Early and late results with combined mitral and aortic valve replacement.

Igaku kenkyu. Acta medica Pub Date : 1993-09-01
T Matsuyoshi, M Kimura, Y Tachikawa, M Nakamura, A Iwakuma, N Morishige, K Nakamura, S Sukehiro, Y Kawano, K Anai
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Abstract

From February 1977 to January 1993, a total of 52 patients have undergone combined mitral and aortic valve replacement (MAVR) at the Fukuoka University Hospital. The ages at operation ranged from 35 to 72 years (mean, 55.3 years) for 16 males and 36 females. Twenty-five patients received two bioprosthetic valves (group BB); 6 received a combination of bioprosthetic valve and mechanical valve (group BM); and 21 received two mechanical valves (group MM). The previous intra-cardiac operations were performed on 24 patients (46.2%). The purpose of this study was to learn about the long-term clinical results of MAVR and to analyze the difference among three groups. Seven patients died within 30 days of operation or during initial hospitalization (early mortality: 13.5%). Two patients died at late period, 5.8 years and 6.9 years after operation, respectively (linearized occurrence rate: 0.9%/pt-yr). Patient survival rate including operative death was 82.9% +/- 5.7% at 5 years and 79.0% +/- 6.7% at 8 years in the total number of patients. Thromboembolism occurred in 2 patients in group MM (0.9%/pt-yr). Anticoagulant-related hemorrhage occurred only in 1 patient (0.4%/pt-yr in overall), in whom two bioprosthetic valves were implanted (group BB), in spite of being in good control with anticoagulants. No infective endocarditis was encountered in any patients during any of the periods. Reoperations were performed in 7 patients (3%/pt-yr in overall), 5 in group BB and 2 in group MM. Percentage freedom from reoperation was 86.4% +/- 5.9% at 5 years and 78.2% +/- 7.7% at 8 years in all. There was no difference among the three groups. Percentage freedom from overall morbidity and mortality was 74.5% +/- 6.9% at 5 years in all. Group MM showed higher morbidity and mortality at 8 years than other groups, but there were no significance (MM: 52.4% +/- 17.6%, BB: 76.5% +/- 9.5%, BM: 83.3% +/- 15.2%). We conclude that there were no significant differences in long-term results of NAVR which consisted of the following combinations of prostheses such as BB, BM, and MM. Redoing MAVR with New York Heart Association functional class IV and emergency cases were considered as in-hospital risk factors.

二尖瓣和主动脉瓣联合置换术的早期和晚期结果。
从1977年2月至1993年1月,共有52名患者在福冈大学医院接受了二尖瓣和主动脉瓣联合置换术(MAVR)。手术年龄35 ~ 72岁(平均55.3岁),男16例,女36例。25例患者接受2个生物假体瓣膜(BB组);6例采用生物假体瓣膜联合机械瓣膜(BM组);21例采用2个机械阀(MM组)。既往行心脏内手术24例(46.2%)。本研究的目的是了解MAVR的长期临床结果,并分析三组之间的差异。7例患者在手术30天内或初次住院期间死亡(早期死亡率:13.5%)。2例患者分别于术后晚期、5.8年和6.9年死亡(线性化发生率:0.9%/pt-年)。包括手术死亡的患者5年生存率为82.9% +/- 5.7%,8年生存率为79.0% +/- 6.7%。MM组2例患者发生血栓栓塞(0.9%/pt-yr)。抗凝血相关出血仅发生在1例患者中(总体为0.4%/pt-年),其中植入了两个生物假瓣膜(BB组),尽管抗凝血药物控制良好。所有患者均未发生感染性心内膜炎。7例患者再次手术(总体为3%/pt-年),BB组5例,MM组2例。5年生存率为86.4% +/- 5.9%,8年生存率为78.2% +/- 7.7%。三组之间没有差异。总体发病率和死亡率的解脱率为74.5% +/- 6.9%。MM组8年发病率和死亡率高于其他组(MM: 52.4% +/- 17.6%, BB: 76.5% +/- 9.5%, BM: 83.3% +/- 15.2%),但差异无统计学意义。我们得出结论,由以下假体如BB、BM和MM组合组成的NAVR的长期结果无显著差异。与纽约心脏协会功能四级和急诊病例重新进行MAVR被认为是院内危险因素。
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