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Dosage Regimen Designs: Nomograms and Tabulations01:23

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Nomograms and tabulations are vital tools used by clinicians to design accurate and individualized dosage regimens. These instruments provide a straightforward method for adjusting dosages based on individual patient characteristics, including age, weight, and physiological condition. The foundation of a drug's nomogram is population pharmacokinetic data collected and analyzed using specific models. This data simplifies complex equations, presenting them diagrammatically or tabularly for easy...
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A multicenter clinical nomogram for predicting post-stroke fatigue: development and validation.

Xiaoqing Tao1, Shan Wang2, Li Pang1

  • 1Department of Neurology, Beijing Anzhen Nanchong Hospital of Capital Medical University & Nanchong Central Hospital, Nanchong, Sichuan, China.

Frontiers in Neurology
|April 29, 2026
PubMed
Summary
This summary is machine-generated.

Post-stroke fatigue (PSF) prediction is improved by a new nomogram identifying key risk factors like lesion location and inflammation markers. This tool aids early identification of high-risk patients for timely intervention.

Keywords:
LASSOmulticenternomogrampost-stroke fatiguepredictors

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Area of Science:

  • Neurology
  • Medical Diagnostics
  • Biostatistics

Background:

  • Post-stroke fatigue (PSF) is a prevalent and debilitating complication following stroke.
  • The underlying pathophysiological mechanisms of PSF are not fully understood.
  • Reliable tools for predicting PSF are currently lacking.

Purpose of the Study:

  • To identify clinical and laboratory risk factors associated with PSF.
  • To develop and validate a predictive nomogram for early PSF detection.

Main Methods:

  • Retrospective cohort study involving 846 stroke patients.
  • Data included demographics, clinical information, imaging, and laboratory results.
  • LASSO and logistic regression models were used to construct and validate a nomogram.

Main Results:

  • Eight independent predictors for PSF were identified: specific lesion locations (brainstem, basal ganglia, thalamus), female sex, older age, mRS score, WBC count, and CRP level.
  • The developed nomogram demonstrated good predictive performance across training, internal, and external validation sets (AUCs ranging from 0.672 to 0.870).
  • The model showed good calibration and clinical utility.

Conclusions:

  • A clinically applicable nomogram for early PSF prediction was successfully developed.
  • The nomogram utilizes routinely available data, facilitating its integration into clinical practice.
  • This tool can assist in identifying high-risk individuals, enabling prompt therapeutic interventions.