Table.
Effects of drugs on functional measures, progression and clinical outcomes of VHD.
AS | AR | MS | MR | TR | |
---|---|---|---|---|---|
ACEi/ARB | RCT: +*; OS: + ; DNR | RCT: −; OS: + ; DNR | N | RCT: N; OS: +; DNR | N |
Beta-blockers | N | BA, F; DNR | F | BA, F; DNR | N |
Bisphosphonates | RCTs: N; OS:±; DNR | N | N | N | N |
Hydralazine | N | F, DNR | N | N | N |
MRAs | N | N | N | N | N |
Nitrates | F | F; DNR | N | F; DNR | N |
Nifedipine | N | + ** | N | N | N |
Statin | RCTs: −; DNR | N | N | N | N |
VHD: valvular heart diseases; AS: aortic stenosis; AR: aortic regurgitation; MS: mitral stenosis; MR: mitral regurgitation; TR: tricuspid regurgitation; ACEi: angiotensin converting enzyme inhibitors; ARB: angiotensin receptor blockers; MRA: mineralocorticoid receptor antagonists; RCT: randomized controlled trials; OS: observational studies; N: not studied/insufficient data; +: benefit; −: no benefit; ±: mixed/inconsistent results on clinical natural history; BA : beneficial effects in animal models only; F: short-term hemodynamic/functional benefits in humans, no long-term data DNR: do not recommend
RCT benefit for exercise tolerance only; no natural history outcome data
RCT benefit for progression/natural history apparently only for hypertensive patients