 0 Table of Contents |
  1 Home |
  2 Business Analysis |
  3 Laboratory Testing Workflow (LTW) |
  4 Patient Administration (PAM) |
  5 Healthcare Provider Directory (HPD) |
  6 Health Information Exchange (HIE) |
  7 Placer Order Management [LAB-1] |
  8 Filler Order Management [LAB-2] |
  9 Order Results Management [LAB-3] |
  10 Work Order Management [LAB-4] |
  11 Test Results Management [LAB-5] |
  12 Query Existing Data [QEDm] |
  13 Mobile Access to Health Documents [MHD] |
  14 Patient Demographics Query for Mobile (PDQm) |
  15 Overview |
  16 HL7 v2 Standards |
  17 Architecture |
  18 Testing |
  19 Support |
  20 Authorisation (OAuth2) |
  21 Deployment |
  22 OAuth2 |
  23 Workflow/Interaction Options |
  24 Report Options |
  25 Identifiers and Codes |
  26 Data Contracts and Issue Reporting |
  27 Care Services Discovery |
  28 Specimen Event Tracking (SET) |
  29 Inter Laboratory Workflow (ILW) |
  30 Simple |
  31 Digital Consent (IHE BPPC and PCF) |
  32 Design |
  33 Artifacts Summary |
   33.1 Automation Manager |
   33.2 Clinical Document |
   33.3 Intermediary |
   33.4 Order Filler |
   33.5 Order Placer |
   33.6 Order Result Tracker |
   33.7 Patient Identity Source |
   33.8 Provider Information Source |
   33.9 CapabilityStatement for NW GMSA Clinical Data Repository |
   33.10 CapabilityStatement for NW GMSA Regional Integration Engine for Genomics |
   33.11 Process Message |
   33.12 Message Definition - Laboratory Order |
   33.13 Message Definition - Patient Encounter |
   33.14 Message Definition - Patient Identity |
   33.15 Message Definition - Unsolicited Observation |
   33.16 assigner |
   33.17 CBC panel - Blood by Automated count |
   33.18 Comprehensive metabolic 2000 panel - Serum or Plasma |
   33.19 Master HL7 genetic variant reporting panel |
   33.20 North West Genomics Test Order |
   33.21 North West Genomics Test Order Future |
   33.22 North West Genomics Test Report |
   33.23 Pedigree |
   33.24 AuditEvent |
   33.25 Binary |
   33.26 Composition Genomic Report |
   33.27 Condition |
   33.28 Diagnostic Implication (Observation) |
   33.29 Diagnostic Report |
   33.30 DocumentReference |
   33.31 Encounter |
   33.32 Event |
   33.33 FamilyMemberHistory |
   33.34 Genomic Study (Observation Panel) |
   33.35 Genomic Study (Procedure) |
   33.36 Genotype (Observation) |
   33.37 Hospital Spell |
   33.38 MessageHeader |
   33.39 Observation |
   33.40 Observation Panel |
   33.41 OperationOutcome |
   33.42 Organization |
   33.43 Patient |
   33.44 Practitioner |
   33.45 PractitionerRole |
   33.46 Procedure |
   33.47 Questionnaire |
   33.48 QuestionnaireResponse |
   33.49 RelatedPerson |
   33.50 ServiceRequest |
   33.51 Specimen |
   33.52 Task |
   33.53 Therapeutic Implication (Observation) |
   33.54 Variant (Observation) |
   33.55 Visit |
   33.56 Attachment |
   33.57 CodeableReference |
   33.58 Correlation Identifier |
   33.59 Genomics Pedigree Number |
   33.60 GS1 Global Service Relation Number (GSRN) |
   33.61 GS1 Serial Shipping Container Code (SSCC) |
   33.62 GS1 Service Relation Instance Number (SRIN) |
   33.63 Hospital Provider Spell Identifier |
   33.64 Medical Record Number |
   33.65 NHS Identifier |
   33.66 Order Group Number |
   33.67 Order Identifier |
   33.68 Organisation Code |
   33.69 Organisation Site Identifier |
   33.70 Practitioner Identifier |
   33.71 Report Identifier |
   33.72 Shipment Tracking Number |
   33.73 Specimen Accession Number |
   33.74 Visit Number |
   33.75 ExtCodeableReference |
   33.76 Admission Method |
   33.77 Admission Source |
   33.78 Discharge Destination |
   33.79 Discharge Disposition |
   33.80 DocumentEntry Class |
   33.81 DocumentEntry mimeType |
   33.82 DocumentEntry Type |
   33.83 Ethnicity |
   33.84 Facility Type |
   33.85 Genomic Cancer Test Directory |
   33.86 Genomic Clinical Indication Codes |
   33.87 Genomic Disorder Carrier |
   33.88 Genomic Finding |
   33.89 Genomic Finding Detected |
   33.90 Genomic Rare and Inherited Disease Test Directory |
   33.91 Genomic Test Codes |
   33.92 Genomic Test Outcome Codes |
   33.93 NW IdentifierType |
   33.94 Order Category |
   33.95 Organisation Cheshire and Merseyside ICS (QYG) NHS Trusts |
   33.96 Organisation Greater Manchester ICS (QOP) NHS Trusts |
   33.97 Organisation Lancashire and South Cumbria ICS (QE1) NHS Trusts |
   33.98 Organisation North West Region NHS Trusts |
   33.99 Patient Encounter Trigger |
   33.100 Patient Identity Trigger |
   33.101 Practitioner Identifiers |
   33.102 Pregnancy |
   33.103 Request Priority |
   33.104 Service |
   33.105 Specialty |
   33.106 Specimen Tracking Events |
   33.107 Specimen Type |
   33.108 UK National Health Identifiers |
   33.109 Yes/No |
   33.110 Yes/No/Unknown |
   33.111 iGene Codes |
   33.112 iGene Test Codes |
   33.113 MFT EPIC Question Ids |
   33.114 NHS England Genomic Clinical Indication Code |
   33.115 NHS England Genomic Test Code |
   33.116 NHS England Genomic Test Outcome Code |
   33.117 NW GMSA Codes |
   33.118 UK National Health Identifiers |
   33.119 UK Professional License |
   33.120 GMC Number |
   33.121 GMP Number |
   33.122 NHS Number |
   33.123 ODS Code |
   33.124 ODS Site Code |
   33.125 LOINC to SNOMED UK edition |
   33.126 Sample Type (SNOMED) to iGene Specimen Type |
   33.127 SNOMED LOINC edition to SNOMED UK edition |
   33.128 Clinical and Genomic Workflow |
   33.129 Collect Specimen - Biopsy Procedure for obtaining a specimen, part of a diagnostic pathway. Day case admission. |
   33.130 Genomic Test Order Process including order entry and transmission of the order |
   33.131 Genomic Test Report Process |
   33.132 Bundle 'Event Message' - Patient Update |
   33.133 Bundle 'Message' - Genomics Order Reply |
   33.134 Bundle 'Message' - Genomics Order Reply Acknowledgement |
   33.135 Bundle 'Transaction' - Genomics Order Asynchronous Message Reply Acknowledgement |
   33.136 Bundle - Conditions for a Patient QEDm |
   33.137 Bundle - Form Search Results SDC |
   33.138 Bundle - Genomic Diagnostic Implication for a Patient QEDm |
   33.139 Bundle - Genomic Variant for a Patient QEDm |
   33.140 Bundle - Genomic Variant Gene = NTHL1 QEDm |
   33.141 Bundle - Patient Search Results by Medical Record Number PDQ |
   33.142 Bundle - Patient Search Results by NHS Number PDQ |
   33.143 Condition - Carcinoma |
   33.144 Condition - Lynch Syndrome |
   33.145 Consanguinity (type=CE) |
   33.146 FamilyMemberHistory - Ricky LEEDS |
   33.147 FamilyMemberHistory - Sarah-Jane Nottingham |
   33.148 Genomic Order Entry Optional Questions |
   33.149 Genomic Report BRCA1 Variant Example |
   33.150 Genomic Report Ovarian Carcinoma Diagnostic Implication Example |
   33.151 Genomic Study (Panel) - Cystic Fibrosis |
   33.152 Genomic Study (Panel) - Lynch Syndrome |
   33.153 MCV - Mean corpuscular volume |
   33.154 Message Header - Genomic Order Reply fatal |
   33.155 Message Header - Genomic Order Reply fatal Acknowledgement |
   33.156 Message Header - Genomic Order Reply Transient |
   33.157 Message Header - Genomic Report |
   33.158 Message Header - Patient |
   33.159 Observation - Lynch Syndrome Mutation Finding |
   33.160 Order Tracking Number (type=ST) |
   33.161 Organization MANCHESTER UNIVERSITY NHS FOUNDATION TRUST |
   33.162 Organization North West GMSA |
   33.163 Output from a FHIR Validation |
   33.164 Parameters Expansion Profile |
   33.165 Patient - Birmingham |
   33.166 Patient - Bolton |
   33.167 Patient - Congleton |
   33.168 Patient - Fetus London |
   33.169 Patient - Lancaster |
   33.170 Patient - London |
   33.171 Patient - Ned Liverpool NHS Number: 9737383206 |
   33.172 Patient - Northwich |
   33.173 Patient - Nottingham |
   33.174 Patient - Rob Leeds NHS Number: 9737383222 |
   33.175 Patient - Sansa Manchester NHS Number: 9737383192 |
   33.176 Patient - Warrington |
   33.177 Patient - Wrexham |
   33.178 PractitionerRole Result INTERPRETER |
   33.179 Pregnancy Expected Delivery Date (type=DT) |
   33.180 Procedure - Liver Biopsy |
   33.181 RelatedPerson Birmingham-Lancaster |
   33.182 RelatedPerson Birmingham-London |
   33.183 RelatedPerson Lancaster-London |
   33.184 RelatedPerson London-Lancaster |
   33.185 RelatedPerson Mother Cersei London |
   33.186 RelatedPerson Wrexham-Lancaster |
   33.187 RelatedPerson Wrexham-London |
   33.188 Task Genomic Test Completed |
   33.189 Task Genomic Test Requested |
   33.190 Binary Genomic Record of Discussion Example |
   33.191 Bundle 'Message' - Genomics Order Reply |
   33.192 Bundle 'Message' - Genomics Order with Attachment |
   33.193 Bundle 'Message' - Genomics Order with Coded Entries |
   33.194 Bundle 'SearchSet' - Genomics Order |
   33.195 Document Reference Laboratory Order |
   33.196 Encounter 'episode/stay' Example |
   33.197 Message Header - Genomic Order |
   33.198 Message Header - Genomic Order Reply ok |
   33.199 Patient - OctaviaCHISLETT NHS Number: 9449305552 |
   33.200 PractitionerRole C3456789 Example |
   33.201 ServiceRequest Attachment Example |
   33.202 ServiceRequest Coded Entries Example |
   33.203 Specimen Example |
   33.204 Binary Genomic Report Example |
   33.205 Bundle 'Message' - Genomics Report |
   33.206 Diagnostic Report Example. |
   33.207 Document Reference Laboratory Report |
   33.208 Message Header - Genomic Report |
   33.209 DiagnosticImplication - Cystic Fibrosis Carrier |
   33.210 DiagnosticImplication - Lynch Syndrome |
   33.211 Genomic Study - Cystic Fibrosis |
   33.212 Genomic Study - Lynch Syndrome |
   33.213 Variant - CFTR |
   33.214 Variant - NTHL1 |
   33.215 748683741 |
   33.216 Bundle `Document` - Genetic Report |
   33.217 Composition - Genomics Report Octavia CHISLETT |
   33.218 EPIC-OBR-1 Example |
   33.219 EPIC-OBX-10 Example |
   33.220 EPIC-OBX-11 Example |
   33.221 EPIC-OBX-2 Example |
   33.222 EPIC-OBX-4 Example |
   33.223 EPIC-OBX-6 Example |
   33.224 EPIC-OBX-7 Example |
   33.225 EPIC-OBX-8 Example |
   33.226 Genomic Referral Category |
   33.227 High infection risk sample |
   33.228 Informed Consent |
   33.229 OBX Pregnancy |
   33.230 Supervising Clinician |
   33.231 Bundle-Bundle-NonWGSTestOrderForm-Reanalysis-Example |
   33.232 Bundle-NonWGSTestOrderForm-CancerSolidTumor-Example |
   33.233 Bundle-NonWGSTestOrderForm-FetalScenario-Example |
   33.234 NRL Genomic Report for Cersei LONDON (Test NHS Number 9737383230). Original order electronic from EPIC system |
   33.235 NRL Genomic Report for Tommen BIRMINGHAM (Test NHS Number 9737383249). Original order not electronic |
   33.236 837d78a0-30cd-478c-83a8-f83d16fc4443 |