My sympathy to you and your husband, it is real hard to even read about someone so young has serious heart problems. The good side is you should have the physical strength to deal with surgery/ablation/treatment... if you just can keep an optimistic can-do attitude.
I also understand WPW does respond to ablation, if the doc can find the right spot, it seems. In any case it seems like you should give ablation another try if the doctor has any optimism it will help/work.
I take heavy dose Metoprolol, 100 mg twice a day, to lower my AFib driven HR. I think I have gotten used to it, and my tiredness is not as bad as it was. I have unhappy dreams every night, however, and I think the BB is part of the driver of that. I do get sleep, however and just try not to think about the coming dream mess when trying to go to sleep.
Thanks for the nice words!
One thing I wanted to ask if you is if you ever thought about trying Toprol xl (name brand) instead of Metoprolol? I know they are supposed to be one in the same, but my dad found that they actually have different release mechanisms! I was able to tolerate Toprol better and my dreams and depression and confusion is way better on Toprol. One problem, its way more expensive...but I'm going to try to afford it no matter what just because of how much better it is.
I just had ablation for a variation of WPW. I was burned on the left side only. I am not sure of my outcome yet, sometimes I feel great, other times very bad. I don't know about a second ablation.
You said they did not burn. I know of one person who did also not get burned because they thought it would give her a pacemaker. My understanding is burns are not reversible. However, with "cryoablation" sites can be tested first with light freezing. This might make for more fine tuned ablation, less burns in healthy areas. They temporarily freeze you to see if that spot is good to ablate or not. I would have liked access to that newer technology. Was not an option for me, but you may have access.
I also have tightness in my chest, with me, from ablation. I don't lay on my back. That makes it worse. I lay on my right side only. Eases the tightness, allows for more satisfying breaths. Elbows out and away.
I, pre ablation, did light running every second day, while taking atenolol. It was harder than without atenolol, and it brought on svt but during the run my heart was in harmony with me. Running, after breaking through some kind of physiological barrier, had the effect of giving me about a two day buffer against svt. I could take less meds. I have started light running again the past few days and would say it has had a positive effect. It also relieves stress.
This has been my experience, but I would not presume it certain to help you. Although I hope it does to at least some extent. Talk to your doc.
My thoughts are with you,
"I have unhappy dreams every night"
Jerry, I'd read one person saying that melatonin helped them sleep peacefully through the night. I think it was on, of all places, some Oprah forum. Well, you never know.
"my dreams and depression and confusion is way better on Toprol"
hi, you probably know this but I'll mention it anyway: the difference in effect is likely because the Toprol, being time released, achieves a lower Peak Plasma Concentration than does the metoprolol.
So, you might mimic those pharmacokinetics somewhat by taking the metoprolol with say... a big meal. Fat in a meal slows down transit time even more.
Or have you checked if you can take two half-doses per day, to reduce PPC?
Also, which metoprolol are you taking, succinate or tartrate?
I'm so sorry you have had such a frightening and challenging experience with your WPW. I also have WPW with a left-sided accessory pathway and on 17 September of this year (just a few weeks ago) had a cryoablation procedure at Mayo Clinic in MN. Although I am still recovering (for some of us it is a longer process than for others!) and we won't know for sure whether or not is was a success for several more months, my cardio seemed very positive about my procedure and I, too, felt that for the most part, it went extremely well, so despite being something of a skeptic about ablations, I am cautiously optimistic that I may have a successful long term outcome.
My accessory pathway was "left free wall" and was much simpler to deal with than what yours sounds like, and while I am not familiar with all the particulars, I am aware that the coronary sinus is a very tricky area to ablate. I would definitely suggest giving the Heart Rhythm Center at Mayo Clinic in Rochester MN a call to discuss your situation. After being told various things about my condition by different specialists (many of which were conflicting) I "self-referred" to Mayo and am COMPLETELY glad that I did. On my initial call, I spoke to one of the nurses at the Rhythm Clinic and gave her my basic info. She checked with their specialists and then had me send all my records so the specialists could study them. After looking at my records they decided which of their specialist EPs would be best for my case then they got back to me and told me they could consult with me, do some tests and discuss whether or not ablation was an option.
I can't say enough good things about Mayo Clinic! I showed up at the clinic on a Tuesday morning and spent all that day and the next day having consults and tests. After a lengthy, informative, respectful and compassionate consult with my EP specialist, I went in the next day, a Thursday morning, for my ablation. The quality of care was absolutely outstanding, the technology available was top notch and the kindness and caring attitude of ALL the staff was remarkable.
There are other facilities that I am sure are equally as good, but the thing that made Mayo a good fit for me was that they are committed to delivering "patient centered" care -- I wanted cryo, not RF so they said if they could safely and successfully use that method, they would definitely accommodate me. I wanted a retrograde aortic approach to the left atrium (rather than a transeptal puncture) so they said if they could successfully and safely do it that way, they would. My specialist spent a great deal of time discussing with me what I wanted and needed from this procedure, also talked about alternatives to ablation and shared his concerns and opinions on my condition in particular, as well as his knowledge and experience with WPW in general. When I left his exam room I was completely confident for the first time in over 20 years that I could finally just leave it in my doctor's hands because I trusted his knowledge, his ethics and the Mayo facility to do what was in my best interest.
I have taken Toprol for over 10 years and found it to be the drug I have tolerated best. I am still on it until at least 3 months post ablation procedure, but hope to taper off if my ablation was successful. While I realize how frustrating and exhausting having WPW arrhythmia can be, I would urge you to keep trying to find treatment that works well for you -- keep asking, keep researching and keep hoping -- just remember to take time to "LIVE", too! And, if there's nothing they can do now, that could easily change -- when I was first diagnosed, open heart surgery was the only "cure" for WPW. In the last 20 years advances in ablation technology have come a long way, so there is always hope.