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PAH or NOT 🤔
Dear all,
Just to recap…I had percutaneous ASD closure Dec 6 with an Amplatzer closure device. The 3cm hole hadn’t been picked up during my adult life until now. A TTE/TOE & heart MRI also confirmed right heart dilatation with raised pulmonary pressures which I’m surmising is a diagnosis of PAH?
I’ve also had a pacemaker inserted Dec 12 for bradycardia/standstill due to 2:1 Mobitz II heart block.
I’ve been to see the cardiologist dealing with the electrical problems with my heart to have the position of my pacemaker checked this am. I stressed to him several times how breathless I felt. I told him in earnest that I feel like I’ve aged 30 years in two weeks.
He checked my ankles for oedema, sounded my chest, checked jugular venous pressures as well as blood pressure, heart rate and oxygen saturations and all were unremarkable. Pardon my ignorance regarding pulmonary hypertension, but am I safe to assume in the absence of yielding a normal examination, that I no longer have it?
I have to return to clinic Jan 7 & staff will perform a TTE if I still remain breathless. At least I’m fairly certain that I shouldn’t have a pulmonary embolism as I’m on dual antiplatlet therapy.
Any comments of help or advice would be sincerely valued. I’m so very new to all of this.
Kind regards,
Michelle
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