Evidence map›Paper›PMID 41221466›Full record

ArticleMedicine and pharmacy reports2025

Impact of pre-analytical variables - temperature, agitation, storage duration, and blood-to-anticoagulant ratio - on complete blood count test reliability.

Malek A Al-Najdawi, Abdulfattah Salah Fararjeh, Moayad Khataibeh

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Article in Medicine and pharmacy reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Malek A Al-NajdawiDepartment of Medical Laboratory Sciences, Faculty of Allied Health Sciences, Al-Balqa Applied University, Jordan.
Abdulfattah Salah FararjehDepartment of Medical Laboratory Sciences, Faculty of Allied Health Sciences, Al-Balqa Applied University, Jordan.
Moayad KhataibehDepartment of Medical Laboratory Sciences, Faculty of Allied Health Sciences, Al-Balqa Applied University, Jordan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The complete blood count is a widely used medical laboratory test that is essential for both diagnosis and treatment decisions. While pre-analytic factors, such as storage temperature, transport conditions, blood volume anticoagulant ratio, and testing delay, might impact the accuracy of the results, the degree of this influence requires further quantification. In the present study, we aim to look more closely at these factors and how they affect complete blood count test readings. Methods: This study evaluates the effects of temperature, agitation, storage duration, and blood volume anticoagulant ratio on complete blood count reliability using a repeated-measures factorial design. A total of 224 CBC runs were performed on the samples of eight participants. Samples were tested at baseline T0 and again at 4, 12, and 24 hours after storage at either room temperature (22°C) or refrigeration (4°C), with and without agitation, and at both optimal (2 mL) and suboptimal (1 mL) blood volumes. Results: The duration of storage was the main factor determining CBC accuracy. After 12 h, WBC counts decreased significantly (p < 0.001, η Conclusion: Specimens should ideally be tested within 12 hours or stored at 4°C to prevent degradation of the test variables, particularly white blood cell counts and platelet counts. The findings suggest that routine handling and transport conditions are appropriate, as agitation during transport and a decreased blood volume-to-anticoagulant ratio appear to have negligible effects. Incorporating measurement uncertainty benchmarks improves the distinction between genuine sample deterioration and assay variability, thereby enhancing diagnostic accuracy.

Indexed as

complete blood countlaboratory best practicesspecimen handlingspecimen stabilitystorage time

Identifiers

PMID41221466
PMCPMC12600060

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