Heart Valve Prosthesis Implantation

心脏瓣膜假体植入
  • 文章类型: Case Reports
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  • 文章类型: Case Reports
    背景:二尖瓣-主动脉瓣间纤维性假性动脉瘤(PMAIF)是感染性心内膜炎或主动脉瓣手术的罕见并发症。建议手术治疗,但保守治疗的长期随访仍不清楚.
    方法:对一名主动脉瓣置换术6年后出现PMAIF的患者进行了33年的随访。患者出现呼吸困难到我们中心,超声心动图显示射血分数为20%,PMAIF为7×10mm。尽管被建议接受手术,患者因担心手术结局而拒绝治疗.因此,开始保守治疗,密切观察,但不进行手术.在33年的随访期间,患者未出现任何不良健康影响.
    结论:当诊断为PMAIF时,应考虑手术干预。然而,在手术不适用的情况下,保守的管理可能会导致长期生存,基于此和文献中的类似病例报告。
    BACKGROUND: Pseudoaneurysm of the mitral-aortic intervalvular fibrosa (PMAIF) is a rare complication of infective endocarditis or aortic valve surgery. Surgical treatment is suggested, but the long-term follow-up of conservative management remains unclear.
    METHODS: A 33-year follow-up of a patient who developed PMAIF six years after aortic valve replacement is reported. The patient presented to our center with dyspnea, and the echocardiography revealed an ejection fraction of 20% and a PMAIF measuring 7 × 10 mm. Despite being advised to undergo surgery, the patient declined due to fear of surgical outcomes. Consequently, conservative treatment with close observation but without surgery was initiated. During the 33-year follow-up period, the patient did not experience any adverse health effects.
    CONCLUSIONS: Surgical intervention should be considered whenever the PMAIF is diagnosed. However, in any case that the surgery was not applicable, conservative management might lead to long-term survival, based on this and similar case reports in the literature.
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  • 文章类型: Journal Article
    目的:患有严重三尖瓣返流(TR)的患者有显著的发病率和死亡率的风险。经导管三尖瓣介入治疗(TTVI)可以为患者提供手术以外的微创治疗方法。这篇综述评估了目前世界上用于治疗TR的最常见的一类设备,三尖瓣经导管边缘对边缘修复术(T-TEER)和经导管原位三尖瓣置换术(TTVR),这两种方法现在都在美国和欧洲获得批准。
    结果:第一个关键的随机临床试验,三倍,证明T-TEER可以安全地降低TR,并与改善的健康状况结果相关。然而,本试验的结果引发了人们对该装置是否能提供足够的TR降低以影响临床结局的疑问.原位TTVR最近受到关注,初步数据表明TR几乎完全消除。当前的审查审查了最常用的T-TEER和原位TTVR设备的技术特征和解剖局限性,讨论了这些设备的当前临床数据,并为器件选择提供了理论结构。
    OBJECTIVE: Patients with severe tricuspid regurgitation (TR) are at risk for significant morbidity and mortality. Transcatheter tricuspid valve interventions (TTVI) may offer patients less invasive treatment alternatives to surgery. This review evaluates the most common class of device currently used worldwide to treat TR, tricuspid transcatheter edge-to-edge repair (T-TEER) and orthotopic transcatheter tricuspid valve replacement (TTVR), both of which are now approved in the USA and Europe.
    RESULTS: The first pivotal randomized clinical trial, TRILUMINATE, demonstrated that T-TEER can safely reduce TR and is associated with improved health status outcomes. However, results of this trial have raised questions about whether this device can provide sufficient TR reduction to impact clinical outcomes. Orthotopic TTVR has recently gained attention with initial data suggesting near-complete TR elimination. The current review examines the technical features and anatomic limitations of the most commonly used devices for T-TEER and orthotopic TTVR, discusses the current clinical data for these devices, and offers a theoretical construct for device selection.
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  • 文章类型: Systematic Review
    背景:主动脉瓣环(SAA)较小的患者进行主动脉瓣置换术的患者-假体不匹配(PPM)的风险增加,对结果产生不利影响。与外科主动脉瓣置换术(SAVR)相比,经导管主动脉瓣置换术(TAVR)在减轻PPM方面显示出希望。
    方法:我们遵循PRISMA指南进行了系统评价和荟萃分析,以比较临床结果,死亡率,接受TAVR和SAVR的SAA患者之间的PPM。通过全面的文献检索确定合格的研究,并评估质量和相关性。
    结果:纳入9项研究,共2476名患者。TAVR表现出相似的30天和2年死亡率,心肌梗塞,与SAVR相比,中风率。然而,TAVR在降低SAVR后的中度生存率方面显示出显著优势,在延长的随访期间,观察到的血流动力学结果可能导致TAVR和SAVR之间的显著生存差异22此外,以前的研究发现,TAVR和SAVR的30天和2年死亡率相当,环大小无显著差异22,2330天和2年时卒中和心肌梗死的发生率以及严重PPM和大出血的发生率降低。相反,SAVR在30天永久性起搏器植入中具有更好的结果。两种干预措施的超声心动图结果具有可比性。
    结论:我们的研究结果表明,TAVR和SAVR都是治疗主动脉瓣环小的AS患者的可行选择。TAVR在减少PPM和大出血方面具有优势,而SAVR在起搏器植入方面表现更好。未来的研究应该集中在比较新一代TAVR技术和设备与SAVR。考虑患者特征对于选择AS的最佳治疗方法至关重要。
    BACKGROUND: Patients with a small aortic annulus (SAA) undergoing aortic valve replacement are at increased risk of patient-prosthesis mismatch (PPM), which adversely affects outcomes. Transcatheter aortic valve replacement (TAVR) has shown promise in mitigating PPM compared to surgical aortic valve replacement (SAVR).
    METHODS: We conducted a systematic review and meta-analysis following PRISMA guidelines to compare clinical outcomes, mortality, and PPM between SAA patients undergoing TAVR and SAVR. Eligible studies were identified through comprehensive literature searches and assessed for quality and relevance.
    RESULTS: Nine studies with a total of 2476 patients were included. There was no significant difference in 30-day Mortality between TAVR vs SAVR groups (OR = 0.65, 95% CI [ 0.09-4.61], P = 0.22). There was no difference between both groups regarding myocardial infarction at 30 days (OR = 0.63, 95% CI [0.1-3.89], P = 0.62). TAVR was associated with a significantly lower 30-day major bleeding and 2-year major bleeding, Pooled studies were homogeneous (OR = 0.44, 95% CI [0.31-0.64], P < 0.01, I2 = 0, P = 0.89), (OR = 0.4 ,95% CI [0.21-0.77], P = 0.03, I2 = 0%, P = 0.62) respectively. TAVR was associated with a lower rate of moderate PPM (OR = 0.6, 95% CI [ 0.44-0.84], p value = 0.01, i2 = 0%, p value = 0.44). The overall effect estimate did not favor any of the two groups regarding short-term Mild AR (OR = 5.44, 95% CI [1.02-28.91], P = 0.05) and Moderate/severe AR (OR = 4.08, 95% CI [ 0.79-21.02], P = 0.08, I2 = 0%, P = 0.59).
    CONCLUSIONS: Our findings suggest that both TAVR and SAVR are viable options for treating AS in patients with a small aortic annulus. TAVR offers advantages in reducing PPM and major bleeding, while SAVR performs better in terms of pacemaker implantation. Future studies should focus on comparing newer generation TAVR techniques and devices with SAVR. Consideration of patient characteristics is crucial in selecting the optimal treatment approach for AS.
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  • 文章类型: Systematic Review
    背景:出现了几种可能的治疗重度二尖瓣返流(MR)的修复策略。进行了系统评价和荟萃分析,以比较不同的经皮二尖瓣修复方法。
    方法:PubMed和Scopus电子数据库在12月11日之前对符合条件的研究进行扫描,2023年。临床疗效终点是全因死亡率,主要不良心血管事件,术后NYHA功能分级<3;超声心动图疗效终点为介入后残余MR小于中度。还评估了安全性终点和程序结果指标。
    结果:包括11项研究:8[N=1662例患者,平均随访(FUP)294天]比较MitraClip®与Pascal®装置,2例(N=195例患者)MitraClip®vsCarillon®和1例研究(N=186例患者)评估了MitraClip®对抗Cardioband®。与MitraClip®治疗组相比,Pascal®治疗组的MR程度较低,干预后平均跨二尖瓣梯度以及临床和安全性终点均无差异。在Pascal®组中观察到更长的手术时间,尽管每个手术的平均植入设备数量较低。两项比较MitraClip®和Carillon®的研究在疗效和安全性方面均不一致。而评估MitraClip®与Cardioband®的研究表明,后者可能会带来显著的临床益处,MR也有类似的减少。
    结论:Pascal®在治疗MR患者方面与MitraClip®一样安全有效,从长远来看,残余瓣膜功能不全的幅度明显减少。关于Cardioband®和Carillon®的数据不足以从此类设备的使用中得出结论。
    BACKGROUND: Several repair strategies emerged as possible treatment for severe mitral regurgitation (MR). A systematic review and meta-analysis was performed to compare the different percutaneous mitral valve repair approaches.
    METHODS: PubMed and Scopus electronic databases were scanned for eligible studies until December 11th, 2023. Clinical efficacy endpoints were all-cause mortality, major adverse cardiovascular events, and post-procedural NYHA functional class <3; the echocardiographic efficacy endpoint was a post-intervention residual MR less than moderate. Safety endpoints and procedural outcome measures were also assessed.
    RESULTS: Eleven studies were included: 8 [N = 1662 patients, mean follow-up (FUP) 294 days] compared MitraClip® vs Pascal® device, 2 (N = 195 patients) MitraClip® vs Carillon® and 1 study (N = 186 patients) evaluated MitraClip® against Cardioband®. The Pascal®-treated group had lower MR degree compared to the MitraClip®-treated group, without difference in post-intervention mean trans-mitral gradient and in clinical and safety endpoints. A longer procedure time was observed in the Pascal® group, albeit with a lower average number of implanted devices per procedure. The two studies comparing MitraClip® and Carillon® were inconsistent in terms of both efficacy and safety outcomes, while the study evaluating MitraClip® vs Cardioband® showed that the latter might confer a significant clinical benefit, with a similar reduction in MR.
    CONCLUSIONS: Pascal® is as safe and clinically effective as MitraClip® in treating patients with MR, with an apparent greater reduction in the magnitude of residual valve insufficiency over the long term. Data on Cardioband® and Carillon® are not robust enough to draw conclusions from the use of such devices.
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  • 文章类型: Journal Article
    衰弱是一种常见的临床综合征,预示着经导管瓣膜介入术后不良的围手术期结局和死亡率增加。我们回顾了经导管介入队列中的虚弱评估工具,以推荐经导管瓣膜手术患者术前虚弱评估的途径。并评估了脆弱干预措施的现有证据及其在经导管干预中的疗效。我们建议使用虚弱筛查工具来识别虚弱的患者,随后对这些患者进行全面的老年评估,协助选择合适的患者,然后优化他们的经导管瓣膜介入治疗。减少程序前脆弱的干预措施没有明确定义,然而,来自有限队列研究的数据支持基于运动的干预措施,以增加功能容量和减少虚弱,同时进行术前医疗优化.
    Frailty is a common clinical syndrome that portends poor peri-procedural outcomes and increased mortality following transcatheter valve interventions. We reviewed frailty assessment tools in transcatheter intervention cohorts to recommend a pathway for preprocedural frailty assessment in patients referred for transcatheter valve procedures, and evaluated current evidence for frailty interventions and their efficacy in transcatheter intervention. We recommend the use of a frailty screening instrument to identify patients as frail, with subsequent referral for comprehensive geriatric assessment in these patients, to assist in selecting appropriate patients and then optimizing them for transcatheter valve interventions. Interventions to reduce preprocedural frailty are not well defined, however, data from limited cohort studies support exercise-based interventions to increase functional capacity and reduce frailty in parallel with preprocedural medical optimization.
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  • 文章类型: Journal Article
    目的:近年来,大量文献表明,与接受心脏瓣膜介入治疗的男性相比,女性的预后较差.在这里,我们试图分析比较接受外科主动脉瓣置换术(SAVR)的男性和女性结局的文献.
    方法:对PubMed,MEDLINE,和Embase的文章比较了接受SAVR的成年男性和女性之间结局的差异.筛选了一千九百九十本书,其中75个全文进行了审查,共有19份手稿符合纳入标准,被纳入本综述.
    结果:对死亡率的汇总估计表明,女性在SAVR后的前30天内生存率较低,尽管术后10年的中期和长期死亡率没有显著差异.对术后数据的汇总估计表明中风和术后出血率没有差异。主动脉瓣再手术率和急性肾损伤对女性有利。
    结论:尽管近年来报道的SAVR后女性的结局较差,这项荟萃分析的结果表明,在文献汇总的数据中,性别之间的结果具有可比性,中长期死亡率具有可比性.尽管死亡率在短期内有利于男性,主动脉瓣再手术和急性肾损伤的发生率对女性有利。未来对这一领域的调查应集中在确定诊断和初始手术管理的差异上,以解决导致短期结果差异的任何潜在因素。
    http://links。www.com/JCM/A651。
    OBJECTIVE: In recent years, extensive literature has been produced demonstrating inferior outcomes for women when compared with men undergoing heart valve interventions. Herein, we seek to analyze the literature comparing outcomes between men and women undergoing surgical aortic valve replacement (SAVR).
    METHODS: A systematic literature search of PubMed, MEDLINE, and Embase was conducted for articles comparing differences in outcomes between adult men and women undergoing SAVR. One thousand nine hundred and ninety titles were screened, of which 75 full texts were reviewed, and a total of 19 manuscripts met the inclusion criteria and were included in this review.
    RESULTS: Pooled estimates of mortality demonstrated that women tended to have lower rates of survival within the first 30 days post-SAVR, although mid-term and long-term mortality did not differ significantly up to 10 years postoperatively. Pooled estimates of postoperative data indicated no difference in the rates of stroke and postoperative bleeding. Rates of aortic valve reoperation and acute kidney injury favored women.
    CONCLUSIONS: Despite the inferior outcomes for women post-SAVR that have been reported in recent years, the results of this meta-analysis demonstrate comparable results between the sexes with comparable mid- to long-term mortality in data pooled from the literature. Although mortality favored men in the short term, rates of aortic valve reoperation and acute kidney injury favored women. Future investigation into this field should focus on identifying discrepancies in diagnosis and initial surgical management in order to address any potential factors contributing to discrepant short-term outcomes.
    UNASSIGNED: http://links.lww.com/JCM/A651.
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  • 文章类型: Systematic Review
    先前的研究表明,二尖瓣(MV)干预后中风率不同。本研究旨在比较经导管和手术MV干预后的术后卒中风险。从开始到2024年2月搜索电子数据库,以比较经二尖瓣导管边缘到边缘修复(mTEER)后的中风率。外科MV修复/更换,或指导医学治疗(GDMT)。主要终点是所有时间和早期(<30天)卒中。次要结局包括新发房颤和1年全因死亡率。采用频繁的网络荟萃分析来比较结果。网络荟萃分析包括18项研究(3项随机临床试验和15项观察性研究),51,703名患者。与手术相比,mTEER与所有时间(比值比[OR]0.61,95%CI0.41-0.89)和早期卒中(OR0.41,95%CI0.33-0.51)的风险降低相关,与GDMT相比,所有时间(OR1.54,95%CI0.76-3.12)和早期卒中(OR2.12,95%CI0.53-8.47)的风险相似。相反,与GDMT相比,手术与所有时间卒中(OR2.55,95%CI1.17-5.57)和早期卒中(OR5.15,95%CI1.27-20.84)的风险增加相关.mTEER与新发房颤的风险(OR0.38,95%CI0.11-1.31)和1年全因死亡率(OR1.43,95%CI0.91-2.24)之间无统计学差异。手术。总之,与手术MV干预相比,mTEER与较低的卒中风险和类似的新发房颤风险以及1年死亡率相关.需要进一步的研究来了解中风的机制,并确定降低MV干预后中风风险的策略。
    Previous research indicates varying stroke rates after mitral valve (MV) interventions. This study aimed to compare postprocedural stroke risks after transcatheter and surgical MV interventions. Electronic databases were searched from inception to February 2024 for studies comparing stroke rates after mitral transcatheter edge-to-edge repair (mTEER), surgical MV repair/replacement, or guideline-directed medical therapy (GDMT). Primary end points were all-time and early (<30 days) stroke. Secondary outcomes included new-onset atrial fibrillation and 1-year all-cause mortality. A frequentist network meta-analysis was employed to compare outcomes. The network meta-analysis included 18 studies (3 randomized controlled trials and 15 observational), with 51,703 patients. mTEER was associated with a decreased risk of all-time (odds ratio [OR] 0.61, 95% confidence interval [CI] 0.41 to 0.89) and early stroke (OR 0.41, 95% CI 0.33 to 0.51) compared with surgery, and a similar risk of all-time (OR 1.54, 95% CI 0.76 to 3.12) and early stroke (OR 2.12, 95% CI 0.53 to 8.47) compared with GDMT. Conversely, surgery was associated with an increased risk of all-time (OR 2.55, 95% CI 1.17 to 5.57) and early stroke (OR 5.15, 95% CI 1.27 to 20.84) compared with GDMT. There were no statistically significant differences in the risk of new-onset atrial fibrillation (OR 0.38, 95% CI 0.11 to 1.31) and 1-year all-cause mortality (OR 1.43, 95% CI 0.91 to 2.24) between mTEER versus surgery. In conclusion, mTEER was associated with a lower risk of stroke and similar risks of new-onset atrial fibrillation and 1-year mortality compared with surgical MV interventions. Further studies are needed to understand the mechanisms of stroke and to determine strategies to reduce stroke risk after MV interventions.
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  • 文章类型: Journal Article
    原位经导管三尖瓣置换术(TTVR)装置已被证明在减少三尖瓣反流(TR)方面非常有效,随着最近第一个原位TTVR的商业批准,对这种疗法的兴趣正在增长。最近的TTVR研究报告,约35%的患者预先存在心脏植入式电子设备(CIED)经瓣导线,在瓣膜植入过程中截留。引起了人们对截留导线的安全性的关注,并在指示时抵消了经静脉导线提取(TLE)的风险。心脏瓣膜联合实验室共识文件试图定义CIED导线相关或导线诱导TR的患者群体,描述TTVR期间铅截留的风险,在此设置中描述TLE的风险和收益,并为考虑进行TTVR的患者开发管理算法。在CIED管理方面经验丰富的电生理学家应该是多学科心脏团队的一部分,并参与共同决策。
    Orthotopic transcatheter tricuspid valve replacement (TTVR) devices have been shown to be highly effective in reducing tricuspid regurgitation (TR), and interest in this therapy is growing with the recent commercial approval of the first orthotopic TTVR. Recent TTVR studies report preexisting cardiac implantable electronic device (CIED) transvalvular leads in ∼35% of patients, with entrapment during valve implantation. Concerns have been raised regarding the safety of entrapping leads and counterbalanced against the risks of transvenous lead extraction (TLE) when indicated. This Heart Valve Collaboratory consensus document attempts to define the patient population with CIED lead-associated or lead-induced TR, describe the risks of lead entrapment during TTVR, delineate the risks and benefits of TLE in this setting, and develop a management algorithm for patients considered for TTVR. An electrophysiologist experienced in CIED management should be part of the multidisciplinary heart team and involved in shared decision making.
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  • 文章类型: Case Reports
    瓣周漏(PVL)是人工瓣膜植入的一种罕见并发症,会导致感染性心内膜炎,心力衰竭,和溶血性贫血.PVL的手术再干预与高死亡率相关。经导管PVL闭合(TPVLc)已成为外科手术再手术的替代方法。该方法提供了高成功率和低并发症率。本文综述了发病机制,临床表现,诊断,以及TPVLc后PVL和并发症的管理。此外,我们介绍了一例二尖瓣置换术后重度PVL患者,在TPVLc期间经历完全心脏传导阻滞(CHB)的人。由于导管插入过程中可能的房室结损伤,我们的患者首次TPVLc手术失败。持续CHB1周后,植入了永久性起搏器。使用上一次尝试成功传递了缺陷。考虑到TPVLc的优点,程序失败应该被视为一个问题。TPVLc应由经验丰富的医疗团队在精心挑选的患者中进行。
    Paravalvular leak (PVL) is an uncommon complication of prosthetic valve implantation, which can lead to infective endocarditis, heart failure, and hemolytic anemia. Surgical reintervention of PVLs is associated with high mortality rates. Transcatheter PVL closure (TPVLc) has emerged as an alternative to surgical reoperation. This method provides a high success rate with a low rate of complications. This article reviews the pathogenesis, clinical manifestation, diagnosis, and management of PVL and complications following TPVLc. Besides, we presented a case of a patient with severe PVL following mitral valve replacement, who experienced complete heart block (CHB) during TPVLc. The first TPVLc procedure failed in our patient due to possible AV-node insult during catheterization. After 1 week of persistent CHB, a permanent pacemaker was implanted. The defect was successfully passed using the previous attempt. Considering the advantages of TPVLc, procedure failure should be regarded as a concern. TPVLc should be performed by experienced medical teams in carefully selected patients.
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