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首例使用CroíValve DUO贴合瓣膜治疗右心室起搏器导线患者的严重三尖瓣反流。

First Case of the Treatment of Massive Tricuspid Regurgitation With the CroíValve DUO Coaptation Valve in a Patient With a Right Ventricular Pacemaker Lead.

作者信息

Peszek-Przybyła Ewa, Jędrzejek Marek, Smolka Grzegorz, Quinn Martin J, Pysz Piotr, Wojakowski Wojtek

机构信息

Division of Cardiology and Structural Heart Diseases, Medical University of Silesia, Katowice, Poland.

CMO of CroíValve and St. Vincents University Hospital, Dublin 4, Ireland.

出版信息

Struct Heart. 2024 Jun 25;8(5):100329. doi: 10.1016/j.shj.2024.100329. eCollection 2024 Sep.

Abstract

BACKGROUND

Tricuspid regurgitation (TR) is a common valvular disorder with limited treatment options. It occurs when tricuspid leaflet closure is prevented by dilation of the right heart or in patients with cardiac implantable rhythm devices when the transvalvular lead impedes proper closure of the valve. The management of these patients can be complicated. The removal of the lead often does not improve the TR, and surgical repair is usually not possible because of comorbidities. A number of percutaneous TR repair and replacement devices have been developed; however, the presence of the right ventricular lead can prevent the delivery of these devices, or the device may displace the pacemaker lead. We report the first implant of the CroíValve DUO Transcatheter Tricuspid Coaptation Valve System (Dublin, Ireland) in a patient with massive TR and a right ventricular lead.

METHODS

The patient was not a fit for surgical treatment and underwent transcatheter treatment following compassionate use approval. The procedure was performed under general anesthetic with echo and X-ray guidance. The device was delivered through the right internal jugular vein.

RESULTS

The device was implanted successfully, and the TR was reduced from massive to mild at 90-day follow-up. The patient's quality of life improved significantly with an improvement in 6-minute walk test (382 m at baseline to 467 m at follow-up), the New York Heart Association classification (III at baseline to I at follow-up), and the Kansas City Cardiomyopathy Questionnaire (baseline score 43 increased to 60). The efficacy and clinical improvement have been stable over the past 90 days of follow-up, and the patient has not suffered any adverse events.

CONCLUSIONS

This is the first implantation of the CroíValve DUO Coaptation Valve System in a patient with a pacemaker lead. In these patients, this device may offer advantages over other current transcatheter approaches.

摘要

背景

三尖瓣反流(TR)是一种常见的瓣膜疾病,治疗选择有限。当右心扩张阻止三尖瓣小叶闭合时,或者在心脏植入式节律装置患者中,当经瓣膜导线妨碍瓣膜正常闭合时,就会发生三尖瓣反流。这些患者的管理可能很复杂。导线移除通常无法改善三尖瓣反流,并且由于合并症通常无法进行手术修复。已经开发了多种经皮三尖瓣修复和置换装置;然而,右心室导线的存在可能会妨碍这些装置的输送,或者该装置可能会使起搏器导线移位。我们报告了首例在一名患有大量三尖瓣反流和右心室导线的患者中植入CroíValve DUO经导管三尖瓣贴合瓣膜系统(爱尔兰都柏林)。

方法

该患者不适合手术治疗,在获得同情使用批准后接受了经导管治疗。该手术在全身麻醉下进行,有超声心动图和X射线引导。该装置通过右颈内静脉输送。

结果

该装置成功植入,在90天随访时,三尖瓣反流从大量减少到轻度。患者的生活质量显著改善,6分钟步行试验有所改善(基线时为382米,随访时为467米),纽约心脏协会分级(基线时为III级,随访时为I级),堪萨斯城心肌病问卷(基线评分43提高到60)。在过去90天的随访中,疗效和临床改善一直稳定,患者未发生任何不良事件。

结论

这是首例在有起搏器导线的患者中植入CroíValve DUO贴合瓣膜系统。在这些患者中,该装置可能比其他当前的经导管方法具有优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa6/11403069/4ba52b8137ed/gr1.jpg

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