I’m writing this blog to help those who, like me, struggled with the whole concept of Pacemakers, CRT Pacemakers and ICD’s.
My understanding of the role of the various pieces of kit are :-
* A Pacemaker is used to help people with heart failure. It gives the heart a little help should it try to slope off and not do its job properly. It is usually wired to one ventricle.
* A CRT Pacemaker is also used to help people with heart failure except it is wired to both ventricles and will synchronise the beating of the heart. Making it more efficient and reducing pressure within the heart.
* An ICD is a device that monitors your heart, and should it slip into a life-threatening arrhythmia it will use electricity to shock the heart and put it back into normal rhythm.
It is possible to have a Pacemaker and ICD in one unit or a Pacemaker on its own. An ICD on its own will not provide any assistance to the heart unless it is a lifesaving situation.
The latest update of my own journey is:-
October 31 2017 – CRT-ICD fitted after two failed attempts to get the wires in the correct position.
December 20 2017 – A Device Check meeting at the Hospital. I was told the CRT-ICD unit was taking the load 68% of the time however to get any noticeable benefits it had to be operating at 80%+ . I had the option of increasing the toxic drugs I was on or having a AV Node Ablation togice the CRT-ICD unit to do its job. I chose ablation.
February 1 2018 – I had the ablation. I felt no better, and my heart was left at 80 BPM and I was scheduled in to have it reduce to 60 BPM. I was told to stop Bisoprolol and Amiodaron (Yippie!!)
February 28 2018 – I was told that the CRT-ICD unit was now operating at 99.6% efficiency and that my ‘Limp Mode’ was 34 BPM. CRT-ICD unit configured for 60 BPM.
I am slowly feeling better but how much of this is the CRT-ICD and how much is the drugs slowly draining from my system, I don’t know. Amiodarone takes 100 days to drain out so I am looking forward to May !!!
Please note this is based on what has happened to me and my understanding, always talk to your Cardiologist or EP.
Regards
Ogilvie.