Related Experiment Videos
Effect of collection and preprocessing methods on neutrophil elastase plasma concentrations
J E Fischer1, M Janousek, M Fischer
1Department of Neonatal and Pediatric Intensive Care, University Children's Hospital, Zurich, Switzerland. jfischer@kispi.unizh.ch
Clinical Biochemistry
|June 18, 1998
Summary
Plasma elastase alpha 1-proteinase inhibitor complex (E-alpha 1 PI) levels vary based on collection tube type in critically ill neonates and children. Proper preanalytical methods are crucial for accurate E-alpha 1 PI measurements in this population.
Area of Science:
- Clinical Chemistry
- Pediatric Critical Care
- Laboratory Medicine
Background:
- Elevated elastase alpha 1-proteinase inhibitor complex (E-alpha 1 PI) is a proposed marker for bacterial infection and neutrophil activation.
- Potential preanalytical interference from elastase liberation post-blood collection necessitates validated methods, especially for neonates and children.
Purpose of the Study:
- To evaluate the impact of preanalytical methods, specifically different blood collection tubes, on E-alpha 1 PI measurements.
- To validate collection methods for critically ill neonates and children, focusing on EDTA tubes.
Main Methods:
- Compared varying acceleration speeds and centrifugation times, establishing 1550 g for 3 min for leukocyte-free plasma.
- Assessed E-alpha 1 PI absorption by different collection tubes.
- Analyzed samples from healthy adults and critically ill neonates/children using a turbidimetric assay.
Main Results:
- One plasma-separation gel tube absorbed 22.1% of E-alpha 1 PI.
- No significant differences in healthy adults across tubes without absorption.
- Critically ill neonates/children showed significantly higher E-alpha 1 PI in plain Li-heparin, EDTA, and citrate tubes compared to Li-hep with cell-plasma separation gel.
Conclusions:
- E-alpha 1 PI results in critically ill neonates and children are dependent on the blood collection tube type.
- Standard collection tube recommendations for adults may not apply to pediatric critical care patients.