Evidence map›Paper›PMID 33313606›Full record

ArticleProceedings : ... IEEE International Conference on Big Data. IEEE International Conference on Big Data2019

Frequent Causal Pattern Mining: A Computationally Efficient Framework For Estimating Bias-Corrected Effects.

Pranjul Yadav, Pedro J Caraballo, Michael Steinbach, Vipin Kumar, M Regina Castro, Gyorgy Simon

Abstract read
In one paragraph

Article in Proceedings : ... IEEE International Conference on Big Data. IEEE International Conference on Big Data, 2019. 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
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0citing 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

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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.

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

6 authors.

Pranjul YadavUniversity of Minnesota.
Pedro J CaraballoMayo Clinic.
Michael SteinbachUniversity of Minnesota.
Vipin KumarUniversity of Minnesota.
M Regina CastroMayo Clinic.
Gyorgy SimonUniversity of Minnesota.

Funding

Innovative Methods for Real-time Risk Modeling of Postoperative ComplicationsR01GM120079 · NIGMS · UNIVERSITY OF MINNESOTA · PI SIMON, GYORGY · 2017 to 2020
$2.1M
Extracting Typical and Atypical Disease Progression Patterns from Multi-Site EHRR01LM011972 · NLM · UNIVERSITY OF MINNESOTA · PI SIMON, GYORGY · 2015 to 2018
$1.3M
NIGMS NIH HHS R01 GM120079NLM NIH HHS R01 LM011972
6 · The paper itself

Abstract

Our aging population increasingly suffers from multiple chronic diseases simultaneously, necessitating the comprehensive treatment of these conditions. Finding the optimal set of drugs for a combinatorial set of diseases is a combinatorial pattern exploration problem. Association rule mining is a popular tool for such problems, but the requirement of health care for finding causal, rather than associative, patterns renders association rule mining unsuitable. To address this issue, we propose a novel framework based on the Rubin-Neyman causal model for extracting causal rules from observational data, correcting for a number of common biases. Specifically, given a set of interventions and a set of items that define subpopulations (e.g., diseases), we wish to find all subpopulations in which effective intervention combinations exist and in each such subpopulation, we wish to find all intervention combinations such that dropping any intervention from this combination will reduce the efficacy of the treatment. A key aspect of our framework is the concept of closed intervention sets which extend the concept of quantifying the effect of a single intervention to a set of concurrent interventions. Closed intervention sets also allow for a pruning strategy that is strictly more efficient than the traditional pruning strategy used by the Apriori algorithm. To implement our ideas, we introduce and compare five methods of estimating causal effect from observational data and rigorously evaluate them on synthetic data to mathematically prove (when possible) why they work. We also evaluated our causal rule mining framework on the Electronic Health Records (EHR) data of a large cohort of 152000 patients from Mayo Clinic and showed that the patterns we extracted are sufficiently rich to explain the controversial findings in the medical literature regarding the effect of a class of cholesterol drugs on Type-II Diabetes Mellitus (T2DM).

Identifiers

PMID33313606
PMCPMC7730315

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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.