In vitro analysis of mechanisms of balloon valvuloplasty of stenotic mitral valves

https://doi.org/10.1016/0002-9149(87)90806-XGet rights and content

Abstract

Preliminary reports indicate that percutaneous balloon valvuloplasty is efficacious for treatment of mitral stenosis. The present study was designed to evaluate whether anatomic features of stenotic mitral valves in older adults affect the efficacy of balloon valvuloplasty and to determine the mechanism by which increased orifice area is accomplished. Fifteen mitral valves excised intact at the time of mitral valve replacement from patients with no more than 2 +/ 4 + mitral regurgitation were selected for study. Balloon valvuloplasty was performed using a sequence of dilation catheters with balloons 18 to 25 mm in inflated diameter. Mitral valve area, measured with a conical valve sizer, increased from 0.71 ± 0.06 cm2 (mean ± standard error of the mean) to 1.77 ± 0.19 cm2 (p < 0.0001) after valvuloplasty, resulting in an increase in calculated orifice area of 185 ± 27% (range 34 to 407%). The increase in calculated orifice area correlated inversely with orifice area before valvuloplasty (r = −0.57; p = 0.026), but was unrelated to extent of calcific deposits on the prevalvuloplasty x-ray of the excised mitral valve. Gross examination together with x-ray analysis after valvuloplasty revealed that the mechanism of balloon valvuloplasty in each case involved commissural splitting, including splits through heavily calcified commissures, without grossly apparent detachment of tissue fragments. These findings suggest that balloon valvuloplasty augments the functional mitral valve orifice area in a manner analogous to standard surgical commissurotomy, and balloon valvuloplastv is likely to be efficacious for a wide spectrum of adult mitral valvular stenosis, including severe stenosis with extensive calcific deposits.

Cited by (0)

This study was supported in part by Grant HL 32747-01 from the National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, and the GenRad Foundation, GenRad, Inc., Concord, Massachusetts.

View full text