Transcatheter Microguidewire Drilling for Transseptal Left Atrial Access
- Conditions
- Atrial Septal DilatationHeart Diseases
- Interventions
- Device: Transseptal puncture with Brockenbrough-needleDevice: Microguidewire-assisted transseptal puncture
- Registration Number
- NCT04561908
- Lead Sponsor
- China National Center for Cardiovascular Diseases
- Brief Summary
This study aims to investigate the safety and efficacy of transcatheter microguidewire drilling (TMD) for transseptal left atrial access in patients with abnormal atrial septal morphology.
- Detailed Description
Despite the widespread application and decades of experience, Brockenbrough-needle transseptal puncture still risks cardiac perforations and secondary pericardial effusion/tamponade, especially in patients with abnormal atrial septal morphology. To facilitate atrial septal crossing, different methods and devices have been developed, including radiofrequency energy, excimer laser, SafeSept wire and so on. However, these are still limited by availability and cost, and the advantages might be further offset by the potential risks. In addition, these methods are performed mainly with the linear insertion technique, which might result in less forward-force to penetrate atrial septum and displacement of needle-tip. Therefore, it is necessary to develop a safe, available and low-cost transseptal procedure for these patients.
Through a Brockenbrough needle, the hard "back-end" of the microguidewire (0.014-inch) has the potential to drill through the atrial septum with ease. Compared with a standard linear insertion technique, the penetration might be improved and less force is required with the bidirectional rotation technique, and the related risks might be reduced with the modified TSP due to the thin microguidewire. After the passage of the needle, the soft-end of microguidewire can be introduced into left pulmonary superior vein, which can become a safe rail for the introduction of puncture dilator/sheath.
In this study, we examined the effectiveness and safety of microguidewire-assisted TSP for patients with complex atrial septum.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 100
- Patients with atrial septal aneurysm (a bulging of the atrial septum of at least 10 mm beyond the plane of the atrial septum into either the right or left atrium); 2) Or patients with previous multiple transseptal punctures (≧2); 3) Or patients with thickened atrial septum (thickness ≧3 mm); 4) Or patients with enlarged right atrium (≧ 6 cm) and diminished left atrium (< 3 cm); 5) Or patients with prior mitral valve surgery; 6) Or patients with atrial baffles.
- Associated atrial septal defect or patent foramen ovale; 2) Associated interrupted inferior vena cava; 3) Presence of implanted cardiac devices; 4) Echocardiographic evidence of intracardiac thrombus, mass, tumor or vegetation; 5) Thromboembolic events within the last 6 months; 6) Patients unable to grant informed, written consent.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Conventional transseptal puncture Transseptal puncture with Brockenbrough-needle Under the guidance of fluoroscopy and echocardiography, transseptal puncture was performed with Brockenbrough-needle. Microguidewire-assisted transseptal puncture Microguidewire-assisted transseptal puncture The Brockenbrough needle, with transseptal dilator and sheath, was introduced into the right atrium and engaged in the fossa ovalis, which was confirmed with angiographical and echocardiographical "tenting sign". 1) the hard-end of a 0.014-inch microguidewire drilled through atrial septum through Brockenbrough-needle; 2) then the needle was advanced into left atrium over the fixed microguidewire; 3) finally the soft-end of microguidewire was introduced into left atrium/left superior pulmonary vein through Brockenbrough-needle, which was further advanced over the fixed microguidewire.
- Primary Outcome Measures
Name Time Method Procedural Success 1 Day of procedure Number of participants with successful transseptal left atrial access
Related-complications 1 Day of procedure Pericardial effusion
- Secondary Outcome Measures
Name Time Method Transseptal Access Procedure Time 1 Day of procedure Total amount of procedure time, from the beginning of the transseptal procedure until left atrium access is obtained in each patient.
Trial Locations
- Locations (2)
Yan Chaowu
🇨🇳Beijing, Select A State Or Province, China
National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences,Fuwai Hospital
🇨🇳Beijing, Beijing, China