Tabulate treatment:control ratios occurring in matched sets, and the frequency of their occurrence.
stratumStructure(stratum, trtgrp =NULL, min.controls =0, max.controls =Inf)## S3 method for class 'optmatch'stratumStructure(stratum, trtgrp, min.controls =0, max.controls =Inf)## Default S3 method:stratumStructure(stratum, trtgrp, min.controls =0, max.controls =Inf)## S3 method for class 'stratumStructure'print(x,...)
Arguments
stratum: Matched strata, as returned by fullmatch or pairmatch
trtgrp: Dummy variable for treatment group membership. (Not required if stratum is an optmatch object, as returned by fullmatch or pairmatch.)
min.controls: For display, the number of treatment group members per stratum will be truncated at the reciprocal of min.controls.
max.controls: For display, the number of control group members will be truncated at max.controls.
x: stratumStructure object to be printed.
...: Additional arguments to print.
Returns
A table showing frequency of occurrence of those treatment:control ratios that occur.
The effective sample size of the stratification, in matched pairs. Given as an attribute of the table, named ‘comparable.num.matched.pairs’ ; see Note.
Note
For comparing treatment and control groups both of size 10, say, a stratification consisting of two strata, one with 9 treatments and 1 control, has a smaller effective sample size , intuitively, than a stratification into 10 matched pairs, despite the fact that both contain 20 subjects in total. stratumStructure first summarizes this aspect of the structure of the stratification it is given, then goes on to identify one number as the stratification's effective sample size. The ‘comparable.num.matched.pairs’
attribute returned by stratumStructure is the sum of harmonic means of the sizes of the treatment and control subgroups of each stratum, a general way of calibrating such differences as well as differences in the number of subjects contained in a stratification. For example, by this metric the 9:1, 1:9 stratification is comparable to 3.6 matched pairs.
Why should effective sample size be calculated this way? The phrase effective sample size suggests the observations are taken to be similar in information content. Modeling them as random variables, this suggests that they be assumed to have the same variance, sigma, conditional on what stratum they reside in. If that is the case, and if also treatment and control observations differ in expectation by a constant that is the same for each stratum, then it can be shown that the optimum weights with which to combine treatment-control contrasts across strata, s, are proportional to the stratum-wise harmonic means of treatment and control counts, c("h[s]=\n", "1/(0.5/n.t[s]+0.5/n.c[s])") (Kalton, 1968). The thus-weighted average of contrasts then has variance 2∗sigma/sum(h). This motivates the use of sum(h) as a measure of effective sample size (Hansen, 2011). Somewhat different motivations of the same calculation appear in Hansen (2004) and in Hansen and Bowers (2008). Since for a matched pair s, h[s]=1, sum(h) can be thought of as the number of matched pairs needed to attain comparable precision.
Examples
data(plantdist)plantsfm <- fullmatch(plantdist)# A full match with unrestricted# treatment-control balanceplantsfm1 <- fullmatch(plantdist,min.controls=2, max.controls=3)stratumStructure(plantsfm)stratumStructure(plantsfm1)stratumStructure(plantsfm, max.controls=4)
References
Kalton, G. (1968), Standardization: A technique to control for extraneous variables , Applied Statistics, 17 , 118--136.
Hansen, B.B. (2004), Full Matching in an Observational Study of Coaching for the SAT , Journal of the American Statistical Association, 99 , 609--618.
Hansen B.B. and Bowers, J. (2008), Covariate balance in simple, stratified and clustered comparativestudies , Statistical Science, 23 (2), 219--236.
Hansen, B.B. (2011), Propensity score matching to extract latent experiments fromnonexperimental data: A case study . Ch. 9 of Looking Backwards: Proceedings from a Conference in Honor of Paul W. Holland, Springer.