Evidence map›Paper›PMID 42227311›Full record

ArticleEpilepsia2026

Long-term prognosis of pharmacotherapy in newly diagnosed focal epilepsy patients and the predictive value of baseline seizure timing: A prospective cohort study.

Lei Sun, Shouye Sun, Xinyue Zhang, Weihong Lin

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Article in Epilepsia, 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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5 · Who and what money

Authors and funding

4 authors.

Lei SunDepartment of Neurology, First Hospital of Jilin University, Changchun, China.ORCID https://orcid.org/0009-0008-4949-196X
Shouye SunOrthopedic Medical Center, Second Hospital of Jilin University, Changchun, China.
Xinyue ZhangDepartment of Neurology, First Hospital of Jilin University, Changchun, China.
Weihong LinDepartment of Neurology, First Hospital of Jilin University, Changchun, China.ORCID https://orcid.org/0000-0002-7738-3949

Funding

National Natural Science Foundation of China 81971205
6 · The paper itself

Abstract

objectiveEpilepsy is a highly heterogeneous neurological disorder with significant prognostic variability. Accurate long-term outcome prediction remains a clinical challenge. We investigated pharmacotherapeutic prognosis and key predictors, particularly baseline seizure timing, to guide individualized treatment.

methodsThis prospective cohort study consecutively enrolled newly diagnosed focal epilepsy patients from the epilepsy specialist clinic of the Department of Neurology in our hospital between September 2015 and September 2025. We applied the Cox proportional hazards regression model to analyze the association between baseline factors and prognosis to identify independent predictors.

resultsA total of 563 patients with ≥36-month follow-up (median = 48.0 months, interquartile range [IQR] = 36.0-78.0) were analyzed. Among them, 64.8% (365/563) achieved seizure freedom at least once (median = 27.0 months, 95% confidence interval [CI] = 22.5-31.5), and 35.9% (131/365) relapsed after seizure freedom; 25.4% (143/563) developed drug resistance, with 6.3% (9/143) later converting to drug-responsive status. At the end of follow-up, 50.8% (286/563) were classified as drug-responsive, 23.8% (134/563) as having drug-resistant epilepsy (DRE), and 25.4% (143/563) as having an undetermined prognosis. Among patients with drug-responsive epilepsy, 63.6% (182/286) achieved seizure freedom with monotherapy. Multivariate analysis identified baseline wake-related seizures (hazard ratio [HR] = 1.743, 95% CI = 1.101-2.760, p = .018), cluster seizures (HR = 2.630, 95% CI = 1.845-3.749, p < .001), status epilepticus (HR = 2.126, 95% CI = 1.394-3.242, p < .001), and sleep problems (HR = 1.740, 95% CI = 1.178-2.572, p = .005) as independent DRE risk factors. SIGNIFICANCE: This prospective large-sample study revealed the inherent complexity and dynamic nature of prognostic assessment in patients with newly diagnosed focal epilepsy. We identified independent prognostic predictors for this condition, first confirming baseline wake-related seizures as a predictor of poor prognosis to guide early risk stratification and personalized treatment.

Indexed as

AnticonvulsantsEpilepsies, PartialSeizuresAdolescentAdultDrug Resistant EpilepsyFemaleFollow-Up StudiesHumansMalePrognosisProportional Hazards ModelsProspective StudiesTime FactorsYoung AdultAnticonvulsantsfocal epilepsyprognosisprospective cohortseizure timing

Identifiers

PMID42227311
PMCPMC13525569

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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.