This question is about a post made last week regarding the return of AVNRT after 2nd ablation. I met with the Doc at Brigham and
WomansWomen's way last Thurs. Needless to say he was quite baffled with what I have been through in such a short time. He susspects that I may have a 3rd pathway going from the AV
nodeLymph node biopsy
Swollen glands
Swollen lymph nodes in the groin
Swollen lymph nodes under arm through the coronary sinus. He also suspects that I may not even have
SVTParoxysmal supraventricular tachycardia (psvt) based on the failed RF ablations with the multiple
burnsAirway burn
Burn, blister - close-up
Burn, thermal - close-up
Burns
Burns - resources
Eye burning - itching and discharge
First degree burn
Heartburn
Heartburn prevention
Minor burn - first aid - series
Painful swallowing that were made in the last procedure, and that what I have may be resembling. He knows that I definitely have an
AtrialAtrial fibrillation/flutter
Atrial myxoma
Left atrial myxoma
Right atrial myxoma Tach based on the last tracing with HR 300+. I will be having another EP study with hopes to finally rid myself of this nucience.
My questions are:
1. How
commonCommon cold is it for someone to have a 3rd accessory pathway?
2. Given the difficulty sometimes to ablate atrial tach, how common is it to have an AV nodal ablation and pacemaker implantation?
3. Having also had Afib and Aflutter, after having a flutterline ablation, would a pacemaker resolve this from coming back?
Thanks for any info you could offer.
I had an av node ablation and pacemaker implanted after 2 ablations, cardioversion and 4 antiarrythmics failed to stop the arrythmias with hr in the 180-250+ for sometimes days, accompanied by plummets in the heart rate when I would convert (into the 30s). Today, almost 1 1/2 years later, I still have afib (feel it less) and occasional aflutter, but the pacemaker is very helpful, along with meds, to greatly curtail the length and severity of the episodes. It has taken an emotional and physical adjustment to live with my heart that is now dependent on the pacemaker, but I am moving along.
I have many good days, some challenging ones when I have many ectopics that lead to runs of flutter/or fib, but for the most part I am doing well. I work strenuously and am much improved clinically, although it took patience and time to allow my heart to settle down after the surgery.
Good luck with whatever occurs. Whatever that is, you will live through it, adjust and embrace a new normal if that is to be.