Evidence map›Paper›PMID 42419976›Full record

ArticleNeurologia medico-chirurgica2026

Cytotoxic Lesions of the Corpus Callosum after Aneurysmal Subarachnoid Hemorrhage and Risk of Shunt-Dependent Chronic Hydrocephalus.

Takashi Iwata, Takayuki Ohno, Masafumi Tada, Noritaka Aihara, Tomoyasu Yamanaka, Teishiki Shibata, Yusuke Nishikawa, Mitsuhito Mase

Abstract readMulticenter Study
In one paragraph

Article in Neurologia medico-chirurgica, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Takashi IwataDepartment of Neurosurgery, Nagoya City University East Medical Center.
Takayuki OhnoDepartment of Neurosurgery, Nagoya City University East Medical Center.
Masafumi TadaDepartment of Research Development and Support Center, Neurology, Emergency Medicine, Nagoya City University East Medical Center.
Noritaka AiharaDepartment of Neurosurgery, Nagoya City University East Medical Center.
Tomoyasu YamanakaDepartment of Neurosurgery, Graduate School of Medical Science, Nagoya City University.
Teishiki ShibataDepartment of Neurosurgery, Graduate School of Medical Science, Nagoya City University.
Yusuke NishikawaDepartment of Neurosurgery, Graduate School of Medical Science, Nagoya City University.
Mitsuhito MaseDepartment of Neurosurgery, Graduate School of Medical Science, Nagoya City University.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytotoxic lesions of the corpus callosum are increasingly recognized after aneurysmal subarachnoid hemorrhage, but their prognostic value for shunt-dependent chronic hydrocephalus remains uncertain. We conducted a two-center retrospective cohort study of consecutive patients with aneurysmal subarachnoid hemorrhage who underwent brain magnetic resonance imaging within 7 days of onset. Cytotoxic lesions of the corpus callosum were defined as diffusion restriction with corresponding apparent diffusion coefficient reduction and were classified as none, small-type, or large-type using prespecified morphological criteria. The primary outcome was shunt-dependent chronic hydrocephalus, and the secondary outcome was unfavorable functional outcome (modified Rankin Scale score 3-6 at discharge or at approximately day 60). Associations were evaluated using prespecified multivariable logistic regression. As a sensitivity analysis, binary intraventricular hemorrhage was replaced by the Graeb score to account for quantitative intraventricular hemorrhage burden. Among 230 patients, 68 (29.6%) had cytotoxic lesions of the corpus callosum (small-type, 44 [19.1%]; large-type, 24 [10.4%]), and 62 (27.0%) developed shunt-dependent chronic hydrocephalus. After adjustment, small-type cytotoxic lesions of the corpus callosum (vs none) were associated with shunt-dependent chronic hydrocephalus (adjusted odds ratio 2.99, 95% confidence interval 1.31-6.83; p = 0.009) and unfavorable functional outcome (adjusted odds ratio 4.85, 95% confidence interval 1.79-13.93; p = 0.002). For large-type cytotoxic lesions of the corpus callosum, point estimates for both outcomes were elevated, but the 95% confidence interval included 1.0. Modified Fisher grade and Graeb score differed significantly across cytotoxic lesion of the corpus callosum subtypes (both p < 0.001). Early cytotoxic lesion of the corpus callosum assessment, particularly identification of small-type lesions, was associated with shunt-dependent chronic hydrocephalus and unfavorable outcome after aneurysmal subarachnoid hemorrhage.

Indexed as

Cerebrospinal Fluid ShuntsCorpus CallosumHydrocephalusSubarachnoid HemorrhageAgedChronic DiseaseFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedRetrospective Studiescerebrospinal fluid shuntscorpus callosumdiffusion magnetic resonance imaginghydrocephalussubarachnoid hemorrhage

Identifiers

PMID42419976
PMCPMC13550108

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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.