Evidence map›Paper›PMID 35364580›Full record

ArticleNeurosurgical focus2022

An integrated risk model stratifying seizure risk following brain tumor resection among seizure-naive patients without antiepileptic prophylaxis.

Michael C Jin, Jonathon J Parker, Laura M Prolo, Adela Wu, Casey H Halpern, Gordon Li, John K Ratliff, Summer S Han, Stephen L Skirboll, Gerald A Grant

Open access · diamondAbstract read
In one paragraph

Article in Neurosurgical focus, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 96% of its field
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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
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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

10 authors at 2 institutions in 1 country.

Michael C Jin1Department of Neurosurgery, Stanford University School of Medicine, Stanford.
Jonathon J Parker1Department of Neurosurgery, Stanford University School of Medicine, Stanford.
Laura M Prolo1Department of Neurosurgery, Stanford University School of Medicine, Stanford.
Adela Wu1Department of Neurosurgery, Stanford University School of Medicine, Stanford.
Casey H Halpern1Department of Neurosurgery, Stanford University School of Medicine, Stanford.
Gordon Li1Department of Neurosurgery, Stanford University School of Medicine, Stanford.
John K Ratliff1Department of Neurosurgery, Stanford University School of Medicine, Stanford.
Summer S Han1Department of Neurosurgery, Stanford University School of Medicine, Stanford.
Stephen L Skirboll1Department of Neurosurgery, Stanford University School of Medicine, Stanford.
Gerald A Grant1Department of Neurosurgery, Stanford University School of Medicine, Stanford.
Stanford University · USVA Palo Alto Health Care System · US

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Vittorio Sebastiano · 2007 to 2026
$71.4M
NCI NIH HHS P30 CA124435
6 · The paper itself

Abstract

objectiveThe natural history of seizure risk after brain tumor resection is not well understood. Identifying seizure-naive patients at highest risk for postoperative seizure events remains a clinical need. In this study, the authors sought to develop a predictive modeling strategy for anticipating postcraniotomy seizures after brain tumor resection.

methodsThe IBM Watson Health MarketScan Claims Database was canvassed for antiepileptic drug (AED)- and seizure-naive patients who underwent brain tumor resection (2007-2016). The primary event of interest was short-term seizure risk (within 90 days postdischarge). The secondary event of interest was long-term seizure risk during the follow-up period. To model early-onset and long-term postdischarge seizure risk, a penalized logistic regression classifier and multivariable Cox regression model, respectively, were built, which integrated patient-, tumor-, and hospitalization-specific features. To compare empirical seizure rates, equally sized cohort tertiles were created and labeled as low risk, medium risk, and high risk.

resultsOf 5470 patients, 983 (18.0%) had a postdischarge-coded seizure event. The integrated binary classification approach for predicting early-onset seizures outperformed models using feature subsets (area under the curve [AUC] = 0.751, hospitalization features only AUC = 0.667, patient features only AUC = 0.603, and tumor features only AUC = 0.694). Held-out validation patient cases that were predicted by the integrated model to have elevated short-term risk more frequently developed seizures within 90 days of discharge (24.1% high risk vs 3.8% low risk, p < 0.001). Compared with those in the low-risk tertile by the long-term seizure risk model, patients in the medium-risk and high-risk tertiles had 2.13 (95% CI 1.45-3.11) and 6.24 (95% CI 4.40-8.84) times higher long-term risk for postdischarge seizures. Only patients predicted as high risk developed status epilepticus within 90 days of discharge (1.7% high risk vs 0% low risk, p = 0.003).

conclusionsThe authors have presented a risk-stratified model that accurately predicted short- and long-term seizure risk in patients who underwent brain tumor resection, which may be used to stratify future study of postoperative AED prophylaxis in highest-risk patient subpopulations.

Indexed as

AnticonvulsantsBrain NeoplasmsAftercareHumansPatient DischargeRetrospective StudiesSeizuresAnticonvulsantsbrain tumormachine learningpredictive modelingseizuresstatus epilepticus

Identifiers

PMID35364580
PMCPMC12767542
OpenAlexW4221060693

What OpenQuestion holds

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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.