 0 Table of Contents |
  1 Home |
  2 Business Analysis |
  3 Laboratory Testing Workflow (LTW) |
  4 Health Data API (HIE/EURDICE) |
  5 Patient Administration (PAM) |
  6 Laboratory Specimen Barcode Labeling (LBL) |
  7 Healthcare Provider Directory (HPD) |
  8 Genomic Archiving and Communication System (GACS) |
  9 Health Document Sharing (MHDS) and Sharing Laboratory Reports (XD-LAB) |
  10 Placer Order Management [LAB-1] |
  11 Filler Order Management [LAB-2] |
  12 Order Results Management [LAB-3] |
  13 Work Order Management [LAB-4] |
  14 Test Results Management [LAB-5] |
  15 Resource Access [IPA/QEDm] |
  16 Message Exchange [MQ] |
  17 Document Exchange [MHD] |
  18 Document Exchange [MHD] Elaboration |
  19 Patient Identity Matching (PDQm) |
  20 Overview |
  21 HL7 v2 Standards |
  22 Architecture |
  23 Testing |
  24 Support |
  25 API Security |
  26 Deployment |
  27 Delivery Overview |
  28 Authorisation [IUA] |
  29 Workflow/Interaction Options |
  30 Genomic Report Sharing Options |
  31 Identifiers and Codes |
  32 Overview - Data Contracts |
  33 Care Services Discovery |
  34 Specimen Event Tracking (SET) |
  35 Inter Laboratory Workflow (ILW) |
  36 Simple |
  37 Digital Consent (IHE BPPC and PCF) |
  38 Design |
  39 Exchange |
  40 Artifacts Summary |
   40.1 Automation Manager |
   40.2 Clinical Document |
   40.3 Intermediary |
   40.4 Order Filler |
   40.5 Order Placer |
   40.6 Order Result Tracker |
   40.7 Patient Identity Source |
   40.8 Provider Information Source |
   40.9 Requestor (ILW) |
   40.10 Subcontractor (ILW) |
   40.11 CapabilityStatement for NW Genomics Genomic Data Platform (EURIDICE Health Data API) |
   40.12 CapabilityStatement for NW GMSA Regional Orchestration Engine for Genomics |
   40.13 Process Message |
   40.14 Message Definition - Acknowledgement |
   40.15 Message Definition - Document and Document Notification |
   40.16 Message Definition - Laboratory Order |
   40.17 Message Definition - Unsolicited Observation |
   40.18 assigner |
   40.19 CBC panel - Blood by Automated count |
   40.20 Comprehensive metabolic 2000 panel - Serum or Plasma |
   40.21 Master HL7 genetic variant reporting panel |
   40.22 North West Genomics Test Order |
   40.23 North West Genomics Test Order Future |
   40.24 North West Genomics Test Report |
   40.25 Pedigree |
   40.26 AuditEvent |
   40.27 Binary |
   40.28 Composition Genomic Report |
   40.29 Condition |
   40.30 Diagnostic Implication (Observation) |
   40.31 Diagnostic Report |
   40.32 Document Message (MessageHeader) |
   40.33 DocumentReference |
   40.34 Encounter |
   40.35 Event Notification (MessageHeader) |
   40.36 FamilyMemberHistory |
   40.37 Genomic Observation |
   40.38 Genomic Study (Observation Panel) |
   40.39 Genomic Study (Procedure) |
   40.40 Genotype (Observation) |
   40.41 Hospital Spell |
   40.42 Laboratory Analyte Result (Observation) |
   40.43 Molecular Biomarker |
   40.44 Observation |
   40.45 Observation Panel |
   40.46 OperationOutcome |
   40.47 Organization |
   40.48 Patient |
   40.49 Practitioner |
   40.50 PractitionerRole |
   40.51 Procedure |
   40.52 Questionnaire |
   40.53 QuestionnaireResponse |
   40.54 RelatedPerson |
   40.55 ServiceRequest |
   40.56 Specimen |
   40.57 Task |
   40.58 Therapeutic Implication (Observation) |
   40.59 Variant (Observation) |
   40.60 Visit |
   40.61 WorkOrder |
   40.62 Attachment |
   40.63 CodeableReference |
   40.64 Correlation Identifier |
   40.65 Genomics Pedigree Number |
   40.66 GS1 Global Service Relation Number (GSRN) |
   40.67 GS1 Serial Shipping Container Code (SSCC) |
   40.68 GS1 Service Relation Instance Number (SRIN) |
   40.69 Hospital Provider Spell Identifier |
   40.70 Medical Record Number |
   40.71 NHS Identifier |
   40.72 Order Group Number |
   40.73 Order Identifier |
   40.74 Organisation Code |
   40.75 Organisation Site Identifier |
   40.76 Practitioner Identifier |
   40.77 Report Identifier |
   40.78 Shipment Tracking Number |
   40.79 Specimen Accession Number |
   40.80 Visit Number |
   40.81 ExtCodeableReference |
   40.82 Admission Method |
   40.83 Admission Source |
   40.84 Discharge Destination |
   40.85 Discharge Disposition |
   40.86 DocumentEntry Class |
   40.87 DocumentEntry mimeType |
   40.88 DocumentEntry Type |
   40.89 Ethnicity |
   40.90 Facility Type |
   40.91 Genomic Cancer Test Directory |
   40.92 Genomic Clinical Indication Codes |
   40.93 Genomic Disorder Carrier |
   40.94 Genomic Finding |
   40.95 Genomic Finding Detected |
   40.96 Genomic Rare and Inherited Disease Test Directory |
   40.97 Genomic Test Codes |
   40.98 Genomic Test Outcome Codes |
   40.99 NW IdentifierType |
   40.100 Order Category |
   40.101 Organisation Cheshire and Merseyside ICS (QYG) NHS Trusts |
   40.102 Organisation Greater Manchester ICS (QOP) NHS Trusts |
   40.103 Organisation Lancashire and South Cumbria ICS (QE1) NHS Trusts |
   40.104 Organisation North West Region NHS Trusts |
   40.105 Patient Encounter Trigger |
   40.106 Patient Identity Trigger |
   40.107 Practitioner Identifiers |
   40.108 Pregnancy |
   40.109 Request Priority |
   40.110 Service |
   40.111 Specialty |
   40.112 Specimen Body Site |
   40.113 Specimen Tracking Events |
   40.114 Specimen Type |
   40.115 UK National Health Identifiers |
   40.116 Yes/No |
   40.117 Yes/No/Unknown |
   40.118 iGene Codes |
   40.119 iGene Sample Sub Type |
   40.120 iGene Test Codes |
   40.121 MFT EPIC Question Ids |
   40.122 NHS England Genomic Clinical Indication Code |
   40.123 NHS England Genomic Test Code |
   40.124 NHS England Genomic Test Outcome Code |
   40.125 NW GMSA Codes |
   40.126 UK National Health Identifiers |
   40.127 UK Professional License |
   40.128 GMC Number |
   40.129 GMP Number |
   40.130 NHS Number |
   40.131 ODS Code |
   40.132 ODS Site Code |
   40.133 LOINC to SNOMED UK edition |
   40.134 Sample Body Site (SNOMED) to iGene Specimen Sub Type |
   40.135 Sample Type (SNOMED) to iGene Specimen Type |
   40.136 SNOMED LOINC edition to SNOMED UK edition |
   40.137 Clinical and Genomic Workflow |
   40.138 Collect Specimen - Biopsy Procedure for obtaining a specimen, part of a diagnostic pathway. Day case admission. |
   40.139 Genomic Test Order Process including order entry and transmission of the order |
   40.140 Genomic Test Report Process |
   40.141 AuditEvent Mobile Query Existing Data [PCC-44] |
   40.142 AuditEvent Placer Order Management [LAB-1] V2/FHIR/V2 Order |
   40.143 Bundle 'Event Message' - Patient Update |
   40.144 Bundle 'Message' - Genomics Order Reply |
   40.145 Bundle 'Message' - Genomics Order Reply Acknowledgement |
   40.146 Bundle 'Transaction' - Genomics Order Asynchronous Message Reply Acknowledgement |
   40.147 Bundle - Conditions for a Patient QEDm |
   40.148 Bundle - Form Search Results SDC |
   40.149 Bundle - Genomic Diagnostic Implication for a Patient QEDm |
   40.150 Bundle - Genomic Variant for a Patient QEDm |
   40.151 Bundle - Genomic Variant Gene = NTHL1 QEDm |
   40.152 Bundle - Patient Search Results by Medical Record Number PDQ |
   40.153 Bundle - Patient Search Results by NHS Number PDQ |
   40.154 Condition - Carcinoma |
   40.155 Condition - Lynch Syndrome |
   40.156 Consanguinity (type=CE) |
   40.157 Example Document and Document Notification Message |
   40.158 Example of a Message Acknowledgement |
   40.159 Example of a Message Search |
   40.160 FamilyMemberHistory - Ricky LEEDS |
   40.161 FamilyMemberHistory - Sarah-Jane Nottingham |
   40.162 FHIR RESTful POST ServiceRequest |
   40.163 Genomic Order Entry Optional Questions |
   40.164 Genomic Report BRCA1 Variant Example |
   40.165 Genomic Report Ovarian Carcinoma Diagnostic Implication Example |
   40.166 Genomic Study (Panel) - Cystic Fibrosis |
   40.167 Genomic Study (Panel) - Lynch Syndrome |
   40.168 Laboratory Analyte Result BCRABL Invalid Example |
   40.169 Laboratory Analyte Result BCRABL Valid Example |
   40.170 MCV - Mean corpuscular volume |
   40.171 Message Header - Genomic Order Reply fatal |
   40.172 Message Header - Genomic Order Reply fatal Acknowledgement |
   40.173 Message Header - Genomic Order Reply Transient |
   40.174 Message Header - Genomic Report |
   40.175 Message Header - Patient |
   40.176 Observation - Lynch Syndrome Mutation Finding |
   40.177 Order Tracking Number (type=ST) |
   40.178 Organization MANCHESTER UNIVERSITY NHS FOUNDATION TRUST |
   40.179 Organization North West GMSA |
   40.180 Output from a FHIR Validation |
   40.181 Parameters Expansion Profile |
   40.182 Patient - Birmingham |
   40.183 Patient - Bolton |
   40.184 Patient - Congleton |
   40.185 Patient - Fetus London |
   40.186 Patient - Lancaster |
   40.187 Patient - London |
   40.188 Patient - Ned Liverpool NHS Number: 9737383206 |
   40.189 Patient - Northwich |
   40.190 Patient - Nottingham |
   40.191 Patient - Rob Leeds NHS Number: 9737383222 |
   40.192 Patient - Sansa Manchester NHS Number: 9737383192 |
   40.193 Patient - Warrington |
   40.194 Patient - Wrexham |
   40.195 PractitionerRole Result INTERPRETER |
   40.196 Pregnancy Expected Delivery Date (type=DT) |
   40.197 Procedure - Liver Biopsy |
   40.198 RelatedPerson Birmingham-Lancaster |
   40.199 RelatedPerson Birmingham-London |
   40.200 RelatedPerson Lancaster-London |
   40.201 RelatedPerson London-Lancaster |
   40.202 RelatedPerson Mother Cersei London |
   40.203 RelatedPerson Wrexham-Lancaster |
   40.204 RelatedPerson Wrexham-London |
   40.205 Task Genomic Test Completed |
   40.206 Task Genomic Test Requested |
   40.207 Binary Genomic Record of Discussion Example |
   40.208 Bundle 'Message' - Genomics Order Reply |
   40.209 Bundle 'Message' - Genomics Order with Attachment |
   40.210 Bundle 'Message' - Genomics Order with Coded Entries |
   40.211 Bundle 'SearchSet' - Genomics Order |
   40.212 Document Reference Laboratory Order |
   40.213 Encounter 'episode/stay' Example |
   40.214 Message Header - Genomic Order |
   40.215 Message Header - Genomic Order Reply ok |
   40.216 Patient - OctaviaCHISLETT NHS Number: 9449305552 |
   40.217 PractitionerRole C3456789 Example |
   40.218 ServiceRequest Attachment Example |
   40.219 ServiceRequest Coded Entries Example |
   40.220 Specimen Example |
   40.221 Binary Genomic Report Example |
   40.222 Bundle 'Message' - Genomics Report |
   40.223 Diagnostic Report Example. |
   40.224 Document Reference Laboratory Report |
   40.225 Message Header - Genomic Report |
   40.226 DiagnosticImplication - Cystic Fibrosis Carrier |
   40.227 DiagnosticImplication - Lynch Syndrome |
   40.228 Genomic Study - Cystic Fibrosis |
   40.229 Genomic Study - Lynch Syndrome |
   40.230 Variant - CFTR |
   40.231 Variant - NTHL1 |
   40.232 748683741 |
   40.233 Bundle `Document` - Genetic Report |
   40.234 Composition - Genomics Report Octavia CHISLETT |
   40.235 EPIC-OBR-1 Example |
   40.236 EPIC-OBX-10 Example |
   40.237 EPIC-OBX-11 Example |
   40.238 EPIC-OBX-2 Example |
   40.239 EPIC-OBX-4 Example |
   40.240 EPIC-OBX-6 Example |
   40.241 EPIC-OBX-7 Example |
   40.242 EPIC-OBX-8 Example |
   40.243 Genomic Referral Category |
   40.244 High infection risk sample |
   40.245 Informed Consent |
   40.246 OBX Pregnancy |
   40.247 Supervising Clinician |
   40.248 Bundle-Bundle-NonWGSTestOrderForm-Reanalysis-Example |
   40.249 Bundle-NonWGSTestOrderForm-CancerSolidTumor-Example |
   40.250 Bundle-NonWGSTestOrderForm-FetalScenario-Example |
   40.251 NRL Genomic Report for Cersei LONDON (Test NHS Number 9737383230). Original order electronic from EPIC system |
   40.252 NRL Genomic Report for Tommen BIRMINGHAM (Test NHS Number 9737383249). Original order not electronic |
   40.253 837d78a0-30cd-478c-83a8-f83d16fc4443 |