Implements a deficiency-theoretic framework for causal inference,
grounded in the classical theory of statistical experiment comparison,
as described in Akdemir (2026)
causaldef implements a deficiency-theoretic framework for causal inference, grounded in the classical theory of statistical experiment comparison, providing quantitative bounds on information loss from confounding, selection bias, and distributional shift.
Unlike traditional sensitivity analysis which focuses on “how much bias”
exists, causaldef answers the decision-theoretic question: “how much
regret” might we incur by acting on this evidence?
The deficiency δ is a theoretical measure of the information gap
between your observational data and a perfect randomized trial. In
practice, causaldef provides a computable proxy $\widehat{\delta}$
based on propensity-score TV balance (PS-TV), which is informative about
overlap/positivity and residual confounding risk.
For bounded utilities with range $M$ (max minus min), the manuscript provides:
policy_regret_bound() reports both quantities.
causaldef is theory-forward, but not every exported quantity is the
same kind of object. The package distinguishes:
policy_regret_bound(), policy_regret_bound_vc(),
confounding_frontier(), sharp_lower_bound(), and
wasserstein_deficiency_gaussian()estimate_deficiency() currently
returns a PS-TV proxy, not a generic nonparametric estimator of the
exact deficiencync_diagnostic() combines an observable
residual-association diagnostic with a user-supplied alignment
parameter kappaYou can install the development version of causaldef from GitHub with:
# install.packages("devtools")
devtools::install_github("denizakdemir/causaldef")
estimate_deficiency() (PS-TV overlap/balance
proxy)policy_regret_bound() (transfer penalty +
minimax floor)nc_diagnostic() (falsification and
bounds)confounding_frontier() (linear-Gaussian
confounding frontier)causal_spec_survival(),
causal_spec_competing()library(causaldef)
set.seed(42)
# Simulate confounded data (W satisfies back-door criterion)
n <- 500
W <- rnorm(n)
A <- rbinom(n, 1, plogis(0.5 * W))
Y <- 1 + 2 * A + W + rnorm(n)
df <- data.frame(W = W, A = A, Y = Y)
# 1. Define the causal problem
spec <- causal_spec(
data = df,
treatment = "A",
outcome = "Y",
covariates = "W"
)
#> ✔ Created causal specification: n=500, 1 covariate(s)
# 2. Estimate a deficiency proxy (PS-TV) for different strategies
results <- estimate_deficiency(
spec,
methods = c("unadjusted", "iptw", "aipw"),
n_boot = 100
)
#> ℹ Estimating deficiency: unadjusted
#> ℹ Estimating deficiency: iptw
#> ℹ Estimating deficiency: aipw
print(results)
#>
#> -- Deficiency Proxy Estimates (PS-TV) ------
#>
#> Method Delta SE CI Quality
#> unadjusted 0.1190 0.0230 [0.1048, 0.1982] Insufficient (Red)
#> iptw 0.0212 0.0099 [0.0142, 0.0537] Excellent (Green)
#> aipw 0.0212 0.0087 [0.0154, 0.0483] Excellent (Green)
#> Note: delta is a propensity-score TV proxy (overlap/balance diagnostic).
#>
#> Best method: aipw (delta = 0.0212 )
Interpretation: Unadjusted $\widehat{\delta} \approx$ 0.119; after IPTW/AIPW, $\widehat{\delta} \approx$ 0.021.
If we use this evidence to make a policy decision (e.g., approve a drug), what is the worst-case loss?
# Calculate bounds for a utility range of [0, 1]
bounds <- policy_regret_bound(results, utility_range = c(0, 1), method = "aipw")
#> ℹ Transfer penalty: 0.0212 (delta = 0.0212)
print(bounds)
#>
#> -- Policy Regret Bounds -------------------------------------------------
#>
#> * Deficiency delta: 0.0212
#> * Delta mode: point
#> * Delta method: aipw
#> * Delta selection: pre-specified method
#> * Utility range: [0, 1]
#> * Transfer penalty: 0.0212 (additive regret upper bound)
#> * Minimax floor: 0.0106 (worst-case lower bound)
#>
#> Note: this is a plug-in bound using a deficiency proxy rather than an identified exact deficiency.
#>
#> Interpretation: Transfer penalty is 2.1 % of utility range given delta
plot(bounds, type = "safety_curve")
The plug-in transfer penalty is 0.0212 on a 0–1 utility scale; the minimax safety floor is 0.0106.
Check if the “Adjusted” strategy actually removes confounding using a negative control outcome $Y_{nc}$ (known to be unaffected by treatment).
# Add a negative control to simulation
df$Y_nc <- W + rnorm(n) # Correlated with W (confounder) but not A
spec_nc <- causal_spec(
data = df,
treatment = "A",
outcome = "Y",
covariates = "W",
negative_control = "Y_nc"
)
#> ✔ Created causal specification: n=500, 1 covariate(s)
# Run diagnostic
set.seed(123)
nc_test <- nc_diagnostic(spec_nc, method = "iptw")
#> ℹ Using kappa = 1 (conservative). Consider domain-specific estimation or sensitivity analysis via kappa_range.
#> ✔ No evidence against causal assumptions (p = 0.91045 )
print(nc_test)
#>
#> -- Negative Control Diagnostic ----------------------------------------
#>
#> * screening statistic (weighted corr): 0.0089
#> * delta_NC (association proxy): 0.0089
#> * delta bound (under kappa alignment): 0.0089 (kappa = 1 )
#> * screening p-value: 0.91045
#> * screening method: weighted_permutation_correlation
#>
#> RESULT: NOT REJECTED. This is a screening result, not proof that confounding is absent.
#> NOTE: Your effect estimate must exceed the Noise Floor (delta_bound) to be meaningful.
Here, the screen does not reject (p = 0.91), but that is not proof that confounding is absent; the observable proxy is $\widehat{\delta}_{NC} \approx$ 0.009.
data(hct_outcomes)
# Create an explicit 0/1 event indicator for death
hct <- hct_outcomes
hct$event_death <- as.integer(as.character(hct$event_status) == "Death")
spec_surv <- causal_spec_survival(
data = hct,
treatment = "conditioning_intensity",
time = "time_to_event",
event = "event_death",
covariates = c("age", "disease_status", "kps", "donor_type"),
estimand = "RMST",
horizon = 24
)
#> ✔ Created survival causal specification: n=800, 131 events
def_surv <- estimate_deficiency(spec_surv, methods = c("unadjusted", "iptw"), n_boot = 50)
#> ℹ Inferred treatment value: Reduced
#> ℹ Estimating deficiency: unadjusted
#> ℹ Estimating deficiency: iptw
print(def_surv)
#>
#> -- Deficiency Proxy Estimates (PS-TV) ------
#>
#> Method Delta SE CI Quality
#> unadjusted 0.3030 0.0460 [0.2505, 0.4189] Insufficient (Red)
#> iptw 0.0644 0.0219 [0.0498, 0.136] Caution (Yellow)
#> Note: delta is a propensity-score TV proxy (overlap/balance diagnostic).
#>
#> Best method: iptw (delta = 0.0644 )
bounds_surv <- policy_regret_bound(def_surv, utility_range = c(0, 24), method = "iptw")
#> ℹ Transfer penalty: 1.5457 (delta = 0.0644)
print(bounds_surv)
#>
#> -- Policy Regret Bounds -------------------------------------------------
#>
#> * Deficiency delta: 0.0644
#> * Delta mode: point
#> * Delta method: iptw
#> * Delta selection: pre-specified method
#> * Utility range: [0, 24]
#> * Transfer penalty: 1.5457 (additive regret upper bound)
#> * Minimax floor: 0.7728 (worst-case lower bound)
#>
#> Note: this is a plug-in bound using a deficiency proxy rather than an identified exact deficiency.
#>
#> Interpretation: Transfer penalty is 6.4 % of utility range given delta
In this death-endpoint survival example, IPTW reduces the PS-TV proxy
from about 0.303 to about 0.064, yielding a transfer penalty of about
1.55 months and a minimax floor of about 0.77 months on the 0–24 month
scale. For full relapse-versus-death analyses, use
causal_spec_competing() and estimate_deficiency_competing().
Based on Akdemir (2026), “Constraints on Causal Inference as Experiment Comparison”.
The core theorem links the deficiency $\delta$ (Total Variation distance) to the max-min regret:
$$ \text{Regret}{do}(\pi) \leq \text{Regret}{obs}(\pi) + M \cdot \delta $$
Where $M$ is the range of the utility function. In practice, the package often provides plug-in bounds by feeding a computable proxy/estimate (e.g., $\widehat{\delta}$) into the regret formula, so the interpretation should track the underlying quantity being supplied.
@misc{causaldef,
title = {causaldef: Decision-Theoretic Causal Diagnostics via Experiment Deficiency},
author = {Akdemir, Deniz},
year = {2026},
doi = {10.5281/zenodo.21877511}
}