Bourguignon Thierry, Bouquiaux-Stablo Anne-Lorraine, Loardi Claudia, Mirza Alain, Candolfi Pascal, Marchand Michel, Aupart Michel R
Department of Cardiac Surgery, Trousseau University Hospital, Tours, France.
Department of Cardiac Surgery, Trousseau University Hospital, Tours, France.
J Thorac Cardiovasc Surg. 2014 Nov;148(5):2004-2011.e1. doi: 10.1016/j.jtcvs.2014.02.050. Epub 2014 Feb 20.
The aim of the present study was to evaluate the very-long-term results of the Carpentier-Edwards pericardial bioprosthesis in the mitral position.
From 1984 to 2011, 450 Carpentier-Edwards PERIMOUNT pericardial mitral bioprostheses were implanted in 404 consecutive patients (mean age, 68 years; 53% female). Patients undergoing multiple valve replacements were excluded. The clinical, operative, and follow-up data were prospectively recorded. The mean follow-up was 7.2±5.1 years, for a total of 3258 valve-years. The follow-up data were 97.8% complete.
The operative mortality rate was 3.3%. A total of 188 late deaths occurred, for a linearized rate of 5.8%/valve-year. At 20 years, the overall actuarial survival rate was 16.9%±3.9%. Age at implantation, preoperative New York Heart Association class III or IV, and redo procedure were significant risk factors affecting late survival. The actuarial freedom from complications at 20 years was thromboembolism, 83.9%±7.6%; hemorrhage, 80.2%±10.8%; endocarditis, 94.8%±1.4%; structural valve deterioration, 23.7%±6.9%; and explantation owing to structural valve deterioration, 40.5%±8.0%. The competing risk analysis demonstrated an actual risk of explantation owing to structural valve deterioration at 20 years of 25.5%±2.9%. The expected valve durability was 16.6 years for the entire cohort (11.4, 16.6, and 19.4 years for patients aged <60, 60 to 70, and >70 years, respectively).
With a low rate of valve-related events at 20 years and, in particular, a low rate of structural valve deterioration, the Carpentier-Edwards PERIMOUNT pericardial bioprosthesis remains a reliable choice for a mitral tissue valve, especially in patients >60 years old.
本研究旨在评估卡彭蒂埃 - 爱德华兹心包生物瓣在二尖瓣位的长期效果。
1984年至2011年,连续404例患者(平均年龄68岁;53%为女性)植入了450枚卡彭蒂埃 - 爱德华兹PERIMOUNT心包二尖瓣生物瓣。排除接受多瓣膜置换的患者。前瞻性记录临床、手术及随访数据。平均随访时间为7.2±5.1年,共3258个瓣膜年。随访数据完整性为97.8%。
手术死亡率为3.3%。共发生188例晚期死亡,线性化死亡率为5.8%/瓣膜年。20年时,总体精算生存率为16.9%±3.9%。植入时年龄、术前纽约心脏协会心功能Ⅲ或Ⅳ级以及再次手术是影响晚期生存的显著危险因素。20年时无并发症的精算自由度为:血栓栓塞83.9%±7.6%;出血80.2%±10.8%;心内膜炎94.8%±1.4%;瓣膜结构退变23.7%±6.9%;因瓣膜结构退变而取出瓣膜40.5%±8.0%。竞争风险分析显示,20年时因瓣膜结构退变而实际取出瓣膜的风险为25.5%±2.9%。整个队列的预期瓣膜耐久性为16.6年(年龄<60岁、60至70岁和>70岁的患者分别为11.4年、16.6年和19.4年)。
卡彭蒂埃 - 爱德华兹PERIMOUNT心包生物瓣在20年时瓣膜相关事件发生率较低,尤其是瓣膜结构退变率低,仍然是二尖瓣组织瓣膜的可靠选择,特别是对于60岁以上的患者。