D
dwfreck
Everyone,
This is a long one (I tend toward wordiness), so grab a cuppa something...
Immediately following my angiogram on 11/18/03, my cardiologist gave me the name of a surgeon, as he had said he would. We didn't meet the surgeon that day because he wasn't available, but we did meet with a representative from the hospital who worked closesly with the surgeon. The representative explained the basic valve replacement options and my likely suitability for each, then gave us a brief sales pitch for the hospital's cardio unit. I REALLY like and respect my cardiologist, we've had excellent experiences at the hospital (child birth, endoscopy, catheterization), and the hospital rep did a good job, so my wife and I had high expectations for our first visit with the surgeon.
Today my wife and I had our first (and likely last) meeting with the surgeon. We spent nearly forty-five minutes talking to the doctor and came away feeling like we hadn't learned anything we didn't already know (other than needing to be aware of vitamin K intake when taking Coumadin).
We discussed my case history, symptoms, and current health status, and the sorgeon concurred with my cardiologist's opinion that it was time to replace my aortic valve, but that we had a few months to work out the details. For some reason, he didn't have the results of my angiogram.
He asked me if I had picked a valve yet. I said, "no," and we discussed the options that were available: mechanical valves of various designs, tissue valves of various origins, and the Ross procedure. We discussed the basic tradeoffs among the options: Coumadin vs. not, lifetime durability vs. 10-15-year durability, one AVR surgery vs. two or more AVR surgeries, relatively simple operations vs. a really complicated operation. There was nothing new here; I've read and heard the basics and discussed them with my wife.
I felt like I had to drag information about homografts out of him. He barely acknowleged their existence, said we would need to measure the size of my aortic annulus via MRI (which I already knew), and then expressed skepticism that a homograft would be available. I understand that the dynamics of donor organs can lead to scarcity of the correct homograft, but his response left me with the impression that he thought the homograft would be a big inconvenience (mostly for him).
I also felt like I had to drag information about the Ross procedure out of him; his first response was that he didn't perform the Ross procedure, but one of his partners did, and that it was a relatively rare procedure in the Cincinnati area. When I pressed him for details, he said my pulmonic valve was probably bicuspid the same as my aortic was. I told him that I would like to find out whether it was or not, and he suggested a CT scan. I told him my cardiologist had suggested an MRI. The surgeon said he would need to ask the radiologist if an MRI would detect a bicuspid pulmonic valve.
I asked for more details about the tradeoff between Coumadin-for-life with a mechanical valve and a second AVR surgery with a tissue valve, and the surgeon responded that he thought the risks of serious medical problems or death were about the same over the course of a lifetime. This was the first time I had ever heard anyone express that particular opinion, and wasn't the answer I was looking for. I pressed him for details about quality-of-life concerns with Coumadin, and he was noncommital, other than saying I would have to watch my diet to regulate my vitamin K intake. This was all new information, but wasn't the answer I wanted.
I specifically asked which valve or procedure he would recommend to me considering my age (39), expected longevity (70-80?), medical history (moderately healthy, except for AV problems), desired post-operative lifestyle (I'd like to ski, but don't want to bleed out on the slopes), and career (I'm a computer programmer). He told me that he uses tissue valves in his other patients, but did not elaborate on why, and suggested I make my own choice. Once again, this was new information, but wasn't the answer I wanted.
He did a brief examination (checked pulse, listened for my murmur in various places), then concluded our visit, with a vague promise to schedule an MRI to measure my annulus and/or image my pulmonic valve.
Add to this the fact that when I arrived at the office, ahead of my scheduled appointment time, I discovered that I wasn't "in the computer," meaning that my (imcomplete) records had shown up, but I wasn't on the schedule and the fact that the receptionist couldn't process a credit card transaction for my $10 insurance copayment, and I was thoroughly, completely, and in all other ways, unimpressed and underwhelmed by my visit. My wife feels exactly the same way.
So, there you have it.
Now, give me a sanity check: Is my (ex-)surgeon an idiot, or is it just me?
I walked into the office with a confirmation letter from the surgical practice and a set of first-visit paperwork; shouldn't I have been on the computerized schedule?
My cardiologist and the surgeon's representative both said the surgeon would get my angiogram results; shouldn't my angiogram results have been there (angio done on 11/18)?
The surgeon is part of a large practice, appears to be in his mid-forties, and was recommended by my cardiologist; shouldn't he have been able to discuss, in greater detail and based on his surgical experience and knowlege of current trends and technology, all of the relevant options, their advantages and disadvantages, the appropriate diagnostic procedures to determine my eligibility for a given option or procedure, and its suitability for my personal situation?
I'd like to have the "Which valve/procedure should I pick?" discussion some other time, so please limit your responses to my and the surgeon's relative sanity, intelligence, and doctor-patient relationship skills.
By the way, I'm calling my cardiologist tomorrow to tell him what happened and ask for another surgical referral.
This is a long one (I tend toward wordiness), so grab a cuppa something...
Immediately following my angiogram on 11/18/03, my cardiologist gave me the name of a surgeon, as he had said he would. We didn't meet the surgeon that day because he wasn't available, but we did meet with a representative from the hospital who worked closesly with the surgeon. The representative explained the basic valve replacement options and my likely suitability for each, then gave us a brief sales pitch for the hospital's cardio unit. I REALLY like and respect my cardiologist, we've had excellent experiences at the hospital (child birth, endoscopy, catheterization), and the hospital rep did a good job, so my wife and I had high expectations for our first visit with the surgeon.
Today my wife and I had our first (and likely last) meeting with the surgeon. We spent nearly forty-five minutes talking to the doctor and came away feeling like we hadn't learned anything we didn't already know (other than needing to be aware of vitamin K intake when taking Coumadin).
We discussed my case history, symptoms, and current health status, and the sorgeon concurred with my cardiologist's opinion that it was time to replace my aortic valve, but that we had a few months to work out the details. For some reason, he didn't have the results of my angiogram.
He asked me if I had picked a valve yet. I said, "no," and we discussed the options that were available: mechanical valves of various designs, tissue valves of various origins, and the Ross procedure. We discussed the basic tradeoffs among the options: Coumadin vs. not, lifetime durability vs. 10-15-year durability, one AVR surgery vs. two or more AVR surgeries, relatively simple operations vs. a really complicated operation. There was nothing new here; I've read and heard the basics and discussed them with my wife.
I felt like I had to drag information about homografts out of him. He barely acknowleged their existence, said we would need to measure the size of my aortic annulus via MRI (which I already knew), and then expressed skepticism that a homograft would be available. I understand that the dynamics of donor organs can lead to scarcity of the correct homograft, but his response left me with the impression that he thought the homograft would be a big inconvenience (mostly for him).
I also felt like I had to drag information about the Ross procedure out of him; his first response was that he didn't perform the Ross procedure, but one of his partners did, and that it was a relatively rare procedure in the Cincinnati area. When I pressed him for details, he said my pulmonic valve was probably bicuspid the same as my aortic was. I told him that I would like to find out whether it was or not, and he suggested a CT scan. I told him my cardiologist had suggested an MRI. The surgeon said he would need to ask the radiologist if an MRI would detect a bicuspid pulmonic valve.
I asked for more details about the tradeoff between Coumadin-for-life with a mechanical valve and a second AVR surgery with a tissue valve, and the surgeon responded that he thought the risks of serious medical problems or death were about the same over the course of a lifetime. This was the first time I had ever heard anyone express that particular opinion, and wasn't the answer I was looking for. I pressed him for details about quality-of-life concerns with Coumadin, and he was noncommital, other than saying I would have to watch my diet to regulate my vitamin K intake. This was all new information, but wasn't the answer I wanted.
I specifically asked which valve or procedure he would recommend to me considering my age (39), expected longevity (70-80?), medical history (moderately healthy, except for AV problems), desired post-operative lifestyle (I'd like to ski, but don't want to bleed out on the slopes), and career (I'm a computer programmer). He told me that he uses tissue valves in his other patients, but did not elaborate on why, and suggested I make my own choice. Once again, this was new information, but wasn't the answer I wanted.
He did a brief examination (checked pulse, listened for my murmur in various places), then concluded our visit, with a vague promise to schedule an MRI to measure my annulus and/or image my pulmonic valve.
Add to this the fact that when I arrived at the office, ahead of my scheduled appointment time, I discovered that I wasn't "in the computer," meaning that my (imcomplete) records had shown up, but I wasn't on the schedule and the fact that the receptionist couldn't process a credit card transaction for my $10 insurance copayment, and I was thoroughly, completely, and in all other ways, unimpressed and underwhelmed by my visit. My wife feels exactly the same way.
So, there you have it.
Now, give me a sanity check: Is my (ex-)surgeon an idiot, or is it just me?
I walked into the office with a confirmation letter from the surgical practice and a set of first-visit paperwork; shouldn't I have been on the computerized schedule?
My cardiologist and the surgeon's representative both said the surgeon would get my angiogram results; shouldn't my angiogram results have been there (angio done on 11/18)?
The surgeon is part of a large practice, appears to be in his mid-forties, and was recommended by my cardiologist; shouldn't he have been able to discuss, in greater detail and based on his surgical experience and knowlege of current trends and technology, all of the relevant options, their advantages and disadvantages, the appropriate diagnostic procedures to determine my eligibility for a given option or procedure, and its suitability for my personal situation?
I'd like to have the "Which valve/procedure should I pick?" discussion some other time, so please limit your responses to my and the surgeon's relative sanity, intelligence, and doctor-patient relationship skills.
By the way, I'm calling my cardiologist tomorrow to tell him what happened and ask for another surgical referral.