Hi all, I’m Fran. I’m using my hubby’s account, who has had AF for about 9 years and has appreciated the wisdom found here. I’d be very grateful for your thoughts on my Atrial Flutter as I’ve found it very difficult to get the advice I feel I need.
(I hope this post isn’t too long, you might want to jump to the end.) For background, I’m 76, and about 3 months ago I saw my GP with pains in my chest and difficulty breathing. It was decided to refer me to the rapid cancer diagnosis service and for x-rays, and not to give any medication for my symptoms in case it interfered with the cancer diagnostics.
A week later, I saw the same GP again, who now suspected bone cancer (myeloma), which was pretty frightening. When I got home, my husband decided to check my pulse. It was just under 200 bpm. We tried phoning the GP but couldn’t get through. My husband meanwhile called 111 who were all great. I was called back by a doctor who was very concerned and told my husband to get me into A&E asap and he would call ahead.
There they confirmed my pulse to be 198 bpm and I was gently carted off on a trolley to the Resus ward. They struggled to get my pulse down with IV infusions and drugs by mouth, and though still higher than they wanted, I was discharged a week later.
The next day, I was phoned by the hospital, wanting me to come straight in. I was expecting to see a cardiologist, but it turned out to be an oncologist concerning the suspected cancer. To my relief she was puzzled as she saw no reason to suspect cancer. But she did find my heart rate was still much too high and I was readmitted to the Resus ward.
I think it was at this point where I first heard the term atrial flutter. I’m not sure whether it had been the untreated pneumonia, or the stress of being told I might have cancer, that triggered it.
My heart rate was brought down to around 130 or so but fluctuating, and, shortly afterwards, I saw a visiting electrophysiologist from a large central London Hospital who arranged for an ablation.
I then saw a different GP, who sent me back to hospital for more tests and x-rays for the lung problem. I was re-admitted again, put back on a drip, given a cocktail of drugs, and at the third attempt, my heart rate fell to around 45 bpm. I haven’t been back in tachycardia since and have an HR now of about 60 bpm. They now think I’d had pneumonia with “pleural effusion” which I now seem to be just about over.
The decision for an urgent ablation was made when they hadn’t been able to get my HR down. So the question that bothers me is, as I have had an abnormal heart rate, for almost 2 months now, how likely is the condition to return, and do I still need an ablation which is booked for about six weeks time? I am now just taking 3.75 mg Bisoprolol and a DOAC. The ECGs I had always showed what seems to be an even rhythm, unlike AF, but very fast.
I’m really sorry for the length of this post, which is a shortened version of what’s been quite a saga. I was discharged and re-admitted multiple times from the hospital and have 4 discharge letters signed by different members of the staff I saw, (2 nurses, and 2 junior doctors who were a nephrologist, and a rheumatologist I think). I’m not aware of ever seeing a cardiologist, apart from the single appointment with the electrophysiologist.
I have been told that I will be able to discuss it with the surgeon when I go in for the procedure, but it would seem a terrible waste of resources if it was decided to not go ahead at that stage.
I’d be very grateful for any suggestions on how to proceed.
Fran