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主动脉瓣置换的两种替代性无缝合策略:一项两中心经验。

Two alternative sutureless strategies for aortic valve replacement: a two-center experience.

作者信息

Concistrè Giovanni, Santarpino Giuseppe, Pfeiffer Steffen, Farneti Pierandrea, Miceli Antonio, Chiaramonti Francesca, Solinas Marco, Glauber Mattia, Fischlein Theodor

机构信息

From the *Department of Cardiac Surgery - Klinikum Nürnberg, Nuremberg, Germany; and †Department of Cardiac Surgery, Ospedale del Cuore "G. Pasquinucci," Fondazione Monasterio-CNR, Massa, Italy.

出版信息

Innovations (Phila). 2013 Jul-Aug;8(4):253-7. doi: 10.1097/IMI.0000000000000007.

Abstract

OBJECTIVE

Important comorbid conditions in patients referred for aortic valve replacement (AVR) require less invasive strategies. We describe our initial experience with the Perceval S (Sorin Group, Saluggia, Italy) and 3f Enable (Medtronic, Minneapolis, MN USA) sutureless aortic bioprostheses.

METHODS

We compared intraoperative data, postoperative clinical outcomes, and echocardiographic results from patients receiving a Perceval S (P group; n = 97) or a 3f Enable (E group; n = 32) prosthesis in two cardiac surgery departments (Nuremberg, Germany, and Massa, Italy).

RESULTS

Baseline patient characteristics were similar in both groups, except for mean ± SD body surface area (P group = 2.01 ± 2.9 m, E group = 1.83 ± 3.8 m; P < 0.001). Sixty-five patients (67%) in the P group and 19 patients (59.5%) in the E group (P = 0.22) underwent minimally invasive AVR with either ministernotomy or right anterior minithoracotomy approach. Concomitant procedures were performed in 37 patients (38%) in the P group and 9 patients (28%) in the E group (P = 0.56). In-hospital mortality was 2%. The mean ± SD prosthesis diameter was 23.5 ± 1.4 mm (P group) compared with 22.1 ± 2 mm (E group) (P < 0.001). In isolated AVR, aortic cross-clamp time was 36 ± 12.7 minutes in the P group and 66 ± 18 minutes in the E group (P < 0.001). At a mean ± SD follow-up of 8.3 ± 4.5 months, survival was 97% (one death in the P group). In five patients (P group = 1, E group = 4), a moderate paravalvular leak was present (P = 0.013). The mean ± SD transvalvular gradient was 9.1 ± 3.3 mm Hg with the Perceval S and 11.2 ± 5.2 mm Hg with the 3f Enable (P = 0.017).

CONCLUSIONS

Aortic valve replacement with sutureless aortic bioprosthesis is feasible, also with a minimally invasive approach. The Perceval S showed lower operative times and moderate paravalvular leaks and lower mean transvalvular gradients than did the 3f Enable, related to the larger diameter of the Perceval S implanted. Both prostheses showed an excellent hemodynamic performance. This new technology needs long-term follow-up.

摘要

目的

因重要合并症而接受主动脉瓣置换术(AVR)的患者需要创伤较小的治疗策略。我们描述了使用Perceval S(索林集团,意大利萨卢贾)和3f Enable(美敦力公司,美国明尼阿波利斯)无缝合主动脉生物假体的初步经验。

方法

我们比较了在两个心脏外科科室(德国纽伦堡和意大利马萨)接受Perceval S(P组;n = 97)或3f Enable(E组;n = 32)假体植入患者的术中数据、术后临床结果和超声心动图结果。

结果

两组患者的基线特征相似,但平均±标准差体表面积除外(P组 = 2.01 ± 2.9平方米,E组 = 1.83 ± 3.8平方米;P < 0.001)。P组65例患者(67%)和E组19例患者(59.5%)(P = 0.22)采用胸骨下段小切口或右前侧胸壁小切口进行微创AVR。P组37例患者(38%)和E组9例患者(28%)(P = 0.56)进行了同期手术。住院死亡率为2%。P组假体平均±标准差直径为23.5 ± 1.4 mm,而E组为22.1 ± 2 mm(P < 0.001)。在单纯AVR中,P组主动脉阻断时间为36 ± 12.7分钟,E组为66 ± 18分钟(P < 0.001)。平均±标准差随访8.3 ± 4.5个月时,生存率为97%(P组1例死亡)。5例患者(P组1例,E组4例)存在中度瓣周漏(P = 0.013)。使用Perceval S时平均±标准差跨瓣压差为9.1 ± 3.3 mmHg,使用3f Enable时为11.2 ± 5.2 mmHg(P = 0.017)。

结论

使用无缝合主动脉生物假体进行主动脉瓣置换术是可行的,采用微创方法也可行。与3f Enable相比,Perceval S手术时间更短、瓣周漏中度且平均跨瓣压差更低,这与植入的Perceval S直径较大有关。两种假体均显示出优异的血流动力学性能。这项新技术需要长期随访。

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