ArticleHeliyon2024
Predictive modeling and interpretative analysis of risks of instability in patients with Myasthenia Gravis requiring intensive care unit admission.
Article in Heliyon, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
6 citing papers in PubMed.
- Associations between myasthenia Gravis and outcomes following cardiac surgery: an analysis of the nationwide inpatient sample.BMC anesthesiology · 2026Article
- Predictors of exacerbation in myasthenia gravis after minimal symptom expression: a bicenter cohort study.Frontiers in immunology · 2026Article
- Explainable machine learning for neurological outcome prediction in out-of-hospital cardiac arrest survivors undergoing targeted temperature management: a multi-cohort validation study.Journal of neuroengineering and rehabilitation · 2025Article
- Machine Learning in Myasthenia Gravis: A Systematic Review of Prognostic Models and AI-Assisted Clinical Assessments.Diagnostics (Basel, Switzerland) · 2025Review
- Personalized Predictions of Therapeutic Hypothermia Outcomes in Cardiac Arrest Patients with Shockable Rhythms Using Explainable Machine Learning.Diagnostics (Basel, Switzerland) · 2025Article
- The Value of Combined Detection of Systemic Inflammation Response Index and Prognostic Nutritional Index in Predicting Short-Term Prognosis of Myasthenia Gravis.Journal of inflammation research · 2025Article
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Objective: Myasthenia gravis (MG), a low-prevalence autoimmune disorder characterized by clinical heterogeneity and unpredictable disease fluctuations, presents significant risks of acute exacerbations requiring intensive care. These crises contribute substantially to patient morbidity and mortality. This study aimed to develop and validate machine-learning models for predicting intensive care unit (ICU) admission risk among patients with MG-related disease instability. Methods: In this retrospective analysis of 314 MG patients hospitalized between 2015 and 2018, we implemented four machine learning algorithms, including logistic regression, support vector machine, extreme gradient boosting (XGBoost), and random forest, to predict ICU admission risk. The models incorporated fourteen clinical parameters as predictive features. The SHapley Additive exPlanations method was utilized to assess the importance of factors associated with ICU admission. Results: Through 10-fold cross-validation, the XGBoost model demonstrated superior predictive performance (area under the receiver operating characteristic curve: 0.8943, accuracy: 0.8603, sensitivity: 0.7222, and specificity: 0.9125). Among the analyzed features, MG severity, as classified by the Myasthenia Gravis Foundation of America clinical classification, was identified as the most significant factor influencing ICU admission. Additionally, disease duration, a key continuous variable, was inversely correlated with the risk of ICU admission. Conclusion: MG severity is the primary determinant of ICU admission, with shorter disease duration increasing the risk, possibly due to greater susceptibility to exacerbations. The XGBoost model exhibited excellent performance and accuracy, effectively identifying critical clinical factors for predicting ICU admission risk in MG patients. This novel, personalized approach to risk stratification elucidates crucial risk factors and has the potential to enhance clinical decision-making, optimize resource allocation, and ultimately improve patient outcomes.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.