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

Does laboratory automation for the preanalytical phase improve data quality?

Author(s): Lima-Oliveira G, Lippi G, Salvagno GL, Danese E, Montagnana M, Brocco G, Voi M, Picheth G, Guidi GC

Publication: J Lab Autom, 2013, Vol. 18, Page 375-81

PubMed ID: 23686657 PubMed Review Paper? No

Purpose of Paper

The purpose of this paper was to determine the effects of manual versus automated preanalytical processing by the MODULAR PRE-ANALYTICALS EVO-MPA system as well as subsequent storage on routine clinical chemistry analytes in plasma.

Conclusion of Paper

Significant differences were noted for several clinical chemistry analytes between manual and automated processing regimes both immediately after processing and even more significant differences were noted between the two processing regimes when specimens were stored for 6 h after processing. Further, significant differences were observed in many clinical chemistry analytes when specimens that were manually processed were compared before and after 6 hours of storage at 4 degrees C. Storage of specimens processed in the MPA system in the MPA output buffer for 6 hours led to fewer significant changes in clinical chemistry analytes as compared to measurements before the additional storage.

Studies

  1. Study Purpose

    The purpose of this study was to determine the effects of manual versus automated preanalytical processing by the MODULAR PRE-ANALYTICALS EVO-MPA system as well as subsequent storage on routine clinical chemistry analytes in plasma. After collection, all specimens were left at room temperature for 10 min. Paired specimens were then either centrifuged manually, uncapped manually, and loaded onto the analyzer, or they were loaded directly into the MODUALR PRE-ANALYTICALS EVO-MPA system where they were centrifuged and fed directly into the same analyzer as the manually processed specimens were analyzed with. After analysis, manually processed specimens were stored at 4 degrees C while those subjected to automated processing were stored in output buffer at room temperature in the MPA system. All specimens were reanalyzed after 6 h of storage.

    Summary of Findings:

    Significant differences were noted for several clinical chemistry analytes between manual and automated processing regimes both immediately after processing and even more significant differences were noted between the two processing regimes when specimens were stored for 6 h after processing. Further, significant differences were observed in many clinical chemistry analytes when specimens that were manually processed were compared before and after 6 hours of storage at 4 degrees C. Storage of specimens processed in the MPA system in the MPA output buffer for 6 hours led to fewer significant changes in clinical chemistry analytes as compared to measurements before the additional storage.

    Biospecimens
    Preservative Types
    • None (Fresh)
    Diagnoses:
    • Not specified
    Platform:
    AnalyteTechnology Platform
    Protein Clinical chemistry/auto analyzer
    Small molecule Clinical chemistry/auto analyzer
    Electrolyte/Metal Clinical chemistry/auto analyzer
    Cell count/volume Clinical chemistry/auto analyzer
    Steroid Clinical chemistry/auto analyzer
    Lipid Clinical chemistry/auto analyzer
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Biospecimen Aliquots and Components Centrifugation Automated
    Manual
    Storage Storage duration 0 h
    6 h
    Storage Short-term storage solution None
    MPA output buffer
    Storage Storage temperature 4 degrees C
    Room temperature
    Biospecimen Aliquots and Components Blood processing method MODULAR PRE-ANALYTICALS EVO-MPA
    Manual

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