Young Age, Liver Dysfunction, and Neurostimulant Use as Independent Risk Factors for Post-Traumatic Seizures: A Multiracial Single-Center Experience
1
Rehabilitation Medicine, SingHealth Residency, Singapore 169608, Singapore
2
Department of Rehabilitation Medicine, Changi General Hospital, Singapore 529889, Singapore
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2023, 20(3), 2301; https://doi.org/10.3390/ijerph20032301
Submission received: 14 December 2022
/
Revised: 20 January 2023
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Accepted: 25 January 2023
/
Published: 28 January 2023
(This article belongs to the Section Public Health Statistics and Risk Assessment)
Abstract
:We aimed to determine the potentially modifiable risk factors that are predictive of post-traumatic brain injury seizures in relation to the severity of initial injury, neurosurgical interventions, neurostimulant use, and comorbidities. This retrospective study was conducted on traumatic brain injury (TBI) patients admitted to a single center from March 2008 to October 2017. We recruited 151 patients from a multiracial background with TBI, of which the data from 141 patients were analyzed, as 10 were excluded due to incomplete follow-up records or a past history of seizures. Of the remaining 141 patients, 33 (24.4%) patients developed seizures during long-term follow up post-TBI. Young age, presence of cerebral contusion, Indian race, low Glasgow Coma Scale (GCS) scores on admission, and use of neurostimulant medications were associated with increased risk of seizures. In conclusion, due to increased risk of seizures, younger TBI patients, as well as patients with low GCS on admission, cerebral contusions on brain imaging, and those who received neurostimulants or neurosurgical interventions should be monitored for post-TBI seizures. While it is possible that these findings may be explained by the differing mechanisms of injury in younger vs. older patients, the finding that patients on neurostimulants had an increased risk of seizures will need to be investigated in future studies.
1. Introduction
Seizure is a known complication following traumatic brain injury (TBI) and may occur early (within 2 weeks post-injury) or late (beyond the 2-week period). Prophylactic anti-epileptics are useful in reducing early but not late seizures [1,2,3,4]. Various classifications have been used to define the type of traumatic brain injury: blunt injuries lead to focal contusion and hematoma, whereas penetrating injuries can result in damage to the skull and underlying brain tissue. In cases of penetrating injuries, seizure occurrence is thought to be a result of cicatrix formation in the cortex [5]. In non-penetrating or closed head injuries, seizure activity is thought to be due to impairment of blood flow, intraparenchymal hemorrhage, and hemorrhagic contusions, which result in hemoglobin breakdown that adversely affects neuronal function and glycolysis, causing negative alterations of excitatory amino acids [6]. Acute-phase response following TBI is characterized by the activation of astrocytes and microglial cells, which then migrate to the injured area and proliferate [2,7]. Acute inflammation is followed by a persistent chronic stage [7,8,9,10,11]. The combination of early and late inflammation and gliosis is thought to be responsible for epileptic activity [2]. Pericontusional areas have also been suggested as electrically active and may become foci for seizures [6,12], with the majority of patients having evidence of the temporo-parietal regions being the source of seizure activity [1,2,13].
Irrespective of pathophysiology, it is generally accepted that post-TBI seizures are associated with a poorer functional outcome; nevertheless, the risk factors that may predict their long-term occurrence are still debated [14]. We sought to characterize potentially modifiable risk factors that may predispose patients to developing post-TBI seizures. We hypothesized that in addition to the commonly known risk factors such as age, there may be other factors (such as drug use) that are hitherto unknown, which may predict the risk and, if modified, may reduce the chances of patients developing post-traumatic seizures. In this study, we analyzed 141 patients with TBI and confirmed, as per previous publications, that the non-modifiable risk factors of younger age, poor initial GCS scores, and the existence of cerebral contusion on brain imaging are indeed risk factors predictive of post-TBI seizures. In addition, we identified novel and potentially modifiable risk factors such as liver dysfunction, active employment, and the use of neurostimulants as potential risk factors that deserve further study.
2. Methods
2.1. Patient Selection and Biological Parameters
This is a retrospective cohort study of TBI patients who were admitted to the neuro-rehabilitation facility at Changi General Hospital, Singapore, from June 2008 to October 2017. All patients, regardless of racial background (Chinese, Malay, Indian, or other), admitted with a diagnosis of TBI had their neurological status and initial GCS assessed. All patients uniformly received urgent CT brain scans, baseline full blood counts, biochemistry, liver function tests, and coagulation profiles at baseline presentation. Based on the initial and subsequent neurological status and neuroimaging by CT of the brain, appropriate referrals to the neurosurgical team to perform any surgical intervention were made. All the TBI patients were eventually referred to inpatient rehabilitation services, where a multidisciplinary team reviewed the patients throughout the inpatient period and during their subsequent outpatient follow-up, which included an outpatient rehabilitation program, neuropsychological review, and return-to-work assessments. The median follow-up period was 59 months (range 28–86 months; Table 1). All the patients included in the current study were discharged from the rehabilitation facility and were regularly followed up as outpatients for a minimum of 6 months. The subsequent records of hospital admissions, changes in their general physical and neurological status, and changes in treatment regimens were available both electronically and in paper format for all patients.
2.2. Inclusion and Exclusion Criteria
Inclusion criteria were: age above 21 years, established diagnosis of TBI, and complete follow-up records. Exclusion criteria were: incomplete follow-up records, patients who were repatriated to other countries, patients less than 21 years of age, and patients with no clear history of TBI.
2.3. Ethics Approval
The Singhealth Centralized Institutional Review Board approved this study (2015/3112). Informed consent from the patients was waived due to the retrospective nature of the study.
2.4. Data Collection
Electronic and paper medical records of the patients from the time TBI was diagnosed were assessed, and follow-up visits including additional admissions were reviewed. The data collected included demographic details, mechanism of injury, occupation, admission GCS, nature and severity of injury, admission, and subsequent computed tomography (CT) or magnetic resonance imaging (MRI) brain scan findings. Other parameters reviewed were admission electrolytes, coagulation profiles, premorbid medications, and comorbidities.
We also documented the treatment modalities, including medical treatments used for raised intracranial pressure; types of neurosurgical interventions, including intracranial pressure monitor (ICP), burr hole drainage, craniotomy, craniectomy, and/or ventriculoperitoneal shunting, if any. The CT brain scan findings were categorized as cerebral contusion, extradural or subdural hematoma (EDH and SDH, respectively), skull fractures, diffuse axonal injury (DAI), and subarachnoid (SAH) and/or intraventricular hemorrhage (IVH).
During the inpatient and follow-up periods, all medications were reviewed, with the use of neurostimulation with levodopa or bromocriptine and the use of lipid lowering agents being particularly documented. Liver function tests were defined as abnormal if the patient’s alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels were higher than two times the upper limit of normal (ULN).
Primary prophylaxis for early seizure was used in all patients for 2 weeks post-initial injury, and any seizure occurring beyond a 2-week period post-initial injury was documented. Seizure was clinically diagnosed either by a physician, neurologist, neurosurgeon, or rehabilitation physician with or without EEG. Treatment initiated and type of anti-epileptic medications used were documented.
2.5. Statistical Analysis
Categorical data are presented as frequency (percentage), and continuous data are presented as mean (± standard deviation) for parametric distributions and median (± interquartile range) for non-parametric distributions. The differences in characteristics were examined using chi-square tests for categorical variables and the two-sample t-test or Mann–Whitney U-tests for continuous variables, where appropriate. A two-tailed p-value of < 0.05 was considered to be statistically significant. The analysis was performed using the Statistical Package for the Social Sciences (SPSS) version 19.0 (IBM Corp. Armonk, NY, USA).
3. Results
Descriptive Analysis
We studied 151 patients with TBI, of which 10 were excluded (8 were lost to follow-up and 2 due to known past medical history of seizure). Of the remaining 141 patients, 24.4% (33) had seizure occurrence during the follow-up period (median = 59 months). The demographic details and admission characteristics are described in Table 1. In the univariate analysis, statistically significant associations with seizures were the presence of cerebral contusion (p = 0.031), Indian ethnicity (p = 0.051), employment (p = 0.028), abnormal liver function on admission (p = 0.004), neurosurgical intervention (p = 0.085), low GCS on admission (p = 0.001), prolonged hospitalization (p = 0.005), and use of neurostimulant medications (p = 0.001). Multivariate analysis revealed that patients of younger age (OR = 0.96, 95% CI: 0.93–0.98, p = 0.001) and those who used neurostimulants (OR = 10.9, 95% CI: 3.5–34.2, p ≤ 0.001) were at increased risk of post-TBI seizure occurrence.
Multivariate logistic regression was used to predict the factors contributing to seizure. The forward selection method was applied for the following factors: age, race, presence of liver dysfunction, admission GCS scores, and use of neurostimulants.
The final model revealed that younger age (OR = 0.96, 95% CI: 0.93–0.98, p = 0.001) and those who used neurostimulants (OR = 10.9, 95% CI: 3.5–34.2, p ≤ 0.001) were at increased risk of seizure occurrence.
4. Discussion
4.1. Summary and Contributions
Amongst the 141 patients with traumatic brain injuries analyzed in this study, seizures were noted in 33 (24.4%) patients, despite receiving primary prophylaxis for 2 weeks following initial TBI. This figure is slightly higher than previously reported incidences of early post-TBI seizures [6,15,16]. Multivariate analysis shows that age, neurostimulant use, and liver dysfunction all had significant effects on predicting whether a patient would develop post-TBI seizures (Table 2).
In terms of injury pathophysiology, patients with cerebral contusions were found to have a higher level of seizure occurrence (22 vs. 51; p-value = 0.05). In contrast with previous studies that found a higher incidence of seizures following TBI in patients with ICH and SAH [6], we did not find any significant correlations of post-TBI seizures with other types of intracranial hemorrhage such as SAH or IVH (Table 1). One possible confounder is that we might not have detected nonconvulsive seizures, which reportedly account for 50% of seizures in intensive care units following TBI and which may lead to raised ICP beyond 96 h post-initial injury. As seizures may lead to metabolic disturbances causing cellular injury, continuous EEG monitoring would be useful to monitor and maintain ICP within a safe range; prompt control of seizures as they occur would be extremely important, as past studies suggested that status epilepticus increases mortality [6]. Due to the retrospective nature of our study, we did not have accurate information on seizure occurrence during the immediate post-brain-injury, intensive care unit, or peri-operative periods, and we were therefore unable to analyze the relationship of early vs. late post-TBI seizures.
In terms of medical risk factors for post-TBI seizures, a Finnish study previously found an association between late post-traumatic seizure with depressed skull fractures and the presence of early seizures [14]. The authors did not find any association of seizures with admission GCS, duration of unconsciousness, or duration of post-traumatic amnesia (PTA). In contrast, our data suggest that low GCS at the time of admission was associated with post-traumatic seizures (mean GCS of 9.5 compared with 11.9 in the no-seizure group; p-value = 0.003). We also noted that a longer length of stay was associated with post-TBI seizure occurrence (mean of 53.1 days versus 36.3 days in the no seizure group; p-value = 0.021). The most probable explanation for this finding may be that those patients with more severe brain injury needed neurosurgical interventions (37.5% vs. 51.9% in our data set; p-value < 0.001), which may also be associated with perioperative complications and hence longer lengths of stay.
4.2. Strength and Limitations
With respect to other factors influencing the risk of post-TBI seizures, studies have identified that the mechanism of injury matters: increased seizure frequency is associated with penetrating brain injuries [17]. From a long-term follow-up study over a period of 50 years, one group found that the risk of seizures increased with the severity of initial brain injury, as well as the presence of SDH, skull fracture, PTA duration more than 24 h, and age above 65 years [18]. In terms of imaging, hippocampal atrophy were observed to be significantly associated with seizures [19]. Severity of injury also matters: the risk of post-TBI seizures is high in the first year in patients with severe TBI and significantly increases up to 10 years for moderate TBI [20]. In this study, the median follow-up period was only 59 months; hence, we were unable to correlate seizure occurrence and its temporal evolution over time in relation to the severity of initial TBI. However, we noted additional demographic factors such as the finding that those patients who were employed at the time of TBI showed an increased tendency of developing post-TBI seizures (Table 1; p-value = 0.097). This finding could be explained by the possibility that the younger patients in this cohort might have been involved in more violent injuries as a result of road traffic accidents in contrast with older adults who might have presented with relatively minor and less violent injuries (p-value = 0.132, which did not reach significance in this study).
Another peculiar finding that may deserve more attention in the future is that, in this cohort, liver dysfunction at the time of admission was associated with long term post-TBI seizure occurrence (Table 2). The reason for this is unclear, though a previous report seems to suggest a correlation f liver cirrhosis with the occurrence of TBI itself [21].
Regarding antiepileptic drugs, phenytoin and levetiracetam are the most common prophylactic agents used for post-TBI seizures, with phenytoin being recommended by the American Academy of Neurology for the prevention of early post-traumatic seizures [1,22,23,24]. In our study, the most common antiepileptic agent used was indeed levetiracetam, followed by valproic acid and phenytoin. Neuroplasticity and its role in brain injury recovery has been well studied. However, there are very few neuromodulators that are currently available for use in TBI patients: amantadine, methylphenidate, modafinil, levodopa, and citalopram have been shown to benefit cognitive improvement and recovery following brain injury [25,26]. Bromocriptine was shown to improve outcomes following TBI, possibly by alleviating autonomic dysfunction [17]. In the patients analyzed in our study, the most common neuromodulator used was levodopa, followed by bromocriptine, which is indicated to manage autonomic instability following TBI. Surprisingly, we found a statistically significant association between the use of these agents and seizure occurrence (39.4% vs. 12%; p-value < 0.001). One possible explanation is that patients who were prescribed levodopa or bromocriptine were more likely to have more severe brain injuries. Hence, the relationship between seizure occurrence in these patients may have been indicative of the severity of brain injury rather than the use of neurostimulants, though this latter possibility cannot be completely ruled out. Of interest, we previously reported a possible correlation of levodopa use in stroke patients with the occurrence of post-stroke seizures [27]. As such, the data presented here need to be carefully interpreted with respect to the role of neurostimulant use in post-TBI vs. post-stroke seizures, and future prospective trials are required to validate these findings.
We did not find any protective effect of lipid-lowering agents in post TBI seizures, although the protective effect was found in another study of post-stroke seizures [27]. This could have been due to the small number of patients analyzed in the current TBI cohort.
4.3. Future Work
In addition to neurostimulants and the use of statins, future studies can investigate the role of various biomarkers to predict the occurrence of post-TBI seizures and to potentially guide future therapeutics. Elevated levels of IL-6 are observed in TBI patients [28] and are considered to play a significant role in those with temporal lobe epilepsy [29] and pediatric epilepsy [30]. The CSF–serum IL-1β ratio was shown to be elevated in TBI patients who are prone to developing epilepsy [31]. Treatment with IL-1 β receptor antagonist reduced seizures in a mouse model [30]. Other studies suggested the use of lipopolysaccharide to prevent the acceleration of kindling epileptogenesis as a result of TBI [32]. Another possible area of exploration is with the manipulation of microglial cells, whose activation is commonly seen following TBI and seizure occurrence [33]. Microglia play a significant role in seizure occurrence, and their inhibition with minocycline has been shown to reduce post TBI seizures and cognitive deficits; this relationship warrants further evaluation [6,34,35,36,37]. Finally, from the clinical perspective, an effort to limit the use of levodopa or bromocriptine in TBI patients may be tested for its possible role in mitigating the risk of post-traumatic seizures.
5. Conclusions
In the current study of 141 patients from the multiracial nation of Singapore, we report a post-traumatic seizure rate following TBI of 24.4%. Patients who are of younger age and patients who received neurostimulants are at a higher risk of seizures following TBI. Adequate information should be provided to the patients at risk regarding long-term seizure occurrence. This is important from a medicolegal point of view and from the viewpoint of compensation claims. The role of neurostimulants and their relationship with seizure occurrence needs to be investigated in further studies.
Author Contributions
All the authors contributed to the study ICMJE criteria for authorship have been met. S.D.P.: concept, data, literature search and write up, and methodology. N.E.O.: literature search, and write-up. P.T.T.: Statistical analysis, tables, graphs, and editing. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Institutional Review Board Statement
The study was conducted in accordance with the Declaration of Helsinki and approved by the Institutional Review Board of SingHealth. Centralized IRB (2015/3112) for data collection; waiver of consent was obtained due to the retrospective nature of the study.
Informed Consent Statement
Patient consent was waived due to the retrospective and anonymous nature of the study.
Data Availability Statement
Data from this research study are available upon request.
Acknowledgments
We acknowledge the work of members of the Changi General Hospital Department of Rehabilitation Medicine for their contribution to the clinical care of the patients.
Conflicts of Interest
The authors declare no conflict of interest.
Abbreviations
| GCS | Glasgow Coma Scale |
| TBI | Traumatic Brain Injury |
| CSF | Cerebrospinal Fluid |
| EEG | Electroencephalogram |
| PTA | Post-Traumatic Amnesia |
| ALT | Alanine Aminotransferase |
| AST | Aspartate Aminotransferase |
| CT | Computed Tomography |
| ICH | Intracerebral Hemorrhage |
| SAH | Subarachnoid Hemorrhage |
| SDH | Subdural Hemorrhage |
| IVH | Intraventricular Hemorrhage |
| CI | Confidence Interval |
| SD | Standard Deviation |
| ICP | Intracranial Pressure |
| EVD | Extraventricular Drainage |
| Hb | Hemoglobin |
| WBC | White Blood Cell |
| MCV | Mean Corpuscular Volume |
| MCH | Mean Corpuscular Hemoglobin |
| eGFR | Estimated Glomerular Filtration Rate |
References
- Beghi, E. Overview of studies to prevent posttraumatic epilepsy. Epilepsia 2003, 44, 21–26. [Google Scholar] [CrossRef] [PubMed]
- Mukherjee, S.; Arisi, G.M.; Mims, K.; Hollingsworth, G.; O’Neil, K.; Shapiro, L.A. Neuroinflammatory mechanisms of post-traumatic epilepsy. J. Neuroinflammation 2020, 17, 193. [Google Scholar] [CrossRef] [PubMed]
- Temkin, N.R.; Dikmen, S.S.; Wilensky, A.J.; Keihm, J.; Chabal, S.; Winn, H.R. A randomized, double-blind study of phenytoin for the prevention of post-traumatic seizures. N. Engl. J. Med. 1990, 323, 497–502. [Google Scholar] [CrossRef]
- Vespa, P.M.; Nuwer, M.R.; Nenov, V.; Ronne-Engstrom, E.; Hovda, D.A.; Bergsneider, M.; Kelly, D.F.; Martin, N.A.; Becker, D.P. Increased incidence and impact of nonconvulsive and convulsive seizures after traumatic brain injury as detected by continuous electroencephalographic monitoring. J. Neurosurg. 1999, 91, 750–760. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Diaz-Arrastia, R.; Agostini, M.A.; Frol, A.B.; Mickey, B.; Fleckenstein, J.; Bigio, E.; Van Ness, P.C. Neurophysiologic and neuroradiologic features of intractable epilepsy after traumatic brain injury in adults. Arch. Neurol. 2000, 57, 1611–1616. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Vespa, P.M.; Miller, C.; McArthur, D.; Eliseo, M.; Etchepare, M.; Hirt, D.; Glenn, T.C.; Martin, N.; Hovda, D. Nonconvulsive electrographic seizures after traumatic brain injury result in a delayed, prolonged increase in intracranial pressure and metabolic crisis. Crit. Care Med. 2007, 35, 2830–2836. [Google Scholar] [CrossRef] [Green Version]
- Karve, I.P.; Taylor, J.M.; Crack, P.J. The contribution of astrocytes and microglia to traumatic brain injury. Br. J. Pharmacol. 2016, 173, 692–702. [Google Scholar] [CrossRef] [Green Version]
- Helmy, A.; Carpenter, K.L.; Menon, D.K.; Pickard, J.D.; Hutchinson, P.J. The cytokine response to human traumatic brain injury: Temporal profiles and evidence for cerebral parenchymal production. J. Cereb. Blood Flow. Metab. 2011, 31, 658–670. [Google Scholar] [CrossRef] [Green Version]
- Kumar, R.G.; Diamond, M.L.; Boles, J.A.; Berger, R.P.; Tisherman, S.A.; Kochanek, P.M.; Wagner, A.K. Acute CSF interleukin-6 trajectories after TBI: Associations with neuroinflammation, polytrauma, and outcome. Brain. Behav. Immun. 2015, 45, 253–262. [Google Scholar] [CrossRef]
- Witcher, K.G.; Bray, C.E.; Dziabis, J.E.; McKim, D.B.; Benner, B.N.; Rowe, R.K.; Kokiko-Cochran, O.N.; Popovich, P.G.; Lifshitz, J.; Eiferman, D.S.; et al. Traumatic brain injury-induced neuronal damage in the somatosensory cortex causes formation of rod-shaped microglia that promote astrogliosis and persistent neuroinflammation. Glia 2018, 66, 2719–2736. [Google Scholar] [CrossRef]
- Wofford, K.L.; Harris, J.P.; Browne, K.D.; Brown, D.P.; Grovola, M.R.; Mietus, C.J.; Wolf, J.A.; Duda, J.E.; Putt, M.E.; Spiller, K.L.; et al. Rapid neuroinflammatory response localized to injured neurons after diffuse traumatic brain injury in swine. Exp. Neurol. 2017, 290, 85–94. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Liesemer, K.; Bratton, S.L.; Zebrack, C.M.; Brockmeyer, D.; Statler, K.D. Early post-traumatic seizures in moderate to severe pediatric traumatic brain injury: Rates, risk factors, and clinical features. J. Neurotrauma 2011, 28, 755–762. [Google Scholar] [CrossRef] [PubMed]
- Tubi, M.A.; Lutkenhoff, E.; Blanco, M.B.; McArthur, D.; Villablanca, P.; Ellingson, B.; Diaz-Arrastia, R.; Van Ness, P.; Real, C.; Shrestha, V.; et al. Early seizures and temporal lobe trauma predict post-traumatic epilepsy: A longitudinal study. Neurobiol. Dis. 2019, 123, 115–121. [Google Scholar] [CrossRef] [PubMed]
- Asikainen, I.; Kaste, M.; Sarna, S. Early and late posttraumatic seizures in traumatic brain injury rehabilitation patients: Brain injury factors causing late seizures and influence of seizures on long-term outcome. Epilepsia 1999, 40, 584–589. [Google Scholar] [CrossRef]
- Annegers, J.F.; Grabow, J.D.; Groover, R.V.; Laws, E.R., Jr.; Elveback, L.R.; Kurland, L.T. Seizures after head trauma: A population study. Neurology 1980, 30, 683–689. [Google Scholar] [CrossRef]
- Vespa, P. Continuous EEG monitoring for the detection of seizures in traumatic brain injury, infarction, and intracerebral hemorrhage: “To detect and protect”. J. Clin. Neurophysiol. 2005, 22, 99–106. [Google Scholar] [CrossRef] [PubMed]
- Munakomi, S.; Bhattarai, B.; Mohan Kumar, B. Role of bromocriptine in multi-spectral manifestations of traumatic brain injury. Chin. J. Traumatol. 2017, 20, 84–86. [Google Scholar] [CrossRef]
- Annegers, J.F.; Coan, S.P. The risks of epilepsy after traumatic brain injury. Seizure 2000, 9, 453–457. [Google Scholar] [CrossRef] [Green Version]
- Vespa, P.M.; McArthur, D.L.; Xu, Y.; Eliseo, M.; Etchepare, M.; Dinov, I.; Alger, J.; Glenn, T.P.; Hovda, D. Nonconvulsive seizures after traumatic brain injury are associated with hippocampal atrophy. Neurology 2010, 75, 792–798. [Google Scholar] [CrossRef] [Green Version]
- Annegers, J.F.; Hauser, W.A.; Coan, S.P.; Rocca, W.A. A population-based study of seizures after traumatic brain injuries. N. Engl. J. Med. 1998, 338, 20–24. [Google Scholar] [CrossRef]
- Yeh, C.C.; Chen, T.L.; Hu, C.J.; Chiu, W.T.; Liao, C.C. Risk of epilepsy after traumatic brain injury: A retrospective population-based cohort study. J. Neurol. Neurosurg. Psychiatry 2013, 84, 441–445. [Google Scholar] [CrossRef] [PubMed]
- Kirmani, B.F.; Robinson, D.M.; Fonkem, E.; Graf, K.; Huang, J.H. Role of Anticonvulsants in the Management of Posttraumatic Epilepsy. Front. Neurol. 2016, 7, 32. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Torbic, H.; Forni, A.A.; Anger, K.E.; Degrado, J.R.; Greenwood, B.C. Antiepileptics for seizure prophylaxis after traumatic brain injury. Am. J. Health Syst. Pharm. 2013, 70, 2064–2067. [Google Scholar] [CrossRef]
- Jones, K.E.; Puccio, A.M.; Harshman, K.J.; Falcione, B.; Benedict, N.; Jankowitz, B.T.; Stippler, M.; Fischer, M.; Sauber-Schatz, E.K.; Fabio, A.; et al. Levetiracetam versus phenytoin for seizure prophylaxis in severe traumatic brain injury. Neurosurg. Focus. 2008, 25, E3. [Google Scholar] [CrossRef] [Green Version]
- Kakehi, S.; Tompkins, D.M. A Review of Pharmacologic Neurostimulant Use During Rehabilitation and Recovery After Brain Injury. Ann. Pharm. 2021, 55, 1254–1266. [Google Scholar] [CrossRef] [PubMed]
- Orient-Lopez, F.; Terre-Boliart, R.; Bernabeu-Guitart, M.; Ramon-Rona, S.; Perez-Miras, A. The usefulness of dopaminergic drugs in traumatic brain injury. Rev. Neurol. 2002, 35, 362–366. [Google Scholar]
- Pande, S.D.; Lwin, M.T.; Kyaw, K.M.; Khine, A.A.; Thant, A.A.; Win, M.M.; Morris, J. Post-stroke seizure-Do the locations, types and managements of stroke matter? Epilepsia Open 2018, 3, 392–398. [Google Scholar] [CrossRef]
- Gill, J.; Motamedi, V.; Osier, N.; Dell, K.; Arcurio, L.; Carr, W.; Walker, P.; Ahlers, S.; Lopresti, M.; Yarnell, A. Moderate blast exposure results in increased IL-6 and TNFalpha in peripheral blood. Brain Behav. Immun. 2017, 65, 90–94. [Google Scholar] [CrossRef]
- Liimatainen, S.; Fallah, M.; Kharazmi, E.; Peltola, M.; Peltola, J. Interleukin-6 levels are increased in temporal lobe epilepsy but not in extra-temporal lobe epilepsy. J. Neurol. 2009, 256, 796–802. [Google Scholar] [CrossRef]
- Semple, B.D.; O’Brien, T.J.; Gimlin, K.; Wright, D.K.; Kim, S.E.; Casillas-Espinosa, P.M.; Webster, K.M.; Petrou, S.; Noble-Haeusslein, L.J. Interleukin-1 Receptor in Seizure Susceptibility after Traumatic Injury to the Pediatric Brain. J. Neurosci. 2017, 37, 7864–7877. [Google Scholar] [CrossRef]
- Webster, K.M.; Sun, M.; Crack, P.; O’Brien, T.J.; Shultz, S.R.; Semple, B.D. Inflammation in epileptogenesis after traumatic brain injury. J. Neuroinflammation 2017, 14, 10. [Google Scholar] [CrossRef] [PubMed]
- Eslami, M.; Sayyah, M.; Soleimani, M.; Alizadeh, L.; Hadjighassem, M. Lipopolysaccharide preconditioning prevents acceleration of kindling epileptogenesis induced by traumatic brain injury. J. Neuroimmunol. 2015, 289, 143–151. [Google Scholar] [CrossRef] [PubMed]
- Klein, P.; Dingledine, R.; Aronica, E.; Bernard, C.; Blumcke, I.; Boison, D.; Brodie, M.J.; Brooks-Kayal, A.R.; Engel, J., Jr.; Forcelli, P.A.; et al. Commonalities in epileptogenic processes from different acute brain insults: Do they translate? Epilepsia 2018, 59, 37–66. [Google Scholar] [CrossRef] [PubMed]
- Chhor, V.; Moretti, R.; Le Charpentier, T.; Sigaut, S.; Lebon, S.; Schwendimann, L.; Ore, M.V.; Zuiani, C.; Milan, V.; Josserand, J.; et al. Role of microglia in a mouse model of paediatric traumatic brain injury. Brain Behav. Immun. 2017, 63, 197–209. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Loane, D.J.; Kumar, A. Microglia in the TBI brain: The good, the bad, and the dysregulated. Exp. Neurol. 2016, 275 Pt 3, 316–327. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Lloyd, E.; Somera-Molina, K.; Van Eldik, L.J.; Watterson, D.M.; Wainwright, M.S. Suppression of acute proinflammatory cytokine and chemokine upregulation by post-injury administration of a novel small molecule improves long-term neurologic outcome in a mouse model of traumatic brain injury. J. Neuroinflammation 2008, 5, 28. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Somera-Molina, K.C.; Robin, B.; Somera, C.A.; Anderson, C.; Stine, C.; Koh, S.; Behanna, H.A.; Van Eldik, L.J.; Watterson, D.M.; Wainwright, M.S. Glial activation links early-life seizures and long-term neurologic dysfunction: Evidence using a small molecule inhibitor of proinflammatory cytokine upregulation. Epilepsia 2007, 48, 1785–1800. [Google Scholar] [CrossRef]
Table 1.
Differing demographical and medical characteristics of patients with traumatic brain injury vis à vis seizure occurrence.
Table 1.
Differing demographical and medical characteristics of patients with traumatic brain injury vis à vis seizure occurrence.
| Parameter | Seizure (n = 33) | No Seizure (n = 108) | p-Value |
|---|---|---|---|
| Age, mean (SD) | 53.0 (19.5) | 63.6 (19.1) | 0.008 |
| Sex, n (%) | 0.363 | ||
| Female | 6 (18.2) | 28 (25.1) | |
| Male | 27 (81.8) | 80 (74.9) | |
| Race, n (%) | 0.035 | ||
| Chinese | 18 (54.5) | 74 (68.5) | |
| Malay | 9 (27.3) | 30 (27.8) | |
| Indian | 4 (12.1) | 2 (1.9) | |
| Other | 2 (6.1) | 2 (1.9) | |
| Occupation, n (%) | 0.097 | ||
| Working | 21 (63.6) | 46 (42.6) | |
| Retired | 11 (33.3) | 59 (54.6) | |
| Mode of injury, n (%) | 0.132 | ||
| Fall | 22 (68.8) | 65 (63.1) | |
| Road traffic accident | 8 (25.0) | 37 (35.9) | |
| Industrial accident | 2 (6.3) | 1 (1.0) | |
| History of diabetes, n (%) | 0.816 | ||
| Yes | 7 (21.2) | 25 (23.1) | |
| No | 26 (78.8) | 83 (76.9) | |
| History of hypertension, n (%) | 0.675 | ||
| Yes | 13 (39.4) | 47 (43.5) | |
| No | 20 (60.6) | 61 (56.5) | |
| History of hyperlipidemia, n (%) | 0.673 | ||
| Yes | 12 (36.4) | 35 (32.4) | |
| No | 21 (63.6) | 73 (67.6) | |
| History of chronic kidney disease, n (%) | 0.557 | ||
| Yes | 2 (6.1) | 4 (3.7) | |
| No | 31 (93.9) | 104 (96.3) | |
| Atrial fibrillation, n (%) | 0.564 | ||
| Yes | 2 (6.1) | 10 (9.3) | |
| No | 31 (93.9) | 98 (90.7) | |
| Ischemic heart disease, n (%) | 0.384 | ||
| Yes | 7 (21.2) | 16 (14.8) | |
| No | 26 (78.8 | 92 (85.2) | |
| Anemia, n (%) | 0.891 | ||
| Yes | 3 (9.1) | 9 (8.3) | |
| No | 30 (91.7) | 99 (91.7) | |
| Past history of stroke, n (%) | 0.795 | ||
| Yes | 4 (12.1) | 15 (13.9) | |
| No | 29 (87.9) | 93 (86.1) | |
| Presence of liver dysfunction, n (%) | 0.01 | ||
| Yes | 2 (6.1) | 0 (0) | |
| No | 31 (93.9) | 108 (100) | |
| Subdural hemorrhage, n (%) | 0.386 | ||
| Yes | 18 (54.5) | 68 (63.0) | |
| No | 15 (45.5) | 40 (37.0) | |
| Subarachnoid hemorrhage, n (%) | 0.882 | ||
| Yes | 13 (39.4) | 41 (38.0) | |
| No | 20 (60.6) | 67 (62.0) | |
| Cerebral contusion, n (%) | 0.05 | ||
| Yes | 22 (66.7) | 51 (47.2) | |
| No | 11 (33.3) | 57 (52.8) | |
| Intraventricular hemorrhage, n (%) | 0.263 | ||
| Yes | 8 (24.2) | 17 (15.7) | |
| No | 25 (75.8) | 91 (84.3) | |
| Extradural hemorrhage, n (%) | 0.31 | ||
| Yes | 7 (21.2) | 15 (13.9) | |
| No | 26 (78.8) | 93 (86.1) | |
| Neurosurgical intervention, n (%) | <0.001 | ||
| No intervention | 12 (37.5) | 56 (51.9) | |
| EVD-ICP | 6 (18.8) | 13 (12.0) | |
| Burr-hole | 1 (3.1) | 24 (22.2) | |
| Craniotomy | 1 (3.1) | 7 (6.5) | |
| Craniectomy | 9 (28.1) | 8 (7.4) | |
| V-P shunt | 3 (9.4) | 0 (0) | |
| GCS at admission, mean (SD) | 9.5 (4.1) | 11.9 (3.0) | 0.003 |
| Hospital length of stay at index admission, day, mean (SD) | 53.1 (36.7) | 36.3 (30.1) | 0.021 |
| Use of neurostimulants, n (%) | <0.001 | ||
| Yes | 13 (39.4) | 13 (12.0) | |
| No | 20 (60.6) | 95 (88.0) | |
| Use of Statins, n (%) | 0.207 | ||
| Yes | 10 (30.3) | 46 (42.6) | |
| No | 23 (69.7) | 62 (57.4) | |
| Mortality, n (%) | 0.873 | ||
| Death | 9 (27.3) | 31 (28.7) | |
| Alive | 24 (72.7) | 77 (71.3) | |
| Follow-up period, days, median (25–75%) | 2242 (951–2894) | 1435 (845–2543) | 0.082 |
| Hb, mean (SD) | 13.3 (2.1) | 13.2 (2.2) | 0.919 |
| WBC, mean (SD) | 13.4 (67) | 11.5 (4.3) | 0.141 |
| Platelet, mean (SD) | 276.6 (104.5) | 272.3 (90.2) | 0.833 |
| MCV, mean (SD) | 86.2 (8.2) | 88.4 (6.8) | 0.179 |
| MCH, mean (SD) | 28.6 (3.3) | 29.4 (3.9) | 0.289 |
| Urea, mean (SD) | 4.7 (2.6) | 5.6 (2.8) | 0.101 |
| Na, mean (SD) | 137 (4.7) | 137.4 (4.3) | 0.687 |
| K, mean (SD) | 3.9 (0.5) | 4.0 (0.5) | 0.299 |
| Bicarb, mean (SD) | 21.9 (3.6) | 22.8 (3.1) | 0.207 |
| Creatinine, mean (SD) | 122.8 (186.4) | 98.9 (50.3) | 0.472 |
| eGFR, mean (SD) | 57.5 (12.4) | 55.8 (10.3) | 0.484 |
Results: Occurrence of seizures after traumatic brain injury was significantly associated with younger age, being Indian, presence of liver dysfunction, neurosurgical interventions, consciousness level at admission, and use of neurostimulant medications. Bold face indicates p-values < 0.05.
Table 2.
Multivariate analysis.
| Parameter | B | S.E. | Wald | df | p-Value | OR | 95% CI for OR | |
|---|---|---|---|---|---|---|---|---|
| Lower | Upper | |||||||
| Age | −0.046 | 0.013 | 11.422 | 1 | 0.001 | 0.956 | 0.931 | 0.981 |
| Neurostimulants | 2.389 | 0.584 | 16.745 | 1 | 0.0001 | 10.899 | 3.472 | 34.220 |
| Liver dysfunction | 24.165 | 28073.795 | 0.000 | 1 | 0.999 | 0.000 | ||
| Constant | 0.359 | 0.699 | 0.263 | 1 | 0.608 | 1.431 | ||
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MDPI and ACS Style
Oey, N.E.; Tan, P.T.; Pande, S.D. Young Age, Liver Dysfunction, and Neurostimulant Use as Independent Risk Factors for Post-Traumatic Seizures: A Multiracial Single-Center Experience. Int. J. Environ. Res. Public Health 2023, 20, 2301. https://doi.org/10.3390/ijerph20032301
AMA Style
Oey NE, Tan PT, Pande SD. Young Age, Liver Dysfunction, and Neurostimulant Use as Independent Risk Factors for Post-Traumatic Seizures: A Multiracial Single-Center Experience. International Journal of Environmental Research and Public Health. 2023; 20(3):2301. https://doi.org/10.3390/ijerph20032301
Chicago/Turabian StyleOey, Nicodemus Edrick, Pei Ting Tan, and Shrikant Digambarrao Pande. 2023. "Young Age, Liver Dysfunction, and Neurostimulant Use as Independent Risk Factors for Post-Traumatic Seizures: A Multiracial Single-Center Experience" International Journal of Environmental Research and Public Health 20, no. 3: 2301. https://doi.org/10.3390/ijerph20032301
APA StyleOey, N. E., Tan, P. T., & Pande, S. D. (2023). Young Age, Liver Dysfunction, and Neurostimulant Use as Independent Risk Factors for Post-Traumatic Seizures: A Multiracial Single-Center Experience. International Journal of Environmental Research and Public Health, 20(3), 2301. https://doi.org/10.3390/ijerph20032301
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