Ewa Peszek-Przybyła MD, PhD , Marek Jędrzejek MD, PhD , Grzegorz Smolka MD, PhD , Martin J. Quinn MD, PhD , Piotr Pysz MD, PhD , Wojtek Wojakowski MD, PhD
{"title":"使用 CroíValve DUO 自适应瓣膜治疗右心室起搏器导联患者大面积三尖瓣反流的首例病例","authors":"Ewa Peszek-Przybyła MD, PhD , Marek Jędrzejek MD, PhD , Grzegorz Smolka MD, PhD , Martin J. Quinn MD, PhD , Piotr Pysz MD, PhD , Wojtek Wojakowski MD, PhD","doi":"10.1016/j.shj.2024.100329","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>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.</p></div><div><h3>Methods</h3><p>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.</p></div><div><h3>Results</h3><p>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.</p></div><div><h3>Conclusions</h3><p>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.</p></div>","PeriodicalId":36053,"journal":{"name":"Structural Heart","volume":"8 5","pages":"Article 100329"},"PeriodicalIF":1.4000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2474870624000770/pdfft?md5=28651adb975d7b4feecdbf3ca27f7025&pid=1-s2.0-S2474870624000770-main.pdf","citationCount":"0","resultStr":"{\"title\":\"First Case of the Treatment of Massive Tricuspid Regurgitation With the CroíValve DUO Coaptation Valve in a Patient With a Right Ventricular Pacemaker Lead\",\"authors\":\"Ewa Peszek-Przybyła MD, PhD , Marek Jędrzejek MD, PhD , Grzegorz Smolka MD, PhD , Martin J. Quinn MD, PhD , Piotr Pysz MD, PhD , Wojtek Wojakowski MD, PhD\",\"doi\":\"10.1016/j.shj.2024.100329\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>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.</p></div><div><h3>Methods</h3><p>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.</p></div><div><h3>Results</h3><p>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.</p></div><div><h3>Conclusions</h3><p>This is the first implantation of the CroíValve DUO Coaptation Valve System in a patient with a pacemaker lead. 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引用次数: 0
摘要
背景三尖瓣反流(TR)是一种常见的瓣膜疾病,治疗方法有限。当三尖瓣瓣叶闭合因右心扩张而受阻时,或在植入心脏节律装置的患者中,当经瓣导联阻碍瓣膜正常闭合时,就会出现三尖瓣反流。这些患者的治疗可能比较复杂。移除导联通常无法改善 TR,而且由于合并症,通常无法进行手术修复。目前已开发出多种经皮 TR 修复和置换装置,但右心室导联的存在可能会阻碍这些装置的植入,或者该装置可能会使起搏器导联移位。我们报告了 CroíValve DUO 经导管三尖瓣瓣膜系统(爱尔兰都柏林)在一名大面积 TR 和右室导联患者身上的首次植入。手术在回声和X光引导下全身麻醉下进行。结果成功植入了该装置,90 天随访时,TR 从大量减少到轻度。患者的生活质量明显改善,6分钟步行测试(基线为382米,随访时为467米)、纽约心脏协会分级(基线为III级,随访时为I级)和堪萨斯城心肌病问卷(基线为43分,随访时为60分)均有改善。在过去 90 天的随访中,疗效和临床改善均保持稳定,患者未发生任何不良事件。结论这是首次在带起搏器导联的患者中植入 CroíValve DUO 自适应瓣膜系统。对于这些患者,该设备可能比目前的其他经导管方法更具优势。
First Case of the Treatment of Massive Tricuspid Regurgitation With the CroíValve DUO Coaptation Valve in a Patient With a Right Ventricular Pacemaker Lead
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.