Randomized Comparison of Left Atrial Appendage Occlusion vs Standard Medical Therapy in Patients in Atrial Fibrillation Undergoing Transfemoral Transcatheter Aortic Valve Implantation: The TAVI LAAO Trial
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 81
- 试验地点
- 2
- 主要终点
- embolic events
研究概览
简要总结
Study category and Rationale Clinical study, Category A.
Clinical Phase: Post market study
Background and Rationale: Left atrial appendage occlusion (LAAO) allows avoiding oral anticoagulation and provides at the same time an at least equally good protection from strokes and peripheral embolism. It may therefore be an attractive alternative to oral anticoagulation in the patient population undergoing transcatheter aortic valve implantation (TAVI): the concept of LAAO is based on the fact that thrombus formation in atrial fibrillation occurs in >90% in the left atrial appendage (LAA). Mechanical occlusion of the LAA reduces the stroke risk by eliminating the source of thrombus formation. In the here proposed "Randomized Comparison of Left Atrial Appendage Occlusion versus Standard Medical Therapy in Patients in Atrial Fibrillation Undergoing Transfemoral Transcatheter Aortic Valve Implantation", study we test the hypothesis, that LAAO is superior to standard medical therapy in the high-risk TAVI population. This hypothesis has not been investigated by previous studies so far.
Overall Objective(s): Overall objective: to compare the safety (and efficacy) of LAAO using the St. Jude left atrial appendage closure device with standard medical therapy in a prospective, multi-center, randomized trial in patients undergoing TAVI in routine clinical practice.
Primary Objective: To assess the safety of the device intervention with regard to stroke prevention and prevention of bleeding complications in a patients population at high risk of stroke and bleeding.
Secondary Objectives: Short-term (procedural) safety of device intervention is assessed (rate of successful deployment of a left atrial appendage occluder; rate of kidney failure). As a further secondary objective, long-term effects of device intervention on stroke and bleeding prevention as well as mortality are assessed and compared to medical therapy.
Outcome(s): Primary: Composite endpoint of ischemic and hemorrhagic neurologic events, peripheral embolism, life-threatening/disabling and major bleeding complications and cardiovascular mortality at 1 year
Secondary: All deaths (cardiac and non-cardiac) at 30 days, 1, 3, and 5 years Device success at 30 days
In-hospital acute kidney injury (AKI)
Study design: An investigator-initiated, randomized, multicenter, non-blinded, all-comers study
Measurements and Procedures: 80 patients in atrial fibrillation undergoing TAVI will be randomized in a non-blinded fashion (1:1 randomization) to LAAO (device group) or SMT at the operators' discretion (medical group; antiplatelet therapy and oral anticoagulation or oral anticoagulation alone). All patients will be followed for up to 5 years. The primary analysis will be performed at 30 days and after completion of a 1-year follow-up.
80 patients in atrial fibrillation undergoing TAVI will be randomized in a non-blinded fashion (1:1 randomization) to LAAO (device group) or standard medical therapy (SMT) at the operators' discretion (medical group; antiplatelet therapy, oral anticoagulation or oral anticoagulation alone).
Estimated duration for the main investigational plan from start of screening of first participant to last participant processed and finishing the study: 6 years
详细描述
Background and Rationale
Transcatheter aortic valve implantation (TAVI) is a minimally invasive treatment option for patients suffering from severe symptomatic aortic stenosis. Superiority of TAVI over medical treatment has been shown in the randomized PARTNER B trial followed by the PARTNER A trial showing non-inferiority over a more invasive open-heart surgical aortic valve replacement in high-risk patients. Over the last years, many patients have been successfully treated with TAVI worldwide.
Peri- and post-procedural morbidity differed considerably between the surgical and interventional treatment group in the PARTNER A trial: while major bleeding (19.5% vs 9.3% at 30 days) and new onset atrial fibrillation (16% vs 8.6% at 30 days) occur more often in surgically treated patients, vascular access complications (3.8 vs 17% at 30 days) and neurologic events (5.5% vs 2.4% at 30 days) are more frequently encountered in the TAVI population. The higher rate of neurologic events in the TAVI group was of particular concern, given its association with a higher mortality and the clinical impact of major neurologic events on patient's quality of life and daily functioning. Only about 40-50% of strokes occur intra-procedurally, followed by a higher hazard rate in the first week and a constant hazard thereafter. After 30 months, the surgical group experienced a numerically higher stroke rate, although not statistically significant. Measures to reduce procedural and post-procedural stroke rate were and are still looked for.
While procedural strokes can be most likely reduced by improvements in valve delivery systems (smaller delivery systems) and more operator experience, cerebral protection devices are currently tested in trials but preliminary results are rather disappointing. Risk factors for post-procedural strokes after TAVI are a previous history of stroke, more extensive peripheral vascular disease, and higher functional class.
A subgroup of patients of particular concern are patients suffering from atrial fibrillation: predictor of early (day 1-30) cerebrovascular events was new-onset atrial fibrillation (OR 2.76), whereas chronic atrial fibrillation was a predictor (OR 2.84) for the occurrence of late (>30 days) cerebrovascular events. Amat-Santos reported a higher rate of strokes/systemic embolism in patients with in hospital new onset atrial fibrillation after TAVI (13.6% vs 3.2% after 30 days). Patients diagnosed with new onset atrial fibrillation during or after the procedure in which no anticoagulation was initiated experienced an alarmingly high 30-day stroke rate of 40%.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Severe aortic valve stenosis with an indication for aortic valve replacement (e.g., symptomatic patient, decreased left ventricular (LV) function)
- •Suitable anatomy for transfemoral TAVI with the Portico Transcatheter Aortic Valve System (ileofemoral arterial diameter, annulus-coronary distance, annulus diameter)
- •No mobile thrombus in the LA or LAA precluding LAAO
- •Atrial fibrillation with a CHA2DS2-Vasc-Score >=
- •No limitation regarding the nature of atrial fibrillation (paroxysmal, permanent, persistent)
排除标准
- •Pregnancy
- •Known intolerance to aspirin, heparin, contrast media or clinically manifest nickel allergy
- •Inability to provide informed consent
- •Mechanical heart valve or other indication for oral anticoagulation (i.e. recent pulmonary embolism)
- •Contraindication for oral anticoagulation
- •Currently participating in another trial
结局指标
主要结局
embolic events
时间窗: 1 year
Assessed by telephone interview
major bleeding
时间窗: 1 year
Assessed by telephone interview
cardiovascular mortality
时间窗: 1 year
Assessed by telephone interview
次要结局
- All deaths(5 years)
- Device success(30 days)
- Acute Kidney Injury (Review of lab results: Peak value of Creatinin)(Peak value of Creatinin at 48 hour, 72 hour after Procedure)