I am writting about my husband who is 45 years old without any symptoms and was told that he has
benignBenign ear cyst or tumor
Benign positional vertigo PVCs in 2001. Later (2004) one of our friends (MD) told us to do
holterHolter monitor (24h) and echo which showed 20000 uniform PVCs and echo was read as having low
normalNormal saline flush EF. Exercise stress test was fine and PVCs disapeared during exercise which we were told is a good sign. Stress echo was read
normalNormal saline flush. We repeated several
holterHolter monitor (24h) all showing between 15000 to 22000 PVCs (same type). He also had two MRIs read as low probability of ARVD and no evidence of scar tissue (again told this is good?). Last november his EF dropped to 45% and his EP doc decided to do ablation, saying PVCs may be causing cardiomyopathy. Ablation was succesful and now have only 100 PVCs per day. However, EF, 3 months later, did not show significant improvement. Still 40-45%. He is on
coregCoreg
Coreg cr and lisinopril.
Is this a bad sign? Did the PVCs caused irreversible damage? Is it possible that EF will improve? Was the cardiomyopathy causing uniform PVCs? I read that may be the cause but the PVCs are usualy diferent types. Would the MRI show scarr tissue if he had cardiomyopathy? Have you seen any similar cases? What is a long term prognosis of someone with EF of 40%?
Thank you
This is a very good and interesting question, Glad your husband's ablation was a success. I've read also that frequent PVCs usually above 15-20% of your total heartbeats for along period of time can cause cardiomyopathy and that ablation is usually recommended for these rare individuals ( usually successful from what I gather). I think 6- 12 months is generally the amount of time in which one would see an improvement in EF, though could be longer or shorter give or take a few months, this is just my understanding I'm not a MD. A also gather that an EF of 45% is just a mild decrease in heart function and if no other underlying pathology is present ie. dilation, CAD, etc. would be probably regarded as "normal" for that individual unless it deterioates or some other underlying pathology presents itself.
Yes, the EF of 40-45% is not horrible but when you read about cardiomyopathy, the disease is chronic and progressive with high mortality. For a 45 year old that means shortened life. The worse thing is there is no known cause and the treatment just slow the progression.
However, there are several reports in medical literature about PVCs induced cardiomyopathy. Most reports are on patients that got better after ablation.
The question is how many people have PVC and cardiomyopathy (whatever came first) and are not getting better (with or without ablation) and are not reported in the literature (so even MDs don't know). My husbands first MD rejected my concern and we looked for another PCP who eventually ordered echo.
My suggestion to all of you with frequent PVCs is to have echo and holter done on a yearly basis.
It has taken me over a year to get an EF back to 60% and I am having another echo in a wk or so. I have PACs and PVCs (which I initally felt alot but not so much now, when they did the last holter, I had thousands of them, but felt very few - I am lucky in that I do not think its my last breath either, so that helps when they do happen and I feel them). I think its mostly about time and as the Doc said, maximising the meds for the best results, but you cannot expect miracles initially. We live at altitude so am not sure if that impacts recovery time, but I suspect so, as when I went to almost 10 000 ft a few wks ago, I REALLY felt symptomatic.
I was 41 when dx'ed and had lots of other serious health issues emerge too, of a myopathic nature. I totally refuse to believe that this issue will shorten my life, I have way to much nagging of my hubby planned and family events I plan on seeing, to check out any time soon :-).
I hope that your hubby is back to his old self soon and in the meantime, keep your expecations realistic and think positively, I am convinced that helped me/us get through it all.
Fiona
I was having 20,000+ pvcs per holter exams when my EF dropped to 40%. My pvcs were multiform, but it appeared that there were 2 dominant foci. In 2003, I had 2 successful ablations. It took about 6 months after the 2nd procedure for my EF to return to normal. After 3 years, it's still 55-60.....I also took Lisinopril. The doctor wanted me to take a BB too, but it turned out not to be necessary. Today, I'm still taking the Lisinopril and a BB as needed for really bad pvc days.
Hope he continues to see improvement!!
connie
did you have echo done at 3 months post ablation? If so, what did it show?
How many PVCs do you have now?
Also where were your foci? Left or right ventricle? Most common 'benign' ones are in RVOT (right ventricular outflow tract).
Thanks
Mary
I have no idea how many pvcs I have now, I know it's nowhere near what i had before....probably hundreds compared to thousands/day. t been a problem at all.
My first ablation was for RVOT and the second was for LVOT (they initially thought it was a second RVOT foci, but turned out to be left sided).
Does your husband have another echo scheduled?
connie
Yes, we will have another ECHO in few months. I guess we just have to live with uncertainty.
Thanks for your response
Good night and good luck.
i really dont like to hear that our mortality rate is low, or that our life will be shortened i have two small children and i would like to be around for a long time to watch them grow... the doctors say with treatment this can improve.. so thats what im hoping..