Evidence map›Paper›PMID 40800216›Full record

ArticleBiometrika2025

Improving efficiency in transporting average treatment effects.

K E Rudolph, N T Williams, E A Stuart, I Díaz

Abstract read
In one paragraph

Article in Biometrika, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Data Fusion for Partial Identification of Causal Effects.Advances in neural information processing systems · 2025
    Article
  3. AAdvances in neural information processing systems · 2025
    Article
  4. Transporting: What Is It and How Do You Do It?Current epidemiology reports · 2025
    Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

K E RudolphDepartment of Epidemiology, Columbia University, 722 W. 168th St, New York, New York, 10032, U.S.A.
N T WilliamsDepartment of Epidemiology, Columbia University, 722 W. 168th St, New York, New York, 10032, U.S.A.
E A StuartDepartment of Biostatistics, Johns Hopkins University, 615 N. Wolfe St., Baltimore, Maryland, 21205, U.S.A.
I DíazDivision of Biostatistics, New York University Langone Health, 180 Madison Ave., New York, New York, 10016, U.S.A.

Funding

Design and analysis advances to improve generalizability of clinical trials for treating opioid use disorderR01DA056407 · NIDA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Kara Elizabeth Rudolph, Elizabeth A. Stuart · 2022 to 2026
$3.1M
Measuring and monitoring carbon nanotubes and their potential toxicityR41ES018002 · NIEHS · MEDICAL NANOTECHNOLOGIES, INC. · PI DRAPER, ROCKFORD KEITH · 2010 to 2010
$184k
NIDA NIH HHS R01 DA056407NIEHS NIH HHS R41 ES018002
6 · The paper itself

Abstract

We develop flexible, semiparametric estimators of the average treatment effect (ATE) transported to a new target population that offer potential efficiency gains. Transport may be of value when the ATE may differ across populations. We consider the setting where differences in the ATE are due to differences in the distribution of effect modifiers, baseline covariates that modify the treatment effect. First, we propose a collaborative one-step semiparametric estimator that can improve efficiency. This approach does not require researchers to have knowledge about which covariates are effect modifiers and which differ in distribution between the populations, but does require all covariates to be measured in the target population. Second, we propose two one-step semiparametric estimators that assume knowledge of which covariates are effect modifiers and which are both effect modifiers and differentially distributed between the populations. These estimators can be used even when not all covariates are observed in the target population; one requires that only effect modifiers are observed, and the other requires that only those modifiers that are also differentially distributed are observed. We use simulation to compare finite sample performance across our proposed estimators and an existing semiparametric estimator of the transported ATE, including in the presence of practical violations of the positivity assumption. Lastly, we apply our proposed estimators to a large-scale housing trial.

Indexed as

causal inferenceeffect modificationefficiencygeneralizabilitytransportability

Identifiers

PMID40800216
PMCPMC12338304

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.