ArticleAmerican journal of epidemiology2024
High-dimensional Iterative Causal Forest (hdiCF) for Subgroup Identification Using Health Care Claims Data.
Article in American journal of epidemiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
5 citing papers in PubMed.
- Multifactorial attribution for vancomycin-associated acute kidney injury.British journal of clinical pharmacology · 2026Article
- The heterogeneous treatment effects of statins on dementia: a target trial emulation with causal machine learning using integrated genetic and real-world data.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026Article
- A novel high dimensional approach to assess heterogeneous treatment effect in claims data.American journal of epidemiology · 2025Article
- Glucagon-like Peptide-1 Receptor Agonists in Asthma Exacerbations: An Application of High-Dimensional Iterative Causal Forest to Identify Subgroups.Pharmacoepidemiology and drug safety · 2025Article
- Glucagon-like Peptide 1 Receptor Agonists and Asthma Exacerbations: Which Patients Benefit Most?Annals of the American Thoracic Society · 2024Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
We recently developed a machine-learning subgrouping algorithm, iterative causal forest (iCF), to identify subgroups with heterogeneous treatment effects (HTEs) using predefined covariates. However, such predefined covariates may miss or poorly define important features leading to inaccurate subgrouping. To address such limitations, we developed a new semi-automatic subgrouping algorithm, hdiCF, which adapts methodology from high-dimensional propensity score for feature recognition in claims data. The hdiCF algorithm has 3 steps: 1) high-dimensional feature identification by International Classification of Diseases, Current Procedural Terminology, and Anatomical Therapeutic Chemical codes (in/outpatient diagnoses, procedures, prescriptions) and creation of ordinal variables by frequency of occurrence; 2) propensity score trimming and high-dimensional feature preparation; 3) iCF implementation to identify subgroups. We applied hdiCF in a 20% random sample of fee-for-service Medicare beneficiaries who initiated sodium-glucose cotransporter-2 inhibitors (SGLT2i) or glucagon-like peptide-1 receptor agonists to identify subgroups with HTEs for incidence of hospitalized heart failure. HdiCF findings were consistent with studies suggesting SGLT2i to be more beneficial for patients with pre-existing heart failure or chronic kidney disease. HdiCF is not dependent on prior hypotheses about HTEs and identifies subgroups with markers for potential HTEs in real-world evidence studies where active-comparator, new-user study designs limit the potential for unmeasured confounding.
Indexed as
Identifiers
What Socratic holds
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 Socratic graph.