Philips Hd 7 User Manual
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DICOM Conformance Statement HD7/HD7XE 3.0 000245000000008 Rev A 2010-09-30 © Koninklijke Philips Electronics N.V. 2010 All rights are reserved.
0.1 REVISION HISTORY Document Version Date of Issue Author Description A Sept. 30, 2010 M. Leif Initial Release HD7/HD7XE 3.0 DICOM Conformance St atement 000245000000008 Rev. A Page 2
HD7/HD7XE 3.0 DICOM Conformance Statement 000245000000008 Rev. A Page 3 1 CONFORMANCE STATEMENT OVERVIEW The Philips HD7/HD7XE 3.0 Ultrasound sy stems implement the necessary DICOM® services to download worklists from an information system, save acquired US Images and Structured Reports to a network storage device, CD or DVD, print to a networked hardcopy devic e and inform the information system about the work actually done. Table 1 provides an overview of the supported network services. Table 1 NETWORK SERVICES Networking SOP Classes User of Service (SCU) Provider of Service (SCP) Transfer Ultrasound Image Storage Yes* No Ultrasound Multiframe Image Storage Yes* No Storage Commitment Push Model Yes* No Comprehensive SR Yes* No Workflow Management Modality Worklist Yes* No Modality Performed Procedure Step Yes* No Print Management Basic Grayscale Print Management Yes* No Basic Color Print Management Yes* No * Purchasable option. Table 2 specifies the Media Storage Application Profiles supported. Table 2 MEDIA SERVICES Media Storage Application Profile Write Files (FSC or FSU) Read Files (FSR) Compact Disk - Recordable STD-US-SC-MF(1)-CD-R for Ultrasound images, compressed and uncompressed Yes / Yes Yes ® DICOM is the registered trademark of the National Electrical Manufacturers Association for its standards publications relating to digital communications of medical information.
HD7/HD7XE 3.0 DICOM Conformance Statement 000245000000008 Rev. A Page 4 STD-GEN-CDR for Structured Reports Yes / Yes No DVD STD-US-SC-MF(1)-DVD for Ultrasound images, compressed and uncompressed Yes / Yes Yes STD-GEN-DVD for Structured Reports Yes / Yes No (1) Note that the “MF” designator includes both Single Frame (SF) and Mullti-frame (MF) ultrasound images. Table 3 Supported STRUCTURED REPORT Templates Concept Name OB-GYN Ultrasound Procedure Report (Template ID 5000) Adult Echocardiography Procedure Report (Template ID 5200)
HD7/HD7XE 3.0 DICOM Conformance Statement 000245000000008 Rev. A Page 5 2 TABLE OF CONTENTS 0.1 REVISION HISTORY .......................................................................\ ....................................... . 2 1 CONFORMANCE STATEMENT OVERVIEW ........................................................................\ ................. 3 2 TABLE OF CONTENTS .......................................................................\ ...................................... .............. 5 3 INTRODUCTION ........................................................................\ ....................................................... ....... 7 3.1 AUDIENCE .......................................................................\ ............................................... ........ 7 3.2 REMARKS .......................................................................\ ........................................................ 7 IMPORTANT NOTE TO THE READER ........................................................................\ ........................... 7 3.3 DEFINITIONS, TERMS AND ABBREVIATIONS ..................................................................... 8 3.4 REFERENCES ...................................................................\ ................................................. .... 8 4 NETWORKING .....................................................................\ ............................................... .................... 9 4.1 IMPLEMENTATION MODEL ........................................................................\ ........................... 9 4.1.1 Application Data Flow ........................................................................\ ............................ 9 4.1.2 Functional Definition of AEs ........................................................................\ ................. 10 4.2 AE SPECIFICAT IONS .......................................................................\ .................................... 1 4 4.2.1 Storage Application Entity Specification ...................................................................... 14 4.2.2 Workflow Application Entity Specif ication ..................................................................\ .. 21 4.2.3 Hardcopy Application Entity Specif ication ..................................................................\ . 32 4.2.4 Verification Application Entity specification .................................................................. 39 4.3 PHYSICAL NETWORK INTERFACES .......................................................................\ ........... 44 4.3.1 Supported Communication Stacks ........................................................................\ ...... 44 4.3.2 Physical Network Interface ........................................................................\ .................. 44 4.4 CONFIGURATION ...................................................................\ .............................................. 44 AE Title/Presentation Address Mapping ........................................................................\ .................. 44 5 MEDIA STORAGE .......................................................................\ .......................................... ................ 45 5.1 IMPLEMENTATION MODEL ........................................................................\ ......................... 45 5.1.1 Application Data Flow ........................................................................\ .......................... 45 5.1.2 Functional Definition of AEs ........................................................................\ ................. 46 5.1.3 Sequencing of Real-Wor ld Activities ...................................................................\ ......... 46 5.1.4 File Meta Inform ation Options ........................................................................\ .............. 46 5.2 AE SPECIFICAT IONS .......................................................................\ .................................... 4 6 5.2.1 Media Application Entity Specification ........................................................................\ . 46 6 SUPPORT OF CHARACTER SETS ........................................................................\ ............................. . 48 6.1 SUPPORT FOR RUSSIAN AND JAPANESE MARKETS ............................................................... 48 6.2 ADDITIONAL SUPPORT FOR JAPANESE MARKETS ................................................................\ .. 48 6.3 SUPPORT FOR CH INESE MARKETS ........................................................................\ ................... 49 7 SECURITY ...............................................................\ ....................................................... ....................... 49 8 ANNEXES ................................................................\ .............................................................................. 50 8.1 CREATED IOD INSTANCES ........................................................................\ ......................... 50 8.1.1 US or US Multi-frame Image IOD ....................................................................\ ............ 50 8.1.2 Comprehensive Structur ed Report IOD ....................................................................... \ 51 8.1.3 Common Modules .....................................................................\ ................................... 51 8.1.4 US or Multiframe Image Modules ........................................................................\ ........ 53 8.1.5 Comprehensive Structured Report Modules ................................................................ 60
HD7/HD7XE 3.0 DICOM Conformance Statement 000245000000008 Rev. A Page 6 8.2 USED FIELDS IN RECEIVED IOD BY APPLICATION ......................................................... 62 8.3 ATTRIBUTE MAPPING .................................................................\ ........................................ 62 8.4 COERCED/MODIFI ED FIELDS........................................................................\ ..................... 63 8.5 CONTROLLED TERM INOLOGY .......................................................................\ ................... 63 8.6 GRAYSCALE IMAGE CONSISTENCY .......................................................................\ .......... 63 8.7 EXTENSIONS / SPECIALIZATION S / PRIVATIZATIONS .................................................... 63 8.7.1 Standard Extended / Specializ ed / Private SOPs ........................................................ 63 8.8 PRIVATE TRANSFER SYNTAXES ........................................................................\ ............... 63 APPENDIX A – Structured Reports ........................................................................\ ....................... ............... 64 A.1 STRUCTURED REPORTS ........................................................................\ ............................ 64 A.1.1 Introduction ...................................................................\ ............................................... 64 A.1.2 OB Measurements .................................................................\ ...................................... 65 A.1.3 GYN Measur ements .................................................................\ ................................... 72 A.1.4 Cardiac Measurements ........................................................................\ ........................ 75
HD7/HD7XE 3.0 DICOM Conformance Statement 000245000000008 Rev. A Page 7 3 INTRODUCTION 3.1 AUDIENCE This document is intended for hospital staff, health care system integrators, software designers or implementers. It is assumed that the reader has a working understanding of DICOM. 3.2 REMARKS DICOM, by itself, does not guarantee inte roperability. However, the Conformance Statement facilitates a first-level validation for interoperability between different applications supporting the same DICOM functionality. This Conformance Statement is not intended to replace va lidation with other DICOM equipment to ensure proper exchange of information intended. The scope of this Conformance Statement is to facilit ate communication between Philips Medical Systems and other vendors’ Medical equipment. The Conformance Statement should be read and understood in conjunction with the DICOM Standard [DICOM]. However, by itself it is not guar anteed to ensure the desired interoperability and successful interconnectivity. The user should be aware of the following important issues: — The comparison of different conformance statements is the first step towards assessing interconnectivity between Philips Medical Systems and non - Philips Medical Systems equipment. — Test procedures should be defined to va lidate the desired level of connectivity. — The DICOM standard will evolve to meet the users’ futu re requirements. Philips Medical Systems is actively involved in developing the standard further and therefore rese rves the right to make changes to its products or to discontinue its delivery. IMPORTANT NOTE TO THE READER Interoperability Interoperability refers to the ability of application functions, di stributed over two or more systems, to work successfully together. The integration of medical devices into an IT env ironment may require application functions that are not specified within the scope of DICOM. Consequently, using only the information provided by this Conformance Statement does not guarantee interoperability of Philips equipment with non-Philips equipment. It is the user’s responsibility to analyze thoroughly the application requirem ents and to specify a solution that integrates Philips equipment with non-Philips equipment. Validation Philips equipment has been carefully tested to assure t hat the actual implementation of the DICOM interface corresponds with this Conformance Statement. Where Philip s equipment is linked to non-Philips equipment, the first step is to compare the relevant Conf ormance Statements. If the Conformance Statements indicate that successful information exchange should be possible, additional validation tests will be necessary to ensure the functionality, performance, accuracy and stability of image and image related data. It is the responsibility of the user (or user’s agent) to specify the appropriate test suite and to carry out the additional validation tests. New versions of the DICOM Standard The DICOM Standard will evolve in future to meet the user ’s growing requirements and to incorporate new features and technologies. Philips is actively involved in this evoluti on and plans to adapt its equipment to future versions of the DICOM Standard. In order to do so, Philips reserves the right to make changes to its products or to discontinue its
HD7/HD7XE 3.0 DICOM Conformance Statement 000245000000008 Rev. A Page 8 delivery. The user should ensure that any non-Philips pr ovider linking to Philips equipment also adapts to future versions of the DICOM Standard. If not, the incorporati on of DICOM enhancements into Philips equipment may lead to loss of connectivity (in case of networki ng) and incompatibility (in case of media). 3.3 DEFINITIONS, TERMS AND ABBREVIATIONS Definitions, terms and abbreviations used in this docu ment are defined within the different parts of the DICOM standard. Abbreviations and terms are as follows: AE DICOM Application Entity AET Application Entity Title ASCE Association Control Service Element CD-R Compact Disk Recordable CSE Customer Service Engineer DICOM Digital Imaging and Communications in Medicine FSC File-Set Creator FSU File-Set Updater FSR File-Set Reader GSDF Grayscale Standard Display Function IOD (DICOM) Information Object Definition ISO International Standard Organization LOINC Logical Observation Identifiers Names and Codes MPPS Modality Performed Procedure Step MSPS Modality Scheduled Procedure Step MWL Modality Worklist R Required Key Attribute O Optional Key Attribute PDU DICOM Protocol Data Unit PDE Patient Data Entry SCU DICOM Service Class User (DICOM client) SCP DICOM Service Class Provider (DICOM server) SOP DICOM Service-Object Pair SNOMED Systematized Nomenclature of Medicine (SRT) U Unique Key Attribute US Ultrasound 3.4 REFERENCES [DICOM] Digital Imaging and Communications in Medicine (DICOM), NEMA PS 3.1-3.18, 2008
HD7/HD7XE 3.0 DICOM Conformance Statement 000245000000008 Rev. A Page 9 4 NETWORKING 4.1 IMPLEMENTATION MODEL 4.1.1 Application Data Flow Send Images, Reports, CommitsStorage A p plicatio n E ntity Remote A p plication E ntity R eceives Im ages, R eports, Com m its; R eturns C om m itm ents Update W o rklist Acquire Im ages Remote A p plication Entity Provides W orklistItem s Remote A p plication E ntity R eceives M P PS C reate / S et Workflow A p plicatio n E ntity Film Im ages Remote A p plication E n tity P rin ts Film SheetsHardcopy A p plicatio n E ntity DICOM Standard Interface Local AEs Connected AEs Figure 1 APPLICATION DATA FLOW DIAGRAM — The Storage Application Entity sends Images to one or two remote AEs and Structured Reports to a single remote AE. Acquisition of images is associated with the lo cal real-world activity “Freeze” then “Acquire” for single frame and “Acquire” for loops or clips. Sending or exporting of images depends on user configuration, either “Send as you go”, or ”Batch” when End Study is pressed, or Manual. An exam may be sent by user selection from “Review”. A storage commitment se rver is configured for one of the two image storage servers. A separate commit server is configured for SRs. If the remote AE is configured for Storage Commitment, the Storage AE will request Storage Commitment after End Exam. If a commitm ent response is successfully obtained, there will be no
HD7/HD7XE 3.0 DICOM Conformance Statement 000245000000008 Rev. A Page 10 job remaining in the queue (viewed using CNTL-J) signali ng the Auto-delete function that the exam qualifies for deletion. — The Workflow Application Entity receives Worklist information from and sends MPPS information to a remote AE. It is associated with the local real-world activiti es “Refresh Worklist” or automatic polling and “Acquire” images. When either the “Refresh Wo rklist” or automatic polling are performed, the Workflow Application Entity queries a remote AE for worklist items and provides th e set of worklist items matching the query request. — Modality Performed Procedure Step (MPPS) messages are sent from the system under the following circumstances: o MPPS N-Create, Status = IN PROGRESS: ƒ Closing the Patient Data Entry screen will result in automated creation of an MPPS Instance managed by a remote AE. o MPPS N-Set, Status = COMPLETE ƒ Completion of the MPPS is performed as the resu lt of an operator action of ending the exam. o MPPS N-Set, Status = DISCONTINUED ƒ “Cancel” exam causes the “Disco ntinued” status to be sent. — The ability to Append images and SRs to an ended exam is availa ble. There are two fundamental methods to perform append: o Append from Image Review ƒ Select an Ended study from the Patient Directory. o Select the study; choose “Open Study”. o Append from Patient Selection • Select the exam from the Patient Worklist Directory. — The Hardcopy Application Entity prints images on a remote AE (Printer or pr int server). It is associated with the local real-world activity Acquire when a DICOM Printer is configured in the current preset, or “DICOM print” is selected with Right Button on the Exam in the system Pati ent Directory. Either user action creates a print queue containing one or more virtual film sheets composed from images acquired by the user. It creates and sends fully rendered pages already containing the user’s selected form atting choices. Only a single image object per sheet is sent to the printer. This print object is rather large compared to sending individual Image Box objects to the printer. If the user has both a BW and Color DICOM pr inter configured and selected, and is using “Send as you go”, the images containing no Color Flow or Chroma data will be sent to the BW printer, all others will be sent to the Color printer. — Exam data is sent to all selected Store, Print and Workflow destinations simultaneously in accordance with system configuration of “Send as you go” or “Batch” at End of Exam or Manual. 4.1.2 Functional Definition of AEs 4.1.2.1 Functional Definition of Storage Application Entity The existence of a Network Store queue with associat ed network destination will activate the Storage AE. An association request is sent to the destination AE and upon su ccessful negotiation of a Presentation Context the image transfer is started. If the association ca nnot be opened, the related queue’s Status is set to RETRY as displayed in the Job Manager (CNTL-J). The user may need to cancel the queue, and then restart manually. After the automatic retries have failed, the job is set to Failed. The user may select “Retry Job” to attempt to send. Deleting a job does not remove the data, as it is still present on the system. Only the request to transfer the data is removed. Once any communication issues have been resolved, retry may be select ed or if the jobs were deleted, they may be queued again from the Review directory. 4.1.2.2 Functional Definition of Workflow Application Entity “Refresh Now” attempts to download a Modality Worklist from a Modality Worklist server with studies matching the search criteria by sending a C-Find Request containing user-definable Query parameters. Query parameters are stored in the Advanced tab adjacent to the MWL SCP se lection in the “Servers and Roles” setup page. 10 Customizable Queries may be us ed, 5 are factory defaults.