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Includes testing and service provision guidance such as patient identification, consent requirements, specimen and sampling policies, turnaround times, electronic results access, crossmatch procedures, and traceability and transfusion reaction management. 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Thornton, Clinical Director of Laboratory Medicine  \nDEPARTMENTAL INFORMATION  \nDEPARTMENT  INFORMATION  \nBlood Transfusion Clinical Guidelines   \n Laboratory Information   \nHaematology & Clinical Guidelines   \nCoagulation & Flow Cytometry  \nLaboratory Information  \nChemical Pathology Clinical Guidelines   \n Laboratory Information   \nImmunology Clinical Guidelines   \n Laboratory Information   \nMicrobiology Clinical Guidelines   \n Laboratory Information   \nHistopathology, Cytology, Clinical Guidelines   \nNeuropathology Laboratory Information   \nMolecular Pathology Clinical Guidelines 66  \n Laboratory Information   \nNHISSOT Clinical Guidelines   \n Laboratory Information   \nSee next page for detailed table of contents.  \n1 INTRODUCTION.............................................................................................. 7  \n1.1 UPDATES OF USER’S HANDBOOK ................................................................. 7  \n2 TESTING GUIDELINES.................................................................................. 8  \n2.1 BLOOD TRANSFUSION & HAEMOVIGILANCE ................................................ 8  \n2.2 SERVICE PROVISION HOURS AND CONTACT DETAILS: ................................... 9  \n2.3 BLOOD PRODUCTS/ COMPONENTS AVAILABLE ............................................ 9  \n2.4 TURNAROUND TIMES ................................................................................... 9  \n2.5 PATIENT IDENTIFICATION ........................................................................... 10  \n2.5.1 Positive Patient Identification (PPID) ..................................................... 10  \n2.5.2 Unidentified Patient .................................................................................. 11  \n2.6 BEAUMONT HOSPITAL MAJOR EMERGENCY PLAN..................................... 11  \n2.7 PATIENT INFORMATION / CONSENT:........................................................... 11  \n2.8 GROUP AND SCREEN SAMPLE: ................................................................... 11  \n2.8.1 Extending a GS ......................................................................................... 12  \n2.8.2 Pre-Transfusion Type and Screen Sampling ............................................ 12  \n2.9 ELECTRONIC RESULTS: .............................................................................. 12  \n2.9.1 Blood Transfusion Widget on PowerChart .............................................. 12  \n2.9.2 Blood Transfusion Test Requests Reports on Powerchart ....................... 14  \n2.9.3 Group & Screen Results (Including Antibody ID) ................................... 14  \n2.9.4 Direct Antiglobulin Test (DAT) ................................................................ 15  \n2.9.5 ABO Titrations .......................................................................................... 15  \n2.9.6 Cold Agglutinins ....................................................................................... 16  \n2.9.7 Unsuitable specimen reports for Rejected Specimens .............................. 16  \n2.10 SECOND SAMPLE POLICY ........................................................................... 16  \n2.11 CROSSMATCH............................................................................................. 16  \n2.12 ORDERING AND PRESCRIBING BLOOD COMPONENTS AND PRODUCTS........ 17  \n2.13 REQUESTING OF BLOOD PRODUCTS WITH SPECIAL REQUIREMENTS .......... 18  \n2.14 MAXIMUM SURGICAL BLOOD ORDERING SCHEDULE................................. 18  \n2.15 BLOODTRACK ............................................................................................ 18  \n2.16 EMERGENCY ISSUE OF BLOOD COMPONENTS AND PRODUCTS .................... 18  \n2.17 MASSIVE TRANSFUSION PROTOCOL ...................","cbCaiof9ygA8gzM8","https://ap.wps.com/l/cbCaiof9ygA8gzM8","pdf",3090946,196,"English","# Introduction\n## Updates of User’s Handbook\n# Testing Guidelines\n## Blood Transfusion & Haemovigilance\n## Service Provision Hours and Contact Details\n## Blood Products/Components Available\n## Turnaround Times\n## Patient Identification\n## Positive Patient Identification (PPID)\n## Unidentified Patient\n## Beaumont Hospital Major Emergency Plan\n## Patient Information / Consent\n## Group and Screen Sample\n## Electronic Results","[{\"question\":\"What does this user guide cover for GP and nursing home users?\",\"answer\":\"It provides guidance on using clinical laboratory services, with detailed instructions for blood transfusion processes and testing pathways, including ordering, specimen handling, and access to results.\"},{\"question\":\"How does the guide address patient identification for testing and transfusion?\",\"answer\":\"It sets out requirements for positive patient identification (PPID) and procedures related to unidentified patients, supporting safe testing and transfusion activities.\"},{\"question\":\"How are blood transfusion results accessed and managed electronically?\",\"answer\":\"The guide describes electronic results processes, including specific PowerChart-related items such as transfusion widgets and blood transfusion test request reports.\"}]","Laboratory User Guide for GPs and Nursing Homes - Clinical Laboratory Services | PDF",1791840356,69]