CLSI H56 A : 1ED 2006
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
BODY FLUID ANALYSIS FOR CELLULAR COMPOSITION
23-07-2013
25-08-2018
Abstract
Committee Membership
Foreword
1 Scope
2 Standard Precautions
3 Definitions
4 Preanalytical Variables
5 Specimen Collection
5.1 Cerebrospinal Fluid
5.2 Serous Fluid
5.3 Synovial Fluid
5.4 Bronchoalveolar Lavage (BAL)
6 Specimen Handling and Transport
6.1 CSF
6.2 Serous Fluids
6.3 Synovial Fluids
6.4 BAL
7 Quantitative Assessment
7.1 Manual Counting
7.2 Automated Methods
8 Morphology Assessment
8.1 Slide Preparation
8.2 Identification of Morphologic Constituents
8.3 Evaluation of Nucleated Cell Subtypes
8.4 Physician Review
8.5 Result Reporting
9 Fluid Types
9.1 Cerebrospinal Fluid and Ventricular Shunt Fluids
9.2 Serous (Pleural, Peritoneal, Pericardial,
Peritoneal Lavage and Dialysate Fluids)
9.3 Synovial Fluid
9.4 Bronchoalveolar Lavage Fluid
10 Additional Studies
10.1 Immunocytologic Studies
10.2 Flow Cytometric Studies
10.3 Cytogenetic Analysis
11 Sample Storage After Completion of Testing
12 Quality Control and Quality Assurance
12.1 Quality Control
12.2 Quality Assurance
12.3 Proficiency Testing (External Quality Assessment)
12.4 Continuous Education and Training
References
Additional References
Appendix A - Reagent Formulations
Appendix B - Interpretation of Cell Types
Appendix C - Reference Intervals
Summary of Comments and Subcommittee Responses
The Quality System Approach
Related CLSI/NCCLS Publications
Provides users with recommendations for collection and transport of body fluids, numeration and identification of cellular components, and guidance for qualitative and quantitative assessment of body fluid.
DevelopmentNote |
Supersedes NCCLS H56 P (07/2006)
|
DocumentType |
Miscellaneous Product
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PublisherName |
Clinical Laboratory Standards Institute
|
Status |
Withdrawn
|
Supersedes |
CLSI M29 A4 : 4ED 2014 | Protection of Laboratory Workers From Occupationally Acquired Infections<br> |
CLSI C50 P : 1ED 2007 | MASS SPECTROMETRY IN THE CLINICAL LABORATORY: GENERAL PRINCIPLES AND GUIDANCE |
CLSI GP48 : 1ED 2017 | ESSENTIAL ELEMENTS OF A PHLEBOTOMY TRAINING PROGRAM |
CLSI C50 A : 1ED 2007 | MASS SPECTROMETRY IN THE CLINICAL LABORATORY: GENERAL PRINCIPLES AND GUIDANCE |
CLSI GP29 A : 1ED 2002 | VALIDATION OF LABORATORY TESTS WHEN PROFICIENCY TESTING IS NOT AVAILABLE |
CLSI EP5 A2 : 2ED 2004 | EVALUATION OF PRECISION PERFORMANCE OF QUANTITATIVE MEASUREMENT METHODS |
CLSI GP16 A2 : 2ED 2001 | ROUTINE URINALYSIS AND COLLECTION, TRANSPORTATION, AND PRESERVATION OF URINE SPECIMENS |
CLSI EP6 A : 1ED 2003 | EVALUATION OF THE LINEARITY OF QUANTITATIVE MEASUREMENT PROCEDURES - A STATISTICAL APPROACH |
CLSI GP21 A2 : 2ED 2004 | TRAINING AND COMPETENCE ASSESSMENT |
CLSI C49 P : 1ED 2006 | ANALYSIS OF BODY FLUIDS IN CLINICAL CHEMISTRY |
CLSI GP27 A : 1ED 99 | USING PROFICIENCY TESTING (PT) TO IMPROVE THE CLINICAL LABORATORY |
CLSI EP9 A2 : 2ED 2002 | METHOD COMPARISON AND BIAS ESTIMATION USING PATIENT SAMPLES |
CLSI GP2 A5 : 5ED 2006 | LABORATORY DOCUMENTS - DEVELOPMENT AND CONTROL |
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