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Optimizing centrifugation of coagulation samples in laboratory automation
Clinical Chemistry and Laboratory Medicine
|April 4, 2014
Summary
High acceleration centrifugation effectively reduces platelet counts in coagulation samples, enabling integration into laboratory automation workflows. A single spin suffices for prothrombin time (PT), activated partial thromboplastin time (APTT), and factor VIII, while protein S requires two spins.
Area of Science:
- Clinical Chemistry
- Hematology
- Laboratory Automation
Background:
- High acceleration centrifugation is used in lab automation to speed up clinical chemistry but not coagulation testing.
- Current guidelines recommend low platelet counts for coagulation assays, often necessitating separate sample handling.
- Integrating coagulation sample processing into automation workflows can improve efficiency.
Purpose of the Study:
- To evaluate high acceleration centrifugation for coagulation sample processing.
- To determine if a single or double centrifugation run is sufficient for various coagulation assays.
- To assess the impact on platelet counts and assay performance.
Main Methods:
- Coagulation samples were subjected to high acceleration centrifugation (3280×g for 5 min) in one or two runs.
- Platelet counts and results for PT, APTT, factor VIII, and protein S were analyzed after each centrifugation step.
- Passing-Bablok regression was used to compare assay performance.
Main Results:
- All samples achieved platelet counts below 200×10(9)/L after one centrifugation.
- Second centrifugation reduced platelet counts below 10×10(9)/L in 73% of samples.
- PT, APTT, and F. VIII showed consistent performance after one or two centrifugations, but protein S required two centrifugations.
Conclusions:
- High acceleration centrifugation can integrate coagulation samples into laboratory automation systems.
- A single centrifugation is adequate for PT, APTT, and F. VIII assays.
- Two successive centrifugations are necessary for reliable protein S activity measurement.
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