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Erschienen in: European Journal of Medical Research 1/2023

Open Access 01.12.2023 | Research

Risk factors of prognosis in older patients with severe brain injury after surgical intervention

verfasst von: Hanchao Shen, Haibing Liu, Jiongzhou He, Lianqfeng Wei, Shousen Wang

Erschienen in: European Journal of Medical Research | Ausgabe 1/2023

Abstract

Background

Older patients (aged ≥ 60 years) with severe brain injury have a high mortality and disability rate. The objective of this retrospective study was to assess the clinical risk factors of prognosis in older patients with severe brain injury after surgical intervention and to analyze the prognosis of the surviving group of patients 1 year after discharge.

Methods

Clinical data of older patients with severe brain injury who were admitted to two neurosurgical centers between January 2010 and December 2020 were collected. Patient age, sex, Glasgow Coma Scale (GCS) score at admission, underlying disease, mechanisms of injury, abnormal pupillary reflex, head computed tomography imaging findings (such as hematoma type),intraoperative brain swelling and other factors were reviewed. All the patients were categorized into a good prognosis (survival) group and a poor prognosis (death) group by the Glasgow Outcome Score (GOS); also, the related factors affecting the prognosis were screened and the independent risk factors were identified by the Binary logistic regression analysis. GOS was used to evaluate the prognosis of the surviving group of patients 1 year after discharge.

Results

Out of 269 patients, 171 (63.6%) survived, and 98 (36.4%) died during hospitalization. Univariate analysis showed that age, GCS score at admission, underlying diseases, abnormal pupillary reflex, the disappearance of ambient cistern, the midline structure shift, intraoperative brain swelling, oxygen saturation < 90%, and cerebral hernia were risk factors for the prognosis of older patients with severe brain injury after surgical intervention. Multivariate analysis showed that age, underlying diseases, disappearance of ambient cistern, Oxygen saturation < 90% and intraoperative brain swelling were independent risk factors of the prognosis in the population. The effect of surgical intervention differed among various age groups at 1-year follow-up after surgery.

Conclusions

The results of this retrospective study confirmed that age, underlying diseases, disappearance of ambient cistern, intraoperative brain swelling, and oxygen saturation < 90% are associated with poor prognosis in older postoperative patients with severe brain injury. Surgical intervention may improve prognosis and reduce mortality in older patients (age < 75 years). But for those patients (age ≥ 75 years), the prognosis was poor after surgical intervention.
Hinweise
Hanchao Shen and Haibing Liu contributed equally and share first authorship.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
TBI
Traumatic brain injury
GCS
Glasgow Coma Scale
GOS
Glasgow Outcome Score
ICU
Intensive care unit
CT
Computed tomography

Background

Traumatic brain injury (TBI) poses a significant challenge to the healthy life of the older patients. China has more patients with TBI than most other countries [1], and severe TBIs impose a significant economic burden on society and families [2]. Despite the continuous improvement of treatment technology [35], the prognosis of older patients (age ≥ 60 years) with severe brain injury remains unsatisfactory, and their mortality and disability rates continue to be high [6, 7].
There is still a lack of unified guidelines for treating older patients with TBI [8, 9]. There are significant differences in treatment management among different centers for older patients with TBI. Some studies show that the prognosis of older patients with severe TBI after surgical intervention is poor [10, 11]. In contrast, other studies emphasize that surgical intervention may positively impact treatment and improve the prognosis of patients [12, 13]. Recent research [6] has found that surgical intervention increased complications and length of hospital stay but was not associated with increased mortality in the older patients with TBI (age ≥ 80 years).
Therefore, this study evaluated the risk factors affecting the prognosis of older patients with severe TBI treated by surgery to understand the impact of surgical intervention on patients’ recovery. This will help make early decisions according to specific information and subsequently make relevant interventions to reduce the mortality of older patients with severe brain injury and improve their quality of life.

Methods

Patient population

A total of 281older patients with severe brain injuries admitted to the Neurosurgery Center of the 900th Hospital and the Cangshan Ward of the 900th Hospital between January 2010 and December 2020 were enrolled in this study. The inclusion criteria were: (1) a history of TBI; (2) head computed tomography (CT) examination confirming brain injury; (3) The diagnosis and treatment were in accordance with the guidelines for the Management of Severe Traumatic Brain Injury [14]; (4) Glasgow Coma Scale (GCS) score ≤ 8 points; the patient remained unconscious for more than 6 h or was comatose after waking up (5) completion of surgical treatment; (6) age ≥ 60 years. The following patients were excluded from this study: (1) patients with other intracranial lesions before the injury; (2) patients who abandoned treatment after surgery; and (3) patients with severe heart, lung, and other vital organ failures.
The inpatient records of all patients who met the inclusion criteria were reviewed. These included age, sex, GCS score at admission, mechanisms of injury, cerebral hernia, type of hematoma, underlying diseases, abnormal pupillary reflex, head CT imaging findings (such as subdural hematoma, epidural hematoma, cerebral contusion and/or intracerebral hematoma, and disappearance of ambient cistern), anticoagulant therapy, intraoperative brain swelling, Glasgow Outcome Score (GOS), and other clinical factors.

Admission management

After admission, two neurosurgeons evaluated all patients. All patients received the same standardized treatment before surgery according to the guidelines for treating TBI. The main surgical techniques were hematoma evacuation and decompressive craniectomy. All patients were treated using standard neurosurgical principles with lowering intracranial pressure and neurotrophic drugs. All patients were treated in the intensive care unit.

Clinical outcome evaluation

Patients were categorized into survival and death groups by GOS at discharge. GOS was also used to evaluate the outcome of the surviving group 1 year after discharge. Follow-up was conducted via telephone and outpatient visits, and informed consent was obtained from all patients.

Statistical analysis

All data were analyzed by IBM SPSS Statistics 26. Continuous variables were expressed as medians with interquartile ranges (IQR = Q3–Q1), and categorical variables were expressed as percentages. The Mann–Whitney U test, the chi-square and Fisher’s exact probability tests were used to compare groups. The variables with significant statistical differences (P < 0.05) in the single factor analysis were included in the binary logistic regression for multivariate analysis. The conditional independent variables were introduced, and the model was established using the back-off method. For all statistical results, P < 0.05 was considered statistically significant.

Results

Characteristics of the patient

A total of 281 patients were enrolled, and 12 were excluded because they abandoned the treatment. The family members gave up treatment during hospitalization and took the patient home because of family economic reasons. Out of 269 patients, 147 were from the Department of Neurosurgery, Cangshan Branch of the 900th Hospital, and 122 were from the Department of Neurosurgery, the 900th Hospital (Fig. 1). There were 209 (77.5%) men and 60 (22.5%) women, and their average age was 72.8 years (Age: from 60 to 89). TBI was caused by traffic accidents in 141 (51.9%) cases, by falls in 111 (41.1%) cases, and by fall from heights in 17 (7.0%) cases. There was no significant difference in the prognosis among the three groups (P = 0.086). A total of 193 (71.0%) patients had less than two underlying diseases and 76 (29.0%) patients had more than three underlying diseases, before the injury. The risk of death was higher in older patients with TBI who had three or more underlying diseases, than in those with two or fewer underlying diseases (P < 0.001). The clinical characteristics of the patients at admission are shown in Table 1.
Table 1
Univariate analysis of prognosis in older patients with severe brain injury after surgery
Factors
Total
n = 269
Survivor
n = 171 (63.6%)
Death
n = 98 (36.4%)
P value
Age (years)
 60–74
212 (67.1%)
145 (67.1%)
67 (32.9%)
< 0.001
 ≥ 75
57 (32.9%)
25 (42.1%)
32 (57.9%)
Sex
    
 Male
209 (77.5%)
127 (55.3%)
82 (44.7%)
0.075
 Female
60 (22.5%)
44 (71.2%)
16 (28.8%)
Mechanisms of injury
 Traffic accident
141 (51.9%)
88 (55.8%)
53 (44.2%)
0.086
 Fall
111 (41.1%)
76 (66.3%)
35 (33.7%)
 Fall from height
17 (7.0%)
7 (37.5%)
10 (62.5)
GCS score at admission
    
 3–5
141 (57.6%)
58 (39.1%)
83 (60.9%)
< 0.001
 6–8
128 (42.4%)
113 (85.7%)
15 (14.3%)
Underlying diseases
 ≤ 2
193 (71.0%)
141 (68.3%)
52 (31.7%)
< 0.001
 ≥ 3
76 (29.0%)
30 (35.8%)
46 (64.2%)
Types of hematoma
 Subdural hematoma
172 (70.1%)
101 (60.5%)
71 (39.5%)
0.070
 Epidural hematoma
15 (5.2%)
12 (75%)
3 (25%)
 Cerebral contusion and Laceration and/or intracerebral hematoma
82 (24.7%)
58 (68.4%)
24 (31.6%)
Abnormal pupillary response
 Unilateral
168 (58.0%)
145 (83.6%)
23 (16.4%)
< 0.001
 Bilateral
101 (42.0%)
26 (24.7%)
75 (75.3%)
Disappearance of ambient cistern
 No
163 (60.6%)
143 (87.7%)
20 (12.3%)
< 0.001
 Yes
106 (39.4%)
28 (26.4%)
78 (73.6%)
Oxygen saturation < 90%
 No
179 (64.1%)
148 (79.1%)
31 (20.9%)
< 0.001
 Yes
90 (35.9%)
23 (22.9%)
67 (77.1%)
Intraoperative brain swelling
 No
173 (59.7%)
145 (81.9%)
28 (18.1%)
< 0.001
 Yes
96 (40.3%)
26 (24.7%)
70 (75.3%)
The midline structure shift
 ≤ 1 cm
154 (52.4%)
136 (86.8%)
18 (13.2%)
< 0.001
 > 1 cm
115 (47.6%)
35 (28.2%)
80 (71.8%)
Using antiplatelet or anticoagulant drugs
 No
165 (61.3%)
112 (67.9%)
53 (32.1%)
0.064
 Yes
104 (38.7%)
59 (56.7%)
45 (43.3%)
Cerebral hernia
 No
54 (20.1%)
49 (90.7%)
10 (9.3%)
0.001
 Yes
215 (79.9%)
127 (59.1%)
88 (40.9%)
Surgical methods
 Hematoma evacuation
123 (45.7%)
87 (70.7%)
36 (29.3%)
0.079
 Decompressive craniectomy
44 (16.4%)
26 (59.1%)
18 (40.9%)
 Both
102 (37.9%)
58 (56.9%)
44 (43.1%)
Median time to surgery in min (IQR)
186 (164–223.5)
184 (164–212)
197 (164–232.3)
0.174
Median duration of surgery in min (IQR)
110 (104–117)
108 (104–116)
112 (104–120)
0.055

The influence of preoperative use of anticoagulant therapy

Before the injury, 104 (38.7%) patients used anticoagulants such as warfarin, clopidogrel, and aspirin. After surgery, 59 (56.7%) patients survived, and 112 (67.9%) patients survived among the 165 (61.3%) patients who did not receive treatment. There was no significant difference in the prognosis between the two groups (P = 0.064). Thus, the use of anticoagulants before injury does not affect disease prognosis.

The patient’s nervous system was examined after admission

Out of 141 (57.6%) patients with a GCS score of 3–5 points at admission, only 58 (39.1%) patients had a good prognosis, and of the 128 (42.4%) patients with a GCS score of 6–8 points, 113 (85.7%) patients had a good prognosis. The difference was significant (P < 0.001). The lower the GCS score at admission, the worse the prognosis. Regarding patients with preoperative unilateral abnormal pupil reactions, 145 out of 168 patients survived after surgery. Conversely, among patients with preoperative bilateral abnormal pupil reactions, only 26 out of 101 patients survived after surgery. The difference were significant between the two groups, and the risk of death was higher in the patients with preoperative bilateral pupil reactions. During emergency treatment, 90 (35.9%) patients with oxygen saturation < 90% at the time of injury underwent endotracheal intubation, and 67 (77.1%) patients in this group died. The difference was significant compared to patients without hypoxia (P < 0.001). Patients with an oxygen saturation of < 90% had a higher risk of death.

Head CT imaging

Preoperative CT revealed 172 (70.1%) cases of subdural hematoma, 15 (5.2%) cases of epidural hematoma, and 82 (24.7%) cases of cerebral contusions and lacerations, intracerebral hematoma, or both. There was no significant difference in prognosis among the three groups (P = 0.07). The cisterna ambiens disappeared in 106 (39.4%) patients and survived in 28 (26.4%). The cisterna ambiens did not disappear in 163 (60.6%) patients and survived in 143 (87.7%). The two groups’ prognoses were significantly different (P < 0.001). It follows that patients with the disappearance of the cisterna ambiens have a poor prognosis. There were 154 (52.4%) patients with a midline shift ≤ 1 cm, of whom 136 (86.8%) survived, whereas of 115 (47.6%) patients who had a midline shift > 1 cm, only 35 (28.2%) survived. Significant difference was found in prognosis between the two groups (P < 0.001). These results suggest that the more obvious the midline structural shift, the worse the prognosis. 127 (59.1%) of the 215 patients with cerebral hernia survived after surgery, whereas of 54 (20.1%) patients without cerebral hernia, 49 (90.7%) survived. The difference in prognosis was significant (P = 0.001). It follows that patients with cerebral hernia have a poor prognosis.

Operative information

Hematoma evacuation was performed in 123 patients and 87 (70.7%) survived, 44 patients underwent decompressive craniectomy and survived in 26 (59.1%). Both procedures were performed on 102 patients and 58 (56.9%) survived. There was no significant difference in prognosis among the three groups (P = 0.079). For the Survivor group, the median time to surgery (IQR) was 184 (164–212) mins, the median duration of surgery was 108 (104–116) mins. The median time to surgery (IQR) was 197 (164–232.3) mins and the median duration of surgery was 112 (104–120) mins in the death group. There were no significant difference in these two variables between the Survivor and death group (P = 0.174, P = 0.055). Brain swelling occurred in 96 (40.3%) patients during the operation, 26 (24.7%) survived, whereas of 173 (59.7%) patients without brain swelling, 145 (81.9%) survived. Between the two groups, the difference in prognosis was significant (P < 0.001). Patients with intraoperative brain swelling have poor prognoses.

Multivariate logistic regression analysis of prognosis in older patients with severe brain injury after surgery

The significant indicators (P < 0.05) in univariate analysis such as age, GCS score at admission, underlying diseases, abnormal pupillary response, disappearance of ambient cistern, oxygen saturation < 90%, intraoperative brain swelling, the midline structure shift, cerebral hernia were used for multivariate analysis. The results showed that age, underlying diseases, the disappearance of ambient cistern, oxygen saturation < 90%, and intraoperative brain swelling were significantly associated with poor prognosis (P < 0.05) (Table 2). Age, underlying diseases, the disappearance of ambient calcium, oxygen saturation < 90% and intraoperative brain swelling are independent risk factors of the prognosis in older patients with severe TBI after surgical intervention.
Table 2
Multivariate Logistic regression analysis of prognosis in older patients with severe brain injury after surgery
Factor
B value
P value
Odds ratio
95% Confidence Interval
Age
0.983
0.03
2.673
1.098–6.511
Underlying diseases
1.650
< 0.001
5.209
2.212–12.269
Disappearance of Ambient Cistern
1.548
0.001
4.701
1.949–11.338
Intraoperative brain swelling
2.335
< 0.001
10.332
4.573–23.344
Oxygen saturation < 90%
1.412
0.002
4.106
1.679–10.044
The Hosmer–Lemeshow method was used to test the goodness of fit of the regression model, χ2 = 0.641, P > 0.05, which could be considered a good fit for the regression model

Prognosis of older patients with severe brain injury at 1-year follow-up after surgery

Among the 269 patients, 171 patients survived during hospitalization. The 1-year follow-up showed that 102 patients had a good prognosis, and 69 patients had a poor prognosis. Among the age groups, the difference in the prognosis was significant (P = 0.005). With the increase in age, the proportion of poor prognosis in each age group gradually increased, and the older the age, the worse the prognosis (Table 3).
Table 3
Prognosis of older patients with severe craniocerebral injury of different ages at 1-year follow-up after surgery
Age (years)
Total
Good prognosis (n)
(GOS 4–5)
Poor prognosis (n)
(GOS 1–3)
P value
60–64
73 (42.7%)
49 (67.1%)
23 (32.9%)
0.007
65–69
43 (25.1%)
28 (65.1%)
17 (34.9%)
70–74
29 (17.0%)
18 (62.7%)
11 (37.3%)
75–79
17 (10.0%)
5 (29.4%)
12 (70.6%)
≥ 80
9 (5.2%)
2 (22.2%)
7 (77.8%)
 
171 (100%)
102 (59.6%)
69 (40.4%)
 
GOS: Glasgow Outcome Score

Discussion

Severe head injury is a high-risk disease in the older population with a long hospital stay and high mortality, which brings great problems to clinical treatment [1517]. Previous studies had shown that the older the age, the worse the prognosis and the higher the hospital mortality [1820]. The results of this study show that the poor prognosis of older patients with severe TBI after surgical intervention gradually increased with age especially in patients aged ≥ 75 years, and the proportion of poor prognosis was > 70%. The main reason may be that the older the patient, the more serious the functional degradation and the more postoperative complications and poor prognosis will occur. Age is an independent risk factor for prognosis in older patients with severe craniocerebral injury after surgery. In clinical practice, we should reasonably evaluate the patient’s condition according to age and choose the best treatment to improve the prognosis of patients.
The functions of various organs and immunity in older adults gradually decline with age, and underlying diseases such as hypertension, diabetes, and heart disease also occur. The combination of physiological aging and pathological conditions aggravates the mortality risk of severe TBI in the older population. Compared to younger people, older people have more complications, higher mortality, and longer time for neurological recovery [21, 22]. This study found that, despite active intervention, the mortality of older patients with three or more underlying diseases was much higher than that of patients with two or fewer underlying diseases. The previous underlying disease is an independent risk factor of the prognosis in older patients with severe TBI after surgical intervention and should be considered in clinical practice.
There is no clear conclusion on whether using antiplatelet or anticoagulant drugs before injury affects the prognostic outcome of older patients with severe TBI. Previous studies have found no significant difference in the poor prognosis between TBI patients who used antiplatelet or anticoagulant drug before the injury and those who did not [23, 24]. However, other study shows that Elderly trauma patients using antiplatelet or anticoagulant drugs can lead to elevated risk of intracerebral hemorrhage and poor prognosis [25]. In this study, the use of anticoagulants before injury did not affect the prognosis, and the difference was not significant. However, we found that these patients were more likely to have incomplete intraoperative hemostasis or postoperative hemorrhage, which may increase the difficulty of treating the disease and the length of hospital stay. Therefore, perioperative management is necessary for patients who have received antiplatelet or anticoagulant drugs before the injury.
Because of different degrees of brain atrophy in older patients, the clinical symptoms such as pupil change, slow respiration, and heart rate, and increased blood pressure in the early stage of cerebral hernia are often atypical, which makes it easy to cover up the condition of older patients. For older patients with severe brain injury, when the optimal treatment period is missed, it can cause great difficulties for subsequent treatment. Therefore, early evaluation based on CT images can help predict disease severity as early as possible and facilitate early treatment and intervention. It has been pointed out in the literature [22] that CT images can indicate intracranial lesions in older patients earlier than GCS and provide earlier clinical strategies for clinical treatment. The cistern of the annulus is adjacent to the brainstem. When supratentorial lesions cause acute intracranial hypertension, the morphological changes of the annulus cistern are often the first to appear and it can be used as the early manifestation of cerebral herniation [26]. Patients with the disappearance of the cisterna ambiens after TBI tend to have a deep coma and a poor prognosis. The poor prognosis is mainly because patients with the disappearance of the cisterna ambiens often indicate diffuse intracranial hypertension and secondary brain stem injury, which can lead to deterioration of the patients [27]. Our study showed that the disappearance of cisterns was significantly associated with worse prognosis and higher mortality in older patients with severe TBI after surgical intervention. Therefore, the surgical intervention decision should be made as early as possible according to the width change of the cisterna ambiens. The reduction of the width of the cisterna ambiens represents the possibility of brain stem injury, but the extent to which the width of the cisterna ambiens is reduced as an indication for surgical intervention needs further clinical research.
Older adults are prone to desaturation of blood oxygen because of coma after severe TBI, vomit regurgitation caused by asphyxia, coupled with their cardiopulmonary insufficiency for the decline of their physical function. When older patients experience a TBI, their brain tissue is more sensitive to hypoxia than usual after injury. When the blood oxygen saturation < 90%, the brain cells are severely hypoxic, which aggravates the edema and necrosis and the patient’s condition. This study found that the mortality rate of patients with oxygen saturation < 90% was as high as 87.7%, which was much higher than that of the non-occurrence group. Studies [28] have shown that patients with severe craniocerebral injury have a high proportion of hypoxia during emergency treatment. Therefore, first aid before admission is essential. Suppose the injured older patients with coma can be found in time. In that case, the airway can be opened, and hypoxemia can be corrected before admission. It may reduce the secondary damage caused by brain cell hypoxia, saving time for further treatment. Studies have shown [29] that tracheotomy in the early stages of severe craniocerebral injury can help reduce secondary injury and adverse events in hospitals and increase the chances of early rehabilitation and discharge of patients. Therefore, to improve the airway, increase the oxygen supply of brain tissue cells, and improve the prognosis of older patients with severe brain injury, attention should be paid to airway management in the early stage, and tracheotomy or tracheal intubation should be performed as soon as possible if necessary.
For the older patients with severe TBI, craniotomy hematoma evacuation and decompressive craniectomy are the main surgical procedures [30]. In the process of decompressive craniectomy, there may be complicated by intraoperative brain swelling on the patients with cerebral herniation or high intracranial pressure. Once brain swelling occurs, the prognosis of patients is often poor [31]. This study found a mortality rate of more than 75% in cases with intraoperative brain swelling, significantly higher than in cases without brain swelling (P < 0.001). The possible causes of intraoperative brain swelling in older patients with severe brain injury are mainly due to rapid disease progression without early detection and complicated by ischemia–reperfusion injury after decompression [32]. Intraoperative brain swelling in older patients with severe brain injury is a complex pathophysiological process, and further research is needed to confirm the main factors. Thus, reducing the incidence of intraoperative brain swelling in older patients with severe brain injury is important.
Older patients have a poor prognosis with severe TBI. Although active surgical treatment is administered, with an increase in age, postoperative complications and mortality become higher, and their postoperative neurological recovery time also becomes longer. This study showed that patients aged ≥ 75 years had worse postoperative recovery than those aged < 75 years. Therefore, we should perform a reasonable evaluation based on age in clinical practice. Surgical intervention may improve prognosis and reduce mortality in older patients aged < 75 years. For older patients aged ≥ 75 years, surgical intervention may need to be carefully considered.
This study has several limitations. First, this study was retrospective in design. Second, we did not analyze the data on complications. Third, there are few data on the use of antiplatelet or anticoagulant drugs. Therefore, it may be impossible to provide a comprehensive, high-quality data basis for all questions arising from this particular topic. Therefore, further studies are needed to evaluate prognostic factors to provide better and more favorable treatment measures for older patients with severe TBI in the future.

Conclusions

This study clearly indicates that age, previous underlying diseases, the disappearance of ambient cistern, oxygen saturation < 90% and intraoperative brain swelling are associated with poor prognosis in older patients with severe brain injury undergoing surgical treatment. Surgical intervention may improve prognosis and reduce mortality in older patients aged < 75 years. But for older patients aged ≥ 75 years, the prognosis was poor after surgical intervention. The advantages and disadvantages of surgery should be carefully considered in older patients with severe brain injury of different ages. In clinical practice, a reasonable evaluation should be made according to age. This study further complements previous studies related to surgery in older patients with traumatic brain injury. It provides decision-making and reference for the surgical treatment of older patients with severe TBI, which can help to improve the treatment prognosis and reduce mortality in older patients with severe TBI. The number of older patients with TBI may increase with the aging of the population. Therefore, it is necessary to further study the prognostic factors after surgical treatment for severe brain injury in older adults.

Acknowledgements

We thank the Neurosurgery Department of the 900th Hospital and all the participants.

Declarations

The Ethics Committee of the 900th Hospital approved the study (No. 2018-005), and all patients received informed consent for inclusion before they participated in the study.
All the authors were consent for publication.

Competing interests

The authors declare that they have no competing interests.
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Literatur
1.
Zurück zum Zitat Jiang JY, Gao GY, Feng JF, Mao Q, Chen LG, Yang XF, et al. Traumatic brain injury in China. Lancet Neurol. 2019;18:286–95.CrossRefPubMed Jiang JY, Gao GY, Feng JF, Mao Q, Chen LG, Yang XF, et al. Traumatic brain injury in China. Lancet Neurol. 2019;18:286–95.CrossRefPubMed
2.
Zurück zum Zitat GBD 2016 Neurology Collaborators. Global, regional, and national burden of traumatic brain injury and spinal cord injury, 1990–2016: a systematic analysis for the global burden of disease study 2016. Lancet Neurol. 2019;18(5):459–80.CrossRef GBD 2016 Neurology Collaborators. Global, regional, and national burden of traumatic brain injury and spinal cord injury, 1990–2016: a systematic analysis for the global burden of disease study 2016. Lancet Neurol. 2019;18(5):459–80.CrossRef
3.
Zurück zum Zitat Rønning P, Helseth E, Skaga NO, Stavem K, Langmoen IA. The effect of ICP monitoring in severe traumatic brain injury: a propensity score-weighted and adjusted regression approach. J Neurosurg. 2018;131(6):1896–904.CrossRefPubMed Rønning P, Helseth E, Skaga NO, Stavem K, Langmoen IA. The effect of ICP monitoring in severe traumatic brain injury: a propensity score-weighted and adjusted regression approach. J Neurosurg. 2018;131(6):1896–904.CrossRefPubMed
4.
Zurück zum Zitat Hui J, Feng J, Tu Y, Zhang W, Zhong C, Liu M, et al. Safety and efficacy of long-term mild hypothermia for severe traumatic brain injury with refractory intracranial hypertension (LTH-1): a multicenter randomized controlled trial. EClinicalMedicine. 2021;32: 100732.CrossRefPubMedPubMedCentral Hui J, Feng J, Tu Y, Zhang W, Zhong C, Liu M, et al. Safety and efficacy of long-term mild hypothermia for severe traumatic brain injury with refractory intracranial hypertension (LTH-1): a multicenter randomized controlled trial. EClinicalMedicine. 2021;32: 100732.CrossRefPubMedPubMedCentral
5.
Zurück zum Zitat Sun Y, Jin W, Gao X, Liu J, Hou J. Effect of decompressive craniectomy under stepped decompression on the outcome of patients. Chin J Neurotrauma Surg. 2018;4(4):213–6. Sun Y, Jin W, Gao X, Liu J, Hou J. Effect of decompressive craniectomy under stepped decompression on the outcome of patients. Chin J Neurotrauma Surg. 2018;4(4):213–6.
6.
Zurück zum Zitat Haddad AF, DiGiorgio AM, Lee YM, Lee AT, Burke JF, Huang MC, et al. The morbidity and mortality of surgery for traumatic brain injury in geriatric patients. Neurosurgery. 2021;89(6):1062–70.CrossRefPubMed Haddad AF, DiGiorgio AM, Lee YM, Lee AT, Burke JF, Huang MC, et al. The morbidity and mortality of surgery for traumatic brain injury in geriatric patients. Neurosurgery. 2021;89(6):1062–70.CrossRefPubMed
7.
Zurück zum Zitat Toida C, Muguruma T, Gakumazawa M, Shinohara M, Abe T, Takeuchi I, et al. Age- and severity-related in-hospital mortality trends and risks of severe traumatic brain injury in Japan: a nationwide10-year retrospective study. J Clin Med. 2021;10(5):1072.CrossRefPubMedPubMedCentral Toida C, Muguruma T, Gakumazawa M, Shinohara M, Abe T, Takeuchi I, et al. Age- and severity-related in-hospital mortality trends and risks of severe traumatic brain injury in Japan: a nationwide10-year retrospective study. J Clin Med. 2021;10(5):1072.CrossRefPubMedPubMedCentral
8.
Zurück zum Zitat Gardner RC, Dams-O’Connor K, Morrissey MR, Manley GT. Geriatric traumatic brain injury: epidemiology, outcomes, knowledge gaps, and future directions. J Neurotrauma. 2018;35(7):889–906.CrossRefPubMedPubMedCentral Gardner RC, Dams-O’Connor K, Morrissey MR, Manley GT. Geriatric traumatic brain injury: epidemiology, outcomes, knowledge gaps, and future directions. J Neurotrauma. 2018;35(7):889–906.CrossRefPubMedPubMedCentral
9.
Zurück zum Zitat Kumar RG, Olsen J, Juengst SB, Dams-OConno K, Oeil-Pirozzi TM, Hammond FM, et al. Comorbid conditions among adults 50 years and older with traumatic brain injury: examining associations with demographics healthcare utilization Institutionalization and 1-year outcomes. Head Trauma Rehabil. 2019;34(4):224–32.CrossRef Kumar RG, Olsen J, Juengst SB, Dams-OConno K, Oeil-Pirozzi TM, Hammond FM, et al. Comorbid conditions among adults 50 years and older with traumatic brain injury: examining associations with demographics healthcare utilization Institutionalization and 1-year outcomes. Head Trauma Rehabil. 2019;34(4):224–32.CrossRef
10.
Zurück zum Zitat Manivannan S, Spencer R, Marei O, Mayo I, Elalfy O, Martin J, et al. Acute subdural haematoma in the elderly: to operate or not to operate? A systematic review and meta-analysis of outcomes following surgery. BMJ Open. 2021;11(12): e050786.CrossRefPubMedPubMedCentral Manivannan S, Spencer R, Marei O, Mayo I, Elalfy O, Martin J, et al. Acute subdural haematoma in the elderly: to operate or not to operate? A systematic review and meta-analysis of outcomes following surgery. BMJ Open. 2021;11(12): e050786.CrossRefPubMedPubMedCentral
11.
Zurück zum Zitat Hazare P, Shukla D, Bhat D, Devi BI, Jayan M, Konar S, et al. Prediction of surgical outcome for acute traumatic brain injury in older adults. Neurol India. 2022;70(3):1112–8.CrossRefPubMed Hazare P, Shukla D, Bhat D, Devi BI, Jayan M, Konar S, et al. Prediction of surgical outcome for acute traumatic brain injury in older adults. Neurol India. 2022;70(3):1112–8.CrossRefPubMed
12.
Zurück zum Zitat Wan X, Liu S, Wang S, Zhang S, Yang H, Ou Y, et al. Elderly patients with severe traumatic brain injury could benefit from surgical treatment. World Neurosurg. 2016;89:147–52.CrossRefPubMed Wan X, Liu S, Wang S, Zhang S, Yang H, Ou Y, et al. Elderly patients with severe traumatic brain injury could benefit from surgical treatment. World Neurosurg. 2016;89:147–52.CrossRefPubMed
13.
Zurück zum Zitat Van Essen TA, Dijkman MD, Cnossen MC, Moudrous W, Ardon H, Schoonman GG, et al. Comparative effectiveness of surgery for traumatic acute subdural hematoma in an aging population. J Neurotraum. 2019;36(7):1184–91.CrossRef Van Essen TA, Dijkman MD, Cnossen MC, Moudrous W, Ardon H, Schoonman GG, et al. Comparative effectiveness of surgery for traumatic acute subdural hematoma in an aging population. J Neurotraum. 2019;36(7):1184–91.CrossRef
14.
Zurück zum Zitat Carney N, Totten AM, O’Reilly C, Ullman JS, Hawryluk GW, Bell MJ, et al. Guidelines for the management of severe traumatic brain injury, fourth edition. Neurosurgery. 2017;80(1):6–15.CrossRefPubMed Carney N, Totten AM, O’Reilly C, Ullman JS, Hawryluk GW, Bell MJ, et al. Guidelines for the management of severe traumatic brain injury, fourth edition. Neurosurgery. 2017;80(1):6–15.CrossRefPubMed
15.
Zurück zum Zitat Ostermann RC, Joestl J, Tiefenboeck TM, Lang N, Platzer P, Hofbauer M. Risk factors predicting prognosis and outcome of elderly patients with isolated traumatic brain injury. J Orthopaedic Surg Res. 2018;13(1):277.CrossRef Ostermann RC, Joestl J, Tiefenboeck TM, Lang N, Platzer P, Hofbauer M. Risk factors predicting prognosis and outcome of elderly patients with isolated traumatic brain injury. J Orthopaedic Surg Res. 2018;13(1):277.CrossRef
16.
Zurück zum Zitat Maiden MJ, Cameron PA, Rosenfeld JV, Cooper DJ, McLellan S, Gabbe BJ. Long-term outcomes after severe traumatic brain injury in older adults a registry-based cohort study. Am J Respir Crit Care Med. 2020;201(2):167–77.CrossRefPubMed Maiden MJ, Cameron PA, Rosenfeld JV, Cooper DJ, McLellan S, Gabbe BJ. Long-term outcomes after severe traumatic brain injury in older adults a registry-based cohort study. Am J Respir Crit Care Med. 2020;201(2):167–77.CrossRefPubMed
17.
Zurück zum Zitat Van der Vlegel M, Mikolić A, Lee Hee Q, Kaplan ZLR, Retel Helmrich IRA, van Veen E, et al. Health care utilization and outcomes in older adults after traumatic brain injury: a CENTER-TBI study. Injury. 2022;53(8):2774–82.CrossRefPubMed Van der Vlegel M, Mikolić A, Lee Hee Q, Kaplan ZLR, Retel Helmrich IRA, van Veen E, et al. Health care utilization and outcomes in older adults after traumatic brain injury: a CENTER-TBI study. Injury. 2022;53(8):2774–82.CrossRefPubMed
18.
Zurück zum Zitat Van den Branda CL, Karger LB, Nijman STM, Hunink MGM, Patka P, Jellema K. Traumatic brain injury in the Netherlands, trends in emergency department visits, hospitalization and mortality between 1998 and 2012. Eur J Emerg Med. 2018;25(5):355–61.CrossRef Van den Branda CL, Karger LB, Nijman STM, Hunink MGM, Patka P, Jellema K. Traumatic brain injury in the Netherlands, trends in emergency department visits, hospitalization and mortality between 1998 and 2012. Eur J Emerg Med. 2018;25(5):355–61.CrossRef
19.
Zurück zum Zitat Lindfors M, Vehvillainen J, Siironen J, Kivisaari R, Skrifvars MB, Raj R. Temporal changes in outcome following intensive care unit treatment after traumatic brain injury: a 17-hear experience in a large academic neurosurgical centre. Acta Neurochir. 2018;160(11):2107–15.CrossRefPubMed Lindfors M, Vehvillainen J, Siironen J, Kivisaari R, Skrifvars MB, Raj R. Temporal changes in outcome following intensive care unit treatment after traumatic brain injury: a 17-hear experience in a large academic neurosurgical centre. Acta Neurochir. 2018;160(11):2107–15.CrossRefPubMed
20.
Zurück zum Zitat Heydari F, Golban M, Majidinejad S. Traumatic brain injury in older adults presenting to the emergency department: epidemiology, outcomes and risk factors predicting the prognosis. Adv J Emerg Med. 2020;2(4): e19. Heydari F, Golban M, Majidinejad S. Traumatic brain injury in older adults presenting to the emergency department: epidemiology, outcomes and risk factors predicting the prognosis. Adv J Emerg Med. 2020;2(4): e19.
21.
Zurück zum Zitat Hawley C, Sakr M, Scapinello S, Salvo J, Wrenn P. Traumatic brain injuries in older adults-6 years of data for one UK trauma centre: retrospective analysis of prospectively collected data. Emerg Med J. 2017;34(8):509–16.CrossRefPubMed Hawley C, Sakr M, Scapinello S, Salvo J, Wrenn P. Traumatic brain injuries in older adults-6 years of data for one UK trauma centre: retrospective analysis of prospectively collected data. Emerg Med J. 2017;34(8):509–16.CrossRefPubMed
22.
Zurück zum Zitat Mahadewa TGB, Golden N, Saputra A, Ryalino C. Modified revised trauma-marshall score as a proposed tool in predicting the outcome of moderate and severe traumatic brain injury. Open Access Emerg Med. 2018;10:135–9.CrossRefPubMedPubMedCentral Mahadewa TGB, Golden N, Saputra A, Ryalino C. Modified revised trauma-marshall score as a proposed tool in predicting the outcome of moderate and severe traumatic brain injury. Open Access Emerg Med. 2018;10:135–9.CrossRefPubMedPubMedCentral
23.
Zurück zum Zitat Rønning P, Helseth E, Skaansar O, Tverdal C, Andelic N, Bhatnagar R, et al. Impact of preinjury antithrombotic therapy on 30-day mortality in older patients hospitalized with traumatic brain injury (TBI). Front Neurol. 2021;12: 650695.CrossRefPubMedPubMedCentral Rønning P, Helseth E, Skaansar O, Tverdal C, Andelic N, Bhatnagar R, et al. Impact of preinjury antithrombotic therapy on 30-day mortality in older patients hospitalized with traumatic brain injury (TBI). Front Neurol. 2021;12: 650695.CrossRefPubMedPubMedCentral
24.
Zurück zum Zitat Mathieu F, Malhotra AK, Ku JC, Zeiler FA, Wilson JR, Pirouzmand F, et al. Pre-injury antiplatelet therapy and risk of adverse outcomes after traumatic brain injury: a systematic review and meta-analysis. Neurotrauma Rep. 2022;3(1):308–20.CrossRefPubMedPubMedCentral Mathieu F, Malhotra AK, Ku JC, Zeiler FA, Wilson JR, Pirouzmand F, et al. Pre-injury antiplatelet therapy and risk of adverse outcomes after traumatic brain injury: a systematic review and meta-analysis. Neurotrauma Rep. 2022;3(1):308–20.CrossRefPubMedPubMedCentral
25.
Zurück zum Zitat Scotti P, Séguin C, Lo BWY, de Guise E, Troquet JM, Marcoux J. Antithrombotic agents and traumatic brain injury in the elderly population: hemorrhage patterns and outcomes. J Neurosurg. 2019;133:1–10. Scotti P, Séguin C, Lo BWY, de Guise E, Troquet JM, Marcoux J. Antithrombotic agents and traumatic brain injury in the elderly population: hemorrhage patterns and outcomes. J Neurosurg. 2019;133:1–10.
26.
Zurück zum Zitat Matsumoto H, Hanayama H, Okada T, Sakurai Y, Minami H, Masuda A, et al. Clinical investigation of chronic subdural hematoma with impending brain herniation on arrival. Neurosurg Rev. 2018;41(2):447–55.CrossRefPubMed Matsumoto H, Hanayama H, Okada T, Sakurai Y, Minami H, Masuda A, et al. Clinical investigation of chronic subdural hematoma with impending brain herniation on arrival. Neurosurg Rev. 2018;41(2):447–55.CrossRefPubMed
27.
Zurück zum Zitat Young AMH, Donnelly J, Liu X, Guilfoyle MR, Carew M, Cabeleira M, et al. Computed tomography indicators of deranged intracranial physiology in paediatric traumatic brain injury. Acta Neurochir Suppl. 2018;126:29–34.CrossRefPubMed Young AMH, Donnelly J, Liu X, Guilfoyle MR, Carew M, Cabeleira M, et al. Computed tomography indicators of deranged intracranial physiology in paediatric traumatic brain injury. Acta Neurochir Suppl. 2018;126:29–34.CrossRefPubMed
28.
Zurück zum Zitat Gao G, Wu X, Feng J, Hui J, Mao Q, Lecky F, et al. Clinical characteristics and outcomes in patients with traumatic brain injury in China: a prospective, multicentre, longitudinal, observational study. Lancet Neurol. 2020;19(8):670–7.CrossRefPubMed Gao G, Wu X, Feng J, Hui J, Mao Q, Lecky F, et al. Clinical characteristics and outcomes in patients with traumatic brain injury in China: a prospective, multicentre, longitudinal, observational study. Lancet Neurol. 2020;19(8):670–7.CrossRefPubMed
29.
Zurück zum Zitat De Franca SA, Tavares WM, Salinet ASM, Paiva WS, Teixeira MJ. Early tracheostomy in severe traumatic brain injury patients: a meta-analysis and comparison with late tracheostomy. Crit Care Med. 2020;48:e325–31.CrossRefPubMed De Franca SA, Tavares WM, Salinet ASM, Paiva WS, Teixeira MJ. Early tracheostomy in severe traumatic brain injury patients: a meta-analysis and comparison with late tracheostomy. Crit Care Med. 2020;48:e325–31.CrossRefPubMed
30.
Zurück zum Zitat Singh RD, van Dijck TJM, van Essen TA, Lingsma HF, Polinder SS, Kompanje EJ. Randomized evaluation of surgery in elderly with traumatic acute sub dural Hematoma (RESET-ASDH trial): study protocol for a pragmatic randomized controlled trial with multicenter parallel group design. Trials. 2022;23(1):242.CrossRefPubMedPubMedCentral Singh RD, van Dijck TJM, van Essen TA, Lingsma HF, Polinder SS, Kompanje EJ. Randomized evaluation of surgery in elderly with traumatic acute sub dural Hematoma (RESET-ASDH trial): study protocol for a pragmatic randomized controlled trial with multicenter parallel group design. Trials. 2022;23(1):242.CrossRefPubMedPubMedCentral
31.
Zurück zum Zitat Al-Mufti F, Mayer SA. Neurocritical care of acute subdural hemorrhage. Neurosurg Clin N Am. 2017;28(2):267–78.CrossRefPubMed Al-Mufti F, Mayer SA. Neurocritical care of acute subdural hemorrhage. Neurosurg Clin N Am. 2017;28(2):267–78.CrossRefPubMed
32.
Zurück zum Zitat Yokobori S, Nakae R, Yokota H, Spurlock MS, Mondello S, Gajavelli S, et al. Subdural hematoma decompression model: a model of traumatic brain injury with ischemic-reperfusional pathophysiology: a review of the literature. Behav Brain Res. 2018;340:23–8.CrossRefPubMed Yokobori S, Nakae R, Yokota H, Spurlock MS, Mondello S, Gajavelli S, et al. Subdural hematoma decompression model: a model of traumatic brain injury with ischemic-reperfusional pathophysiology: a review of the literature. Behav Brain Res. 2018;340:23–8.CrossRefPubMed
Metadaten
Titel
Risk factors of prognosis in older patients with severe brain injury after surgical intervention
verfasst von
Hanchao Shen
Haibing Liu
Jiongzhou He
Lianqfeng Wei
Shousen Wang
Publikationsdatum
01.12.2023
Verlag
BioMed Central
Erschienen in
European Journal of Medical Research / Ausgabe 1/2023
Elektronische ISSN: 2047-783X
DOI
https://doi.org/10.1186/s40001-023-01473-0

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