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contaminants of concern likely to occur at dredged material management sites.
These should be updated with each risk assessment as indicated in the following
steps.
The products of a toxicity assessment are:
a. A discussion of the potential adverse health effects due to exposure to
contaminants of concern.
b. The toxicity factors for use in a quantitative estimate of risk.
Step 1: Determine Toxicity Factors
Carcinogenic effects of COC. EPA has used the weight-of-evidence approach to
evaluate potential human carcinogens and categorizes them in Integrated Risk
Information System (IRIS) (USEPA 1997) and the Health Effects Assessment
Summary Tables (HEAST) (USEPA/OSWER 1997). The carcinogenic slope factor
(CSF) expresses the carcinogenicity of a compound. The CSF is a toxicity value that
defines the quantitative relationship between dose and response. It is a plausible
upper-bound estimate of the probability of a response per unit intake of a
contaminant over a lifetime. The slope factor is usually the upper 95th-percent
confidence limit of the slope of the dose-response curve and is expressed as
(mg/kg/day) -1.
Noncarcinogenic Effects of COC. A reference dose, or RfD, is the toxicity value
used most often in evaluating noncarcinogenic effects, resulting from exposures to
chemicals. The RfD is defined as an estimate of a daily exposure level for the
human population, including sensitive subpopulations (such as elderly and children)
that is likely to be without an appreciable risk of adverse effects during a lifetime.
Step 2: Assemble Sources of Toxicity Information
There is a hierarchy of toxicity information that should be consulted when
conducting a risk assessment. The first is the Integrated Risk Information System
(IRIS), an information database that contains chemical-specific health risk and
USEPA regulatory information. Information in IRIS supersedes all other sources. If
information is unavailable in IRIS, then HEAST may be consulted. The HEAST
contains toxicity information and values from USEPA. It is updated quarterly and
contains interim toxicity factors that are not found on IRIS.
Human Health Risk Characterization
This text provides the toxicity factors which are quantitative estimates of the
potency of the contaminants of concern. These factors, combined with the average
daily intake estimates derived in the exposure assessment section, are used to
estimate risk in the risk characterization.
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Chapter 4 Human Health Risk Assessment
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