Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9154836 | American Heart Journal | 2005 | 6 Pages |
Abstract
The development of a quality-controlled PVI registry requires the commitment and collaboration of clinician-investigators and hospital systems devoted to understanding factors that contribute to quality outcomes. Central to achievement of this goal is the creation of a careful diagnostic and data quality assessment system. This registry will provide important clinical insights into patient demographic and clinical characteristics, procedural characteristics, and current practice patterns that foster or impede achievement of long-term quality-based clinical outcomes for patients with peripheral arterial disease.
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Authors
Debabrata MD, MS, Khan PhD, Alan T. MD, Stanley MD, Paul M. MD, Sanjay MD, Brahmajee K. MD, Mauro MD, Peter MD, Elias MD, Chaman MD, Arthur MD, Donna RN, Ann E. RN, Michele MD, Kiritkumar MD, Karen C. RN, MSN, Kim A. MD,