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metafor (version 1.9-4)

rma.peto: Meta-Analysis via Peto's Method

Description

Function to fit fixed-effects models to $2 \times 2$ table data via Peto's method. See below and the documentation of the metafor-package for more details on these models.

Usage

rma.peto(ai, bi, ci, di, n1i, n2i,
         data, slab, subset,
         add=1/2, to="only0", drop00=TRUE,
         level=95, digits=4, verbose=FALSE)

Arguments

ai
vector to specify the $2 \times 2$ table frequencies (upper left cell). See below and the documentation of the escalc function for more details.
bi
vector to specify the $2 \times 2$ table frequencies (upper right cell). See below and the documentation of the escalc function for more details.
ci
vector to specify the $2 \times 2$ table frequencies (lower left cell). See below and the documentation of the escalc function for more details.
di
vector to specify the $2 \times 2$ table frequencies (lower right cell). See below and the documentation of the escalc function for more details.
n1i
vector to specify the group sizes or row totals (first group). See below and the documentation of the escalc function for more details.
n2i
vector to specify the group sizes or row totals (second group). See below and the documentation of the escalc function for more details.
data
optional data frame containing the data supplied to the function.
slab
optional vector with labels for the $k$ studies.
subset
optional vector indicating the subset of tables that should be used for the analysis. This can be a logical vector of length $k$ or a numeric vector indicating the indices of the tables to include.
add
non-negative number indicating the amount to add to zero cells, counts, or frequencies when calculating the individual outcomes. Can also be a vector of two numbers, where the first number is used in the calculation of the individual outcomes and the seco
to
character string indicating when the values under add should be added (either "only0", "all", "if0all", or "none"). Can also be a character vector, where the first string again applies when
drop00
logical indicating whether studies with no cases (or only cases) in both groups should be dropped when calculating the observed outcomes of the individual studies (the outcomes for such studies are set to NA). See below and the documentation
level
numerical value between 0 and 100 specifying the confidence interval level (default is 95).
digits
integer specifying the number of decimal places to which the printed results should be rounded (default is 4).
verbose
logical indicating whether output should be generated on the progress of the model fitting (default is FALSE).

Value

  • An object of class c("rma.peto","rma"). The object is a list containing the following components:
  • baggregated log odds ratio.
  • sestandard error of the aggregated value.
  • zvaltest statistics of the aggregated value.
  • pvalp-value for the test statistic.
  • ci.lblower bound of the confidence interval.
  • ci.ubupper bound of the confidence interval.
  • QEtest statistic for the test of heterogeneity.
  • QEpp-value for the test of heterogeneity.
  • knumber of tables included in the analysis.
  • yi, vithe vector of individual log odds ratios and corresponding sampling variances.
  • fit.statsa list with the log-likelihood, deviance, AIC, BIC, and AICc values under the unrestricted and restricted likelihood.
  • ...some additional elements/values.
  • The results of the fitted model are formated and printed with the print.rma.peto function. If fit statistics should also be given, use summary.rma (or use the fitstats.rma function to extract them). The residuals.rma, rstandard.rma.peto, and rstudent.rma.peto functions extract raw and standardized residuals. Leave-one-out diagnostics can be obtained with leave1out.rma.peto. Forest, funnel, radial, L'abbé, and Baujat plots can be obtained with forest.rma, funnel.rma, radial.rma, labbe.rma, and baujat.rma.peto. The qqnorm.rma.peto function provides normal QQ plots of the standardized residuals. One can also just call plot.rma.peto on the fitted model object to obtain various plots at once. A cumulative meta-analysis (i.e., adding one obervation at a time) can be obtained with cumul.rma.peto. Other extractor functions include coef.rma, vcov.rma, logLik.rma, deviance.rma, AIC.rma, and BIC.rma.

Details

The studies are assumed to provide data in terms of $2 \times 2$ tables of the form: lccc{ outcome 1 outcome 2 total group 1 ai bi n1i group 2 ci di n2i } where ai, bi, ci, and di denote the cell frequencies and n1i and n2i the row totals. For example, in a set of randomized clinical trials (RCTs) or cohort studies, group 1 and group 2 may refer to the treatment (exposed) and placebo/control (not exposed) group, with outcome 1 denoting some event of interest (e.g., death) and outcome 2 its complement. In a set of case-control studies, group 1 and group 2 may refer to the group of cases and the group of controls, with outcome 1 denoting, for example, exposure to some risk factor and outcome 2 non-exposure. An approach for aggregating $2 \times 2$ table data of this type was suggested by Peto (see Yusuf et al., 1985). The method provides a weighted estimate of the (log) odds ratio under a fixed-effects model. The method is particularly advantageous when the event of interest is rare, but it should only be used when the group sizes within the individual studies are not too dissimilar and effect sizes are generally small (Greenland & Salvan, 1990; Sweeting et al., 2004; Bradburn et al., 2007). Note that the printed results are given both in terms of the log and the raw units (for easier interpretation). Peto's method itself does not require the calculation of the individual (log) odds ratios and directly makes use of the $2 \times 2$ table counts. Zero cells are not a problem (except in extreme cases, such as when one of the two outcomes never occurs in any of the tables). Therefore, it is unnecessary to add some constant to the cell counts when there are zero cells. However, for plotting and various other functions, it is necessary to calculate the individual (log) odds ratios for the $k$ tables. Here, zero cells can be problematic, so adding a constant value to the cell counts ensures that all $k$ values can be calculated. The add and to arguments are used to specify what value should be added to the cell frequencies and under what circumstances when calculating the individual (log) odds ratios and when applying Peto's method. The documentation of the escalc function explains how the add and to arguments work. If only one value for these arguments is specified, then these values are used when calculating the individual outcomes and no adjustment to the cell counts is made when applying Peto's method. Alternatively, when specifying two values for these arguments, the first value applies when calculating the individual outcomes and the second value when applying Peto's method. Note that drop00 is set to TRUE by default, since studies where ai=ci=0 or bi=di=0 are also automatically dropped when applying Peto's method.

References

Bradburn, M. J., Deeks, J. J., Berlin, J. A., & Localio, A. R. (2007). Much ado about nothing: A comparison of the performance of meta-analytical methods with rare events. Statistics in Medicine, 26, 53--77. Greenland, S., & Salvan, A. (1990). Bias in the one-step method for pooling study results. Statistics in Medicine, 9, 247--252. Sweeting, M. J., Sutton, A. J., & Lambert, P. C. (2004). What to add to nothing? Use and avoidance of continuity corrections in meta-analysis of sparse data. Statistics in Medicine, 23, 1351--1375. Yusuf, S., Peto, R., Lewis, J., Collins, R., & Sleight, P. (1985). Beta blockade during and after myocardial infarction: An overview of the randomized trials. Progress in Cardiovascular Disease, 27, 335--371. Viechtbauer, W. (2010). Conducting meta-analyses in R with the metafor package. Journal of Statistical Software, 36(3), 1--48. http://www.jstatsoft.org/v36/i03/.

See Also

rma.uni, rma.glmm, rma.mh, and rma.mv for other model fitting functions. dat.collins1985a, dat.collins1985b, and dat.yusuf1985 for further examples of the use of the rma.peto function.

Examples

Run this code
### load data
data(dat.bcg)

### meta-analysis of the (log) odds ratios using Peto's method
rma.peto(ai=tpos, bi=tneg, ci=cpos, di=cneg, data=dat.bcg)

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