Evidence map›Paper›PMID 40828436›Full record

ArticleInternational journal of clinical pharmacy2025

Clinical prediction of sodium valproate-induced movement disorders in hospitalized patients: a nomogram-based model using real-world data.

Liqiang Cui, Man Zhu, Tianlin Wang, Ao Gao, Pengzhi Zhao, Jing Xiao, Daihong Guo

Abstract readValidation Study
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In one paragraph

Article in International journal of clinical pharmacy, 2025. 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

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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.

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4 · The record

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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

7 authors.

Liqiang CuiChinese PLA Medical School, Beijing, 100853, China.
Man ZhuDepartment of Pharmacy, Medical Supplies Center, Chinese PLA General Hospital, No.28 Fuxing Road, Haidian District, Beijing, 100853, China.
Tianlin WangDepartment of Pharmacy, Medical Supplies Center, Chinese PLA General Hospital, No.28 Fuxing Road, Haidian District, Beijing, 100853, China.
Ao GaoDepartment of Pharmacy, Medical Supplies Center, Chinese PLA General Hospital, No.28 Fuxing Road, Haidian District, Beijing, 100853, China.
Pengzhi ZhaoDepartment of Pharmacy, Medical Supplies Center, Chinese PLA General Hospital, No.28 Fuxing Road, Haidian District, Beijing, 100853, China.
Jing XiaoCollege of Pharmacy, Chongqing Medical University, Chongqing, 400016, China.
Daihong GuoDepartment of Pharmacy, Medical Supplies Center, Chinese PLA General Hospital, No.28 Fuxing Road, Haidian District, Beijing, 100853, China. guodh301@163.com.

Funding

the Key Project of Medical Innovation Project in 2017 No. 17CXZ010the Project of Monitoring and Evaluation of the Use of Key Clinical Drugs" commissioned by the Chinese Association of Research Hospitals No. Y2024FH-YWPJ02
6 · The paper itself

Abstract

introductionDrug-induced movement disorders (DIMDs) are often underrecognized and challenging to diagnose and manage in clinical practice. Sodium valproate (VPA), a widely prescribed antiepileptic drug, causes DIMDs. Predictive modeling based on electronic medical records and machine learning algorithms offers a promising approach to improve early identification of adverse drug reactions (ADRs) and enhance clinical safety.

aimThis study aimed to conduct real-world active surveillance of VPA-associated DIMDs using hospital information system data, to identify independent risk factors, and to develop a clinically applicable prediction model for early warning and intervention.

methodIn this retrospective case-control study, data were collected from hospitalized patients prescribed sodium valproate between 2018 and 2022. DIMD cases were identified through automated alerts generated by the ADE Active Surveillance and Assessment System II, and subsequently confirmed using the Naranjo scale for manual causality assessment. A clinical prediction model was developed using LASSO logistic regression and was presented as a nomogram. Model performance was evaluated using area under the receiver operating characteristic (ROC) curve, calibration curve, decision curve analysis (DCA), and clinical impact curve (CIC).

resultsOf the 6692 patients screened, 98 were confirmed to have DIMDs, yielding an incidence rate of 1.46%. Four independent protective factors were identified: higher lymphocyte count, red blood cell count, serum sodium concentration, and co-administration of levetiracetam. The nomogram demonstrated good discrimination (AUC = 0.774), acceptable calibration (Brier score = 0.194), and strong clinical utility across a threshold probability range of 10-70%.The results of the external validation suggest that the efficiency of the model remained stable and showed no significant decline. It had better predictive ability in high- and medium-risk groups and had significant potential for clinical application. The incidence of DIMDs was significantly higher among patients receiving VPA for therapeutic purposes than among those receiving VPA prophylactically.

conclusionVPA-associated DIMDs are common in hospitalized patients. The prediction model based on routine clinical indicators enabled the identification of high- and middle-risk individuals, thereby facilitating timely monitoring and targeted interventions to reduce the burden of movement-related ADRs.

Indexed as

AnticonvulsantsDyskinesia, Drug-InducedNomogramsValproic AcidAdolescentAdultCase-Control StudiesChinaFemaleHumansIncidenceInpatientsMaleRetrospective StudiesRisk AssessmentYoung AdultAnticonvulsantsValproic AcidActive monitoringDrug-induced movement disordersDrug-related side effects and adverse reactionsLogistic modelsNomogramsPredictive modelValproic acid

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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.