AF! Sorry, this is rather long...
Hi! Sorry to hear you are still not great following surgery, but you are not the only one…here is my story so far (11 weeks post aortic valve replacement).
Hi…I thought my experience might prove useful to others…and I’m also interested to know if anyone else had a similar experience.
I was diagnosed with Aortic stenosis in 2005 and told I would need a valve replacement op in the next 5-10 years. At the end of 2011, my echocardiogram showed that my valve was getting pretty narrow. I also had an angiogram, which fortunately showed my Heart to be pretty much A-OK apart from the valve.
In march/april 2012 I started getting symptoms…breathlessness when walking a few hundred yards or climbing a single flight of stairs. Even breathlessness when lying flat in bed at night. Sometimes I would sit up in the night suddenly because I could not catch my breath. The doctor prescribed Furosemide to reduce fluid retention, as I was also getting swollen lower leg/ankles.
I saw the surgeon April/May, and got put on the list for late July, so I could attend my daughters Masters graduation. I was scheduled for 29th July, with operation on 30th, but my white blood cell count was high so they put me on antibiotics and delayed the op.
On Friday 27th July driving home from work I had a chest pain. After about 40 mins it had not gone away, so I called the ambulance and they took me to accident/emergency. They told me it seemed I had a heart attack. The next day, I felt well enough to go home, but they wanted to keep me in for tests. On 2nd August they did another angiogram. My heart looked fine, with no problems with arteries, just the aortic valve problem. The cardiac team explained away my chest pain as either pain caused by the valve problem, or possibly a bit of the plaque in the valve breaking off and getting into an artery. I was discharged a few days later, and went into hospital for my op on August 22nd. The op went ok. The surgeon said the valve was in pretty poor condition. The day after the Op, I had an episode of Atrial Fibrillation (AF). I was not too good for a while, but medication helped. They decided to cardiovert my heart (electric shock) to get it back in rhythm. All went well, and I was discharged August 30th. 6 weeks later, the surgical team discharged me to the care of my local cardiology team, at the same time stopping the Amiodarone that I had taken for AF. Two weeks later I went to the hospital for my first cardiac rehab session. The physiotherapist noticed my BP was high, with rapid, irregular heartbeat, and sent me off for an ECG. This showed that my AF had returned. Over the past few weeks I have started getting breathless when walking/climbing stairs. I get breathless lying flat in bed. My ankles are swelling. i.e. all the symptoms I had before my valve was replaced have returned. I googled AF and found a paragraph in Wikipedia which exactly described my symptoms. I’m currently back on Amiodarone, and waiting for cardioversion again.
So, I reckon that the symptoms I experienced in the months before my operation were due to AF, and that is why they came on so quickly. None of the doctors I saw diagnosed AF, or sent me for an ECG. Now, having had my valve replacement, I am still suffering, because of the AF.
So, if you experience rapid heartbeat (120/minute), breathlessness walking or climbing stairs, sudden breathlessness lying in bed at night and swollen ankles, it is probably due to Atrial Fibrillation, and not your valve!
Needless to say, since all the pre-operative symptoms have returned, I feel pretty P’d off some of the time. If I walk up 12 stairs I’m breathless. I went to the supermarket the other day and parked my car. Walking from the car to the store, I had to stop twice due to breathlessness!! This is no fun, and my Cardiology appointment is not til 14th January 2013!!! I am lucky I still have my sense of humour! I think if I get too fed up, then I will turn up at the local Accident & Emergency and invent a few extra symptoms so that I get seen, and maybe sorted out.
As for chest pain….soon after the OP, I had a strange, indescribable, tingly feeling, which stretched 6 inches or so either side of my sternum. It felt like I had a small swarm of bees or wasps buzzing around in there. And I had the usual sharp pain if I sneezed or coughed. Now, the pain is more centralized, an inch or so either side of the sternum. I’m hoping this means that the outer part has healed.
Hope this Helps! Best wishes for a speedy recovery.