Abstract
Objective
This study aimed to identify predictors of brain CT abnormalities in patients who sustained a mild traumatic brain injury (mTBI).
Methods
Retrospective observational cohort of adult patients with mTBI (Glasgow Coma Score 13–15) that occurred within the preceding 24 h.
Results
2548 (91%) of the cohort had a brain CT and 698 (27%) demonstrated abnormal findings. The most frequently observed CT abnormalities were bleeding (638, 25%) and fractures (190, 7.4%). Multivariate logistic regression analysis revealed several significant predictors associated with the presence of brain CT abnormalities including older age [P < 0.0001], male sex [P < 0.0001], loss of consciousness [P = 0.0041], associated vomiting [P = 0.0011], alteration of consciousness (AOC) [P = 0102], and GCS score [P < 0.0001]. This was a robust model with an R² of 14.2%.
Conclusion
In this retrospective analysis, older age, male sex, the presence of loss of consciousness or alteration in consciousness, lower GCS score, and associated vomiting were found to be significant predictors of having an abnormal brain CT. These findings highlight the importance of considering these factors when determining the necessity of brain CT scans in patients with mTBI and suggest that existing clinical decision rules may be limited. These findings may also help to inform clinical decision rules. Early identification of individuals at a higher risk of CT abnormalities may assist in appropriate management and allocation of healthcare resources.
Keywords: Mild TBI, Brain CT, Clinical decision rules
Introduction
In the United States, the Center for Disease Control and Prevention (CDC) documented over 200,000 hospitalizations related to traumatic brain injury (TBI) in 2020, with over 80% of these cases being classified as mild. This translates to a daily average of 586 hospitalizations and 10 deaths due to TBI, highlighting the severity of this injury [1]. TBIs contribute to almost 1/3 of all injury-related deaths [2]. Mild Traumatic Brain Injury (mTBI) is a significant health concern, characterized by neurological dysfunction following a trauma. It is usually defined by a Glasgow Coma Score of 13–15, although there is a wide variation within this range, with significant injuries noted in patient even with a GCS of 15 [3].
Sometimes referred to as post-concussive syndrome, the sequelae of mTBI includes a range of physical, cognitive, and emotional symptoms such as headaches, dizziness, confusion, oculomotor deficits, memory disturbances, and impaired executive functioning [4, 5].
Diagnosis and assessment typically involve a combination of clinical evaluation and imaging techniques, with brain computed tomography (CT) scans being the most common tool for detecting intracranial abnormalities such as hemorrhages and fractures [5].
This study aims to identify specific predictors associated with the presence of brain CT abnormalities in patients presenting with mTBI. Understanding these predictors is critical for optimizing the risk vs. benefit of CT scans, enhancing patient outcomes, and effectively allocating healthcare resources.
Methods
This study is a retrospective analysis of an observational cohort of adult patients who presented to the emergency department (ED) of a level I trauma facility with a mild traumatic brain injury (mTBI), defined by a Glasgow Coma Scale (GCS) score of 13–15. Eligible patients were those whose mTBI occurred within 24 h prior to their ED presentation, from any mechanism, including fall, motor vehicle collision, assault, or recreational or sports-related injury. Written informed consent was obtained from participants for the inclusion of their data in the study, which was approved by our institutional review board.
The Glasgow Coma Scale (GCS) is a standardized tool used to assess the level of consciousness in patients with head injuries [6]. It consists of three components: eye opening (scored 1–4), verbal response (scored 1–5), and motor response (scored 1–6). The total score ranges from 3 to 15, with higher scores indicating better neurological function. A score of 13–15 is classified as mild TBI, 9–12 as moderate TBI, and 3–8 as severe TBI. The GCS is widely used in clinical practice to quickly evaluate the severity of brain injuries and guide management decisions [7].
Data was collected on various demographic and clinical variables, including patient age, sex, mechanism of injury, initial GCS score, and the presence of clinical symptoms such as headache, vomiting, loss of consciousness, post-traumatic amnesia, and focal neurological deficits. Additional data included the results of brain CT scans, which were assessed for abnormalities such as intracranial hemorrhage, contusions, fractures, and other signs of significant injury.
Data management and statistical analyses were conducted using JMP 16.0. Regression analyses were performed to identify predictors of CT scan abnormalities, with results expressed as odds ratios (OR), and associated p-values with 95% confidence intervals (CI).
Results
A total of 2786 patients were in the cohort, of which 2548 (91%) had a brain CT and 698 (27% of imaged cohort) demonstrated abnormal findings. As this was an observational study, whether a patient had a head CT performed was at the discretion of the treating Emergency Physician. Table 1 delineates the characteristics between those who had a head CT done and those who did not. The 9% that did not have a head CT done were significantly more often male, younger, did not have peri-injury symptomatology, were more likely to have a GCS of 15, and were less likely to have sustained their TBI from a fall or motor vehicle collision mechanism.
Table 1.
Head CT performed (n = 2548) | NO head CT performed (n = 238) | P-value (z test for proportions) | |
---|---|---|---|
Sex | 0.59 | 0.42 | P < 0.00001 |
Median age | 40 years | 27 years | |
Fall mechanism | 0.51 | 0.37 | P < 0.00001 |
MVC mechanism | 0.33 | 0.36 | NS |
LOC | 0.49 | 0.03 | P < 0.00001 |
AOC | 0.31 | 0.12 | P < 0.00001 |
Associated seizure | 0.02 | 0.01 | NS |
Associated vomiting | 0.06 | 0.03 | NS |
PTA | 0.29 | 0.07 | P < 0.00001 |
ED GCS 13 | 0.03 | 0 | P = 0.0067 |
ED GCS 14 | 0.11 | 0.02 | P < 0.00001 |
ED GCS 15 | 0.86 | 0.98 | P < 0.00001 |
The most frequently observed CT abnormalities were bleeding (n = 638, 91% of abnormal scans, or 25% of imaged cohort) and fractures (n = 190, 27% of abnormal scans or 7.4% of imaged cohort). Extrapolating these results to the 9% of the cohort that did not get a brain CT (n = 238), 60 bleeds and 18 fractures were potentially missed, although that cohort was significantly different in many ways as highlighted above.
Figure 1 illustrates the distribution of brain CT abnormalities across different age groups and sexes. The incidence of abnormalities increases with age, with the highest occurrence observed in the 66–101 age group, which had the highest occurrence of CT-detected abnormalities. This trend underscores the heightened vulnerability of older adults to sustaining more severe intracranial injuries following mild TBI. Furthermore, males exhibited a consistently higher incidence of abnormalities across all age groups compared to females, reflecting the underlying sex-based difference in injury mechanisms or possibly physiological responses to trauma. The figure also highlights that younger age groups, particularly those aged 18–23 and 23–31, show the lowest incidence of abnormalities, suggesting that they may have a greater capacity for resilience or recovery following mild TBI, or that their TBI mechanism was of a more benign nature. The distribution of peri-injury symptomatology is summarized in Table 2.
Table 2.
Did not have it | Had it | Unknown | |
---|---|---|---|
LOC | 1137, 41% | 1301, 47% | 348, 12% |
AOC | 1749, 63% | 818, 29% | 219, 8% |
Associated seizure | 2733, 98% | 49, 2% | 0, 0% |
Associated vomiting | 2617, 94% | 167, 6% | 0, 0% |
PTA | 1816, 65% | 762, 27% | 208, 7% |
Figures 2-5 are violin plots that help to visualize the relationships between the peri-injury symptomatology and the outcome of abnormal head CT, depicted by age and sex
A multivariate logistic regression model including age, GCS score, and injury symptomatology, revealed the following significant predictors associated with the presence of brain CT abnormalities (Table 3): older age [P < 0.0001], male sex [P < 0.0001], loss of consciousness [P = 0.0041], associated vomiting [P = 0.0011], alteration of consciousness (AOC) [P = 0102]. This was a robust model with an R² of 14.2%.
Table 3.
Term | Estimate | Std Error | Chi-Square | P-value | Lower 95% | Upper 95% | Odds ratio | Lower 95% | Upper 95% | Reci-procal |
---|---|---|---|---|---|---|---|---|---|---|
Age | 0.0385 | 0.0023 | 272.99 | < 0.0001 | 0.0339 | 0.0430 | 1.0392 | 1.0345 | 1.0440 | 0.9622 |
Sex | 0.4749 | 0.1033 | 21.14 | < 0.0001 | 0.2725 | 0.6774 | 1.6079 | 1.3132 | 1.9688 | 0.6219 |
Associated vomiting | 0.6406 | 0.1966 | 10.62 | 0.0011 | 0.2553 | 1.0259 | 1.8975 | 1.2908 | 2.7895 | 0.5270 |
Associated seizure | 0.5202 | 0.3282 | 2.51 | 0.1130 | -0.1232 | 1.1635 | 1.6823 | 0.8841 | 3.2010 | 0.5944 |
Loss of consciousness | 0.1575 | 0.0771 | 4.17 | 0.0411 | 0.0064 | 0.3086 | 1.1706 | 1.0064 | 1.3616 | 0.8543 |
Alteration of consciousness | 0.2143 | 0.0834 | 6.60 | 0.0102 | 0.0509 | 0.3778 | 1.2390 | 1.0522 | 1.4591 | 0.8071 |
Post Traumatic Amnesia | 0.0847 | 0.0852 | 0.99 | 0.3203 | -0.0824 | 0.2518 | 1.0884 | 0.9209 | 1.2863 | 0.9188 |
GCS score in the ED | -0.6211 | 0.1047 | 35.17 | < 0.0001 | -0.8264 | -0.4159 | 0.5373 | 0.4376 | 0.6598 | 1.8611 |
Discussion
In this study, we identified several significant predictors of brain CT scan abnormalities in patients with mild traumatic brain injury (mTBI). The analysis revealed that loss of consciousness (LOC), alteration of consciousness (AOC), post-traumatic amnesia (PTA), associated vomiting, and associated seizures were all significantly associated with abnormal CT findings. These results highlight the importance of these clinical factors in the initial assessment and decision-making process for mTBI patients.
These findings are supported by previous studies, which emphasized the significance of neuroimaging in all TBI patients, including those with a GCS of 15. A study of over 2000 patients found that even the mildest cases of TBI could present with significant CT abnormalities, with variables such as LOC, AOC, and PTA being significantly associated with adverse outcomes, including ICU admission and mortality [3]. Similarly, a 2017 study that included 453 patients with GCS 15 found that presence of vomiting or any symptom combination including LOC, bleeding, seizure or vomiting was significantly associated with having an abnormal brain CT (P < 0.0001) [8].
Further, these findings highlight the challenges in developing standardized assessment protocols for mTBI in emergency settings, particularly given the heterogeneity of mTBI presentations and the lack of consensus on management guidelines, especially in mild cases [9, 10]. This underscores the need for integrating identified clinical predictors into decision-making processes, which can help standardize and improve the assessment, leading to better patient outcomes.
The most common clinical decision tool used to determine whether a head CT should be done after a mTBI is the Canadian head CT rule [11]. This rule states that if all criteria are negative, then the sensitivity of the rule for any intracranial traumatic finding is 83–100%. The included high-risk criteria are age > 65, suspected skull fracture, signs of basilar skull fracture, or 2 or more episodes of vomiting. Medium risk criteria include 30 or more minutes of amnesia to the event (PTA), and a dangerous mechanism for the TBI, defined as pedestrian struck by motor vehicle, occupant ejected from motor vehicle, or fall from > 3 feet or > 5 stairs. In our cohort, after removing every patient who had even 1 of these criteria, there were still 1309 patients left, or 47%. All of these would be deemed to not need a head CT because traumatic findings would not be expected. Indeed, a quarter of these patients actually did have intracranial hemorrhage, and 7% had a fracture.
One of the key strengths of this study is the large sample size, which provides robust evidence for the identified predictors. The multivariate logistic regression model used in this analysis demonstrated a strong predictive capability, with an R² of 14.2%, indicating a substantial proportion of the variance in CT abnormalities can be explained by the included predictors. The inclusion of a wide range of clinical variables enhances the comprehensiveness of our analysis, ensuring that the identified predictors are not confounded by other factors.
Despite these strengths, it is crucial to acknowledge the limitations of this study. CT scans primarily offer structural information and may not detect functional abnormalities, which are often critical in the assessment of mTBI. Functional changes in brain activity, which can significantly impact cognitive function, are not directly observable on CT scans. Additionally, the timing of CT scans may affect the detection of abnormalities. Early CT scans might miss evolving injuries that become apparent only later, emphasizing the potential need for follow-up imaging and more frequent monitoring of mTBI patients.
The identification of intracranial hemorrhage on CT in mTBI is important, even if neurosurgical intervention is not performed. A 2021 study in JAMA Neurology [12] reports that patients who sustained a subarachnoid hemorrhage, epidural hematoma or subdural hematoma were significantly more likely to have incomplete recovery from their TBI, even at 1 year. This information is important to frame prognosis and make rehabilitation plans for the patient.
The findings from this study have significant implications for clinical practice. Incorporating the identified predictors into clinical decision rules could improve the accuracy of triaging mTBI patients, ensuring that those at higher risk receive timely and appropriate imaging and care. This targeted approach can optimize resource allocation in emergency departments, reducing unnecessary CT scans for low-risk patients while prioritizing high-risk cases. Future research should focus on developing and validating clinical decision rules that integrate these predictors, potentially incorporating advanced imaging techniques and functional assessments to enhance the diagnostic process for mTBI.
Overall, this study underscores the critical role of specific clinical predictors in identifying brain CT abnormalities in mTBI patients. These findings contribute to the growing body of evidence that informs clinical guidelines and decision-making protocols, ultimately aiming to improve patient outcomes and healthcare efficiency. By integrating clinical predictors with neuroimaging and understanding the broader context of TBI management, clinicians can adopt a more comprehensive approach to diagnosis and treatment, hopefully leading to better outcomes for mTBI patients.
Conclusion
In this retrospective analysis, loss of consciousness, altered level of consciousness (AOC), post-traumatic amnesia (PTA), associated vomiting, and associated seizures were identified as significant predictors of abnormal brain CT findings in patients with mild traumatic brain injury (mTBI). These results emphasize the importance of considering these clinical factors when assessing the need for brain CT scans in mTBI patients. Early identification of individuals at higher risk for CT abnormalities can aid in optimizing patient management and the efficient allocation of healthcare resources in the emergency department setting. Moreover, these findings could contribute to the development of more refined clinical decision rules, enhancing the accuracy of diagnostic evaluations for mTBI patients.
Author contributions
SV and LG drafted the initial manuscript. JSF and NK edited and critically revised the manuscript. LG supervised the project. All authors read and approved the final manuscript.
Funding
No funding was received for this study.
Data availability
No datasets were generated or analysed during the current study.
Declarations
Ethical approval
The study was performed in accordance with the ethical standards as laid down in the 1964 Declaration of Helsinki and its later amendments or comparable ethical standards. The Orlando College of Osteopathic Medicine’s Research Committee determined this study to be exempt.
Consent to participate
Patients provided written informed consent to participate in this study.
Consent for publication
Not applicable.
Competing interests
Dr. Ganti has an editorial role at Springer.
Footnotes
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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Associated Data
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Data Availability Statement
No datasets were generated or analysed during the current study.