Division of Cardiac Surgery of the Peter Munk Cardiac Centre at Toronto General Hospital and the University of Toronto, Toronto, Ontario, Canada.
Division of Cardiac Surgery of the Peter Munk Cardiac Centre at Toronto General Hospital and the University of Toronto, Toronto, Ontario, Canada.
J Thorac Cardiovasc Surg. 2021 Mar;161(3):890-899.e1. doi: 10.1016/j.jtcvs.2020.07.121. Epub 2020 Sep 5.
To examine the late outcomes of reimplantation of the aortic valve (RAV) in patients followed prospectively since surgery.
All 465 patients who had RAV from 1989 to 2018 were followed prospectively with periodic clinical and echocardiographic assessments. Mean follow-up was 10 ± 6 years and 98% complete.
Patients' mean age was 47 ± 5.1 years, and 78% were men. The aortic root aneurysm was associated with Marfan syndrome in 164 patients, Loeys-Dietz syndrome in 13, bicuspid aortic valve (BAV) in 67, and type A aortic dissection in 33. Aortic insufficiency (AI) was greater than mild in 298 patients. Concomitant procedures were performed in 105 patients. There were 5 operative and 51 late deaths. At 20 years, 69.1% of patients were alive and free from aortic valve reoperation, and the cumulative probability of aortic valve reoperation with death as a competing risk was 6.0%, and the cumulative probability of developing moderate or severe AI was 10.2%. Only time per 1-year interval was associated with the development of postoperative AI by multivariable analysis (hazard ratio, 1.06; 95% confidence interval, >1.02-1.10; P = .006). Gradients across preserved BAV increased in 5 patients, and 1 required reoperation for aortic stenosis. Distal aortic dissections occurred in 22 patients, primarily in those with associated genetic syndromes.
RAV provides excellent long-term results, but there is a progressive rate of AI over time, and patients with BAV may develop aortic stenosis. Patients with genetic syndromes have a risk of distal aortic dissections. Continued surveillance after RAV is necessary.
检查前瞻性随访的主动脉瓣再植入(RAV)患者的晚期结果。
1989 年至 2018 年期间,所有 465 例接受 RAV 的患者均进行前瞻性随访,定期进行临床和超声心动图评估。平均随访时间为 10±6 年,随访率为 98%。
患者平均年龄为 47±5.1 岁,78%为男性。主动脉根部瘤与 164 例马凡综合征、13 例洛伊兹-迪茨综合征、67 例二叶式主动脉瓣(BAV)和 33 例 A 型主动脉夹层相关。298 例患者存在中重度主动脉瓣关闭不全。105 例患者同时进行了其他手术。有 5 例手术死亡和 51 例晚期死亡。20 年时,69.1%的患者存活且无主动脉瓣再次手术,主动脉瓣再次手术且以死亡为竞争风险的累积概率为 6.0%,发展为中度或重度主动脉瓣关闭不全的累积概率为 10.2%。多变量分析显示,只有每增加 1 年间隔时间与术后主动脉瓣关闭不全的发生相关(风险比,1.06;95%置信区间,>1.02-1.10;P=0.006)。5 例保留的 BAV 瓣跨瓣压差增加,其中 1 例因主动脉瓣狭窄再次手术。22 例患者发生远端主动脉夹层,主要发生在合并遗传综合征的患者中。
RAV 提供了极好的长期结果,但随着时间的推移,主动脉瓣关闭不全的发生率逐渐增加,而 BAV 患者可能会发生主动脉瓣狭窄。合并遗传综合征的患者存在远端主动脉夹层的风险。RAV 后需要继续进行监测。