryhtmia considering symptoms are present? should i ask to see a EP? I do apologize for all of you who have been trying to get your questions in considering this is my second post but i cant find anything on marked sinus arrythmia( causing symptoms) on the net or at the library so this is my best option, thank you in
advanceAdvance care plus
Advance relief....ONeil
Goodluck-
If your cardio has advised on how to try the atenolol and 25mg atenolol is not that big of a dose as i understand, i would at least give it try I've been on it for 3 years now without any problems whatsoever though we are all different and respond differently, at least you are under the doctor's recommendations. I'm a male so I can't say my tachycardia or PVcs are hormonal. I've had this affliction all my life, though my cardiac evaluations are always essentially normal and I've had lots of them in my 41, nearly 42 years. Good luck , you might just find the relief you're looking for.
I've had palps for nearly two years, and just need some advice. What are you supposed to do if you know there's absolutley nothing wrong with your heart, you keep away from caffeine and alcohol, you still do exrecise and try and enjoy life, you try meditation, and you still continue to get palps??
I've been on a beta blocker which hasn't really helped. I just want to know how much of the palpiations are actually caused by anxiety and how much of it is just "there" and we cant really do anything about it?
What do people do when they start getting them? They're agonising. I can barely hold a conversation with someone when I get my "heart hiccups." I know that the best thing to do is to try and ignore them but this is proving near impossible.
Any advice anyone? Any natural remedies? Another beta blocker perhaps? Or no meds at all? I feel like I've tried everything and it really is upsetting me and hindering my enjoyment of life at the moment :-(
However, once we have been reassured by our docs, often over and over again, that our tests show that the odd beats are not dangerous, the next question is how to deal with them.
Some people do find that one beta blocker or another reduces the strength or perception of them, and sometimes the frequency, too. Often, it requires a trial of several beta blockers.
If the fright over pvcs continues and becomes chronic, so that the poor patient spends more time listening to his/her heartbeat than enjoying life, then I believe it's time for psychological intervention. Some people use a relatively short-acting anti-anxiety-drug, like xanax or klonopin, several times a day. IMHO, this is sending boys to do a man's work. I think if you're dealing with months of anxiety because of benign pvcs or palps, it makes sense to visit a good psychiatrist who is familiar with antidepressants. In my experience, finding the right one really gets rid of the self-monitoring thing, and lets one move on. Some people find that one SSRI seems to increase the odd beats, but some shrinks, like mine, are very up to date on the pharmacology of this class of drug, and will choose based on the patient's symptoms.
I know I probably should just stay away from all meds but honestly it'd be nice to have a break from the palps and be able to concentrate on things like study etc. I'm in my honours year this year and dont have time for annoying paplitations!
Having said that I know I should probably learn how to deal with the anxiety better. I feel like I do meditation and it sort of decreases the pvcs but then they just come right back the next day with a vengenace. Very frustrating isn't it. Honestly I feel like I've got so many awesome things in my life and I wish so much that I could just concentrate on them without always having to factor in pvcs. It would be so nice to wake up in the morning and not have palps be the very first thing on my mind. It would be so nice to wake up and think "wow, what a beautiful day!" instead of "I wonder how many palps I will get today and whether they will make me cry or not" :-(
Sorry I went on a bit there it just feels so good to vent. If anyone else has any similiar thoughts/feelings/experiences please share. I am so gald for this Forum! Take care everyone :-)
Megzz, you're listening for your heartbeat, aren't you? It's natural, and we all do it at first. But, when that's the first thing you listen for at daybreak, I think it means it's time to get a bit of counseling. Myself, I favor a psychiatrist, because, as an MD, he/she can prescribe medication. However, some people get enough help from a counselor, who will try relaxation techniques and so on. ACCEPTANCE of the palps will be large part of therapy. This sort of thing is described in a rather cool old book titled 'Hope and Help for Your Nerves," by Claire Weekes.
To answer your questions about beta blockers, yeah, there are lots of them. You should probably ask your doc about the current smorgasbord, and which of them would be best for you to try. There is no reason to steer clear of medications, particularly when the palps are so troublesome in your life.
I will be seeing my cardiologist in the morning, and have some questions, and feed back from the medicine he has me taking. I hope he can reassure me the meds will not make me worse the longer I take them. Have you ever heard of that happening?
Thanks and hope you all are feeling well as can be!! Think positive ~!
Tannins (high tannin red wine is a BIG no no)
MSG
Caffeine
Chocolate
alcohol (does however suppress it totally at the time, its the next day combined with the above that cause me extreme grief)
After all this time I am strongly considering an ablation as want to enjoy the rest of my life without the dread of palipations, anyone had an ablation? If so how was it?
Cheers
You have probobaly read some of my other posts. I also had SVT since I was a young teen.(39 now) After being on beta blockers for 25 years and have my cardiologist urging me to have an ablation, I finally did. First one was 4/06 didn't work. Second was 6/06. Have not had SVT since then and initially was taken off of beta blocker. Started having major sinus tachy. (not SVT) and put back on Inderal. Heartrate slowed down ok then started having PACS constantly (2/3 per minute 24/7). Only had maybe 5-6 per day before on a bad day - sometimes none at all prior to ablation. That is where I am at 3 months after 2nd ablation. Saw EP today , getting another cardionet monitor. Still don't have any definite answers - why am I having so many now when I didn't have them prior to ablation, Can I ever get off of the Inderal or will my heartrate go in the 150's from just walking slowly, will these eventually subside if they are from irritation from the ablation?? I got a definite "I don't know" Mind you I went to a well known, experienced EP from a leading major teaching hospital. I do trust him and I think the fact of the matter is the heart is such a complex organ, who knows what happens when they burn and destroy heart tissue. I guess if the electrical system was that easy to figure out this forum wouldn't exist because none of us would have to put up with these crazy beats. Imagine the value in coming up with a cure-all for PACs and PVCs!! If the doc could tell me this is normal and within 6 months they will stop when the heart tissue is no longer irritated I would be ecstatic and could get through 3 more months. I guess I kind of in limbo now thinking these could have been avoided if I didn't have the ablation and put up with episodes of SVT 4 times a year!! This is only my experience and who knows, maybe they will go away. I know that many people have had successful ablations - they are just not posting on heart forums, they are out enjoying their lives!! I would just say make sure you get an experienced EP - mine has done thousands. Good luck and I would be glad to reply if you have any other questions...
Fellow SVTer
Thanks for your reply, friend of mine recently had an ablation at 40 yrs old, went fine and has had no problems months later, however only has SVT for a couple of years - not 20+. My son has been complaining of something jumping in his chest so took him for an ecg and looks like he's got SVT also at 6 yrs old poor little lad. Hope they get to the bottom of your problem, the jury is out for me on whether I have an ablation, will think long and hard - more worried about my little one now.
thanks again
cheers
stuey
Sorry to hear you son may have the same problem. Maybe there is a hereditary factor. Take care and let us know how he is ....