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.