Evidence map›Paper›PMID 41990098›Full record

ArticleJMIR medical informatics2026

Methodological Development and Assessing Prescribing Determinants Through Cumulative Drug Exposure in Hospitalized Patients: Proof-of-Concept Retrospective Study.

Mathilde Bories, Guillaume Bouzillé, Marc Cuggia, Pascal Le Corre, Aurélie Bannay

Abstract read
In one paragraph

Article in JMIR medical informatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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

5 authors.

Mathilde BoriesInserm, Laboratoire Traitement du Signal et de l'Image-UMR 1099, Centre Hospitalier Universitaire de Rennes, Université de Rennes, LTSI - Laboratoire Traitement du Signal et de l'Image, Université de Rennes, Campus Santé - Bâtiment 15b, 2 avenue du Professeur Léon Bernard, Rennes, 35000, France, 33 675438670.ORCID 0000-0001-9092-4298
Guillaume BouzilléInserm, Laboratoire Traitement du Signal et de l'Image-UMR 1099, Centre Hospitalier Universitaire de Rennes, Université de Rennes, LTSI - Laboratoire Traitement du Signal et de l'Image, Université de Rennes, Campus Santé - Bâtiment 15b, 2 avenue du Professeur Léon Bernard, Rennes, 35000, France, 33 675438670.ORCID 0000-0002-3637-6558
Marc CuggiaInserm, Laboratoire Traitement du Signal et de l'Image-UMR 1099, Centre Hospitalier Universitaire de Rennes, Université de Rennes, LTSI - Laboratoire Traitement du Signal et de l'Image, Université de Rennes, Campus Santé - Bâtiment 15b, 2 avenue du Professeur Léon Bernard, Rennes, 35000, France, 33 675438670.ORCID 0000-0001-6943-3937
Pascal Le CorrePôle Pharmacie, Secteur Pharmacotechnie et Onco-Pharmacie, Centre Hospitalier Universitaire de Rennes, Rennes, France.ORCID 0000-0003-4483-0957
Aurélie BannayUniversité de Lorraine, Centre Hospitalier Régional Universitaire de Nancy, Centre national de la recherche scientifique, Inria, Laboratoire lorrain de recherche en informatique et ses applications, Nancy, France.ORCID 0000-0002-1631-566X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Preventing adverse drug reactions requires accurate monitoring of drug exposure throughout patient care. Conventional metrics, measured at admission or discharge, fail to capture the dynamic and cumulative nature of drug burden during hospitalization. Improving exposure assessment is essential to support clinical decision-making and medication safety. Clinical data warehouses (CDWs), which integrate detailed drug administration records, enable the retrospective reuse of hospital data to develop more granular and dynamic measures of in-hospital drug exposure. Objective: This exploratory proof-of-concept study aimed to introduce 2 cumulative drug exposure metrics computed from CDW: cumulative drug exposure (CDE) and cumulative drug exposure density (CDED). The study also aimed to compare these metrics with conventional metrics, primarily as a methodological development for characterizing prescribing determinants in hospitalized patients. Methods: We conducted a retrospective study using the eHOP CDW at Rennes University Hospital. Adults hospitalized for hematological malignancies were included. Four prescribing determinants were analyzed: polypharmacy (PP), hyperpolypharmacy (HPP), drug-drug interactions (DDIs), and potentially inappropriate medications (PIMs). CDE quantified the number of days each determinant was present, while CDED normalized this value to hospital length of stay. Analyses combined descriptive statistics, Spearman correlations, and factorial analysis of mixed data (FAMD). Results: Mean CDE values were 10.5 days for PP, 5.7 for HPP, 64.7 for DDIs, and 19.0 for PIMs (≥65 years). CDED values ranged from 0.3 to 3.2. Conventional metrics at admission were weakly correlated with cumulative exposure measures (eg, DDIs: rs=0.04, P=.752; PP: rs=-0.04, P=.757; HPP: rs=0.11, P=.364). Stronger, significant correlations emerged at discharge (CDE DDIs: rs=0.44, CDED: rs=0.46; both P<.001). PIMs showed strong significant correlations at both time points. FAMD highlighted that cumulative metrics contributed independently to the principal components, capturing dynamics of drug exposure not reflected by conventional indicators. Conclusions: CDE and CDED, derived from real-time CDW data, offer reproducible and scalable alternatives to conventional metrics for characterizing drug exposure in patients hospitalized for severe conditions. They provide a more accurate characterization of drug burden and hold promise for pharmacoepidemiological research and clinical decision support.

Indexed as

Drug PrescriptionsHospitalizationAdultAgedDrug InteractionsDrug-Related Side Effects and Adverse ReactionsFemaleHumansMaleMiddle AgedPolypharmacyProof of Concept StudyRetrospective Studiesclinical data warehousecumulative drug exposuredrug interactionshyperpolypharmacypolypharmacypotentially inappropriate medications

Identifiers

PMID41990098
PMCPMC13086184

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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.