Supraventricular tachycardia (svt) when should i catch on prescription?
i have svt attacks about 4-5 times a day. my heart speeds up to where on earth i can barely breathe then beats really wide and slow then it goes back to average im just exhausted after the fact. my doctor told me he could put me on meds for it but i denied cause he said it be possible to go without it. at that time i was one and only having one a day. do any of you guys with svt enjoy that many attacks per day? do u think i should move about back to the doc?
Answers: Listen to Princess and not the dramatic others, she is "mostly" right. I have had SVT since I was a child (30 now) and have surgery to fix it (worked for a few years). SVT can actually cause death, heart dud, etc BUT it is very rare. I've had to hold the good old electric paddles before to stabilize my heart. Most though never enjoy that problem and some go their whole lives without treatment and you can do equal if you choose. I would recommend though trying at the meds. Good luck to you!
Get on medication if you want to live.
on medication in a minute. Source(s): ER Nurse.
I was diagnosed with SVT as economically. Yes, it is very scary during an attack. I feel breathing heavily, light headed, and it feels close to you have no control over your heart. I was put on medicine a year ago. SVT attacks started surrounded by 2006, but they got more frequent and longer lasting as time progressed. So I went a while minus medicine. I took 50 mg of Atenelol. Before I was put on medication, my attacks were exceptionally severe and long. They got up to 220 bpm and I thought my heart was going to jump out of my chest. However, they occur 5-6 times a week. The Atenelol made the attacks less severe, but it did not make them go away. In other words I did hold some "break through episodes" as my cardiologist called it.
SVT is not a life threatening condition, so dont freak out by some of the answers on here. They have never experienced SVT and partly of the people on here automatically think "serious" when they hear of a problem associated with the heart. Ninja 636: it isnt time threatning and its not like if you get an attack you cant drive. You dont even know what SVT is about. Angela: I hold been in the ER for svt before and you nurses are broad. You arent trained in cardiology, so how the heck would you know? You have NO IDEA of the details of svt. My ER nurse didnt even know how to plug me up to the heart monitor. Little newsflash, you cannot have a heart attack from SVT, nor can you die. It is physically IMPOSSIBLE. Stick to what you know for sure (like sticking on bandaids) and stop trying to work like you know what you are talking about. I'm serious because stuff resembling that scares people and it is bs...that cant happen.
Anyways, a month ago, I be tired of having attacks so I underwent catheter ablation. I bet your cardiologist has mentioned it to you. This is a low-risk procedure where on earth you are put under anestesia and they insert 4 catheters through the groin. They map the heart's electrical system to find what is causing the SVT. (People with SVT usually own an extra electrical pathway that the heart will occasionaly jump on. This is the palpatations we feel. Some may have over 1 pathway. I newly had one.) My extra electrical pathway was in a tough spot to burn with the catheter. (That is how they get rid of the pathway. They either burn or freeze. Once the extra pathway is gone, they heart cannot soar on it. Therefore, palpatations are history!) They tried burning ir 8 times! They couldnt get to it, so they tried freezing which worked! Once they think they eliminated the pathway, they try to induce a palpitation. I wasnt getting palpitations, so my SVT is cured! The expected time for this procedure is 3-8 hours. We thought mine would be short, but I be under anestesia for 8 hours because of the inconvient location of the pathway. Afterwards I had complications like junctional tachycardia. My heart be beating at 120 bpm afterwards at an irregular rhythm. The beat was coming from the AV Node and skipping the sinus. In other words, sinus rhythm is the everyday. Junctional rhythm is the backup in case something goes wrong next to the sinus. Nothing was wrong with my sinus. In fact, the sinus and junctional rhythms be racing each other. This is what caused the swift heart rate. I was admitted in the hospital and be there for a week after the procedure. (Usually you go home the same time of the procedure.) The electrophysiologist concluded that the reason for the junctional tachycardia was because the heart was so irritated from the burning and freezing for 8 hours non stop. It wasnt terrifying, it was just annoying feeling that easier said than done rapid heart rate all day! They put me support on the medicine to slow the heart rate. It sucked because that was the initial reason to hold the procedure...to get off the medicine. Your body become immune to medicine after a while. Anyways, about 2 weeks ago I was weened bad the medicine to see if the junctional tachycardia had ceased...and it did! Right presently I am living SVT free with no limitations! I definitely recommed the procedure. I was extremely worried to have it at first but I felt so limited near the attacks. I was on the medicine a year though. I suggest you start it and see how it goes. If you are fed-up with breakthrough episodes, try the procedure! A tip for SVT attacks: you can use manuevers to try and stop them. The manuever I used most often is bearing down or "Valsalva manuever." The Valsalva maneuver should be the first vagal maneuver tried because it is most impressive. It works by increasing intra-thoracic pressure and affecting baro-receptors (pressure sensors) within the arch of the aorta. It is carried out by asking the patient to hold their breath and "bear down" as if straining to overrun a bowel motion, or by getting them to hold their nose and blow out against it. Also try rubbing one side of your neck firmly. Rub around the area where on earth you would check your pulse. You can also try drinking ice water, plunging your face contained by ice cold water, and standing on your head. Although I individually DO NOT reccommend standing on your head during an SVT attack. Durning my attacks, I was light head and dizzy. Standing on my head would have resulted in some other twist of fate. When you are on medicine, the attacks are easier to stop. By the way, I am only 15. I wasnt born beside SVT, it developed when I was like, 12. Hope this helps and angelic luck! :) Source(s): I'm like an SVT expert now that I've been through tablets AND catheter ablation. I've seen many cardiologists and electrophysiologists for years now. I love helping those with SVT to the best of my ability. I feel it is my opening to share my personal experiences of life with SVT because I know how scary it can be and I want to lighten people's mind the best I can. I've been there before and be very confused about it all so I want to be in that for others and help all I can :)
Related Questions:
Answers: Listen to Princess and not the dramatic others, she is "mostly" right. I have had SVT since I was a child (30 now) and have surgery to fix it (worked for a few years). SVT can actually cause death, heart dud, etc BUT it is very rare. I've had to hold the good old electric paddles before to stabilize my heart. Most though never enjoy that problem and some go their whole lives without treatment and you can do equal if you choose. I would recommend though trying at the meds. Good luck to you!
Get on medication if you want to live.
on medication in a minute. Source(s): ER Nurse.
I was diagnosed with SVT as economically. Yes, it is very scary during an attack. I feel breathing heavily, light headed, and it feels close to you have no control over your heart. I was put on medicine a year ago. SVT attacks started surrounded by 2006, but they got more frequent and longer lasting as time progressed. So I went a while minus medicine. I took 50 mg of Atenelol. Before I was put on medication, my attacks were exceptionally severe and long. They got up to 220 bpm and I thought my heart was going to jump out of my chest. However, they occur 5-6 times a week. The Atenelol made the attacks less severe, but it did not make them go away. In other words I did hold some "break through episodes" as my cardiologist called it.
SVT is not a life threatening condition, so dont freak out by some of the answers on here. They have never experienced SVT and partly of the people on here automatically think "serious" when they hear of a problem associated with the heart. Ninja 636: it isnt time threatning and its not like if you get an attack you cant drive. You dont even know what SVT is about. Angela: I hold been in the ER for svt before and you nurses are broad. You arent trained in cardiology, so how the heck would you know? You have NO IDEA of the details of svt. My ER nurse didnt even know how to plug me up to the heart monitor. Little newsflash, you cannot have a heart attack from SVT, nor can you die. It is physically IMPOSSIBLE. Stick to what you know for sure (like sticking on bandaids) and stop trying to work like you know what you are talking about. I'm serious because stuff resembling that scares people and it is bs...that cant happen.
Anyways, a month ago, I be tired of having attacks so I underwent catheter ablation. I bet your cardiologist has mentioned it to you. This is a low-risk procedure where on earth you are put under anestesia and they insert 4 catheters through the groin. They map the heart's electrical system to find what is causing the SVT. (People with SVT usually own an extra electrical pathway that the heart will occasionaly jump on. This is the palpatations we feel. Some may have over 1 pathway. I newly had one.) My extra electrical pathway was in a tough spot to burn with the catheter. (That is how they get rid of the pathway. They either burn or freeze. Once the extra pathway is gone, they heart cannot soar on it. Therefore, palpatations are history!) They tried burning ir 8 times! They couldnt get to it, so they tried freezing which worked! Once they think they eliminated the pathway, they try to induce a palpitation. I wasnt getting palpitations, so my SVT is cured! The expected time for this procedure is 3-8 hours. We thought mine would be short, but I be under anestesia for 8 hours because of the inconvient location of the pathway. Afterwards I had complications like junctional tachycardia. My heart be beating at 120 bpm afterwards at an irregular rhythm. The beat was coming from the AV Node and skipping the sinus. In other words, sinus rhythm is the everyday. Junctional rhythm is the backup in case something goes wrong next to the sinus. Nothing was wrong with my sinus. In fact, the sinus and junctional rhythms be racing each other. This is what caused the swift heart rate. I was admitted in the hospital and be there for a week after the procedure. (Usually you go home the same time of the procedure.) The electrophysiologist concluded that the reason for the junctional tachycardia was because the heart was so irritated from the burning and freezing for 8 hours non stop. It wasnt terrifying, it was just annoying feeling that easier said than done rapid heart rate all day! They put me support on the medicine to slow the heart rate. It sucked because that was the initial reason to hold the procedure...to get off the medicine. Your body become immune to medicine after a while. Anyways, about 2 weeks ago I was weened bad the medicine to see if the junctional tachycardia had ceased...and it did! Right presently I am living SVT free with no limitations! I definitely recommed the procedure. I was extremely worried to have it at first but I felt so limited near the attacks. I was on the medicine a year though. I suggest you start it and see how it goes. If you are fed-up with breakthrough episodes, try the procedure! A tip for SVT attacks: you can use manuevers to try and stop them. The manuever I used most often is bearing down or "Valsalva manuever." The Valsalva maneuver should be the first vagal maneuver tried because it is most impressive. It works by increasing intra-thoracic pressure and affecting baro-receptors (pressure sensors) within the arch of the aorta. It is carried out by asking the patient to hold their breath and "bear down" as if straining to overrun a bowel motion, or by getting them to hold their nose and blow out against it. Also try rubbing one side of your neck firmly. Rub around the area where on earth you would check your pulse. You can also try drinking ice water, plunging your face contained by ice cold water, and standing on your head. Although I individually DO NOT reccommend standing on your head during an SVT attack. Durning my attacks, I was light head and dizzy. Standing on my head would have resulted in some other twist of fate. When you are on medicine, the attacks are easier to stop. By the way, I am only 15. I wasnt born beside SVT, it developed when I was like, 12. Hope this helps and angelic luck! :) Source(s): I'm like an SVT expert now that I've been through tablets AND catheter ablation. I've seen many cardiologists and electrophysiologists for years now. I love helping those with SVT to the best of my ability. I feel it is my opening to share my personal experiences of life with SVT because I know how scary it can be and I want to lighten people's mind the best I can. I've been there before and be very confused about it all so I want to be in that for others and help all I can :)
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