mets (version 1.2.9)

binregATE: Average Treatment effect for censored competing risks data using Binomial Regression

Description

Under the standard causal assumptions we can estimate the average treatment effect E(Y(1) - Y(0)). We need Consistency, ignorability ( Y(1), Y(0) indep A given X), and positivity.

Usage

binregATE(
  formula,
  data,
  cause = 1,
  time = NULL,
  beta = NULL,
  treat.model = ~+1,
  cens.model = ~+1,
  offset = NULL,
  weights = NULL,
  cens.weights = NULL,
  se = TRUE,
  kaplan.meier = TRUE,
  cens.code = 0,
  no.opt = FALSE,
  method = "nr",
  augmentation = NULL,
  ...
)

Arguments

formula

formula with outcome (see coxph)

data

data frame

cause

cause of interest

time

time of interest

beta

starting values

treat.model

logistic treatment model given covariates

cens.model

only stratified cox model without covariates

offset

offsets for partial likelihood

weights

for score equations

cens.weights

censoring weights

se

to compute se's with IPCW adjustment, otherwise assumes that IPCW weights are known

kaplan.meier

uses Kaplan-Meier for IPCW in contrast to exp(-Baseline)

cens.code

gives censoring code

no.opt

to not optimize

method

for optimization

augmentation

to augment binomial regression

...

Additional arguments to lower level funtions

Author

Thomas Scheike

Details

The first covariate in the specification of the competing risks regression model must be the treatment effect that is binary. This is then model using a logistic regresssion using the standard binary double robust estimating equations that are then IPCW censoring adjusted using binomial regression.

Also computes the ATT and ATC, average treatment effect on the treated (ATT), E(Y(1) - Y(0) | A=1), and non-treated, respectively.

Rather than binomial regression we also consider a IPCW weighted version of standard logistic regression logitIPCWATE.

Examples

data(bmt)

brs <- binregATE(Event(time,cause)~tcell+platelet+age,bmt,time=50,cause=1,
  treat.model=tcell~platelet+age)
summary(brs)