Objectives: The goal of this study was to assess the immediate and long-term outcomes in patients undergoing percutaneous coronary intervention (PCI) for in-stent restenosis (ISR) in an unprotected distal left main coronary artery (UDLM).
The goal of this study was to provide a measurement of the true internal diameter (ID) of various surgical heart valves (SHV) to facilitate the valve-in-valve (VIV) procedure. During a VIV procedure, it is important to choose the right of the transcatheter heart valve (THV). Most users use the stent ID of an SHV to select the appropriate THV size. Echocardiography and computed tomography measurements are not yet standardized for measuring the ID of a variety of SHVs. Hence, we measured the true ID of SHV to assess the effect of valve design on the stent ID. Thirteen types of stented and 3 types of stentless valves were evaluated. True ID measurements were obtained using calipers and Hegar dilators. These were compared with the stent ID measurements. Fluoroscopy was used to confirm the impact of SHV designs on the true ID. Caliper measurements were found to be inaccurate and are hence not recommended. Hegar dilator measurements revealed a trend of reduction in stent ID. Porcine valves were most affected by their design, with reduction in the stent ID by at least 2 mm; pericardial valves with leaflets sutured inside the stent had the stent ID reduced by at least 1 mm, and SHV with leaflets sutured outside the stent had no effect on stent ID. In the majority of SHV designs, there is a reduction in the stent ID as a result of leaflet tissue. This is important in borderline sizes to avoid problems associated with oversizing and also to confirm suitability for the VIV procedure in the smaller label sizes of SHV.
Objectives: The aim of this study was to determine the impact of new-onset persistent left bundle branch block (NOP-LBBB) on late outcomes after transcatheter aortic valve implantation (TAVI).
Transcatheter aortic valve implantation (TAVI) has experienced unprecedented growth since its first description by Alain Cribier in 2002 1 and is now routinely performed in many institutions worldwide. New-onset left bundle branch block (LBBB) or atrioventricular (AV) block necessitating permanent pacemaker implantation (PPI) are among the most frequent complications of TAVI (2,3,4,5). Case reports describing late occurrence of complete AV block and the fact that LBBB has been associated with a worse outcome after surgical aortic valve implantation led clinicians to adopt a generous strategy of pacemaker implantation after TAVI. This strategy was further enhanced by the urge to ambulate patients early after TAVI instead of prolonged monitoring for resolution of AV conduction impairment. Improvement of valve design and implant strategy has lowered the rate of AV conduction abnormalities, but they continue to be a matter of concern. Moreover, new-onset LBBB after TAVI was associated with increased mortality in a study by Houthuizen et al. (3), whereas others have found no association (4,6,7,8). Additional insights into the outcome of patients with LBBB after TAVI are therefore needed.
Objectives: This study sought to evaluate the impact of baseline activated clotting time (ACT)–guided heparin administration on major bleeding after transfemoral transcatheter aortic valve implantation (TAVI).
Background: Rehospitalization within 30 days after an admission for percutaneous coronary intervention (PCI) is common, costly, and a future target for Medicare penalties. Causes of readmission after PCI are largely unknown.
Objectives: The goal of this study was to provide a systematic review and analysis of observational studies on percutaneous left atrial appendage (LAA) occlusion for stroke prophylaxis in nonvalvular atrial fibrillation (NVAF).
Objectives: The aim of this study was to systematically review and perform a meta-analysis of randomized trials and observational studies of intravascular ultrasound (IVUS)-guided versus angiography-guided implantation of drug-eluting stents (DES).
Objectives: This study sought to investigate the clinical impact of the use of intravascular ultrasound (IVUS) during revascularization of patients with left main coronary artery (LM) disease with drug-eluting stents (DES).
Objectives: The authors sought to investigate whether the impact of treatment strategies on clinical outcomes differed between patients with left main (LM) bifurcation lesions and those with non-LM bifurcation lesions.
Objectives: This study evaluated the impact of nonculprit vessel myocardial perfusion on outcomes of non–ST-segment elevation acute coronary syndromes (NSTE-ACS) patients.
Objectives: This study sought to determine the utilization and outcomes for radial access for percutaneous coronary intervention (PCI) for ST-segment elevation acute myocardial infarction (STEMI) in common practice.
Objectives: This study sought to assess aortic regurgitation (AR) after transcatheter aortic valve implantation (TAVI) with the self-expandable Medtronic CoreValve (MCV) (Medtronic Inc., Minneapolis, Minnesota) versus balloon-expandable Edwards Sapien XT valve (ESV) (Edwards Lifesciences, Irvine, California).
Transcatheter aortic valve implantation (TAVI) has revolutionized the treatment of symptomatic severe aortic stenosis in patients at a high risk of surgical valve replacement 1. The 2 main devices in clinical use at present are the self-expandable Medtronic CoreValve (MCV) (Medtronic, Minneapolis, Minnesota) and balloon-expandable Edwards SAPIEN XT valve (ESV) (Edwards Lifesciences, Irvine, California). Paravalvular aortic regurgitation (AR) is not an uncommon complication after TAVI, and suboptimal device sizing and positioning are the main culprits
Objectives: This study sought to evaluate the safety and performance of the Igaki-Tamai (Igaki Medical Planning Company, Kyoto, Japan) biodegradable stent in patients with occlusive superficial femoral artery (SFA) disease.
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