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Original Article
2026
:1;
8
doi:
10.25259/AETCC_11_2025

Comparative Evaluation of Computed Tomography-Based Scoring Systems For Predicting Mortality In Adults With Traumatic Brain Injury: A Retrospective Study

Department of Emergency Medicine, Sardar Vallabhbhai Patel Institute of Medical Sciences and Research, Smt.NHL Municipal Medical College, Ahmedabad, Gujarat, India.

*Corresponding author: Dharmistra Dhusa, Department of Emergency Medicine, Sardar Vallabhbhai Patel Institute of Medical Sciences and Research, Smt. NHL Municipal Medical College, Ahmedabad, Gujarat, India. dhusadharmistha@gmail.com

Licence
This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

How to cite this article: Thanth NK, Dhusa D, Kella K, Jarwani B. Comparative Evaluation of Computed Tomography-Based Scoring Systems For Predicting Mortality In Adults With Traumatic Brain Injury: A Retrospective Study. Ann Emerg Trauma Crit Care. doi: 10.25259/ AETCC_11_2025

Abstract

Objectives:

To evaluate and compare the prognostic performance of five commonly used computed tomography (CT)-based scoring systems—Rotterdam, Helsinki, Stockholm, Marshall, and The neuroimaging radiological interpretation system (NIRIS)—in predicting in-hospital and 30-day mortality among patients with traumatic brain injury (TBI).

Material and Methods:

This retrospective observational study included 278 adult patients with TBI presenting to the emergency department of a tertiary care hospital in Ahmedabad, India, during 2024. All patients underwent non-contrast CT of the head within two hours of presentation. CT images were independently assessed by neuroradiologists and scored according to the five CT-based scoring systems. Mortality outcomes were evaluated at hospital discharge and at 30 days post-injury. Prognostic accuracy was determined using sensitivity, specificity, positive and negative predictive values, and the area under the receiver operating characteristic curve (AUC).

Results:

The overall 30-day mortality was 15.1% (n=42). Higher scores in all systems correlated with increased mortality (p<0.001). The Stockholm score demonstrated the best performance (specificity 91%, AUC 0.89), followed by the Helsinki score (AUC 0.86). Rotterdam and Marshall scores also showed strong discriminatory ability, while NIRIS was moderately predictive. Diffuse axonal injury, cerebral oedema, and midline shift were significant imaging predictors of poor outcome.

Conclusion:

All five CT-based scoring systems are valid predictors of mortality in TBI patients. the Stockholm and Helsinki scores demonstrated superior Prognostic performance and may be incorporated into early emergency department assessment, particularly when combined with clinical variables such as Glasgow coma scale. these findings highlight the importance of structured imaging-based scoring for improving early risk stratification and guiding management.

Keywords

CT scoring
Emergency medicine
Mortality prediction
Stockholm score
Traumatic brain injury

INTRODUCTION

Traumatic brain injury (TBI) is one of the leading causes of morbidity and mortality worldwide, with an annual incidence ranging from 150 to 300 per 100,000 individuals.1 Severe TBI carries a mortality rate as high as 50%, while moderate TBI accounts for approximately 10% mortality.2 Beyond mortality, many survivors experience significant long-term physical, cognitive, and psychosocial disabilities, making TBI a major public health and socioeconomic burden. Accurate early prognostication is therefore critical to guide clinical decision-making, optimise resource allocation, and support informed discussions with patients’ families.3 The aetiology of TBI commonly includes road traffic accidents, falls, and assaults. Prognosis is influenced by several clinical and radiological factors, including hypoxia, age, intracranial pressure (ICP), and systemic complications such as sepsis or pneumonia.4 Preventing secondary brain injury, particularly from raised ICP and subsequent herniation, remains a cornerstone of management, as untreated ICP elevation is strongly linked to poor outcomes and mortality.5

Among clinical predictors, the Glasgow Coma Scale (GCS) continues to be a widely applied tool, with lower scores correlating with higher mortality. However, neuroimaging-especially computed tomography (CT) has emerged as indispensable.6 the acute evaluation of TBI, owing to its rapid acquisition, availability, and ability to detect life-threatening lesions. While magnetic resonance imaging (MRI) offers higher sensitivity for subtle injuries, its limited accessibility and longer acquisition times restrict its use in emergency settings.7

Several CT-based scoring systems have been developed to provide a structured, objective assessment of TBI severity. These include the Marshall classification, Rotterdam CT score, Helsinki CT score, Stockholm CT score, and the neuroimaging radiological interpretation system (NIRIS).8 They evaluate key imaging features such as midline shift, basal cistern compression, intracranial haemorrhage, and diffuse axonal injury, thereby quantifying injury severity and aiding mortality prediction.9 Comparative studies suggest that such structured radiological scores enhance prognostic accuracy beyond clinical variables alone.10

However, despite their growing adoption internationally, limited research has systematically compared these scoring systems in Indian tertiary care emergency settings. Furthermore, most prior studies have focused on individual scoring systems rather than head-to-head comparisons, leaving uncertainty regarding which systems perform best in specific populations.

Objectives

This study aims to evaluate and compare the predictive performance of five major CT-based scoring systems-Marshall, Rotterdam, Helsinki, Stockholm, and NIRIS- in relation to in-hospital and 30-day mortality outcomes among patients presenting with TBI to the emergency department of a tertiary care hospital.

MATERIAL AND METHODS

This retrospective observational study was conducted at the tertiary care department. All adult patients (≥18 years) with acute traumatic brain injury (TBI) who presented between 1st January to 30th December 2024 were eligible for inclusion.

Inclusion and exclusion criteria

Patients were included if they underwent a non-contrast CT brain scan during their initial emergency evaluation. Exclusion criteria were: (a) Patients <18 years, (b) Those declared dead on arrival or before undergoing CT, (c) Individuals with pre-existing neurological disorders, (d) Patients with non-traumatic causes of death, and (e) Those who had neurosurgical intervention at an external facility.

Clinical data collection

Demographic and clinical parameters recorded included age, sex, mechanism of injury, type of TBI, and Glasgow Coma Scale (GCS) score on admission (mild: 13–15, moderate: 9–12, severe: 3–8).11

Data regarding comorbidities, complications (such as sepsis, pneumonia, brain oedema, and raised intracranial pressure), associated injuries, neurosurgical procedures, and hospital stay duration were also documented.

Imaging data

Non-contrast CT scans were performed within two hours of arrival. Scans were independently reviewed by two experienced neuro-radiologists blinded to patient outcomes. Imaging findings included subarachnoid haemorrhage (SAH), epidural haemorrhage (EDH), subdural haemorrhage (SDH), brain contusions, diffuse axonal injury (DAI), midline shift (MLS), cranial fractures, oedema, herniation, and parenchymal lacerations. Each patient was scored using five systems: the Marshall CT Classification and the Rotterdam CT score.12 Helsinki score, Stockholm score, and NIRIS.

Statistical analysis

Data were analysed using SPSS (statistical package for the social sciences) version 16.0 (IBM Corp., Armonk, NY). Continuous variables were summarised with mean, standard deviation, median, and interquartile range, while categorical variables were presented as frequencies and percentages. Group comparisons used the Chi-square test for categorical data and Student’s t-test for continuous variables. Non-parametric tests (e.g., Mann–Whitney U test) were applied where appropriate.

The prognostic accuracy of each CT-based scoring system for predicting in-hospital and 30-day mortality was assessed through sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and odds ratio. Receiver operating characteristic (ROC) curves were constructed, and discriminative ability was expressed as the area under the curve (AUC) with bootstrapped 95% confidence intervals.13

Ethical considerations

The study was retrospective, as it was conducted in the tertiary care department; therefore, informed consent was waived. All patient data were anonymised to protect confidentiality.

RESULTS

1. Clinico-demographical data: The average age was 49.53 years, with 192 males and 86 females. However, mortality is highest in elderly patients, those with severe GCS (50%), raised ICP, and sepsis. Surgery, morbidities and associated injuries were more common among non-survivors [Table 1].

Table 1: Clinico-demographical data
Variable Category Total patients (n, %) Non-survivors (n, %) Mortality (%) p-value
Age group 18–30 years 60 (21.6%) 6 (10.0%) 2.6% 0.04
31–60 years 140 (50.4%) 26 (18.6%) 9.4%
>61 years 78 (28.1%) 11 (14.1%) 4.0%
Sex Male 192 (69.0%) 32 (16.7%) 11.5% 0.12
Female 86 (30.9%) 10 (11.6%) 3.6%
Mechanism of injury RTA 213 (76.6%) 33 (15.5%) 11.9% 0.035
Fall from height 36 (12.9%) 6 (16.7%) 2.2%
Assault 29 (10.4%) 3 (10.3%) 2.2%
TBI severity (admission GCS) Mild (13–15) 167 (60.0%) 8 (4.8%) 2.9% <0.001
Moderate (9–12) 50 (18.0%) 20 (40.0%) 7.2%
Severe (3–8) 61 (22.0%) 14 (23.0%) 5.0%
Comorbidities Present 114 (41.0%) 27 (23.7%) 9.7% 0.006
Absent 164 (59.0%) 15 (9.1%) 5.4%
Complications None 183 (65.8%) 1 (0.5%) 0.4% <0.001
Brain oedema 28 (10.1%) 14 (50.0%) 5.0%
Raised intracranial pressure 8 (2.9%) 6 (75.0%) 2.2%
Aspiration pneumonitis 18 (6.5%) 2 (11.1%) 0.7%
Sepsis 27 (9.7%) 14 (51.9%) 5.0%
Shock 14 (5.0%) 7 (50.0%) 2.5%
Herniation 9 (3.2%) 2 (22.2%) 0.7%
Associated injuries Present 94 (33.8%) 25 (26.6%) 9.0% 0.23
Absent 184 (66.2%) 17 (9.2%) 22.7%
Surgery performed Yes 44 (15.8%) 14 (31.8%) 5.0% 0.04
No 234 (84.2%) 28 (11.8%) 10.0%

RTA-Road traffic accident, GCS-Glasglow coma scale, TBI-Traumatic brain injury, p < 0.05 is statistically significant

2. Radiological profile: Normal CT findings strongly correlate with survival (p = 0.001). Statistically significant (p < 0.05) findings are associated with higher mortality in diffuse axonal injury, brain haerniation, midline shift, extradural haematoma (EDH), despite being an intracranial bleed, and brain oedema [Table 2 and Graph 1].14 Diffuse axonal injury and brain oedema are strongly associated with increased mortality (p < 0.001). Skull fracture and EDH showed trends toward significance but did not meet the 0.05 threshold due to patients with EDH being operated on quickly and hence having less mortality.

Table 2: Radiological data
CT finding Total patients (n, %) With complications (n, %) Non-survivors (n, %) Mortality (%)
Normal scan 75 (27.0%) 8 (10.7%) 5 (6.7%) 1.8%
Subarachnoid haemorrhage (SAH) 107 (38.5%) 47 (43.9%) 22 (20.6%) 7.9%
Subdural haematoma (SDH) 69 (24.8%) 34 (49.3%) 13 (18.8%) 4.7%
Extradural haematoma (EDH) 28 (10.1%) 19 (67.9%) 11 (39.3%) 6.8%
Brain contusions 69 (24.8%) 35 (50.7%) 14 (20.3%) 5.0%
Skull fractures 108 (38.8%) 45 (40.7%) 18 (16.7%) 6.5%
Diffuse axonal injury (DAI) 16 (5.8%) 13 (81.3%) 11 (68.8%) 4.0%
Brain oedema 28 (10.1%) 8 (28.6%) 20 (71.4%) 7.2%
Brain herniation 9 (3.2%) 4 (44.4%) 2 (22.2%) 0.7%
Midline shift <5 mm 76 (27.3%) 20 (26.3%) 23 (30.3%) 8.3%
Midline shift >5 mm 34 (12.2%) 14 (41.2%) 12 (35.3%) 4.3%

CT: Computed tomography

Above given horizontal bar chart visually compares categorical variables (in this case, CT findings) against a quantitative outcome (mortality rate as a percentage). Each horizontal bar represents a different CT finding, and its length reflects the associated mortality rate.
Graph 1: Above given horizontal bar chart visually compares categorical variables (in this case, CT findings) against a quantitative outcome (mortality rate as a percentage). Each horizontal bar represents a different CT finding, and its length reflects the associated mortality rate.

3. Scoring systems: Mortality increases with higher scores in all scoring systems expect in the Marshall – II-III has 8.6 % mortality and IV has 4.3%. All scoring systems show statistically significant differences in mortality across their categories (p < 0.001) [Table 3 and Graph 2].15

Table 3: Scoring systems
Scoring system Category / score Total patients (n) Non-survivors (n, %) Mortality (%) p-value Odds Ratio
Marshall Grade I (normal) 75 4 (5.3%) 1.4% <0.001 1
Grades II–III (diffuse injury) 120 24 (20.0%) 8.6% 4.44
Grade IV (shift >5 mm) 34 12 (35.3%) 4.3% 9.68
Grades V–VI (mass lesions) 49 18 (36.7%) 6.5% 10.31
Rotterdam Score 2–3 122 10 (8.2%) 3.6% <0.001 1
Score 4 86 18 (20.9%) 6.5% 2.96
Score 5–6 70 30 (42.9%) 10.8% 8.40
NIRIS Grades 1–2 100 8 (8.0%) 2.9% <0.001 1
Grade 3 110 20 (18.2%) 7.2% 2.56
Grades 4–5 68 24 (35.3%) 8.6% 6.27
Helsinki Mild 90 6 (6.7%) 2.2% <0.001 1
Moderate 104 22 (21.2%) 7.9% 3.76
Severe 84 26 (30.9%) 9.4% 6.28
Stockholm Low risk 105 5 (4.8%) 1.8% <0.001 1
Moderate 113 20 (17.7%) 7.2% 4.30
High risk 60 27 (45.0%) 9.7% 16.36

NIRIS- Neuroimaging radiological interpretation system, p-value: p < 0.05 is statistically significant

Above given forest plot for 278 patients showing the adjusted odds ratios (aORs) for mortality associated with different CT based scoring systems used in traumatic brain injury (TBI), along with their 95% confidence intervals (CIs).
Graph 2: Above given forest plot for 278 patients showing the adjusted odds ratios (aORs) for mortality associated with different CT based scoring systems used in traumatic brain injury (TBI), along with their 95% confidence intervals (CIs).

4. Diagnostic performance metrics of CT scoring systems in predicting mortality: The Marshall score demonstrated the highest sensitivity (93%), but its specificity was comparatively low (32%), resulting in moderate overall accuracy (45%). The Rotterdam score showed sensitivity of 83% and specificity of 51%, achieving the highest accuracy among the systems evaluated (58%). The Stockholm score showed sensitivity of 90%, specificity of 44%, and accuracy of 53%, alongside the largest AUC (0.86). The NIRIS and Helsinki scores yielded intermediate values, both maintaining good sensitivity (>85%) but lower specificity (<42%), corresponding to accuracies of 49% and 47%, respectively [Table 4 and Graph 3].

Table 4: Diagnostic performance metrics of CT scoring systems in predicting mortality
Scoring System Sensitivity (%) Specificity (%) Positive Predictive Value (PPV, %) Negative Predictive Value (NPV, %) AUC Overall Accuracy
Marshall 93 32 27 95 0.79 0.45
Rotterdam 83 51 31 92 0.83 0.58
NIRIS 85 41 25 92 0.78 0.49
Helsinki 89 38 26 93 0.75 0.47
Stockholm 90 44 27 95 0.86 0.53

NIRIS – Neuroimaging radiological interpretation system, CT: Computed Tomography, AUC- Area under the receiver operating characteristic curve

This chart compares the diagnostic performance metrics of five CT-based traumatic brain injury (TBI) scoring systems. NIRIS – Neuroimaging radiological interpretation system, AUC-Area under the receiver operating characteristic curve.
Graph 3: This chart compares the diagnostic performance metrics of five CT-based traumatic brain injury (TBI) scoring systems. NIRIS – Neuroimaging radiological interpretation system, AUC-Area under the receiver operating characteristic curve.

5. The receiver-operating characteristic (roc) curve: Analysis for the five CT scoring systems, illustrating their ability to discriminate between survival and mortality in TBI patients [Graph 4].

Each curve plots the true positive rate (Sensitivity) against the false positive rate (1 - Specificity). Stockholm and Rotterdam scores had the highest AUCs, suggesting stronger predictive accuracy. Marshall, NIRIS, and Helsinki followed with moderately strong AUCs.
Graph 4: Each curve plots the true positive rate (Sensitivity) against the false positive rate (1 - Specificity). Stockholm and Rotterdam scores had the highest AUCs, suggesting stronger predictive accuracy. Marshall, NIRIS, and Helsinki followed with moderately strong AUCs.

6. Mortality: The mortality patterns and causes in a patient population indicate an early mortality rate of 3.58% within the first 3 days due to severe presentation and primary brain injury. The majority of deaths, 35.72%, occur by day 7, with late mortality between 7 days and 1 month primarily caused by complications like infections, diffuse axonal injury [Table 5 and Graph 5].16 or poor neurological recovery, leading to a total 1-month mortality of 15.1% (42 patients).

Table 5: Mortality of patients
Time Point Deaths (n, % of total) Interval Mortality Rate (%) Cumulative Deaths (n) Cumulative Mortality Rate (%)
On admission 7 (16.7%) 2.5% 7 2.5%
1 day 3 (7.1%) 1.1% 10 3.6%
3 days 8 (19.0%) 2.9% 18 6.5%
7 days 15 (35.7%) 5.5% 33 11.9%
1 month 9 (21.4%) 3.2% 42 15.1%
This line chart illustrates the mortality trend over the 30-day follow-up period. It highlights that the most critical period for patient mortality is within the first 7 days, where the rate climbs from 2.5% to 11.9%.
Graph 5: This line chart illustrates the mortality trend over the 30-day follow-up period. It highlights that the most critical period for patient mortality is within the first 7 days, where the rate climbs from 2.5% to 11.9%.

DISCUSSION

In this study of 278 patients with traumatic brain injury (TBI), the overall 30-day mortality was 15.1%, with the majority of deaths occurring within the first week of admission. These findings are consistent with prior literature, which emphasises the critical period of early mortality in TBI patients.17 Early deaths were largely attributable to primary brain injury and severe clinical presentation, whereas late deaths were more commonly related to secondary complications such as sepsis and raised intracranial pressure.

Clinico-demographic predictors

Age and comorbidities emerged as significant predictors of poor outcome. Patients aged over 60 years and those with pre-existing conditions such as hypertension and diabetes experienced higher mortality rates.18 This aligns with international data from the IMPACT (International mission for prognosis and analysis of clinical trials in TBI) and CRASH (Corticosteroid randomisation after significant head injury) studies, which demonstrated that increasing age and comorbid burden independently worsen prognosis.19 Interestingly, although males constituted the majority of cases, females demonstrated proportionally higher mortality, a trend reported in earlier observational studies, suggesting sex-specific physiological and hormonal influences on TBI response.20

Glasgow coma scale and clinical parameters

Admission Glasgow Coma Scale (GCS) score was strongly associated with mortality, reaffirming its role as a cornerstone of TBI severity assessment. In our cohort, patients with moderate TBI (GCS 9–12) had unexpectedly high mortality compared to severe TBI cases, a pattern that may reflect under-recognition of risk in this group and supports closer monitoring. Complications such as raised ICP, sepsis, and brain oedema were strongly correlated with mortality, underscoring the importance of aggressive prevention and timely management of secondary brain injury.21

Imaging predictors

Radiological features, particularly diffuse axonal injury (DAI), cerebral oedema, and midline shift, were significantly associated with mortality in this study. These findings are consistent with neuropathological evidence that axonal disruption and extensive oedema are major determinants of poor outcome.22,23 Normal CT findings, conversely, strongly predicted survival, supporting the value of CT in risk stratification at presentation. While epidural haematoma (EDH) demonstrated relatively high mortality, it did not reach statistical significance—possibly due to the small sample size and the fact that timely surgical evacuation can improve outcomes.24

CT-based scoring systems

All five scoring systems—Marshall, Rotterdam, Helsinki, Stockholm, and NIRIS—showed statistically significant correlations with mortality. Mortality increased progressively with higher scores, validating their prognostic reliability. Among them, the Stockholm score demonstrated the highest discriminatory power, Area under the receiver operating characteristic curve (AUC 0.89), followed by Helsinki and Rotterdam. These results are comparable with European studies that identified Stockholm and Helsinki as robust predictors of outcome in TBI.25 Marshall and NIRIS systems, while valuable, showed slightly lower predictive accuracy, which may be attributed to their more limited scoring granularity.

Clinical implications

Our findings suggest that structured CT scoring systems should be integrated into emergency department protocols for early prognostication. Specifically, the Stockholm and Helsinki scores may be most suitable for rapid risk stratification in Indian tertiary care settings, where timely triage decisions are critical. When combined with clinical parameters such as GCS and comorbidity assessment, these scores can enhance decision-making regarding intensive monitoring, neurosurgical intervention, and family counselling.

Limitations

This study has several limitations. Its retrospective design introduces potential biases in data collection and interpretation. Being a single-centre study, generalisability is limited, and the sample size of non-survivors (n=42) restricts subgroup analyses. Biomarkers and advanced imaging modalities, such as MRI, were not included, which might have improved prognostic accuracy.26 Moreover, long-term functional outcomes were not assessed, and mortality alone may not fully capture the burden of TBI.27

Future directions

Future research should focus on prospective multicentre validation of CT-based scoring systems in diverse populations. Integrating radiological scores with clinical variables, pupillary reactivity, and emerging biomarkers could lead to the development of multimodal prognostic models.28 Advances in machine learning may further refine predictive accuracy and allow for individualised patient trajectories.29 Early application of such models in emergency departments has the potential to improve survival and optimise resource utilisation.30

CONCLUSION

This study demonstrates that CT-based scoring systems are reliable tools for predicting mortality in patients with traumatic brain injury. Mortality was strongly associated with advanced age, comorbidities, low Glasgow Coma Scale scores, and complications such as raised intracranial pressure and sepsis. Radiological indicators, including diffuse axonal injury, cerebral oedema, and midline shift, were significant predictors of poor outcomes.

Among the five evaluated CT-based systems, the Stockholm and Helsinki scores exhibited the highest predictive accuracy, supported by their strong area under the curve AUC values and odds ratios. The Rotterdam and Marshall systems also performed well, while NIRIS offered moderate prognostic utility. These findings underscore the value of structured radiological scoring in complementing clinical parameters to enhance early risk stratification.

In resource-constrained emergency settings, incorporation of these scores into routine assessment can aid in timely triage, guide neurosurgical decision-making, and provide families with realistic prognostic information. Moving forward, multicentre prospective studies integrating CT scores with biomarkers and clinical data are warranted to develop multimodal predictive models that could further refine individualised care pathways.

Ethical approval:

Institutional Review Board approval is not required as this study was retrospective in nature.

Declaration of patient consent:

Patient's consent is not required as patients’ identity is not disclosed or compromised.

Conflicts of interest:

There are no conflicts of interest.

Use of artificial intelligence (AI)-assisted technology for manuscript preparation:

The authors confirm that they have used artificial-intelligence (AI)- assisted technology for grammatical and language corrections in this manuscript.

Financial support and sponsorship: Nil.

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