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CLSI GP33 A : 1ED 2010

Withdrawn

Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

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withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

ACCURACY IN PATIENT AND SAMPLE IDENTIFICATION

Withdrawn date

07-23-2013

Published date

08-25-2018

Abstract
Committee Membership
Foreword
1 Scope
2 Introduction
3 Terminology
4 Designing a Patient and Sample Identification System
5 Preexamination Phase
6 Examination Phase
7 Postexamination Phase
8 Training
9 Validation a New System for Patient Identification
10 Reports of Incorrect Identification Incidents
11 Audit Systems
12 Technology Tools
13 Point-of-Care Testing
14 Conclusion
References
Appendix A - Preexamination Phase Process for Hospital
             Patients
Appendix B - Sample Hospital Identification Band Policy
Appendix C - Sample Inpatient Identification Procedure
Appendix D - Sample Procedure for Patients Identification
             in a Physician Office Laboratory
Appendix E - Sample Procedure for Identifying Neonates
Appendix F - Sample Labeling Policy and Procedures
Appendix G - Examples of Examination Phase Process
Appendix H - Postexamination Phase Process
Appendix I - Sample Training Checklist Form
Appendix J - Sample Policy for the Misidentified or
             Unidentified Patient
Summary of Delegate Comments and Subcommittee Responses
The Quality Management System Approach
Related CLSI Reference Materials

Specifies the essential elements of systems and processes required to ensure accurate patient identification.

The identification (ID) process begins with the patient, either at the time of registration for admission to a health care facility, or on presentation for sample collection, and ends with reporting the results of the examination. This document outlines all points in the path of workflow related to patient and sample ID. The essential elements of systems and processes required to ensure accurate patient ID are described. The principles in this document are applicable to manual or electronic systems. Considerations covered include criteria for accuracy, differences in inpatient vs outpatient settings that impact patient ID, language and cultural considerations, and standardization of processes across the health care enterprise. Guidance on system implementation and user training is included. Validation of patient ID systems/programs and ongoing monitoring as a quality measure are also covered. This document is intended for health care providers (HCPs) who design, select, implement, monitor, and evaluate patient ID systems or any individual responsible for specimen collection.

DevelopmentNote
Supersedes NCCLS GP33 P. (06/2010)
DocumentType
Miscellaneous Product
PublisherName
Clinical Laboratory Standards Institute
Status
Withdrawn
SupersededBy
Supersedes

PD ISO/TS 20658:2017 Medical laboratories. Requirements for collection, transport, receipt, and handling of samples
BIS IS/ISO 15189 : 2012 MEDICAL LABORATORIES - REQUIREMENTS FOR QUALITY AND COMPETENCE
I.S. EN ISO 15189:2012 MEDICAL LABORATORIES - REQUIREMENTS FOR QUALITY AND COMPETENCE (ISO 15189:2012, CORRECTED VERSION 2014-08-15)
CLSI AUTO12 A : 1ED 2011 SPECIMEN LABELS: CONTENT AND LOCATION, FONTS, AND LABEL ORIENTATION
PREN ISO 15189 : DRAFT 2011 MEDICAL LABORATORIES - PARTICULAR REQUIREMENTS FOR QUALITY AND COMPETENCE
UNE-EN ISO 15189:2013 Medical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15)
CLSI GP44 A4 : 4ED 2010 PROCEDURES FOR THE HANDLING AND PROCESSING OF BLOOD SPECIMENS FOR COMMON LABORATORY TESTS
11/30173018 DC : 0 BS EN ISO 15189 - MEDICAL LABORATORIES - PARTICULAR REQUIREMENTS FOR QUALITY AND COMPETENCE
ISO/TS 20658:2017 Medical laboratories — Requirements for collection, transport, receipt, and handling of samples
DIN EN ISO 15189:2014-11 Medical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15)
UNI EN ISO 15189 : 2013 MEDICAL LABORATORIES - REQUIREMENTS FOR QUALITY AND COMPETENCE
CLSI QMS01 A4 : 4ED 2011 QUALITY MANAGEMENT SYSTEM: A MODEL FOR LABORATORY SERVICES
CLSI EP33 : 2016 USE OF DELTA CHECKS IN THE MEDICAL LABORATORY
CLSI GP23 A2 : 2ED 2014 NONGYNECOLOGICAL CYTOLOGY SPECIMENS: PREEXAMINATION, EXAMINATION, AND POSTEXAMINATION PROCESSES
ISO 15189:2012 Medical laboratories — Requirements for quality and competence
BS EN ISO 15189:2012 Medical laboratories. Requirements for quality and competence

CLSI HS1 A2 : 2ED 2004 A QUALITY MANAGEMENT SYSTEM MODEL FOR HEALTH CARE
CLSI GP41 A6 : 6ED 2007 PROCEDURES FOR THE COLLECTION OF DIAGNOSTIC BLOOD SPECIMENS BY VENIPUNCTURE
CLSI QMS11 A : 1ED 2007 MANAGEMENT OF NONCONFORMING LABORATORY EVENTS
CLSI GP43 A4 : 4ED 2004 PROCEDURES FOR THE COLLECTION OF ARTERIAL BLOOD SPECIMENS
CLSI MM13 A : 1ED 2006 COLLECTION, TRANSPORT, PREPARATION, AND STORAGE OF SPECIMENS FOR MOLECULAR METHODS
CLSI GP42 A6 : 6ED 2008 PROCEDURES AND DEVICES FOR THE COLLECTION OF DIAGNOSTIC CAPILLARY BLOOD SPECIMENS
CLSI QMS03 A3 : 3ED 2009 TRAINING AND COMPETENCE ASSESSMENT
CLSI EP18 A2 : 2ED 2009 RISK MANAGEMENT TECHNIQUES TO IDENTIFY AND CONTROL LABORATORY ERROR SOURCES

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