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, August 26, 2024

Predictors of early neurological deterioration in patients with acute ischemic stroke

 

You do realize survivors want prevention of early neurological deterioration rather than this USELESS PREDICTION?  I'd have you all fired!

Predictors of early neurological deterioration in patients with acute ischemic stroke

Yang ZhouYang Zhou1Yufan LuoYufan Luo2Huazheng Liang,,Huazheng Liang3,4,5Zhenyu WeiZhenyu Wei6Xiaofei YeXiaofei Ye7Ping Zhong
Ping Zhong6*Danhong Wu
Danhong Wu2*
  • 1Emergency Department, Shaoxing People’s Hospital, Shaoxing, Zhejiang, China
  • 2Department of Neurology, Shanghai Fifth People’s Hospital, Fudan University, Shanghai, China
  • 3Suzhou Industrial Park Monash Research Institute of Science and Technology, Suzhou, Jiangsu Province, China
  • 4Southeast University-Monash University Joint Graduate School, Suzhou, Jiangsu Province, China
  • 5Monash University-Southeast University Joint Research Institute, Suzhou, Jiangsu Province, China
  • 6Department of Neurology, Shanghai Yangpu District Shidong Hospital, Shanghai, China
  • 7Department of Military Health Statistics, School of Health Service, People's Liberation Army, Naval Medical University, Shanghai, China

Background: The present study aimed to develop a reliable and straightforward Nomogram by integrating various parameters to accurately predict the likelihood of early neurological deterioration (END) in patients with acute ischemic stroke (AIS).

Methods: Acute ischemic stroke patients from Shaoxing People’s Hospital, Shanghai Yangpu District Shidong Hospital, and Shanghai Fifth People’s Hospital were recruited based on specific inclusion and exclusion criteria. The primary outcome was END. Using the LASSO logistic model, a predictive Nomogram was generated. The performance of the Nomogram was evaluated using the ROC curve, the Hosmer-Lemeshow test, and a calibration plot. Additionally, the decision curve analysis was conducted to assess the effectiveness of the Nomogram.

Results: It was found that the Nomogram generated in the present study showed strong discriminatory performance in both the training and the internal validation cohorts when their ROC-AUC values were 0.715 (95% CI 0.648–0.782) and 0.725 (95% CI 0.631–0.820), respectively. Similar results were observed in two external validation cohorts when their ROC-AUC values were 0.685 (95% CI 0.541–0.829) and 0.673 (95% CI 0.545–0.800), respectively. In addition, CAD, SBP, neutrophils, TBil, and LDL were found to be positively correlated with the occurrence of END post-stroke, while lymphocytes and UA were negatively correlated.

Conclusion: Our study developed a novel Nomogram that includes CAD, SBP, neutrophils, lymphocytes, TBil, UA, and LDL and it demonstrated strong discriminatory performance in identifying AIS patients who are likely to develop END.

More at link.

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