The National Research Council report Science and Judgment
in Risk Assessment (NRC 1994a) addressed the extensive
uncertainty and variability associated with estimating risk and
concluded that risk characterizations should not be reduced to a
single number or even to a range of numbers intended to portray
uncertainty. Instead, the report recommended, risk managers
should be given risk characterizations that are both qualitative
and quantitative and both verbal and mathematical. The Commission
concurs that qualitative descriptions of risk-related uncertainty
are needed, but it does not agree that formal, quantitative
uncertainty analyses are either necessary or useful for most risk
assessments. When the Commission's risk-management framework is
implemented, nonquantitative methods of communicating information
about uncertainty to participants are likely to be more effective
than quantitative methods. There are, of course, situations in
which quantitative uncertainty analyses are likely to provide
information that is useful in a decision-making process, and the
Commission encourages the continued development and application
of quantitative methods. There are also likely to be situations
in which a quantitative uncertainty analysis can be used to
improve qualitative information about uncertainty, even if the
quantitative information is not what is communicated to the risk
manager.
FINDING 3.3: The best way to present the
results of a risk assessment so as to acknowledge variability and
uncertainty is controversial. There is also confusion regarding
the differences between variability and uncertainty. Variability
comprises a population's natural heterogeneity or diversity, and
it does not change through further measurement or study, although
better sampling can improve knowledge about variability.
Uncertainty reflects gaps in information about scientifically
observable phenomena. Uncertainty sometimes can be reduced
through further measurement or study. Several quantitative
methods to describe risk-assessment uncertainties are being
explored. Although there is general agreement as to the value of
qualitative statements describing critical uncertainties in
health risk assessments, formal quantitative approaches to
uncertainty analysis are complex, difficult to perform, difficult
to understand, and often unnecessary. Variability, in contrast,
can be described much more readily and can be based on actual
measurements.
RECOMMENDATION: Qualitative descriptions of
the primary sources of uncertainty and the weight of the evidence
associated with exposure, toxicity, and susceptibility should be
included in risk characterizations intended for risk managers and
the nontechnical public. Quantitative methods of describing the
variability associated with exposure can yield useful information
for risk management and should be included with qualitative
descriptions in risk characterizations (see sections 3.2 and
5.1). However, a formal quantitative analysis of the
uncertainties in risk estimates is not needed for most risk
assessments.
RATIONALE
Support for routine, formal quantitative analysis of
uncertainty is based on the desire to move away from poorly
supported default assumptions and point estimates of risk that
convey an unwarranted sense of accuracy and that fail to convey
any sense of the confidence that the risk assessor has in the
estimates or their inherent complexity. Providing a numerical
range of possible risks that reflects uncertainty and variability
is thought to allow more-informed and more-transparent decisions
than are possible when only a single point estimate of risk is
generated.
In the absence of some explanation of the weight of scientific
evidence, communicating a range of population risks might be
misconstrued by those unfamiliar with quantitative methods as
implying that all the numbers in the range are equally likely or
plausible and therefore equally valid for regulation. Many risk
estimates are crude yardsticks for decision-making--as Thomas
Gentile, of New York State's Division of Air Resources, noted in
his testimony before the Commission, many state-level risk
managers just want to know, "Is it safe or not?" In
this context, the routine provision of a distribution or range of
possible risks might only confuse and delay the regulatory
process.
Generating ranges or probabilistic distributions of risk
estimates instead of point estimates is thought to portray more
accurately the range of possible risks experienced by an exposed
population. When data are scarce, assumptions about the
underlying shape of the risk distribution dominate; that is, when
uncertainty is great, a range of probabilities based on
assumptions would replace point estimates based on assumptions.
As Thomas Starr, of ENVIRON, testified before the Commission,
formal uncertainty analyses are not useful if there are
disagreements about the underlying shapes of the distributions;
folding assumptions about those shapes into a risk assessment
incorporates the assessor's bias into the risk estimate.
Approximating uncertainty thus introduces yet another source of
uncertainty.
A report prepared by Cambridge Environmental Inc. for the
Commission, Health Risk Assessments Prepared per the Risk
Assessment Reforms under Consideration in the U.S. Congress
(see appendix A.5 for abstract), showed that when chemicals that
are not known human carcinogens are evaluated, most of the
uncertainty in risk estimates results from uncertainty about a
substance's toxicity. The probability distributions generated to
account for that kind of uncertainty can take a variety of
shapes, depending on the assumptions made and the data used--for
example, whether a chemical that tested positive for
carcinogenicity in a rodent bioassay is or is not a human
carcinogen and whether some tumor rates were reduced, not
increased. Methods for quantitatively describing the
uncertainties associated with toxicity are still under
development.
Providing distributions of risk is thought to counteract the
perceived bias toward overestimating risk that is due to a
compounding of conservative default assumptions. However, any
range of a population's risks inevitably will include estimates
in the upper end of the distribution that are at least as
stringent as currently provided by point estimates. When
confronted by an array of estimates, regulators and community
groups are likely to choose from the more stringent portion of
the range. Using formal uncertainty analysis is unlikely to lead
to less-stringent regulation. If the risk-management process is
perceived to be too stringent, the risk-management process, not
the risk-assessment method, should be modified.