Hi Doctor, If you would be so kind as to answer several questions I would be very grateful. I had a prior MI in 1992 an ICD Inplant in 2001 for NSVT and
SVTParoxysmal supraventricular tachycardia (psvt) which is now under
controlControl
Control rx through meds. Last year they discovered 3/3+
mitralMitral regurgitation - chronic
Mitral stenosis
Mitral valve prolapse valve leak - 50% leakage - I go for echos every 6 mos. I recently had my 6 mos echo - I'm not sure I feel confident that this kind of test gives the best 'picture' of when to have surgery. The surgeon said if I go below 50% EF or hit 55 mm on left
ventricleUltrasound, normal fetus - ventricles of brain
Ultrasound, normal fetus- ventricles of brain enlargement (ESD) OR show symptoms - then he recommends that to be the 'time' for surgery but it is my decision. I'm presently asymptomatic.. Everything I've been reading says you don't want to wait to long or the enlargement will not decrease after surgery.
Q1. Do you feel that the
ECHOCARDIOGRAM is best test to be for indication for when surgery is necessary?
My last echo said my left
ventricleUltrasound, normal fetus - ventricles of brain
Ultrasound, normal fetus- ventricles of brain was enlarged to 51 mm - but my doc said its a +/- 5 mm so its ok as my previous one was 49 mm last July. So being just 4 mm away - I'm wondering if I'm already at 55 or perhaps I'm 44 !!
Q2.Is that normal to have a +/- 5 mm on echo tests?
Q3.Would a second opinion differ if taken from another hospital and another tech - depending on who and where you go and different echo equipment?
The surgeon said in all probability I can't be 'repaired' and will need a mechanical valve.
Q4.Does CCF perform 100% success in repairs as far as leakage?
Q5.Is it common to need mitral surgery when you have no symptoms and is that the 'best' time for surgery - before symptoms apear?
Thanks
The people I have met on line have been so helpful. It's great to be able to talk to others who know exactly what I'm talking about. I know what you mean about studying "too much", gets me even more confused too! I've had pvcs since my early 20's and they went crazy in the last 5-7 years, but still not a problem, medically. You are SOOO young to have had a heart attack! That must have been so scary! From what I understand the frequency of pvcs is not normally of medical concern, except for in rare situations (like mine, I guess..lol). For me, they led to cardiomyopathy and now I'm waiting to see what new test shows. Seems so confusing at times.
Glad to hear that one of your ablations was successful, and that you have had some success with the others. I am so fortunate that my ablations were successful. I get some "speedups", so I'll see what my doctor says next month. Yep, we've definitely gotta laughing, cuz otherwise, it would be tears all the way!
Good for you for staying on top of things....
I'm not sure if my heart is enlarged. TEE in 2000 said normal EF and no enlargement. Last year, I was so overwhelmed with tests and appointments that I kinda stopped asking my usual million questions. The report in Dec. 2002 said "evidence of a cardio-myopathic process in the entire left ventricle; EF 40%" YIKES!!! Because of some other factors, my doctor is certain (or as close as one can get) that it was from the pvcs.
I started resistance training (weights) about 6 weeks ago and I'm hoping that it will help my endurance. I used to use the treadmill, but I backed away from it because of being tired and uncomfortable. I'm working on getting back to exercising more...We have SO MUCH SNOW that I can't really walk outside, but there's always the treadmill!! Great talking to you. Email me if you want to talk more. Thanks for your exercise tip...I'll keep working on that! As far as running after the kids, nope...not any more. Now, I'm running from them...HAHAHAH!! Just kidding, they are great!!
Connie