Sample transportation – an overview

Author:

Nybo Mads1,Cadamuro Janne2,Cornes Michael P.3,Gómez Rioja Rubén4ORCID,Grankvist Kjell5

Affiliation:

1. Department of Clinical Biochemistry and Pharmacology , Odense University Hospital , Sdr. Boulevard 29 , Odense 5000 , Denmark

2. Department of Laboratory Medicine , Paracelsus Medical University , Salzburg , Austria

3. Department of Clinical Chemistry , Worcestershire Acute Hospitals NHS Trust , Worcester , UK

4. Laboratorio Clínico Hospital La Paz , Madrid , Spain

5. Department of Medical Biosciences, Clinical Chemistry, Umeå University , Umeå , Sweden

Abstract

Abstract Transportation of blood samples is a major part of the preanalytical pathway and can be crucial in delaying laboratory results to the clinicians. A variety of aspects however makes sample transportation a complex, challenging and often overlooked task that needs thorough planning and dedicated resources. The purpose of this review is to outline the options available for this task and to emphasize the preanalytical aspects that need consideration in this process, e.g. performance specifications for sample transportation as stated in ISO standards 15189 and 20658, quality control of automated transportation systems, monitoring of sample integrity parameters and temperature surveillance in general and for external samplers in particular. All these are tasks that the laboratory must assure on a daily basis in terms of continuous quality control, and simultaneously the laboratory must remain alert to alterations in clinical demands (sample frequency, turn-around-times) and new regulations within this area (e.g. the recent General Data Protection Regulation from the EU).

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,Public Health, Environmental and Occupational Health,Health Policy,Medicine (miscellaneous)

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