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经导管植入 Edwards SAPIEN 心脏瓣膜治疗肺动脉位置的管道失效:国际多中心临床试验的早期阶段 1 结果。

Percutaneous implantation of the Edwards SAPIEN transcatheter heart valve for conduit failure in the pulmonary position: early phase 1 results from an international multicenter clinical trial.

机构信息

Rush University Medical Center, 1653 West Congress Parkway, Chicago, IL 60612, USA.

出版信息

J Am Coll Cardiol. 2011 Nov 15;58(21):2248-56. doi: 10.1016/j.jacc.2011.07.040.

Abstract

OBJECTIVES

The purpose of this study was to evaluate the safety and effectiveness of the Edwards SAPIEN transcatheter heart valve (Edwards Lifesciences LLC, Irvine, California) in the pulmonary position in patients with moderate to severe pulmonary regurgitation with or without stenosis.

BACKGROUND

Transcatheter pulmonary valve replacement is evolving, but to date, experience has been limited to the Melody valve (Medtronic Inc., Minneapolis, Minnesota).

METHODS

Eligible patients with dysfunctional right ventricle-to-pulmonary artery conduits were screened if body weight was ≥35 kg and the in situ conduit diameter was ≥16 mm and ≤24 mm. Standardized implantation and follow-up protocols were used.

RESULTS

Thirty-six patients from 4 centers were recruited between April 2008 and May 2010. Mean body weight was 73.4 ± 22.9 kg. Successful valve deployment was achieved in 33 of 34 attempts (97.1%). Valve migration occurred in 3 patients, with 2 requiring surgical retrieval; however, 1 patient underwent successful perventricular valve implantation. Further intraprocedure complications included pulmonary hemorrhage (n = 2), ventricular fibrillation (n = 1), and stent migration (n = 1). Pullback gradient across the conduit decreased from 26.8 ± 18.4 mm Hg to 11.7 ± 8.0 mm Hg (p < 0.001). The right ventricular/aortic pressure ratio decreased from 0.6 ± 0.2 to 0.4 ± 0.1 (p < 0.001). Peak Doppler gradient across the right ventricular outflow tract decreased from 41.9 ± 27.9 mm Hg to 19.1 ± 13.3 mm Hg (p < 0.001). At 6-month follow-up, all patients were alive. The number of patients with New York Heart Association functional class I increased from 5 at baseline to 27 at follow-up. Pulmonary regurgitation was ≤2+ in 97% of patients. Freedom from reintervention was 97% with 1 patient undergoing elective placement of a second valve due to conduit-induced distortion of the initial implant.

CONCLUSIONS

Transcatheter pulmonary valve replacement using the Edwards SAPIEN transcatheter heart valve is safe and effective in patients with dysfunctional right ventricle-to-pulmonary artery conduits.

摘要

目的

本研究旨在评估经导管爱德华兹 SAPIEN 心脏瓣膜(爱德华兹生命科学公司,加利福尼亚州欧文)在中重度肺动脉瓣反流伴或不伴狭窄患者中的安全性和有效性。

背景

经导管肺动脉瓣置换术正在发展,但迄今为止,经验仅限于 Melody 瓣膜(美敦力公司,明尼苏达州明尼阿波利斯)。

方法

筛选出体重≥35kg 且原位导管直径≥16mm 且≤24mm 的右心室至肺动脉导管功能障碍患者。使用标准化的植入和随访方案。

结果

2008 年 4 月至 2010 年 5 月,4 个中心共招募了 36 名患者。平均体重为 73.4±22.9kg。34 次尝试中有 33 次成功部署瓣膜。3 例发生瓣膜迁移,其中 2 例需要手术取出,但 1 例成功进行了经心室瓣植入。进一步的术中并发症包括肺动脉出血(n=2)、心室颤动(n=1)和支架迁移(n=1)。导管内梯度从 26.8±18.4mmHg 降低至 11.7±8.0mmHg(p<0.001)。右心室/主动脉压力比从 0.6±0.2 降至 0.4±0.1(p<0.001)。右心室流出道的峰值多普勒梯度从 41.9±27.9mmHg 降低至 19.1±13.3mmHg(p<0.001)。6 个月随访时,所有患者均存活。纽约心脏协会心功能分级 I 级的患者从基线时的 5 例增加到随访时的 27 例。97%的患者肺动脉瓣反流≤2+。无再干预率为 97%,1 例患者因初始植入导致导管诱导的初始植入变形而选择性放置第二枚瓣膜。

结论

经导管爱德华兹 SAPIEN 心脏瓣膜置换术治疗右心室至肺动脉导管功能障碍患者安全有效。

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