Do beta blockers effect the ejection fraction results on an
echocardiogram? I have read that one side effect of beta blocker use can be heart failure. How does this happen, and can long term use (12 years) be responsible for a marginally low EF of 47%?
Sierra
I reduced that to 25 MG split into two doses which seemed to be ok. Later I reduced to taking 1/2 of the 25MG daily. At that level it seemed to be a very beneficial drug. It reduced my B.P. at moderate exercise by about 10 BPM, which was helpful.
Overall, I think that it has been a very beneficial drug at low level, but, I too, worry about the long term effects on heart function.
I recently have stopped taking it altogether. I still have a low resting heart rate and am temporarily taking it a little easier on my uphill hiking to keep the exercise heart rate down, until I adjust to being off of the drug.
My guess is that all of these drugs giveth and taketh away. I personally think that Atenolol is helpful in low dose for 6 months after a M.I., but believe that it could decrease heart function if I were on it indefinitely. That's why I chose to stop taking it.
past two years since his first "episode". he has been very
unhappy with the results since the only thing it seems to do
is lower his B P from 140/90 (he is 73, always excercised
vigorously,doesn't smoke, use alcohol or caffine) and adds
a few negative reactions like slow pulse (sometimes to 43
bpm and low even when excercising), exhaustion, drowsy-
ness and in general less joy. coumadin for safety from
possible clotting from atrial fibrillation, and ativan when he
gets anxious about it all, are the only other meds. i tried to
get the information you mentioned from cbshealthwatch.
medscape.com but i am so new at this i was all over their
site with no luck. my husband has another followup visit
with his dr. and we'd like to go informed so as to discuss
alternatives. we have seen electrophysiologists and are
considering the possibillitiies (though afraid to make things
worse). we would appreciate it if you could tell us if this
was an article and the date, or where we can read it. 73 may
sound old to some of you kids out there...but believe me .. it
is not ! our prayers are with all of you young people that
you make it to at least 100! lee
I suffer from extreme fatigue related to tenormin. I sleep 12-14 hours a night and still feel drowsy all day. I can't skip it though because it is supposed to prevent cardiac arrest in my case (I have prolonged QT) and without it I am at high risk. I am concerned about the long term effects of it now that I have read this. My doctors never said anything to me about congestive heart failure. I am on 100 Mg. a day. I still went into cardiac arrest twice when I was on 75 so they had to increase it. I am 5'2" and less than 100 pounds, so it really hits me hard! My pulse is usually around 52 or 56, and my BP is usually around 80/50. I will have to take it for the rest of my life they are telling me. Should I be really concerned about the side effects? I have been on it for four years. Please respond here or e-mail me at ***@****. thanks.
I've always had a very rapid pulse (even at rest), so this year I decided to have my heart checked out. After doing EKG's, echocardiogram, blood tests, and holter monitor, they said I have Mitral valve prolapse and innapropiate sinus tachycardia because of the MVP. The cardiologist put me on Toprol xl, 50 mg (another beta blocker). First I didn't want to take it because of the bad experience with atenolol, but then tried 25 mg the first day, and felt Ok. Then went to the 50 mg, felt a little sleepy during the first days, but now feel totally normal and my tachycardia is under control (I feel even better than before).
The doctor says that I'm going to have to take the Toprol for life, and I really don't mind now. My blood pressure is low now: 85/65 (it used to be 100/75), but my pulse is normal and feel wonderful.
Worst Pills / Best Pills book put out by Public Citizen's Health
Research Group, but the cbs drug directory made the atenolol
discription much clearer. .not that the book isn't great for detail.
good luck with you thalium stress test. please keep us informed
on what happens after your 48 hours without atenolol. lee
Thanks for this website - it is a great comfort to know I am not alone.
Thanks!
From what I understand, most docs won't do ablation for pvc's. They say it is a benign and harmless condition. Have you tried medication? I have pvc's and also svt. I was prescribed a beta blocker for svt, but haven't had any pvc's that I've noticed since. Good luck to you.
Jen, if I were you and could get an ablation for the SVT and therefore, get off of the atenolol, I would. I even read one of the dr.s on this forum tell someone exactly that. Why take medication w/side effects the rest of your life?
I feel dumb - I am not sure what re-entrant SVT's are - I was just told I have SVT!! The atenolol does not have any terrible side effects but I still have PVC's and sporadic SVT attacks - like today - which just happened to be the first day of my menstral cycle - they always seem to happen then, but the docs dismiss it...
Jan, is there no surgery you can have to help you? I was also told by one cardiologist I have MVP - would that affect an ablation? I just am scared to face the possibility of something going wrong, even though "they" say 95% of abltions are successful. Does anyone have any ablation info? You can e-mail me directly at ***@****
Than for caring, I hope you all feel better Let's try and not let his heart thing monopolize our lives, although it is hard!
you're right about "this heart business" getting us down. My husband gets depressed everytime he reads the forum with me..so guess who does most of the reading? he see's his doctor this friday and hopefully can cut ack some on atenolol, jan. take a look at the question posted by marisha on magnesium, if you haven't already. i know for a fact that it is very significant in heart problems. we keep hoping that one day we'll be able to use natural methods methods with safer or no side effects which can help these heart problems "we" all share. i have so much compassion for all of you. once in awhile i get very frightened about something or other and know this must be the fear you experience on an everyday basis. I use Bach flower essences when this happens (and so does my husband) and it helps. check your health food store or the web for info. they have been around for 70 years and becoming more and more known and used. they do not interact with any meds or food etc. good luck.
Re-entrant SVT is from an extra electrical pathway. I have inappropriate sinus tachycardia, this is something wrong with my sinus node. If I don't respond satisfactorily to the meds. then they will try an ablation, but there is usually a need for a pacemaker then and that is why my dr. wants to try everything else first. I, also, have mvp with mild regurg. and mild tricuspid regurg. I don't believe that would interfere at all with an ablation. You know, Jen, being perfectly honest I would be hesitant to get an ablation, too. It's scarey. As far as the magnesium, I do take calcium/magnesium supplements and drink bottled water. I will ask my dr. about the magnesium. Last year when I found out about my heart conditions and started reading this forum I felt depressed also ( besides the fact that I had just lost my mother to CHF 4 mos. before). I think everybody needs some time to adjust and accept the diagnosis. I do think I feel better since cutting back the atenolol, as far as the depression, but I still am on a wait and see basis. However, I'm not sure it's enough to control the arrhythmia. I have an appt. in about 1 1/2 weeks. May I suggest Relax-o-zyme by Enzymatic Therapy for stress, I don't take it according to the instructions, that would be too much for me.
Is that how they tell the difference?
I was wondering about having SVT vs. sinus node trouble. I was told by en ER nurse after reading my EKG that I had SVT. How can they tell if that is what it is for sure without doing an EP study?
It's been 3 weeks since cutting back the atenolol and it was definitely the cause of my depression. I told my EP this morning and he agreed and said it was a known side effect. I feel so much better. Of course he is having me do a holter to be sure the arrhythmia is under control. Oh, by the way, I passed the thallium stress test! Yes! One less thing to be concerned about. I hope you all are doing well.
My marriage is in jeopardy because I am being treated as if I am faking or "crazy" at this point. I am scared and alone. In the last three weeks I have experienced them during sexual activity as well as at rest lasting for as long as 10-20 minutes usually around mid afternoon.
I need a friend. I am so scared.
#39 yrs old after a Mytocardial Infarction at the age of 31.
Using 25 mgs of the drug daily seems to be OK.
It was my decision to go down from 50 mgs. and my Dr. OK'd it.
One day I skipped it, and I "thought" I felt a difference.
Since I am Vegan, very active, I would like to GIVE IT UP>>>!
One Dr. I met with thought I did not need it.
Q: What can I expect as PHYSICAL manifestations
of not using the drug any more. Should I go down to 12.5 mgs
first....Who has experienced the "withdrawal?"
Mahalo
Glad I found this website. I'm new. Will be here again. Good luck....