| DESCRIPTION |
+---------------------------------------------------------------+
| The Food and Drug Administration classifies this software as |
| a medical device. As such, it may not be changed in any way. |
| Modifications to this software may result in an adulterated |
| medical device under 21CFR820, the use of which is considered |
| to be a violation of US Federal Statutes. |
| |
+---------------------------------------------------------------+
The entries in this table contain the demographic information for the various
patients, for whom tasks are recorded on the worklist for a DICOM "modality".
| |
The top-level information in this table separates the patients from the
various clinics at a consolidated site; the next level contains the patient
information.
This file contains temporary copies of information from the VistA
system that live on our satellite systems for the duration of the
study that produces the images, and the only reason for
replicating the information onto these "DICOM Gateway Stations"
is that we want to be able to allow the acquisition of images and
the presentation of "worklist information" to continue, even
| Property of the US Government. |
while the VistA system is down, or when the RPC connection
between our Gateways and the VistA system is not operating.
Information is copied from VistA to DICOM Gateway when an HL7
message is processed that announces the "exam", and removed when
an HL7 message is processed that announces that the exam is
carried out.
| No permission to copy or redistribute this software is given. |
| Use of unreleased versions of this software requires the user |
| to execute a written test agreement with the VistA Imaging |
| Development Office of the Department of Veterans Affairs, |
| telephone (301) 734-0100. |
| |
|
