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Conceptual and practical advances in the measurement and clinical management of lead toxicity
1Division of Environmental Sciences, Columbia University Medical Center, New York, New York 10032.
Insights
The FDA approved 2,3-dimercaptosuccinic acid (DMSA) for treating children with high blood lead levels. However, its use for lower levels requires further study to balance risks and benefits.
Area of Science:
- Pediatric Toxicology
- Environmental Health
- Pharmacology
Background:
- Elevated blood lead (BPb) concentrations in children pose significant health risks.
- The FDA approved 2,3-dimercaptosuccinic acid (DMSA) in 1991 for treating children with BPb ≥ 45 µg/dL.
- DMSA offers a safer, orally active, and specific treatment option, simplifying management of lead poisoning.
Purpose of the Study:
- To discuss the risks and benefits of DMSA pharmacologic intervention in children with elevated BPb.
- To address concerns regarding the potential overuse of DMSA for lower BPb concentrations ( < 45 µg/dL).
- To evaluate the necessity and justification for treating children with BPb levels below 45 µg/dL.
Main Methods:
- Literature review and discussion of existing data on DMSA efficacy and safety.
- Analysis of current guidelines and their potential impact on clinical practice.
- Identification of knowledge gaps regarding DMSA treatment for lower BPb levels.
Main Results:
- DMSA is an effective and relatively safe treatment for children with BPb ≥ 45 µg/dL.
- The risks and benefits of DMSA treatment for children with BPb < 45 µg/dL are not well-established.
- Current public health aims to lower BPb may inadvertently lead to the treatment of children with lower levels.
Conclusions:
- Further research, including randomized, placebo-controlled trials, is essential to assess the risks and benefits of DMSA for lower BPb concentrations.
- Clinical decisions regarding DMSA use in children with BPb < 45 µg/dL require careful consideration of uncertain outcomes.
- Evidence-based guidelines are needed to ensure appropriate pharmacologic intervention for pediatric lead exposure.
Abstract:
The purpose of this paper is to discuss issues which relate to the risks and benefits of pharmacologic intervention in children with elevated blood lead (BPb) concentrations. In January, 1991, 2,3-dimercaptosuccinic acid (DMSA; succimer or CHEMET) was approved by the FDA for administration to children with blood lead concentrations of 45 micrograms/dl or higher. Thus, it is now considerably simpler to treat children with elevated BPb's. DMSA is orally actively, relatively safe and specific, and can, in some situations, be used on an out-patient basis. The author is concerned that the recent CDC statement on lead poisoning, whose aim is to reduce (by various means) children's BPb's below 10 micrograms/dl, may unintentionally encourage pediatricians to treat children with relatively low BPb's with DMSA, both for medical and legal reasons. Should children with BPb's of less than 45 ug/dl be treated, and why? The risks and benefits of treatment in such children are uncertain. A randomized, placebo controlled, double-blind drug intervention trial is needed (and justified) in order to more carefully assess the benefits and the risks associated with the treatment of lower BPb's.
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