Evidence map›Paper›PMID 35753014›Full record

ArticleLifetime data analysis2022

Semi-supervised approach to event time annotation using longitudinal electronic health records.

Liang Liang, Jue Hou, Hajime Uno, Kelly Cho, Yanyuan Ma, Tianxi Cai

Abstract read
In one paragraph

Article in Lifetime data analysis, 2022. 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. Machine learning approaches for electronic health records phenotyping: a methodical review.Journal of the American Medical Informatics Association : JAMIA · 2023
    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

6 authors.

Liang LiangDepartment of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, MA, USA.
Jue HouDepartment of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, MA, USA.
Hajime UnoDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Kelly ChoMassachusetts Veterans Epidemiology Research and Information Center, US Department of Veteran Affairs, Boston, MA, USA.
Yanyuan MaDepartment of Statistics, Penn State University, University Park, PA, Boston, USA.
Tianxi CaiDepartment of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, MA, USA. tcai@hsph.harvard.edu.ORCID 0000-0002-5379-2502

Funding

Semi-supervised Approaches to Denoising Electronic Health Records Data for Risk PredictionR01LM013614 · NLM · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI CAI, TIANXI, GUO, ZIJIAN · 2021 to 2024
$1.4M
Semi-supervised Algorithms for Risk Assessment with Noisy EHR DataR21CA242940 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI CAI, TIANXI · 2019 to 2020
$370k
NCI NIH HHS R21 CA242940NLM NIH HHS R01 LM013614
6 · The paper itself

Abstract

Large clinical datasets derived from insurance claims and electronic health record (EHR) systems are valuable sources for precision medicine research. These datasets can be used to develop models for personalized prediction of risk or treatment response. Efficiently deriving prediction models using real world data, however, faces practical and methodological challenges. Precise information on important clinical outcomes such as time to cancer progression are not readily available in these databases. The true clinical event times typically cannot be approximated well based on simple extracts of billing or procedure codes. Whereas, annotating event times manually is time and resource prohibitive. In this paper, we propose a two-step semi-supervised multi-modal automated time annotation (MATA) method leveraging multi-dimensional longitudinal EHR encounter records. In step I, we employ a functional principal component analysis approach to estimate the underlying intensity functions based on observed point processes from the unlabeled patients. In step II, we fit a penalized proportional odds model to the event time outcomes with features derived in step I in the labeled data where the non-parametric baseline function is approximated using B-splines. Under regularity conditions, the resulting estimator of the feature effect vector is shown as root-n consistent. We demonstrate the superiority of our approach relative to existing approaches through simulations and a real data example on annotating lung cancer recurrence in an EHR cohort of lung cancer patients from Veteran Health Administration.

Indexed as

Electronic Health RecordsLung NeoplasmsAlgorithmsDatabases, FactualHumansNeoplasm Recurrence, LocalCensoringElectronic health recordsFunctional principle component analysisMorePoint processProportional odds modelSemi-supervised learning

Identifiers

PMID35753014
PMCPMC10044535

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Registered trials

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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.