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Diagnostics 2017, 7(2), 36;

Creating a Registry for Patients with Thoracic Outlet Syndrome

Division of Vascular and Endovascular Surgery, University of California Davis Health, 4860 Y Street, Suite 3400, Sacramento, CA 95817, USA
Academic Editor: Andreas Kjaer
Received: 3 March 2017 / Revised: 10 May 2017 / Accepted: 24 May 2017 / Published: 17 June 2017
(This article belongs to the Special Issue Diagnosis and Treatment of Thoracic Outlet Syndrome)
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The creation of any patient database requires substantial planning. In the case of thoracic outlet syndrome, which is a rare disease, the Society for Vascular Surgery has defined reporting standards to serve as an outline for the creation of a patient registry. Prior to undertaking this task, it is critical that designers understand the basics of registry planning and a priori establish plans for data collection and analysis. View Full-Text
Keywords: Thoracic Outlet Syndrome (TOS); nTOS; aTOS; vTOS; Paget-Schroetter syndrome Thoracic Outlet Syndrome (TOS); nTOS; aTOS; vTOS; Paget-Schroetter syndrome

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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. (CC BY 4.0).

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Humphries, M.D. Creating a Registry for Patients with Thoracic Outlet Syndrome. Diagnostics 2017, 7, 36.

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