Comparison of Left Atrial Appendage Occlusion vs Standard Medical Therapy in Patients in AF Undergoing TAVI

Atrial Fibrillation Clinical Trial

— TAVI/LAAO  

Official title:

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

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03088098
• Other study ID #: 2015-0459
• Status: Active, not recruiting
• Phase: N/A
• Start date: May 2, 2016
• Est. completion date: September 14, 2024

Study information

• Verified date: May 2024
• Source: University of Zurich
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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

Description:

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%.

Despite these results and the high prevalence of atrial fibrillation (AF) of about 33% in the overall TAVI population, only 30% of AF patients were on vitamin K antagonists (VKA) before, and only 70% after TAVI. While oral anticoagulation is an effective medical treatment for ischemic stroke prevention in these patients, it is often withheld from patients given their high risk of bleeding. TAVI patients typically not only suffer from much co-morbidity and are poly-medicated, but also suffer from a lot of bleeding risk factors. The bleeding risk score (HASBLED score) expresses the risk of major bleeding with a scoring system consisting of 9 individual risk factors for bleeding; a patient is at high risk for bleeding, if 3 or more factors are present. The stroke risk score (CHA2DS2-Vasc score) comprises of 9 individual risk scores for stroke in patients suffering from atrial fibrillation. Both risk scores share common risk factors, such as age, hypertension and previous stroke. It is therefore not surprising that patients at highest risk for stroke are at the same time at highest risk for major bleedings. The TAVI population forms such a high risk group with a high prevalence of the above risk factors: average patients age in the PARTNER trial was 84 years, with 11% showing severe renal impairment, about 75% had an indication for concomitant acetylsalicylic acid use and all suffered per definition from heart failure. In Stortecky's study on TAVI patients suffering AF, the average CHA2DS2-Vasc score was 4.5, with >95% of patients having a score >3.

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 TAVI patient population: 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.

Clinical studies proved this concept to be true: the PROTECT-AF study randomized >700 patients to either LAA occlusion or medical therapy (VKA). At one year, non-inferiority of LAAO was proven, with numerically less embolic events in the LAAO group. At a European conference (EuroPCR conference) 2013, Holmes (principal investigator of the PROTECT-AF trial) reported 4-year follow-up data with a significant 40% reduction of the composite of stroke/peripheral embolism/cardiovascular death and a 34% reduction of all cause mortality in the LAAO group as compared to oral anticoagulation. By reducing bleeding complications, it can be anticipated that morbidity and mortality will continue to diverge between the two groups. Comparable results from a large registry using Amplatzer devices (St. Jude Medical, St. Paul, USA) for LAAO were reported: after an average follow-up of 32 months, cardiovascular death, stroke, and peripheral embolism occurred in 7% of patients. In the latter study, oral anticoagulation was instantly stopped after LAAO in all patients.

In the here proposed "Randomized Comparison of Left Atrial Appendage Occlusion versus Standard Medical Therapy of Atrial Fibrillation in Patients Undergoing Transfemoral Transcatheter Aortic Valve Implantation", study the investigators 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. The design is an investigator-initiated, randomized, multicenter, non-blinded, all-comers study. It is understood, that this is a pilot trial with the intention to prove safety, but which is underpowered to show superiority over medical therapy.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 80
• Est. completion date: September 14, 2024
• Est. primary completion date: September 14, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• 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 >=1. No limitation regarding the nature of atrial fibrillation (paroxysmal, permanent, persistent)

Exclusion Criteria:

• 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

Related Conditions & MeSH terms

• Aortic Stenosis
• Aortic Valve Stenosis
• Atrial Fibrillation

Intervention

Device:
• LAAO
Left atrial appendage occlusion for stroke prevention

Locations

Country	Name	City	State
Switzerland	University Hospital Zurich	Zurich	ZH

Sponsors (2)

Lead Sponsor	Collaborator
University of Zurich	Abbott Medical Devices

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	embolic events	Assessed by telephone interview	1 year
Primary	major bleeding	Assessed by telephone interview	1 year
Primary	cardiovascular mortality	Assessed by telephone interview	1 year
Secondary	All deaths	Assessed by medical chart review and telephone interview	30 days
Secondary	All deaths	Assessed by medical chart review and telephone interview	1 year
Secondary	All deaths	Assessed by medical chart review and telephone interview	3 years
Secondary	All deaths	Assessed by telephone interview	5 years
Secondary	Device success	Assessed by review of the implant procedure (fluoroscopy and echocardiography)	30 days
Secondary	Acute Kidney Injury (Review of lab results: Peak value of Creatinin)	Review of lab results in hospital	Peak value of Creatinin at 48 hour, 72 hour after Procedure