M. Benfarhat et al., RESULTS OF PERCUTANEOUS DOUBLE-BALLOON MITRAL COMMISSUROTOMY IN ONE MEDICAL-CENTER IN TUNISIA, The American journal of cardiology, 76(17), 1995, pp. 1266-1270
Percutaneous balloon mitral commissurotomy was attempted in Tunisia, w
here rheumatic fever is still endemic, in 463 consecutive patients wit
h severe rheumatic mitral valve stenosis. Their mean age +/- SD was 33
+/- 12 years (range 8 to 68), 324 patients (70%) were women, and 327
(71%) were in sinus rhythm. Valvotomy was technically successful in 45
4 patients (98%). The mean mitral valve gradient decreased from 20 +/-
7 to 6 +/- 4 mm Hg, mean left atrial pressure decreased from 27 +/- 8
to 15 +/- 6 mm Hg, cardiac index increased from 3.0 +/- 0.7 to 3.6 +/
- 0.8 L/min/m(2), and Gorlin mitral valve area, from 0.97 +/- 0.19 to
2.2 +/- 0.4 cm(2) (all p <0.001). Two-dimensional echocardiographic mi
tral valve area increased from 1.03 +/- 0.18 to 2.15 +/- 0.36 cm(2) (p
<0.00001). A final valve area of greater than or equal to 1.5 cm(2) w
as achieved in 98% of patients. Multivariate analysis identified a pre
-mitral valve area <0.8 cm(2) and an echocardiographic score (echo sco
re) greater than or equal to 12 as the strongest predictors of residua
l stenosis (final mitral valve area <1.5 cm(2)). Major procedural comp
lications included mortality (0.4%), tamponade (0.7%), thromboembolism
(2.0%), severe mitral regurgitation (4.6%), significant (pulmonary to
systemic flow ratio greater than or equal to 1.5) interatrial shunt (
4.8%). Four hundred thirty patients were followed vp between 6 and 82
months (mean 37 +/- 22): 95% were in functional class I to II without
reintervention, and 7 patients died (1.6%); restenosis (echocardiograp
hic mitral valve area <1.5 cm(2)) occurred in 10.4% of patients. The 3
-year Kaplan-Meier freedom from restenosis was 92%, and from reinterve
ntion 93%. Because fluoroscopic calcium and postprocedure mitral valve
area less than or equal to 1.8 cm(2) were the independent predictors
of restenosis, patients with calcified valves should be selected for t
his procedure on a case-to-case basis.