The CDA TM book

Clinical documentation is used throughout healthcare to describe care provided to a patient, communicate essential information between healthcare providers and maintain medical records.  The CDA Book describes the HL7 Clinical Document Architecture Release 2.0 standard, a standard format for clinica...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριος συγγραφέας: Boone, Keith W. (Συγγραφέας)
Συγγραφή απο Οργανισμό/Αρχή: SpringerLink (Online service)
Μορφή: Ηλεκτρονική πηγή Ηλ. βιβλίο
Γλώσσα:English
Έκδοση: London : Springer London : Imprint: Springer, 2011.
Θέματα:
Διαθέσιμο Online:Full Text via HEAL-Link
Πίνακας περιεχομένων:
  • 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 <ClinicalDocument>
  • 12.2 Infrastructure Elements
  • Summary
  • 13 The CDA Header
  • 13.1 Clinical Document RIM Attributes
  • 13.2 Acts
  • 13.3 Participations 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.