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下一代球囊扩张式经导管心脏瓣膜在主动脉瓣环超过正式批准尺寸时的适用性。

Applicability of next generation balloon-expandable transcatheter heart valves in aortic annuli exceeding formally approved dimensions.

机构信息

Department of Cardiovascular Surgery, University Heart Center Hamburg, Martinistraße 52, 20246, Hamburg, Germany.

Department of Cardiac and Thoracic Surgery, University Hospital Halle, Ernst-Grube-Straße 40, 06120, Halle (Saale), Germany.

出版信息

Clin Res Cardiol. 2016 Jul;105(7):585-91. doi: 10.1007/s00392-015-0954-9. Epub 2015 Dec 17.

Abstract

OBJECTIVES

Physicians are frequently confronted with patients suffering from aortic stenosis with annular diameters exceeding dimensions in which currently available transcatheter heart valves (THV) are formally approved. Experience in patients receiving significantly undersized Sapien 3 (S3) THV (Edwards Lifesciences, Inc., Irvine, CA, USA) in aortic annuli up to 32 mm has not been reported so far.

METHODS

Patients with aortic annuli exceeding the formally determined upper size limit and who received a 29 mm S3, were identified from our database. Calcification pattern and annulus dimension were analyzed retrospectively using the 3mensio Medical Imaging software. Clinical endpoints were adjudicated in accordance with the updated standardized VARC-2 definitions.

RESULTS

21 consecutive patients with aortic annuli ≥28.1 mm received a 29 mm THV. All patients were male (77.4 ± 8.1 year, logEuroSCORE I 22.5 ± 14.1 %). Multi-slice computed tomography and transesophageal echocardiography derived annular dimensions were 30.2 ± 1.5 vs. 28.8 ± 0.9 mm (p = 0.0001). Total calcium load of the aortic valves was 1327 ± 957 mm(3). Device success according to VARC-2 definitions was achieved in 100 % (21/21). All-cause 30-day mortality was 0 % (0/21). Rate of permanent pacemaker implantation was 14.3 % (3/21). No paravalvular leakage ≥ grade II was detectable.

CONCLUSIONS

Preliminary experience suggests implantation of this type of THV in aortic annuli up to 32 mm to be feasible and safe, in particular calcification patterns. It does not result in a relevant incidence of PVL ≥ grade II, or increased rate of VARC-2 adjudicated clinical endpoints. Also, functional outcomes regarding transvalvular gradients or EOA demonstrate applicability of this THV in such patients.

摘要

目的

医生经常会遇到瓣环直径超过目前可用的经导管心脏瓣膜(THV)正式批准尺寸的主动脉瓣狭窄患者。目前尚未报道在瓣环直径达 32mm 以下的情况下,使用明显尺寸过小的 Sapien 3(S3)THV(爱德华兹生命科学公司,加利福尼亚州欧文,美国)治疗患者的经验。

方法

从我们的数据库中确定了瓣环直径超过正式确定的上限且接受 29mm S3 的患者。使用 3mensio 医疗成像软件回顾性分析钙化模式和瓣环尺寸。临床终点按照更新的标准化 VARC-2 定义进行裁决。

结果

21 例连续主动脉瓣环直径≥28.1mm 的患者接受了 29mm THV。所有患者均为男性(77.4±8.1 岁,logEuroSCORE I 22.5±14.1%)。多层螺旋 CT 和经食管超声心动图测量的瓣环直径分别为 30.2±1.5mm 与 28.8±0.9mm(p=0.0001)。主动脉瓣总钙负荷为 1327±957mm³。根据 VARC-2 定义,器械成功率达到 100%(21/21)。所有患者 30 天全因死亡率为 0%(0/21)。永久起搏器植入率为 14.3%(3/21)。未检测到任何≥2 级的瓣周漏。

结论

初步经验表明,在瓣环直径达 32mm 内植入此类 THV 是可行且安全的,特别是在钙化模式方面。这并不会导致明显的≥2 级瓣周漏发生率或增加 VARC-2 裁定的临床终点发生率。此外,关于跨瓣梯度或 EOA 的功能结果表明,这种 THV 可适用于此类患者。

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