XpanDH Patient Summary
0.1.0 - ci-build 150

XpanDH Patient Summary, published by XpanDH Project. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-eu/xpandh-ps/ and changes regularly. See the Directory of published versions

Table of Contents

.. 0 Table of Contents
... 1 Home
... 2 Examples
... 3 Downloads
... 4 Artifacts Summary
.... 4.1 A - Patient Summary
.... 4.2 A.1.1, A.1.2 - Patient or Subject of care
.... 4.3 A.2.1.1 - Allergy
.... 4.4 A.2.2.1 - Vaccination/prophylaxis information
.... 4.5 A.2.2.2 Resolved, closed or inactive problems model to this guide
.... 4.6 A.2.3.1 Current problems model to this guide
.... 4.7 A.2.3.2 Medical devices and implants model to this guide
.... 4.8 A.2.3.3 Procedures model to this guide
.... 4.9 A.2.3.3 Functional Status model to this guide
.... 4.10 A.2.4.1 Current and relevant past medicines
.... 4.11 A.2.6 Pregnancy history model to this guide
.... 4.12 A.2.8 Results model to this guide
.... 4.13 A - Patient Summary model to this guide
.... 4.14 A.1.1, A.1.2 - Subject of care model to this guide
.... 4.15 A.2.1.1 - Allergy model to this guide
.... 4.16 A.2.2.1 - Vaccination/prophylaxis information model to this guide
.... 4.17 A.2.3.1 Current problems model to this guide
.... 4.18 A.2.3.2 Medical devices and implants model to this guide
.... 4.19 A.2.3.3 Functional Status model to this guide
.... 4.20 A.2.3.3 Procedures model to this guide
.... 4.21 A.2.4.1 Current and relevant past medicines model to this guide
.... 4.22 A.2.6 Pregnancy history model to this guide
.... 4.23 A.2.8 - Results model to this guide
.... 4.24 Allergy Intolerance (EU PS)
.... 4.25 Bundle (EU PS)
.... 4.26 CareTeam
.... 4.27 Composition (EU PS)
.... 4.28 Condition (EU PS)
.... 4.29 Device (EU PS)
.... 4.30 Device Use Statement (EU PS)
.... 4.31 Flag (EU PS)
.... 4.32 Immunization (EU PS)
.... 4.33 ImmunizationRecommendation (EU PS)
.... 4.34 Location (EU PS)
.... 4.35 Medication (EU PS)
.... 4.36 Medication Statement (EU PS)
.... 4.37 Observation Results (EU PS)
.... 4.38 Observation Results: laboratory (EU PS)
.... 4.39 Observation Results: pathology (EU PS)
.... 4.40 Observation Results: radiology (EU PS)
.... 4.41 Observation Social History (EU PS)
.... 4.42 Observation: Blood Group
.... 4.43 Organization: Care provisioning
.... 4.44 Patient (EU PS)
.... 4.45 Practitioner (EU PS)
.... 4.46 PractitionerRole (EU PS)
.... 4.47 Procedure (EU PS)
.... 4.48 Condition Status Reason
.... 4.49 Immunization AdministeredProduct
.... 4.50 Supporting Information
.... 4.51 Absent or Unknown Allergies
.... 4.52 Absent or Unknown Device
.... 4.53 Absent or Unknown Medication
.... 4.54 Absent or Unknown Problem
.... 4.55 Absent or Unknown Procedure
.... 4.56 Active Ingredient
.... 4.57 Adverse Event Type
.... 4.58 Allergen No Drug
.... 4.59 Allergens
.... 4.60 Allergens or no known or unknown conditions
.... 4.61 Allergy Certainty
.... 4.62 Allergy Status
.... 4.63 Blood Group
.... 4.64 Blood Pressure
.... 4.65 Body Site
.... 4.66 Certainty
.... 4.67 Conditions
.... 4.68 Confidentiality
.... 4.69 Country
.... 4.70 Criticality
.... 4.71 Current Pregnancy Status
.... 4.72 Document Code
.... 4.73 Dose Form
.... 4.74 eHDSI Social History
.... 4.75 Healthcare Professional Role
.... 4.76 Hospital Discharge Report Type
.... 4.77 Illness and Disorder (PARTIAL)
.... 4.78 Medical Device
.... 4.79 Problems
.... 4.80 Problems (including unknown conditions)
.... 4.81 Procedure
.... 4.82 Rare Disease (PARTIAL)
.... 4.83 Reaction Allergy
.... 4.84 Route of Administration
.... 4.85 Severity
.... 4.86 Substance (PARTIAL)
.... 4.87 Vaccine
.... 4.88 eHN ClosedProblem to this guide Map