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

When to collect blood specimens: midmorning vs fasting samples.

Author(s): Leppänen E, Dugué B

Publication: Clin Chem, 1998, Vol. 44, Page 2537-42

PubMed ID: 9836723 PubMed Review Paper? No

Purpose of Paper

The purpose of this paper was to determine the effects of collecting fasting blood specimens at 8:00 am versus collecting blood after breakfast at 9:30 am or 11:00 am on 32 common hematology and clinical chemistry analytes.

Conclusion of Paper

22 of the 32 analytes examined showed statistically significant differences between specimens obtained from fasting individuals and those obtained after the subjects had breakfast. Individual clinically significant differences were observed for more than half of the analytes. The direction or degree of changes observed for many analytes were different between inpatients and outpatients.

Studies

  1. Study Purpose

    The purpose of this study was to determine the effects of collecting fasting blood specimens at 8:00 am versus collecting blood after breakfast at 9:30 am or 11:00 am on 32 common hematology and clinical chemistry analytes. Three specimens (one at each time point) were collected from each patient. Complete blood counts, thromboplastin time, and erythrocyte sedimentation rates were analyzed in fresh specimens. Serum was separated and frozen at -20 degrees C for 2-5 days prior to analysis of clinical chemistry analytes.

    Summary of Findings:

    22 of the 32 analytes examined showed statistically significant differences between specimens obtained from fasting individuals and those obtained after the subjects had breakfast. Clinically significant changes were observed for 17 of the analytes in some individuals. The direction or degree of changes observed for many analytes were different between inpatients and outpatients. Analytes showing changes in the opposite direction between inpatients and outpatients included sodium, creatinine, aspartate aminotransferase, gamma-glutamyltransferase, alanine aminotransferase, cholesterol, and free thyroxine.

    Biospecimens
    Preservative Types
    • None (Fresh)
    • Frozen
    Diagnoses:
    • Not specified
    • Normal
    Platform:
    AnalyteTechnology Platform
    Morphology Hematology/ auto analyzer
    Cell count/volume Hematology/ auto analyzer
    Protein Hematology/ auto analyzer
    Steroid Clinical chemistry/auto analyzer
    Lipid Clinical chemistry/auto analyzer
    Electrolyte/Metal Clinical chemistry/auto analyzer
    Small molecule Clinical chemistry/auto analyzer
    Carbohydrate Clinical chemistry/auto analyzer
    Glycoprotein Clinical chemistry/auto analyzer
    Protein Clinical chemistry/auto analyzer
    Peptide Clinical chemistry/auto analyzer
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Biospecimen Preservation Type of fixation/preservation Frozen
    None (fresh)
    Biospecimen Aliquots and Components Blood and blood products Serum
    Whole blood
    Biospecimen Acquisition Time of biospecimen collection 8:00 am (fasting)
    9:30 am (after breakfast)
    11:00 am (after breakfast)
    Preaquisition Diagnosis/ patient condition Inpatient (unspecified)
    Outpatient (healthy)

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