In 2009 I had an EP Study because I had roughly 50,000 pvc's; VT runs, shortness of breath, chest pain, recurring Syncope, Hypotension, Bradycardia and some EKG abnormalities that keep showing up such as multi focal pvc's, long qt, then short qt, low voltage QRS, non specific Septal T wave changes, nonspecific T wave abnormalities, IRBBB.
Exertion & exercise makes my symptoms worse (noted on my treadmill stress test). I've fainted quite often for about 35 years - since age 9; both with and without exertion/exercise.
My EP ablated the pvc's and diagnosed me with malignant pvc's - Polymorphic VT, implanted a Pacemaker/ICD; due to long sustained runs of Polymorphic VT. A few hours after surgery, I developed PAC's and PSVT and within a few months frequent PVC's and VT came back.
I was tested for ARVD and other infiltrative disease, but my MRI was inconclusive due to wall motion degradation. I had a tilt table test that showed when they gave me nitro I had no palpable pulse and my bp tanked - dx was neurocardiogenic syncope & orthostatic intolerance. All of my Xrays and CTA shows I have Cardiomegaly and vascular crowding.
I'm confused though; why do my echo's and catherization show my EF and CM so differently? and why could an echo be technically difficult to do?
My LVIS, LVPW and EF increased yet my LVESD and LA decreased; any idea why this would happen? Should I just accept the new echo that I'm "cured" of CM, DD and my other problems? should I ask for other tests such as MUGA, TEE, CT since my symptoms have not changed?
Different cardiologists & ep's disagree with the DX of ARVD, and I just need to find out what's caused all of this so I can have my children tested if it's genetic.
Can you recommend anyone in FL to go to who may look at all of my tests I've had done and figure out what's going on with me since I do have a complicated case?
Thanks for any help or insight you can give me. (listing my test results below for reference)