meta (version 3.7-0)

metaprop: Meta-analysis of single proportions

Description

Calculation of an overall proportion from studies reporting a single proportion.

Usage

metaprop(event, n, studlab,
         data=NULL, subset=NULL,
         sm=.settings$smprop,
         incr=.settings$incr, allincr=.settings$allincr,
         addincr=.settings$addincr,
         method.ci=.settings$method.ci,
         level=.settings$level, level.comb=.settings$level.comb,
         comb.fixed=.settings$comb.fixed, comb.random=.settings$comb.random,
         hakn=.settings$hakn,
         method.tau=.settings$method.tau, tau.preset=NULL, TE.tau=NULL,
         tau.common=.settings$tau.common,
         prediction=.settings$prediction, level.predict=.settings$level.predict,
         method.bias=.settings$method.bias,
         title=.settings$title, complab=.settings$complab, outclab="",
         byvar, bylab, print.byvar=.settings$print.byvar,
         keepdata=.settings$keepdata,
         warn=.settings$warn)

Arguments

event

Number of events.

n

Number of observations.

studlab

An optional vector with study labels.

data

An optional data frame containing the study information, i.e., event and n.

subset

An optional vector specifying a subset of studies to be used.

sm

A character string indicating which summary measure ("PFT", "PAS", "PRAW", "PLN", or "PLOGIT") is to be used for pooling of studies, see Details.

incr

A numeric which is added to each cell frequency for studies with a zero cell count.

allincr

A logical indicating if incr is added to each cell frequency of all studies if at least one study has a zero cell count. If FALSE (default), incr is added only to each cell frequency of studies with a zero cell count.

addincr

A logical indicating if incr is added to each cell frequency of all studies irrespective of zero cell counts.

method.ci

A character string indicating which method is used to calculate confidence intervals for individual studies, see Details.

level

The level used to calculate confidence intervals for individual studies.

level.comb

The level used to calculate confidence intervals for pooled estimates.

comb.fixed

A logical indicating whether a fixed effect meta-analysis should be conducted.

comb.random

A logical indicating whether a random effects meta-analysis should be conducted.

prediction

A logical indicating whether a prediction interval should be printed.

level.predict

The level used to calculate prediction interval for a new study.

hakn

A logical indicating whether the method by Hartung and Knapp should be used to adjust test statistics and confidence intervals.

method.tau

A character string indicating which method is used to estimate the between-study variance $\tau^2$, see Details.

tau.preset

Prespecified value for the square-root of the between-study variance $\tau^2$.

TE.tau

Overall treatment effect used to estimate the between-study variance tau-squared.

tau.common

A logical indicating whether tau-squared should be the same across subgroups.

method.bias

A character string indicating which test is to be used. Either "rank", "linreg", or "mm", can be abbreviated. See function metabias.

title

Title of meta-analysis / systematic review.

complab

Comparison label.

outclab

Outcome label.

byvar

An optional vector containing grouping information (must be of same length as event.e).

bylab

A character string with a label for the grouping variable.

print.byvar

A logical indicating whether the name of the grouping variable should be printed in front of the group labels.

keepdata

A logical indicating whether original data (set) should be kept in meta object.

warn

A logical indicating whether the addition of incr to studies with zero cell frequencies should result in a warning.

Value

• An object of class c("metaprop", "meta") with corresponding print, summary, plot function. The object is a list containing the following components:
• event, n, studlab,
• sm, incr, allincr, addincr, method.ci,
• level, level.comb,
  As defined above.
• comb.fixed, comb.random,
• hakn, method.tau, tau.preset, TE.tau, method.bias,
• tau.common, title, complab, outclab,
• byvar, bylab, print.byvar, warn
• TE, seTE
  Estimated (un)transformed proportion and its standard error for individual studies.
• lower, upper
  Lower and upper confidence interval limits for individual studies.
• zval, pval
  z-value and p-value for test of treatment effect for individual studies.
• w.fixed, w.random
  Weight of individual studies (in fixed and random effects model).
• TE.fixed, seTE.fixed
  Estimated overall (un)transformed proportion and standard error (fixed effect model).
• lower.fixed, upper.fixed
  Lower and upper confidence interval limits (fixed effect model).
• zval.fixed, pval.fixed
  z-value and p-value for test of overall effect (fixed effect model).
• TE.random, seTE.random
  Estimated overall (un)transformed proportion and standard error (random effects model).
• lower.random, upper.random
  Lower and upper confidence interval limits (random effects model).
• zval.random, pval.random
  z-value or t-value and corresponding p-value for test of overall effect (random effects model).
• prediction, level.predict
  As defined above.
• seTE.predict
  Standard error utilised for prediction interval.
• lower.predict, upper.predict
  Lower and upper limits of prediction interval.
• k
  Number of studies combined in meta-analysis.
• Q
  Heterogeneity statistic Q.
• tau
  Square-root of between-study variance.
• se.tau
  Standard error of square-root of between-study variance.
• C
  Scaling factor utilised internally to calculate common tau-squared across subgroups.
• sm
  A character string: "proportion"
• method
  A character string indicating method used for pooling: "Inverse"
• df.hakn
  Degrees of freedom for test of treatment effect for Hartung-Knapp method (only if hakn=TRUE).
• incr.event
  Increment added to number of events.
• keepdata
  As defined above.
• data
  Original data (set) used in function call (if keepdata=TRUE).
• subset
  Information on subset of original data used in meta-analysis (if keepdata=TRUE).
• call
  Function call.
• version
  Version of R package meta used to create object.

Details

Fixed effect and random effects meta-analysis of single proportions to calculate an overall proportion. By default, the DerSimonian-Laird estimate (1986) is used in the random effects model (method.tau="DL"). The following transformations of proportions are implemented to calculate an overall proportion:

• Logit transformation (sm="PLOGIT", default)
• Log transformation (sm="PLN")
• Freeman-Tukey Double arcsine transformation (sm="PFT")
• Arcsine transformation (sm="PAS")
• Raw, i.e. untransformed, proportions (sm="PRAW")

If the summary measure is equal to "PRAW", "PLN", or "PLOGIT", a continuity correction is applied if any studies has a zero cell count. By default, 0.5 is added to all cell frequencies of studies with a zero cell count (argument incr).

Various methods are available to calculate confidence intervals for individual study results (see Agresti & Coull 1998; Newcombe 1988):

• Clopper-Pearson interval also called 'exact' binomial interval (method.ci="CP", default)
• Wilson Score interval (method.ci="WS")
• Wilson Score interval with continuity correction (method.ci="WSCC")
• Agresti-Coull interval (method.ci="AC")
• Simple approximation interval (method.ci="SA")
• Simple approximation interval with continuity correction (method.ci="SACC")
• Normal approximation interval based on summary measure, i.e. defined by argumentsm(method.ci="NAsm")

Note, with exception of the normal approximation based on the summary measure, i.e. method.ci="NAsm", the same confidence interval is calculated for any summary measure (argument sm) as only number of events and observations are used in the calculation disregarding the chosen summary measure. Internally, both fixed effect and random effects models are calculated regardless of values choosen for arguments comb.fixed and comb.random. Accordingly, the estimate for the random effects model can be extracted from component TE.random of an object of class "meta" even if argument comb.random=FALSE. However, all functions in R package meta will adequately consider the values for comb.fixed and comb.random. E.g. function print.meta will not print results for the random effects model if comb.random=FALSE.

A prediction interval for treatment effect of a new study is calculated (Higgins et al., 2009) if arguments prediction and comb.random are TRUE.

R function update.meta can be used to redo the meta-analysis of an existing metaprop object by only specifying arguments which should be changed.

For the random effects, the method by Hartung and Knapp (2003) is used to adjust test statistics and confidence intervals if argument hakn=TRUE. The iterative Paule-Mandel method (1982) to estimate the between-study variance is used if argument method.tau="PM". Internally, R function paulemandel is called which is based on R function mpaule.default from R package metRology from S.L.R. Ellison .

If R package metafor (Viechtbauer 2010) is installed, the following methods to estimate the between-study variance $\tau^2$ (argument method.tau) are also available:

• Restricted maximum-likelihood estimator (method.tau="REML")
• Maximum-likelihood estimator (method.tau="ML")
• Hunter-Schmidt estimator (method.tau="HS")
• Sidik-Jonkman estimator (method.tau="SJ")
• Hedges estimator (method.tau="HE")
• Empirical Bayes estimator (method.tau="EB").

For these methods the R function rma.uni of R package metafor is called internally. See help page of R function rma.uni for more details on these methods to estimate between-study variance.

References

Agresti A & Coull BA (1998), Approximate is better than “exact” for interval estimation of binomial proportions. The American Statistician, 52, 119--126.

DerSimonian R & Laird N (1986), Meta-analysis in clinical trials. Controlled Clinical Trials, 7, 177--188.

Edward JM et al. (2006), Adherence to antiretroviral therapy in sub-saharan Africa and North America - a meta-analysis. Journal of the American Medical Association, 296, 679--690.

Freeman MF & Tukey JW (1950), Transformations related to the angular and the square root. Annals of Mathematical Statistics, 21, 607--611. Higgins JPT, Thompson SG, Spiegelhalter DJ (2009), A re-evaluation of random-effects meta-analysis. Journal of the Royal Statistical Society: Series A, 172, 137--159.

Knapp G & Hartung J (2003), Improved Tests for a Random Effects Meta-regression with a Single Covariate. Statistics in Medicine, 22, 2693--2710, doi: 10.1002/sim.1482 .

Miller JJ (1978), The inverse of the Freeman-Tukey double arcsine transformation. The American Statistician, 32, 138. Newcombe RG (1998), Two-sided confidence intervals for the single proportion: Comparison of seven methods. Statistics in Medicine, 17, 857--872. Paule RC & Mandel J (1982), Consensus values and weighting factors. Journal of Research of the National Bureau of Standards, 87, 377--385.

Pettigrew HM, Gart JJ, Thomas DG (1986), The bias and higher cumulants of the logarithm of a binomial variate. Biometrika, 73, 425--435.

Viechtbauer W (2010), Conducting Meta-Analyses in R with the Metafor Package. Journal of Statistical Software, 36, 1--48.

See Also

update.meta, metacont, metagen, print.meta

Examples

metaprop(4:1, c(10, 20, 30, 40))
metaprop(4:1, c(10, 20, 30, 40), sm="PAS")
metaprop(4:1, c(10, 20, 30, 40), sm="PRAW")
metaprop(4:1, c(10, 20, 30, 40), sm="PLN")
metaprop(4:1, c(10, 20, 30, 40), sm="PFT")

forest(metaprop(4:1, c(10, 20, 30, 40)))


m1 <- metaprop(c(0, 0, 10, 10), rep(100, 4))
m2 <- metaprop(c(0, 0, 10, 10), rep(100, 4), incr=0.1)

summary(m1)
summary(m2)

forest(m1)
forest(m2)

## Example from Miller (1978):
death <- c(3, 6, 10, 1)
animals <- c(11, 17, 21, 6)
##
m3 <- metaprop(death, animals, sm="PFT")
forest(m3)

## Data examples from Newcombe (1998)
##
event <- c(81, 15, 0, 1)
n <- c(263, 148, 20, 29)
##
m1 <- metaprop(event, n, sm="PLOGIT", method.ci="SA")
m2 <- update(m1, method.ci="SACC")
m3 <- update(m1, method.ci="WS")
m4 <- update(m1, method.ci="WSCC")
m5 <- update(m1, method.ci="CP")
##
lower <- round(rbind(NA, m1$lower, m2$lower, NA, m3$lower, m4$lower, NA, m5$lower), 4)
upper <- round(rbind(NA, m1$upper, m2$upper, NA, m3$upper, m4$upper, NA, m5$upper), 4)
##
tab1 <- data.frame(
  scen1=meta:::p.ci(lower[,1], upper[,1]),
  scen2=meta:::p.ci(lower[,2], upper[,2]),
  scen3=meta:::p.ci(lower[,3], upper[,3]),
  scen4=meta:::p.ci(lower[,4], upper[,4]),
  stringsAsFactors=FALSE
  )
names(tab1) <- c("r=81, n=263", "r=15, n=148", "r=0, n=20", "r=1, n=29")
row.names(tab1) <- c("Simple", "- SA", "- SACC",
                     "Score", "- WS", "- WSCC",
                     "Binomial", "- CP")
tab1[is.na(tab1)] <- ""
##
## Newcombe (1998), Table I, methods 1-5:
##
tab1

## Same confidence interval, i.e. unaffected by choice of summary measure
##
print(metaprop(event, n, sm="PLOGIT", method.ci="WS"), ma=FALSE)
print(metaprop(event, n, sm="PLN", method.ci="WS"), ma=FALSE)
print(metaprop(event, n, sm="PFT", method.ci="WS"), ma=FALSE)
print(metaprop(event, n, sm="PAS", method.ci="WS"), ma=FALSE)
print(metaprop(event, n, sm="PRAW", method.ci="WS"), ma=FALSE)