The CDA TM book
(Sprache: Englisch)
Here is clear, easy-to-use guidance to implement the Clinical Document Architecture standard, with numerous examples. Beyond the nuances of healthcare IT implementation, readers learn to "speak" the language of the CDA standard, and to understand its idioms.
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Produktinformationen zu „The CDA TM book “
Here is clear, easy-to-use guidance to implement the Clinical Document Architecture standard, with numerous examples. Beyond the nuances of healthcare IT implementation, readers learn to "speak" the language of the CDA standard, and to understand its idioms.
Klappentext zu „The CDA TM book “
The CDA book provides clear and easy to use guidance to implement the standard, with numerous examples covering many of the nuances of the standard. Readers can learn not only how to implement healthcare IT using the CDA standard, but to "speak" in the language of the standard, and to understand its idioms.
Inhaltsverzeichnis zu „The CDA TM book “
- Introduction- Acknowledgements
- Acronyms and Abbreviations
- Preface
- Organization of this Book
Section I: Introduction
Section II: Data Types
Section III: CDA Modeling
Section IV: Implementing CDA
1. Clinical Documentation
1.1 Properties of Clinical Documents
1.2 The 6 Characteristics of Clinical Documents
2. The HL7 Clinical Document Architecture2.1 History of the Clinical Document Architecture
2.2 CDA is based on XML
2.3 Structure of a CDA Document
2.4 Levels of CDA
- Summary
3. Extensible Markup Language
3.1 The XML Declaration
3.2 Namespaces
3.3 XML Schema Language
3.4 Parsing the CDA XML
- Summary
4 Basic Data Types
4.1 ANY
4.2 Booleans
4.3 Quantities
- Summary
5 Text and Multimedia
5.1 BIN Binary
5.2 ED Encapsulated Data
5.3 ST String
- Summary
6 Demographic Data
6.1 ADXP Address Part
6.2 AD Address Mixed Content Models
6.3 ENXP Entity Name Part
6.4 EN Entity Name
6.5 ON Organization Name
6.6 PN Person Name
6.7 TN Trivial Name
6.8 II Instance Identifier
- Stupid Geek Tricks
6.9 TEL Telecommunications Address
- Summary
- 7 Codes and Vocabularies
7.1 Concepts
7.2 Codes
7.3 Coding Systems
7.4 Pre- and Post-Coordination
7.5 Value Sets
- Summary
- 8 Codes
8.1 CD Concept Descriptor
8.2 CE Coded With Equivalents
8.3 CV Coded Value
8.4 CO Coded Ordinal
8.5 CS Coded Simple
- Summary
- 9 Dates and Times
9.1 TS Time Stamp
9.2 IVL_TS
- Interval of Time
9.3 PIVL_TS Periodic Interval of Time
9.4 EIVL_TS Event-Related Periodic Interval of Time
9.5 GTS Generic Timing Specification
9.6 Use of Time Data Types with Medications
- Summary
- 10 Collections
10.1 BAG Bag
10.2 SET Set
10.3 IVL Interval
10.4 LIST List
- Summary
- 11 HL7 Version 3 Modeling
11.1 The RIM Backbone Classes
11.2 HL7 Modeling and UML
- Summary
- 12 Clinical Document Infrastructure
12.1
12.2 Infrastructure Elements
- Summary
- 13 The CDA Header
13.1 Clinical Document RIM Attributes
13.2 Acts
13.3 Participations
... mehr
and Roles in the Document Context Co-occurrence
13.4 People, Organizations and Devices
- Summary
- 14 The CDA Body
14.1 Unstructured Narrative
14.2 Structured Narrative
14.3 The Narrative Block
14.4 Subject Participation
14.5 Other Rendering Options
- Summary
- 15 Clinical Statements in the CDA
-
15.1 Act classes in the CDA Clinical Statement Model
15.2 EntryRelationship
15.3 Participants
- Summary
- 16 HL7 Version 2 to CDA Release 2
16.1 HL7 Version 2 Data Type Mappings
16.2 Converting Codes and Assigning Authorities
16.3 Observation (OBX)
16.4 Transcription Document Header (TXA)
16.5 Patient Identifier (PID)
16.6 Patient Visit Information (PV1)
16.7 Additional Patient Visit Information (PV2)
16.8 Next of Kin (NK1)
16.9 Message Header (MSH) and Event (EVN) Segments
16.10 Common Order Segment (ORC)
16.11 Observation Request Segment (OBR)
16.12 Note (NTE)
16.13 Specimens (SPM)
- Summary
- 17 Extracting Data from a CDA Document
17.1 Data Extraction
17.2 XPath Searching through Context
- Summary
- 18 Templates
18.1 Building Implementation Guides using Templates
18.2 CDA Extensions
-
Summary
- 19 Validating the Content of a CDA Document
19.1 Using the CDA Schemas
19.2 ISO Schematron
19.3 Model Based Validation
19.4 Validating when CDA Extensions are Used
19.5 Validating Narrative
- Summary
- 20 Implementation Guides on CDA
20.1 Claims Attachments (HL7)
20.2 Electronic Medical Summary (British Columbia / Vancouver Island Health Authority)
20.3 Care Record Summary (HL7)
20.4 Volet Médical (DMP)
20.5 Cross Enterprise Sharing of Medical Summaries (IHE)
20.6 The Continuity of Care Document
-
20.7 Exchange of Personal Health Records
20.8 Laboratory Reports
20.9 Smart Open Services for European Patients
20.10 Unstructured Documents
- Summary
13.4 People, Organizations and Devices
- Summary
- 14 The CDA Body
14.1 Unstructured Narrative
14.2 Structured Narrative
14.3 The Narrative Block
14.4 Subject Participation
14.5 Other Rendering Options
- Summary
- 15 Clinical Statements in the CDA
-
15.1 Act classes in the CDA Clinical Statement Model
15.2 EntryRelationship
15.3 Participants
- Summary
- 16 HL7 Version 2 to CDA Release 2
16.1 HL7 Version 2 Data Type Mappings
16.2 Converting Codes and Assigning Authorities
16.3 Observation (OBX)
16.4 Transcription Document Header (TXA)
16.5 Patient Identifier (PID)
16.6 Patient Visit Information (PV1)
16.7 Additional Patient Visit Information (PV2)
16.8 Next of Kin (NK1)
16.9 Message Header (MSH) and Event (EVN) Segments
16.10 Common Order Segment (ORC)
16.11 Observation Request Segment (OBR)
16.12 Note (NTE)
16.13 Specimens (SPM)
- Summary
- 17 Extracting Data from a CDA Document
17.1 Data Extraction
17.2 XPath Searching through Context
- Summary
- 18 Templates
18.1 Building Implementation Guides using Templates
18.2 CDA Extensions
-
Summary
- 19 Validating the Content of a CDA Document
19.1 Using the CDA Schemas
19.2 ISO Schematron
19.3 Model Based Validation
19.4 Validating when CDA Extensions are Used
19.5 Validating Narrative
- Summary
- 20 Implementation Guides on CDA
20.1 Claims Attachments (HL7)
20.2 Electronic Medical Summary (British Columbia / Vancouver Island Health Authority)
20.3 Care Record Summary (HL7)
20.4 Volet Médical (DMP)
20.5 Cross Enterprise Sharing of Medical Summaries (IHE)
20.6 The Continuity of Care Document
-
20.7 Exchange of Personal Health Records
20.8 Laboratory Reports
20.9 Smart Open Services for European Patients
20.10 Unstructured Documents
- Summary
... weniger
Autoren-Porträt von Keith W. Boone
Keith W. Boone has been involved in the development of Health Level 7 standards including the HL7 Clinical Document Architecture since 2004. He co-chaired the HL7 Structured Documents working group from 2007 to 2010, which is the home of CDA in Health Level 7 International. He is presently a member at large of the HL7 Board. Keith also co-chairs the Integrating the Healthcare Enterprise (IHE) Patient Care Coordination (PCC) planning committee which develops CDA Implementation Guides (which IHE calls profiles) for use internationally. He co-chaired the technical committee of that group from 2006 to 2009.
He also co-chaired the ANSI/HITSP Care Management and Health Records (CMHR) domain technical committee which developed the ANSI/HITSP C32 Summary Documents using CCD and the ANSI/HITSP C83 CDA Document Content Module specifications, and the Data Architecture tiger team which developed the ANSI/HITSP C152 Data Dictionary specification.
He also participates in other standards organizations, including the US Technical Advisory Group to ISO TC-215, ASTM and Continua.
Mr. Boone is a Standards Architect for GE Healthcare, where he is currently employed, and represents GE Healthcare to numerous standard organizations. He was introduced to IHE profiles and HL7 standards while working as a Chief Engineer at Dictaphone Corporation where he took on the role of leading that organization's efforts in standards. Before he developed an interest in the HL7 Clinical Document Architecture, Keith was a Software Architect for eBusiness Technologies, an XML technology company. There he was introduced to standards development, and worked alongside many of the co-chairs and developers of the XML specifications, including XML, XML Namespaces, XSLT, and XPath.
Bibliographische Angaben
- Autor: Keith W. Boone
- 2014, 2011, XXXIV, 307 Seiten, Masse: 15,6 x 23,4 cm, Kartoniert (TB), Englisch
- Verlag: Springer, Berlin
- ISBN-10: 1447158873
- ISBN-13: 9781447158875
Sprache:
Englisch
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