knitr::opts_chunk$set( collapse = TRUE, comment = "#>", fig.path = "man/figures/README-" )
devtools::load_all("~/Dropbox/pte") devtools::load_all("~/Dropbox/ppe") load("~/Dropbox/ppe/data/covid_data.rda") library(ggplot2) library(dplyr)
The pte
package compartmentalizes the steps needed to implement estimators of group-time average treatment effects (and their aggregations) in order to make it easier to apply the same sorts of arguments outside of their "birthplace" in the literature on difference-in-differences.
This code is lightweight, only works for balanced panels, and has minimal error checking. That said, it should be useful projects that build on top of group-time average treatment effects in order to deliver estimates of causal effects in panel data settings.
The main function is called pte
. The most important paramters that it takes in are subset_fun
and attgt_fun
. These are functions that the user should pass to pte
.
subset_fun
takes in the overall data, a group, a time period, and possibly other arguments and returns a data.frame
containing the relevant subset of the data, an outcome, and whether or not a unit should be considered to be in the treated or comparison group for that group/time. There is one example of a relevant subset function provided in the package: the two_by_two_subset
function. This function takes an original dataset, subsets it into pre- and post-treatment periods and denotes treated and untreated units. This particular subset is perhaps the most common/important one for thinking about treatment effects with panel data.
The other main function is attgt_fun
. This function should be able to take in the correct subset of data, possibly along with other arguments to the function, and report an ATT for that subset. With minor modification, this function should be availble for most any sort of treatment effects application --- for example, if you can solve the baseline 2x2 case in difference in differences, you should use that function here, and the pte
package will take care of dealing with the variation in treatment timing.
If attgt_fun
returns an influence function, then the pte
package will also conduct inference using the multiplier bootstrap (which is fast) and produce uniform confidence bands (which adjust for multiple testing).
The default output of pte
is an overall treatment effect on the treated (i.e., across all groups that participate in the treatment in any time period) and dynamic effects (i.e., event studies). More aggregations are possible, but these seem to be the leading cases; aggregations of group-time average treatment effects are discussed at length in Callaway and Sant'Anna (2021).
Here are a few examples:
The did
package, which is based on Callaway and Sant'Anna (2021), includes estimates of group-time average treatment effects, ATT(g,t), based on a difference in differences identification strategy. The following example demonstrates that it is easy to compute group-time average treatment effects using difference in differences using the pte
package. [Note: This is definitely not the recommended way of doing this as there is very little error handling, etc. here, but it is rather a proof of concept. You should use the did
package for this case.]
This example reproduces DID estimates of the effect of the minimum wage on employment using data from the did
package.
library(did) data(mpdta) did_res <- pte(yname="lemp", gname="first.treat", tname="year", idname="countyreal", data=mpdta, setup_pte_fun=setup_pte, subset_fun=two_by_two_subset, attgt_fun=did_attgt, xformla=~lpop) summary(did_res) ggpte(did_res)
What's most interesting here, is that the only "new" code that needs to be writte is in the did_attgt
function. You will see that this is a very small amount of code.
As a next example, consider trying to estimate effects of Covid-19 related policies during a pandemic. The estimates below are for the effects of state-leve shelter-in-place orders during the early part of the pandemic.
Callaway and Li (2021) argue that a particular unconfoundedness-type strategy is more appropriate in this context than DID-type strategies due to the spread of Covid-19 cases being highly nonlinear. However, they still deal with the challenge of variation in treatment timing. Therefore, it is still useful to think about group-time average treatment effects, but the DID strategy should be replaced with their particular unconfoundedness type assumption.
The pte
package is particularly useful here.
# formula for covariates xformla <- ~ current + I(current^2) + region + totalTestResults
# drop some data as in paper trim_id_list <- lapply(c(10,15,20,25,30), did::trimmer, tname="time.period", idname="state_id", gname="group", xformla=xformla, data=covid_data, control_group="nevertreated", threshold=0.95) time_id_list <- unlist(trim_id_list) # unique(subset(covid_data, state_id %in% time_id_list)$state) covid_data2 <- subset(covid_data, !(state_id %in% time_id_list))
covid_res <- pte(yname="positive", gname="group", tname="time.period", idname="state_id", data=covid_data2, setup_pte_fun=setup_pte_basic, subset_fun=two_by_two_subset, attgt_fun=covid_attgt, xformla=xformla, max_e=21, min_e=-10) summary(covid_res) ggpte(covid_res) + ylim(c(-1000,1000))
What's most interesting is just how little code needs to be written here. The only new code required is the ppe::covid_attgt
function which is available here, and, as you can see, this is very simple.
The code above used the multiplier bootstrap. The great thing about the multiplier bootstrap is that it's fast. But in order to use it, you have to work out the influence function for the estimator of ATT(g,t). Although I pretty much always end up doing this, it can be tedious, and it can be nice to get a working version of the code for a project going before working out the details on the influence function.
The pte
package can be used with the empirical bootstrap. There are a few limitations. First, it's going to be substantially slower. Second, this code just reports pointwise confidence intervals. However, this basically is set up to fit into my typical workflow, and I see this as a way to get preliminary results.
Let's demonstrate it. To do this, consider the same setup as in Example 1, but where no influence function is returned. Let's write the code for this:
# did with no influence function did_attgt_noif <- function(gt_data, xformla, ...) { # call original function did_gt <- did_attgt(gt_data, xformla, ...) # remove influence function did_gt$inf_func <- NULL did_gt }
Now, we can show the same sorts of results as above
did_res_noif <- pte(yname="lemp", gname="first.treat", tname="year", idname="countyreal", data=mpdta, setup_pte_fun=setup_pte, subset_fun=two_by_two_subset, attgt_fun=did_attgt_noif, #this is only diff. xformla=~lpop) summary(did_res_noif) ggpte(did_res_noif)
What's exciting about this is just how little new code needs to be written.
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