NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

The preanalytical influence of two different mechanical transport systems on laboratory analysis.

Author(s): Koessler J, Kobsar AL, Brunner K, Stolz H, Dossler B, Walter U, Steigerwald U

Publication: Clin Chem Lab Med, 2011, Vol. 49, Page 1379-82

PubMed ID: 21574889 PubMed Review Paper? No

Purpose of Paper

The purpose of this paper was to determine the effects of transporting blood specimens via two mechanical transport systems, including a slow moving track vehicle system (TVS) and a rapid pneumatic tube system (PTS) rather than by courier transport (CT) on blood cell counts, coagulation parameters, platelet function tests, and clinical chemistry analytes.

Conclusion of Paper

The only significant difference observed between PTS and TVS transport was slightly elevated basal glycoprotein IIb/IIIa activation on platelet surface (PAC-1) activation in the PTS transported specimens. Similar basal PAC-1 activation levels were observed after TVS and CT transport. Activation of PAC-1 by adenosine diphosphate (ADP) was reduced after 2 and 5 min in PTS and TVS transported specimens compared to those transported by CT. In addition, the number of leukocytes and lymphocytes were reduced, and lactate dehydrogenase (LD), aspartate transamine (AST) (TVS only), prothrombin time (PT), and d-dimer concentration were each significantly increased in specimens transported by PTS and TVS compared to those transported by CT. 21 other analytes were unaffected by specimen transportation method.

Studies

  1. Study Purpose

    The purpose of this study was to determine the effects of TVS and PTS as methods for transport of blood specimens compared to courier transport (CT) on blood cell counts, coagulation parameters, platelet function tests, and clinical chemistry analytes. Specimens were collected from 33 volunteers including healthy individuals, and those on oral anticoagulants or other medications. Specimens were collected into different tube types but no comparison is made.

    Summary of Findings:

    The only significant difference observed between PTS and TVS transport was slightly elevated basal PAC-1 activation in the PTS transported specimens. Similar basal PAC-1 activation levels were observed after TVS and CT transport. Activation of PAC-1 by ADP was reduced after 2 and 5 min in PTS and TVS transported specimens compared to those transported by CT. The number of leukocytes and lymphocytes were reduced after PTS or TVS transport compared to CT, but the reduction was only significant for leukocytes when blood was transported by PTS. LD was significantly increased after transport of blood specimens by PTS or TVS compared to CT. AST was significantly increased in the TVS transported specimens compared to those transported by CT, but not in the PTS transported specimens. PT and d-dimer concentration were each significantly increased in specimens transported by PTS and TVS compared to those transported by CT. 21 other analytes were unaffected by specimen transportation method.

    Biospecimens
    Preservative Types
    • None (Fresh)
    Diagnoses:
    • Normal
    • Not specified
    Platform:
    AnalyteTechnology Platform
    Cell count/volume Hematology/ auto analyzer
    Protein Hematology/ auto analyzer
    Morphology Hematology/ auto analyzer
    Peptide Hematology/ auto analyzer
    Protein Clinical chemistry/auto analyzer
    Electrolyte/Metal Clinical chemistry/auto analyzer
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Biospecimen Acquisition Anticoagulant Citrate
    EDTA
    Gel-barrier
    Storage Within hospital transportation method Hand-delivered
    Pneumatic tube system
    Track vehicle system
    Storage Specimen transport duration/condition 1 min 45 sec (PTS)
    4 min (hand-delivered)
    11 min (TVS)

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