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HomeHealth QueryCardiologyI had a TMT test in February 2019 and an Echo in A...
  • female
  • 45 Years
  • 07/02/2025

I had a TMT test in February 2019 and an Echo in April 2020, and both were normal, but I'm still experiencing a lot of symptoms. I've been having chest discomfort that moves to my throat and arm for over two years now. I get ECGs done twice every month since 2019, and they only show sinus tachycardia. How long should I trust the normal TMT results? Since it's not COVID causing this, I keep wondering if I should repeat the TMT and Echo. What do you think?

Doctor 1

Answered by 1 Apollo Doctors

Dr. Dr Shubham Chauhan

Dr Shubham Chauhan

General Practitioner

  • MBBS
  • 4+ Yrs
Consult Now

That could be due to anxiety visit Psychiatrist for evaluation and appropriate management

Dr. Shubham Suggests...

Consult a Cardiologist

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Answered 04/07/2025

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I'm about 5 feet 3 inches and weigh 70 kg. I've been taking olmetrack 20 mg for the last year, but now my blood pressure is at 13084. I was wondering if I could switch to taking olmighty 20 mg instead, since it's cheaper. Are these two medications different in any way?

Both Olmetrack 20 mg and Olmighty 20 mg contain the same active ingredient, which is olmesartan. They belong to the same class of medications called angiotensin II receptor blockers (ARBs) and are used to treat high blood pressure. You can switch from Olmetrack 20 mg to Olmighty 20 mg as they are equivalent in terms of effectiveness. The recommended dosage for Olmighty 20 mg would be the same as Olmetrack 20 mg, which is usually once daily. It is important to monitor your blood pressure regularly after switching to ensure that it remains controlled. If you experience any unusual symptoms or side effects, please consult your healthcare provider.

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I'm worried because my wife has been taking Concor AM 5 and she's started experiencing some sweating and headaches. Could this be caused by the medication, or might something else be going on?

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I recently got an ECG and 2D Echo done and the results show acyanotic congenital heart disease with severe valvular PS, mild PR, mild infundibular stenosis, significant RV hypertrophy, mild TR, and a moderately restrictive PDA with LR shunt gradient of 50 mmHg. The report also mentions RV hypertrophy, RA MPA dilation, but normal LV systolic function. Can you explain what this condition means and whether surgery is the only option to treat it? What would be the estimated cost for surgery and is there any chance of managing this with just medication? If I don't get surgery, how long can I expect to live with this condition and are there risks of a heart attack?

Consult a cardiologist with detailed Echo report (both hard copy and cd) This is a congenital malformation in your heart The definitive treatment is surgery Risk of heart attack per say because of this disease doesn't increase many fold but a potential risk of heart failure is always there Consult a cardiologist as advised earlier

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