Use of hospital big data to optimize and personalize laboratory test interpretation with an application.

Big data Optimization Personalization Platelets Precision medicine Reference population

Journal

Clinica chimica acta; international journal of clinical chemistry
ISSN: 1873-3492
Titre abrégé: Clin Chim Acta
Pays: Netherlands
ID NLM: 1302422

Informations de publication

Date de publication:
06 Jun 2024
Historique:
received: 27 10 2023
revised: 29 04 2024
accepted: 03 06 2024
medline: 9 6 2024
pubmed: 9 6 2024
entrez: 8 6 2024
Statut: aheadofprint

Résumé

In laboratory medicine, test results are generally interpreted with 95% reference intervals but correlations between laboratory tests are usually ignored. We aimed to use hospital big data to optimize and personalize laboratory data interpretation, focusing on platelet count. Laboratory tests were extracted from the hospital database and exploited by an algorithmic stepwise procedure. For any given laboratory test Y, an "optimized and personalized reference population" was defined by keeping only patients whose laboratory values for all Y-correlated tests fell within their own usual reference intervals, and by partitioning groups by individual-specific variables like sex and age category. The method was applied to platelet count. Laboratory data were recorded for 28,082 individuals. At the end of the algorithmic process, seven correlated laboratory tests were chosen, resulting in a reference sample of 159 platelet counts. A new 95 % reference interval was constructed [152-334 × 10 This method offers new perspectives in laboratory data interpretation, especially in patient screening and longitudinal follow-up.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
In laboratory medicine, test results are generally interpreted with 95% reference intervals but correlations between laboratory tests are usually ignored. We aimed to use hospital big data to optimize and personalize laboratory data interpretation, focusing on platelet count.
MATERIAL AND METHODS METHODS
Laboratory tests were extracted from the hospital database and exploited by an algorithmic stepwise procedure. For any given laboratory test Y, an "optimized and personalized reference population" was defined by keeping only patients whose laboratory values for all Y-correlated tests fell within their own usual reference intervals, and by partitioning groups by individual-specific variables like sex and age category. The method was applied to platelet count.
RESULTS RESULTS
Laboratory data were recorded for 28,082 individuals. At the end of the algorithmic process, seven correlated laboratory tests were chosen, resulting in a reference sample of 159 platelet counts. A new 95 % reference interval was constructed [152-334 × 10
CONCLUSION CONCLUSIONS
This method offers new perspectives in laboratory data interpretation, especially in patient screening and longitudinal follow-up.

Identifiants

pubmed: 38851476
pii: S0009-8981(24)02015-1
doi: 10.1016/j.cca.2024.119763
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

119763

Informations de copyright

Copyright © 2024 BIO LOGBOOK. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Ronan H Boutin (RH)

Bio Logbook, 1 rue Julien Videment, 44200 Nantes, France. Electronic address: ronan.boutin@biologbook.fr.

Jakez E Rolland (JE)

Nantes University, École Centrale Nantes, CNRS, LS2N, UMR 6004, 1 Rue de la Noë, 44321 Nantes, France. Electronic address: jakez.rolland@biologbook.fr.

Marie T Codet (MT)

Bio Logbook, 1 rue Julien Videment, 44200 Nantes, France. Electronic address: marie.codet@biologbook.fr.

Clément V Bézier (CV)

Bio Logbook, 1 rue Julien Videment, 44200 Nantes, France; University of Western Brittany, INSERM, LBAI, UMR1227, 9 Rue Félix le Dantec, 29200 Brest, France. Electronic address: clement.bezier@biologbook.fr.

Nathalie N Maes (NN)

Biostatistics and Medico-economic Information Department, University Hospital of Liege, Avenue de l'Hôpital 1, 4000 Liège, Belgium. Electronic address: nmaes@chuliege.be.

Philippe Kolh (P)

Department of Information Systems Management, University Hospital of Liege, Avenue de l'Hôpital 1, 4000 Liège, Belgium. Electronic address: philippe.kolh@chuliege.be.

Leila S Equinet (LS)

Bio Logbook, 1 rue Julien Videment, 44200 Nantes, France. Electronic address: leila.equinet@biologbook.fr.

Marie Thys (M)

Use of medico-economic data, University Hospital of Liege, Avenue de l'Hôpital 1, 4000 Liège, Belgium. Electronic address: mthys@chuliege.be.

Michel Moutschen (M)

Infectious Diseases Department, University Hospital of Liege, Avenue de l'Hôpital 1, 4000 Liège, Belgium. Electronic address: mmoutschen@chuliege.be.

Pierre-Jean Lamy (PJ)

Biopathology and Genetics of Cancers, Institute of Medical Analysis IMAGENOME, INOVIE, 90 rue Nicolas Chedeville, 34075 Montpellier, France; Clinical Research Department, Clinique BeauSoleil, Aesio Santé Méditerranée, 149 Rue de la Taillade, 34070 Montpellier, France. Electronic address: pierre-jean.lamy@labosud.fr.

Adelin I Albert (AI)

Biostatistics and Medico-economic Information Department, University Hospital of Liege, Avenue de l'Hôpital 1, 4000 Liège, Belgium; Public Health Department, University of Liege, Avenue de l'Hôpital 1, 4000 Liège, Belgium. Electronic address: aalbert@uliege.be.

Classifications MeSH