Evidence map›Paper›PMID 29930957›Full record

ArticleEGEMS (Washington, DC)2017

Extracting Deep Phenotypes for Chronic Kidney Disease Using Electronic Health Records.

Duc Thanh Anh Luong, Dinh Tran, Wilson D Pace, Miriam Dickinson, Joseph Vassalotti, Jennifer Carroll, Matthew Withiam-Leitch, Min Yang, Nikhil Satchidanand, Elizabeth Staton and 3 more

Abstract read
In one paragraph

Article in EGEMS (Washington, DC), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Journal of healthcare informatics research · 2019
    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

13 authors.

Duc Thanh Anh LuongUniversity at Buffalo.
Dinh TranUniversity at Buffalo.
Wilson D PaceUniversity of Colorado, Denver.
Miriam DickinsonUniversity of Colorado, Denver.
Joseph VassalottiIcahn School of Medicine at Mount Sinai.
Jennifer CarrollUniversity of Colorado, Denver.
Matthew Withiam-LeitchUniversity at Buffalo.
Min YangUniversity at Buffalo.
Nikhil SatchidanandUniversity at Buffalo.
Elizabeth StatonUniversity of Colorado, Denver.
Linda S KahnUniversity at Buffalo.
Varun ChandolaUniversity at Buffalo.
Chester H FoxUniversity at Buffalo.

Funding

Institutional Career DevelopmentKL2TR001413 · NCATS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI DUBOCOVICH, MARGARITA L · 2015 to 2024
$4.2M
NCATS NIH HHS KL2 TR001413
6 · The paper itself

Abstract

introductionAs chronic kidney disease (CKD) is among the most prevalent chronic diseases in the world with various rate of progression among patients, identifying its phenotypic subtypes is important for improving risk stratification and providing more targeted therapy and specific treatments for patients having different trajectories of the disease progression. PROBLEM DEFINITION AND DATA: The rapid growth and adoption of electronic health records (EHR) technology has created a unique opportunity to leverage the abundant clinical data, available as EHRs, to find meaningful phenotypic subtypes for CKD. In this study, we focus on extracting disease severity profiles for CKD while accounting for other confounding factors. PROBABILISTIC SUBTYPING MODEL: We employ a probabilistic model to identify precise phenotypes from EHR data of patients who have chronic kidney disease. Using this model, patient's eGFR trajectory is decomposed as a combination of four different components including disease subtype effect, covariate effect, individual long-term effect and individual short-term effect. EXPERIMENTAL

resultsThe discovered disease subtypes obtained by Probabilistic Subtyping Model for CKD are presented and their clinical relevance is analyzed. DISCUSSION: Several clinical health markers that were found associated with disease subtypes are presented with suggestion for further investigation on their use as risk predictors. Several assumptions in the study are also clarified and discussed.

conclusionThe large dataset of EHRs can be used to identify deep phenotypes retrospectively. Directions for further expansion of the model are also discussed.

Identifiers

PMID29930957
PMCPMC5983069

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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.