The Role of Early Brain Injury assessment in a-SAH in predicting Structural Brain Abnormalities in Cognitive Impairments

Abstract

Background Early brain edema and/or Hematoma after aneurysmal subarachnoid hemorrhage (a-SAH) is an important impact determinant of clinical cognition outcomes. However, due to the lack of early assessment of the impact on cognitive structural systems, Therefore, there is a need to develop early predictive and/or decision-making models, termed the a-SAH Early Brain Edema/Hematoma Compression Neural (Structural Brain) Networks Score System (SEBE-HCNNSS). Methods 202 consecutive patients with spontaneous a-SAH and initial CT/ magnetic resonance imaging (MRI) scans (24 h of ictus) and follow-up 2 months. Clinically relevant factors and a variety of traditional different scale ratings were defined using Linear regression analysis (Univariate, multivariate). The risk factors with highest values for area under the curve (AUC) were included in the multivariate analysis and least absolute shrinkage and selection operator (LASSO) analysis or Cox regression analysis. Results A total of 177 patients were enrolled in this study, 43 patients had a high SEBE-HCNNSS classification (grade 3 to 5). After a mean follow-up of 2month, 121 individuals (68.36%) with a-SAH and 3 control subjects had incident CI. The CT inter-observer reliability of the SEBE-HCNNSS scale was high, with a Kappa value of 1. ROC analysis showed that the SEBE-HCNNSS scale (OR 3.322, 95% CI 2.312-7.237, p = 0.00025) was determined to be an independent predictor of edema, CI and unfavorable prognosis. These results were replicated in validation cohort. Conclusions SEBE-HCNNSS scale is fairly easy to perform and this study indicates that is good predictor value for CI and clinical outcomes after SAH. we suggest that it is practically useful prognostic instrument for the risk evaluation after a-SAH.

Competing Interest Statement

The authors have declared no competing interest.

Clinical Trial

none

Funding Statement

none

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The study protocol was approved by the Institutional Review Board (Clinical Research Ethics Committee of the First Hospital of Hebei Medical University, ID: 2023-1001), and all participants and their proxies provided written informed consent.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

留言 (0)

沒有登入
gif