ArticleStatistics in medicine2021
Vector-based kernel weighting: A simple estimator for improving precision and bias of average treatment effects in multiple treatment settings.
Article in Statistics in medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
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Who cites it
1 citing paper in PubMed, 4 citations in OpenAlex.
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Corrections and comments
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Authors and funding
3 authors at 2 institutions in 1 country.
Funding
Abstract
Treatment effect estimation must account for observed confounding, in which factors affect treatment assignment and outcomes simultaneously. Ignoring observed confounding risks concluding that a helpful treatment is not beneficial or that a treatment is safe when actually harmful. Propensity score matching or weighting adjusts for observed confounding, but the best way to use propensity scores for multiple treatments is unknown. It is unclear when choice of a different weighting or matching strategy leads to divergent inferences. We used Monte Carlo simulations (1000 replications) to examine sensitivity of multivalued treatment inferences to propensity score weighting or matching strategies. We consider five variants of propensity score adjustment: inverse probability of treatment weights, generalized propensity score matching, kernel weights (KW), vector matching, and a new hybrid that is easily implemented-vector-based kernel weighting (VBKW). VBKW matches observations with similar propensity score vectors, assigning greater KW to observations with similar probabilities within a given bandwidth. We varied degree of propensity score model misspecification, sample size, treatment effect heterogeneity, initial covariate imbalance, and sample distribution across treatment groups. We evaluated sensitivity of results to propensity score estimation technique (multinomial logit or multinomial probit). Across simulations, VBKW performed equally or better than the other methods in terms of bias, efficiency, and covariate balance measured via prognostic scores. Our simulations suggest that VBKW is amenable to full automation and is less sensitive to PS model misspecification than other methods used to account for observed confounding in multivalued treatment analyses.
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Registered trials
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.