My cardiologist is a very good and caring individual who goes the extra mile for you. I was surprised when he suggested moving away from Bisoporol and Flecanide and suggested Sotalol to combat my AF and Atrial Flutter
He explained that there could be side effects and I was started on a low dose (40mgx2) increasing if I can tolerate it to 80 mg twice daily
Has anyone found that Sotalol works for them as I have seen that it is no longer a drug of choice
Additionally I am being assessed for an ablation
Thanks
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Kelvyn
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No as you say in UK Sotalol is not much used these days and taken off the advised list. My understanding is that it is both beta blocker and anti-arrhythmic but has problems in that at doses large enough to be anti-arrhythmic can cause some dangerous other arrhythmias in some people. My question would be is your cardio an arrhythmia specialist (an electrophysiologist.) He may be very caring but is he up to speed on latest ideas and treatments? An EP would be.
What is to assess about ablation? If you have paroxysmal AF and dugs are not able to control it then you fall into the approved category. All that then matters is your decision yes or no and probably a long wait.
Thanks for reply In respect of the assessment I am just going through the process and this appears to be the step to get me on the waiting list I hear that waiting times at Leicester are around 4 months
I moved from bisoprolol and flecainide to sotalol and it was OK. Since my cryoablation 2½ years ago, I have continued with sotalol as a PIP. I use it infrequently but it seems to help with the control of the one or two ectopic runs I have had.
My EP put me on Sotalol for a short while last year, he said it was good for my atrial flutter. Unfortunately it didn't work for me, so I went back on Flecainide.
I have used Soltalol as PIp for 15 years and it worked well for me then. I found it not to be as effective as a daily drug for PAF when it became more regular. I was taking up to 4 x 40mg a day and PAF would break through, however after, a so far successful cryoablation last year,I just keep 40mg as a PIp again, but not used yet ! Long may it last! Good luck and hopefully an ablation will work for you too.
After a broken hip operation which was a few days after a heart and stent operation, I started to have AF attacks. I was put on Sotolol. As the attacks continued my doctor kept raising the dosage until I was at 40mg of Sotolol twice daily. At a yearly checkup I stated that my heart rate seemed low at night and that I was waking up at night gasping for air and that I thought that I was having spells where I was not breathing. My cardiologist put a device on me to check my heart rate for a night. When saw the results he call me with some urgency in his voice and told me that my heart rate was dropping below 40bpm and that I must stop taking Sotolol. I had been taking Sotolol for around 8 years and thinking that it was helping, the thought of stopping worried me. I have been off Sotolol for about 2 years now without a single AF episode. While on Sotolol things that would trigger AF were alcohol, caffeine, heat/sun, stress etc. Now I can exercise, I live in Phoenix and the past few days I have been working for hours timing trees in the hot sun without AF. At my mens group we were discussing how drugs affect people in differently ways. I told them "you know they test these drugs on rats. Maybe some drugs only work on people that are rats." I don't mean to make light of this issue because it scares the heck out of me. Every time I had AF I would wonder if I was going to see the morning light. Tom
Yes I take 40mg of Sotolol twice daily and it certainly keeps the af at bay, the only side effects I get are aching legs and a little breathless. At my pacemaker check on Wednesday they were pleased with how things were and to delay the AV node ablation. Aching legs are a nuisance though.
I have been taking 80mg twice a day of Sotalol for over twelve months and take an extra tablet when I get an attack of AF. I was taking Bisoprol and Flecainide but it didn't suit me and ended up in hospital.
I am the same and have been on the 80mg x 2 a day and an extra one when I have a PAF episode . I was changed from Bisoprol after a cardioversion nearly three years ago and seemed to be OK. I was signed off by the hospital heart consultant but recently I have noticed my blood pressure is very high at night but ok during the day and the heartbeat is very regular 24 hours a day. My doctor suggested I upped mI felt it wasn't looked into enough. She then suggested 80mg in the morning and 120mg at night which I have taken for the first time tonight! I have Flecainide 100mg as a PIP but haven't used it, it was given to me whilst in A&E during a holiday 200 miles from home.
I find it all so very confusing and worrying but try and keep the faith!
I am surprised you have Flecainide as a PIP as when I was changed from Bisoprolol and Flecainide I had to wait five days without any medication before starting on Sotalol.
I was shifted to ~Sotalol after problems with Amariodarone after a cardioversion for atrial flutter. and have not experienced any side effects (or, apart from a isolated episode, any recurrence of AF)/. As with any drugs some people will experience side effects and others won't. Why not give Sotalol a try but be alert for any side effects.
I'm on Sotalol 80mg twice a day and 40mg, if in AF. My cardiologist switched me from amiodarone in 2010 because of breakthrough AF. Even after both ablations my EP has kept me on this dosage. No side effects except my blood pressure is generally on the low end of normal.
I am on 160mg twice a day of sotalol for PAF the smaller doses didn't work for me. I have a pacemaker so am able to be given this high dose. So far so good. I started out taking 80mg twice a day gradually my GP increased this because my AF was not kept at bay. I do not have any significant side affects except tiredness. Fingers crossed it gives me some release for a while at least. Go for it.
To my surprise soltalol works very well after two ablations and previous bisoprolol for persistent AF. Early days yet but feeling quite good. Headaches and aching joints which I hope will ease but being in NSR is such a relief that I feel I can breathe again
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