Info4Mom
New member
Hello,
My name is Sean and I am here to hopefully find some information to help my mother. It's a bit of a long story, so here goes:
8 years ago my mom was diagnosed with a congenital defect of her aortic valve. It was bicuspid instead of the proper tricuspid arrangement. At the time, Mom was 64 years old. She had noticed a pronounced shortness of breath while trying to do routine activities and after a heart catheterization and TE, the doctors decided that she needed surgery to correct this problem. The whole process happened very quickly and doctors at Lancaster Regional Medical Center (in Pennsylvania) seemed to have a very keen sense of urgency to replace her aortic valve. Mom made the decision to go with a mechanical valve (I do not know the model) and the surgery was scheduled for just a few days later. The surgery did not go smoothly and what was supposed to be a 90 minute procedure quickly became a 4 hour ordeal. At some point during the surgery, the left side of her heart stopped functioning properly and required an emergency double bypass. She came through it, but it was very touch and go and she remained in the ICU for sometime. Her recovery process was very slow. Since the surgery she has routinely struggled with keeping her Coumadin levels within range and has developed diabetes. The valve has leaked ever since it was installed and that leak has increased as time has gone on. Now, routine activities like walking up 1 flight of stairs can lead to a pronounced shortness of breath.
In February, she went in for a check-up and it was discovered that she was having a high level of PVC's, literally dozens per minute. Again, she was catheterized and had an EEG. The surgeons (this time at Lancaster General Hospital), were convinced that a blockage was to blame and that she would again require surgery. No blockages were found, but she developed a hematoma at the site of her catheterization and almost bled out just a few hours before her scheduled discharge from the hospital. The doctors rushed her to surgery to repair a tear in one of her blood vessels and she was in the hospital for a total of 2.5 weeks.
Now, another doctor has apparently given her some hard facts to deal with and think about. With the way her heart valve is leaking, it is clear that outside of some unforeseen catastrophe, it will be her cause of death. As far as I know, no one can tell her if its weeks, months, or years, though. The surgeons at Lancaster General were not certain that my mom is a viable candidate for any sort of repair/replacement surgery due to her overall state of health. She weighs only about 100lbs and has what I would classify as a pretty weak immune system (she gets sick quite often). Couple that with diabetes (type II) and it makes people a bit nervous. Her new doctor has suggested that she get a second opinion on whether or not surgery is an option for her at a more well known cardiac center, such as Johns Hopkins or Penn Medical.
My question for the boards is this, does anyone here have experience with 2nd valve surgeries for repair/replacement of a mechanical valve. If so, what were they like? Second, has anyone had experience with either of the two hospitals listed above and what was that experience like. Any information you could provide would be greatly appreciated. Thanks!
My name is Sean and I am here to hopefully find some information to help my mother. It's a bit of a long story, so here goes:
8 years ago my mom was diagnosed with a congenital defect of her aortic valve. It was bicuspid instead of the proper tricuspid arrangement. At the time, Mom was 64 years old. She had noticed a pronounced shortness of breath while trying to do routine activities and after a heart catheterization and TE, the doctors decided that she needed surgery to correct this problem. The whole process happened very quickly and doctors at Lancaster Regional Medical Center (in Pennsylvania) seemed to have a very keen sense of urgency to replace her aortic valve. Mom made the decision to go with a mechanical valve (I do not know the model) and the surgery was scheduled for just a few days later. The surgery did not go smoothly and what was supposed to be a 90 minute procedure quickly became a 4 hour ordeal. At some point during the surgery, the left side of her heart stopped functioning properly and required an emergency double bypass. She came through it, but it was very touch and go and she remained in the ICU for sometime. Her recovery process was very slow. Since the surgery she has routinely struggled with keeping her Coumadin levels within range and has developed diabetes. The valve has leaked ever since it was installed and that leak has increased as time has gone on. Now, routine activities like walking up 1 flight of stairs can lead to a pronounced shortness of breath.
In February, she went in for a check-up and it was discovered that she was having a high level of PVC's, literally dozens per minute. Again, she was catheterized and had an EEG. The surgeons (this time at Lancaster General Hospital), were convinced that a blockage was to blame and that she would again require surgery. No blockages were found, but she developed a hematoma at the site of her catheterization and almost bled out just a few hours before her scheduled discharge from the hospital. The doctors rushed her to surgery to repair a tear in one of her blood vessels and she was in the hospital for a total of 2.5 weeks.
Now, another doctor has apparently given her some hard facts to deal with and think about. With the way her heart valve is leaking, it is clear that outside of some unforeseen catastrophe, it will be her cause of death. As far as I know, no one can tell her if its weeks, months, or years, though. The surgeons at Lancaster General were not certain that my mom is a viable candidate for any sort of repair/replacement surgery due to her overall state of health. She weighs only about 100lbs and has what I would classify as a pretty weak immune system (she gets sick quite often). Couple that with diabetes (type II) and it makes people a bit nervous. Her new doctor has suggested that she get a second opinion on whether or not surgery is an option for her at a more well known cardiac center, such as Johns Hopkins or Penn Medical.
My question for the boards is this, does anyone here have experience with 2nd valve surgeries for repair/replacement of a mechanical valve. If so, what were they like? Second, has anyone had experience with either of the two hospitals listed above and what was that experience like. Any information you could provide would be greatly appreciated. Thanks!