Which statement about lead poisoning is false?

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Identifying False Statements About Lead Poisoning

Statement C, "Serum lead level is a good inexpensive screening test for lead toxicity," is false. Whole blood lead measurement, not serum lead testing, is the recommended method for detecting lead toxicity 1, 2.

Analysis of Each Statement

A. Lead levels below 5 μg/dl in children do not prompt ongoing monitoring

  • This statement is false. According to CDC guidelines, there is no safe blood lead level in children 1, 2.
  • The CDC and American Academy of Pediatrics recommend monitoring children with blood lead levels below 5 μg/dL, particularly those at high risk of lead exposure 1, 2.
  • For children with blood lead levels <5 μg/dL who are at high risk or whose risk profile increases, repeat testing is recommended in 6-12 months 1.
  • For children initially screened before 12 months of age, retesting in 3-6 months is recommended as mobility increases and risk of exposure may change 1.

B. Whole blood lead measurement is the best test for detecting lead toxicity

  • This statement is true. Whole blood lead measurement is the standard method for detecting lead toxicity 1, 2.
  • Guidelines specifically recommend venous blood sampling for confirmation of elevated blood lead levels, with capillary samples acceptable for initial screening 1, 2.
  • Research has shown that properly collected capillary blood samples correlate well with venous samples (correlation coefficient ≥0.96), making them acceptable for screening purposes 3.

C. Serum lead level is a good inexpensive screening test for lead toxicity

  • This statement is false. Serum lead testing is not recommended for lead toxicity screening 1, 2.
  • All major guidelines specify whole blood lead measurement, not serum testing, as the appropriate test for lead toxicity 1, 2.
  • Laboratory considerations for blood lead testing focus on whole blood analysis, with specific performance standards for accuracy at various blood lead concentrations 1.

D. While lead distributes to all tissues, the central nervous system, kidney, and bone marrow are particularly susceptible to lead toxicity

  • This statement is true. Lead is known to be toxic to multiple organ systems, with particular susceptibility in the central nervous system, kidneys, and bone marrow 2, 4.
  • Lead causes neurodevelopmental effects, cognitive impairment, and behavioral problems through its impact on the central nervous system 2, 5, 4.
  • Lead toxicity can cause anemia with basophilic stippling of erythrocytes, demonstrating its effect on bone marrow 2, 4.
  • Kidney damage is a recognized effect of lead toxicity 4.

Important Clinical Considerations

  • Blood lead level testing has inherent laboratory variability, with federal regulations allowing an error margin of ±4 μg/dL or ±10% (whichever is greater) 1, 2.
  • Most laboratories can achieve performance of ±2 μg/dL at concentrations <10 μg/dL, which is important when interpreting results near reference values 1, 2.
  • The CDC has established 5 μg/dL as the reference value for identifying children with elevated blood lead levels requiring case management 1, 2.
  • No safe blood lead level has been identified in children, and even low levels can cause permanent neurological damage 2, 5.

In conclusion, statement C is false because serum lead testing is not recommended for lead toxicity screening; whole blood lead measurement is the appropriate test.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Lead Exposure Management in Children

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Lead poisoning.

The Western journal of medicine, 1994

Research

Assessment and Prevention of Lead Poisoning in Refugee Populations.

Journal of health care for the poor and underserved, 2023

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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