The probability of favorable outcome after traumatic brain injury (TBI) decreases with age. Elderly, ≥ 60 years, are an increasing part of our population. Recent studies have shown an increase of favorable outcome in elderly over time. However, the optimal patient selection and neurointensive care (NIC) treatments may differ in the elderly and the young. The aims of this study were to examine outcome in a larger group of elderly TBI patients receiving NIC and to identify demographic and treatment related prognostic factors.
Patients with TBI ≥ 60 years receiving NIC at our department between 2008 and 2014 were included. Demographics, co-morbidity, admission characteristics, and type of treatments were collected. Clinical outcome at around 6 months was assessed. Potential prognostic factors were included in univariate and multivariate regression analysis with favorable outcome as dependent variable.
Two hundred twenty patients with mean age 70 years (median 69; range 60–87) were studied. Overall, favorable outcome was 46% (Extended Glasgow Outcome Scale (GOSE) 5–8), unfavorable outcome 27% (GOSE 2–4), and mortality 27% (GOSE 1). Significant independent negative prognostic variables were high age (p < 0.05), multiple injuries (p < 0.05), GCS M ≤ 3 on admission (p < 0.05), and mechanical ventilation (p < 0.001).
Overall, the elderly TBI patients > 60 years receiving modern NIC in this study had a fair chance of favorable outcome without large risks for severe deficits and vegetative state, also in patients over 75 years of age. High age, multiple injuries, GCS M ≤ 3 on admission, and mechanical ventilation proved to be independent negative prognostic factors. The results underline that a selected group of elderly with TBI should have access to NIC.
Outcome after traumatic brain injury (TBI) has improved over time with the development of neurointensive care (NIC) [3, 4, 9, 10, 26, 27, 30, 48] despite the fact that favorable outcome decreases with increasing age [16, 21, 28, 29, 38, 44], and there is an increasing proportion of elderly in the TBI population [17, 19, 33, 34]. The United Nations reports that the population aged 60 or older is growing faster than all the younger age groups and expects the number of persons over 60 years to be more than doubled by 2050 . Elderly are prone to trauma from falls. One third of every person above 60 years and every other person above 80 years have a falling accident every year . The management of elderly patients with traumatic head injury constitutes a tremendous challenge in the future. An updated periodic evaluation of NIC of TBI patients made by us showed substantial increase of the proportion of patients > 60 years treated from 16 to 30% between 1996–1997 and 2008–2009 . Furthermore, when clinical outcome was evaluated in the elderly TBI patients who received NIC, 51% of patients age ≥ 65 had favorable outcome . Those relatively favorable results indicate that elderly patients with TBI should not be excluded from NIC. However, the optimal patient selection and most beneficial treatments may differ in the elderly and the young. Elderly patients have comorbidities to a higher degree, are more likely to use anticoagulants, and respond less well to rehabilitation . Therefore, it is important to gain more knowledge about elderly TBI patients. The aims of this study were to examine outcome in a larger group of elderly TBI patients receiving NIC and to identify demographic- and treatment-related prognostic factors specifically in the elderly.
Material and methods
Referral of patients
The Department of Neurosurgery at the Uppsala University Hospital in Sweden provides highly specialized NIC for a population of approximately 2 million people living in the central part of Sweden. Patients arriving at local hospitals are stabilized according to the ATLS principles and then referred to Uppsala for tertiary care (the most distant local hospital 382 km away) .
Patient selection and data collection
Information about clinical characteristics, management, and clinical outcome are recorded for all TBI patients treated at the NIC unit in Uppsala in the Uppsala Traumatic Brain Injury register .TBI patients ≥ 60 years of age registered between 2008 and 2014 were eligible for the study. In total, 249 patients were identified. After exclusion of 29 elderly patients, 220 remained to be the studied. The patients were excluded for the following reason: patients admitted to the NIC unit ≥ 5 days after the trauma (n = 10), or treated successfully at the NIC unit within 24 h (n = 6); patients with both pupils wide and non-reacting on arrival at the NIC unit (n = 4) (i.e., patients with an obvious predestined fatal clinical course [1, 7]); patients with gunshot wound to the head (n = 1); patients lost to follow-up (n = 8).
The following parameters were studied: primary or secondary transfer, sex, age, cause of trauma, multiple injuries, trauma under influence of drugs/alcohol, acute surgery before arrival, GCS on admission, medical history (brain injury/disease, previous traumatic brain injury, diabetes mellitus, hypertension/cardiovascular disease (CVD), antithrombotic drugs (subgrouped by antiplatelet, warfarin, non-vitamin K antagonist oral anticoagulants (NOAC), and low molecular weight heparin (LMWH)), and ethylism), craniotomy, cause of craniotomy, decompressive hemicraniectomy, intracranial pressure (ICP) monitoring, mechanical ventilation, and NIC mortality.
The computed tomography (CT) scans from the admission were classified retrospectively according to Marshall Classification  by one of the authors (S.L.).
All patients were treated according to the standardized escalated management protocol, described in detail earlier , and summarized below:
All unconscious patients (Glasgow Coma Scale motor response (GCS M) ≤ 5) are intubated and mechanically ventilated. Intubated patients are moderately hyperventilated (PaCO2 4.0–4.5 kPa) on admission with the aim of normoventilation as soon as possible when ICP allows. Propofol (Propofol-LipuroB; Braun Medical, Danderyd, Sweden) is used for sedation and morphine for analgesia. ICP is monitored in unconscious patients using an external ventricular drain (EVD) or an intraparenchymal pressure probe. When EVD is used, ICP is measured with the pressure dome at the level of the lateral ventricles. Arterial blood pressure is measured with the pressure dome at heart level. Patients are positioned in bed with 30° head elevation to facilitate venous outflow. Clinical neurological status is monitored using frequent wake-up tests. Lesions causing significant mass effect, extracerebral hematomas or contusions, are surgically evacuated except when coagulopathy is resistant to therapy. Prophylactic anticonvulsants are not used. Thromboprophylaxis are used when the risk for new intracranial bleedings are deemed low and continued until patients have been mobilized. Treatment goals are as follows: ICP < 20 mmHg, cerebral perfusion pressure (CPP) > 60 mmHg, systolic blood pressure (SBP) > 100 mmHg, central venous pressure (CVP) 0–5 cm H20, pO2 > 12 kPa, blood glucose 5–10 mmol/L, electrolytes within normal range, normovolemia, and body temperature < 38 °C. If ICP is increased > 20 mmHg without mass lesions, intermittent cerebrospinal fluid (CSF) drainage of small volumes (1–2 ml) are used during the early period when there are risks of expanding hematomas and brain swelling. Later, CSF is drained using an open system against a pressure level of 15–20 mmHg if needed.
In case of persisting ICP problems, the treatment is escalated to Step 1A with no wake-up test. This entails continuous sedation with propofol and stress reduction with β1-antagonist metoprolol (Seloken®, AstraZeneca AB Södertälje, Sweden) (0.2–0.3 mg/kg/24 h as an infusion) and α2-agonist clonidin (Catapresan®, BoehingerIngelheim AB Stockholm Sweden) (0.5–1.0 μg/kg × 8 or the same dose as an infusion).
When the ICP problems continue, barbiturate coma treatment with infusion of thiopental (Pentocur, Abcur AB, Helsingborg, Sweden) is initiated provided that there is no shift of the midline. Bolus dose of 4–8 mg/kg is given as repeated 50 mg injections until ICP is < 20 mmHg followed by an infusion of 5–10 mg/kg/h for 6 h and thereafter 2–5 mg/kg/h as required to control ICP. The lowest possible dose is used to keep ICP < 20 mmHg and burst-suppression on electroencephalogram (EEG) is not the goal. During this treatment, a CPP as low as 50 mmHg is allowed. Thiopental concentration > 380 μmol/L is avoided. Because of the high risk of severe side effects with barbiturate coma treatment in elderly, this therapy was only exceptionally escalated to this step in old patients.
Decompressive craniectomy  is used when Step 1B is insufficient to reduce ICP or when adverse effects of the thiopental treatment are observed. Bi-fronto-temporal craniectomies are done, sparing the bone ridge in the midline when there are no mass lesions. When there is a shift of the midline and no localized mass lesions to evacuate, a hemicraniectomy is done.
Evaluation of outcome
The outcome was categorized in favorable (GOSE 5–8), unfavorable (GOSE 2–4), and dead (GOSE 1).
To compare different age groups, Pearson’s Chi-squared test was used. Patients and treatment factors were analyzed using univariate logistic regression. Multivariate logistic regression analysis was performed with favorable outcome (GOSE 5–8) as dependent variable. Admission variables were included as explanatory variables, and admission together with treatment variables was also analyzed. All explanatory variables were dichotomized except age. IBM SPSS Statistics for Windows was used.
The mean age of the 220 patients was 70 years (median 69; range 60–87). The age distribution showed that most of the patients were between 60 and 75 years (Fig. 1).
Patient characteristics on admission
The patient characteristics are presented in Table 1 for all patients > 60 years old, for patients 60–74 years old, and for patients 75–89 years old. There were 170 patients 60–74 years old and 50 patients 75–89 years old. There was no significant difference in sex between the two age groups. The most common cause of trauma was falls which occurred in 77% of all cases (170 patients). There was no significant difference between the two age groups. In both age groups, around 90% of the patients were admitted in GCS M ≥ 4. Multiple injuries were found in 25% of the 60–74-year-old patients and in 10% of the 75–89 years old (p < 0.05). Trauma under the influence of alcohol was almost 5 times as common in the 60–74-year-old patients compared to the older patients, 26% vs 6%, respectively, (p < 0.01).
Overall, the most common type of injury dominating TBI was acute subdural hematoma (ASDH; 43%) followed by contusions (29%). In the 60–74-year-old group, contusions were the dominating injury type, and occurred in 35% of the patients, compared to 10% in the 75–89-year-old group (p < 0.001). In the 75–89-year-old group, the dominating injury type was ASDH, occurring in 76% of the patients compared to 34% in the 60–74 years old (p < 0.01) (Table 1).
When the initial CT scans were classified according to Marshall Classification (Table 1), diffuse injury II was the most common class with 41% in patients 60–74 years old and 22% in patients 75–89 years old (p < 0.05). Evacuated mass lesion was the most common Marshall Classification in patients 75–89 years old and occurred in 40% of those patients.
Regarding the medical history (Table 1), 54% of all elderly had hypertension/CVD and 37% used antithrombotic drugs. One fifth of all 220 patients (20%) had a history of previous brain injury/disease before the trauma, but only 4% of those were a previous TBI. Among patients 60–74 years old, 48% had hypertension/CVD in the medical history compared to 72% in patients 75–89 years old (p < 0.01). Antithrombotic drugs were almost twice as common in 75–89-year-old patients compared to 60–74-year-old patients, 62% and 30%, respectively (p < 0.001). Looking at the specific antithrombotic drugs, warfarin was four times as common in 75–89-year-old patients compared to patients 60–74 years old; 42% vs 8%. Among patients 60–74 years old, 30% of had a history of ethylism compared to 10% among patients 75–89 years old (p < 0.01).
Among all 220 elderly patients, 177 (80%) received mechanical ventilation for a mean of 7 days (median 6, range 1–21), and 118 (53%) had ICP monitoring for a mean of 10 days (median 8, range 2–25) (Table 2). Eighteen patients (8%) had been operated with evacuation of ASDH at the referring hospital due to acute herniation before arrival (Table 2). Ninety-five patients (43%) had a craniotomy done during NIC, most commonly due to ASDH which occurred in 80 patients (36%) followed by evacuation of contusions in 25 patients (11%). Decompressive hemicraniectomy was done in 9 patients (4%). Thirty patients 75–89 years old (60%) had a craniotomy compared to 65 patients 60–74 years old (38%) (p ≤ 0.01). Three patients received thiopental.
Follow-up of surviving patients was made after 7.8 months in mean (median 7, range 5–28). When outcome was graded with the Extended Glasgow Outcome Scale, 43 patients (20%) were GOSE 8 (upper good recovery), 40 (18%) were GOSE 7 (lower good recovery), 10 (5%) were GOSE 6 (upper moderate disability), 8 (4%) were GOSE 5 (lower moderate disability), 21 (10%) were GOSE 4 (upper severe disability), 37 (17%) were GOSE 3 (lower severe disability), 2 patients (1%) were in GOSE 2 (vegetative state), and 59 patients (27%) were GOSE 1 (dead; 17 (8%) died at the NICU) (Fig. 2). The clinical outcome by age groups is summarized in Fig. 3. Patients 60–69 years old showed favorable outcome in around 50% of the cases and < 20% died. Patients 70–74 years old almost also showed favorable outcome in 50% of the cases and around 35% died. In patients 75–84 years of age, favorable outcome was around 30% and declined to 25% in patients 85–89 years old. Of the 60–74 years old, 11 patients (6%) died at the NICU compared with 6 (12%) in the 75–89 years old.
Prediction of prognosis
Univariate logistic regression analysis with favorable outcome (GOSE 5–8) as dependent variable (Table 3) showed the following significant patient variables (predictors): age (p < 0.05), GCS M ≤ 3 on admission (p < 0.01), diffuse injury Marshall score I–IV (p < 0.001), and Marshall score evacuated mass lesion (EML) (p < 0.001) and warfarin (p < 0.05). The following patient variables showed marginal significance (Table 3): extracerebral hematoma (p = 0.08), history of brain injury/disease (p = 0.056), and history of ethylism (p = 0.066) and antiplatelet (p = 0.053).
For the treatment variables, the significant variables were (Table 3): craniotomy (p < 0.01), evacuation of extracerebral hematoma (p < 0.05), and mechanical ventilation (p < 0.001).
Multivariate logistic regression analysis of admission variables showed that the significant independent variables were age (p < 0.05) and multiple injuries (p < 0.05). GCS M ≤ 3 on admission (p = 0.052) and EML (p = 0.078) showed marginal significance (Table 4).
When admission variables and treatment variables were included in the multivariate logistic regression analysis, the significant independent variables were age (p < 0.05), GCS M ≤ 3 on admission (p < 0.05), multiple injuries (p < 0.05), and mechanical ventilation (p < 0.01). Variables that showed marginal significance were EML (p = 0.067), ethylism (p = 0.073), warfarin (p = 0.088), surgery before arrival (p = 0.053), and evacuated contusions (p = 0.055) (Table 5). Age was studied as a continuous variable so for every year in age there was a 0.94 odds ratio for favorable outcome, meaning the chance of favorable outcome decreased 6% with each increase of 1 year in age.
Forty-six percent of the elderly over 60 years of age had favorable outcome (GOSE 5–8), while 27% had unfavorable outcome (GOSE 2–4), and 27% died (GOSE 1) (Fig. 3), which indicates that NIC may be beneficial for the elderly. The rate of favorable outcome was virtually unchanged up to 75 years of age and then a slight decrease was seen with more advanced age. Unfavorable outcome did not increase after 75 years of age; it appears as the reason for the slight decrease in the proportion of favorable outcome above 75 years of age was higher mortality rather than an increased proportion of unfavorable outcome (Fig. 3). Those results are important to consider when to decide to offer NIC or not in an elderly TBI patient, taking also into consideration the general assumption that elderly are not afraid to die but to become dependent . It should be emphasized, however, that these results cannot be extrapolated to the elderly population in general, since there was a selection of elderly patients judged to have a reasonable chance to achieve favorable outcome depending on, e.g., previous functional status, type of injury, level of consciousness, and co-morbidity. It is important to look at the characteristics of the elderly patients studied and try to identify prognostic factor in order to facilitate the selection of elderly TBI patients for NIC in the future.
The main cause of trauma in all elderly age groups was fall (Table 1), which is in accordance with our earlier findings [22, 28] as well as with the results of many other studies [8, 15, 17, 19, 23, 34, 36, 40]. Although there was a predominant injury mechanism, there was a notable significant difference between the age groups regarding several other characteristics (Table 1). The 60–74 years old were more often intoxicated at the time of trauma (26% vs 6%) and other injuries (25% vs 10%). They were also more likely to have contusions (35% vs 10%) and less likely to have ASDH (34% vs 76%). They had fewer cases of hypertension/CVD (48% vs 72%) and antithrombotic drugs (30% vs 62%, warfarin 8% vs 42%) and were more likely to have a history of ethylism (30% vs 10%). These findings highlight important differences between the 60–74-year-old group, and the 75–89-year-old group. The differences were also reflected in patient management with the older group having more craniotomies than the younger group (60% vs 38%). This may be explained by the fact that ASDH was more common among patients 75–89 years old and consistently it was also found that the reason for craniectomy was ASDH in 56% in the older age group compared to 31% in the younger group (Table 2).
Looking for prognostic predictors in the medical history, none of the following, such as previous brain injury/disease, previous traumatic brain injury, diabetes mellitus, and ethylism, had any significant impact on favorable outcome in the univariate analysis or the multivariate analyses, which was unexpected (Tables 3, 4, and 5). This of course does not exclude that those factors do not influence clinical outcome, but simply means that we were unable to show significant differences with our data. The reasons for that may be that some of those factors were present in too large proportions of the patients and others in too small proportions, and that a larger patient material is required to show significant differences in outcome. It is obvious that established prognostic factors from large patient materials of all ages cannot be disregarded in the decision-making process for which elderly TBI patients should be treated.
Antithrombotic drugs as a group had no negative impact on outcome in the univariate analysis. However, in a subgroup analysis, warfarin was a significant prognostic factor and antiplatelet therapy showed marginal significance (p = 0.053), but neither showed any significant independent contribution in the multivariate analysis (Table 4, Table 5). This finding is in contrast to the results of many earlier studies and needs to be discussed in particular. Karni et al. found a 50% mortality rate for traumatic head injury in elderly with anticoagulants . Lavoie et al. showed that preinjury warfarin in elderly with closed head injury had more severe head injury and a higher likelihood of death . Franko et al. showed that warfarin carries a six-fold increase in TBI-mortality and that mortality and occurrence of intracerebral hemorrhage increased with higher international normalized ratio (INR), especially INR over 4.0 where the mortality was found to be 50% and the risk of intracerebral hematoma (ICH) 75% . Grandhi et al. found that warfarin and not antiplatelet medication influenced survival and need for neurosurgical intervention in the elderly . Pieracci et al. found that the degree of anticoagulation rather than warfarin itself predicts adverse outcome in TBI in elderly patients . Ohm et al. showed that elderly with intracranial hemorrhage and antiplatelet therapy had increased mortality . Wong et al. found in their study that clopidogrel increased mortality but not warfarin and aspirin . There are also contradicting studies. In 2017, Ganetsky et al. examined 939 patients who had ground-level falls and antiplatelet therapy or anticoagulants, and found a low incidence of clinically significant intracranial hemorrhage (< 5%) and no difference between anticoagulation and antiplatelet therapy . One could speculate that possible reasons for why anticoagulants did not have any prognostic significance in our study could be: (1) In our referral area, patients on warfarin have frequent check-ups which reduces the risk for overtreatment with too high INR. (2) National guidelines require CT examination after mild head trauma when on anticoagulation and prompt reversal of warfarin in case of intracranial hemorrhages. (3) Standardized NIC which minimizes secondary insults may prevent worsening of intracranial hemorrhages. Altogether, however, it is reasonable to assume that anticoagulation therapy increases the risk for worsening of the head injury and may under some circumstances complicate the insertion of ICP devices and surgical treatment, although such therapy doses not make successful management impossible.
Considering other possible prognostic factors analyzed in the univariate analysis, diffuse injury I–IV had a OR > 1 and seems to be associated with favorable outcome (most likely due to the large number of diffuse injury II, the least serious class in that group). EML had an OR 0.299 indicating less chance of good outcome (Table 3). Both craniotomy and evacuated extracerebral hematoma had a negative influence on good outcome in the univariate analysis as well as mechanical ventilation (Table 3).
When analyzing potential prognostic factors, it is of utmost importance to identify factors with independent prognostic information. The multivariate analysis of prognostic admission factors for favorable outcome showed that high age and multiple injuries had a significant independent negative prognostic value and low GCS showed marginal significance (p = 0.052) (Table 4), which was as expected and in accordance with other studies of elderly patients [6, 29, 38, 44]. When both treatment factors and admission factors were included in the multivariate analysis of prognostic factors for favorable outcome, age, low GCS, and multiple injuries all had significant independent negative prognostic value. Surgery before arrival (evacuated ASDH at the referring hospital) showed positive prognostic value of marginal significance (p = 0.053). Evacuation of contusions and extracerebral hematoma, which were significant prognostic factors in the univariate analysis, did not show any significant independent influence on clinical outcome, although evacuation of contusions had marginal significant (p = 0.055). Mechanical ventilation on the other hand proved to have independent negative predictive value for favorable outcome (OR 0.195) (Table 5). The reasonable explanation for that may be that mechanical ventilation is not completely dependent on the severity of brain injury but also related to other factors not included in the statistical analysis, e.g., various infections including lung infections and other adverse events. Barnato et al. also found that elderly treated at the intensive care unit who survived mechanical ventilation had worse functional outcome . It is likely that the negative impact of mechanical ventilation on outcome depends both on a more severe brain injury requiring mechanical ventilation, and on the development of systemic complications, with which the elderly are less able to cope.
There are some study limitations that needs to be considered. This is a single-center study and the results may have been influenced by the local management applied, and therefore the results may not be completely generalizable. Furthermore, as mentioned earlier, there was a selection bias since predominantly patients judged to have a reasonable chance for favorable outcome were accepted for NIC. Therefore, the results need to be interpreted with caution.
While these results may at first look discouraging but for this group of elderly TBI patients, a relatively large proportion achieved favorable outcome, when they were treated according to modern NIC principles and the treatment did not cause a large proportion of patients with severe disability or vegetative state. Similar results have also been reported by others [24, 29, 37, 47]. Further studies are required focusing on the NIC specifically in elderly TBI patients concerning, e.g., secondary insults, ICP management, and cerebral perfusion thresholds, to find out if these areas holds the key to improve outcome.
This study shows that an appropriately selected group of elderly TBI patients receiving modern NIC have a fair chance of favorable outcome without large risks for severe deficits and vegetative state. Significant negative prognostic factors were high age, multiple injuries, low GCS M on admission, and the use of mechanical ventilation. The results underline that elderly with TBI should have access to NIC, when favorable outcome is as high as 47% for patients 60–74 years and around 30% for the patients between 75 and 84 years. Further research is needed about the selection of elderly patients and the optimal NIC management of elderly with TBI.
Traumatic brain injury
Extended Glasgow Outcome Scale
Glasgow Coma Scale
- GCS M:
Glasgow Coma Scale motor response
Advanced Trauma Life Support
External ventricular drain
Cerebral perfusion pressure
Systolic blood pressure
Central venous pressure
Acute subdural hematoma
Evacuated mass lesions
International normalized ratio
Non-vitamin K antagonist oral anticoagulants
Low molecular weight heparin
Andrews BT, Pitts LH (1991) Functional recovery after traumatic transtentorial herniation. Neurosurgery 29:227–231
Barnato AE, Albert SM, Angus DC, Lave JR, Degenholtz HB (2011) Disability among elderly survivors of mechanical ventilation. Am J Respir Crit Care Med 183:1037–1042. https://doi.org/10.1164/rccm.201002-0301OC
Becker DP, Miller JD, Ward JD, Greenberg RP, Young HF, Sakalas R (1977) The outcome from severe head injury with early diagnosis and intensive management. J Neurosurg 47:491–502. https://doi.org/10.3171/jns.1977.47.4.0491
Bowers SA, Marshall LF (1980) Outcome in 200 consecutive cases of severe head injury treated in San Diego County: a prospective analysis. Neurosurgery 6:237–242
Cheng C, Chi NC, Williams E, Thompson HJ (2018) Examining age-related differences in functional domain impairment following traumatic brain injury. Int J Older People Nursing:e12208. https://doi.org/10.1111/opn.12208
Chestnut RM, Ghajar J, Maas AIR, Marion DW, Servadei F, Teasdale G, Unterberg A, von Holst H, Walter BC (2000) Part 2: early indicators of prognosis in severe traumatic BRAIN injury. J Neurotrauma 17:555–555. https://doi.org/10.1089/neu.2000.17.555
Combes P, Fauvage B, Colonna M, Passagia JG, Chirossel JP, Jacquot C (1996) Severe head injuries: an outcome prediction and survival analysis. Intensive Care Med 22:1391–1395
Dams-O’Connor K, Cuthbert JP, Whyte J, Corrigan JD, Faul M, Harrison-Felix C (2013) Traumatic brain injury among older adults at level I and II trauma centers. J Neurotrauma 30:2001–2013. https://doi.org/10.1089/neu.2013.3047
Eker C, Asgeirsson B, Grande PO, Schalen W, Nordstrom CH (1998) Improved outcome after severe head injury with a new therapy based on principles for brain volume regulation and preserved microcirculation. Crit Care Med 26:1881–1886
Elf K, Nilsson P, Enblad P (2002) Outcome after traumatic brain injury improved by an organized secondary insult program and standardized neurointensive care. Crit Care Med 30:2129–2134. https://doi.org/10.1097/01.CCM.0000025893.73582.52
Fischerström A, Nyholm L, Lewén A, Enblad P (2014) Acute neurosurgery for traumatic brain injury by general surgeons in Swedish county hospitals: a regional study. Acta Neurochir 156:177–185. https://doi.org/10.1007/s00701-013-1932-5
Franko J, Kish KJ, O’Connell BG, Subramanian S, Yuschak JV (2006) Advanced age and preinjury warfarin anticoagulation increase the risk of mortality after head trauma. J Trauma 61:107–110. https://doi.org/10.1097/01.ta.0000224220.89528.fc
Ganetsky M, Lopez G, Coreanu T, Novack V, Horng S, Shapiro NI, Bauer KA (2017) Risk of intracranial hemorrhage in ground-level fall with antiplatelet or anticoagulant agents. Acad Emerg Med 24:1258–1266. https://doi.org/10.1111/acem.13217
Grandhi R, Harrison G, Voronovich Z, Bauer J, Chen SH, Nicholas D, Alarcon LH, Okonkwo DO (2015) Preinjury warfarin, but not antiplatelet medications, increases mortality in elderly traumatic brain injury patients. J Trauma Acute Care Surg 78:614–621. https://doi.org/10.1097/TA.0000000000000542
Hawley C, Sakr M, Scapinello S, Salvo J, Wrenn P (2017) Traumatic brain injuries in older adults-6 years of data for one UK trauma Centre: retrospective analysis of prospectively collected data. Emerg Med J 34:509–516. https://doi.org/10.1136/emermed-2016-206506
Hukkelhoven CW, Steyerberg EW, Rampen AJ, Farace E, Habbema JD, Marshall LF, Murray GD, Maas AI (2003) Patient age and outcome following severe traumatic brain injury: an analysis of 5600 patients. J Neurosurg 99:666–673. https://doi.org/10.3171/jns.2003.99.4.0666
Iaccarino C, Carretta A, Nicolosi F, Morselli C (2018) Epidemiology of severe traumatic brain injury. J Neurosurg Sci 62:535–541. https://doi.org/10.23736/S0390-5616.18.04532-0
Karni A, Holtzman R, Bass T, Zorman G, Carter L, Rodriguez L, Bennett-Shipman VJ, Lottenberg L (2001) Traumatic head injury in the anticoagulated elderly patient: a lethal combination. Am Surg 67:1098–1100
Koskinen S, Alaranta H (2008) Traumatic brain injury in Finland 1991-2005: a nationwide register study of hospitalized and fatal TBI. Brain Inj 22:205–214. https://doi.org/10.1080/02699050801938975
Lavoie A, Ratte S, Clas D, Demers J, Moore L, Martin M, Bergeron E (2004) Preinjury warfarin use among elderly patients with closed head injuries in a trauma center. J Trauma 56:802–807
LeBlanc J, de Guise E, Gosselin N, Feyz M (2006) Comparison of functional outcome following acute care in young, middle-aged and elderly patients with traumatic brain injury. Brain Inj 20:779–790. https://doi.org/10.1080/02699050600831835
Lenell S, Nyholm L, Lewen A, Enblad P (2015) Updated periodic evaluation of standardized neurointensive care shows that it is possible to maintain a high level of favorable outcome even with increasing mean age. Acta Neurochir 157:417–425. https://doi.org/10.1007/s00701-014-2329-9
Lennartsson C, Heimerson I (2012) Elderly people’s health: health in Sweden: the National Public Health Report 2012. Chapter 5. Scand J Public Health 40:95–120. https://doi.org/10.1177/1403494812459468
Li LF, Lui WM, Wong HH, Yuen WK, Leung GK (2017) Outcome after operative intervention for traumatic brain injuries in the elderly. Asian J Neurosurg 12:37–43. https://doi.org/10.4103/1793-5482.148787
Marshall LF, Marshall SB, Klauber MR, Clark MB, Eisenberg HM, Jane JA, Luerssen TG, Marmarou A, Foulkes MA (1991) A new classification of head injury based on computerized tomography. Spec Suppl 75:S14–S20. https://doi.org/10.3171/sup.1991.75.1s.0s14
Marshall LF, Smith RW, Shapiro HM (1979) The outcome with aggressive treatment in severe head injuries. Part I: the significance of intracranial pressure monitoring. J Neurosurg 50:20–25. https://doi.org/10.3171/jns.1979.50.1.0020
Marshall LF, Smith RW, Shapiro HM (1979) The outcome with aggressive treatment in severe head injuries. Part II: acute and chronic barbiturate administration in the management of head injury. J Neurosurg 50:26–30. https://doi.org/10.3171/jns.1979.50.1.0026
Merzo A, Lenell S, Nyholm L, Enblad P, Lewen A (2016) Promising clinical outcome of elderly with TBI after modern neurointensive care. Acta Neurochir 158:125–133. https://doi.org/10.1007/s00701-015-2639-6
Mosenthal AC, Lavery RF, Addis M, Kaul S, Ross S, Marburger R, Deitch EA, Livingston DH (2002) Isolated traumatic brain injury: age is an independent predictor of mortality and early outcome. J Trauma 52:907–911
Nordstrom CH, Sundbarg G, Messeter K, Schalen W (1989) Severe traumatic brain lesions in Sweden. Part 2: impact of aggressive neurosurgical intensive care. Brain Inj 3:267–281
Nyholm L, Howells T, Enblad P, Lewén A (2013) Introduction of the Uppsala Traumatic Brain Injury register for regular surveillance of patient characteristics and neurointensive care management including secondary insult quantification and clinical outcome. Ups J Med Sci 118:169–180. https://doi.org/10.3109/03009734.2013.806616
Ohm C, Mina A, Howells G, Bair H, Bendick P (2005) Effects of antiplatelet agents on outcomes for elderly patients with traumatic intracranial hemorrhage. J Trauma 58:518–522
Pedersen K, Fahlstedt M, Jacobsson A, Kleiven S, von Holst H (2015) A national survey of traumatic brain injuries admitted to hospitals in Sweden from 1987 to 2010. Neuroepidemiology 45:20–27. https://doi.org/10.1159/000381780
Peeters W, Majdan M, Brazinova A, Nieboer D, Maas AIR (2017) Changing epidemiological patterns in traumatic brain injury: a longitudinal hospital-based study in Belgium. Neuroepidemiology 48:63–70. https://doi.org/10.1159/000471877
Pieracci FM, Eachempati SR, Shou J, Hydo LJ, Barie PS (2007) Degree of anticoagulation, but not warfarin use itself, predicts adverse outcomes after traumatic brain injury in elderly trauma patients. J Trauma 63:525–530. https://doi.org/10.1097/TA.0b013e31812e5216
Sjörgen H, Björnstig U (1991) Injuries among the elderly in the home environment:detailed analysis of mechanisms and consequences. J Aging Health 3:107–125. https://doi.org/10.1177/089826439100300106
Stocchetti N, Paternò R, Citerio G, Beretta L, Colombo A (2012) Traumatic brain injury in an aging population. J Neurotrauma 29:1119–1125. https://doi.org/10.1089/neu.2011.1995
Susman M, DiRusso SM, Sullivan T, Risucci D, Nealon P, Cuff S, Haider A, Benzil D (2002) Traumatic brain injury in the elderly: increased mortality and worse functional outcome at discharge despite lower injury severity. J Trauma 53:219–223 discussion 223-214
Teasdale GM, Pettigrew LE, Wilson JT, Murray G, Jennett B (1998) Analyzing outcome of treatment of severe head injury: a review and update on advancing the use of the Glasgow Outcome Scale. J Neurotrauma 15:587–597
Thomas KE, Stevens JA, Sarmiento K, Wald MM (2008) Fall-related traumatic brain injury deaths and hospitalizations among older adults--United States, 2005. J Saf Res 39:269–272. https://doi.org/10.1016/j.jsr.2008.05.001
Unterhofer C, Ho WM, Wittlinger K, Thome C, Ortler M (2017) “I am not afraid of death”-a survey on preferences concerning neurosurgical interventions among patients over 75 years. Acta Neurochir 159:1547–1552. https://doi.org/10.1007/s00701-017-3240-y
Wettervik TS, Lenell S, Nyholm L, Howells T, Lewen A, Enblad P (2018) Decompressive craniectomy in traumatic brain injury: usage and clinical outcome in a single centre. Acta Neurochir 160:229–237. https://doi.org/10.1007/s00701-017-3418-3
Wilson JT, Pettigrew LE, Teasdale GM (1998) Structured interviews for the Glasgow Outcome Scale and the extended Glasgow Outcome Scale: guidelines for their use. J Neurotrauma 15:573–585
Vollmer DG, Torner JC, Jane JA, Sadovnic B, Charlebois D, Eisenberg HM, Foulkes MA, Marmarou A, Marshall LF (1991) Age and outcome following traumatic coma: why do older patients fare worse? Spec Suppl 75:S37–S49. https://doi.org/10.3171/sup.1991.75.1s.0s37
Wong DK, Lurie F, Wong LL (2008) The effects of clopidogrel on elderly traumatic brain injured patients. J Trauma 65:1303–1308. https://doi.org/10.1097/TA.0b013e318185e234
World Population Prospects (2017) The 2017 Revision, Volume II: Demographic Profiles. ST/ESA/SER.A/400. United Nations, Department of Economic and Social Affairs, Population Division
Wutzler S, Lefering R, Wafaisade A, Maegele M, Lustenberger T, Walcher F, Marzi I, Laurer H, TraumaRegister DGU (2015) Aggressive operative treatment of isolated blunt traumatic brain injury in the elderly is associated with favourable outcome. Injury 46:1706–1711. https://doi.org/10.1016/j.injury.2015.02.013
Wärme PE, Bergström R, Persson L (1991) Neurosurgical intensive care improves outcome after severe head injury. Acta Neurochir 110:57–64
The study was supported by grants from the Uppsala university hospital.
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Lenell, S., Nyholm, L., Lewén, A. et al. Clinical outcome and prognostic factors in elderly traumatic brain injury patients receiving neurointensive care. Acta Neurochir 161, 1243–1254 (2019). https://doi.org/10.1007/s00701-019-03893-6
- Traumatic brain injury
- Quality register
- Neurointensive care
- Prognostic factors