Evidence map›Paper›PMID 34086345›Full record

ArticleBiometrics2022

Estimating mean potential outcome under adaptive treatment length strategies in continuous time.

Hao Sun, Ashkan Ertefaie, Brent A Johnson

Open access · greenAbstract read
In one paragraph

Article in Biometrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 92% of its field
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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

3 authors at 1 institution in 1 country.

Hao SunDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, New York.ORCID 0000-0002-9284-5320
Ashkan ErtefaieDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, New York.ORCID 0000-0003-2611-9512
Brent A JohnsonDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, New York.
University of Rochester · US

Funding

VISUAL INDICES OF NEUROTOXICITYP30ES001247 · NIEHS · UNIVERSITY OF ROCHESTER · PI B Paige Lawrence · 1985 to 2026
$42.8M
The University of Rochester's Clinical and Translational Science InstituteUL1TR002001 · NCATS · UNIVERSITY OF ROCHESTER · PI WILSON, KAREN M., ZAND, MARTIN S · 2016 to 2024
$34.6M
Analyzing Sequential, Multiple Assignment, Randomized Trials in the Presence of Partial ComplianceR01DA048764 · NIDA · UNIVERSITY OF ROCHESTER · PI ERTEFAIE, ASHKAN · 2019 to 2022
$1.6M
Optimal dynamic treatment strategies for controlling alcohol use: novel methods for selecting and incorporating effect modifiersR21AA027571 · NIAAA · UNIVERSITY OF ROCHESTER · PI ERTEFAIE, ASHKAN · 2019 to 2020
$423k
NCATS NIH HHS UL1 TR002001NIAAA NIH HHS R21 AA027571NIDA NIH HHS R01 DA048764NIEHS NIH HHS P30 ES001247
6 · The paper itself

Abstract

An adaptive treatment length strategy is a sequential stage-wise treatment strategy where a subject's treatment begins at baseline and one chooses to stop or continue treatment at each stage provided the subject has been continuously treated. The effects of treatment are assumed to be cumulative and, therefore, the effect of treatment length on clinical endpoint, measured at the end of the study, is of primary scientific interest. At the same time, adverse treatment-terminating events may occur during the course of treatment that require treatment be stopped immediately. Because the presence of a treatment-terminating event may be strongly associated with the study outcome, the treatment-terminating event is informative. In observational studies, decisions to stop or continue treatment depend on covariate history that confounds the relationship between treatment length on outcome. We propose a new risk-set weighted estimator of the mean potential outcome under the condition that time-dependent covariates update at a set of common landmarks. We show that our proposed estimator is asymptotically linear given mild assumptions and correctly specified working models. Specifically, we study the theoretical properties of our estimator when the nuisance parameters are modeled using either parametric or semiparametric methods. The finite sample performance and theoretical results of the proposed estimator are evaluated through simulation studies and demonstrated by application to the Enhanced Suppression of the Platelet Receptor IIb/IIIa with Integrilin Therapy (ESPRIT) infusion trial data.

Indexed as

Models, StatisticalComputer SimulationTreatment Outcomeadaptive treatment strategiescausal inferenceinformative eligibilitysurvival analysistreatment competing eventstreatment discontinuation

Identifiers

PMID34086345
PMCPMC9482146
OpenAlexW3164860187

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.