Publications by authors named "A Buxton"

Background: The boundaries of critical isthmuses for re-entrant ventricular tachycardia (VT) are formed by wavefront discontinuities (fixed lines of block, slow propagation, and rotational propagation) seen during baseline rhythm. It is unknown whether wavefront discontinuities can be automatically identified and targeted for ablation using electroanatomic mapping systems.

Objectives: The purpose of this study was to assess the electrophysiologic characteristics of automatically projected wavefront discontinuity lines (WADLs) and outcomes of an ablation strategy targeting WADLs in a mixed cohort of VT patients.

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Background: Myocardial electrical heterogeneity is critical for normal cardiac electromechanical function, but abnormal or excessive electrical heterogeneity is proarrhythmic. The spatial ventricular gradient (SVG), a vectorcardiographic measure of electrical heterogeneity, has been associated with arrhythmic events during long-term follow-up, but its relationship with short-term inducibility of ventricular arrhythmias (VAs) is unclear.

Objective: This study was designed to determine associations between SVG and inducible VAs during electrophysiology study.

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Article Synopsis
  • A multicenter phase II trial evaluated the effectiveness of adding vorinostat or bevacizumab to focal radiation therapy (RT) in improving 1-year event-free survival (EFS) for children with newly diagnosed high-grade gliomas (HGGs), compared to the standard treatment of temozolomide.
  • Out of 90 patients, the one-year EFS rates were 43.8% for bevacizumab, 41.4% for vorinostat, and 59.3% for temozolomide, with no significant differences among the treatment options.
  • The study concluded that combining vorinostat or bevacizumab with RT does not offer superior outcomes compared to temoz
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Antigen-specific antibody infusion is known to enhance or suppress germinal center (GC) responses depending on the affinity of the infusion. We hypothesized that infusing monoclonal antibodies (mAbs) of escalating affinity during an immunization regimen may progressively escalate selection pressure on competing B cells, increasing their affinity. To test this, we immunized mice with HIV envelope gp120 and infused CD4 binding-site (CD4bs)-specific mAbs.

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