report on japanese activities dicom standards committee 12/2/2004 at chicago hidenori shinoda jira
TRANSCRIPT
Report on Japanese Activities
DICOM Standards Committee12/2/2004
At ChicagoHidenori Shinoda
JIRA
Notification about Worklist Availability
• We proposed a push model of MWL at the last meeting of DSC in Munich. But, it was rejected.
• We still need a mechanism that can trigger a modality to pull a specific worklist.– Poling is one of the solutions, but it may cause the
network congestion.– An RIS terminal is usually put closely by the moda
lity.
Situation of exam rooms in Japan
X-Ray Exam Room A
CT Exam Room
RIS
RIS Terminal CT
RISTerminalX-Ray A
Enter dataPatient NameIDEtc.
Notify “Data is Ready”
Sequence Diagram
RIS CR
Select a patient and Enter data about thePatient and Study
SetDataAnd
RespondStatus
N-EVENT-REPORTRequest
Acknowledge
Notified Info. about events1. Entered2. Changed3. Deleted
Attributes may be requiredDescription /module Tag SCU/SCP Note/matching type
Specific character set (0008,0005) 1C/1C This attribute is necessary when an extended or replaced character set is used.
Name of searched AE (0008,0054) 1/1 Name of the searched AE
Study instance UID (0020,000D) 1/1
Accession number (0008,0050) 1/1C (Responding to patient base search)
Patient name (0010,0010) 1/2C (Responding to patient base search)
Patient ID (0010,0020) 1/1C (Responding to patient base search)
Requested procedure step ID (0040,1001) 1/1C (Responding to patient base search)
Reserved procedure step ID (0040,0009) 2/2
Reserved station AE name (0040,0001) 2/2 (Responding to wide-area search)
Reserved procedure step start date (0040,0002) 2/2 (Responding to wide-area search)
Reserved procedure step start time (0040,0003) 2/2 (Responding to wide-area search)
Modality (0008,0060) 2/2 Modality is obtained by matching a single value.
Japanese government will modify a rule on drugs and medical equipment• Ministry of Health, Welfare, and Labor will
modify a rule that regulate the use of drugs and medical equipment.
• They updated the list of medical devices. A general purpose image processing workstation is now included in the list.
• The workstation may be classified as Class 2 devices and then, vendors will be required to improve their organizations.
Japanese government will modify a rule on drugs and medical equipment-to be continued• Requirements
– Vendors must be authorized to sell the workstations and prepare experienced people to sell them.
– Manufacturers must be authorized to develop and manufacture those devices and form a division that is responsible to the quality of the devices.
• This is the result from global harmonization. FDA already has such a rule.
New Project of Interoperability for Healthcare IS Has Started
Systems Common Infrastructure- Security Related-
Electronic Chart System(EMR)
Dep
t. Syste
m
2 Dep
t. Syste
m
n
Departmental System 1
ECS DataItems
Trans-form
Cross SystemsData Reference
System Connectivity
Data Portability
Consortium is formed;JIRAJAHISand MEDIS