Anyone get ectopics when walking? Are they worse if you get them when you move rather than being still?
Ectopics again: Anyone get ectopics... - Atrial Fibrillati...
Ectopics again
yorkcardiology.co.uk/ectopi...
Just answered my own question
Thanks! I found that interesting as one who has only recently been affected to a troublesome degree with ectopics. I've had more than my share of AF/Flutter over many years and had multiple ablations and dc cardioversions plus every drug known to man 🙄🤒
Have they recently started your ectopics?
Yes, in the past few weeks
Yeah they are very distracting and horrible just can’t get my head round them I’m still waiting results from my 7 day holter monitor
I know that they are harmless ( usually....) but they can still be very alarming. I sent a 30 second recording from my Kardia for analysis just for reassurance really and report came back with a yellow 'multiple atrial ectopics, see your physician within 24 hrs " I was back to normal by then so of course didn't bother.
How many will you get a day roughly and do you take anything that makes them slightly better
I wouldn't be able to count they are so numerous ! I take Bisoprolol 1.25mg as a PIP and increase as necessary
Do you get relief with the bisraprol?
Yep, me! Never used to but in the last 8 months when I’m walking especially if I’m carrying something like shopping I get them. I take 1.25mg Bisoprolol night and day and this helps to regulate me. Stress, lack of sleep etc will usually make mine worse. I get weeks where I get loads then nothing at all but the odd one here and there.
You take any magnesium for them ?
Hi,
Just on ectopics, I get them almost constantly, except according to the halter monitor, when I am asleep at night.
When I go for a walk I feel the heart seems to be more steady, as if when I put it under load, it seems to help.
Had an ablation 4 years ago.
My electrical cardiologist says must keep on my pradaxa, and if I can't keep up with my wife on walks I need to go back and see him, otherwise will see him in a year.
Definitely stress is bad, and lack of sleep.
I no longer wear a Garman as only causes stress.
Is there anything you take that can make them better? How long have you been suffering with ectopics after you abalation?
I can't have beta blockers, as they make my heart go too slow. .So I only take a magnesium supplement, magnesium chelate 1000mg,
I don't know how much it actually helps, but even if a bit, it's worth having.
I have had ectopics ever since the ablation, although now much more frequent.
When I had the ablation, took over 5 hours, and the cardiologist isolated 3 short circuit, but couldn't do the 4th, said getting too tricky, so problem probually relates to that.
The positive side of things, is I can still do most things, such as walking , and we have a hobie kayak and can still use that.
So is there any other meds your on like flacinide or anything? So what’s your EP now saying another abalation or just live with them?
I am just on pradaxa, a must. Saw cardiologist last week, has said I am on a slope down hill, but seeing I am able to live reasonable well, and if I can keep up with my wife when going for walks, he will see me in a year's time.
Can you explain to me how an ectopic heart beat feels?
To me it's a lurch in my heart rhythm like I might experience if I had some bad news. I feel the extra beat like a thump, but then I feel a pause that follows the extra beat so I feel as if my heart has skipped a beat. It's very unsettling and makes me feel anxious.
How many would you get a day?
Well sometimes a succession maybe 4 - 6 a minute for several minutes or even hours. It can feel a bit like AF. Sometimes just an odd one. Other times none that I'm aware of. After one holter monitor reading the EP said I'd had 2000 in a day.
Do you take anything for it like magnesium
I rub magnesium oil in my skin every day. That is said to be a better way th absorb it at cellular level than tablets which people say can give you the runs. (At least that is what it says on the packaging - but who to believe? There's so much money to be made from all these supplements!)
Frankly the AF bothers me more than the ectoptics when it gets going, pounding away. I have had a run of it this week after a wasp sting. So I am considering trying Magnesium Glycinate now as recommended by Sanjay Gupta. Researching doses.
What dose of Magnesium Taurate do you take? Has it affected your digestion/ bowels?
I take 2 tablets of magnesium taurate for about a week now by bio care, bowel movement is normal for me although stools can be quite firm
I will give it a try. Two tabs what strength?
A wasp sting has triggered a week of AF episodes for me. Apparently the histamine your body makes in reaction to a sting causes inflammation. So I am wondering if continuing Piriton antihistamine would help....
Btw FYI I am on Flecainide Bisoprolol and Apixaban for AF. Plus BP meds. Had 2 ablations after AF went 24/7 for months on end. The second worked well. But I still need the Flecainide.
Anyway the Mag Taurate sounds worth a try. Thank you.
It is s wobbly feeling, fluttery.
Hi Padayn.
I get ectopics every time I stand up, walk, eat - basically whenever I move.
I generally don’t get them when I sit completely still!!
Over the past 4 years the ectopics have come and gone- this bad episode has lasted for 8 weeks now and really getting me down.
I’ve just paid privately for a 7 day monitor in desperation to see what (if anything) is going on.
Usually by the time I get to see a cardiologist the ectopics have died down but luckily this time it was bad for the whole period including really fast irregular runs that last 20-30 mins that sometimes wake me in the night.
I have also been getting 4 and 5 ectopics in a row which feels horrible and again new with this episode.
It will be interesting to see what the report comes back with.
I’ve got a consultation with Dr Sanjay Gupta shortly.
My cardiologist wants to put me on Flecainide- I’m so worried about taking tablets!!
I started taking magnesium glycinate 3 weeks ago but not noticing much of an effect. (200mg a day)
Every day I wake up hoping they’ve gone but by the time I’ve cleaned my teeth know it’s not the case 😢
Oh wow so similar to my situation everything you describe is exactly what I’m going through the only thing is I get mostly mine when at rest I also paid Dr Sanjay Gupta Privately for a 7 day holter monitor, I used to take magnesium glycinate made no difftrence but switch to mag taurate made some difference please let me know how you get on with your results, have you also got AFIB?
I believe that ectopics when you start putting greater pressure on your heart can be a sign that your heart is irritated by something which may go away if you resolve the irritation (as well as what Dr Gupta says). Possibly electrolyte imbalance or too much sugar or food preservatives. The main contenders for Electrolyte imbalance are taking PPIs, low iron, low magnesium, low vitamin D and low potassium. Also irritation somewhere else in your body can also irritate your heart. No answers I am afraid but something to consider for you personal condition.
Do you take any stuff for electolyte imbalance?
I take magnesium (a mixture - but not oxide) and eat a banana a day and an avocado at least 2 times a week and I have halved my PPIs (omeprazole). I limit my sugar intake and foods that contain preservatives (thats difficult as so many do including wine and beer). I also drink more water and especially first thing in the morning before anything else. I have also found leaving 12 to 14 hours between the last meal in the evening and first the next day may help - it certainly helps with weight loss and digestion.
Both, but I think sometimes when doing steady exercise tend to be more even, and when asleep at night perfect no ectopics at all.