Bortolotti U, Scioti G, Milano A, De Carlo M, Codecasa R, Nardi C, Tartarini G
Department of Cardiology, Angiology and Pneumology, University of Pisa Medical School, Italy.
Ann Thorac Surg. 2000 Jan;69(1):47-50. doi: 10.1016/s0003-4975(99)00856-5.
Aortic valve replacement in elderly patients with a small aortic annulus may pose difficult problems in terms of prosthesis selection. We have evaluated the hemodynamic performance of the 21-mm Carpentier-Edwards Perimount bioprosthesis implanted in elderly patients.
From July 1996 to June 1998, 19 patients (17 women and 2 men, mean age 76+/-4 years and mean body surface area 1.73+/-0.13 m2), had aortic valve replacement with a 21-mm Carpentier-Edwards Perimount bioprosthesis. The hemodynamic performance of the valve was evaluated in 16 patients, who completed at least a 6-month follow-up interval, with transthoracic color-Doppler echocardiography with particular reference to peak and mean transprosthetic gradients, effective orifice area index, and regression of left ventricular mass index.
There were no late deaths and no major postoperative complications. At a mean follow-up of 12+/-7 months, compared to discharge, all patients showed clinical improvement with a significant reduction of peak gradient (from 23+/-4 to 21+/-6 mm Hg, p = 0.04) and left ventricular mass index (from 181+/-23 to 153+/-20 g/m2; p<0.001), whereas mean gradient (from 13+/-3 to 13+/-4 mm Hg, p = not significant) and effective orifice area index (from 1.12+/-0.34 to 1.13+/-0.28 cm2/m2, p = not significant) remained substantially unchanged.
The use of a 21-mm Carpentier-Edwards Perimount bioprosthesis is associated with low transprosthetic gradients and significant reduction in left ventricular hypertrophy after aortic valve replacement. The results of our study suggest that a 21-m Carpentier-Edwards Perimount bioprosthesis should be considered a valid option in elderly patients with aortic valve disease and a small aortic annulus.
对于主动脉瓣环小的老年患者,主动脉瓣置换在假体选择方面可能会带来难题。我们评估了植入老年患者体内的21毫米Carpentier-Edwards Perimount生物假体的血流动力学性能。
1996年7月至1998年6月,19例患者(17名女性和2名男性,平均年龄76±4岁,平均体表面积1.73±0.13平方米)接受了21毫米Carpentier-Edwards Perimount生物假体主动脉瓣置换术。对16例完成至少6个月随访期的患者,采用经胸彩色多普勒超声心动图评估瓣膜的血流动力学性能,特别关注跨假体峰值和平均压差、有效瓣口面积指数以及左心室质量指数的回归情况。
无晚期死亡病例,也无重大术后并发症。平均随访12±7个月时,与出院时相比,所有患者临床症状均有改善,峰值压差显著降低(从23±4降至21±6毫米汞柱,p = 0.04),左心室质量指数降低(从181±23降至153±20克/平方米;p<0.001),而平均压差(从13±3降至13±4毫米汞柱,p = 无显著意义)和有效瓣口面积指数(从1.12±0.34增至1.13±0.28平方厘米/平方米,p = 无显著意义)基本保持不变。
使用21毫米Carpentier-Edwards Perimount生物假体与较低的跨假体压差以及主动脉瓣置换术后左心室肥厚的显著减轻相关。我们的研究结果表明,对于患有主动脉瓣疾病且主动脉瓣环小的老年患者,21毫米Carpentier-Edwards Perimount生物假体应被视为一种有效的选择。