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Estimates the required sample size to detect disease. The method adjusts sample size estimates on the basis of test sensitivity and specificity and can account for series and parallel test interpretation.
epi.detectsize(N, prev, se, sp, interpretation = "series",
covar = c(0,0), conf.level = 0.95, finite.correction = TRUE)a vector of length one or two defining the size of the population. The first element of the vector defines the number of clusters, the second element defining the mean number of sampling units per cluster.
a vector of length one or two defining the prevalence of disease in the population. The first element of the vector defines the between-cluster prevalence, the second element defines the within-cluster prevalence.
a vector of length one or two defining the sensitivity of the test(s) used.
a vector of length one or two defining the specificity of the test(s) used.
a character string indicating how test results should be interpreted. Options are series or parallel.
a vector of length two defining the covariance between test results for disease positive and disease negative groups. The first element of the vector is the covariance between test results for disease positive subjects. The second element of the vector is the covariance between test results for disease negative subjects. Use covar = c(0,0) (the default) if these values are not known.
scalar, defining the level of confidence in the computed result.
logical, should a finite correction factor be applied?
A list containing the following:
The sensitivity and specificity of the testing strategy.
The number of clusters, units, and total number of units to be sampled.
Dohoo I, Martin W, Stryhn H (2003). Veterinary Epidemiologic Research. AVC Inc, Charlottetown, Prince Edward Island, Canada, pp. 47 and pp. 102 - 103.
## EXAMPLE 1:
## We would like to confirm the absence of disease in a single 1000-cow
## dairy herd. We expect the prevalence of disease in the herd to be 5%.
## We intend to use a single test with a sensitivity of 0.90 and a
## specificity of 0.80. How many samples should we take to be 95% certain
## that, if all tests are negative, the disease is not present?
epi.detectsize(N = 1000, prev = 0.05, se = 0.90, sp = 0.80, interpretation =
"series", covar = c(0,0), conf.level = 0.95, finite.correction = TRUE)
## We need to sample 59 cows.
## EXAMPLE 2:
## We would like to confirm the absence of disease in a study area. If the
## disease is present we expect the between-herd prevalence to be 8% and the
## within-herd prevalence to be 5%. We intend to use two tests: the first has
## a sensitivity and specificity of 0.90 and 0.80, respectively. The second
## has a sensitivity and specificity of 0.95 and 0.85, respectively. The two
## tests will be interpreted in parallel. How many herds and cows within herds
## should we sample to be 95% certain that the disease is not present in the
## study area if all tests are negative? There area is comprised of
## approximately 5000 herds and the average number of cows per herd is 100.
epi.detectsize(N = c(5000, 100), prev = c(0.08, 0.05), se = c(0.90, 0.95),
sp = c(0.80, 0.85), interpretation = "parallel", covar = c(0,0),
conf.level = 0.95, finite.correction = TRUE)
## We need to sample 31 cows from 38 herds (a total of 1178 samples).
## The sensitivity of this testing regime is 99%. The specificity of this
## testing regime is 68%.
## EXAMPLE 3:
## You want to document the absence of Mycoplasma from a 200-sow pig herd.
## Based on your experience and the literature, a minimum of 20% of sows
## would have seroconverted if Mycoplasma were present in the herd. How many
## sows do you need to sample?
epi.detectsize(N = 200, prev = 0.20, se = 1.00, sp = 1.00, conf.level = 0.95,
finite.correction = TRUE)
## If you test 12 sows and all test negative you can state that you are 95%
## confident that the prevalence rate of Mycoplasma in the herd is less than
## 20%.
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