Has anyone had an insertable Cardiac Monitor?
Just curious if anyone else has a Reveal LINQ implant ?? I had one inserted in July of this year to monitor my palpitations. I have had palpitations for years but earlier this year they changed (at least for a while) and I experienced shortness of breath and pain with the palpitations.
I just think this is really cool technology.
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Ive had a loop recorder since 9/21.
I have the loop recorder because I pass out randomly with no warning at all. I do feel symptoms, (fluttery pounding, racing) but every time I reported them, they seemed annoyed. Finally they straight up told me, we only want to know if you pass out. So I would patient activate when that happened, and it showed nothing. We recently decided to have it removed, and while I’m waiting for them to set that up, I’ve begun getting red alerts in my chart. I get an automated response, but they’ve stopped answering my messages. So I guess I don’t know what’s going on, if I’m still having it removed? Or if I should go back on metoprolol. Communication would be great.
My son has had one for about 7 months. It is a Linq II. This specific one was implanted because his A. Fib is asymptomatic. It records 24/7 without him pushing any buttons. At first, I was frustrated that we couldn't access the data. But, now I am more glad than not, because we would probably be checking it ALOT. Knowing every beat of his heart is recorded is great peace of mind.
cwitton1- Has your cardiologist ever mention the possibility of Cardiogenic Syncope? I have family member that has these same symptoms. It was finally determined that Cardiogenic Syncope was his diagnosis. Is there any chance you can go to a different Cardiologist? For your safety and well-being- it sounds like this may be a good option to explore.
I had my monitor in for 3 years. I was diagnosed with Supraventricular Tachycardia. I am lean and the monitor poked through so I had it removed. It wasn't providing any additional data and was at the 3 year mark. It was a simple procedure, in part because it was so close to the surface. A small hole and they kind of "squeezed" it out.
I had my loop recorder (Linq) inserted about a month ago. I just started with a new cardiologist EP. That was a first thing he suggested. It already caught one AFIB episode and the cardiologist office called me in the morning telling me that the doctor wanted to see me to discuss further treatment.
I got one inserted June 27, 2024. It hurt like a m f'er. For 2 weeks it felt like someone had shoved a brick into my left breast and left an elephant to hold it in place. For one week it felt like I was being kicked by a horse with rusty shoes. 3 weeks post insertion, the bruising is finally gone, it looks like something took a chunk out of me, and it still "pinches" every once in a while. Most annoying is that the transmitter machine beeps in the middle of the night 3 times), last night @ 1:30 am waking me and the puppy. I have contacted Medtronic's and the providers office for how to turn the volume off or down with no response. It is very frustrating overall. Still too early to tell if it is doing me one lick of good.
I had a Medtronic Reveal Linc inserted in 2020 in New Zealand where it would have cost $35,000 NZ if I had had to pay to have it inserted privately. I was very lucky to have it inserted in the public hospital and the cost was covered by our national health system.
At the time of insertion I was taking Diltiazem 120 mg daily. At the time I asked a variety of questions of the staff but was only told to read the booklet when I got home. At that time no one here knew anything about them including my cardiologist.
I had several "events" or episodes during the next 18 months until I was prescribed Rivaroxaban and the episodes dropped to one a year since.
After I had had the device for three years I received a call from the clinic to let me know that the device was about to stop working because the battery was at the end of it's life. I was told that I would not be getting another one and asked when I could have it removed but was told patients just left them in.
That's when the fun started. I had begun to feel lumps around the device so my doctor arranged an ultrasound. Strangely the radiographer could feel the lumps but they didn't show up on the ultrasound screen.
My cardiologist said it should be removed but the surgery is risky because of infection.
I'm interested in knowing if anyone else has had this happen and would be very pleased to receive any comments to this post. Thanks in advance.