Volume 9, Issue 2

 

 

 

 

 

 

 

 

ISLH Recommended Reference Procedure for the Enumeration of Particles in Urine

T. KOURI1, A. GYORY2, R. M. ROWAN3

1Oulu University Hospital, Oulu, Finland; 2Royal North Shore Hospital, St. Leonard?s, Australia; 3Glasgow, Scotland

Members of ISLH Urinalysis Task Force:

T. DEMATTEO, USA; M. DOTSON, USA; B. FERNANDES, CANADA; A. GYORY, AUSTRALIA; A. KOONTZ, USA; T. KOURI, FINLAND; A. MICHAELS, USA; M. ROWAN, SCOTLAND

Adviser to the Task Force:

PROFESSOR P. LAIPPALA, PHD, TAMPERE SCHOOL OF PUBLIC HEALTH, TAMPERE UNIVERSITY; RESEARCH UNIT OF TAMPERE UNIVERSITY HOSPITAL, TAMPERE, FINLAND

FOREWORD

Automated systems for counting urine particles are now being developed and marketed. A reference measurement procedure must be developed to determine the accuracy and validity of these systems and to provide means for instrument calibration.

A task force of the International Society of Laboratory Hematology (ISLH) has proposed such a procedure for the enumeration of erythrocytes, leukocytes, hyaline casts, and squamous epithelial cells in urine. The proposed standard can be extended to include other urine particles such as the smaller epithelial cells and granular or cellular casts when there is consensus on the morphological description of these entities.

The ISLH Task Force standard is based on ISO/DIS (International Organization for Standardization) draft international standard 78-2, with special consideration given to the requirements for biological materials and for reference measurement procedures, the current model being based on the structures being developed by CEN/TC (European Standardisation Committee, Technical Committee on Health Care Informatics) 140 prEN 12286 and ISO/CD (ISO committee draft) 15193, with reference to ISO/CD 15195. Where relevant the terms and definitions are those provided in the International Vocabulary of Basic and General Terms in Metrology (VIM) [1].

The proposed standard draws heavily on previously published guidelines such as the Finnish Recommendations from the Working Group on Clean Midstream Specimens [2], the NCCLS Urinalysis and Collection, Transportation and Preservation of Urine Specimens (NCCLS Document GP16-A) [3], JCCLS (Japanese Committee for Clinical Laboratory Standards Guideline) GP1-P2 [4], and the ECLM (European Confederation of Laboratory Medicine) European Urinalysis Guidelines [5].

The importance of preanalytical specimen information is usually underestimated, and this information is generally not documented. This information is relevant and must be included in the procedure.


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