<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3-mathml3.dtd">
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.3" xml:lang="EN">
<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Neurol.</journal-id>
<journal-title-group>
<journal-title>Frontiers in Neurology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Neurol.</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">1664-2295</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fneur.2026.1738430</article-id>
<article-version article-version-type="Version of Record" vocab="NISO-RP-8-2008"/>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Original Research</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Construction and validation of a prognostic model for clinical outcomes in patients with prolonged disorders of consciousness based on multidimensional indicators: a prospective cohort study</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Feng</surname>
<given-names>Zhen</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="conceptualization" vocab-term-identifier="https://credit.niso.org/contributor-roles/conceptualization/">Conceptualization</role>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="methodology" vocab-term-identifier="https://credit.niso.org/contributor-roles/methodology/">Methodology</role>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="investigation" vocab-term-identifier="https://credit.niso.org/contributor-roles/investigation/">Investigation</role>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Formal analysis" vocab-term-identifier="https://credit.niso.org/contributor-roles/formal-analysis/">Formal analysis</role>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Writing &#x2013; original draft" vocab-term-identifier="https://credit.niso.org/contributor-roles/writing-original-draft/">Writing &#x2013; original draft</role>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Zhang</surname>
<given-names>Qiaojun</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
<xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/3152605"/>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="validation" vocab-term-identifier="https://credit.niso.org/contributor-roles/validation/">Validation</role>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Data curation" vocab-term-identifier="https://credit.niso.org/contributor-roles/data-curation/">Data curation</role>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Writing &#x2013; review &#x0026; editing" vocab-term-identifier="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing &#x2013; review &#x0026; editing</role>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="supervision" vocab-term-identifier="https://credit.niso.org/contributor-roles/supervision/">Supervision</role>
</contrib>
</contrib-group>
<aff id="aff1"><institution>The Second Affiliated Hospital of Xi&#x2019;an Jiaotong University (Xibei Hospital)</institution>, <city>Xi&#x2019;an</city>, <state>Shanxi</state>, <country country="cn">China</country></aff>
<author-notes>
<corresp id="c001"><label>&#x002A;</label>Correspondence: Qiaojun Zhang, <email xlink:href="mailto:zqj1232025@163.com">zqj1232025@163.com</email></corresp>
</author-notes>
<pub-date publication-format="electronic" date-type="pub" iso-8601-date="2026-02-20">
<day>20</day>
<month>02</month>
<year>2026</year>
</pub-date>
<pub-date publication-format="electronic" date-type="collection">
<year>2026</year>
</pub-date>
<volume>17</volume>
<elocation-id>1738430</elocation-id>
<history>
<date date-type="received">
<day>03</day>
<month>11</month>
<year>2025</year>
</date>
<date date-type="rev-recd">
<day>20</day>
<month>01</month>
<year>2026</year>
</date>
<date date-type="accepted">
<day>30</day>
<month>01</month>
<year>2026</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2026 Feng and Zhang.</copyright-statement>
<copyright-year>2026</copyright-year>
<copyright-holder>Feng and Zhang</copyright-holder>
<license>
<ali:license_ref start_date="2026-02-20">https://creativecommons.org/licenses/by/4.0/</ali:license_ref>
<license-p>This is an open-access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License (CC BY)</ext-link>. The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</license-p>
</license>
</permissions>
<abstract>
<sec>
<title>Objective</title>
<p>To develop and validate a prognostic prediction model for patients with prolonged disorders of consciousness (pDoC) based on multidimensional clinical indicators, aiming to improve prognostic accuracy and provide objective support for clinical decision-making.</p>
</sec>
<sec>
<title>Methods</title>
<p>A prospective cohort study was conducted involving 304 patients with pDoC admitted to the First Affiliated Hospital of Nanchang University between January 2021 and October 2023. Clinical data were collected, including demographics, etiology, disease duration, behavioral assessment scores (Glasgow Coma Scale [GCS], Full Outline of UnResponsiveness [FOUR], and Coma Recovery Scale-Revised [CRS-R]), laboratory indicators, and other relevant clinical variables. Prognosis was assessed using the Glasgow Outcome Scale-Extended (GOS-E) and dichotomized into good outcome (GOS-E 3&#x2013;8) and poor outcome (GOS-E 1&#x2013;2). Feature selection was performed using the Boruta algorithm combined with recursive feature elimination (RFE). Prognostic models were developed using logistic regression, support vector machine (SVM), multilayer perceptron (MLP), XGBoost, and gradient boosting machine (GBM) implemented in scikit-learn. Model performance was evaluated using accuracy, receiver operating characteristic curve area under the curve (ROC-AUC), and decision curve analysis (DCA). SHapley Additive exPlanations (SHAP) were applied to interpret the optimal model.</p>
</sec>
<sec>
<title>Results</title>
<p>Among the developed models, the GBM model demonstrated the best predictive performance, with an AUROC of 0.954 (95% CI: 0.924&#x2013;0.977) in the training set and 0.922 (95% CI: 0.847&#x2013;0.979) in the test set. Decision curve analysis indicated that the GBM model yielded substantial net clinical benefit across most threshold probabilities. SHAP analysis identified CRS-R score, age, FOUR score, total GCS score, and length of hospitalization as the most influential prognostic predictors.</p>
</sec>
<sec>
<title>Conclusion</title>
<p>A robust prognostic prediction model for pDoC patients was developed and validated using multidimensional clinical data and machine learning techniques. The GBM model achieved excellent discriminative performance and clinical utility, providing an objective tool for prognosis estimation and individualized treatment and rehabilitation planning. Further multi-center studies are warranted to optimize the model and confirm its generalizability.</p>
</sec>
</abstract>
<kwd-group>
<kwd>behavioral scales</kwd>
<kwd>clinical evaluation</kwd>
<kwd>disorders of consciousness</kwd>
<kwd>prediction model</kwd>
<kwd>prognosis</kwd>
</kwd-group>
<funding-group>
<funding-statement>The author(s) declared that financial support was not received for this work and/or its publication.</funding-statement>
</funding-group>
<counts>
<fig-count count="9"/>
<table-count count="2"/>
<equation-count count="0"/>
<ref-count count="32"/>
<page-count count="14"/>
<word-count count="7932"/>
</counts>
<custom-meta-group>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Neurorehabilitation</meta-value>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="sec1">
<label>1</label>
<title>Introduction</title>
<p>Disorders of Consciousness (DoC) are caused by brain injuries resulting from traumatic brain injury (TBI), stroke, hemorrhage, hypoxia, or other factors that disrupt overall brain function, leading to a loss of consciousness. This includes conditions such as coma, Unresponsive Wakefulness Syndrome (UWS), and Minimally Conscious State (MCS) (<xref ref-type="bibr" rid="ref1">1</xref>). Prolonged Disorders of Consciousness (pDoC) (<xref ref-type="bibr" rid="ref2">2</xref>) is a more complex and severe form of DoC. A patient is diagnosed with pDoC if they remain in an unconscious state, unresponsive to both themselves and the environment, for more than 28&#x202F;days. With continuous advancements in emergency medicine and critical care, the survival rate of patients with severe brain injuries has significantly increased, resulting in a growing number of individuals living with chronic consciousness impairment (<xref ref-type="bibr" rid="ref3">3</xref>). Epidemiological studies indicate that the number of pDoC patients in China currently exceeds 500,000, with an annual increase of over 100,000 cases and cumulative direct medical expenses surpassing 10&#x202F;billion RMB (<xref ref-type="bibr" rid="ref4">4</xref>); Further research by Leonard et al. revealed that the annual medical costs for pDoC patients are approximately 120,000 euros, while the median annual income of 40.2% of family caregivers is around 170,000 euros (<xref ref-type="bibr" rid="ref5">5</xref>). This not only causes immense suffering for the patients themselves but also places a long-term caregiving burden and psychological stress on their family members, creating significant challenges for the healthcare system (<xref ref-type="bibr" rid="ref6">6</xref>).</p>
<p>Accurate prognostic assessments provide essential information for patients and their families, helping family members create long-term care plans, allocate resources effectively, and manage psychological expectations, thereby alleviating the burden and stress associated with prolonged caregiving. Additionally, precise prognosis prediction aids healthcare providers in designing more targeted treatment and rehabilitation strategies, optimizing the allocation of medical resources, and preventing both overtreatment and undertreatment, ultimately improving the efficiency and effectiveness of the healthcare system. This approach is crucial for addressing the increasing number of pDoC patients. Therefore, accurate prognosis prediction is key to developing appropriate rehabilitation plans, optimizing resource allocation, and offering psychological support and expectation management for the families of patients (<xref ref-type="bibr" rid="ref7">7</xref>).</p>
<p>Currently, the prognostic evaluation of pDoC patients primarily relies on a combination of behavioral assessment scales, neurophysiological examinations, neuroimaging technologies, and serum biomarkers. Behavioral assessment scales are widely used in clinical practice due to their simplicity and ease of administration. These include the Glasgow Coma Scale (GCS), the Full Outline of Unresponsiveness (FOUR) score, and the Coma Recovery Scale-Revised (CRS-R), among others. Since its introduction in 1974, the GCS has become the most commonly used tool for assessing consciousness (<xref ref-type="bibr" rid="ref8">8</xref>), though it has limitations such as a limited number of assessment items and an inability to evaluate brainstem reflexes (<xref ref-type="bibr" rid="ref9">9</xref>). The FOUR score overcomes some of these limitations by incorporating assessments of brainstem reflexes and respiratory patterns (<xref ref-type="bibr" rid="ref10">10</xref>). The CRS-R is considered the gold standard for diagnosing and assessing pDoC (<xref ref-type="bibr" rid="ref11">11</xref>), as it effectively distinguishes between patients in UWS and MCS and is sensitive to subtle behavioral changes. However, its comprehensive assessment is time-consuming and requires extensive training for evaluators (<xref ref-type="bibr" rid="ref12">12</xref>). Despite their usefulness, The CRS-R is influenced by factors such as fluctuations in patient consciousness, medication effects, complications, and the subjective judgments of the evaluator, leading to a misdiagnosis rate as high as 40% (<xref ref-type="bibr" rid="ref13">13</xref>). Furthermore, these scales rely mainly on the patient&#x2019;s overt behavioral responses and are unable to assess patients with severe motor dysfunction who may retain cognitive abilities (<xref ref-type="bibr" rid="ref14">14</xref>).</p>
<p>Neuroimaging and neurophysiological techniques provide essential structural and functional information, offering valuable prognostic data for the assessment of pDoC patients (<xref ref-type="bibr" rid="ref15">15</xref>). However, their high costs, limited availability, and dependence on specialized personnel hinder their widespread application in routine clinical practice (<xref ref-type="bibr" rid="ref16">16</xref>, <xref ref-type="bibr" rid="ref17">17</xref>). Serum biomarkers hold significant potential for prognostic prediction in consciousness disorders (<xref ref-type="bibr" rid="ref18">18</xref>), but their clinical utility is limited due to a lack of sufficient research, with relatively few studies conducted specifically in pDoC patients. Research by Bagnato et al. has demonstrated that serum biomarkers can not only more accurately represent the extent of brain damage but also support prediction models with valuable data (<xref ref-type="bibr" rid="ref19">19</xref>).</p>
<p>In recent years, with the rapid advancement of artificial intelligence technology, machine learning-based prediction models have offered new solutions to the challenges mentioned above. Compared to traditional statistical methods, machine learning techniques present several advantages, such as the ability to handle high-dimensional data, capture complex nonlinear relationships between variables, automatically assess the importance of each predictive factor, possess dynamic learning capabilities, and provide individualized predictions. Machine learning has already shown significant potential in the field of pDoC prognostic prediction (<xref ref-type="bibr" rid="ref20">20</xref>). Haveman et al. defined a Glasgow Outcome Scale-Extended (GOSE) score &#x2265;3 as the threshold for good prognosis in pDoC patients (<xref ref-type="bibr" rid="ref21">21</xref>). They developed a weighted sparse brain network feature based on resting-state functional magnetic resonance imaging (fMRI) data and utilized a support vector machine classifier to predict patient outcomes, achieving a classification accuracy of 90% (<xref ref-type="bibr" rid="ref22">22</xref>). While machine learning has demonstrated substantial potential in pDoC prognostic prediction, its clinical application still faces challenges, such as data quality issues, lack of model interpretability, limited generalization capacity, and class imbalance (<xref ref-type="bibr" rid="ref23 ref24 ref25">23&#x2013;25</xref>).</p>
<p>Building on the above analysis, this study integrates multidimensional indicators, such as behavioral assessments and serum biomarkers, and applies advanced machine learning algorithms to construct a multimodal prediction model for prognostic evaluation in pDoC patients.</p>
</sec>
<sec sec-type="materials|methods" id="sec2">
<label>2</label>
<title>Materials and methods</title>
<sec id="sec3">
<label>2.1</label>
<title>Study subjects</title>
<p>This study is a prospective cohort study that included 304 patients with DoC who were treated in the Department of Rehabilitation Medicine at the First Affiliated Hospital of Nanchang University from January 2021 to October 2023.</p>
<p>Inclusion criteria: &#x2460; First diagnosis of DoC; &#x2461; UWS or MCS according to the &#x201C;European Guidelines for Coma and Consciousness Disorder Diagnosis; &#x2462; Duration of DoC &#x2265;28&#x202F;days.</p>
<p>Exclusion criteria: &#x2460; Co-existing severe brain atrophy, congenital neurological disorders, or drug poisoning; &#x2461; History of cognitive dysfunction (such as dementia or a history of mental illness).</p>
</sec>
<sec id="sec4">
<label>2.2</label>
<title>Research methods</title>
<sec id="sec5">
<label>2.2.1</label>
<title>Data collection</title>
<p>Clinical data were collected for all patients at the time of hospital admission as part of the baseline assessment. The data collected included demographic characteristics (age, gender, education level, occupational status, marital status), etiology, duration of DoC, length of hospitalization(defined as the total duration of inpatient stay during the rehabilitation phase), smoking history, behavioral assessment scales (GCS score, FOUR score, CRS-R score), medical history (hypertension, diabetes, history of multiple injuries, history of craniectomy), pupil dilation (defined as a diameter &#x2265;5&#x202F;mm, unilateral, bilateral, or none), complications (secondary epilepsy, muscle spasticity, pulmonary infections), imaging findings (subdural effusion, subarachnoid hemorrhage, hydrocephalus), and laboratory test indicators (albumin, hemoglobin, etc.). These variables were all obtained as part of the routine clinical evaluation at admission.</p>
</sec>
<sec id="sec6">
<label>2.2.2</label>
<title>Outcome measures</title>
<p>The GOS-E score was used as the outcome variable. This score was assessed by two follow-up personnel who were rigorously and professionally trained. Follow-up was conducted through telephone calls to the patients&#x2019; families, with a follow-up interval of no more than 2&#x202F;weeks. If at least 3 phone contact attempts were unsuccessful, the patient was considered lost to follow-up. The GOS-E scale consists of 8 categories (<xref ref-type="bibr" rid="ref26">26</xref>), which include: &#x2460; Death; &#x2461; Vegetative state (unconscious state); &#x2462; Severe disability (conscious but requiring frequent assistance for daily activities); &#x2463; Moderate to severe disability (conscious but requiring partial assistance for daily activities); &#x2464; Moderate disability (independent in daily life but unable to participate in some social roles); &#x2465; Mild disability (able to participate in social roles but with limitations); &#x2466; Good recovery (return to normal life but with minor symptoms); &#x2467; Complete recovery (full recovery to normal life without functional impairments). IIn this study, the patients&#x2019; outcomes were categorized based on the GOS-E score into two groups: a poor prognosis group (GOS-E score 1&#x2013;2) and a good prognosis group (GOS-E score 3&#x2013;8) (<xref ref-type="bibr" rid="ref21">21</xref>). Outcome assessment was performed 1&#x202F;year after the initial baseline data collection at hospital admission, providing a consistent and clinically relevant evaluation window for assessing long-term recovery in patients with DoC. This standardized assessment time point improves the reproducibility and clinical applicability of the model.</p>
</sec>
</sec>
<sec id="sec7">
<label>2.3</label>
<title>Data preprocessing</title>
<p>In this study, we conducted rigorous screening and preprocessing of the data from patients with DoC who were treated at the Department of Rehabilitation Medicine, The First Affiliated Hospital of Nanchang University, between January 2021 and October 2023. The initial cohort included 304 patients, with cases exhibiting missing critical data being excluded. Missing critical data included essential assessment scales, laboratory results, or follow-up data. Ultimately, data from 239 patients with good completeness were included in the final analysis. The data set was divided into a training set (70%) and a testing set (30%) using stratified random sampling, ensuring that the proportion of samples in each category was consistent between the two sets to enhance the model&#x2019;s generalizability.</p>
</sec>
<sec id="sec8">
<label>2.4</label>
<title>Feature selection</title>
<p>This study employed a combination of the Boruta algorithm based on random forests and recursive feature elimination (RFE) for feature selection. The Boruta algorithm constructs random features as a control group and compares their importance with that of the original features, thereby identifying those features that are truly important for the target variable. Recursive feature elimination utilizes feature contribution analysis and model average AUC performance evaluation to quantify the contribution of features to the model output and assess the model&#x2019;s classification performance, further validating the importance of the features. The combination of these two methods ensures the comprehensiveness and robustness of the feature selection process, while enhancing the predictive power of the feature subset.</p>
</sec>
<sec id="sec9">
<label>2.5</label>
<title>Machine learning algorithms</title>
<p>This study constructed five machine learning models using Python&#x2019;s scikit-learn library: Logistic Regression (LR), Support Vector Machine (SVM), XGBoost, Gradient Boosting Machine (GBM), and Multi-Layer Perceptron (MLP). The optimal parameters for each model were determined using Grid Search and 5-fold cross-validation (CV) to minimize overfitting and optimize model performance. Logistic Regression (LR), a classic statistical method, is simple yet performs exceptionally well in medical predictions, offering good interpretability. Support Vector Machine (SVM) constructs a linear decision boundary by mapping input vectors into a high-dimensional feature space, thereby enhancing generalization ability. Multi-Layer Perceptron (MLP), a feedforward neural network model, possesses powerful representation learning capabilities. XGBoost is one of the most powerful boosting algorithms, offering excellent predictive performance via gradient boosting frameworks and regularization techniques. Gradient Boosting Machine (GBM) sequentially integrates multiple weak learners to improve overall performance.</p>
<p>In addition to conventional discrimination metrics such as the area under the receiver operating characteristic curve (AUC), the Net Reclassification Improvement (NRI) was employed as a supplementary performance measure. NRI, originally proposed by Pencina MJ et al., evaluates whether a new prediction model improves individual risk stratification relative to a reference model by quantifying changes in risk category assignment for individuals with and without events (<xref ref-type="bibr" rid="ref27">27</xref>). Unlike AUC, which summarizes overall discriminative ability, NRI specifically assesses the direction and magnitude of risk reclassification, providing complementary information on model performance.</p>
<p>In this study, the machine learning model demonstrating the best performance based on cross-validation was treated as the new model and was compared with LR, which served as the reference model. The NRI was calculated using predefined clinical risk thresholds to assess differences in patient risk reclassification between the two models.</p>
</sec>
<sec id="sec10">
<label>2.6</label>
<title>SHAP interpretability analysis</title>
<p>To enhance clinical applicability and interpretability, SHAP analysis was employed to evaluate the contribution of each feature to the model&#x2019;s predictions. SHAP, based on the Shapley values from game theory, quantifies each feature&#x2019;s contribution to the model&#x2019;s prediction, with theoretical guarantees of completeness, consistency, and local accuracy. By calculating each feature&#x2019;s marginal contribution across all possible feature combinations, SHAp values reflect the positive or negative influence of features on predictions. In this study, SHAP values were computed for all samples, and features were ranked based on mean absolute SHAP values. SHAP dependence plots were used to explore nonlinear relationships between feature values and their effects. Additionally, SHAP force plots visually demonstrate how features collectively influence individual sample predictions, providing explanations for personalized prognostic predictions.</p>
</sec>
<sec id="sec11">
<label>2.7</label>
<title>Statistical analysis</title>
<p>All data analysis was conducted using Python 3.8 and related libraries. Continuous variables were expressed as mean &#x00B1; standard deviation or median (interquartile range), while categorical variables were presented as frequencies and percentages. Group comparisons were performed using independent sample t-tests, Mann&#x2013;Whitney U tests, or chi-square tests, with the appropriate statistical method selected based on data distribution characteristics. For model evaluation, the area under the receiver operating characteristic curve (AUC) was used to assess the classification performance of each model. DCA was used to compare the clinical utility of each model, and calibration curves were employed to assess the consistency between predicted probabilities and actual outcomes. Statistical analyses were carried out using Python libraries, including scikit-learn (version 1.5.1) and statsmodels (version 0.14.4), with visualization generated by matplotlib (version 3.10.0). Data preprocessing relied on pandas (version 2.2.3) and numpy (version 1.26.4), model construction used xgboost (version 2.0.3), and model interpretation was facilitated using shap (version 0.45.1). All statistical tests were two-sided, and a <italic>p</italic>-value of &#x003C; 0.05 was considered statistically significant.</p>
</sec>
</sec>
<sec sec-type="results" id="sec12">
<label>3</label>
<title>Results</title>
<sec id="sec13">
<label>3.1</label>
<title>Patient characteristics</title>
<p>A total of 304 patients with Disorders of Consciousness (DoC) who visited the Department of Rehabilitation Medicine at The First Affiliated Hospital of Nanchang University from January 2021 to October 2023 were initially included. After strict screening and excluding cases with missing data, 239 patients were ultimately included in the analysis. Among them, 97 patients had a good prognosis (GOS-E score 3&#x2013;8), while 142 had a poor prognosis (GOS-E score 1&#x2013;2). The mean age of the entire cohort was 53.7&#x202F;&#x00B1;&#x202F;15.0&#x202F;years, with 60.7% of the patients being male. As shown in <xref ref-type="table" rid="tab1">Table 1</xref>, there were statistically significant differences between the good and poor prognosis groups in terms of demographic characteristics, consciousness status, and assessment indicators (<italic>p</italic>&#x202F;&#x003C;&#x202F;0.05). No substantial differences were observed between the training and validation sets. <xref ref-type="table" rid="tab2">Table 2</xref> reveals that there were no significant differences between the training and validation sets in terms of demographic characteristics, medical history, consciousness status, and physiological indicators, except for the presence of subdural effusion, which showed a statistically significant difference (<italic>p</italic>&#x202F;&#x003C;&#x202F;0.05).</p>
<table-wrap position="float" id="tab1">
<label>Table 1</label>
<caption>
<p>Basic clinical information of the good prognosis and poor prognosis groups.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Variables</th>
<th align="center" valign="top">Total (<italic>n</italic> =&#x202F;239)</th>
<th align="center" valign="top">Poor prognosis group (<italic>n</italic> =&#x202F;142)</th>
<th align="center" valign="top">Good prognosis group (<italic>n</italic> =&#x202F;97)</th>
<th align="center" valign="top"><italic>p</italic> value</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top" colspan="5">History_of_hypertension</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">147 (61.5%)</td>
<td align="center" valign="bottom">83 (58.5%)</td>
<td align="center" valign="bottom">64 (66.0%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">92 (38.5%)</td>
<td align="center" valign="bottom">59 (41.5%)</td>
<td align="center" valign="bottom">33 (34.0%)</td>
<td align="center" valign="bottom">0.299</td>
</tr>
<tr>
<td align="left" valign="top" colspan="5">History_of_diabetes_mellitus</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">211 (88.3%)</td>
<td align="center" valign="bottom">124 (87.3%)</td>
<td align="center" valign="bottom">87 (89.7%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">28 (11.7%)</td>
<td align="center" valign="bottom">18 (12.7%)</td>
<td align="center" valign="bottom">10 (10.3%)</td>
<td align="center" valign="bottom">0.723</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">History_of_epilepsy_disorder</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">228 (95.4%)</td>
<td align="center" valign="bottom">133 (93.7%)</td>
<td align="center" valign="bottom">95 (97.9%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">11 (4.6%)</td>
<td align="center" valign="bottom">9 (6.3%)</td>
<td align="center" valign="bottom">2 (2.1%)</td>
<td align="center" valign="bottom">0.217</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Pulmonary_infection</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">72 (30.1%)</td>
<td align="center" valign="bottom">41 (28.9%)</td>
<td align="center" valign="bottom">31 (32.0%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">167 (69.9%)</td>
<td align="center" valign="bottom">101 (71.1%)</td>
<td align="center" valign="bottom">66 (68.0%)</td>
<td align="center" valign="bottom">0.714</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Subdural_effusion</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">204 (85.4%)</td>
<td align="center" valign="bottom">129 (90.8%)</td>
<td align="center" valign="bottom">75 (77.3%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">35 (14.6%)</td>
<td align="center" valign="bottom">13 (9.2%)</td>
<td align="center" valign="bottom">22 (22.7%)</td>
<td align="center" valign="bottom">0.007</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Smoking_history</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">226 (94.6%)</td>
<td align="center" valign="bottom">132 (93.0%)</td>
<td align="center" valign="bottom">94 (96.9%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">13 (5.4%)</td>
<td align="center" valign="bottom">10 (7.0%)</td>
<td align="center" valign="bottom">3 (3.1%)</td>
<td align="center" valign="bottom">0.302</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Sex</td>
</tr>
<tr>
<td align="left" valign="bottom">Female</td>
<td align="center" valign="bottom">94 (39.3%)</td>
<td align="center" valign="bottom">62 (43.7%)</td>
<td align="center" valign="bottom">32 (33.0%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Male</td>
<td align="center" valign="bottom">145 (60.7%)</td>
<td align="center" valign="bottom">80 (56.3%)</td>
<td align="center" valign="bottom">65 (67.0%)</td>
<td align="center" valign="bottom">0.128</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Multiple_injuries</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">180 (75.3%)</td>
<td align="center" valign="bottom">108 (76.1%)</td>
<td align="center" valign="bottom">72 (74.2%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">59 (24.7%)</td>
<td align="center" valign="bottom">34 (23.9%)</td>
<td align="center" valign="bottom">25 (25.8%)</td>
<td align="center" valign="bottom">0.866</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Craniotomy</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">171 (71.5%)</td>
<td align="center" valign="bottom">104 (73.2%)</td>
<td align="center" valign="bottom">67 (69.1%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">68 (28.5%)</td>
<td align="center" valign="bottom">38 (26.8%)</td>
<td align="center" valign="bottom">30 (30.9%)</td>
<td align="center" valign="bottom">0.579</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Subarachnoid_hemorrhage</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">169 (70.7%)</td>
<td align="center" valign="bottom">103 (72.5%)</td>
<td align="center" valign="bottom">66 (68.0%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">70 (29.3%)</td>
<td align="center" valign="bottom">39 (27.5%)</td>
<td align="center" valign="bottom">31 (32.0%)</td>
<td align="center" valign="bottom">0.545</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Hydrocephalus</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">206 (86.2%)</td>
<td align="center" valign="bottom">122 (85.9%)</td>
<td align="center" valign="bottom">84 (86.6%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">33 (13.8%)</td>
<td align="center" valign="bottom">20 (14.1%)</td>
<td align="center" valign="bottom">13 (13.4%)</td>
<td align="center" valign="bottom">1.000</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Muscle_tone</td>
</tr>
<tr>
<td align="left" valign="bottom">Unable to measure</td>
<td align="center" valign="bottom">78 (32.6%)</td>
<td align="center" valign="bottom">48 (33.8%)</td>
<td align="center" valign="bottom">30 (30.9%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Weak</td>
<td align="center" valign="bottom">37 (15.5%)</td>
<td align="center" valign="bottom">23 (16.2%)</td>
<td align="center" valign="bottom">14 (14.4%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Normal</td>
<td align="center" valign="bottom">77 (32.2%)</td>
<td align="center" valign="bottom">40 (28.2%)</td>
<td align="center" valign="bottom">37 (38.1%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">High</td>
<td align="center" valign="bottom">47 (19.7%)</td>
<td align="center" valign="bottom">31 (21.8%)</td>
<td align="center" valign="bottom">16 (16.5%)</td>
<td align="center" valign="bottom">0.411</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Etiology</td>
</tr>
<tr>
<td align="left" valign="bottom">Traumatic brain injury</td>
<td align="center" valign="bottom">95 (39.7%)</td>
<td align="center" valign="bottom">57 (40.1%)</td>
<td align="center" valign="bottom">38 (39.2%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Intracerebral hemorrhage</td>
<td align="center" valign="bottom">117 (49.0%)</td>
<td align="center" valign="bottom">66 (46.5%)</td>
<td align="center" valign="bottom">51 (52.6%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Cerebral infarction</td>
<td align="center" valign="bottom">7 (2.9%)</td>
<td align="center" valign="bottom">3 (2.1%)</td>
<td align="center" valign="bottom">4 (4.1%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Others</td>
<td align="center" valign="bottom">20 (8.4%)</td>
<td align="center" valign="bottom">16 (11.3%)</td>
<td align="center" valign="bottom">4 (4.1%)</td>
<td align="center" valign="bottom">0.190</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Patient&#x2019;s_state_of_consciousness</td>
</tr>
<tr>
<td align="left" valign="bottom">VS</td>
<td align="center" valign="bottom">150 (62.8%)</td>
<td align="center" valign="bottom">111 (78.2%)</td>
<td align="center" valign="bottom">39 (40.2%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">MCS-</td>
<td align="center" valign="bottom">68 (28.5%)</td>
<td align="center" valign="bottom">26 (18.3%)</td>
<td align="center" valign="bottom">42 (43.3%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">MCS+</td>
<td align="center" valign="bottom">16 (6.7%)</td>
<td align="center" valign="bottom">5 (3.5%)</td>
<td align="center" valign="bottom">11 (11.3%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Emergence from MCS</td>
<td align="center" valign="bottom">5 (2.1%)</td>
<td align="center" valign="bottom">0 (0.0%)</td>
<td align="center" valign="bottom">5 (5.2%)</td>
<td align="center" valign="bottom">0.000</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Age</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">53.7&#x202F;&#x00B1;&#x202F;15.0</td>
<td align="center" valign="bottom">56.8&#x202F;&#x00B1;&#x202F;14.2</td>
<td align="center" valign="bottom">49.0&#x202F;&#x00B1;&#x202F;15.2</td>
<td align="center" valign="bottom">0.000</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Hb</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">101.5&#x202F;&#x00B1;&#x202F;15.7</td>
<td align="center" valign="bottom">103.1&#x202F;&#x00B1;&#x202F;14.9</td>
<td align="center" valign="bottom">99.3&#x202F;&#x00B1;&#x202F;16.5</td>
<td align="center" valign="bottom">0.075</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">D_dimer</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">3.2&#x202F;&#x00B1;&#x202F;4.5</td>
<td align="center" valign="bottom">3.3&#x202F;&#x00B1;&#x202F;4.1</td>
<td align="center" valign="bottom">3.1&#x202F;&#x00B1;&#x202F;5.1</td>
<td align="center" valign="bottom">0.760</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Serum_albumin</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">35.8&#x202F;&#x00B1;&#x202F;6.9</td>
<td align="center" valign="bottom">35.3&#x202F;&#x00B1;&#x202F;4.9</td>
<td align="center" valign="bottom">36.6&#x202F;&#x00B1;&#x202F;9.1</td>
<td align="center" valign="bottom">0.207</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Length_of_hospital_stay</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">31.4&#x202F;&#x00B1;&#x202F;14.1</td>
<td align="center" valign="bottom">30.4&#x202F;&#x00B1;&#x202F;15.9</td>
<td align="center" valign="bottom">32.8&#x202F;&#x00B1;&#x202F;10.8</td>
<td align="center" valign="bottom">0.150</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">CRS-R</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">7.3&#x202F;&#x00B1;&#x202F;3.2</td>
<td align="center" valign="bottom">6.1&#x202F;&#x00B1;&#x202F;2.3</td>
<td align="center" valign="bottom">9.1&#x202F;&#x00B1;&#x202F;3.5</td>
<td align="center" valign="bottom">0.000</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">GCS</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">8.2&#x202F;&#x00B1;&#x202F;1.8</td>
<td align="center" valign="bottom">7.6&#x202F;&#x00B1;&#x202F;1.6</td>
<td align="center" valign="bottom">9.2&#x202F;&#x00B1;&#x202F;1.5</td>
<td align="center" valign="bottom">0.000</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">FOUR</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">12.0&#x202F;&#x00B1;&#x202F;2.2</td>
<td align="center" valign="bottom">11.2&#x202F;&#x00B1;&#x202F;2.0</td>
<td align="center" valign="bottom">13.2&#x202F;&#x00B1;&#x202F;1.8</td>
<td align="center" valign="bottom">0.000</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>Continuous variables are presented as mean &#x00B1; standard deviation and were compared between groups using the independent-samples <italic>t</italic>-test. Categorical variables are presented as counts (percentages) and were compared using the Chi-square test or Fisher&#x2019;s exact test, as appropriate. A <italic>p</italic> value &#x003C; 0.05 was considered statistically significant.</p>
</table-wrap-foot>
</table-wrap>
<table-wrap position="float" id="tab2">
<label>Table 2</label>
<caption>
<p>Clinical information of the training and validation sets.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Variables</th>
<th align="center" valign="top">Total (<italic>n</italic> =&#x202F;239)</th>
<th align="center" valign="top">Training set (<italic>n</italic> =&#x202F;167)</th>
<th align="center" valign="top">Validation set (<italic>n</italic> =&#x202F;72)</th>
<th align="center" valign="top"><italic>p</italic> value</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="bottom" colspan="5">History_of_hypertension</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">147 (61.5%)</td>
<td align="center" valign="bottom">102 (61.1%)</td>
<td align="center" valign="bottom">45 (62.5%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">92 (38.5%)</td>
<td align="center" valign="bottom">65 (38.9%)</td>
<td align="center" valign="bottom">27 (37.5%)</td>
<td align="center" valign="bottom">0.950</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">History_of_diabetes_mellitus</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">211 (88.3%)</td>
<td align="center" valign="bottom">147 (88.0%)</td>
<td align="center" valign="bottom">64 (88.9%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">28 (11.7%)</td>
<td align="center" valign="bottom">20 (12.0%)</td>
<td align="center" valign="bottom">8 (11.1%)</td>
<td align="center" valign="bottom">1.000</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">History_of_epilepsy_disorder</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">228 (95.4%)</td>
<td align="center" valign="bottom">159 (95.2%)</td>
<td align="center" valign="bottom">69 (95.8%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">11 (4.6%)</td>
<td align="center" valign="bottom">8 (4.8%)</td>
<td align="center" valign="bottom">3 (4.2%)</td>
<td align="center" valign="bottom">1.000</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Pulmonary_infection</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">72 (30.1%)</td>
<td align="center" valign="bottom">52 (31.1%)</td>
<td align="center" valign="bottom">20 (27.8%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">167 (69.9%)</td>
<td align="center" valign="bottom">115 (68.9%)</td>
<td align="center" valign="bottom">52 (72.2%)</td>
<td align="center" valign="bottom">0.715</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Subdural_effusion</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">204 (85.4%)</td>
<td align="center" valign="bottom">141 (84.4%)</td>
<td align="center" valign="bottom">63 (87.5%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">35 (14.6%)</td>
<td align="center" valign="bottom">26 (15.6%)</td>
<td align="center" valign="bottom">9 (12.5%)</td>
<td align="center" valign="bottom">0.677</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Smoking_history</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">226 (94.6%)</td>
<td align="center" valign="bottom">158 (94.6%)</td>
<td align="center" valign="bottom">68 (94.4%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">13 (5.4%)</td>
<td align="center" valign="bottom">9 (5.4%)</td>
<td align="center" valign="bottom">4 (5.6%)</td>
<td align="center" valign="bottom">1.000</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Sex</td>
</tr>
<tr>
<td align="left" valign="bottom">Female</td>
<td align="center" valign="bottom">94 (39.3%)</td>
<td align="center" valign="bottom">64 (38.3%)</td>
<td align="center" valign="bottom">30 (41.7%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Male</td>
<td align="center" valign="bottom">145 (60.7%)</td>
<td align="center" valign="bottom">103 (61.7%)</td>
<td align="center" valign="bottom">42 (58.3%)</td>
<td align="center" valign="bottom">0.733</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Multiple_injuries</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">180 (75.3%)</td>
<td align="center" valign="bottom">127 (76.0%)</td>
<td align="center" valign="bottom">53 (73.6%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">59 (24.7%)</td>
<td align="center" valign="bottom">40 (24.0%)</td>
<td align="center" valign="bottom">19 (26.4%)</td>
<td align="center" valign="bottom">0.812</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Craniotomy</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">171 (71.5%)</td>
<td align="center" valign="bottom">121 (72.5%)</td>
<td align="center" valign="bottom">50 (69.4%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">68 (28.5%)</td>
<td align="center" valign="bottom">46 (27.5%)</td>
<td align="center" valign="bottom">22 (30.6%)</td>
<td align="center" valign="bottom">0.751</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Subarachnoid_hemorrhage</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">169 (70.7%)</td>
<td align="center" valign="bottom">120 (71.9%)</td>
<td align="center" valign="bottom">49 (68.1%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">70 (29.3%)</td>
<td align="center" valign="bottom">47 (28.1%)</td>
<td align="center" valign="bottom">23 (31.9%)</td>
<td align="center" valign="bottom">0.662</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Hydrocephalus</td>
</tr>
<tr>
<td align="left" valign="bottom">No</td>
<td align="center" valign="bottom">206 (86.2%)</td>
<td align="center" valign="bottom">145 (86.8%)</td>
<td align="center" valign="bottom">61 (84.7%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Yes</td>
<td align="center" valign="bottom">33 (13.8%)</td>
<td align="center" valign="bottom">22 (13.2%)</td>
<td align="center" valign="bottom">11 (15.3%)</td>
<td align="center" valign="bottom">0.819</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Muscle_tone</td>
</tr>
<tr>
<td align="left" valign="bottom">Unable to measure</td>
<td align="center" valign="bottom">78 (32.6%)</td>
<td align="center" valign="bottom">55 (32.9%)</td>
<td align="center" valign="bottom">23 (31.9%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Weak</td>
<td align="center" valign="bottom">37 (15.5%)</td>
<td align="center" valign="bottom">26 (15.6%)</td>
<td align="center" valign="bottom">11 (15.3%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Normal</td>
<td align="center" valign="bottom">77 (32.2%)</td>
<td align="center" valign="bottom">50 (29.9%)</td>
<td align="center" valign="bottom">27 (37.5%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">High</td>
<td align="center" valign="bottom">47 (19.7%)</td>
<td align="center" valign="bottom">36 (21.6%)</td>
<td align="center" valign="bottom">11 (15.3%)</td>
<td align="center" valign="bottom">0.589</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Etiology</td>
</tr>
<tr>
<td align="left" valign="bottom">Traumatic brain injury</td>
<td align="center" valign="bottom">95 (39.7%)</td>
<td align="center" valign="bottom">67 (40.1%)</td>
<td align="center" valign="bottom">28 (38.9%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Intracerebral hemorrhage</td>
<td align="center" valign="bottom">117 (49.0%)</td>
<td align="center" valign="bottom">81 (48.5%)</td>
<td align="center" valign="bottom">36 (50.0%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Cerebral infarction</td>
<td align="center" valign="bottom">7 (2.9%)</td>
<td align="center" valign="bottom">5 (3.0%)</td>
<td align="center" valign="bottom">2 (2.8%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Others</td>
<td align="center" valign="bottom">20 (8.4%)</td>
<td align="center" valign="bottom">14 (8.4%)</td>
<td align="center" valign="bottom">6 (8.3%)</td>
<td align="center" valign="bottom">0.997</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Patient&#x2019;s_state_of_consciousness</td>
</tr>
<tr>
<td align="left" valign="bottom">VS</td>
<td align="center" valign="bottom">150 (62.8%)</td>
<td align="center" valign="bottom">109 (65.3%)</td>
<td align="center" valign="bottom">41 (56.9%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">MCS-</td>
<td align="center" valign="bottom">68 (28.5%)</td>
<td align="center" valign="bottom">47 (28.1%)</td>
<td align="center" valign="bottom">21 (29.2%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">MCS+</td>
<td align="center" valign="bottom">16 (6.7%)</td>
<td align="center" valign="bottom">7 (4.2%)</td>
<td align="center" valign="bottom">9 (12.5%)</td>
<td/>
</tr>
<tr>
<td align="left" valign="bottom">Emergence from MCS</td>
<td align="center" valign="bottom">5 (2.1%)</td>
<td align="center" valign="bottom">4 (2.4%)</td>
<td align="center" valign="bottom">1 (1.4%)</td>
<td align="center" valign="bottom">0.111</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Age</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">53.7&#x202F;&#x00B1;&#x202F;15.0</td>
<td align="center" valign="bottom">52.6&#x202F;&#x00B1;&#x202F;16.1</td>
<td align="center" valign="bottom">56.1&#x202F;&#x00B1;&#x202F;12.0</td>
<td align="center" valign="bottom">0.067</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Hb</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">101.5&#x202F;&#x00B1;&#x202F;15.7</td>
<td align="center" valign="bottom">101.9&#x202F;&#x00B1;&#x202F;15.8</td>
<td align="center" valign="bottom">100.7&#x202F;&#x00B1;&#x202F;15.5</td>
<td align="center" valign="bottom">0.606</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">D_dimer</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">3.2&#x202F;&#x00B1;&#x202F;4.5</td>
<td align="center" valign="bottom">3.2&#x202F;&#x00B1;&#x202F;4.5</td>
<td align="center" valign="bottom">3.4&#x202F;&#x00B1;&#x202F;4.6</td>
<td align="center" valign="bottom">0.703</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Serum_albumin</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">35.8&#x202F;&#x00B1;&#x202F;6.9</td>
<td align="center" valign="bottom">36.1&#x202F;&#x00B1;&#x202F;7.6</td>
<td align="center" valign="bottom">35.3&#x202F;&#x00B1;&#x202F;5.1</td>
<td align="center" valign="bottom">0.374</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">Length_of_hospital_stay</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">31.4&#x202F;&#x00B1;&#x202F;14.1</td>
<td align="center" valign="bottom">31.8&#x202F;&#x00B1;&#x202F;15.0</td>
<td align="center" valign="bottom">30.4&#x202F;&#x00B1;&#x202F;11.6</td>
<td align="center" valign="bottom">0.445</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">CRS-R</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">7.3&#x202F;&#x00B1;&#x202F;3.2</td>
<td align="center" valign="bottom">7.2&#x202F;&#x00B1;&#x202F;3.1</td>
<td align="center" valign="bottom">7.6&#x202F;&#x00B1;&#x202F;3.4</td>
<td align="center" valign="bottom">0.329</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">GCS</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">8.2&#x202F;&#x00B1;&#x202F;1.8</td>
<td align="center" valign="bottom">8.2&#x202F;&#x00B1;&#x202F;1.7</td>
<td align="center" valign="bottom">8.3&#x202F;&#x00B1;&#x202F;1.9</td>
<td align="center" valign="bottom">0.543</td>
</tr>
<tr>
<td align="left" valign="bottom" colspan="5">FOUR</td>
</tr>
<tr>
<td align="left" valign="bottom">Mean &#x00B1; SD</td>
<td align="center" valign="bottom">12.0&#x202F;&#x00B1;&#x202F;2.2</td>
<td align="center" valign="bottom">11.9&#x202F;&#x00B1;&#x202F;2.1</td>
<td align="center" valign="bottom">12.2&#x202F;&#x00B1;&#x202F;2.4</td>
<td align="center" valign="bottom">0.305</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="sec14">
<label>3.2</label>
<title>Feature selection</title>
<p>In the feature selection process, we used the Boruta algorithm based on random forests and the Recursive Feature Elimination (RFE) algorithm to identify relevant features from an initial set of 37. The Boruta algorithm accurately identified 8 key features that played a significant role in predicting patient prognosis, including the CRS-R total score, age, length of hospitalization, GCS motor response, GCS total score, and FOUR total score. At the same time, Hb was labeled as &#x201C;Tentative,&#x201D; indicating that this feature may have some predictive value, but its statistical significance was somewhat weaker compared to the features that were clearly selected. The remaining features were deemed &#x201C;Rejected,&#x201D; suggesting that they contributed minimally to predicting patient prognosis (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p>
<fig position="float" id="fig1">
<label>Figure 1</label>
<caption>
<p>Sorted feature ranking distribution by Boruta. The feature ranking distribution was determined using the Boruta algorithm. The importance of each attribute is represented by the median importance score, with the box plots illustrating the distribution of importance scores for each feature. The attributes are sorted based on their median importance score, with the most important features on the right. The color coding indicates the feature status: selected (blue), rejected (red), and tentative (yellow).</p>
</caption>
<graphic xlink:href="fneur-17-1738430-g001.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Box plot comparing importance ranking distributions of features selected, rejected, and deemed tentative by the Boruta algorithm for attribute selection. Attributes are color-coded: selected in blue, rejected in red, and tentative in yellow.</alt-text>
</graphic>
</fig>
<p>To further validate the importance of these features, we employed the Recursive Feature Elimination (RFE) algorithm. Our analysis revealed that features such as age, CRS-R, Hb, and FOUR ranked highly in terms of feature contribution, highlighting their crucial role in shaping the model&#x2019;s predictive capability and marking them as key factors in predicting patient outcomes. Additionally, the model&#x2019;s average AUC value gradually stabilized as more features were added, indicating that the selected feature set sufficiently supported the model&#x2019;s predictive performance. Further addition of features did not significantly improve the model&#x2019;s performance (<xref ref-type="fig" rid="fig2">Figure 2</xref>).</p>
<fig position="float" id="fig2">
<label>Figure 2</label>
<caption>
<p>Feature Contribution and AUC Performance. The contribution of individual features to model performance, along with the AUC results, underscored the significance of the top eight most important features.</p>
</caption>
<graphic xlink:href="fneur-17-1738430-g002.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Bar chart compares feature importance for multiple variables related to patient outcome prediction. Top eight features are highlighted in red, with age showing the highest importance. AUC performance, shown by a line plot with confidence intervals, remains above 0.8 across features.</alt-text>
</graphic>
</fig>
<p>Throughout the feature selection process, we integrated the conclusions from both methods and carefully selected the features that made significant contributions to predicting patient outcomes. These included the CRS-R score, length of hospitalization, FOUR score, and hemoglobin level, among others. These features not only demonstrated high importance within the model but also underwent rigorous validation by the Boruta algorithm, ensuring the scientific rigor and robustness of the feature selection process. Based on this procedure, we meticulously constructed a highly efficient and accurate feature set for subsequent model development. This not only significantly enhanced the model&#x2019;s predictive capability but also greatly increased its value and reliability in practical applications.</p>
</sec>
<sec id="sec15">
<label>3.3</label>
<title>Multi-model ensemble analysis for classification</title>
<p>This study utilized five machine learning models to predict the prognosis of patients with chronic consciousness disorders, specifically LR, MLP, SVM, XGBoost, and GBM. <xref ref-type="fig" rid="fig3">Figure 3</xref> displays the ROC curves for each model in the training set, with the GBM model showing the best performance (AUC&#x202F;=&#x202F;0.954, 95% CI: 0.924&#x2013;0.977). The MLP model followed, with an AUC of 0.896 (95% CI, 0.842&#x2013;0.940), followed by GBM (AUC&#x202F;=&#x202F;0.946, 95% CI: 0.912&#x2013;0.973), LR (AUC&#x202F;=&#x202F;0.830, 95% CI: 0.761&#x2013;0.891), and SVM (AUC&#x202F;=&#x202F;0.859, 95% CI: 0.800&#x2013;0.911).</p>
<fig position="float" id="fig3">
<label>Figure 3</label>
<caption>
<p>ROC curves for model performance comparison. <bold>(A)</bold> ROC curves of different machine learning models on the training set. <bold>(B)</bold> ROC curves of different machine learning models on the test set.</p>
</caption>
<graphic xlink:href="fneur-17-1738430-g003.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Two side-by-side ROC curve graphs compare five machine learning models&#x2014;logistic regression, multilayer perceptron, support vector machine, XGBoost, and gradient boosting machine&#x2014;on train set (A) and test set (B), reporting AUC values and confidence intervals in the legends, with axes labeled true positive rate and false positive rate.</alt-text>
</graphic>
</fig>
<p>On the test set (<xref ref-type="fig" rid="fig3">Figure 3</xref>), the performance of all models slightly decreased, yet they still maintained good predictive power. The GBM model continued to perform the best (AUC&#x202F;=&#x202F;0.922, 95% CI: 0.847&#x2013;0.979), followed by XGBoost (AUC&#x202F;=&#x202F;0.907, 95% CI: 0.817&#x2013;0.976), MLP (AUC&#x202F;=&#x202F;0.903, 95% CI: 0.814&#x2013;0.962), SVM (AUC&#x202F;=&#x202F;0.898, 95% CI: 0.812&#x2013;0.963), and LR (AUC&#x202F;=&#x202F;0.895, 95% CI: 0.806&#x2013;0.963).</p>
<p>Compared with the LR, the GBM demonstrated a significantly higher threshold-based net reclassification improvement (Thr-NRI&#x202F;=&#x202F;0.403, 95% CI: 0.069&#x2013;0.714, <italic>p</italic>&#x202F;=&#x202F;0.019), indicating improved patient risk reclassification at predefined clinical risk thresholds.</p>
<p>This study evaluated the classification performance of each model using confusion matrices on both the training and test sets. On the test set, the GBM model exhibited the highest specificity (0.977), accurately identifying patients with poor prognosis. However, its sensitivity was relatively low (0.621), resulting in the misclassification of some patients with good prognosis. The XGBoost model had a specificity of 0.930 and sensitivity of 0.690, showing a more balanced performance. The SVM and MLP models had sensitivities of 0.690 and 0.62, respectively, but their specificities were lower. The Logistic Regression model showed a sensitivity of 0.654 and specificity of 0.883, with overall lower accuracy (<xref ref-type="fig" rid="fig4">Figure 4</xref>).</p>
<fig position="float" id="fig4">
<label>Figure 4</label>
<caption>
<p>Model performance evaluation. Confusion matrices of five machine learning models (LR, MLP, SVM, XGBoost, GBM) on the training set. Each matrix shows the classification results, allowing comparison of model accuracy and classification patterns.</p>
</caption>
<graphic xlink:href="fneur-17-1738430-g004.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Five confusion matrices compare model performance for LR, MLP, SVM, XGBoost, and GBM on the train set. Each matrix shows true versus predicted binary class counts with varying accuracy and class distributions.</alt-text>
</graphic>
</fig>
<p>On the training set, all models demonstrated high accuracy and low error rates. XGBoost exhibited the best sensitivity (0.750), while the GBM model excelled in specificity (0.909; <xref ref-type="fig" rid="fig5">Figure 5</xref>).</p>
<fig position="float" id="fig5">
<label>Figure 5</label>
<caption>
<p>Model performance evaluation. Confusion matrices of five machine learning models on the testing set. Each matrix shows the classification results, allowing comparison of model accuracy and classification patterns.</p>
</caption>
<graphic xlink:href="fneur-17-1738430-g005.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Five confusion matrices compare LR, MLP, SVM, XGBoost, and GBM models on a test set. Each matrix shows true versus predicted class counts, highlighting differences in model classification performance.</alt-text>
</graphic>
</fig>
<p>The model calibration performance evaluation (<xref ref-type="fig" rid="fig6">Figure 6</xref>) revealed that the GBM model had the smallest expected calibration error on the training set. On the test set, all models showed similar calibration performance, with expected calibration errors ranging from 0.076 to 0.167.</p>
<fig position="float" id="fig6">
<label>Figure 6</label>
<caption>
<p>Model calibration evaluation. <bold>(A)</bold> Calibration curves for different machine learning models on the training set. <bold>(B)</bold> Calibration curves for different machine learning models on the test set.</p>
</caption>
<graphic xlink:href="fneur-17-1738430-g006.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Two side-by-side line charts display calibration curves comparing predicted probabilities against actual outcomes for five models on training set (panel A, left) and test set (panel B, right). Curves for XGBoost, Logistic Regression, SVM, MLP, and LightGBM are compared to a dashed line representing perfect calibration. Legends indicate each model&#x2019;s color and average calibration error with ninety-five percent confidence intervals. Both axes are labeled: mean predicted value on the x-axis and fraction of positives on the y-axis. Panel B demonstrates greater deviation and variability among the models compared to panel A.</alt-text>
</graphic>
</fig>
<p>Decision curve analysis (<xref ref-type="fig" rid="fig7">Figure 7</xref>) further confirmed that, across most clinically relevant decision threshold ranges, all machine learning models offered higher net benefits compared to the &#x201C;treat-all&#x201D; or &#x201C;treat-none&#x201D; strategies, with the GBM model performing best across most threshold intervals.</p>
<fig position="float" id="fig7">
<label>Figure 7</label>
<caption>
<p>Decision curve analysis. <bold>(A)</bold> The net benefits of different machine learning models across varying threshold probabilities in the training set; <bold>(B)</bold> The corresponding performance in the test set. The black and blue dashed lines represent the reference net benefits of the &#x201C;Treat all&#x201D; and &#x201C;Treat none&#x201D; strategies, respectively.</p>
</caption>
<graphic xlink:href="fneur-17-1738430-g007.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Two line charts titled "Decision Curve Analysis" display net benefit versus threshold probability for multiple machine learning models comparing training set (left, panel A) and test set (right, panel B). Both charts include lines for &#x201C;Treat all,&#x201D; &#x201C;Treat none,&#x201D; logistic regression (LR), support vector machine (SVM), XGBoost, gradient boosting machine (GBM), and multilayer perceptron (MLP), with respective color-coded legends for comparison of net benefit.</alt-text>
</graphic>
</fig>
<p>Precision-recall curve analysis (<xref ref-type="fig" rid="fig8">Figure 8</xref>) indicated that the GBM model achieved an average precision (AP) of 0.87 on the test set, significantly higher than the baseline level (0.40). On the training set, the average precision (AP) was 0.94, substantially higher than the baseline level (0.41), confirming that the model maintained excellent classification performance across different thresholds.</p>
<fig position="float" id="fig8">
<label>Figure 8</label>
<caption>
<p>Precision-recall curve. <bold>(A)</bold> Precision and recall performance of the LGB model on the test set; <bold>(B)</bold> Performance on the training set. The x-axis represents recall, and the y-axis represents precision. The area under the curve (AP) reflects the model&#x2019;s overall ability to identify positive samples, while the dashed line indicates the performance of a random classifier.</p>
</caption>
<graphic xlink:href="fneur-17-1738430-g008.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Panel A is a precision-recall curve for a test set, showing the lightGBM classifier with an average precision of 0.87 compared to a chance level of 0.40. Panel B displays a precision-recall curve for a train set, where the classifier achieves an average precision of 0.94 versus a chance level of 0.41. Both panels have precision on the y-axis and recall on the x-axis.</alt-text>
</graphic>
</fig>
</sec>
<sec id="sec16">
<label>3.4</label>
<title>Model interpretability and application</title>
<p>Based on feature importance analysis and the SHAP value explanation framework, this study systematically identified the key factors influencing prognosis prediction in patients with chronic consciousness disorders. Through the visualization of SHAP summary plots, the impact of core features, including the CRS-R total score, age, GCS total score, and FOUR total score, was quantitatively analyzed. The SHAP feature importance plot, arranged in descending order of the absolute mean SHAP values, clearly demonstrated that these four indicators dominate the prediction model, with their cumulative contribution to the explained variance significantly higher than that of other variables. This confirmed the central role of these features in prognosis prediction.</p>
<p>Further analysis revealed that higher scores on the CRS-R, FOUR, and GCS scales were significantly positively correlated with favorable prognosis, highlighting the critical role of neurological function assessments in identifying recovery potential. In contrast, the age variable showed a significant negative correlation, suggesting that older age independently exerts a negative effect on prognosis. Additionally, while the weights of hospital stay duration, hemoglobin levels, and D-dimer concentrations were relatively lower, fluctuations in their SHAP values still significantly influenced the prediction outcomes, suggesting that these clinical parameters play an essential, though auxiliary, role in prognosis evaluation.</p>
<p>Case-specific analysis using SHAP force plots provided individualized insights into the model&#x2019;s predictions. For example, in a typical case, features such as a FOUR score of 14.0, GCS total score of 10.0, CRS-R total score of 8.0, and a hospital stay of 33.0&#x202F;days positively shifted the SHAP values, significantly increasing the likelihood of predicting a favorable prognosis. In contrast, indicators such as D-dimer concentration (1.18), hemoglobin level (97.0&#x202F;g/L), age (63.0&#x202F;years), and serum albumin level (32.0&#x202F;g/L) contributed negative SHAP values, thereby decreasing the predicted probability of a favorable outcome. This combined approach of group feature analysis and individual case validation strengthens the statistical robustness of the model and enhances its clinical interpretability and practical utility (<xref ref-type="fig" rid="fig9">Figure 9</xref>).</p>
<fig position="float" id="fig9">
<label>Figure 9</label>
<caption>
<p>SHA <italic>p</italic> value analysis. <bold>(A)</bold> Displays the direction and magnitude of each feature&#x2019;s impact on model output, with dot color indicating the feature value; <bold>(B)</bold> shows the mean SHAp value of each feature, reflecting its overall importance in the model; <bold>(C)</bold> presents the SHAP force plot of a single sample, visualizing the positive and negative contributions of individual features to the prediction, where red indicates features that increase the model output and blue indicates those that decrease it.</p>
</caption>
<graphic xlink:href="fneur-17-1738430-g009.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Three SHAP visualizations labeled A, B, and C: Panel A displays a SHAP summary dot plot ranking feature impacts with color gradients denoting feature values; Panel B shows a horizontal bar chart of feature importance, with Age as most influential; Panel C presents a SHAP force plot visualizing the contribution of each feature to the prediction, with positive and negative impacts highlighted.</alt-text>
</graphic>
</fig>
<p>Based on the above findings, the GBM model was selected as the optimal model. It not only demonstrated excellent predictive performance but also provides intuitive decision support for clinicians, enabling them to better understand and apply the model&#x2019;s predictions, thereby optimizing treatment plans and resource allocation for patients with prolonged disorders of consciousness pDOC.</p>
</sec>
</sec>
<sec sec-type="discussion" id="sec17">
<label>4</label>
<title>Discussion</title>
<p>This study evaluates an integrative machine-learning prognostic framework that combines routinely collected clinical indicators to predict functional outcome (Good vs. Poor GOS-E). By quantifying predictive performance and examining how conventional variables contribute jointly within a unified model, our findings provide evidence on the utility of data-driven integration of established clinical information for outcome stratification in this population.</p>
<p>The model demonstrated favorable overall discriminative performance, indicating that routinely available clinical indicators contain meaningful prognostic information when leveraged in combination. The observed operating characteristics, characterized by relatively high specificity with moderate sensitivity, suggest that the model adopts a more conservative strategy in identifying good functional outcomes. Accordingly, model outputs should be interpreted as supportive risk information, with decision thresholds selected based on the relative clinical consequences of false-positive and false-negative classifications.</p>
<p>The multi-model ensemble prediction model developed in this study demonstrated favorable performance in predicting the prognosis of patients with chronic disorders of consciousness. After training, testing, and validation, the GBM model showed comparatively robust predictive performance among the evaluated models. In the training set, the GBM achieved an ROC of 0.954 (95% CI, 0.924&#x2013;0.977), reflecting its ability to capture complex patterns in the data. This performance may be attributed to the gradient boosting mechanism, which iteratively optimizes model performance. While LR and MLP also demonstrated reasonable predictive ability, their performance in terms of generalizability and stability appeared relatively limited. Furthermore, Thr-NRI analysis suggested that GBM outperformed LR in risk reclassification, indicating potential advantages in clinically relevant risk stratification. Moreover, DCA supported the potential clinical utility of the model across a wide range of threshold probabilities, particularly between 0.2 and 0.6.</p>
<p>The key prognostic prediction factors identified in this study systematically cover a multidimensional assessment framework for clinical characteristics in patients with consciousness disorders. Among these, the CRS-R, GCS, and FOUR total scores, as core indicators of neurological function assessment, play an essential role in prognosis prediction. As the most widely used behavioral assessment scale in clinical practice, the CRS-R score directly reflects the patient&#x2019;s level of consciousness recovery, and its optimal value, determined through repeated assessments, can effectively enhance diagnostic reliability. A study by Xu et al. suggested that a CRS-R score &#x2264;7 could serve as a high-risk warning indicator, significantly increasing the biological risk of progression to permanent consciousness impairment (<xref ref-type="bibr" rid="ref28">28</xref>). The GCS scale, a classic tool for assessing the depth of coma, shows a significant correlation with consciousness state and prognosis, providing a crucial reference for evaluating the acute phase of the condition. However, the GCS is limited by its focus on three dimensions&#x2014;eye, verbal, and motor responses&#x2014;thereby limiting its assessment of overall neurological integrity (<xref ref-type="bibr" rid="ref8">8</xref>). The FOUR score system expands the assessment dimensions of the GCS by integrating additional indicators such as eye movement responses, motor function, brainstem reflexes, and breathing patterns, offering a more comprehensive neurological evaluation system. From a neuroanatomical functional localization perspective, the CRS-R is more sensitive to cortical function status (<xref ref-type="bibr" rid="ref29">29</xref>),while the FOUR scale excels at detecting signs of brainstem recovery, and the GCS focuses on evaluating motor responses of the limbs (<xref ref-type="bibr" rid="ref30">30</xref>, <xref ref-type="bibr" rid="ref31">31</xref>). The combined use of these three scales forms a comprehensive assessment system that spans from cortical to brainstem function, providing a multi-layered quantitative basis for accurately charting the trajectory of neurological function recovery and designing individualized rehabilitation strategies.</p>
<p>Age and length of hospital stay are critical prognostic factors that significantly influence the prognosis of patients with consciousness disorders. From a neurobiological perspective, older patients experience a marked decline in cognitive reserve due to physiological neurodegenerative changes. Their synaptic remodeling and neural plasticity abilities diminish progressively, leading to a significantly reduced capacity for neurological recovery after brain injury, compared to younger individuals. In contrast, children in the brain development phase demonstrate a unique advantage in neurorepair. According to the theory of neurofunctional reorganization, children&#x2019;s brains, when injured, can achieve functional recovery through compensation mechanisms in unaffected brain regions, particularly in motor function recovery, where unexpected rehabilitation effects are often seen. Recent clinical studies have provided empirical evidence supporting this conclusion. A large-scale cohort study by Duan et al. showed that the consciousness recovery rate in pediatric patients with pDoC significantly increased within 12&#x202F;months post-injury: 73.1% in the TBI group and 53.9% in the non-TBI group (<xref ref-type="bibr" rid="ref32">32</xref>). Subgroup analysis revealed that children under the age of 4, diagnosed with TBI, exhibited particularly high consciousness recovery potential, with significantly greater neurofunctional recovery efficiency than other age groups. This study suggests that age and injury type should be core components of individualized prognosis assessment systems for patients with consciousness disorders. Length of hospitalization emerged as a significant predictor; however, its interpretation warrants caution. In this study, it represents the total inpatient stay in the rehabilitation setting. This variable likely reflects a mixture of baseline functional status at rehabilitation admission, the pace of functional gains, intercurrent medical events, and discharge processes influenced by social support and institutional practice. Therefore, we interpret &#x201C;length of hospitalization&#x201D; primarily as an accessible marker of rehabilitation complexity and recovery trajectory rather than a causal determinant of GOS-E.</p>
<p>The predictive model developed in this study holds significant clinical value as a tool for early, accurate prognosis assessment. It can assist clinicians in formulating personalized treatment plans, optimizing resource allocation, and improving treatment outcomes. Additionally, it provides objective prognostic information for patients&#x2019; families, enhancing treatment adherence.</p>
<sec id="sec18">
<label>4.1</label>
<title>Limitations section</title>
<p>This study is limited by its single-center design, which may introduce selection bias and reduce generalizability. Although multiple routine clinical predictors were included, unmeasured factors may still influence prognosis, and the lack of neurophysiological and advanced neuroimaging data may constrain accuracy and interpretability. The model also shows high specificity but moderate sensitivity for Good vs. Poor GOS-E, potentially underestimating recovery in some patients; thus, predictions should be used cautiously with clinically appropriate thresholds. Multicenter, larger-sample validation is warranted.</p>
</sec>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="sec19">
<title>Data availability statement</title>
<p>The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.</p>
</sec>
<sec sec-type="ethics-statement" id="sec20">
<title>Ethics statement</title>
<p>The studies involving humans were approved by the Affiliated Rehabilitation Hospital of Nanchang University. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.</p>
</sec>
<sec sec-type="author-contributions" id="sec21">
<title>Author contributions</title>
<p>ZF: Conceptualization, Methodology, Investigation, Formal analysis, Writing &#x2013; original draft. QZ: Validation, Data curation, Writing &#x2013; review &#x0026; editing, Supervision.</p>
</sec>
<sec sec-type="COI-statement" id="sec22">
<title>Conflict of interest</title>
<p>The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="ai-statement" id="sec23">
<title>Generative AI statement</title>
<p>The author(s) declared that Generative AI was not used in the creation of this manuscript.</p>
<p>Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.</p>
</sec>
<sec sec-type="disclaimer" id="sec24">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
<ref-list>
<title>References</title>
<ref id="ref1"><label>1.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Kondziella</surname><given-names>D</given-names></name> <name><surname>Bender</surname><given-names>A</given-names></name> <name><surname>Diserens</surname><given-names>K</given-names></name> <name><surname>van Erp</surname><given-names>W</given-names></name> <name><surname>Estraneo</surname><given-names>A</given-names></name> <name><surname>Formisano</surname><given-names>R</given-names></name> <etal/></person-group>. <article-title>European academy of neurology guideline on the diagnosis of coma and other disorders of consciousness</article-title>. <source>Eur J Neurol</source>. (<year>2020</year>) <volume>27</volume>:<fpage>741</fpage>&#x2013;<lpage>56</lpage>. doi: <pub-id pub-id-type="doi">10.1111/ene.14151</pub-id>, <pub-id pub-id-type="pmid">32090418</pub-id></mixed-citation></ref>
<ref id="ref2"><label>2.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Song</surname><given-names>M</given-names></name> <name><surname>Yang</surname><given-names>Y</given-names></name> <name><surname>Yang</surname><given-names>Z</given-names></name> <name><surname>Cui</surname><given-names>Y</given-names></name> <name><surname>Yu</surname><given-names>S</given-names></name> <name><surname>He</surname><given-names>J</given-names></name> <etal/></person-group>. <article-title>Prognostic models for prolonged disorders of consciousness: an integrative review</article-title>. <source>Cell Mol Life Sci</source>. (<year>2020</year>) <volume>77</volume>:<fpage>3945</fpage>&#x2013;<lpage>61</lpage>. doi: <pub-id pub-id-type="doi">10.1007/s00018-020-03512-z</pub-id>, <pub-id pub-id-type="pmid">32306061</pub-id></mixed-citation></ref>
<ref id="ref3"><label>3.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Gao</surname><given-names>G</given-names></name> <name><surname>Wu</surname><given-names>X</given-names></name> <name><surname>Feng</surname><given-names>J</given-names></name> <name><surname>Hui</surname><given-names>J</given-names></name> <name><surname>Mao</surname><given-names>Q</given-names></name> <name><surname>Lecky</surname><given-names>F</given-names></name> <etal/></person-group>. <article-title>Clinical characteristics and outcomes in patients with traumatic brain injury in China: a prospective, multicentre, longitudinal, observational study</article-title>. <source>Lancet Neurol</source>. (<year>2020</year>) <volume>19</volume>:<fpage>670</fpage>&#x2013;<lpage>7</lpage>. doi: <pub-id pub-id-type="doi">10.1016/s1474-4422(20)30182-4</pub-id>, <pub-id pub-id-type="pmid">32702336</pub-id></mixed-citation></ref>
<ref id="ref4"><label>4.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Shilan</surname><given-names>T</given-names></name> <name><surname>Yansui</surname><given-names>X</given-names></name></person-group>. <article-title>Advances in rehabilitation outcomes and care in patients with prolonged disorders of consciousness</article-title>. <source>Chin Gen Pract</source>. (<year>2023</year>) <volume>3</volume>:<fpage>1</fpage>&#x2013;<lpage>8</lpage>. doi: <pub-id pub-id-type="doi">10.12114/j.issn.1007-9572.2023.0088</pub-id></mixed-citation></ref>
<ref id="ref5"><label>5.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Leonardi</surname><given-names>M</given-names></name> <name><surname>Giovannetti</surname><given-names>AM</given-names></name> <name><surname>Pagani</surname><given-names>M</given-names></name> <name><surname>Raggi</surname><given-names>A</given-names></name> <name><surname>Sattin</surname><given-names>D</given-names></name><collab id="coll1">National Consortium Functioning And Disability In Vegetative And In Minimal Conscious State Patients</collab></person-group>. <article-title>Burden and needs of 487 caregivers of patients in vegetative state and in minimally conscious state: results from a national study</article-title>. <source>Brain Inj</source>. (<year>2012</year>) <volume>26</volume>:<fpage>1201</fpage>&#x2013;<lpage>10</lpage>. doi: <pub-id pub-id-type="doi">10.3109/02699052.2012.667589</pub-id>, <pub-id pub-id-type="pmid">22571687</pub-id></mixed-citation></ref>
<ref id="ref6"><label>6.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Soeterik</surname><given-names>SM</given-names></name> <name><surname>Connolly</surname><given-names>S</given-names></name> <name><surname>Playford</surname><given-names>ED</given-names></name> <name><surname>Duport</surname><given-names>S</given-names></name> <name><surname>Riazi</surname><given-names>A</given-names></name></person-group>. <article-title>The psychological impact of prolonged disorders of consciousness on caregivers: a systematic review of quantitative studies</article-title>. <source>Clin Rehabil</source>. (<year>2017</year>) <volume>31</volume>:<fpage>1374</fpage>&#x2013;<lpage>85</lpage>. doi: <pub-id pub-id-type="doi">10.1177/0269215517695372</pub-id>, <pub-id pub-id-type="pmid">28933608</pub-id></mixed-citation></ref>
<ref id="ref7"><label>7.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Giacino</surname><given-names>JT</given-names></name> <name><surname>Katz</surname><given-names>DI</given-names></name> <name><surname>Schiff</surname><given-names>ND</given-names></name> <name><surname>Whyte</surname><given-names>J</given-names></name> <name><surname>Ashman</surname><given-names>EJ</given-names></name> <name><surname>Ashwal</surname><given-names>S</given-names></name> <etal/></person-group>. <article-title>Practice guideline update recommendations summary: disorders of consciousness: report of the guideline development, dissemination, and implementation Subcommittee of the American Academy of neurology; the American congress of rehabilitation medicine; and the National Institute on Disability, Independent Living, and Rehabilitation Research</article-title>. <source>Neurology</source>. (<year>2018</year>) <volume>91</volume>:<fpage>450</fpage>&#x2013;<lpage>60</lpage>. doi: <pub-id pub-id-type="doi">10.1212/WNL.0000000000005926</pub-id>, <pub-id pub-id-type="pmid">30089618</pub-id></mixed-citation></ref>
<ref id="ref8"><label>8.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Teasdale</surname><given-names>G</given-names></name> <name><surname>Jennett</surname><given-names>B</given-names></name></person-group>. <article-title>Assessment of coma and impaired consciousness. A practical scale</article-title>. <source>Lancet</source>. (<year>1974</year>) <volume>2</volume>:<fpage>81</fpage>&#x2013;<lpage>4</lpage>. doi: <pub-id pub-id-type="doi">10.1016/S0140-6736(74)91639-0</pub-id>, <pub-id pub-id-type="pmid">4136544</pub-id></mixed-citation></ref>
<ref id="ref9"><label>9.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Laureys</surname><given-names>S</given-names></name> <name><surname>Bodart</surname><given-names>O</given-names></name> <name><surname>Gosseries</surname><given-names>O</given-names></name></person-group>. <article-title>The Glasgow coma scale: time for critical reappraisal?</article-title> <source>Lancet Neurol</source>. (<year>2014</year>) <volume>13</volume>:<fpage>755</fpage>&#x2013;<lpage>7</lpage>. doi: <pub-id pub-id-type="doi">10.1016/s1474-4422(14)70152-8</pub-id>, <pub-id pub-id-type="pmid">25030507</pub-id></mixed-citation></ref>
<ref id="ref10"><label>10.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Wijdicks</surname><given-names>EF</given-names></name> <name><surname>Bamlet</surname><given-names>WR</given-names></name> <name><surname>Maramattom</surname><given-names>BV</given-names></name> <name><surname>Manno</surname><given-names>EM</given-names></name> <name><surname>McClelland</surname><given-names>RL</given-names></name></person-group>. <article-title>Validation of a new coma scale: the four score</article-title>. <source>Ann Neurol</source>. (<year>2005</year>) <volume>58</volume>:<fpage>585</fpage>&#x2013;<lpage>93</lpage>. doi: <pub-id pub-id-type="doi">10.1002/ana.20611</pub-id>, <pub-id pub-id-type="pmid">16178024</pub-id></mixed-citation></ref>
<ref id="ref11"><label>11.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Giacino</surname><given-names>JT</given-names></name> <name><surname>Kalmar</surname><given-names>K</given-names></name> <name><surname>Whyte</surname><given-names>J</given-names></name></person-group>. <article-title>The JFK coma recovery scale-revised: measurement characteristics and diagnostic utility</article-title>. <source>Arch Phys Med Rehabil</source>. (<year>2004</year>) <volume>85</volume>:<fpage>2020</fpage>&#x2013;<lpage>9</lpage>. doi: <pub-id pub-id-type="doi">10.1016/j.apmr.2004.02.033</pub-id>, <pub-id pub-id-type="pmid">15605342</pub-id></mixed-citation></ref>
<ref id="ref12"><label>12.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Bodien</surname><given-names>YG</given-names></name> <name><surname>Carlowicz</surname><given-names>CA</given-names></name> <name><surname>Chatelle</surname><given-names>C</given-names></name> <name><surname>Giacino</surname><given-names>JT</given-names></name></person-group>. <article-title>Sensitivity and specificity of the coma recovery scale--revised Total score in detection of conscious awareness</article-title>. <source>Arch Phys Med Rehabil</source>. (<year>2016</year>) <volume>97</volume>:<fpage>490</fpage>&#x2013;<lpage>2.e1</lpage>. doi: <pub-id pub-id-type="doi">10.1016/j.apmr.2015.08.422</pub-id>, <pub-id pub-id-type="pmid">26342571</pub-id></mixed-citation></ref>
<ref id="ref13"><label>13.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Schnakers</surname><given-names>C</given-names></name> <name><surname>Vanhaudenhuyse</surname><given-names>A</given-names></name> <name><surname>Giacino</surname><given-names>J</given-names></name> <name><surname>Ventura</surname><given-names>M</given-names></name> <name><surname>Boly</surname><given-names>M</given-names></name> <name><surname>Majerus</surname><given-names>S</given-names></name> <etal/></person-group>. <article-title>Diagnostic accuracy of the vegetative and minimally conscious state: clinical consensus versus standardized neurobehavioral assessment</article-title>. <source>BMC Neurol</source>. (<year>2009</year>) <volume>9</volume>:<fpage>35</fpage>. doi: <pub-id pub-id-type="doi">10.1186/1471-2377-9-35</pub-id>, <pub-id pub-id-type="pmid">19622138</pub-id></mixed-citation></ref>
<ref id="ref14"><label>14.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Owen</surname><given-names>AM</given-names></name> <name><surname>Coleman</surname><given-names>MR</given-names></name> <name><surname>Boly</surname><given-names>M</given-names></name> <name><surname>Davis</surname><given-names>MH</given-names></name> <name><surname>Laureys</surname><given-names>S</given-names></name> <name><surname>Pickard</surname><given-names>JD</given-names></name></person-group>. <article-title>Detecting awareness in the vegetative state</article-title>. <source>Science</source>. (<year>2006</year>) <volume>313</volume>:<fpage>1402</fpage>. doi: <pub-id pub-id-type="doi">10.1126/science.1130197</pub-id>, <pub-id pub-id-type="pmid">16959998</pub-id></mixed-citation></ref>
<ref id="ref15"><label>15.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Giacino</surname><given-names>JT</given-names></name> <name><surname>Fins</surname><given-names>JJ</given-names></name> <name><surname>Laureys</surname><given-names>S</given-names></name> <name><surname>Schiff</surname><given-names>ND</given-names></name></person-group>. <article-title>Disorders of consciousness after acquired brain injury: the state of the science</article-title>. <source>Nat Rev Neurol</source>. (<year>2014</year>) <volume>10</volume>:<fpage>99</fpage>&#x2013;<lpage>114</lpage>. doi: <pub-id pub-id-type="doi">10.1038/nrneurol.2013.279</pub-id>, <pub-id pub-id-type="pmid">24468878</pub-id></mixed-citation></ref>
<ref id="ref16"><label>16.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Huang</surname><given-names>L</given-names></name> <name><surname>Kang</surname><given-names>J</given-names></name> <name><surname>Zhong</surname><given-names>Y</given-names></name> <name><surname>Zhang</surname><given-names>J</given-names></name> <name><surname>Qiang</surname><given-names>M</given-names></name> <name><surname>Feng</surname><given-names>Z</given-names></name></person-group>. <article-title>A predictive model for awakening in patients with prolonged disorders of consciousness after craniocerebral injury</article-title>. <source>Medicine (Baltimore)</source>. (<year>2024</year>) <volume>103</volume>:<fpage>e36701</fpage>. doi: <pub-id pub-id-type="doi">10.1097/md.0000000000036701</pub-id>, <pub-id pub-id-type="pmid">38215152</pub-id></mixed-citation></ref>
<ref id="ref17"><label>17.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Gawryluk</surname><given-names>JR</given-names></name> <name><surname>D'arcy</surname><given-names>RC</given-names></name> <name><surname>Connolly</surname><given-names>JF</given-names></name> <name><surname>Weaver</surname><given-names>DF</given-names></name></person-group>. <article-title>Improving the clinical assessment of consciousness with advances in electrophysiological and neuroimaging techniques</article-title>. <source>BMC Neurol</source>. (<year>2010</year>) <volume>10</volume>:<fpage>11</fpage>. doi: <pub-id pub-id-type="doi">10.1186/1471-2377-10-11</pub-id>, <pub-id pub-id-type="pmid">20113490</pub-id></mixed-citation></ref>
<ref id="ref18"><label>18.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Formisano</surname><given-names>R</given-names></name> <name><surname>D&#x2019;Ippolito</surname><given-names>M</given-names></name> <name><surname>Giustini</surname><given-names>M</given-names></name> <name><surname>Catani</surname><given-names>S</given-names></name> <name><surname>Mondello</surname><given-names>S</given-names></name> <name><surname>Piccolino</surname><given-names>I</given-names></name> <etal/></person-group>. <article-title>The prognostic role of candidate serum biomarkers in the post-acute and chronic phases of disorder of consciousness: a preliminary study</article-title>. <source>Brain Sci</source>. (<year>2024</year>) <volume>14</volume>:<fpage>239</fpage>. doi: <pub-id pub-id-type="doi">10.3390/brainsci14030239</pub-id></mixed-citation></ref>
<ref id="ref19"><label>19.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Bagnato</surname><given-names>S</given-names></name> <name><surname>Boccagni</surname><given-names>C</given-names></name></person-group>. <article-title>Cerebrospinal fluid and blood biomarkers in patients with post-traumatic disorders of consciousness: a scoping review</article-title>. <source>Brain Sci</source>. (<year>2023</year>) <volume>13</volume>:<fpage>364</fpage>. doi: <pub-id pub-id-type="doi">10.3390/brainsci13020364</pub-id>, <pub-id pub-id-type="pmid">36831907</pub-id></mixed-citation></ref>
<ref id="ref20"><label>20.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Lee</surname><given-names>M</given-names></name> <name><surname>Laureys</surname><given-names>S</given-names></name></person-group>. <article-title>Artificial intelligence and machine learning in disorders of consciousness</article-title>. <source>Curr Opin Neurol</source>. (<year>2024</year>) <volume>37</volume>:<fpage>614</fpage>&#x2013;<lpage>20</lpage>. doi: <pub-id pub-id-type="doi">10.1097/WCO.0000000000001322</pub-id>, <pub-id pub-id-type="pmid">39498844</pub-id></mixed-citation></ref>
<ref id="ref21"><label>21.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Haveman</surname><given-names>ME</given-names></name> <name><surname>Van Putten</surname><given-names>M</given-names></name> <name><surname>Hom</surname><given-names>HW</given-names></name> <name><surname>Van Putten</surname><given-names>MJAM</given-names></name> <name><surname>Eertman-Meyer</surname><given-names>CJ</given-names></name> <name><surname>Beishuizen</surname><given-names>A</given-names></name> <etal/></person-group>. <article-title>Predicting outcome in patients with moderate to severe traumatic brain injury using electroencephalography</article-title>. <source>Crit Care</source>. (<year>2019</year>) <volume>23</volume>:<fpage>401</fpage>. doi: <pub-id pub-id-type="doi">10.1186/s13054-019-2656-6</pub-id>, <pub-id pub-id-type="pmid">31829226</pub-id></mixed-citation></ref>
<ref id="ref22"><label>22.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Yu</surname><given-names>R</given-names></name> <name><surname>Zhang</surname><given-names>H</given-names></name> <name><surname>Wu</surname><given-names>X</given-names></name> <name><surname>Fei</surname><given-names>X</given-names></name> <name><surname>Yang</surname><given-names>Q</given-names></name> <name><surname>Ma</surname><given-names>Z</given-names></name> <etal/></person-group>. <article-title>Outcome prediction of unconscious patients based on weighted sparse brain network construction</article-title>. <source>IEEE J Biomed Health Inform</source>. (<year>2023</year>) <volume>27</volume>:<fpage>469</fpage>&#x2013;<lpage>79</lpage>. doi: <pub-id pub-id-type="doi">10.1109/JBHI.2022.3218652</pub-id>, <pub-id pub-id-type="pmid">36318552</pub-id></mixed-citation></ref>
<ref id="ref23"><label>23.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>El-Rashidy</surname><given-names>N</given-names></name> <name><surname>Sedik</surname><given-names>A</given-names></name> <name><surname>Siam</surname><given-names>AI</given-names></name> <name><surname>Ali</surname><given-names>ZH</given-names></name></person-group>. <article-title>An efficient edge/cloud medical system for rapid detection of level of consciousness in emergency medicine based on explainable machine learning models</article-title>. <source>Neural Comput Applic</source>. (<year>2023</year>) <volume>35</volume>:<fpage>10695</fpage>&#x2013;<lpage>716</lpage>. doi: <pub-id pub-id-type="doi">10.1007/s00521-023-08258-w</pub-id>, <pub-id pub-id-type="pmid">37155550</pub-id></mixed-citation></ref>
<ref id="ref24"><label>24.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Liuzzi</surname><given-names>P</given-names></name> <name><surname>Magliacano</surname><given-names>A</given-names></name> <name><surname>De Bellis</surname><given-names>F</given-names></name> <name><surname>Mannini</surname><given-names>A</given-names></name> <name><surname>Estraneo</surname><given-names>A</given-names></name></person-group>. <article-title>&#x003C;article-title update="added"&#x003E;predicting outcome of patients with prolonged disorders of consciousness using machine learning models based on medical complexity</article-title>. <source>Sci Rep</source>. (<year>2022</year>) <volume>12</volume>:<fpage>13471</fpage>. doi: <pub-id pub-id-type="doi">10.1038/s41598-022-17561-w</pub-id>, <pub-id pub-id-type="pmid">35931703</pub-id></mixed-citation></ref>
<ref id="ref25"><label>25.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Alt&#x0131;ntop</surname><given-names>&#x00C7;G</given-names></name> <name><surname>Latifo&#x011F;lu</surname><given-names>F</given-names></name> <name><surname>Ak&#x0131;n</surname><given-names>AK</given-names></name> <name><surname>&#x00DC;lgey</surname><given-names>A</given-names></name></person-group>. <article-title>Quantitative electroencephalography analysis for improved assessment of consciousness levels in deep coma patients using a proposed stimulus stage</article-title>. <source>Diagnostics (Basel)</source>. (<year>2023</year>) <volume>13</volume>:<fpage>1383</fpage>. doi: <pub-id pub-id-type="doi">10.3390/diagnostics13081383</pub-id>, <pub-id pub-id-type="pmid">37189484</pub-id></mixed-citation></ref>
<ref id="ref26"><label>26.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Wilson</surname><given-names>L</given-names></name> <name><surname>Boase</surname><given-names>K</given-names></name> <name><surname>Nelson</surname><given-names>LD</given-names></name> <name><surname>Temkin</surname><given-names>NR</given-names></name> <name><surname>Giacino</surname><given-names>JT</given-names></name> <name><surname>Markowitz</surname><given-names>AJ</given-names></name> <etal/></person-group>. <article-title>A manual for the Glasgow outcome scale-extended interview</article-title>. <source>J Neurotrauma</source>. (<year>2021</year>) <volume>38</volume>:<fpage>2435</fpage>&#x2013;<lpage>46</lpage>. doi: <pub-id pub-id-type="doi">10.1089/neu.2020.7527</pub-id>, <pub-id pub-id-type="pmid">33740873</pub-id></mixed-citation></ref>
<ref id="ref27"><label>27.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Pencina</surname><given-names>MJ</given-names></name> <name><surname>D'agostino</surname><given-names>RB</given-names></name> <name><surname>D'agostino</surname><given-names>RB</given-names></name> <name><surname>Vasan</surname><given-names>RS</given-names></name></person-group>. <article-title>Evaluating the added predictive ability of a new marker: from area under the roc curve to reclassification and beyond</article-title>. <source>Stat Med</source>. (<year>2008</year>) <volume>27</volume>:<fpage>157</fpage>&#x2013;<lpage>72</lpage>. doi: <pub-id pub-id-type="doi">10.1002/sim.2929</pub-id>, <pub-id pub-id-type="pmid">17569110</pub-id></mixed-citation></ref>
<ref id="ref28"><label>28.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Xu</surname><given-names>L</given-names></name> <name><surname>Ge</surname><given-names>Q</given-names></name> <name><surname>Lu</surname><given-names>H</given-names></name> <name><surname>Zhuang</surname><given-names>Y</given-names></name> <name><surname>Geng</surname><given-names>X</given-names></name> <name><surname>Chen</surname><given-names>X</given-names></name> <etal/></person-group>. <article-title>Cerebrospinal fluid metabolite alterations in patients with different etiologies, diagnoses, and prognoses of disorders of consciousness</article-title>. <source>Brain Behav</source>. (<year>2023</year>) <volume>13</volume>:<fpage>e3070</fpage>. doi: <pub-id pub-id-type="doi">10.1002/brb3.3070</pub-id>, <pub-id pub-id-type="pmid">37421239</pub-id></mixed-citation></ref>
<ref id="ref29"><label>29.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Cao</surname><given-names>B</given-names></name> <name><surname>Chen</surname><given-names>Y</given-names></name> <name><surname>Yu</surname><given-names>R</given-names></name> <name><surname>Chen</surname><given-names>L</given-names></name> <name><surname>Chen</surname><given-names>P</given-names></name> <name><surname>Weng</surname><given-names>Y</given-names></name> <etal/></person-group>. <article-title>Abnormal dynamic properties of functional connectivity in disorders of consciousness</article-title>. <source>Neuroimage Clin</source>. (<year>2019</year>) <volume>24</volume>:<fpage>102071</fpage>. doi: <pub-id pub-id-type="doi">10.1016/j.nicl.2019.102071</pub-id>, <pub-id pub-id-type="pmid">31795053</pub-id></mixed-citation></ref>
<ref id="ref30"><label>30.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Saika</surname><given-names>A</given-names></name> <name><surname>Bansal</surname><given-names>S</given-names></name> <name><surname>Philip</surname><given-names>M</given-names></name> <name><surname>Devi</surname><given-names>BI</given-names></name> <name><surname>Shukla</surname><given-names>DP</given-names></name></person-group>. <article-title>Prognostic value of four and Gcs scores in determining mortality in patients with traumatic brain injury</article-title>. <source>Acta Neurochir</source>. (<year>2015</year>) <volume>157</volume>:<fpage>1323</fpage>&#x2013;<lpage>8</lpage>. doi: <pub-id pub-id-type="doi">10.1007/s00701-015-2469-6</pub-id>, <pub-id pub-id-type="pmid">26077394</pub-id></mixed-citation></ref>
<ref id="ref31"><label>31.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Schnakers</surname><given-names>C</given-names></name> <name><surname>Giacino</surname><given-names>J</given-names></name> <name><surname>Kalmar</surname><given-names>K</given-names></name> <name><surname>Piret</surname><given-names>S</given-names></name> <name><surname>Lopez</surname><given-names>E</given-names></name> <name><surname>Boly</surname><given-names>M</given-names></name> <etal/></person-group>. <article-title>Does the four score correctly diagnose the vegetative and minimally conscious states?</article-title> <source>Ann Neurol</source>. (<year>2006</year>) <volume>60</volume>:<fpage>744</fpage>&#x2013;<lpage>5</lpage>. doi: <pub-id pub-id-type="doi">10.1002/ana.20919</pub-id>, <pub-id pub-id-type="pmid">16847951</pub-id></mixed-citation></ref>
<ref id="ref32"><label>32.</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Duan</surname><given-names>X</given-names></name> <name><surname>Zhang</surname><given-names>T</given-names></name> <name><surname>Chen</surname><given-names>Y</given-names></name> <name><surname>Hou</surname><given-names>X</given-names></name> <name><surname>Huang</surname><given-names>Q</given-names></name> <name><surname>Li</surname><given-names>T</given-names></name> <etal/></person-group>. <article-title>Natural course and predictors of consciousness recovery in children with prolonged disorder of consciousness</article-title>. <source>Sci Rep</source>. (<year>2024</year>) <volume>14</volume>:<fpage>17417</fpage>. doi: <pub-id pub-id-type="doi">10.1038/s41598-024-68370-2</pub-id>, <pub-id pub-id-type="pmid">39075188</pub-id></mixed-citation></ref>
</ref-list>
<fn-group>
<fn fn-type="custom" custom-type="edited-by" id="fn0001">
<p>Edited by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/547573/overview">Chen-Chih Chung</ext-link>, Taipei Medical University, Taiwan</p>
</fn>
<fn fn-type="custom" custom-type="reviewed-by" id="fn0002">
<p>Reviewed by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1747468/overview">Li Tingsong</ext-link>, Children&#x2019;s Hospital of Chongqing Medical University, China</p>
<p><ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/2227135/overview">Qi Xiong</ext-link>, The First Affiliated Hospital of Nanchang University, China</p>
</fn>
</fn-group>
</back>
</article>