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Primary prevention of pediatric lead exposure requires new approaches to transfusion screening
Eric Gehrie1, Amaris Keiser, Sheila Dawling
1Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.
Insights
Transfusion of packed red blood cells (pRBCs) can expose patients to lead. This study developed a method to measure lead in pRBCs, finding detectable levels in all units tested, highlighting a potential source of pediatric lead exposure.
Area of Science:
- Environmental Health
- Hematology
- Toxicology
Background:
- Transfusion-associated lead exposure is a concern.
- Assessing lead levels in transfused blood products is crucial for patient safety.
Purpose of the Study:
- To develop and validate a procedure for quantifying lead concentration in packed red blood cells (pRBCs).
- To investigate the relationship between whole blood lead and pRBC lead concentrations.
Main Methods:
- A modified clinical assay was used to analyze 27 blood samples.
- Lead concentrations were measured in 100 pRBC units.
Main Results:
- A strong correlation (R² = 0.82) was found between whole blood and pRBC lead levels.
- All 100 tested pRBC units contained detectable lead, with a median concentration of 0.8 μg/dL.
- Significant lead was found in supernatant plasma after short storage periods.
Conclusions:
- Packed red blood cell transfusions represent a significant source of lead exposure.
- The developed method allows for the quantification of lead in pRBCs.
- Pretransfusion testing or donor screening could mitigate pediatric lead exposure from transfusions.
Objective:
To facilitate further assessment of transfusion-associated lead exposure by designing a procedure to test packed red blood cells (pRBCs) prepared for transfusion.
Study Design:
The relationship between pRBCs and whole blood lead concentration was investigated in 27 samples using a modified clinical assay. Lead concentrations were measured in 100 pRBC units.
Results:
Our sample preparation method demonstrated a correlation between whole blood lead and pRBC lead concentrations (R(2) = 0.82). In addition, all 100 pRBC units tested had detectable lead levels. The median pRBC lead concentration was 0.8 μg/dL, with an SD of 0.8 μg/dL and a range of 0.2-4.1 μg/dL. In addition, after only a few days of storage, approximately 25% of whole blood lead was found in the supernatant plasma.
Conclusion:
Transfusion of pRBCs is a source of lead exposure. Here we report the quantification of lead concentration in pRBCs. We found a >20-fold range of lead concentrations in the samples tested. Pretransfusion testing of pRBC units according to our proposed approach or donor screening of whole blood lead and selection of below-average units for transfusion to children would diminish an easily overlooked source of pediatric lead exposure.
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