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.

Tuesday, May 12, 2026

Prediction models for early neurological deterioration in patients with acute ischemic stroke: a systematic review and critical appraisal

 

You're supposed to solve problems, NOT just predict them you blithering idiots. Hoping comeuppance hits you really hard when you are the 1 in 4 per WHO that has a stroke


Why are you incompetently? predicting failure to recover than delivering recovery?

Laziness? Incompetence? Or just don't care? NO leadership? NO strategy? Not my job? Not my Problem!

Had you been thinking at all you would be solving the  5 causes of the neuronal cascade of death in the first week saving hundreds of million to billions of neurons! Thus, preventing early neurological deterioration. Or don't you have two functioning neurons to rub together for a spark of intelligence?

Prediction models for early neurological deterioration in patients with acute ischemic stroke: a systematic review and critical appraisal

PMCID: PMC12971439  PMID: 41815732

Abstract

Background

Despite the proliferation of risk prediction models for early neurological deterioration (END) in patients with acute ischemic stroke (AIS), significant uncertainties persist regarding their methodological rigor and clinical applicability.

Objective

To systematically review and critically evaluate published prediction models for END in patients with AIS.

Methods

PubMed, Embase, Scopus, and the Cochrane Library were searched from inception to March 26, 2025. Data extraction was conducted using a standardized data extraction form by two independent reviewers based on the recommendations in the CHecklist for critical Appraisal and data extraction for systematic Reviews of prediction Modelling Studies (CHARMS). The Prediction model Risk Of Bias ASsessment Tool (PROBAST) checklist was used to assess the risk of bias and applicability. A qualitative synthesis was carried out to summarize the main characteristics of the included studies and constructed models.

Results

A total of 3,682 studies were retrieved, and 45 prediction models from 23 studies were included. Logistic regression and machine learning were utilized to establish END risk prediction models. The reported incidence of END in AIS patients varied from 6.6 to 43.7%, depending on the definition and study population. The most frequently used predictors were baseline National Institutes of Health Stroke Scale score and systolic blood pressure. The model’s discrimination performance, quantified by the area under the curve or concordance statistic, showed remarkable heterogeneity in predictive accuracy across studies. Critically, all included studies were assessed as having a high risk of bias, mainly owing to inappropriate data sources and poor reporting of the analysis domain. Concerns regarding applicability were generally low across studies.

Conclusion

This systematic review provides a comprehensive mapping and critical assessment of existing END prediction models in AIS. The findings reveal a critical gap that current models exhibit high risk of bias, limiting their reliability for clinical adoption. Future research should prioritize prospective model development and validation with pre-specified protocols, rigorous adherence to methodological standards such as the TRIPOD guidelines, adequate sample size estimations, robust external validation, as well as the update and clinical utility of existing predictive models.

Systematic review registration

PROSPERO, identifier (CRD42025643096).

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