Once an ICD always an ICD???
My husband had a mild M.I. and cath w/ two DE stents to the LAD Dec. 2004 at age 55. His father had died at 39 after what he thought was two weeks of arm pain from lifting his father's casket, but apparently it was a M.I. as he died in his doctor's office when he developed chest pain the day he died. My husband's resting heart rate pre-M.I. was betw 60-65 bpm. After the cath, he went home on Plavix, aspirin, Toprol, and cozaar. He'd already been taking Lipitor for a decade, oh and they added Zetia. He took the Plavix for 365 days at his doc's suggestion. A few weeks prior to the one year mark, we called to reconfirm the Plavix cessation at 1 year. He stopped taking the Plavix, waited seven days and then got his teeth cleaned for the first time all year. 16 hours later he awakened to a funny feeling and I raced him to ER. He went into v-tach and v-fib and sudden cardiac arrest within 10 minutes of getting to the Er. His heart was defibrillated back and he was transported to the heart center from our local small community hospital and went into the cath lab again. Doctor found one of the two DE stents had collapsed on one end, and he found a small clot. Put in a third stent and shored up the other. Was sending him home the next day but wanted a 64 slice CT first to check things out. Well, that started the dominos to fall. They discovered in this four color glossy photo image that there was some LVH. His ejection fraction was 80% though, and the LVH was there and revealed on echo the year before and nobody noticed/mentioned any issue. We told the doctors that his mom and sister both have it too without incident/issue/complication. Well, after keeping us on ice for several days while the EP returned from Christmas vacation and we rotten in the hospital, the decision was made to put in an ICD. We felt it was reasonable to be his 'paramedic onboard' so to speak. NO EP study was done. Just a team of interventionalists met and decided that he needed this ICD. So, we're now on month 23 without incident. No shocking needed so the thing hasn't fired. It has, however, paced him constantly...last interrogation shows 72% of the time it's ramping UP his heart rate. I hate Toprol and believe it's the culprit. He was on 100 mg and they finally let him reduce that by half to 50 mg and added amlodipine, and the pacing went from 64% to 72% and they had switched him to hyzaar. His BP at home is normal. At the doctor's office it spikes to 140/90. What's up with that? Adding insult to injury, we learned Oct. 15 about Medtronic's removal of the Sprint Fidelis lead off the market, and yes, his leads are those. So, on the 30th we went in and the Medtronic rep reprogrammed the sensor alarm to beep sooner rather than later if there is a malfunction or lead integrity issue. Lovely. Now we have the elephant in the room. There has no been an arrythmia requiring shocking in 23 months that the device has been in...the apothecary he's on isn't working well enough in the doc's estimation at keeping the blood pressure low enough, but the damn drugs make his heart rate so low that the pacemaker has to work constantly. Now what do we do? Wait for the lead to fracture or the battery of the device to wane and die. Then we'll be faced w/ what to do in probably four years time. Is it reasonable to not replace the device with an ICD but just use a pacemaker? Is it reasonable to remove the device, cap the wires, and be done with it in four years providing he hasn't had an arrythmia in that time? That would mean six years without an issue. Could we tweak the medications down and start over? He quit smoking when they put him in that first ambulance in 2004. The Toprol has made him gain weight, along with the quitting smoking, but he started exercising (treadmill and exercise bike) after cardiac rehab training and has no luck shaking off weight. Tried 1200 calories a day, good calories only, and 5 days a week 1 hr walking and biking minimum and lost 6 pounds after a 5 week diet. He's 6'3 and weighed 196-200 when the first M.I. issue happened. He's never had a weight problem. He sleeps at the drop of a hat now. He feels side effects, top to bottom on the list. We have an apothecary going into him and for what? Yes, Plavix for anti-platelets so those stents don't reocclude. Aspirin too. I suppose the Lipitor and Zetia are pertinent, but I believe fish oil and oat bran could work just as well, and did get his ratio better and cholesterol down 100 points 20 years ago when we started on this journey to fight his genes. How realistic is it to just remove the ICD and cap off the potentially faulty leads and use medication to ward off v-tach/v-fib instead of the device? The risk of perforation outweighs the risk of fractured leads right now, right? Shouldn't he start over with all this medication? I feel like he's WAY OVERMEDICATED and it's not working for the BP in their eyes, so why take it all? Nobody believes us when we tell them that his BP is normal at home. What do I need to do videotape the process here? Probably. I am ticked off. The cardiologist who did the second cath never believed my husband needed the ICD but didn't tell us that. The group mentality was that his father had had SCA and once they NOTICED the LVH they decided that was enough evidence to warrent the ICD. But, no tests were done while we rotted over the holiday time, and by the time they told us that was the decision, we were like, just do it and get us the hell out of here so we can go home...Have you ever had a patient who had his device removed under similar circumstances? If the device never fires, it is reasonable to not replace it when the current device's battery dies? Have the Medtronic leads fractured that are there for pacing function, or just defribrillating?