自体肺动脉瓣移植术治疗先天性主动脉瓣病变

目的　总结自体肺动脉瓣移植手术 (Ross手术 )治疗先天性主动脉瓣病变的疗效。方法　自 1994年 10月至 2 0 0 3年 11月 ,共收治 2 0例先天性主动脉瓣病变患者行Ross手术治疗 ,其中男 15例 ,女 5例 ,平均年龄 2 5岁 ;术前诊断 :主动脉瓣二瓣畸形 12例 ,主动脉瓣叶脱垂 5例 ,瓣叶发育不良 3例 ,合并亚急性细菌性心内膜炎 4例 ,合并室间隔缺损 2例。术前超声心动图检查 (UCG)示所有患者均存在主动脉瓣狭窄或 /并关闭不全 (中重度 )。左心室舒张末内径 (LVDD) (6 0 5 1±11 87)mm ,主动脉瓣跨瓣压差 (2 7 0 4± 6 80 )mmHg。心功能 (NYHA分级 )Ⅱ级 17例 ,Ⅲ级 3例。所有病例均在全麻体外循环中度低温下进行 ,手术分三步进行 :(1)采取自体肺动脉瓣 ;(2 )切除病变的主动脉瓣并移植自体肺动脉瓣于主动脉位 ;(3)利用同种动脉瓣重建右心室流出道。结果　全组患者无手术死亡 ;左心室舒张末内径明显缩小 ,为 (46 38± 9 17)mm (t=3 4 0 0 7,P =0 0 0 0 8) ,术后主动脉跨瓣压差降至正常范围 (6 80± 0 19)mmHg。术后随访 3个月至 9年 ,所有患者的主动脉瓣、肺动脉瓣结构及功能正常。结论　自体肺动脉瓣移植手术是一种临床疗效好的治疗先天性主动脉瓣病变的手术方法 ,近中期效果良好。

Experience on transplantation of auto-pulmonary graft treating with congenital aortic disease

OBJECTIVE: To summarize the experience on auto-pulmonary transplantation (Ross procedure) treating with congenital aortic disease. METHODS: From October 1994 to November 2003, 20 cases of Ross procedure were performed to treat with congenital aortic disease, Male: 15 cases; Female: 5 cases; age: 25 years; Diagnosis: congenital heart disease (CHD), aortic abnormalities: 12 cases; aortic valve prolapse: 5 cases; aortic valve hypogenesis: 3 cases; combined with subacute bacterial endocarditis (SBE): 4 cases, and ventricle septal defect (VSD): 2 cases; UCG showed aortic stenosis(AS) and/or aortic insufficience (AI) (moderate to severe), Left ventricle diastole diameter (LVDD): (60.51 +/- 11.87) mm, the grade pressure across aortic valve: (27.04 +/- 6.80) mmHg, heart function (NYHA): Class II: 13 cases; Class III: 3 cases; all cases were performed under CPB and moderate hypothermia, the operation procedure was following: (1) taking off auto-pulmonary artery valve; (2) removing dysfunctional aortic valve and auto-transplantation of pulmonary valve on aortic root; (3) putting a pulmonary homograft to rebuild right ventricular outflow tract. RESULTS: The mortality was 0 during stay at hospital, aortic valve function were all normal, LVDD decreased significantly (t = 3.4007, P = 0.0008), the grade pressure across aortic valve was in normal limitation, (6.8 +/- 0.19) mmHg. Follow-up showed heart function was in Class I (NYHA), aortic and pulmonary valve function was very well. CONCLUSION: Ross procedure is a kind of effective alterative operation for treating with congenital aortic valve disease, with good short and middle term results.