Thank you for your interest in joining the Dose Index Registry (DIR)! This step-by-step start-up guide is intended to help you to get underway with submitting your data and obtaining helpful feedback information.
The DIR is expanding beyond CT to include the additional modalities of fluoroscopy, digital radiography, and nuclear medicine. This guide covers participation in both DIR Computed Tomography (CT), in operation since 2011, and the recently introduced DIR Fluoroscopy (Fluoro) module. The following steps pertain to getting underway with either module and include links to articles in the National Radiology Data Registry (NRDR) Knowledge Base and the NRDR user guide.
The NRDR Team welcomes suggestions for how we can improve this guide and your overall experience with DIR start up and ongoing participation. Please send your suggestions and comments to NRDRSupport@acr.org.
Acknowledgments: Thank you to the authors of the article "A diagnostic medical physicist’s guide to the American College of Radiology Fluoroscopy Dose Index Registry," published in the Journal of Applied Clinical Medical Physics upon which this guide is based.
I. Assemble Your Team
A wide array of expertise will ensure a successful launch and continued operation of the DIR at your institution. Key team members and their roles are described briefly in this section.
NRDR administrative roles: Review the NRDR administrative roles within a Corporate Account to determine which DIR team members at your site should be assigned specific administrative roles for one—or both—of the DIR modules.
Additional highly recommended roles: While not official NRDR roles, identifying the right personnel to carry out the following responsibilities is key to DIR implementation and ongoing participation success. Some personnel likely could serve on both the DIR CT and DIR Fluoro teams. Other roles are more specialized to the modality, e.g., the physician champion and technologist.
Physician Champion: coordinates and directs the implementation process. Consider recruiting a champion who serves on a radiation protocol (or similar) committee or is involved with quality improvement efforts
Diagnostic Medical Physicist: facilitates effective communication among the other key team members and is key to the successful implementation of any of the DIR modules given their domain knowledge in radiation dosimetry, informatics, and basic clinical knowledge
Information Technology (IT) Specialist: interfaces with multiple hospital systems/applications and servers and is familiar with imaging informatics
TRIAD® Site Server Administrator: maintains the TRIAD Site Server. Both this role and the role of IT Specialist may be played by the same individual
Lead Technologist: manages the mapping of site-specific facility clinical procedure names to the ACR Common lexicon or the RadLex Playbook ID (RPID) based on the technologists’ in-depth understanding of the specific modality
II. Complete the Application Process and Create an NRDR Account
If your facility wishes to participate in DIR and doesn't currently participate in any other registries, you will need to complete the application process. NRDR Knowledge Base articles provide step-by-step instructions.
III. Get Your Team Signed Up with ACR Login
Team members who will need to access the NRDR portal for account set up activities and to review reports, will need to have ACR Login credentials. ACR Login enables users to enter their login credentials one time on a single page to access all their ACR Login applications.
Certain ACR Login applications, such as NRDR, require Multifactor Authentication (MFA). MFA necessitates users entering an additional piece of information when logging in for enhanced data security, making it harder for user accounts to become compromised.
Read the Knowledge Base article ACR Login and Multifactor Authentication for more information.
IV. Setup and Configure TRIAD®
Upon completing the DIR registration and account setup requirements, the next step is the setup of the TRIAD Site Server software. TRIAD enables the collection, de-identification, and transmission of data securely from CT scanners and fluoroscopes at one or more facilities to the DIR database. A single TRIAD Site Server can support all facilities within an NRDR Corporate Account.
View the DIR Data Collection and Submission Using TRIAD articles for basic information and the TRIAD installation website for technical instructions.
V. Validate Your Data
Data transfer between a DIR participating facility and the DIR Central Server can be interrupted for a variety of reasons. Therefore, as described below, facilities should undertake the quality assurance process of data validation to minimize missing time periods, modalities, or procedure types in the data submitted from Facilities to the DIR Central Server.
Initial data validation
Initial data validation focuses on ensuring that data from a newly set up DIR modality(ies) are being received and processed at the ACR DIR Central Server, i.e., verification that the full anonymized Radiation Dose Structured Report (RDSR), with the modalities’ Station Name(s), are being received and included within the NRDR database.
Periodic data validation
Periodically, e.g., quarterly, facilities should compare actual procedure volumes to procedure volumes reported in NRDR-DIR reports for the respective facility(ies) for a specific time period. If total procedure volumes match and the Station Name of each connected system is represented, it is likely that no further comparison is needed. If there is a mismatch, comparisons at the level of Station Name or even Study Description/Requested Procedure Description may be required for troubleshooting.
Facility process health monitoring
Implementing process health monitoring is another strategy to consider for minimizing interruptions in the data flow from the facility to the TRIAD Central Server. For example, automated email alerts that notify the site administrator if there is a failure to transfer data from PACS or an RDIM to the TRIAD Site Server would support optimal data flow. The local facility informatics architecture will dictate which types of facility process health monitoring can be implemented.
VI. Map Clinical Procedure/Exam Name
DIR participating facilities have their own internal facility exam or procedure “names” (a.k.a. procedure description, study description, etc.). To allow for exams and procedures that are named differently across DIR facilities to be analyzed and compared for benchmarking feedback reports (“apples to apples comparison”), DIR participants must map their exams and procedures to a standardized terminology.
CT exams are mapped, or “tagged” using RadLex Playbook IDs (RPIDs) and fluoro procedures are tagged using ACR Common™ procedure names. Detailed knowledge of the exams and procedures is required for accurate mapping; therefore, it is recommended that a lead or senior technologist manage exam name mapping with support from a physicist or physician champion.
The Knowledge Base articles below provide detailed information about the mapping process.
VII. Manage Device Profiles for DIR Fluoroscopy
DIR Fluoro participants complete a device profile for each fluoroscope that sends Radiation Dose Structured Reports (RDSR) files to the DIR Central server, to accurately report and assess practice patterns. The device profile contains important information such as year of manufacture, classification (e.g. single plane interventional, or remote radiography and fluoroscopy), and single point dose index correction factor.
Correct setup of fluoroscopy devise profiles enables the most meaningful comparison of benchmarking data for DIR Fluoro participants and provides valuable information for the fluoroscopy community. Consult the Managing Device Profiles Knowledge Base article for more information.
VIII. Readiness Checklist
DIR Team Members Identified and Have ACR Login and MFA Set up
Device Profile Setup (For DIR Fluoro only)
Last reviewed: 05/06/2021