Seeking shared experiences. I'm a 39-year-old male, underwent a second ablation for paroxysmal afib (first was for WPW). Initially diagnosed with WPW 13 years ago, treated successfully. Ten years later, afib emerged and was managed with flecainide and atenolol for 2.5 years. Recently had ablation due to increased afib frequency.
Post-ablation, experiencing discomfort:occasional mild headaches with slightly blurred vision, slowed digestion leading to stomach discomfort/bloating, frequent burping and passing gas (partly managed with buscopan), especially at night. Occasional diarrhea. Looking for insights from those with similar post-ablation symptoms.
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Al_baj1984
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This is what Dr. John Mandrola* says about this in part:
"....I have seen, in a handful of cases, patients have trouble moving food through their GI tract after ablation. Symptoms include reflux, feeling bloated, and intolerance of big meals, while signs may include distention of the abdomen. Ablation in the left atrium may transiently damage nerves that control motility of the GI tract. The good news is that these effects resolve with time. I usually treat this problem by recommending small meals, and an acid blocker."
It's the vagus nerve he's talking about. I'd also add to make the meals not only small, but lower fat, ask about a course of PPI's to reduce acid and possible some motility medications to keep things moving. And keep on top of your doctors about this if it doesn't resolve in time.
I was given a PPI, lansoprazole to take for six weeks post ablation to keep stomach acid down and protect the oesophagus. Appears to be common practice in the UK whether you have symptoms or not.
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Thanks for this . Went through the document and it’s very informative. Will also talk to my doctor about the meds perhaps he can prescribe something as the nights are becoming difficult.
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