Evidence map›Paper›PMID 38355486›Full record

ArticleBMC medical informatics and decision making2024

Characterizing the limitations of using diagnosis codes in the context of machine learning for healthcare.

Lin Lawrence Guo, Keith E Morse, Catherine Aftandilian, Ethan Steinberg, Jason Fries, Jose Posada, Scott Lanyon Fleming, Joshua Lemmon, Karim Jessa, Nigam Shah and 1 more

Abstract read
In one paragraph

Article in BMC medical informatics and decision making, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

11 authors.

Lin Lawrence GuoProgram in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.
Keith E MorseDivision of Pediatric Hospital Medicine, Department of Pediatrics, Stanford University, Palo Alto, CA, USA.
Catherine AftandilianDivision of Hematology/Oncology, Department of Pediatrics, Stanford University, Palo Alto, CA, USA.
Ethan SteinbergStanford Center for Biomedical Informatics Research, Stanford University, Palo Alto, CA, USA.
Jason FriesStanford Center for Biomedical Informatics Research, Stanford University, Palo Alto, CA, USA.
Jose PosadaUniversidad del Norte, Barranquilla, Colombia.
Scott Lanyon FlemingStanford Center for Biomedical Informatics Research, Stanford University, Palo Alto, CA, USA.
Joshua LemmonProgram in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.
Karim JessaInformation Services, The Hospital for Sick Children, Toronto, ON, Canada.
Nigam ShahStanford Center for Biomedical Informatics Research, Stanford University, Palo Alto, CA, USA.
Lillian SungProgram in Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada. Lillian.sung@sickkids.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiagnostic codes are commonly used as inputs for clinical prediction models, to create labels for prediction tasks, and to identify cohorts for multicenter network studies. However, the coverage rates of diagnostic codes and their variability across institutions are underexplored. The primary objective was to describe lab- and diagnosis-based labels for 7 selected outcomes at three institutions. Secondary objectives were to describe agreement, sensitivity, and specificity of diagnosis-based labels against lab-based labels.

methodsThis study included three cohorts: SickKids from The Hospital for Sick Children, and StanfordPeds and StanfordAdults from Stanford Medicine. We included seven clinical outcomes with lab-based definitions: acute kidney injury, hyperkalemia, hypoglycemia, hyponatremia, anemia, neutropenia and thrombocytopenia. For each outcome, we created four lab-based labels (abnormal, mild, moderate and severe) based on test result and one diagnosis-based label. Proportion of admissions with a positive label were presented for each outcome stratified by cohort. Using lab-based labels as the gold standard, agreement using Cohen's Kappa, sensitivity and specificity were calculated for each lab-based severity level.

resultsThe number of admissions included were: SickKids (n = 59,298), StanfordPeds (n = 24,639) and StanfordAdults (n = 159,985). The proportion of admissions with a positive diagnosis-based label was significantly higher for StanfordPeds compared to SickKids across all outcomes, with odds ratio (99.9% confidence interval) for abnormal diagnosis-based label ranging from 2.2 (1.7-2.7) for neutropenia to 18.4 (10.1-33.4) for hyperkalemia. Lab-based labels were more similar by institution. When using lab-based labels as the gold standard, Cohen's Kappa and sensitivity were lower at SickKids for all severity levels compared to StanfordPeds.

conclusionsAcross multiple outcomes, diagnosis codes were consistently different between the two pediatric institutions. This difference was not explained by differences in test results. These results may have implications for machine learning model development and deployment.

Indexed as

HyperkalemiaNeutropeniaDelivery of Health CareHumansMachine LearningSensitivity and SpecificityCohort identificationDiagnostic coding practiceElectronic health recordsMachine learning for healthOutcome identification

Identifiers

PMID38355486
PMCPMC10868117

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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.