Keywords
traumatic brain injury - midline shift in CT scan brain - Glasgow coma scale
Introduction
Head injury is a silent epidemic that has paramount short- and long-term consequences.
To allow proper resource allocation (which is of preeminent importance in developing
countries), there is a need for such a system that correctly predicts the outcome.
Traumatic brain injury (TBI) is a complex injury caused by a sudden trauma to the
brain or by an object piercing the brain tissue in which a broad spectrum of symptoms
and disabilities can be observed.[1] It is one of the major causes of death and disability. Predicting an outcome after
head injury is difficult, and it is therefore rightly described in the Hippocratic
maxim, “No head injury is too severe to despair of, nor too trivial to ignore.”[2]
Clinicians treating patients often take decisions on the basis of their assessment
of prognosis. As much as 80% of doctors believe that an assessment of prognosis in
a head injury patient is important for taking therapeutic decisions such as barbiturates,
hyperventilation, or mannitol. Assessment of prognosis could help communication with
a patient and the family.[3]
One of the most widely used clinical pearls for such prediction is the Glasgow coma
scale (GCS).[4] However, its major shortcoming is the limitation of its use among patients who are
under sedation, under the influence of alcohol or psychoactive drugs, or are intubated.[5]
[6]
[7]
[8]
[9] This hindrance has been compensated with the use of the morphological criteria based
on radiological imaging. MRI studies are limited in terms of detecting white matter
changes in the late phase.[10]
[11] Hence, in the current scenario, scoring models based on CT imaging remains the valid
option for prognostication of patients with TBI.
CT scan characteristics such as status of basal cistern,[9] midline shift,[12]
[13]
[14] traumatic subarachnoid hemorrhage (tSAH),[15]
[16]
[17] and intraventricular hemorrhage[18] are useful indicators in predicting outcome in TBI.
So, we planned a prospective study to analyze the correlation between degree of midline
shift on CT scan of brain and GCS score on admission in prediction of possible clinical
outcome in head injury, in order to correlate CT scan finding of head injury patient
with GCS of the patient and evaluate age, site of injury, type of injury and pupillary
reaction as contributory factors in predicting outcome.
Materials and Methods
This study was conducted at our tertiary care center. A total of 108 patients with
head injury admitted in trauma ward and ICU in the stipulated duration of study were
enrolled in this study.
The duration of study was between January 2019 and June 2019. The study was prospective
in nature. The following criteria were set to include and exclude patients in this
study.
Eligibility Criteria
Inclusion Criteria: All patients with recent onset traumatic head injuries coming to casualty and outpatient
Exclusion Criteria: Patients on anticoagulant therapy or having any coagulopathy, Patients with preexisting
intracranial lesions.
All patients with recent history of head injury coming to outpatient and casualty
were enrolled in the study. All patients enrolled were evaluated immediately on admission.
This was followed by clinical history and physical examination. GCS scoring, pupil
size and it’s response & signs of base of skull fractures were documented. CT head
was done as soon as the patient was stabilized. The type of brain injury was noted
along with the presence and amount of midline shift. Subsequently, neurological assessment
of patients was done from admission till discharge. The interval of neurological assessment
for patients with GCS score equal to 15 were followed, starting after the initial
assessment in the emergency department: half-hourly for 2 hours, then 1-hourly for
4 hours, and 2-hourly thereafter. If patients with GCS score equal to 15 deteriorated
at any time after the initial 2-hour period, neurological assessment interval was
reverted to half-hourly and original frequency schedule was followed. Operative decisions
were taken as per latest brain trauma foundation guidelines.[19] Patients in whom surgical intervention was not required were managed conservatively
with serial neurological assessment as described above, and antiepileptics and antiedema
measures were given as recommended in the latest brain trauma foundation guidelines.[19]
The final outcome at discharge was divided into two groups on the basis of Glasgow
outcome scale (GOS) scores as described below:
-
Good outcome: Recovery with no or moderate disability.
-
Poor outcome: Patients with severe disability, vegetative status, or death.
The GCS-hospital discharge (GOS-HD) is a useful prognostic index in patients with
TBI, as it predicts long-term outcome at time of discharge which helps in rehabilitation.
Patients with moderate-to-severe disability were asked to follow-up on OPD basis at
1-month interval from discharge and mild disability at 3 months from discharge. The
total duration of follow-up for each group was approximately 6 months.
Statistical Analysis
Statistical analysis was performed using the computational program statistical analysis
system (SAS), for Windows, version 8.2. Descriptive analysis was done by constructing
frequency tables for categorical variables and position and dispersion measures for
continuous variables. To verify the existence of associations or to compare proportions
between selected variables, χ2, McNemar, or Fisher’s exact tests were employed as
fitted. To verify the most important factors that have influenced patients’ outcome,
logistic regression analysis was employed. The results were considered statistically
significant when p < 0.05.
Results
The results were derived from pooled data of 108 patients with TBI. The study took
into account the age, sex, cause of head injury, type of brain lesion, midline shift
on CT scan of brain, pupillary reaction and GCS score as clinical outcome predictors
in patients with head injury.
Majority of the patients in the study were within the age group of 21 to 40 years
(51.8%), followed by 41 to 60 years (28.7%) but this difference was considered to
be not statistically significant (p > 0.05; [Table 1]).
Table 1
Age-wise distribution
Age, in years
|
Good outcome
|
Poor outcome
|
Total
|
Chi- square
|
p- value
|
a
Statistically, no significant value.
|
0–20
|
6
|
1
|
7
|
3.0363
|
0.44
a
|
21–40
|
46
|
10
|
56
|
41–60
|
22
|
9
|
31
|
> 60
|
9
|
5
|
14
|
Total
|
83
|
25
|
108
|
In our study, road traffic accidents (RTA) was the most common cause of head injury
(76%), followed by fall (15%) and assault (9%). RTA was the most common cause of head
injury in age groups of 0 to 20 years, 21 to 40 years and 41 to 60 years, while fall
being the most common cause in elderly (> 60 years).
Out of these 108 patients in the study, 88 (81%) were male and 20 (19%) females. This
difference was found not significant on statistical analysis (p value = 0.8278; [Table 2]).
Table 2
Sex distribution
Sex
|
Good outcome
|
Poor outcome
|
Total
|
Chi-square
|
p-Value
|
aStatistically, no significant value.
|
Male
|
68
|
20
|
88
|
0.05
|
0.8278
a
|
Female
|
15
|
5
|
20
|
Total
|
83
|
25
|
108
|
CT scan of brain showed multiple lesions in most patients, but for the purpose of
classification of head injury in this study, the dominant lesion was considered. The
present study showed no abnormality in 16 patients, while the rest had common intracranial
hemorrhage like subdural hemorrhage (n = 44), extradural hemorrhage (n = 21), intracerebral hemorrhage (n = 14), and subarachnoid hemorrhage (SAH) (n = 8). Five patients had diffuse axonal injury with no intracranial hemorrhage ([Table 3]).
Table 3
CT head findings and outcome
CT head finding
|
Good outcome
|
Poor outcome
|
Total
|
Chi-square
|
p-Value
|
Abbreviations: CT, computed tomography; SDH, subdural hematoma; DAI, diffuse axonal
injury; EDH, extradural hematoma; SAH, subarachnoid hematoma; ICH, intracerebral hematoma.
aStatistically significant value.
|
Normal
|
16
|
0
|
16
|
15.96
|
0.025
a
|
SDH
|
10
|
2
|
12
|
EDH
|
8
|
1
|
9
|
SAH
|
7
|
1
|
8
|
ICH
|
11
|
3
|
14
|
SDH with shift
|
19
|
13
|
32
|
EDH with shift
|
10
|
2
|
12
|
DAI
|
2
|
3
|
5
|
Total
|
83
|
25
|
108
|
In our study, 60 patients had no midline shift on CT scan of brain, while 30 patients
had midline shift of less than 5 mm, and 18 patients had shift of more than 5 mm ([Table 4]). RTA had maximum incidence of mass effect in the form of midline shift (53%).
Table 4
Midline shift in CT head and outcome
Midline shift in CT
|
Good outcome
|
Poor outcome
|
Total
|
Chi-square
|
p value
|
Abbreviation: CT, computed tomography.
aStatistically significant value.
|
No shift
|
52
|
8
|
60
|
7.505
|
0.023
a
|
< 5 mm
|
20
|
10
|
30
|
≥ 5 mm
|
11
|
7
|
18
|
Total
|
83
|
25
|
108
|
If the type of brain lesion is taken into account with respect to mass effect, that
is, midline shift, then subdural hemorrhage was most commonly associated with midline
shift with incidence of almost 75% followed by extradural hemorrhage (52%). In the
present study, CT scan of brain showed no midline shift in patients with SAH and diffuse
axonal injury (
[Fig. 1]
).
Fig. 1 Computed tomography (CT) head finding and midline shift in CT. DAI, diffuse axonal
injury; EDH, extradural hematoma; ICH, intracerebral hematoma; SAH, subarachnoid hematoma;
SDH, subdural hematoma.
GCS score of patients was also associated with an amount of midline shift in the present
study. Out of 21 patients of head injury with mild GCS, six patients (29%) had midline
shift; out of 18 patients with moderate GCS, seven patients (39%) had midline shift;
and out of 69 patients with severe GCS, 35 patients (51%) had midline shift ([Table 5]).
Table 5
Midline shift in CT head and GCS
Midline shift in CT head
|
GCS
|
Mild
|
Moderate
|
Severe
|
Total
|
Abbreviations: CT, computed tomography; GCS, Glasgow coma scale.
|
No shift
|
15
|
11
|
34
|
60
|
Shift < 5 mm
|
5
|
5
|
20
|
30
|
Shift > 5 mm
|
1
|
2
|
15
|
18
|
Total
|
21
|
18
|
69
|
108
|
Pupillary reaction was also taken into consideration, which showed 27% patients with
bilaterally equal reacting pupils had midline shift as compared with 100% patients
with unequal pupils had midline shift, while 40% patients with bilaterally nonreacting
pupils had midline shift ([Table 6]).
Table 6
Pupillary reaction and midline shift in CT head
Midline shift in CT head
|
Pupillary reaction
|
Total
|
Equal reacting
|
Unequal
|
Bilaterally nonreacting
|
Abbreviation: CT, computed tomography.
|
No shift
|
51
|
0
|
9
|
60
|
Shift < 5 mm
|
19
|
8
|
3
|
30
|
Shift > 5 mm
|
0
|
15
|
3
|
18
|
Total
|
70
|
23
|
15
|
108
|
In our study, 18 out of 108 patients of head injury got operated for craniotomy. Out
of these 18 patients, 13 patients had subdural hematoma, three patients had intraparenchymal
bleed/contusion, one patient had extradural hematoma, and one patient had diffuse
axonal injury with medically refractory cerebral edema. Among the operated patients,
14 patients had anisocoria and four patients had bilaterally unequal nonreacting pupillary
reaction.
When the midline shift was taken into consideration, three patients had midline shift
less than 5 mm, while the rest had more than 5 mm. The patients with midline shift
less than 5 mm were decided for surgical management on the basis of severe GCS score,
anisocoria, and presence of clot size more than 30 mL. Postoperative deaths were three
out of 18 patients.
Neurological outcome was dichotomized into good and poor outcome based on the GOS
score.[20] In the present study, 83 patients had good outcome (GOS 4 and 5) after head injury
according to GOS as compared with 25 patients who had poor outcome (GOS 1, 2 and 3;
[Table 7]).
Table 7
GOS distribution
GOS score
|
No. of patients
|
Abbreviation: GIS, Glasgow outcome scale.
|
GOS 5
|
37
|
GOS 4
|
46
|
Total (good outcome)
|
83
|
GOS 3
|
7
|
GOS 2
|
10
|
GOS 1
|
8
|
Total (poor outcome)
|
25
|
There were 83 patients in the good outcome group. Out of these 83 patients, midline
shift of more than 5 mm in CT head was found only in 11 cases (13.25% cases). In the
bad outcome group of a total of 25 patients, seven patients (28% cases) has more than
5 mm midline shift in CT head ([Table 4]).
In the present study, low-GCS score at admission was associated with poor outcomes
(p = 0.003). Among the patients with mild GCS (13 to 15) at presentation, 95.2% patients
had good outcome (GOS 4 and 5), while 4.2% patients had poor outcome (GOS 1, 2 and
3), in contrast to patients with severe GCS (3 to 8), wherein 66% patient had good
outcome and 33.4% patients had poor outcome ([Table 8]).
Table 8
GCS and outcome
GCS severity
|
Good outcome
|
Poor outcome
|
Total
|
Chi square
|
p value
|
Abbreviation: GCS, Glasgow coma scale.
aStatistically significant value.
|
Mild
|
20
|
1
|
21
|
11.146
|
0.003
a
|
Moderate
|
17
|
1
|
18
|
Severe
|
46
|
23
|
69
|
Total
|
83
|
25
|
108
|
In the present study, out of 70 patients with equal reacting pupils, only 10 patients
(14.3%) had poor outcome, while 34.8% of patients with unequal pupils and 46.7% patients
with nonreacting pupils on both sides had poor outcome ([Table 9]).
Table 9
Pupillary reaction and outcome
|
Good outcome
|
Poor outcome
|
Total
|
Chi-square
|
p value
|
aStatistically significant value.
|
Equal reacting
|
60
|
10
|
70
|
9.504
|
0.008
a
|
Unequal
|
15
|
8
|
23
|
Bilateral non reacting
|
8
|
7
|
15
|
Total
|
83
|
25
|
108
|
Discussion
The study by Kraus [21] has shown that the most common group affected by head injuries are the young people
between 20 years and 40 years and the incidence is lowest at extremes of age, that
is, below 5 years and above 60 years. Similar findings were observed in our present
study.
The most common mechanisms leading to TBI are fall accidents, RTA, and assault-related
incidents as observed by Gan et al.[22] A study by Chiewvit et al[20] has shown that the most common cause of head injury in age group of 0 to 20 years
was motor accidents; highest incidence in group of 21 to 40 years was assault with
a blunt object; and in group of 41–60 years, car accident was the most common cause
while fall was the most common etiology in the group of > 60 years. On analysis of
mode of head injury, we have found that RTA was the most common cause for the same.
In the study by Kraus,[21] it was shown that the incidence is more in males as compared with females and most
of the studies quote an incidence of 3:2 in favor of males. Ratio of male female in
our study came out to be 4:1, indicating males are affected more than female, and
this finding is similar to other studies. Age and sex are important predictors of
outcome in head injury. As shown in the study by Gan et al,[22] which concluded that the mortality rate of the elderly group was significantly more,
as much as more than double than that of the younger group. Hence, age can be considered
an important factor in predicting outcome in the elderly with TBI.
In the study by Slewa-Younan et al,[23] although identical admission criteria was applied to both sexes, the levels of injury
severity in males were greater than females. Other authors state that the association
was apparent only after the age of 40 years[3]
[24] and especially above 60 years.[25] There is no association between outcome in patients with head injury and age lower
than 40 years.[3]
[26] A plausible explanation for this may be comorbidities due to old age other than
intracranial injury, senile changes in brain like increased plasticity and cortical
atrophy, or differences in clinical management in the elderly group.[3] Surprisingly, Fabbri et al[26] in their analysis did not find age to be associated with outcome in patients with
head injury, in contrast with a few reports. Similarly, in the present study, age
and sex were no significant predictors of outcome (p > 0.05).
Strong evidence was found for the midline shift,[14]
[27]
[28]
[29] and increasing size of the shift was associated with poorer outcome.[30] Jacobs et al,[31] in their study of 605 patients with moderate-to-severe head injuries concluded that
midline shift is a significant predictor of outcome. They did not find any cutoff
mark in midline shift; rather it was a continuous variable. They also concluded that
type of lesion was also significant in predicting outcome. The prognosis in patients
with similar midline shift after intracranial injuries was better for patients with
an extradural hematoma, as compared with those with acute subdural hematoma.[12]
[27]
[32]
The present study concluded that the degree of midline shift in patients’ brain injury
was a statistically significant determinant of outcome (p = 0.023). Seventeen out of 48 patients (35.4%) with midline shift had poor outcome
as compared with eight out of 60 patients (13.3%) with no midline shift.
Gennarelli et al[33] and Lobato et al[34] in their study concluded that the type of intracranial lesion is an important factor
in predicting outcome, as the severity of injury is assessed by GCS scores. In the
present study, the type of injury was significantly associated with outcome of patients
with head injury (p = 0.025). Diffuse axonal injury had the worst results with 60% patients having poor
outcome while extradural hematoma patients had better results with 11% patients having
poor outcome. Also, patients of subdural hematoma with midline shift had poorer outcome
(41.6%) than patients having extradural hematoma with midline shift (16.7%).
According to the literature, there is strong evidence for the prognostic value of
the GCS score on admission to hospital and the GCS motor score.[25]
[28]
[35]
[36] Lower admission GCS and lower GCS motor scores were associated with worse outcomes.[26]
[35]
[36] The GCS showed a clear linear relation with mortality.[3]
There exists a relation between absence of or abnormal pupillary reactions and worse
outcomes in TBI.[28]
[36] Pupil abnormalities were noted more frequently in patients with mass lesions, compressed
cisterns, and shift, and more in patients with CT class III/IV than in patients with
CT class I/II.[37]
Conclusion
The increasing degree of midline shift on CT scan of brain in patients with mass lesions
after TBI was significantly related to the severity of head injury (GCS = 3–12) and
eventually resulted in poor clinical outcome. The maximum number of patients on presentation
were found to have severe head injury (GCS < 8). Prognosis of patients worsens with
decreasing GCS score. The type of head injury also plays a significant role in outcome
prediction. By correlating CT scan finding with GCS score, we can predict the severity
of head injury and a possible outcome of patient more accurately than considering
both parameters as separate entities.