Introduction to REM-NM Radiation Exposure Monitoring for Nuclear Medicine. Jeff Pohlhammer, Charles Smith

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Transcription:

Introduction to REM-NM Radiation Exposure Monitoring for Nuclear Medicine Jeff Pohlhammer, Charles Smith

Agenda A Little History The REM Profile Introduction of REM-NM Profile Features Functional Requirements Workflow Use Cases Dose Information Reporter and Dose Registry Connectathon Review Next Steps

REM-NM Profile New Radiology Profile; REM-NM. Supports recording/reporting administered activity and estimated organ radiation dose due to Radiopharmaceutical administration. Includes automatic transmission of administered activity information from hot lab/injector systems to scanner.

Background REM Profile Regulatory bodies require reporting of X-Ray dose information DICOM supports X-Ray dose via Structured Reports (RDSR) IHE REM (Radiation Exposure Monitoring) based on the RDSR REM Profile in use since 2009 All CTs shipped since 2013 support RDSR/REM

Background REM Profile cont d Dose Register Dose Info Reporter [RAD-63] Submit Dose Information [RAD-64] Query Dose Information [RAD-65] Retrieve Dose Information Image Archive Image Manager [RAD-64] Query Dose Information [RAD-65] Retrieve Dose Information Dose Info Consumer [RAD-62] Store Dose Information [RAD-10] Storage Commitment Acquisition Modality [RAD-62] Store Dose Information

REM-NM Profile Regulatory bodies, professional societies, and institutions are interested in monitoring administered activity for NM and PET procedures. For example: QIBA ASNC - ImageGuide DICOM has defined new Structured Report for NM/PET in 2013, similar to CT. REM-NM Profile provides a framework for managing reporting of administered activity and estimated dose. PET imaging procedures. NM and SPECT imaging procedures. NM procedures that do not involve imaging. REM-NM leverages infrastructure, actors, roles of REM. Promotes quantitative imaging by providing accurate activity and time information (e.g. QIBA)

REM-NM Profile Structure Dose Registry [RAD-63] Submit Dose Information Dose Info Reporter [RAD-64] Query Dose Information [RAD-65] Retrieve Dose Information Identical actors and roles as in REM Profile Image Archive Image Manager [RAD-64] Query Dose Information [RAD-65] Retrieve Dose Information Dose Info Consumer [RAD-Z] Store Radiopharmaceutical Dose Information Radiopharmaceutical Activity Supplier [RAD-5] Query Modality Worklist [RAD-64] Query Dose Information [RAD-65] Retrieve Dose Information [RAD-8] Modality Images Stored [RAD-10] Storage Commitment DSS/Order Filler Acquisition Modality [RAD-5] Query Modality Worklist [RAD-Z] Store Radiopharmaceutical Dose Information Differs from REM Profile: RAS becomes source of the Dose Report Acquisition Modality only consumes reports pulled from Image Manager/Archive RAS and Modality pull study info from Worklist

REM-NM High Level Requirements Modality and RAS: Must support Consistent Time Profile Must support Worklist Query transactions Hybrid Modalities (e.g. PET/CT) Must support both REM and REM-NM Use Cases: General Imaging Procedure (Most Common) Non-imaging Procedure Simultaneous Administration and Imaging Procedure Dose Information Reporter Pull-based Workflow Dose Information Reporter Push-based Workflow

Use Case General Imaging Procedure The RAS (Hot lab) retrieves Worklist entry to get patient demographics, order and procedure info. Radiopharmaceutical is administered to patient. RAS records amount of activity actually administered, generates new Radiopharmaceutical Administration Event UID. RAS sends Dose Report (RRDSR) to archive (PACS). When scan is set up, modality queries for the Dose Report (using Study Instance UID) and extracts relevant information (admin event UID, activity, date/time, pharmaceutical name, etc., but might not include half-life or positron fraction). Modality includes this info in images, and uses information for decay correction, SUVs, etc.

Use Case Continued

Dose Information Reporter and Dose Registry IHE Technical Framework defines these as part of REM Profile In many organizations, a Dose Information Reporter will collect Dose objects covering a particular period (e.g., today, this week or last month), analyze them, compare to site policy and generate summary reports. All, or a sampled subset of the Dose objects might be submitted to a National Registry to facilitate composing population statistics and other research. Such Dose objects will generally undergo a configurable de-identification process prior to submission.

Example Dose Info Reporter Uses Department QA (Process Control) Patient Impact Evaluation E.g. Assess impact to fetus when mother was determined to be pregnant after the scan.

Example Dose Registry Uses Population Dose and Dose Indicators Dose Reference Levels Site Benchmarking Population Epidemiology Clinical Trials Longitudinal Patient Dose Record

IHE Europe 2017 Connectathon Review 1 RAS Actor 2 Image Archive Actors 1 Modality 2 Dose Information Consumers

Next Steps Vendors begin implementation Upcoming IHE Connectathons will continue to test REM-NM Customers begin to include requirements for REM- NM support in RfPs. Dose Registries plan to receive and analyze Radiopharmaceutical Radiation Dose SRs. Raise awareness of the standard.