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VA Technical Reference Model v 24.4

Ambulatory Blood Pressure Report Management System
Ambulatory Blood Pressure Report Management System Technology

General InformationGeneral Information help

Technologies must be operated and maintained in accordance with Federal and Department security and privacy policies and guidelines. More information on the proper use of the TRM can be found on the TRM Proper Use Tab/Section.

Website: Go to site
Description: The Ambulatory Blood Pressure (ABP) Report Management System is used to retrieve, display, edit, and print ABP data. The software assesses cardiac health via blood pressure readings taken during daily patient activity for 24 to 48 hours, or more. The software includes on-screen calipers for the selection, viewing, analysis, and printing of specific time periods throughout the day and night.

This technology does not have a specific website.

This product has been discontinued. Ambulatory Blood Pressure Report Management System is the legacy software for Sentinel Cardiology Information Management System. User should refer to the Sentinel Cardiology Information Management System TRM entry.
Technology/Standard Usage Requirements: Users must ensure their use of this technology/standard is consistent with VA policies and standards, including, but not limited to, VA Handbooks 6102 and 6500; VA Directives 6004, 6513, and 6517; and National Institute of Standards and Technology (NIST) standards, including Federal Information Processing Standards (FIPS). Users must ensure sensitive data is properly protected in compliance with all VA regulations. Prior to use of this technology, users should check with their supervisor, Information Security Officer (ISO), Facility Chief Information Officer (CIO), or local Office of Information and Technology (OI&T) representative to ensure that all actions are consistent with current VA policies and procedures prior to implementation.
Section 508 Information: Section 508 does not apply. This product is considered Medical Technology as defined by the VA in the Medical Device Isolation Architecture (MDIA). For additional information or assistance regarding Section 508, please contact the Section 508 Office at
Decision: View Decisions

Decision Source: TRM Mgmt Group
Decision Process: One-VA TRM v20.5
Decision Date: 05/04/2020 at 12:10:19 UTC
Introduced By: TRM Request
Vendor Name: Spacelabs Healthcare
- The information contained on this page is accurate as of the Decision Date (05/04/2020 at 12:10:19 UTC).