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.

Thursday, September 25, 2025

Development and validation of a nomogram for pressure injury risk prediction in stroke patients: a retrospective cohort study

Predictions ARE TOTALLY FUCKING USELESS! Create protocols that prevent this problem! You're so blitheringly stupid you need to be fired immediately!

 Development and validation of a nomogram for pressure injury risk prediction in stroke patients: a retrospective cohort study


Tang HaiyanTang Haiyan1Zhong QuanzhenZhong Quanzhen1Liao TingtingLiao Tingting1Fu QingFu Qing1Xie YuleiXie Yulei2Lv ZeweiLv Zewei1Zhou Mijuan
Zhou Mijuan1*Huang Bo
Huang Bo3*
  • 1Rehabilitation Department of Zigong First People’s Hospital, Zigong, Sichuan, China
  • 2Rehabilitation Department, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan, China
  • 3Otolaryngology, Zigong First People's Hospital, Zigong, Sichuan, China

Study design: Retrospective cohort study.

Objective: This study aimed to identify independent risk factors for pressure injury (PI) during the post-stroke recovery phase, develop and validate a nomogram prediction model to facilitate the identification of high-risk individuals for PI, and establish a theoretical framework for optimizing clinical intervention strategies.

Methods: Retrospective clinical data were collected from 284 hospitalized stroke patients in the recovery phase (including 85 PI cases) at the Affiliated Hospital of North Sichuan Medical College between January 2018 and December 2022. Participants were randomly allocated into training (70%) and internal validation (30%) cohorts. An external validation cohort comprising 60 stroke patients (30 PI cases) from Zigong First People’s Hospital (January 2023–January 2024) was additionally analyzed. Univariate analysis and LASSO regression were utilized to screen independent PU risk factors, followed by nomogram construction. Model performance was evaluated using the C-index, calibration curves, and Decision Curve Analysis (DCA). Comparative analyses were conducted against the Braden scale (Model 2) and a combined model incorporating the Braden scale (Model 3).

Results: Independent risk factors for PI in post-stroke recovery patients included hemorrhagic stroke subtype, advanced age, hypoalbuminemia, elevated leukocyte counts, and low Activities of Daily Living (ADL) scores. The nomogram model incorporating these five predictors demonstrated AUC values of 0.902 (training cohort), 0.935 (internal validation), and 0.936 (external validation), exceeding the predictive capacity of individual variables: stroke type (AUC = 0.642), age (AUC = 0.756), albumin level (AUC = 0.754), leukocyte count (AUC = 0.712), and ADL score (AUC = 0.839). Calibration curves indicated strong concordance between predicted and observed outcomes, while DCA confirmed substantial clinical net benefit. The Braden scale (AUC = 0.817) exhibited inferior predictive performance compared to our model, and the combined model (AUC = 0.901) showed no significant improvement, underscoring the parsimony and clinical utility of the proposed nomogram.

Conclusion: The nomogram developed in this study for predicting PIs in stroke recovery patients demonstrates high accuracy and discrimination, facilitating the early identification of high-risk individuals and aiding in the formulation of personalized intervention strategies.

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