My 59 y.o. mother had MV replacement 3 years ago (St Judes Valve). She had a very complicated
recoveryRecovery position - series (chylothorax,shocked kidney with
dialysisDialysis
Kidney diet - dialysis patients,shocked liver, coded x 2 - to name a few). She somehow survived and has been doing okay until recently. Apparantly her MV placement is causing a lot of problems. The most recent echo reads:
NormalNormal saline flush LV function with moderate LVH and proximal
septalUltrasound, ventricular septal defect - heartbeat
Ventricular septal defect thickening. Severe LV outflow tract obstruction, peak gradient 85 mm Hg appears to be due to both
septalUltrasound, ventricular septal defect - heartbeat
Ventricular septal defect hypertrophyEnlarged prostate
Lymphoid hyperplasia and the placement of the MVR (this is down from 117 in Dec. 2000). SJ MVR appears to have perivalvar MR. There is severe tricuspid regurgitation (4+). Recommend TEE if clinically indicated. Compared to prior study of 12/5/00, severe LV outflow tract obstruction is again noted. Probable perivalvar MR is new. (This is exactly as typed on echo report - I have a copy)
The physicians here say that we can't do anything at this point. They feel we shouldn't do anything until my mother goes into CHF and then they would consider MV replacement again. Clinically she has become very tired lately and admits to DOE. She often sounds winded. She is still carrying on her ADL's, but in our opinion she is not looking good. Do we really just wait until she goes into CHF before doing anything for her? We had a consultation with Dr Brian McGovern (From Boston - he comes to Albany 2 x's a month) in March and he said if everything stayed stable, then we just take a wait and see attitude. That was before the Tricuspid Regurg was a 4+ and before there was what appears to be a perivalvar leak. Mom was also not having much SOB and fatigue at the time. Is it time to get another opinion? She is understandable terrified after the 90 days she spent in ICU three years ago (and so are we). We feel helpless just waiting for the worst to happen. Is this really the best course of action right now? What options does she have? Is heart transplant an option? Would she now need both valves repaired? We would appreciate any advise you could give us. We would also be willing to travel to Cleveland for an evaluation. I should also mention she had to have a pacemaker placed 3 years ago and the battery is running low already. She is currently taking Procrit every other week because of hemolysis of the RBC's from the valve. I don't have a list of the other meds available right now, but I could get it. Please advise. Which type of Doctor do we need - Cardiology or Cardiothoracic Surgeons?