sessment of transport model are independent of one another, the variance of the log of the estimated LAR is the sum of three pieces:
which are due, respectively, to the variability in the parameter estimators in the EAR model, the uncertainty in the transport model, and the uncertainty in the DDREF. It is a fairly simple matter to estimate the variance of the log (LAR) from these quantities. The variance of log (LAR), with a normal approximation to the sampling distribution of log (LAR), leads directly to the coefficient of variation in Table 12-10 and the subjective confidence intervals in Tables 12-6 and 12-7.
The simplifying approximation mentioned above amounts to assuming that log and log have equal variances and a correlation of 1 or, in other words, that the variance of an average of these two quantities is the same as the variance of either one individually. The effect of inaccuracies in this assumption is expected to be small relative to the overall variability. Furthermore, because the first term in the variance expression represents the variance of the estimated LAR for either transport model, a weighted average of and is used to estimate it (with the weight corresponding to the strength of belief in the relative risk transport model).
The approach for estimating the variances of the sampling distributions of the estimated LARs is discussed in the first section of this annex. The variance of is taken to be Bernoulli variance. If, for example, the probability that the relative risk transport is correct is taken to be .7, then the variance of is .7 × 0.3. The Bernoulli variance tends to be larger than a variance from a uniform distribution (for a model in which the correct transport is some completely unknown combination of relative and absolute risk) or from a beta distribution (for a model in which the correct transport is some unknown combination, but with more specific information about the possible combination). In the absence of any real knowledge about which of these is correct, the committee has elected to use the more conservative approach, which leads to somewhat wider confidence intervals.
As discussed in Annex 11B, the DDREF analysis is necessarily rough and the variance of the uncertainty distribution described there is, if anything, misleadingly small. For the uncertainty analysis considered here, therefore, the variance representing the uncertainty in log (DDREF) was inflated by 50%, using 0.09 as the variance of , rather than the derived posterior variance 0.06.
Tables 12D-1 and 12D-2 show lifetime risk estimates for cancer incidence and mortality resulting from a single dose of 0.1 Gy at several specific ages. Estimates are shown for all cancer, leukemia, all solid cancer, and cancer of several specific sites. Table 12D-3 shows analogous lifetime risk estimates for exposure to 1 mGy per year throughout life and to 10 mGy per year from ages 18 to 65. The examples below illustrate how these tables may be used to obtain estimates for other exposure scenarios. For clarity of presentation, the committee has generally shown more decimal places than are justified.
Example 1: A 10-year-old male receives a dose of 0.01 Gy (10 mGy) to the colon from a computed tomography (CT) scan. Table 12D-1 shows the estimated lifetime risk of being diagnosed with colon cancer for a male exposed to 0.1 Gy at age 10 as 241 per 100,000. The estimate for a male exposed at 0.01 Gy is obtained as (0.01 / 0.1) × 241 = 24.1 per 100,000 (about 1 in 4000). An estimate of the lifetime risk of dying of colon cancer can also be obtained using Table 12D-2, and is (0.01 / 0.1) × 117 = 11.7 per 100,000 (about 1 in 8500).
Example 2: A 45-year-old woman receives a dose of 0.001 Gy (1 mGy) to the breast from a mammogram. Table 12D-1 shows an estimated lifetime risk of being diagnosed with breast cancer for a female exposed to 0.1 Gy at age 40 as 141 per 100,000; the comparable estimate for exposure at age 50 is 70 per 100,000. Using linear interpolation, the risk from exposure to 0.1 Gy at age 45 is (141 + 70) / 2 = 105.5 per 100,000. The risk from exposure to 0.001 Gy is estimated as (0.001 / 0.1) × 105.5 = 1.055 per 100,000. A rough estimate of the risk from repeated annual mammograms could be obtained by adding estimates obtained from receiving a mammogram at ages 45, 46, 47, 48, and so forth. For most purposes, such an estimate will be reasonable, although this approach does not account for the possibility of dying before subsequent doses are received.
Example 3: A female is exposed to high natural background of 0.004 Gy (4 mGy) per year throughout life. Lifetime risk estimates for exposure to 0.001 Gy (1 mGy) per year throughout life are shown in columns 2 (incidence) and 4 (mortality) of Table 12D-3. To obtain estimates for exposure to 4 mGy throughout life, these estimates must be multiplied by 4. For example, the estimated risk of a female being diagnosed with a solid cancer would be 3872 (4 × 968), per 100,000 whereas the risk of being diagnosed with leukemia would be 204 (4 × 51) per 100,000, yielding a total risk of being diagnosed with cancer of 4076 per 100,000 (about 1 in 25). The risk of dying of cancer can be obtained in a similar manner and would be 1988 per 100,000 (about 1 in 50).