I'm awaiting a hospital appointment to assess my episodes of SVT, which started recently and don't respond to the 'home remedies' so it's A&E and adenosine to reset me. Horrible and scary.
Meanwhile, I thought I'd run my questions past you forumites. I know you're not experts, but general thoughts or shared experiences would be welcome while I wait for cardio to see me ...
My episodes have gone on for approx 2-3 hours, by the time I've got to A&E, been assessed then been treated. How long might an episode continue if I didn’t/ couldn't get to a hospital? Do they 'burn out' eventually?
How damaging or dangerous are prolonged episodes?
Why do they use adenosine rather than a beta blocker (which I did have the first time as they thought initially I'd had a heart attack, before they discovered it was my electrics!). Adenosine is pretty drastic and I'm grateful it works, but it's no fun.
Grateful to hear any info that anyone might have (and all these questions are also on my list for my cardio appointment, whene'er that may be 😉).