<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <channel>
        <title>Atrial Fibrillation Forum</title>
        <description>A forum for sharing experiences and treatment options regarding atrial fibrillation and other atrial tachy-arrhythmias.</description>
        <link>https://www.afibbers.org/forum/index.php</link>
        <lastBuildDate>Sun, 24 May 2026 20:36:18 +0000</lastBuildDate>
        <generator>Phorum 5.2.23</generator>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201356,201466#msg-201466</guid>
            <title>Re: Post ablation questions</title>
            <link>https://www.afibbers.org/forum/read.php?9,201356,201466#msg-201466</link>
            <description><![CDATA[ Jackie logged into the forum today at 1:30 PM ET.]]></description>
            <dc:creator>Carey</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 24 May 2026 19:52:58 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201356,201465#msg-201465</guid>
            <title>Re: Post ablation questions</title>
            <link>https://www.afibbers.org/forum/read.php?9,201356,201465#msg-201465</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>GeorgeN</strong><br />
<br />
I don&#039;t know who Jackie is,<br />
<br />
<br />
Jackie is a woman who has been an active member here since the early 2000&#039;s.   She&#039;s now around 89 years old.  She had an ablation with Dr. Natale around 2003 and then a subsequent one around 2015 (from memory).  She last posted 11 months ago &amp; I last chatted with her on the phone likely within the last year as well.</div></blockquote>
<br />
She hasn’t posted in a while, so I hope she is ok. I’ve been on this site since 2004 and Jackie had contributed a wealth of valuable information.]]></description>
            <dc:creator>susan.d</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 24 May 2026 16:24:48 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201448,201464#msg-201464</guid>
            <title>Re: New SVT</title>
            <link>https://www.afibbers.org/forum/read.php?9,201448,201464#msg-201464</link>
            <description><![CDATA[ It is beginning to look like there is a gas exchange problem, and it might be resident in the lungs themselves. Have you had a lung scan to see if you have fibrosis or emphysema of some kind/related/analog?  No night sweats?]]></description>
            <dc:creator>gloaming</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 24 May 2026 15:40:07 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201452,201463#msg-201463</guid>
            <title>Re: HF and afib/flutter</title>
            <link>https://www.afibbers.org/forum/read.php?9,201452,201463#msg-201463</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>mjamesone</strong><br />
You can&#039;t seen an EP there unless referred by another cardiologist. So the HF is first<br />
<br />
That makes a lot of sense and it may work to your advantage. <br />
<br />
At Cleveland Clinic, you&#039;re already looking at an elite EP group, including as Wazni, Saliba, Santangeli, Hussein and others.  But even at that level one EP may be a better match than another, especially with your previous congntal heart surgery history. <br />
<br />
So since you&#039;re seeing the HF cardiologist first, Id use that visit to ask who they think is the best EP match for your particular case.<br />
<br />
Best of luck,<br />
<br />
Jim</div></blockquote>
<br />
Good thoughts there. I just wish I didn&#039;t have to wait till august to see the HFpEF doc.]]></description>
            <dc:creator>bettylou4488</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 24 May 2026 14:53:16 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201452,201462#msg-201462</guid>
            <title>Re: HF and afib/flutter</title>
            <link>https://www.afibbers.org/forum/read.php?9,201452,201462#msg-201462</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>Carey</strong><br />
<br />
I should add- I go to the UofMich.  they are having a war with BCBS and I may not be able to see them in a few months unless they iron things out.  I have made an HFpEF appointment  at Cleveland in August.  You can&#039;t seen an EP there unless referred by another cardiologist.  So the HF is first. (Also made appointment with adult congenital folks but not sure how good they are).  Any suggestions on an EP there?<br />
<br />
By &quot;there&quot; do you mean Cleveland Clinic or UofM? If you mean Cleveland, then yes, I have a recommendation: Pasquale Santangeli. He&#039;s the EP director there so it might take some time to get scheduled, but he&#039;s a personal friend of Natale and trained with him. I would consider the two of them on par with each other.</div></blockquote>
<br />
Thanks you sorry that wasn&#039;t clear.  Yes CC.  Hopefully HF card will refer me to them (I may even try and make an appointment or have my UM doc call).  Thanks for the name]]></description>
            <dc:creator>bettylou4488</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 24 May 2026 14:51:38 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201452,201461#msg-201461</guid>
            <title>Re: HF and afib/flutter</title>
            <link>https://www.afibbers.org/forum/read.php?9,201452,201461#msg-201461</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>mjamesone</strong><br />
So does anyone who is NOT overweight take them- or have info on that- wrt afib or HF if you deal with that?<br />
<br />
I looked into some time ago. And yes, cardio protective irrespective if you are overweight or not. However, if you are not overweight, there may be an insurance issue.<br />
<br />
I finally decided against these drug because I already have gastroparesis, meaning my stomach empties slowly, and GLP-1 drugs can slow gastric emptying even further. That&#039;s in part how they help reduce appetite. <br />
<br />
But other than that, I definitely would have considered these drugs, especially since I was recently stented for CAD.<br />
<br />
<br />
Jim</div></blockquote>
<br />
Thanks for responding.  I do have some gastro stuff I deal with.... There is a local. urgent care who does an out of pocket program.  They would not prescribe for me but I was wondering if they would work with my cardiologist so I could get on their cash program directed by my doc.  it&#039;s worth a shot]]></description>
            <dc:creator>bettylou4488</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 24 May 2026 14:50:32 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201452,201460#msg-201460</guid>
            <title>Re: HF and afib/flutter</title>
            <link>https://www.afibbers.org/forum/read.php?9,201452,201460#msg-201460</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>susan.d</strong><br />
I wanted to reach out and share my experience with a medication called Spironolactone, as it has significantly helped my heart health.<br />
<br />
I was prescribed a 12.5mg daily dose (half of a 25mg pill) to be taken first thing in the morning. While I resisted taking it for six months—partly because my pharmacist was concerned about combining it with Lasix for my edema—it has made a notable difference. After starting the medication, my Ejection Fraction (EF) improved from 39 to 50.<br />
<br />
It is classified as a potassium-sparing diuretic, so it does increase potassium levels. I get my labs checked every three months, and so far, my levels have remained within the upper limits of normal.<br />
<br />
Given how much it has helped improve my heart failure (HF) markers, I thought it might be worth mentioning. Perhaps you could ask your cardiologist about Spironolactone to see if it might be a suitable option for your situation as well.</div></blockquote>
<br />
Thanks so much.. I have HFpEF which is preserved ejection fraction (so myEF is ok.). But I do take aldactone.  It is supposed help HFpEF as well.]]></description>
            <dc:creator>bettylou4488</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 24 May 2026 14:48:15 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201448,201459#msg-201459</guid>
            <title>Re: New SVT</title>
            <link>https://www.afibbers.org/forum/read.php?9,201448,201459#msg-201459</link>
            <description><![CDATA[ GeorgeN<br />
<br />
I did the test and reached 26 seconds.  Could go longer but the reflex jumps in.  I have always focused on deep breathing when swim training, running, mountain climbing (been up maybe 10 fourteeners and one 18,700 (Orizaba in Mexico).  Nothing like that in the last 30 years other than skiing in Telluride Co. where we are at 10,000 to 12,000 for 6 days.  No breathing issues while skiing.  I stop when the legs burn too much.  Mostly blue slopes.]]></description>
            <dc:creator>Ken</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 24 May 2026 13:50:57 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201452,201458#msg-201458</guid>
            <title>Re: HF and afib/flutter</title>
            <link>https://www.afibbers.org/forum/read.php?9,201452,201458#msg-201458</link>
            <description><![CDATA[ <i>You can&#039;t seen an EP there unless referred by another cardiologist. So the HF is first</i><br />
<br />
That makes a lot of sense and it may work to your advantage. <br />
<br />
At Cleveland Clinic, you&#039;re already looking at an elite EP group, including as Wazni, Saliba, Santangeli, Hussein and others.  But even at that level one EP may be a better match than another, especially with your previous congntal heart surgery history. <br />
<br />
So since you&#039;re seeing the HF cardiologist first, Id use that visit to ask who they think is the best EP match for your particular case.<br />
<br />
Best of luck,<br />
<br />
Jim]]></description>
            <dc:creator>mjamesone</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 24 May 2026 13:48:35 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201352,201457#msg-201457</guid>
            <title>Re: Pulsed Field Ablation Bests Meds as First-Line Treatment for Persistent AF in Randomized Trial</title>
            <link>https://www.afibbers.org/forum/read.php?9,201352,201457#msg-201457</link>
            <description><![CDATA[ I just received my summary after appt and was surprised to see a TEE scheduled before PFA. Initially was not informed of this and only to start noacs 1 month before and 3 months after, and to stop flec and metop afterward. I guess its a good precaution, but now wondering why this wasnt explained to me at my appt.]]></description>
            <dc:creator>hwkmn05</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 24 May 2026 12:40:34 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201452,201456#msg-201456</guid>
            <title>Re: HF and afib/flutter</title>
            <link>https://www.afibbers.org/forum/read.php?9,201452,201456#msg-201456</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>bettylou4488</strong><br />
I should add- I go to the UofMich.  they are having a war with BCBS and I may not be able to see them in a few months unless they iron things out.  I have made an HFpEF appointment  at Cleveland in August.  You can&#039;t seen an EP there unless referred by another cardiologist.  So the HF is first. (Also made appointment with adult congenital folks but not sure how good they are).  Any suggestions on an EP there?</div></blockquote>
<br />
By &quot;there&quot; do you mean Cleveland Clinic or UofM? If you mean Cleveland, then yes, I have a recommendation: Pasquale Santangeli. He&#039;s the EP director there so it might take some time to get scheduled, but he&#039;s a personal friend of Natale and trained with him. I would consider the two of them on par with each other.]]></description>
            <dc:creator>Carey</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 24 May 2026 03:10:20 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201452,201455#msg-201455</guid>
            <title>Re: HF and afib/flutter</title>
            <link>https://www.afibbers.org/forum/read.php?9,201452,201455#msg-201455</link>
            <description><![CDATA[ <i>So does anyone who is NOT overweight take them- or have info on that- wrt afib or HF if you deal with that?</i><br />
<br />
I looked into some time ago. And yes, cardio protective irrespective if you are overweight or not. However, if you are not overweight, there may be an insurance issue.<br />
<br />
I finally decided against these drug because I already have gastroparesis, meaning my stomach empties slowly, and GLP-1 drugs can slow gastric emptying even further. That&#039;s in part how they help reduce appetite. <br />
<br />
But other than that, I definitely would have considered these drugs, especially since I was recently stented for CAD.<br />
<br />
<br />
Jim]]></description>
            <dc:creator>mjamesone</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 24 May 2026 02:39:12 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201452,201454#msg-201454</guid>
            <title>Re: HF and afib/flutter</title>
            <link>https://www.afibbers.org/forum/read.php?9,201452,201454#msg-201454</link>
            <description><![CDATA[ I wanted to reach out and share my experience with a medication called Spironolactone, as it has significantly helped my heart health.<br />
<br />
I was prescribed a 12.5mg daily dose (half of a 25mg pill) to be taken first thing in the morning. While I resisted taking it for six months—partly because my pharmacist was concerned about combining it with Lasix for my edema—it has made a notable difference. After starting the medication, my Ejection Fraction (EF) improved from 39 to 50.<br />
<br />
It is classified as a potassium-sparing diuretic, so it does increase potassium levels. I get my labs checked every three months, and so far, my levels have remained within the upper limits of normal.<br />
<br />
Given how much it has helped improve my heart failure (HF) markers, I thought it might be worth mentioning. Perhaps you could ask your cardiologist about Spironolactone to see if it might be a suitable option for your situation as well.]]></description>
            <dc:creator>susan.d</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sun, 24 May 2026 02:15:48 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201448,201453#msg-201453</guid>
            <title>Re: New SVT</title>
            <link>https://www.afibbers.org/forum/read.php?9,201448,201453#msg-201453</link>
            <description><![CDATA[ Hi Ken, <br />
<br />
Know you are fit, but even some who are fit (and young) have a lower CO2 tolerance.  <br />
<br />
In this post [<a href="https://www.afibbers.org/forum/read.php?9,198062,198094#msg-198094"  rel="nofollow">www.afibbers.org</a>] scroll down to CO2 tolerance test and then follow the link and see how you do.  This is something that is trainable.  A decade younger than you, I have trained this for years.   Today, I commonly rock climb with people 30-40 years younger.  I&#039;m  carrying a 60# climbing pack up steep canyon trails at 7,000&#039; elevation.  I&#039;m never out of breath, always nasal breathing.  My younger companions may carry a 10# pack, breathing thorugh their mouth and stopping to catch their breath.  I&#039;m typically the person leading all the climbs including trad &amp; multi-pitch.  Again, I&#039;m never out of breath while the followers who are not leading get winded. Same when I&#039;m alpine skiing at 12-13000&#039;.  Let me know if you want more info.]]></description>
            <dc:creator>GeorgeN</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 23 May 2026 18:53:47 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201452,201452#msg-201452</guid>
            <title>HF and afib/flutter</title>
            <link>https://www.afibbers.org/forum/read.php?9,201452,201452#msg-201452</link>
            <description><![CDATA[ I was diagnosed with HFpEF about 2 or 3 years ago.  Lots of previous heart surgeries (congenial) and I deal with afib. Had 2 successful ablations about 4 years ago- one for fib and follow up for flutter.  Just about a month ago had a flutter/fib re-occurance and ended up getting a successful cardioversion.  It was an exceedingly stressful time.  I had gotten over covid.  Dad fell.  a week later in the hospital.  Organ donation - had to wait. then had to wait for him to die because he didn&#039;t in the time for the organs to be used..then had to deal with mom who is very difficult.  <br />
<br />
I tell you all that to say that probably was what triggered it.<br />
<br />
But I am researching HF and HFpEF (heart failure preserved ejection fraction), along with Afib and I see a lot of stuff.  <br />
<br />
I take a calcium channel blocker (cardizem).  I am reading that isn&#039;t optimal.<br />
<br />
I am reading a LOT about GLP1s.  I think Carey posted here an article I just read.  <br />
<br />
6 months ago my HF doc said he only did that for overweight people but it looks like it could be very heart protective for both HF and Afib. I see him again this next week.<br />
<br />
So does anyone who is NOT overweight take them- or have info on that- wrt afib or HF if you deal with that?<br />
<br />
I should add- I go to the UofMich.  they are having a war with BCBS and I may not be able to see them in a few months unless they iron things out.  I have made an HFpEF appointment  at Cleveland in August.  You can&#039;t seen an EP there unless referred by another cardiologist.  So the HF is first. (Also made appointment with adult congenital folks but not sure how good they are).  Any suggestions on an EP there?  I am loosely scheduled for an ablation in the fall / early winter at UM- but won&#039;t be able to do that if the insurance stuff isn&#039;t figured out.<br />
<br />
I also see my adult congenial doc next week.  I am just trying to figure out what questions to ask and specifically the GLP-1 thing.]]></description>
            <dc:creator>bettylou4488</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 23 May 2026 18:49:28 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201448,201451#msg-201451</guid>
            <title>Re: New SVT</title>
            <link>https://www.afibbers.org/forum/read.php?9,201448,201451#msg-201451</link>
            <description><![CDATA[ <i>Essentially, I have been through all those tests with no issues found.</i><br />
<br />
If you&#039;ve had a CT angiogram and it was clear, then obstructive CAD becomes less likely an explanation, but that doesn&#039;t mean, of course, that it&#039;s the SVT&#039;s. The echo will be another data point but SOB can be a very tough differential diagnosis. Good luck. <br />
<br />
Jim]]></description>
            <dc:creator>mjamesone</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 23 May 2026 16:42:24 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201448,201450#msg-201450</guid>
            <title>Re: New SVT</title>
            <link>https://www.afibbers.org/forum/read.php?9,201448,201450#msg-201450</link>
            <description><![CDATA[ Thanks for the reply Jim,<br />
<br />
Essentially, I have been through all those tests with no issues found.  The patch was because of a low heart rate concern since my resting rate was often in the high 40&#039;s.  Dr. wanted to see what was happening when I slept.  Nothing in the low 40&#039;s.  The whole thing started when I was breathing a bit harder with my normal activities, similar to a previous bi-lateral pulmonary embolism.  No embolism this time, so they looked for something else, but little to nothing found except the SVT.  My max heart rate only reached 127 during the stress test, which is within normal limits for my age.  I feel like my heart doesn&#039;t keep up with O2 demand when under physical exertion.]]></description>
            <dc:creator>Ken</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 23 May 2026 15:20:28 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201448,201449#msg-201449</guid>
            <title>Re: New SVT</title>
            <link>https://www.afibbers.org/forum/read.php?9,201448,201449#msg-201449</link>
            <description><![CDATA[ Hi Ken,<br />
<br />
Of course you will know more with the echo report, but shortness of breath has be taken seriously, and isn&#039;t necessarily related to the SVT&#039;s. <br />
<br />
I would think given your symptons and age that you need a complete cardio pulmonary work up, including PFT&#039;s, Chest CT, a stress exercise test, Lp(a)  and a Calcium Score or CT Angiogram. And if you have any GI issues, then a GI workup as well.<br />
<br />
I had most of the above with my SOB and it pointed to part coronary and part GI. Ended up with six stents, which is not bad considering what might have happened without the tests. Hopefully, in your case something less serious. <br />
<br />
Meanwhile, until you get more information, I would cut bck on the activities that really push your heart rate.<br />
<br />
Jim]]></description>
            <dc:creator>mjamesone</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 23 May 2026 14:31:17 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201448,201448#msg-201448</guid>
            <title>New SVT</title>
            <link>https://www.afibbers.org/forum/read.php?9,201448,201448#msg-201448</link>
            <description><![CDATA[ A long story on why I am at this point, but a little shortness of breath kicked it all off.  Lots of negative testing, but then I wore a Zio Patch for a week and found 77 episodes of SVT, but the longest episode was only 12 seconds.  So, the other 76 episodes were just blips, and I did not notice / feel anything when these &quot;blips&quot; occurred.  Lowest heart rate was 43, highest was 164, which occurred with the 12 second episode.  Average heart rate was 57.  I have not had a discussion with my Dr. regarding the results.  He called, but I wasn&#039;t able to talk at the time.  Waiting for a call back.  Earlier testing showed an enlarged right ventricle.<br />
<br />
Any comments on what this may mean would be appreciated.  To me, it seems that there is little to worry about, but???<br />
<br />
Many of you may recall my story.  Two successful afib ablations, excellent physical condition, 81 years old,1968 Olympic swimmer. Play golf, windsurf, scuba dive, snow ski and regular workouts.]]></description>
            <dc:creator>Ken</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 23 May 2026 12:31:05 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201444,201447#msg-201447</guid>
            <title>Re: EP visit at Dartmouth Hitchcock.</title>
            <link>https://www.afibbers.org/forum/read.php?9,201444,201447#msg-201447</link>
            <description><![CDATA[ <i>This is a teaching hospital so I would like some assurances before hand.</i><br />
<br />
You should have the &quot;talk&quot; about who will do what. Some EPs will do all of it, especially if you ask, some will flat out say, I&#039;ll be there supervising, but this is a teaching hospital and we teach. <br />
<br />
At the end of the day, teaching hopsitals like Cleveland Clinc and Sinai have very high success rates, so it seems to work. And remember, your success gets credited to the EP, so they have a real vested interest. So if you pick the right EP, you will be fine. I would not overthink.<br />
<br />
The one caveat is do not schedule I think in August? I may have the date wrong, but I was told never to schedule an ablation the month the new cardiac fellows arrive and rotate, so find out when that is and schedule say 1-2 months after. This was told to me by an EP at a teaching hospital.<br />
<br />
Anyway, for a basic PVI, it&#039;s pretty much by formula and if they&#039;re trained right, the results should be the same. Now, if they were hunting for an elusive tachycardia, then I&#039;d want a solid assurance who will be looking.<br />
<br />
Jim]]></description>
            <dc:creator>mjamesone</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Sat, 23 May 2026 00:17:53 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201444,201446#msg-201446</guid>
            <title>Re: EP visit at Dartmouth Hitchcock.</title>
            <link>https://www.afibbers.org/forum/read.php?9,201444,201446#msg-201446</link>
            <description><![CDATA[ Thank you for that input. It did make sense to me. In year 17 and never on daily meds or ablated with average of two per year, now at 2 per month without meds and not converting easily and timely. At 72, and mostly healthy, I believe this may be my chance to have some peace of mind with moving/traveling soon. This is a teaching hospital so I would like some assurances before hand.]]></description>
            <dc:creator>hwkmn05</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Fri, 22 May 2026 22:03:40 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201444,201445#msg-201445</guid>
            <title>Re: EP visit at Dartmouth Hitchcock.</title>
            <link>https://www.afibbers.org/forum/read.php?9,201444,201445#msg-201445</link>
            <description><![CDATA[ <i>Of course they only do PVI ...</i><br />
<br />
Don&#039;t know your AF history, but if it&#039;s your first ablation, especially for paroxysmal AF, a PVI only is not a bad thing. In fact that is probably what you want. It&#039;s what I wanted. My EP was highly qualified to do more, but he did a simple PVI because his experience showed that was the right amount of ablation in cases like mine. Going on 3 years AF free. <br />
<br />
More burning does not automatically mean better results and can add risk without necessarily improving success. And just because something can be provoked during the procedure, does not mean it will be a problem when you go home. <br />
<br />
And there is study data supporting both these points.<br />
<br />
Yes, a simple PVI might not work, no guarantees with any ablation, but according to a couple of EPs I spoke to at top cardiac hospitals, if success is defined as a 95% reduction in AF burden, then the odds of a successful ablation can be close to 90%.<br />
<br />
And if your&#039;re in the unlucky 10%, you can always go back later. But you can&#039;t un-ablate tissue that was unecessarily burned the frst time. <br />
<br />
Additional burning outside of the pulmonary veins certainly has its place especially in redo cases, very persistent AF, flutter, identifiable left atrial fibrosis, or other documented tachycardias. <br />
<br />
But what might be most important in your case is simply to find a high-volume EP you have confidence in, who works at a cardiac center of excellence. And not just assume that the most extensive ablation is automatically the best, especially for a first ablation for paroxysmal. <br />
<br />
Jim]]></description>
            <dc:creator>mjamesone</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Fri, 22 May 2026 19:08:39 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201444,201444#msg-201444</guid>
            <title>EP visit at Dartmouth Hitchcock.</title>
            <link>https://www.afibbers.org/forum/read.php?9,201444,201444#msg-201444</link>
            <description><![CDATA[ After 5 weeks since last episode and protocol of 75mg flecainide at bedtime, I took the 100 mile trip to explore options. Mostly what I expected. The fellow was 1 month from leaving and gave his opinion on 4 options. 1. If Im to continue Flec it will be with a BB even if its 12.5mg. 2. Full dose of Flec and Metop daily, not yet. 3.  Tikosyn 3 day stay, no thanks. 4.PFA. Dr Sangha believes I am a good candidate for this and the failures he has seen are 80 yrs plus. Of course they only do PVI and only while in NSR. Ive read most on here from Careys explanation of why ablations fail to the many success and concerns, and have a pretty good idea of what I am facing. My thoughts are I roll the dice closer to home for 1st one with PVI only and hope that sticks, and next one to the rock star in Tx if necessary.  They are 3-5 months out, so I did schedule with time to research while waiting. I have to say however, the Flec has done wonders for nighttime pacs/tachy and afib getting me thru the night with a few hiccups daytime I address with Potassium water. However, its early and meds could wain over time, possibly?]]></description>
            <dc:creator>hwkmn05</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Fri, 22 May 2026 11:13:22 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201424,201443#msg-201443</guid>
            <title>Re: Heading for my 3rd ablation with Dr. Natale</title>
            <link>https://www.afibbers.org/forum/read.php?9,201424,201443#msg-201443</link>
            <description><![CDATA[ There is an option. I did it. Fly into Austin before you wean. <br />
<br />
I lived 45 minutes from Los Robles hospital. I knew with my &gt;190 flutter, once I wean I would need the ER to drug convert me. However 911 would only take me to a local ER and i didnt want to be stuck and miss my ablation. So a fellow on this board suggested an inexpensive hotel that was close to the hospital to guarantee if I did need the ER, an ambulance would take me to the hospital where the ablation was scheduled.<br />
<br />
Actually I was calmer knowing I was close enough to the hospital if my flutter acted up. I never did need an ambulance but it was a good plan B. Especially if you are flying and don’t want an episode on the flight because of your weaning.<br />
<br />
I don’t know about AirbNb prices, but perhaps check it out. Get a place with a kitchenette/microwave/fridge to save on eating out. <br />
<br />
Good luck with your ablation!]]></description>
            <dc:creator>susan.d</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Fri, 22 May 2026 01:28:50 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201417,201442#msg-201442</guid>
            <title>Re: Multaq and low dose amitriptyline</title>
            <link>https://www.afibbers.org/forum/read.php?9,201417,201442#msg-201442</link>
            <description><![CDATA[ I agree.]]></description>
            <dc:creator>Carey</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Thu, 21 May 2026 02:54:18 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201417,201441#msg-201441</guid>
            <title>Re: Multaq and low dose amitriptyline</title>
            <link>https://www.afibbers.org/forum/read.php?9,201417,201441#msg-201441</link>
            <description><![CDATA[ I meant if I wasn’t stopping the amitriptyline. In my opinion I should have been told to stop the amitriptyline before starting Multaq. By the EP or the pharmacy.]]></description>
            <dc:creator>PamelaJean</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Wed, 20 May 2026 23:22:05 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201417,201440#msg-201440</guid>
            <title>Re: Multaq and low dose amitriptyline</title>
            <link>https://www.afibbers.org/forum/read.php?9,201417,201440#msg-201440</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>PamelaJean</strong><br />
No labs or EKG since I started Multaq so wouldn’t that be needed sooner rather than later?</div></blockquote>
<br />
There&#039;s no need for that if you&#039;re taking Multaq alone. I spent a while on Multaq and my EP never felt the need to monitor that, and he&#039;s a stickler for stuff like that.]]></description>
            <dc:creator>Carey</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Wed, 20 May 2026 22:51:16 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201417,201439#msg-201439</guid>
            <title>Re: Multaq and low dose amitriptyline</title>
            <link>https://www.afibbers.org/forum/read.php?9,201417,201439#msg-201439</link>
            <description><![CDATA[ My PCP only refills my amitriptyline, he didn’t prescribe it or the Multaq. And he was the first to respond when I asked three different doctors/NPs. My endocrinologist originally prescribed amitriptyline but he is in a different medical system and would have no access to my EP or PCP records. So I asked his opinion too and he agreed with my PCP. I finally sent another message to my EPs NP saying “never mind I’m doing what my PCP and said, stopping amitriptyline.” Only then did someone reply. This is part of the message: <br />
<br />
“our pharmacist was messaged 5/18/26 about this when you messaged us to look into the interactions and she said &quot;The pt is on a lower dose of amitriptyline and, at this time, the potassium and Magnesium are normal. We would need to monitor those levels regularly, along with the QT interval and dose of amitriptyline to make sure the risk of TaP does not increase.” Which we already have yearly labs ordered and yearly EKG as well to monitor.”<br />
<br />
This is not the first time I find out they were actually having conversations about me but not informing me. How is that helpful? Not even sure if that means amitriptyline would be safe or not. No labs or EKG since I started Multaq so wouldn’t that be needed sooner rather than later? My appointment isn’t until mid-June. Unless my sleep schedule changes drastically I’m not planning on restarting amitriptyline. <br />
<br />
Thanks.]]></description>
            <dc:creator>PamelaJean</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Wed, 20 May 2026 22:34:23 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201417,201438#msg-201438</guid>
            <title>Re: Multaq and low dose amitriptyline</title>
            <link>https://www.afibbers.org/forum/read.php?9,201417,201438#msg-201438</link>
            <description><![CDATA[ <blockquote class="bbcode"><div><small>Quote<br /></small><strong>PamelaJean</strong><br />
<br />
Not so far, but the loop should be closed IMO.  If it&#039;s the same issuing pharmacy, the team should pick that up, probably on software they rely on to advise of potential conflicts. Since you don&#039;t know, yeah, I would at least say something.<br />
<br />
“Not so far” So I shouldn’t be concerned? Say something to the pharmacy? The doctor?</div></blockquote>
<br />
I was perhaps too cryptic...sorry.  So far, you don&#039;t seem to be suffering unduly, and that&#039;s all I meant.  Which is good....no?  As for contacting someone, if your pharmacist hasn&#039;t caught it (mine are scrupulous about this and coach us about any potential problems in view of our medical history), then your PCP, at least, should be queried.]]></description>
            <dc:creator>gloaming</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Wed, 20 May 2026 20:58:31 +0000</pubDate>
        </item>
        <item>
            <guid>https://www.afibbers.org/forum/read.php?9,201417,201437#msg-201437</guid>
            <title>Re: Multaq and low dose amitriptyline</title>
            <link>https://www.afibbers.org/forum/read.php?9,201417,201437#msg-201437</link>
            <description><![CDATA[ I portal messaged my endocrinologist since he first prescribed amitriptyline. I messaged my primary care physician since he handles the refills now. I messaged an NP at the cardiology office since my EP is out of the office until May 26. PC answered quickly and said just stop the amitriptyline. My endocrinologist actually called me the day after I sent him a message and agreed stopping immediately would be best. It’s been almost 48 hours since I sent the message to cardiology and no response. I have skipped the amitriptyline for three nights now and don’t seem to be sleeping any worse than usual. I wake up multiple times during the night either way. Maybe a little more often now but use the toilet and go back to sleep fairly quickly.]]></description>
            <dc:creator>PamelaJean</dc:creator>
            <category>AFIBBERS FORUM</category>
            <pubDate>Wed, 20 May 2026 14:56:38 +0000</pubDate>
        </item>
    </channel>
</rss>
