Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Monday, September 14, 2026

An interpretable machine learning model for predicting prognosis in acute ischemic stroke with large vessel occlusion

 

Not solving a well-known problem is inexcusable!

I'll predict your comeuppance/screaming when you are the 1 in 4 per WHO that has a stroke  will be soul satisfying. 

An interpretable machine learning model for predicting prognosis in acute ischemic stroke with large vessel occlusion


  • Department of Medical Imaging Center, Affiliated Hospital of Qinghai University, Xining, China

Abstract


Objective: 


To develop and validate an interpretable nomogram that integrates an imaging score, clinical characteristics, and machine-learning models to predict 90-day functional outcomes in patients with acute ischemic stroke (AIS) and large-vessel occlusion (LVO).


Methods: 


We analyzed 240 AIS patients with anterior circulation LVO who underwent one-stop multimodal CT between October 2019 and December 2024. Fifty-two variables, including pretreatment clinical features, conventional and advanced imaging, and angiographic characteristics, were assessed. The 90-day modified Rankin Scale (mRS-90) was used as the prognostic endpoint; good and poor outcomes were defined as mRS-90 ≤ 2 and > 2, respectively. Patients were randomly assigned to training (80%, n = 192) and testing (20%, n = 48) cohorts. Least absolute shrinkage and selection operator (LASSO) regression was used to derive the imaging score, which was then combined with key clinical predictors to construct a nomogram. Clinical, imaging, and hybrid models were developed separately and evaluated using the area under the receiver operating characteristic curve (AUC), calibration curves, and decision curve analysis (DCA). Repeated stratified 5-fold cross-validation repeated 20 times was performed as a stability analysis of the fixed final model structures. SHapley Additive Explanations (SHAP) was applied to identify influential features and visualize feature importance and interactions.


Results: 


Among 240 patients, 162 (67.5%) had unfavorable 90-day functional outcomes. Patients with unfavorable outcomes were generally older, had higher admission NIHSS scores, and showed less favorable collateral and perfusion profiles. Age, admission NIHSS score, and onset-to-CT time were retained as clinical predictors, while eight imaging features were integrated into the imaging score. Adding the imaging score did not significantly improve discrimination in the testing cohort (ΔAUC, 0.0078; 95% CI, −0.0071 to 0.0227; P = 0.305). In repeated stratified 5-fold cross-validation performed 20 times, the mean AUCs were 0.942, 0.747, and 0.939 for the clinical, imaging, and hybrid models, respectively. SHAP analysis characterized the contributions of age, NIHSS, onset-to-CT time, and the composite imaging score within the four-input hybrid model.


Conclusions: 


An interpretable model combining routine clinical predictors with a multimodal CT-derived imaging score demonstrates promising predictive potential for 90-day functional outcome in patients with AIS-LVO.

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