Anyone here diagnosed with Superventricular Tachycardia?

I have been suffering from irregular beats since 1995 (pac's, pvc's). I tried beta blockers early on but had a low resting heartbeat to begin with and they brought it down too much and I was also cold and tired all the time. I just learned to live with the irregular beats, episodes of chest pain and tachycardia. All in all I have probably been to the ER 25 times over the years for this but they never caught the fast heart rate, only pvcs, pacs and regular tachycardia. They basically thought I was having panic attacks and called me a nut. I have had multiple echo's, nuclear imaging, stress tests, an angiogram, a CT angiogram, much too much testing. All negative, except for mild mitral, tricuspid regurgitation on the echo, which they said was normal. I have been treating for Lyme, Bartonella, Cpni, Mycoplasma since 1996 and have very few symptoms left, but the heart irregularities remain. I have noticed more irregular beats in the last few months related to vagal irritation and provoked by swallowing, moving my torso, adrenaline etc... 2 nights ago I swallowed some pasta and turned around and suddenly went into a very fast rhythm. Usually I pop out of this very quickly, but this time I did not. My heart went from 60 to 200 in a split second. I tried various vagal maneuvers to get it out of the fast rhythm but nothing worked. After 15 mins (an eternity at the time) I called an ambulance. The paramedics saw SVT at a rate of 177bpm on the monitor and gave me a shot of adenosine to slow my rhythm. It worked immediately but was very scary. I thought I would die right there. At the hospital the next day my EP cardiologist said I was a very good candidate for cryoablation. Looking back I realize this has been going on for too long and really affecting my life. I thought the irregular beats would go away with Lyme/cpn treatment but so far no go. I am supposed to treat Babesia next, and there is a case for Babesia causing this kind of thing, but I honestly am scared of all this. Apparently ablations have a 95% cure rate for simple arrhythmias like this one. I am not a fan of meds like beta blockers for life, so I am seriously considering the ablation. Many young athletes choose to do it and go on to live normal lives. If there is anyone out there with SVT I would love to hear from you! Thanks for any advice. Be well all.

My brother had the ablation.  I think he was in his late teens when he had the ablation performed.   He was hooked up to the 30 day cardiac monitor and the highest he went was 300 BPM.  didn't even know that this high of a number would register, but most of his readings were around 200-220.  He had the ablation and has lived a normal life symptom free for past 6-7 years. He even played soccer for the first couple of years after his surgery. 

 His attacks never lasted as long as yours though. His eposides would last a few minutes and then would self correct itself. during those few minutes, he would passout or be on the brink of passing out.  But from the first episode,  to the 30 day monitor to surg was less than 6 months.  

I wish you peace with your decision. From a family member, it is very scarey. I can't imagine being in your shoes.  

Mphs, TN. CFSi, hypoT (Hashi), adrenal fatigue, hormonal inbalance. right arm neuropathy-getting better. cpni, myco, EBVi, CMV, HHV-6. Capi began in 6/07. NACi 2400mg, minoi 100mg bidi, biaxin 500mg bidi. cytomel, flagyli bid continuously.

Hey Mycoplasma,

Sorry to hear you're still having troubles with this.   I'm assuming you've tried magnesium to see if it helps at all?

Hang in there...

Treatment for Rosaceai

  • CAPi:  01/06-07/07
  • High-Dose Vit D3, NACi:  07/07-11/08
  • Intermtnt CAP, HDose Vit D3:  11/08-01/09
  • HDose Vit D3, Mg, Zn: 01/09-
Yes, I am on Magnesium but I am not sure it is doing anything. This seems very vagal related to me. Happens when I swallow and push back on my neck and spine. Must be a vagal connection. Funny how the Cardio's and GI Dr's just won't communicate with each other on this. I have read many message boards with hundreds of patients like me and they all think there is a connection also.
CAPi since 11/06 for Cpni, Lyme, Bartonella, Babesia, Myco P, CMV, HHV-6 infectionsi. Rifampin 600mg daily, Zithromax 500mg daily. NACi 2250mg daily. All other supplementsi. Now Bicillin LA 2.4 mil injection weekly.
Yes, there is a definite correlation with hiatal hernia and vagus nerve. Here is the condition and possible treatments: http://en.wikipedia.org/wiki/Roemheld_Syndrome
CAPi since 11/06 for Cpni, Lyme, Bartonella, Babesia, Myco P, CMV, HHV-6 infectionsi. Rifampin 600mg daily, Zithromax 500mg daily. NACi 2250mg daily. All other supplementsi. Now Bicillin LA 2.4 mil injection weekly.
Hi mycoplasma1, I came upon an interesting stretch in one of my physical therapy books you might try, to help your problems, it is the Vagus Nerve Stretch. I will explain it as best I can, lie down on your back and relax, pulling your shoulders down and palms up toward the ceiling, stick out your tongue,keeping it down and extened over the lower lip, as far as possible. At the same time, without moving your head, gaze up and back with your eyes, trying to see as far as you can behind your head. Hold this position for a count of six, and repeat several times. This sounds funny I know but it a real stretch! I am also trying this stretch because of heart palpitations, swallowing difficulties, and reflux,because the vagus nerve is tied in with all of these symptoms. This stretch might free the nerve so it can deliver its signals fully and efficiently. Hope this helps, Patti
FMSi,CFSi, 15 years,CPni antibodies,mycoplasm pn.,leison on posterior pituitary. Started CAPi end of Dec. 08 minoi.100 daily, azith. 250 MWF all supplementsi,compounded T3 therapy.
Thanks Patti! I will give that a try.
CAPi since 11/06 for Cpni, Lyme, Bartonella, Babesia, Myco P, CMV, HHV-6 infectionsi. Rifampin 600mg daily, Zithromax 500mg daily. NACi 2250mg daily. All other supplementsi. Now Bicillin LA 2.4 mil injection weekly.

Hi mycoplasma, I also have the mitral valve prolapse and have fibromyalgiai.  About 2002 I really started having problems.  From 2002 to about 2005 it got worse and worse.  Doc said I was born with it.  Went to the firestation 3 different times in about a year around 2004 or 05.  They gave me the shot that stops your heart and hopefully it starts again correctly.  Mine did.  One time my heart was racing at 225 beats per min.  When my heart stopped it was the worst pain ever.  I asked them, what if it didn't restart and they said - That's what the paddles are for!!!  Yipes!! They were racing me to the hospital each time so it was pretty scary.  After the third time I went to a heart surgeon.  We tried meds but didn't help.  So I had a heart ablaution and have had no trouble since.  I really recommend it.  One time I waited about 30 minutes and that is the worst thing to do.  All of that can damage your heart too.  They said my heart seemed to be okay thankfully.  It was a breeze.  I felt nothing and was not even put completely to sleep.  I even watched some of it on the monitor after the doc told me to look.  No big deal!  Really!  The worst part is thinking about it and getting nervous beforehand. 

 Talk to people and get their recommendations.  I went to a heart clinic with a number of surgeons.  Let us know how it goes.

FMSi/CFS 1995. tinnitusi, ibsi, sinusitis, EBVi, NACi 2400mg, valtrex, cortef, armour, doxy, biaxin, tinii, vita c 5 - 10,000 daily 

Lynn, Where did you have yours done?
CAPi since 11/06 for Cpni, Lyme, Bartonella, Babesia, Myco P, CMV, HHV-6 infectionsi. Rifampin 600mg daily, Zithromax 500mg daily. NACi 2250mg daily. All other supplementsi. Now Bicillin LA 2.4 mil injection weekly.
Dr. Litzow at the Sutherland Clinic in Memphis, Tennesse.  Are you close by?

FMSi/CFS 1995. tinnitusi, ibsi, sinusitis, EBVi, NACi 2400mg, valtrex, cortef, armour, doxy, biaxin, tinii, vita c 5 - 10,000 daily 

No, I am in Los Angeles. I hear the Mayo clinic and Cleveland Clinic are the best. There is a guy here in LA but not sure. So hard who to know I can trust!
CAPi since 11/06 for Cpni, Lyme, Bartonella, Babesia, Myco P, CMV, HHV-6 infectionsi. Rifampin 600mg daily, Zithromax 500mg daily. NACi 2250mg daily. All other supplementsi. Now Bicillin LA 2.4 mil injection weekly.

I know it is a scary procedure to do but I got to the point that I was afraid I would die.  Or that my heart would be damaged.  Then, I guess I figure - if it's my time to go, it's my time to go!  Sometimes I am so ready to go anyway!!!!!!  (Go to heaven I mean!)  If I'm still here that means that God isn't finished with me yet!

FMSi/CFS 1995. tinnitusi, ibsi, sinusitis, EBVi, NACi 2400mg, valtrex, cortef, armour, doxy, biaxin, tinii, vita c 5 - 10,000 daily 

They are doing a cold induced ablation at Mass General Hopital.  I have a friend that had it after doing everything offered and breaking through.

The procedure went very well and she is cured for a year now.

  • CAPi(TiniOnly): 06/07-02/09 for CFSi
  • MethylationProtocolSupplements: Started08/08
  • Intermtnt CAP: 02/09-02/10
  • Full MethylProtocol & LDNi 02/09
  • Off CAP: 02/10, cont LDN & MethlyProtocol support
If you have not already try to get your thyroid hormones tested: TSH, T4, T3, Free T4 and Free T3! I had MANY of the same frightening issues you describe. (Not to say you do, or this was the root cause of my tachycardia, BP issues, ect. but I was found to have thyroid cancer July '09. Probably had this for many years and most likely would have lived to 90 with no issues. I'm fine now! The Mayo Clinic cut it out and tossed in the trash!)  But, I have had BP issues, tachycardia issues, high triglicerides and cholesterol for many years. My tachycardia became much more pronounced when I tried to go to sleep at night about the same time I suspect I picked up my CNP infection. What "I think I uncovered" is that a CNP infection impacts how your infected CNP cells process thyroglobulin into the various thyroid hormone forms in an atypical fashion. Very complex process, just have these test run and determine if your experiencing any hidden thyroid issues that might be possibly related to CNP aggravating a harmless preexisting thyroid problem you may have. My TSH was .7 "Normal low" so doctors refused to look at my thyroid any further, called me crazy as well just before they sent me packing to try to find another doctor.  After the cancer diagnosis I had additional thyroid tests run. My free T4 was hypothyroid at .77 and Free T3 was hyperthyroid with a high 5.2 reading. Endocrinologist could not even come close to explaining this. The thyroid imbalance coupled with CNP made me a total mental and physical wreck to say the least! Brand new person now! Tachycardia gone, blood pressure now stable normal, triglicerides went from 500 to 125, HLD now normal LDL now normal from "Gawd!" No worries and good luck to you!  :) 

squirl Man

SquirrelyMan

  Mycoplasma, ablation would be a suitible treatment for you.

  yılmaz.

KEREM'S TAKECARER;

Suspıcıon of MSi (transient nystagmus during conjugated gaze on february 2008, blepharospazms and some optic complaints on february 2009-no plaque on MRI), Vit D3 started 400 IU and elevated to 2000 ıu ın 40 days.

Thanks for your help everyone. Seems some people have a resolution of arrhythmia with Lyme treatment and others do not. I don't think this is something I can live with and I don't want to be taking meds for the rest of my life so I am looking into an ablation. My Dr. asked me yesterday how often this happens and I told him I had been to the hospital 4 or 5 times this year, not all heart related but mostly. Usually my heart will go into tachycardia and not SVT and resolve before the ambulance comes. But this time it was clearly a rhythm I jumped into (60-200 in a split second) and it didn't show any sign of easing up without medical intervention. That is scary. I am treating Babesia right now and might wait until that treatment is over and monitor the situation in the meantime. I do have meds to take if I need them. I am a little afraid to exercise now as it would be really scary to go into this with exercise. Funny how I feel fairly normal health wise now after all the antibioticsi but am afraid to workout because of the arrythmia. It's never easy is it!
CAPi since 11/06 for Cpni, Lyme, Bartonella, Babesia, Myco P, CMV, HHV-6 infectionsi. Rifampin 600mg daily, Zithromax 500mg daily. NACi 2250mg daily. All other supplementsi. Now Bicillin LA 2.4 mil injection weekly.

  If its sinus tachycardia mostly, ablation wouldn't be helpfull but if you experience SVT manytimes a year ablation is ok.

  yılmaz

KEREM'S TAKECARER;

Suspıcıon of MSi (transient nystagmus during conjugated gaze on february 2008, blepharospazms and some optic complaints on february 2009-no plaque on MRI), Vit D3 started 400 IU and elevated to 2000 ıu ın 40 days.

Yes, this is true. They are both very different. I will wait until I finish Babesia treatment to see where I am. If it becomes a regular thing I will get the ablation.
CAPi since 11/06 for Cpni, Lyme, Bartonella, Babesia, Myco P, CMV, HHV-6 infectionsi. Rifampin 600mg daily, Zithromax 500mg daily. NACi 2250mg daily. All other supplementsi. Now Bicillin LA 2.4 mil injection weekly.

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