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EVToday EVToday + CIToday

evt | News | October 3, 2023

InspireMD Appoints Dr. Patrick Verta as Executive VP of Clinical and Medical Affairs

October 3, 2023—InspireMD, Inc., developer of the CGuard embolic prevention stent system (EPS) for prevention of stroke, announced senior leadership additions and changes.

evt | Article | September 2011

Carotid Artery Stenting for Standard-Surgical-Risk Patients

Implications of the new FDA approval in the United States.

By Chuck Simonton, MD, and Patrick Verta, MD

evt | Article | September 2013

The Effect of Limited CMS Coverage and Patient Access on CAS Outcomes and Device Development

National coverage decisions can play a critical role in creating the environment in which these improvements take place.

By Patrick Verta, MS Stat, MD

evt | News | December 12, 2013

Study Shows Positive Impact of FDA Approval and Medicare Coverage on CAS Outcomes

December 3, 2013—Findings from an evaluation of the impact of US Food and Drug Administration (FDA) regulatory approval and Centers for Medicare and Medicaid Services (CMS) coverage on outcomes of carotid artery stenting (CAS) have been published online ahead of print by William A. Gray, MD and Patrick Verta, MD, in Catheterization and Cardiovascular Interventions.

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evt | Article | September 2013

The State of CAS

By William A. Gray, MD, and Sumaira Macdonald, MBChB, FRCP, FRCR, PhD

evt | Article | September 2011

Surveying the CAS Landscape

By Sumaira Macdonald, MBChB (Comm.), FRCP, FRCR, PhD, and William A. Gray, MD

evt | Article | March 2014

Upper Extremity Approaches for Carotid Stenting

The utility of transradial and transbrachial access for difficult arch anatomy.

By Patrick M.S. Neville, MD; Brian A. Kuhn, MD; Matthew H. Recht, MD; and Patrick E. Muck, MD

evt | Article | February 2007

Raising Critical Questions

Sumaira Macdonald, MBChB (Comm.), FRCP, FRCR, PhD, discusses the questions she posed to the EVA-3S and SPACE presenters at VEITH, the difference between failure to show noninferiority and superiority, and critical aspects of future trial design.

By Sumaira Macdonald, MBChB (Comm.), FRCP, FRCR, PhD

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