Stent For Coarctation Of Aorta
Sep 12, 2009
I was diagnosed very late with this condition. An acute GP noticed the murmur and was not convinced that all was normal. Test after test later it was confirmed. Months later i had a stent fitted which is 4cm x 2cm, I was not warned about the amount of bruising or the pain in the legs, 4 months later i am still having pain in the groin and the che chest. The cardiologist does not know why I have this pain that travels from my chest to my back and left arm. MY left leg feels heavy and numb down to the foot which is freezing cold at times again. I have started feeling tired and fed up with the whole ordeal. Yes i know i needed this procedure but through choice i would never have had it - my active happy go lucky lifestyle now revolves around this. When i get ill My poor GP has to send me into the hospital as they are not well versed with this condition. Can anyone tell me when will I feel well and strong again. Do you get back to normal? The hospital and the doctors have been wonderful but they just do not have the answers. They think it could be damage due to the surgery but not life threatening so at least that is something to be cheerful about. I would love to hear from other people that have undergone similar treatment.
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Has anyone ever had coarctation of the aorta (where the heart squeezes and one feels pressure in arms)? i got this feeling last sunday and a little later felt slight pressure in my left eye. Has anyone has eye pressure due to anxiety/stress? if yes, what have the implications been? i am concerned.
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How much time a patient of "coarctation of aorta" & " transposition of great arteries" can live after the success operation of an arterial switch.......
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About a year ago, I had a kidney stone, and stent put in. I thought the stent would help me pass the stone. The Dr. said that wouldn't happen, removed the stent 6 weeks later, saying he thinks I still have it. To my knowledge I have not passed a stone, people say if I did I would feel it. I am now having pain, like a kidney infection, am a little worried it could be this stone. The Dr. said it would make me really sick if I don't pass it. It does hurt on the left, where the stone was located, but not like before. I don't have insurance and can't afford another ultrasound. has anyone passed a stone with stent in place? I think I passed it when I had the stent and just have an infection.
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I had my first kidney stone in February of this year. I had lithotripsy twice on my right side and also a stent. The stent was removed after three days. I have had a constant stabbing pain where the stent once was. I have seen many different doctors and been to the ER several times. Each CT scan has come back negative for more stones and doctors cannot find a reason I am still in pain. Anyone have the same problem?
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For years I have been suffering with a pulsating stomach and ibs. That's what the doctor said it was, being that the scan I had done showed up nothing so the doctor put it down irritable bowel syndrome.
In May this year I went for an endoscopy and colonoscopy. A couple of biopsies were taken.
The results were normal, apart from a hiatus hernia and anaemia, the anaemia they put down to the fact that some time ago I was taking anti-inflammatory tablets for arthritis. On a course of iron tablets for the past three months.
Last Thursday I went for my blood test result, and I mentioned about the pulsating in my stomach. She told me t lie down on the bed while she felt my stomach. She told me that it was the aorta pulsating.
My stomach drives me nuts especially in the evening when I am Sat down.I don't know if the pulsating is due to the ibs or the hernia or both.
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My younger sister aged 50 was diagnosed with TAA of 5.1 cm in January and operated in February due to her small frame. She is recovering well which is encouraging. I have been meaning to go and have a check myself but kept putting it off. I went to my GP 2 weeks ago and he immediately picked up a murmur. Echo followed by a CT scan confirmed I also have an aneurysm but mine is still at 4.27 and I am 55 years old. Clearly we have a genetic disposition but mine is growing more slowly (so far) . I am in shock and still cannot get my head round it. I am fit, practise yoga, follow mainly a vegetarian diet, don't smoke, hardly drink and do not have high blood pressure. I am now now in 'watchful waiting' and will have another CT scan in 6 months time. I have been advised to take Beta Blockers and was wondering how patients react to them. I have a professional job in sales and need to keep my energy up. I have off course been considering giving up work but sitting at home waiting for my aneurysm to grow will not help me. I would also like to know if aneurysms always grow and if I need to accept that mine will be bigger by the time I have my next CT?
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So I am a 34yo male and I was having palpitations and asked the dr to do a work up so he did an echo and a sonogram of my aorta to check for aneurysm. The echo came back good no issues and there was no aneurysm or evidence of one my measurements were all good. However the report said that plaque was found in all the areas of my aorta ascending descending and mid and in my right and left iliac arteries. The doctor said this was unusual and abnormal for my age. I haven't got to actually talk to him it wrote it on the report that I got. I don't have a follow up for about 1 month and I'm curious what the outlook is on this. I smoked for a couple years when I was 18 and completely quit. I have always been somewhat active(not sedentary) the last 3-4 years I have been lifting weights and running I weigh 220 and I'm 6-3 somewhat built. I look and feel healthy? I'm kinda thinking that I can't live a long life anymore?
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My 21 year old brother was at the heart doctor today, they told him he had an enlarged aorta. When he was 5 he had open heart surgery for a hole in his heart. Today was supposed to be just a regular check up for his old condition but they found the enlarged aorta. I'm sorry that I don't know much information about his original condition or much of anything else but I get everything passed on from my mother and she's pretty upset with the news. Apparently the doctor is not very worried about this and says that he needs to come back in a year for a follow up. This to me does not seem right....seems they need to maybe look into this further instead of sending him on his way. Any outlook on this? He has always been an athlete and is an high jumper for Washington State University (went to Pac 12 this year) so he is in really great health. I would really like to console my mother and give her some good (better) news.
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My Dad had a Stent placed after a heart attack one week ago. He has been having jaw pain all day. Should we be worried?
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My father got his xray result just now. An examination on his Chest PA. And the impressions were: Bilateral PTB, Concurrent Pneumonia, and Atheromatous Aorta. Can someone please explain to me what is Bilateral PTB? And Concurrent Pneumonia?
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I was diagnosed with kidney stones and parathyroid disease in March 2010 whilst being in hospital as a result of high calcium levels (3.7 mmol/L) and significant pains in the back. A stent was inserted in order to help the kidneys and I went through a number of tests (Mibi scan, ultrasound, DEXA among others) for identifying the gland(s) that were overproducing the hormone for calcium (201 serum PHT). While I was told that the stent should not remain longer than two months and that I should have the stones removed as soon as possible, I have not been scheduled yet for the removal (ureteroscope). During the last month, the stent has become very uncomfortable, I cannot walk for more than 10 minutes and I feel very tired. I went to the A&E but I was offered only muscle relaxants and painkillers and I have not seen any improvement as a result of these. Simultaneously, I am waiting for the arrangement of the removal of the parathyroid gland.
Is there anyone with similar experience? Is it normal to have that long the stent and have these symptoms? And is there anyone that has gone through a removal of parathyroid glands? Any information would be most helpful.
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Dec 29 emergency room found 2 stones 7 & 8 in size. Put in stint, went to urologist 2 weeks later and 2 weeks after that had Lithotripsy, turned 2 stones into 5 that were at the bottom of my kidney. 3 weeks later had Ureteroscopy urologist said this would get rid of stones. Went in today to have stint removed. Blah, still have several stones. I am beside myself and quickly loosing confidence in my urologist. He told me to stand on my head numerous times a day in hopes that the kidney stones will float to the top and out (I am 60 by the way). Standing on my head is going to be a feat. Said come by in 2 weeks and we will explore options to remove the stones again...
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66 year old husband who has always been fit and healthy developed unstable angina and within three days was fitted with a stent. This was at the end of January. Not been feeling too great since a few days after and now the doc has said he is suffering from anaemia and will have to go for a colonoscopy.
hubby cant understand this as he was never anaemic before.
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I've got a 13 x 12 mm kidney stone in my left kidney.
unfortunately, they are unable to remove the stone due to the fact I'm on warfarin.
The doctors are going to put in a stent to help relieve my pain.
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I was wondering if anyone has had a metal stent placement to treat SOD level one at all. I have posted here in the past as I have gone through 5 ERCP since my gallbladder removal summer of 2013. 3 of the 5 had a single plastic stent placement which all worked until the stent either passed on its own, or was removed by my GI doc. The other 2 times I had multiple stents placed intended to stretch the duct open in hopes of staying that way when these were removed. Obviously it didn't stay open as I relapse into the same set of symptoms that I hope to alleviate......stinging pain where the GB was, bloated all the time, the feeling of a softball lodged into the R abdomen, and pain in the back and R shoulder blade. GI doc (who is well respected here at the Univ. of MN) says that the only options left for me are a botox injection, or metal stent. Any opinions out there? Status quo being stent-less right now is not how I want to live the rest of my life. I am 52 and feel way too young to concede this whole thing.
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I have been having abdominal and pelvic pain for months since my daughter was born in May. I went to the er at 2 different hospitals and both did a CT scan and 1 found bilateral lower lobe atelectasis and the other a narrowing of my aorta valve of the celiac. I asked my family physician about the atelectasis but he said it was air pockets but nothing to worry about. I had a collapsed lung 3 years ago so are these things I should be concerned about because he is not.
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Does anyone here have an ascending aorta aneurysm, and/or aneurysms in any other location in the coronary arteries? What is your experience as far as symptoms and treatment? Thank you.
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I'm due to have my ascending aorta replaced, I think with a Dacron graft. The cardiologist and the surgeon seem to think I'll know everything I need to by Osmosis or something. I was wondering if anyone has or is going through this.
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I am 62 and I have been diagnosed with a 4.2 aneurysm in the ascending aorta. It was found while in the hospital for a suspected heart attack. I do know that aneurysms run in my father's side....one brother died of a ruptured abdominal aneurysm, one died with a brain aneurysm, grandfather died of a ruptured ascending aneurysm and my dad had the same. Of course, they won't do surgery till it reaches 5, but the stress of this is hard on me and my husband. We do know that I did not have the aneurysm two years ago, because I had all the tests done because of my heart rate rate drops into the thirties at times. I do have this sensation in my chest that I had mentioned to my doctor several months ago and I am now wondering if it is related to the growth of this thing. Periodically, I get this stretching sensation in the upper part of my chest...doesn't hurt, but it makes me feel like something is pulling. It lasts a few minutes and then stops...it does this a few times a day. I was just wondering if it was possible to feel the aneurysm growing?
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70 year old male in good shape been exercising 6 days a week cardio and weights for the past 5 years or so.Last couple of weeks or started to feel discomfort in my neck and jaw while exercising, it would go away when I stopped. Went to to non interventional cardiologist who ordered up an angiogram which I had 4 days ago. Results were Right artery 99% blocked, LAD 70 % and two other arteries on the left also 70% blocked. Interventional Cardiologist recommended CABG surgery because of multiple artery involvement and that the left arteries were not good candidates for stenting due to the position of the blockage.
My non interventional cardio after conferring with the interventional cardio said that I had options other than CABG. Both doctors agreed that my angina was most likely coming from the 99% right block.
Option is stenting the 99% blocked right and the OMT for the rest. A surgeon was also called in for consultation and neither he or the two other Cardios would predict outcomes or give an opinion as to which course of treatment I should follow. Regardless something had to be done sooner rather than later for the right artery. I sent the pics to another interventional Cardio who validated the position of my non interventional cardio that I do have choices other than CABG and that the which ever decision I would make I would probably have a good outcome. So next week I'm going to have the right artery stented and then medically treat the rest of my disease and see where it goes from there.
I also plan to make major changes in my diet to hopefully control the progression of the disease or even possible improve my condition
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