The key to any successful
cardiacCardiac catheterization
Cardiac tamponade
Left heart ventricular angiography surgery is the experience of your surgeon and their preference for
valvesHeart valves
Heart valves - anterior view
Heart valves - superior view ( bioprosthetic vs. mechanical ) or repairs ( the Ross or David procedure ) in your case.
The stentless valve has far more experience in Canada and is used less extensively in the U.S. You may want to discuss specifically with your surgeon their experience, pump times and long term efficacy with this particular valve. It is likely that you will need a combined procedure and a homograft may be another option to consider.
If you would like additional information or want a second opinion, that can be arranged through the number listed below.
Best of luck.
I have downloaded some information about the porcine stentless valve and talked with 5 surgeons, two of which use it practically exclusively when they cannot use the Ross procedure.
The other three use the bovine pericardial valve when not using the mechanical valve and only do a few Ross, mostly in children.
The Clinical trials in Canada and Europe seem very favorable over 8 years which is probably why the FDA approved it here. But the installed base here in the US is still small and there are no long term numbers here yet. It really is up to
If you have not already tried it, and if you want further information you can find some by using a search engine and typing in 'porcine stentless valve'.
It sure looks highly efficient but the surgery and by pass time
is longer than the bovine pericardial implant.
Your surgeon will not offer much if any choice since they choose
the valves they are most proficient with.
This is what I have learned through experience: You must have the very best surgeon your insurance will let you go to. If at all possible, I highly recommend the Cleveland Clinic. They have the best surgeons. I had my mitral valve repair there with Dr. Cosgrove. The more skilled your surgeon, the less chance of complications. I was never asked what kind of valve I preferred in case of a replacement, but told to trust that Dr. Cosgrove would make the very best decision for me. If you want a second opinion, please go to the Clinic. Just my two cents worth.
Thank you.
Noticed you are seeking info about porcine stentless valve:
Try:
http://www.ccf.org/heartcenter/physinfo/cconsult/fall95/
valves.htm
A statement comparing this valve may be of interest to you.
I'M BACK TO HELP SAVE THIS SITE IF NEED BE...LET ME KNOW ***@****
Remember to take care of yourself...I know it's hard, but go ahead and be a baby for a little while. You deserve it, and your body needs lots of time to heal.
my best wishes for your continued excellent recovery are traveling to you on the internet tonight!
shannon
I'm not a doctor, but what I've been told is that you should have regular checks by a cardiologist, along with regular echocardiograms (annual). I have a valve ring and a PFO patch,a and have been told by my doc to plan on coming in to see him once a year, once I pass the one-year mark for surgery (next month!).
However, if you are having cardiac symptoms of any kind, such as shortness of breath, easily fatiguing, weird rhythms, etc., you should make an appointment to see the cardiologist relatively soon.
Hope this helps. My option, if the docs were unable to fix my valve, was a mechanical, and I was told to expect it to last a long time -- like 15 to 20 years, or even my lifetime (I'm 45).
take care.
shannon
Thanks for posting your experiences for the rest of us. Have you completely recovered from the mini stroke?
After considerable reading,investigation and consideration I have asked for the homograft also. I am scheduled for surgery at the CCF on 2/29. Can you tell what a "HUST LOPRESSOR"
Thanks,
Steve
toronto general. He did the David procedure using a porcine valve he also replace my replace my pulmonary valve with a pig valve it's been my third opertion. I have tetralogy of fallot with absent pulmonary which i was born with. good luck with your surgery
It's nice to know we have a place to go for questions. I applaud all of you who have been there. May God Bless You All. I can be reached at ***@**** or this site. Thanks
And to Shirlene, ask your Dr. what options you have? Ask him what his specialties are. Some Dr. dont even do some procedures, and some have had bad results with some procedures that others do all of the time with great results. I just want you to keep your mind open and dont feel like you have to do what 1 Dr. tells you. If you dont feel right, get a second opinion. Remember this is a matter of life and death to you. YOURS. You can contact me at ***@****
TO HARVEY: Keep us posted about how you are doing also...good luck. I can tell you it just keeps getting better...I am still having trouble believing how great I am doing. As somebody said to me, just keep checking back and help out the new people who are just starting their journey. I can so plainly remember how terrified I was and how much it helped to talk to all the great people who nurse maided me through the fall.
Jean
Thank you for all your comments and the support you provide each other. Unfortunately, as you know, physician support on this forum has been cut back so it is important that you all provide whatever additional support you may to each other.
thanks again for utilizing this forum!
TO JEAN: Glad to hear your hand is getting the motor skills back. Do you have any idea what caused the mini-stroke you had?
I never made it for my scheduled surgery at the CCF on 3/1 because my body decided to unload a kidney stone on me and that derailed me for about 1.5 weeks because it wouldn't pass and required surgery. I'm now shooting for 4/5 and, at this point, I just want to get on with it.
Regards
The word on my stroke is that they aren't sure if it was a stroke. They (neurology at the Cleveland Clinic) did an MRI the third day and found a spot that could have been the site of a stroke (apparently blood clot as opposed to calcification from the old valve) but it was healing already and they could not say for sure THIS IS IT. I had been warned before surgery and had read that with the calcified valve and the change of clots during surgery a stroke was always a variable.
Anyway I would say I am 90% recovered now...just need to work on strengthening my hand and a little more fine motor control.
Went to my cardiologist Friday and he added Finestril (spelling) to my Lopressor for the blood pressure. It is still higher than either of us like. First day on the med. it dropped to the 120 to 135 range. I am eager to get this settled and off meds and back to better than normal...my dad at 77 takes no meds at all --just a vitamin pill a day. I feel great though. Am walking 50 minutes a day three or four times a week, doing chores, even horsing grain bags and hay bales around again and not hurting from it at all. Only take Advil (one pill) every so often -- some days not at all, others one or two times.
I would like to hear from any of you who had to work on your pb after surgery...my never used to be a problem.
Jean
Jean, Im glad that your feeling better and Im praying for your complete recovery. Sometimes it seems so tough, but I think if we didnt go through with all this we may be gone.
I do not try to pressure people to choose a bio or a mechanical valve. I'll just tell you the thought process I went through when I decided on a homograft.
I did not want to mess with coumadin. I farm and I know that coumadin is Wayfarin and that is a rat poison...that freaked me out. I have had cancer and done the blood testing every week routine and didn't want to do that. I also love and could not be without fresh or cooked green veggies, and I like wine with dinner. In my opinion what I read about the whole coumadin thing, I did not want to go that route. Also I am very physically active and did not like the restrictions and risks of the mechanical. And besides I heard from so many people who had a mechanical "because it lasts forever" and like you found that it did not. In fact I know a gentleman who is on the third mechanical in 18 years. Also I figured that in 20 years who knows what research will bring us...do you know the homografts may last longer (or shorter, I know) its just that now we know they will last 20 years if all goes well. To me the risks of the coumadin and the mechanical valve were greater than those of the homograft and resurgery in 20 years more or less.
But I will restate , that I think each individual needs to do their own research and settle in their own mind. You get to live with it.
If you have problems with blood thinners I would recomend a tissue valve. This is what I have and I dont have to take any. Also you have proven that there is no guarantee how long a mech. valve will last.You only got 20 years out of it. So no matter which one you choose, you, in all likely will have to have another surgury at some time anyway. Why not go tissue and releive some of your ongoing problems.