Sjogren’s Syndrome with heart pain
Has anyone had chest pain with Sjogren’s disease?
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Has anyone had chest pain with Sjogren’s disease?
Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.
i don’t have a rheumatologist. However, i have an excellent cardiologist and excellent endocrinologist.
I have only had incidents of AFIB when i have been hyperthyroid. Emergency rooms apparently routinely test TSH level when patients have “heart attack like symptoms”.
I have so many specialists and don’t feel like i need a rheumatologist. My endochrinologist and my cardiologist agree that my occasional incidents of cardiac symptoms are triggered by hyperthroidism.
Hyperthyroidism (graves’ disease in my case) is known to trigger afib. I do not know anything about the correlation between other autoimmune conditions and cardiac symptoms.
If all my test results were normal, my next step would have been to go to an electrophysiologist.
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1 ReactionI do have heart pain. I don’t know if it is because of me having Sjogren’s but my cardiolologist is very aware and mindful of the fact that I have Sjogren’s. Every single visit (1/yr now) I have an EKG and an echocardiogram. I suffer from congestive heart failure and a left bundle branch block (that part is probably not the Sjogren’s fault). I am really blessed to have a good cardiologist. I don’t care for him (personality difference) but I don’t have to…because he is thorough and efficient. I respect and trust him. It’s really important to have that trust.
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1 ReactionBecky, i’m sorry that i don’t have any useful information to provide you. i have repeatedly been informed by numerous drs that An abnormally low level of TSH is a valid root cause of Afib. During each of the few Afib incidents i have had, my TSH has been highly abnormal. Moreover, i have never had chest pain. if i had chest pain i would be inclined to see my pulmonologist. And with thyroid auto-immune disease, i have repeatedly been advised to see an endochrinologist rather than a rheumatologist. The one time i went to a rheumatologist, the Dr told me that i didnt belong there.
I have been tested for Sjorgrens and do not test positive. Nonetheless, i have very dry itchy eyes. which are treated by a cornea specialist at the no 1 ranked eye institute in the country. i am fortunate to live near there. My eyes are treated with Cequa (.09 percent) cyclosporine eye drops . i’ve also had surgically inserted “plugs” in my tear ducts and for a few years serum eye drops spun from my bloodZ i ultimately developed an auro8une reaction to the eye drops made from my blood serum. i also have an excellent allergist/immunologist who has helped me a lot. I wish you all the best. Maybe you want to consider trying some new physicians with different perspectives? That’s what i always do when i feel like i’ve reached a brick wall with any of my physicians c
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2 ReactionsI've had tachycardia for yrs on n off but lately it's been each time longer and longer episodes..BP meds don't always work and I get very anxious when eyes are blurry from high BP.. im on a new BP which is working better, Aldactone..but I took it 2x one day..12 hrs apart and EMT came to adjust my rhythm which was terrifying doing it without anesthesia..my heart rate was high but BP was 70/60...my next visit will be cardio to be sure my heart is ok..every test has been normal but lately nothing is normal..I just want my energy back, Crohns in remission and be able to do my Grad classes..wow
I was diagnosed with CAN (cardiac autonomic neuropathy).
I saw a neurologist. They did EMG/nerve conduction test along with biopsies for small fiber neuropathy. The cardiologist did a one month holter monitor test on me. I go between bradycardia/tachycardia.
My blood pressure goes up and down. I also have Afib and ventricler fib. There are other things that cause Afib. One of mine used to be low potassium. I take prescription potassium 20mgs twice a day and have had IV potassium. You don’t want that very painful.
So sorry Hugs