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The Journal of Thoracic and Cardiovascular Surgery, Vol 88, 432-438, Copyright © 1984 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
D Burckhardt, A Hoffmann, S Vogt, M Pfisterer, J Hasse and E Gradel
To evaluate the clinical performance of the St Jude Medical bileaflet heart
valve prosthesis, we followed 150 consecutive patients (95 male and 55
female patients, mean age 54 years, range 1 to 74 years) for an average of
24 months. These included 74 patients with aortic, 56 patients with mitral,
and 20 patients with multiple valve replacement. During the 2 year
follow-up, there were a total of four perioperative and seven late deaths,
two of which were prosthesis related. Reoperation was necessary in four
patients, because of paravalvular leaks in two patients with mitral and one
patient with aortic prostheses and because of leaflet dislodgment in one
patient with a mitral prosthesis, a postoperative complication that has not
been reported previously. The thromboembolic rate per 100 patient-years was
2.6 in aortic and 2.9 in mitral valve replacement, the symptoms being
reversible in all patients. All patients were receiving anticoagulant
therapy. A total of four complications of anticoagulant therapy (three
minor and one fatal) were observed. Significant hemolysis was observed in
none of the patients. In patients with dyspnea, the New York Heart
Association functional classification was 2.7 +/- 0.8 preoperatively versus
1.3 +/- 0.6 postoperatively. In patients with angina, it was 2.6 +/- 0.6
preoperatively versus 1.03 +/- 0.2 postoperatively. Noninvasive Doppler
measurements revealed excellent flow characteristics, values being close to
those obtained in natural valves (mean +/- standard deviation of maximal
flow velocity: 1.5 +/- 0.5 versus 0.9 +/- 0.1 m/sec in the aortic position;
1.1 +/- 0.3 versus 0.8 +/- 0.3 m/sec in the mitral position).
ARTICLES
Clinical evaluation of the St. Jude Medical heart valve prosthesis. A two-year follow-up of 150 patients
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