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Welcome to the Heart Forums!! Hope you are finding lots of good information in the current and archived posts.
I'm not real familiar with BAV, but it seems to me that I have heard "5" is the magic number. Sounds like everything is stable and you're doing well. Be sure to let your doctor know if you have any change in symptoms between appointments.
I am in the middle of a surgery determination with similar conditions. I have a BAV with aortic dialation. My echo in October 2007 was 4.9. My last echo (April 2008) indicated an aortic root measurement of 5.3 cm with moderate reguritation. Yesterday, I just had a cardiac CT scan and should have the report in the next five days. I am also told the magic number is 5. I haven't been specifically told this but am assuming an aortic root replacement is probable with the valve replacement. My cardiologist is going to refer me to the surgeon. I am nervously looking at my valve replacement options as I am 53 and do not wish to repeat any such surgery when I am 70. I am also nervous as I have some spinal issues that might require surgeries in the near future and I don't want to be playing with the possibility of strokes. Seems like a catch 22.
I'd also like to hear from anybody with similar symptoms or success stories. One question, how secure is an aortic root repair and how long will it last?
I am 39 years old and also have a BAV, however with moderate regurg and an enlarged ventricle and my aortic root is only 3.5cm (the high side of normal) and I have good ejection fraction (65%), I have been very active my whole life so it was a bit shocking to learn. One thing that I have learned is that anyone with this diagnosis should be sure to have a CT or MRI of the entire aorta because it is apparently not just a valve problem, but is now being considered a connective tissue disease that affects the medial layer of the aortic wall, making it weak and therefore prone to aortic aneurysms or dissections - mainly in the ascending aorta, but could be anywhere. Another factor involved is people with BAVD are more prone to brain aneurysms and some other disturbing things. (Ugh!) I'm no expert, but just kind of paraphrasing what I read. I just had my first echo in Jan and a CT with contrast in Feb and I went to a cardiologist today to get prescriptions for my 2 children (2 and 4) to have echos done because it is hereditary. The cardiologist also ordered a stress echo for me because I am having some chest pain with exercise and I read on this forum that another guy had a stress echo, so I suggested it to the cardio and she seemed to think it was a good idea (least invasive).
A great and informative site to check out is the bicupid aortic valve foundation - tons of info ( a little scary at first, but in a supportive way) and also the cedars-sinai medical center in LA - they have a thoracic surgeon there that more or less specializes in this and he has a page of FAQ about aortic valve and aneurysms, etc. Let me know what you think if you check it out, this is all new to me and I am doing everything I can to be proactive without over-reacting....A delicate balance!
Sorry I couldn't offer any real experiences, but I think these 2 websites can answer a lot of questions.
Good Luck!
Welcome to the Heart Forums!! Hope you are finding lots of good information in the current and archived posts.
I'm not real familiar with BAV, but it seems to me that I have heard "5" is the magic number. Sounds like everything is stable and you're doing well. Be sure to let your doctor know if you have any change in symptoms between appointments.
connie
I'd also like to hear from anybody with similar symptoms or success stories. One question, how secure is an aortic root repair and how long will it last?
upchurch131
A great and informative site to check out is the bicupid aortic valve foundation - tons of info ( a little scary at first, but in a supportive way) and also the cedars-sinai medical center in LA - they have a thoracic surgeon there that more or less specializes in this and he has a page of FAQ about aortic valve and aneurysms, etc. Let me know what you think if you check it out, this is all new to me and I am doing everything I can to be proactive without over-reacting....A delicate balance!
Sorry I couldn't offer any real experiences, but I think these 2 websites can answer a lot of questions.
Good Luck!