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Hello from the other side! I underestimated how much it’s gonna hurt. But I’ll be fine. 😊

I got a #23 On-X. According to my surgeon my valve was unicuspid 😳. I consider it a miracle that my heart managed to cope for 44 years without failing.
Welcome to the other side! Glad that you were able to get things taken care of quickley.

I got a #23 On-X
At your young age, good choice in going mechanical.

I underestimated how much it’s gonna hurt
Hang in there. It gets significantly better day by day.

Please update us on how your recovery is coming along when you get a chance.
 
With the drugs and the delirium from them time seems to be flowing oddly. I'm doing breathing exercises with a small device that provides adjustable resistance as instructed by the physio. I got the urethral catheter removed yesterday, and the temporary "just in case" pacemaker today. The removal of the latter got me really curious how the leads are so steadily attached to the muscle tissue of the heart and I'll try to find more information about it.

Getting also potassium, beta-blocker, ACE inhibitor and some diuretic too every now and then because I’ve bloated 😂 and need to lose sth like 3,5 liters worth of liquid. Taking my thyroid inhibiting pill. I’ll be able to get back home one of these days, maybe Wednesday. Tomorrow I’ll get the broken teeth checked out.

Not sleeping very well though. Feeling hot, feeling cold, sweating, waking up in the middle of the night. 😵‍💫

Cheers,
Georgi
 
Regarding the valve, if I choose to focus on that and it’s quiet enough, I can follow the ticking sound. I have feelings of pulling here and there inside of my heart, especially today after they pulled out the pacemaker leads. The heart itself feels more twisty-turny, and, for exaple during the weekend, I would say I felt my pulse in the carotid area much more clearly than before. Not exactly a surprise when I’m now not having regurgitation. As long as it is not pathologic, I’ll get used to whatever I need to get used to.
 
Regarding the valve, if I choose to focus on that and it’s quiet enough, I can follow the ticking sound. ... The heart itself feels more twisty-turny, and, for exaple during the weekend, I would say I felt my pulse in the carotid area much more clearly than before. Not exactly a surprise when I’m now not having regurgitation. As long as it is not pathologic, I’ll get used to whatever I need to get used to.
its amazing how just that tiny piece of tissue in the heart can make such a difference isn't it

regarding

Not sleeping very well though. Feeling hot, feeling cold, sweating, waking up in the middle of the night. 😵‍💫

I always felt more temperature control problems post OHS, feeling cold and yet feeling damp with sweat. However you should also report this to your team because it is also (depending on intensity) a sign of something else that's not good.

Make sure you aren't being that stoic Finn with sisu.

Best Wishes
 
On this point allow me to present some readings here which may be helpful

The heart itself feels more twisty-turny, and

firstly this whole thread but if I may start with my post here.

Next you will need to strart thinking about "remodeling" (ask the surgeon and cardiologist you have about it). You will probably have significant ventricular hypertrophy and also septum wall thickening. You can read some posts here where Chuck C has made a great set of points about that.

Remember, as Dick says ... eat the elephant one bite at a time ... don't be afraid to leave "dark and hazy things" in this body of knowledge and to "take out what you need now" and come back to those details later in your cycle of new knowledge.

Time is now on your side.
 
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Not sleeping very well though. Feeling hot, feeling cold, sweating, waking up in the middle of the night. 😵‍💫
Thanks for the report. The very fact that you wrote it in a detailed and coherent manner means you are not doing too badly! :)

Everybody gains "water weight" apparently, that's normal for this type of surgery. The sleep should improve a lot when you get home.

All the best!
 
Glad to hear you are doing well. It’ll be 4 weeks this Friday since I had mine replaced also with a St Jude, and I also had a unicusp valve. The first few days are pretty rough, but after the first week or so everything starts to get a little better. The ticking is a little annoying but I only hear while trying to get to sleep, and if I move around a little it goes.
Hope everything works out well for you
 
Hey! Glad the surgery went well. The recovery time in the hospital can be rough, not to mention really boring.

You got this! Hang in there.
 
Hello,

Currently at 44, my BAV with moderate to severe stenosis and moderate regurgitation was discovered in May 2022, the first time I had heart ultrasound done in my life. I went to have it checked because a year before that my gastroenterologist mentioned that she hears some kind of murmur and recommended that I have it checked at some point, just to be on the safe side.

At that time I didn't have any symptoms, got prescribed ACE inhibitor, a statin and acetylsalicylic acid. Wasn't really happy with the meds but in the end started taking them, and continued living my life, staying active and having checks every now and then, hoping that things will continue like this for at least a decade. My last regular visit to my cardiologist was on June 28 this year and it showed pretty much the same situation like it was 2 years ago and I still continued having no symptoms whatsoever.

Then in August I started feeling hot all of a sudden, sweating a lot and definitely noticed that something's amiss because my Venu smartwatch reported that my body practically doesn't rest, I had high stress all of the time, day, night, during sleep, awake. I ran the basic thyroid tests and much to my surprise (because I had run them two months before that and they were absolutely normal) this time nothing was within the reference ranges. As a result I started antithyroid therapy with carbimazol at the beginning of September. My summer was pretty busy and I noticed that I had lost 5 kilograms without even noticing it and due to the thyroid problems and feeling tired I didn't dare visit the gym.

I live on top of a small hill. On the one side of it the slope is steep and on the other it's gentler. I started noticing that on the steep incline, which is the one I use most often, I would get somewhat out of breath and I would feel tightness in my chest, but I thought that it was because I have had hyperthyroidism for more than a month and my body was simply tired. I also started noticing that even on the genlter slope, when walking uphill I would still feel out of breath by the time I reach home.

10 days ago, on Saturday, after having done 20000 steps on Thursday in the forest, then 18000 more on Friday picking mushrooms and then 16000 on Saturday just walking slowly for three hours, I was going back home and was in a hurry for the common weekly sauna that is a usual thing in all blocks of flats in Finland. I took the steep incline and decided to go for it fast. By the time I reached the top I was heavily out of breath, but went on, I had 50 meters or so to my door. Then a bit further down the path I started seeing "stars", and my chest was really tight. I got scared and remember mumbling to myself "this is not good, this is not good". From that point on I can only reconstruct what must have happened, because I don't really remember it. I must have decided, to the extent that I was able to think (clearly) that, after all, my home is so close, I'll be able to reach it. Then apparently I have lost consciousness, fell down on the ground, first hitting my knees slightly and then my head hitting the asphalt with the chin.

Then I remember hearing "Are you okay? Do you want me to call an ambulance?" coming from a lady somewhere close. I heard it a couple of times not really understanding what's going on, then I slightly got an idea what must have happened. I managed to get up, lightheaded, and my silly reply was "Why would you want to call an ambulance?", probably still having hopes that all of this is just a bad dream and being in denial about it, to which the lady responded "You really don't look well at all". I realized there's metallic taste in my mouth, I was spitting blood and my tongue identified a fair amount of broken teeth. I got home, tried to clean myself somewhat and called the emergency number. They came and took me to the ER.

Long story short, apart from three fractures to the mandible, one at the symphysis and one on each condyle, and after a week worth of tests, the conclusion is that I've had an NSTEMI, with global ischemia (ST depressions present in pretty much all ECG leads but one), troponin also rose and came down. Luckily my ECG returned to normal and ultrasound at least shows the heart to be working fine. The stenosis however seems to have progressed in two and a half months' time alarmingly and from an AVA of 1.1 cm2 at the end of June, it is 0.7-0.8 cm2 at the moment and regurgitation seems to have also deteriorated.

Doctors are reluctant to let me go back home in these circumstances and strongly recommend that I get a valve replacement during this hospital stay. They have already asked the cardiac surgery unit to include me in their plans in one of the next weeks.

I had completely different plans for the upcoming months, I was supposed to travel three times, do lots of stuff... There was a short period of not being able to accept things as they are and being "annoyed". I think I'm past that point now, but while I was writing this post and re-enacted the event in my head (for the first time in this detail) I can identify that I'm not comfortable with it so I suppose I'll need to dedicate some time to reflecting upon it.

Now waiting for the surgeon to contact me in order to discuss what the options are.

I'm glad I've found these forums, seeing that many other people have already been there, faced challenges and overcame them, living normally and sharing their experiences. Thank you for that!
My AVA is 0,5cm. They say I don't need operation. I am not in life danger. My cardiologist say that. Somebody is crazy here?
 
My AVA is 0,5cm. They say I don't need operation. I am not in life danger. My cardiologist say that. Somebody is crazy here?
I'm definitely not a doctor so I can't really tell you whether this is indeed the case or not, BUT if multiple official sources on the internet categorize this not even as a "severe" but as a "critical" degree of stenosis, I would look for a second opinion or at least I would ask for a reasonable explanation from your cardiologist why the AVA value is interpreted contrary to common practice.

The opening area of my valve, as measured during the transesophagial echocardiography was around 0.7 cm2. In the notes from the surgery the surgeon, examining the valve directly has written: "A unicuspid aortic valve is found, gravely thickened, with a very small and stiff opening in the center".

They didn't even want to let me go back home once I was in the hospital with that AVA and insisted that I get a valve replacement during "the current hospital stay". There is no point to wait for a collapse to occur, suffer additional injuries (like me) and have the whole thing take a completely new level of complexity, that could turn out very hard to solve (i.e. any complications that can be avoided are best avoided).
 
I'm definitely not a doctor so I can't really tell you whether this is indeed the case or not, BUT if multiple official sources on the internet categorize this not even as a "severe" but as a "critical" degree of stenosis, I would look for a second opinion or at least I would ask for a reasonable explanation from your cardiologist why the AVA value is interpreted contrary to common practice.

The opening area of my valve, as measured during the transesophagial echocardiography was around 0.7 cm2. In the notes from the surgery the surgeon, examining the valve directly has written: "A unicuspid aortic valve is found, gravely thickened, with a very small and stiff opening in the center".

They didn't even want to let me go back home once I was in the hospital with that AVA and insisted that I get a valve replacement during "the current hospital stay". There is no point to wait for a collapse to occur, suffer additional injuries (like me) and have the whole thing take a completely new level of complexity, that could turn out very hard to solve (i.e. any complications that can be avoided are best avoided).
Yes. I will get second opinion. I have TEE and MTSC coronarography in ten days. I was in urgent medicine too and lead cardiologist(woman) also measure on ultrasound AVA o,5cm and AV velocity 5,3 m/s. Rocket fast! And they send me home. They said you have time to check that.
Not urgent so much. I swear.

My friend have OPS mitral valve,not aortic 2 years ago. He was been in dentists two months to repair bad teeth, first condition for operation?
How your doctor 'insist that you stay for operation imidiatly without and preparation? That sound good. Why they not tell my that?
 
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