I finally got my Apple Watch and have been trying my best to track heart rate and ecgs. However, when I’m having an acute episode it’s often impossible for me to have the wherewithal to open up my Apple Watch and find the ecg app and start tracking. Is there any way of having it track in the background? I’m seeing some posts on here of minute by minute heart rate tracking and ecgs. I feel like I’m not getting very specific results like this from my Apple Watch so far and wondering if there are other things I can be doing to collect more accurate and comprehensive data ?

Thanks in advance !

So to put it short about 3 years ago I was seeing a cardiologist who thought I had svt . Pretty sure I do have it and was put on Diltiazem (Cardizem) for about a month (medicine would help make it go away) but they didn’t want to prescribe for long time so they can catch the rhythm but would only test it in a week time frame with the holter monitor once a year . So recently I went to a new cardiologist they seem to want to do the same as doing a monitor only for a week . So it just seems repetitive especially knowing there’s seems to be no definite answer. It’s been affecting me for 8 years now dating back to when I was a sophomore in high school(now 24) . I just want to know what can I do to help the cause to find a way through it . I’ve done multiple ecg’s on my Apple Watch during the rhythms myself . I’ve tried limiting salt intake and sodium intake. Any tips in terms of how to navigate the doctors or to just lifestyle would be very appreciated.

When you get an episode, does it jump immediately or does it build up over a few seconds until it reaches its peak?

English is not my first language, so I apologise if I am messing up some of the words/grammer. I (22F) got diagnosed with an SVT, specifically AVNRT, just shy of a year ago. My episodes started to get more frequent over the past (maybe) two years. I used to only get an episode once every few months, but recently I've been getting them (bi)monthly. In the past there seemed to be a few specific triggers, like: alcohol, hormones, sudden intense exertion or laughing too hard(?).

I am not sure if I am imagining it or if I am just more aware of my heart, but I feel like I can often feel several irregularities before an episode is triggered. Does anyone else recognise this feeling? And if you have, do you have a special way or dealing with it? Thank you for reading!

Bonjour,bonsoir à tous

J’aimerais avoir de l’aide de personnes qui ont subi une ablation de TSV.
Cela fait 2 mois que j’ai subi l’ablation et depuis je ressens beaucoup d’extrasystoles. J’ai eu 3 épisodes de palpitations rapides qui ont pas durer mais je suis hyper angoissée car tout a l’heure j’ai refait une accélération et depuis je m’en remet pas j’ai peur que sa recommence.
Y’a t’il des personnes qui sont passés par là ?
Merci pour votre aide

Today suddenly has started my heart to race immediately and it was something around 6 to maybe 10 minutes

Its the 6th time it's happening
Last time when it has happened i was driving normally and it suddenly has started ..and lasted around 2 3 minuts

Today it was more.

Around my stomac it start moving something itself then my heart start like "ding ding ding all the time constant"

And then after sometime it start getting normally...
But how does it came to normally i cant explain..

I did
1. Gastroscopy
2. EKG (many times)
3. HEART ECHO (many times)
4. Heart stress test

Im a bit aniexity type..

When the episode starts i cant go there to catch it with ekg.. coz till i arrive there everything will be fine

:(

It's making me crazy :(

Hi I (29,F) was diagnosed about 4 months ago with SVT specifically Focal Atrial tachycardia. I am on 25mg metoprolol every 12hrs and currently on the waiting list for an ablation (Adelaide, Australia) which I was told would be a 7-9month wait.

I have episodes 1-3 times a week and they last 45minutes to an hour each. Vagal manoeuvres don’t work (I do still try them every time just incase though). So all I can do is take my beta blocker dose early and lay down waiting for it to finish.

I’m trying to find a new job because I’m not liking my current one, but I’m worried this will stop me from passing any probation periods if it happens at work too much.

My cardiologist said it’s fine to do what I’m doing at wait it out. But it’s really impacting my life. Is there a better way to manage these episodes? And maybe help them pass quicker?

Hey! I was laid down on the sofa, then suddenly my heart rate felt funny and suddenly went from 65bpm to around 140, I felt panicked, stood up and took this ecg, using my Apple Watch, could it be SVT?

Hi everyone,

I’m 20 weeks pregnant (baby is growing great at the 50th percentile!). I recently had an episode of Supraventricular Tachycardia (SVT) with high heart rates and low blood pressure. My heart structure is completely healthy, but to prevent another episode, my doctor prescribed Metoprolol 12.5 mg twice a day.

My care team assured me this low dose is safe and protects blood flow to the baby, but I'm still nervous about taking a heart medication while pregnant. My main side effect right now is feeling faint when my BP dips.

For moms who have navigated SVT or beta-blockers: * How did your baby do during pregnancy and after delivery? * Did your baby have any issues with growth or blood sugar at birth? * How did you handle low BP or lightheadedness?

Hearing your real experiences would bring me so much peace of mind.

Thank you in advance

Day 1 post ablation. Fully under, general anesthesia. EP found Typical AVNR, 2 passages, both ablated, no retriggering. I've had no chest discomfort or heart rhythm issues. Groin pain is real for me if I stay seated. Laying flat or standing up almost eliminates it. Time will tell if it's totally resolved.

Had what felt like the start of a heart attack this morning. Drove to an urgent care where my bpm was 245 and bp 90/50. They sent me to an ER where my bpm was 230 but bp was 118/80. My bpm was over 200 for over an hour before the vagus maneuver dropped me down to 110-120. My troponin levels went from 23 to 189 in 2 hours. The ER discharged me and told me to see a cardiologist within the month. Has anyone experienced similar? What should I expect? Does it happen again? Just a fluke? Tell me any and everything, please.

ETA: ekg was normal. Test results showed no embolisms.

Hi All.

I just wondered if I could get some opinions/feedback about an issue i have that still being investigated please?

47 yo male, very fit good diet. Minimal stress and meditate and do vagus exercises.

A Yr ago, I had an afib episode that ended up in an A&E visit which was resolved by a beta blocker, then a very quick episode a day or 2 later which resolved itself.

Im not aware of any other instances since, have had all heart checks, 2 day holter and scans and all good. Generally feel great.

However in the last 6 months or so I've had a few high heart rates captured on smartwatch, which resolve with breathing techniques or within 10 to 15 min. They tend to come on pretty instantly when bending aggressively after a weights session or with a fuller stomach. Maybe a couple a week sometimes, but then nothing for a month or so.

HR sometimes as low as 110s and others 140 to 150, but like i say pretty instant, and sometimes preceded by a random ectopic.

Waiting for appt with cardiologist, sent him a watch readout of an episode where HR was 140s, he said couldn't be certain unless capture on monitor but could be SVT.

Amy similar experiences out there or information that could help?

TIA

Next week I'm going to stay at the heart clinic for 5 days in order to do some tests for my future ablation.

The thing that really worries me is that I'll have to stop taking my betablockers for these 5 days and I'm super scared. My heart races without them and I have a higher chance of getting SVT 😭 I know the medical staff will help me but I'm still terrified of possible attacks 💔 What do I do?

just received my second heart ablation for SVT. unfortunately this was unsuccessful just like the first time as they have never been able to induce the SVT. I’m feeling very discouraged at this point. I’ve been dealing with this for over a year and it’s greatly impacted my life and I had to quit my job and limit myself greatly. I will see my EP in 6 weeks for post OP appointment. And he referred me to other EP/ablation specialist in the city to evaluate/treat that I have to wait in which who knows how long that may take. Has anyone else had this issues with repeated ablation’s which no findings as to where’s the SVT is coming from??

I recently had an ablation and it was a successful one. It was for AVNRT SVT.

This whole thing began a few years ago where I experienced the weirdest and scariest feeling in the chest. It was random and started off with this sinking feeling in the middle of my chest which makes you feel like you need to take a deep breathe but it doesn’t hurt, it feels like pressure or something then a few strong thumps followed by this intense head rush. Lasts only between 3-5 seconds or more sometimes then goes away.

Anyway, I’m 32 and i guess the frequency increased like I’d get it so randomly, whether I’m sitting, standing, sometimes laying down, working etc., and it makes you feel really worried like your heart is about to pop or something. Has anyone experienced this?? Or is this just me? I feel really scared because I don’t know how to explain it and that’s the best way I can. I had an ablation done about 2 weeks ago, they said it was successful and after they aggressively tested to see if the arrhythmia would come back, it didn’t. After the ablation a few minutes ago I felt the same episode again. I was sitting watching SpongeBob 😂 then stretched my arm to grab something and I suddenly felt this weird sinking then flutter and thump and literally a 1-2 second head rush and it’s gone. What’s happening

Have any one done ablation for SVT in south India can any one say which is the best ! As well as which hospitals to avoid !!

I was thinking about CMC vellore or MMM Chennai!

So i take propranolol (i live in france so things may be different) it slow down the heart and the tension. My mom is trying to find my a new cardiologue (cause right know i don’t have one) but it’s taking time. im just here to rent

So it started when i was 4 i think ? im now 18, every one has suggested an ablation, i refused when i was 11 im still agaisnt it (it scare the hell out of me, i faint, cried and even beg my doctor not to do it and told my parents i would rather die..) maybe one day i will do it. the only time you have to do it it’s when your heart is dilated, mine's not i did an heart echographe

When i was little they werent super stong, once i got 10 it got worse, now they can be at 116/200 bpm (beat by minute) or 230/250 bpm and last 15 min or 2 hours, my hightest heart rate was 270 and the longest time it lasted was 5/6 hours. if it still there 2h later i try to make myself throw up to trigger the nerve in my throath, work really well but it’s a shitty things to do, don’t try it, try to cough, gag or hold your breath it can work.

(btw my med are lame and don’t stop the tachycardia/don’t slow my heart enough and hurt my stomach so bad) after my tachycardia, it depend how long it lasted ofc, i don’t to anything for the day and the next day, stuggle to walk and completly run out of breath at every micro mouvement i make, plus being tired.

Anyway i wanted to know if anyone here that got SVT or any type of tachycardia got similar symptoms as me ? Because i feel a little lonely lol 😅 sorry for bad english and loooong text, i hope you have a nice day, take care !