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, July 21, 2025

Development of a novel nomogram to predict hemorrhagic transformation following endovascular treatment in patients with acute ischemic stroke

What is your competent? doctor's EXACT PROTOCOL to prevent hemorrhagic transformation? Oh, doesn't have one? So, you DON'T have a functioning stroke doctor, do you? Predicting hemorrhagic transformation is useless! You blithering idiots need to prevent the problem! Doesn't anyone in stroke know how to think?

Hemorrhagic transformation (23 posts to August 2018)

 Development of a novel nomogram to predict hemorrhagic transformation following endovascular treatment in patients with acute ischemic stroke


Xiaofen ZhaoXiaofen Zhao1Yuanjie LeYuanjie Le2Ting XinTing Xin3Guosheng GaoGuosheng Gao4Mengya ZhuMengya Zhu5Kai XunKai Xun2Xinliang Mao
Xinliang Mao2*
  • 1Department of Intensive Care Medicine, Ningbo No. 2 Hospital, Ningbo, China
  • 2Department of Emergency Medicine, Ningbo No. 2 Hospital, Ningbo, China
  • 3Department of Neurology, Tai’an Central Hospital, Tai’an, China
  • 4Department of Clinical Laboratory, Ningbo No. 2 Hospital, Ningbo, China
  • 5Department of Rheumatology and Immunology, Ningbo No. 2 Hospital, Ningbo, China

Background: Hemorrhagic transformation (HT) is a critical complication of endovascular therapy (EVT) in acute ischemic stroke (AIS), significantly worsening patient outcomes. Although various risk factors have been identified, existing predictive models often fail to account for the multimodal nature of EVT and the complex interplay of clinical, imaging, and laboratory variables.

Objective: This study aimed to develop and validate a nomogram-based predictive model to estimate the risk of HT in AIS patients undergoing EVT, incorporating clinical, imaging, and laboratory data to provide a comprehensive risk assessment.

Methods: A retrospective analysis was performed on 154 AIS patients who underwent EVT at a single center between 2018 and 2023. The least absolute shrinkage and selection and operator (LASSO) and multivariate logistic regression were used to identify the independent predictors of HT. A nomogram was constructed and evaluated using the area under the receiver operating characteristic curve (AUC-ROC), calibration curves, and decision curve analysis (DCA).

Results: Among the 154 patients, 34.4% experienced HT. The nomogram demonstrated excellent discriminatory ability, with an AUC-ROC of 0.82 (95% CI: 0.752–0.888), and strong calibration, as indicated by calibration curves. DCA confirmed the model’s clinical utility when the threshold probability was <0.8. Six independent prediction factors of HT were identified: atrial fibrillation (OR: 6.152), albumin (OR: 1.145), baseline NIHSS score (OR: 1.081), diastolic blood pressure (OR: 1.057), Trial of ORG 10172 in Acute Stroke Treatment (TOAST) Classification (TOAST_2, cardioembolic stroke subtype, OR: 0.201), and the location of obstructed blood vessel_5 (basilar artery occlusion, OR: 0.081).

Conclusion: The developed nomogram provides an accurate, individualized risk assessment of HT in AIS patients undergoing EVT. This tool enables personalized risk stratification, aiding clinicians in optimizing treatment strategies and improving patient outcomes. Further multicenter validation is warranted to generalize these findings.

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