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Post Transseptal Puncture/PVI Ablation Symptoms

MeganMN profile image
14 Replies

After my ablation, I did have absolutely new onset ocular migraines after the ablation. My understanding is that it can be related to the trans septal puncture, maybe the autonomic nervous system injury/inflammation. I also have, in conjunction, a weird dizzy/head rush feeling that precedes the headache. My heart rate/BP is always fine. It is getting better, and my EP team is not concerned about it. Just wondering if others have experienced similar.

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MeganMN profile image
MeganMN
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14 Replies
Responsable profile image
Responsable

Hi, Megan! I had no ablation until now, but am regular reader of other people's posts and, during the past 10 years, I have noticed the following. After the ablation, large percentage of people complain about symptoms similar to yours - disturbed vision, headaches, disturbed stomach, shortness of breath etc. I would say that your idea about disturbed Autonomous Nervous System is quite correct. A good thing is that, after some time, the things correct from themselves and the symptoms disappear.

I have noticed another thing - people are usually very happy if their BP is "normal" or "on the low side". Low heartrate and low BP may only mean that, at least temporarily, your blood flowrate is not large enough, so your body suffers. Being the most sensitive, nervous cells in the brain suffer most, so you get a headache. Best wishes!

CDreamer profile image
CDreamer

If you read the leaflet on Recovering from Ablation on the AFA website you will it is see very common.

I had the opposite- migraines with aura all my life - ablation - PFO found - not a migraine since.

Buzby62 profile image
Buzby62

Here’s a link where you’ll find the USA versions of the sheets CDreamer mentions

heartrhythmalliance.org/afa...

Best wishes

CDreamer profile image
CDreamer in reply toBuzby62

The one written by patients looks exactly the same on both US & UK sites - if you scroll down from the link given you will eventually see it.

I’m unable to post a direct hyperlink.

What medics tell you and real experience doesn’t always match!

MeganMN profile image
MeganMN in reply toCDreamer

Seriously! This handout should be given out at the hospital. My EP team didn't tell me any of that!! Thank you!!

Buzby62 profile image
Buzby62 in reply toMeganMN

I had the UK versions in the pack issued in a counselling session a few weeks before my ablation. There’s no difference in the versions other than the AFA contact details for UK or USA.

Best wishes

CDreamer profile image
CDreamer in reply toMeganMN

That’s because they only offer their own literature, not the AFA literature. Canvas your hospital.

Blueflags profile image
Blueflags in reply toMeganMN

Hi MeganMN, I absolutely agree that you should be told or be given some indication of various side effects, I had the same thing and was worried that I had a problem with my eye sight!! 😊😊

Desertflowerchild profile image
Desertflowerchild in reply toBlueflags

My EP mentioned the possibility of ocular migraines twice. I imagine she understood such a side effect would be very disturbing to patients not forewarned.

Buzby62 profile image
Buzby62 in reply toCDreamer

It’s just the AFA contact details differ I believe.

opal11uk profile image
opal11uk

Yes, I did, everything would go white, heat would radiate from my feet up to my head and then whiteout. It was very scary particularly as I had to go up and down stairs etc., at the same time I would have occasions when I would speak and all that came out was gobbledegook, I knew perfectly well what I was saying but no one else did!!!!! So, after return visits to the hospital where I had the ablation carried out, without explanation other than migraines my cardiologis, concerned about the drop in my hr and the risks of me passing out decided a pacemaker would be the best option, I'm pleased to say it was and I haven't had another so called migraine since 2015.

BevCynfelyn profile image
BevCynfelyn

I had a mitraclip operation last Tuesday which has brought with it multicoloured zigzags, flying black dots and a whole gammit of weird visual disturbances. No one in the hospital was the faintest bit surprised or alarmed by it, and one week on they are getting less common. Apparently caused by the puncture being made from the right side of my heart to the left.Today I've driven the car for the first time since the operation

marcyh profile image
marcyh

My EP says my transseptal puncture is difficult. I have had ocular disturbances after my two ablations but only briefly - one day. No headaches.

Madscientist16 profile image
Madscientist16

Yes, I had repeated ocular migraines immediately after my ablation for 3 or 4 weeks but they are greatly diminished. I have had maybe 3 or 4 in the last 5 years.

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