I tried metaprolol. It only made me feel really tired, and I still got PVCs. I'm hoping there is a better, more permanent solution.
Hey saw something about a BB being written, and wondering if you have been on this type of medication before? If not, you should talk to your physician about it. In your case with the adrenaline rushes, it could help cut that down alot possibly leading you to a better night. I hear you about the life part being turned upside down. Pvc's are such a battle, such a mind battle, and pretty much a life battle. I wish there was an easier way to deal with these things!! Everyone has there triggers, some knowing, some not. I hope you can try and find the right path in dealing with yours, good luck!!
I was under the impression that the insurance company has maximums or allowed amounts that a dr or hospital can charge for a specific procedure. I would assume that can vary depending on the part of the country you are in or the type of plan you have.
I may be wrong though.
I really don't think the doctors try to get the maximum payment...most of them bill by codes and there is a price list you can ask for at their office/hospital. How many of us shop around for a more reasonable price for lab tests or outpatient services? Not easy to do comparison shopping when you are in need of medical care. That said, the system is broken - costs are way to high and we the consumer get the shaft. I count my blessings that I have medical insurance and don't mind paying a small co-pay now and then.
I think the cost is what it costs...
The cath lab is expensive...
The catheters themselves, I'm told are $5,000 each - disposable.
Docs have airplanes to fly and malpractice insurance to buy...
I have good insurance, and I like the way its structured. Cheap premiums. High deductible. It forces the patient to be a consumer and consider cost. How much would your health care habits change if your deductible was $5k?
I would bet that the costs vary depending on what type of insurance you have. Also the area you live in can be a factor. The docs and hospitals will milk everything they can out of the plan. The better your insurance, the higher the cost. Would you agree?
I went in for a broken foot in June 2009 and my primary heard pvc's and what he thought was valve damage. He sent me to a cardiologist who did an ekg, echo, holter and stress test. Tests showed nothing was wrong structurally; just minor things that didn't add up to anything. (stress test had red flags)
The first EP I saw who was head of the largest heart hospital here said if I didn't have an ablation to try and get rid of the pvc's I could develop cardiomyopathy but he was positive the ablation would get rid of my problem.
I didn't quite believe him and went in for other opinions; the other drs said it wasn't as severe as the first EP said and tried me on Toprol - big mistake; it sent me to the ER in distress and they gave me a shot to try to counter act the med - after 11 hours my BP wouldn't go above 70/40 and my hr 40 so I told them to let me go since they didn't find anything other than pvc's. (red flag) the EKG showed I had multifocal pvc's and cardiomegaly (heart enlargement) another red flag
I went in to have a tilt table test before my ablation and when they gave me Nitro, my heart stopped they told me that was "rare" to have that happen (another big red flag). Then a few hours later I had an EP study and ablation which found that I had problems in the RV Apex and RVOT; and I went into long runs of polymorphic VT 3 separate times. (huge red flag) my heart stopped and the first time was really bad and almost didn't start. I think what happened during my EPS was Propofol messed with my heart rhythm.
When I woke up they explained what happened and told me they thought it was ARVD or HCM but most likely ARVD with my symptoms and that I needed to have a MRI and Cathierzation and an ICD implant.
somewhere dr's have missed the mark; one day my heart is normal then not normal and I have something benign then malignant; then normal again? doesn't make much sense...for me, I think I've had something wrong my entire life and it's just been missed and different meds mess with my heart; which is consistent with HCM or HOCM patients.
I wasn't scared about ablation; I had major surgery before and knew it would be a pretty quick and easy procedure. for most patients, ablation can be an answer and cure and may even help diagnose a problem. I think it's better to go through with it and find out you have something wrong and be in a place if something does happen like with me, at least you're right there where they can treat it immediately.