I have battled Afib (initially dx as
SVTParoxysmal supraventricular tachycardia (psvt))for 2.5 yrs. I had been treating with a cardiologist who had me on
SotalolSotalol
Sotalol hydrochloride
Sotalol hydrochloride af 180mg 2x per day & 10 mg
coumadin along w/ 80 mg
DiovanDiovan
Diovan hct for HBP but I had break-through about 3-4x per month. Finally went to a good EP in Buffalo (the only good EP) who recommended an EP test. The test was performed on 3/16 and my EP found and ablated a "
flutterAtrial fibrillation/flutter". Since the ablation, knock on wood, I have not had as much as a skipped beat &
pulseNeck pulse
Pulse
Pulse - bounding
Pulse - weak or absent
Radial pulse
Takayasu arteritis
Taking your carotid pulse is regular (no extra beats) - but not that strong - for the first time in 2 yrs. Question is, he kept me on the same med regime - no changes whatsoever. Was hopeful to get rid of or at least change/decrease the meds, so I can resume a normal life and lose some weight! No matter how hard I work at excercise, I can't get my heart rate above 85 while on Sotalol. I have a follow up appt in 4 weeks. Is there a chance he may wean me or change the meds at that time? Just wondering if ablating the flutter will stop the fib. Thank you.
Hi, I am no doctor but i understand a-flutter is a more regular version of a-fib, sometimes a-flutter converts to a-fib and vice versa. Even after an ablation patients are kept on the medications for a while even though the ablation appears to be a success, your doctor probably want to gradually taper you off the sotalol, it will probably help keep your heart less irritable after the ablation.Being you have HBP , you will probably be kept on Diovan indefinitey as you know HBP is usually a lifelong battle that needs control, the sotalol will probably be tappered off gradually after success has been established with your ablation.Hope you continue to feel better. Good luck.
i am 29 years old. with goodhealth. one month ago i felt tired and like chest heaviness then i developed with tachycardia. that lasted for few mints. and the episodes attacked me many times. . i went to the cardiologist. he did ECG and echocardiography. i was told that echo was all normal. and EKG showed what my doctor called " sinus tachycardia" , my heart rate reaches up to 110 when the episode attacks me .. then my doctor advised me to do thyroid function test. which was normal , i did ESR and blood picture. no evidence of anemia. my ESR was 4 . everything was normal as u see! now he prescripted Propranolol 40 mgs daily.
now my complaint is. i havnt felt any imporvment. concern the feelings. the tachycardia attacks me whenever i go out walking. at rest. my heart rate becomes normal but the feeling of chest tightness and the tiredness is wrapping me,.i always feel sleepy and lazy and heaviness in my head without or without the tachycardia. it always presists.
also i have a strange phenomenon . that my heart beating is palpalbe, whether there is tachycardia or not! i mean whenever i put my hands over my heart. i can feel the heart beating. sometimes loudly. it occurs with me all the time. i m, wondering. is the heart beat usually palpable? or not. i heard in thin people its a normal manifistation. but i aint that thin. i am 187 cm and 81 kgs weight.i am scared like hell. whenever i lay in my bed i keep putting my hand over my heart to feel the beating " which worsens the situation" plz can u explain me the causes of the tiredness feeling. and chest tightness. that happen to me whether during the tachycardia or normal heart rate?? thank u again. i know i posted a newspaper in here . its long. but really i am worried
Wow ... my HR goes to 140-150 just mowing the lawn, and I am fairly fit! Even when I was on a Beta Blocker I could still get my heart rate to over 150. It is amazing how the drugs affect people so differently. Of course, the amount you are taking has a lot to do with that.
If you want a doctor to answer your question you will have to post it. It is not that easy to post, but just keep trying.
Without being on a beta blocker , i would assume that is nothing to worry about, at 37 your max predicted heartrate would be around 183bpm. As I understand 12 bpm as an increase or decrease over or under the max predicted heartrate during an exercise is normal. I myself if I hadn't been on a beta blocker during the stress test , my maximum would have probably been around 200 or over myself.
Some just naturally have a higher heartrate in response to exercise or excitement, the fact that it is 55 at rest i would assume is excellent and that you are fit and well conditioned.
13METs is excellent, I achieved 12mets and was told that was excellent, unless you doc or cardio same concerned i wouldn't be alarmed about slightly excessive increase in your heartrate during the exercise test once it was sinus rhythm and not some other ectopic atrial response which i am certain you would have been informed of.
My understanding is that you have to reach at least 85% and over of your maximum predicted heartrate for the test to be considered accurate in the majority of cases.
I'm not a doctor so I surely wouldn't know. However there are three possibilites that I can think of in your case:
1. The atrial flutter was a trigger for atrial fib. Thus getting rid of the atrial flutter probably had an impact on the fib.
2. Getting rid of the atrial flutter may have caused your medication for atrial fib. to finally work.
3. In doing the atrial flutter ablation they unwittingly did enough of an ablation to get rid of the afib.
I guess you might want to ask your doctor what kind of an ablation was done. Was it a PVI (pulmonary vein ablation)? If so then that's the ablation procedure for AFIB.
Whatever, it's a wonderful thing not to have afib.
How was your expereince of the ablation? It's been recommended to me for extremely rapid SVT (200bpm even while ON a beta-blocker - tho only for 7 seconds) and a possible brief afib episode, but I'm completely scared of the procedure. I'd really appreciate your feedback, as well as anyone else's who's had an ablation. Thanks!
Jennifer
Just wanted to let you know my experience. I've had two ablations for svt/vt. I have been on sotalol since fall 2000. My EP has always advised me to continue exercising. I walk/jog 5-6 days per week and lift weights 2 to 3 times per week. I have been able to lose weight and get in better shape while taking sotalol. During the first year or so I experienced fatigue, dizziness, etc., but exercising helped lessen side effects and now I don't notice that sotalol really affects me much at all other than keeping my heart rate lower than it would be normally. Take care.
Neener
I went to Mayo, and saw one of the best EP's in the country. The procedure took about 7 hours. I had three days of tests before the procedure. So it was a very thorough exam.
My cardiologist who was fairly aggressive in treating the AFIB said that it should only be done if:
1) Two meds fail to keep in rythmn.
2) Symptomatic (I just felt drained when in AFIB).
3) Persistant. It was occuring on a frequent basis.
I spent three years messing with meds. But finally had the ablation.
The procedure itself needs to be done by someone who really knows what they are doing. I wouldn't have just any one do it. It is not without risk.
Therefore I would only do it if it's the only treatment that promises help.
On the otherhand if in the hands of a good doctor it can deliver a wonderful result. I have been AFIB free for over one year. I still take a beta blocker (small dose), and that's it.
Expect to be out of commission for about 3 days following the procedure. And you will feel tired for about a month. Also you can expect some arrythmias after the procedure because it does irritate the heart. Typically one doesn't know if it worked for about 3 months afterwards.
Most of the discomfort came early on when they were putting the catheters in. At Mayo they put in three, one in each groin, and one down the throat area. However at that point I told the anesthestiologist to put me to sleep. I wasn't under anesthesia, but I was sleeping the entire 7 hours.
The biggest pain came in my lower back area from lying flat for 7 hours. But they gave me pain meds and that was fine after awhile.
Put it this way I have had far worse experiences of pain.
I would ask your doctor what their procedures are. I would certainly not want to be awake during the entire time. But my procedure took 7 hours. Lots of places to ablate. I've heard some where they don't use as many catheters and then you are out for a shorter time.
I did have a 12 hour bout of afib yesterday and felt slightly discouraged but I called my MD & feel much more optomistic about the success of the procedure. He stated that the heart is irritated from the procedure and bouts of afib may be more frequent/severe for a few weeks following the procedure but they should become less frequent and less in duration as time passes. Hopefully the end result will be known in 3 months. Let me know if you have any more questions.