Required section · Section 4 of 6
Guided case: confirm the lead screen
A 3-year-old child in housing built before 1978 has a capillary blood lead screen collected in a lead-free capillary device at 14.0 µg/dL. A capillary result at or above 3.5 µg/dL needs venous confirmation, and the 10 to 19 µg/dL band has a recommended confirmation window within 1 month. Delayed confirmation can delay exposure investigation and follow-up while exposure continues; the one-month window is a recommendation, not a hard universal deadline.
The laboratory requests whole blood in its specified trace-element-free EDTA tube, not a routine lavender-top tube assumed acceptable by color. ICP-MS reports the venous specimen at 12.8 µg/dL. Using 1 µg/dL approximately equal to 0.04826 µmol/L, the converted value is 0.62 µmol/L after rounding.
The confirmed venous result is above the CDC blood lead reference value of 3.5 µg/dL. That population-based reference value is not a toxicity threshold, safety limit, or diagnostic cutoff. The result supports exposure-source investigation and follow-up under applicable guidance, not a laboratory diagnosis of lead toxicity.
Local laboratory policy places 12.8 µg/dL below its own panic list and releases it through the routine workflow while state reporting proceeds under applicable law. A laboratory-defined alert value requires immediate notification under CLIA, but CLIA does not set a universal lead value or minute-based deadline. Confirm an elevated capillary screen with correctly collected venous whole blood before releasing the interpretation.
| Stage | Specimen and method | Result | Disposition |
|---|---|---|---|
| Screen | Capillary blood lead | 14.0 µg/dL | Obtain venous confirmation within the recommended 1-month window; delay can postpone exposure investigation and follow-up while exposure continues. |
| Confirmation | Trace-element-free EDTA whole blood by ICP-MS | 12.8 µg/dL, 0.62 µmol/L | Confirmed above CDC BLRV; routine release and local reporting workflow. |
| Reference context | CDC blood lead reference value | 3.5 µg/dL | Population reference, not toxicity threshold. |
Ordering exercise
Place the laboratory actions in the order that protects the confirmation pathway.
1. Release and report
Release according to policy and complete jurisdictional reporting requirements.
2. Analyze confirmed specimen
Run the validated whole-blood lead method with applicable QC.
3. Review capillary screen
Recognize the elevated screen and its confirmation band.
4. Collect venous whole blood
Use the laboratory-specified trace-element-free EDTA device without avoidable delay so confirmation does not postpone exposure investigation and follow-up.
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