CC BY 4.0 · Indian Journal of Neurotrauma 2024; 21(01): 043-047
DOI: 10.1055/s-0043-1768170
Original Article

Revisiting the Classification of Moderate and Mild Traumatic Brain Injury Based on the Admission Glasgow Coma Scale Score

1   Department of Neurological Sciences, Christian Medical College, Vellore, Tamil Nadu, India
,
1   Department of Neurological Sciences, Christian Medical College, Vellore, Tamil Nadu, India
,
Thenmozhi Mani
2   Department of Biostatistics, Christian Medical College, Vellore, Tamil Nadu, India
,
Mathew Joseph
1   Department of Neurological Sciences, Christian Medical College, Vellore, Tamil Nadu, India
› Institutsangaben
Funding None.
 

Abstract

Objective We study the clinical relevance of classifying traumatic brain injury (TBI) into moderate and mild categories based on the Glasgow Coma Scale (GCS) score at admission with respect to the treatment intensity and 6-month mortality and morbidity rates.

Methods Analysis of patients from a prospectively maintained database admitted at a level I trauma center from 2013 to 2019 with an admission GCS score between 9 and 15 and a minimum follow-up of 6 months post-TBI was done to study the treatment intensity and 6-month morbidity and mortality rates for each GCS score from 9 to 15.

Results In all, 2,060 patients met the study criteria, of which 1,684 were males (81.7%). Road traffic accident was the most common cause of TBI (83.7%). There was a significant linear increase in the proportion of patients who had good outcomes with increasing GCS scores from 9 to 15 (p ≤ 0.001). When the variables in each GCS score were compared with a GCS score of 15, there was an increase in the odds ratio of mortality and poor outcome with decreasing GCS scores (p ≤ 0.001). Patients with a lower admission GCS score required more intense treatment in the form of surgery and ventilation (p ≤ 0.00001). There was a higher incidence of pupillary asymmetry in patients with lower GCS scores (p ≤ 0.00001).

Conclusions The classification of TBI patients into moderate and mild based on the GCS score at admission is not of any practical value, and TBI patients may be more usefully classified based on the admission GCS score into severe and not severe groups.


#

Introduction

Traumatic brain injury (TBI) is a leading cause of morbidity and mortality worldwide and remains a public health challenge in resource-constrained low- to middle-income countries.[1] More than 1 million individuals sustain TBI in India annually and many of them remain disabled.[2] The Glasgow Coma Scale (GCS) score introduced in 1974 is widely used for assessment of a patient's level of consciousness following TBI.[3] The score has been shown to have excellent interobserver reliability, which improves with training.[4] Postresuscitation GCS score has a strong influence on the outcome of patients with TBI and studies have shown a linear relationship between the GCS score at admission and the risk of mortality.[5] [6]

The postresuscitation GCS score is used to classify TBI into mild (GCS score of 13–15), moderate (GCS score of 9–12), and severe (GCS score ≤ 8). The traditional classification included patients with a GCS score of 13 in the moderate category, but the advanced trauma life support (ATLS) reclassified GCS score of 13 as mild head injury based on the findings from the Canadian Computed Tomography (CT) Head Rule Study and other studies.[7] [8] [9] [10]

Severe head injury (GCS score ≤8) has been shown to be associated with poor outcomes, but data on the difference in outcomes between mild and moderate TBI are scarce. A study by Norwood et al showed that a prehospital GCS score < 14 accurately predicts the need for full trauma team activation and patient hospitalization after motor vehicle collisions.[11] Studies have also shown that patients with a GCS score of 13 harbor intracranial lesions at a frequency similar to patients with moderate head injury defined as GCS score of 9 to 12.[12] [13]

In this study, we analyzed whether dividing head injuries into moderate and mild categories based on the admission GCS score is of any clinical relevance, based on treatment required and 6-month morbidity and mortality rates in patients with an admission GCS score of 9 to 15.


#

Materials and Methods

The study was conducted on a prospectively maintained database of TBI patients admitted at a level I trauma care center between 2013 and 2019. Patients whose GCS score at admission was between 9 and 15 and had a minimum follow-up of 6 months post-TBI were included in the study. All the patients were treated at our center largely in line with the Brain Trauma Foundation (BTF) guidelines.[10] They were followed up in a dedicated outpatient clinic at 1, 3, and 6 months after discharge during which a detailed assessment was done. Patient outcomes were recorded using the Extended Glasgow Outcome Scale (GOS-E).[14] The incidence of anisocoria, need for surgery and ventilation, mortality, and GOS-E at 6 months was assessed for each GCS score from 9 to 15.

The mortality and outcome for each GCS score was compared against the mortality and outcome for patients with a GCS score of 15 for statistical analysis. The need for surgery and ventilation for each GCS score was similarly compared against the requirements for the patients with a GCS score of 15. Surgeries included in the analysis were craniotomy for hematoma evacuation and decompressive craniectomy with or without hematoma evacuation. Surgeries for depressed fractures, cerebrospinal fluid (CSF) leak, or other indications were not included as they are unlikely to be a reflection of the severity of the injury. Patients in whom one or both pupils could not be assessed due to local causes were excluded only from the analysis on anisocoria.

Statistical Analysis

Data were entered into a spreadsheet and statistical analysis was performed using SPSS (Version 21.0, IBM Corp., Armonk, NY). Categorical variables were reported as frequency and percentage. Mean ± standard deviation (SD) and median (interquartile range [IQR]) were used for continuous variables, as applicable. Association of the categorical variables was reported using the chi-squared test. The odds ratio was calculated using unadjusted regression analysis. A p-value of <0.05 was considered statistically significant.


#
#

Results

Among 2,204 patients with TBI and a GCS score of 9 to 15 admitted at our center during the study period, 2,060 had adequate follow-up and were included in the study. Of these, 293 patients were <18 years of age and 1,684 were males. The most common cause of head injury was road traffic accidents (83.7%). The clinical and demographic characteristics are described in [Table 1].

Table 1

Clinical and demographic profile of patients

Variable

Number of patients (%)

Gender

 Male

 Female

1,684 (81.7)

376 (18.3)

Age (y)

 ≤18

 19–64

 ≥65

293 (14.2)

1,625 (78.8)

142 (7)

Etiology

 RTA

 Fall

 Assault

 Others

1,724 (83.6)

220 (10.7)

47 (2.3)

69 (3.4)

GCS score

 9

 10

 11

 12

 13

 14

 15

298 (14.5)

265 (12.9)

282 (13.7)

123 (5.9)

281 (13.6)

294 (14.3)

517 (25.1)

Abbreviations: GCS, Glasgow Coma Scale; RTA, road traffic accident.


There was an almost linear increase in the proportion of patients who had a good outcome (GOS-E of 5–8) with an increasing admission GCS score, ranging from 82.5% for a GCS score of 9 to 95.8% for a GCS score of 15. The number of patients with a GOS-E of 8 also showed a similar increase from 66.8 to 88.7% ([Table 2]).

Table 2

Patient outcomes at 6 months for each GCS score

GCS score

GOS-E, n (%)

1

1–4

5–8

8

9 (298)

41 (13.8)

52 (17.5)

246 (82.5)

199 (66.8)

10 (265)

28 (10.6)

42 (15.9)

223 (84.1)

185 (69.8)

11 (282)

28 (9.9)

40 (14.2)

242 (85.8)

214 (75.9)

12 (123)

14 (11.3)

18 (14.6)

105 (85.4)

90 (73.2)

13 (281)

24 (8.5)

36 (12.8)

245 (81.2)

220 (78.3)

14 (294)

25 (8.5)

31 (10.5)

263 (89.5)

234 (79.6)

15 (517)

16 (3.1)

22 (4.2)

495 (95.8)

459 (88.7)

Abbreviations: GCS-E, Extended Glasgow Coma Scale.


As mentioned earlier in the earlier section, all measures of significance were generated by comparing the variable for each GCS score with that for patients with a GCS score of 15. There was a linear increase in mortality with decreasing GCS scores, with an odds ratio for mortality of 5.0 (confidence interval [CI]: 2.75–9.08) for an admission GCS score of 9 when compared to a GCS score of 15 ([Table 3]). Similarly the odds ratio of a poor outcome was 4.76 (CI: 2.82–8.01) for an admission GCS score of 9 when compared with a GCS score of 15 ([Table 4]).

Table 3

Mortality in patients with GCS score ranging from 9 to 15, compared with mortality in patients with a GCS score of 15 for statistical significance

GCS score

Mortality (GOS-E1), n (%)

Univariate

Odds ratio (OR)

p value

OR

95% CI

p value

9

41/298 (13.8)

<0.00001

5.00

2.75–9.08

<0.001

10

28/265 (10.6)

0.00001

3.70

1.96–6.97

<0.001

11

28/282 (9.9)

0.00005

3.45

1.83–6.50

<0.001

12

14/123 (11.3)

0.00009

4.02

1.91–8.49

<0.001

13

24/281 (8.5)

0.00075

2.92

1.53–5.60

<0.001

14

25/294 (8.5)

0.00072

2.91

1.53–5.55

0.001

15

16/517 (3.1)

1.00

Abbreviations: CI, confidence interval; GCS-E, Extended Glasgow Coma Scale.


Table 4

Poor outcome at 6 months of follow-up for each GCS score from 9 to 15, comparing each GCS score with the outcome for a GCS score of 15 for statistical significance

GCS score

Death/poor outcome

Univariate

Odds ratio (OR)

GOS-E1–4, n (%)

p value

OR

95% CI

p value

9

52/298(17.5)

<0.00001

4.76

2.82–8.01

<0.001

10

42/265(15.9)

<0.00001

4.24

2.47–7.27

<0.001

11

40/282(14.2)

<0.00001

3.72

2.16–6.40

<0.001

12

18/123(14.6)

0.00001

3.86

2.00–7.45

<0.001

13

36/281(12.8)

<0.00001

3.31

1.90–5.74

<0.001

14

31/294(10.5)

0.00049

2.65

1.51–4.67

0.001

15

22/517 (4.2)

1.00

Abbreviations: CI, confidence interval; GCS-E, Extended Glasgow Coma Scale.


Patients with a lower admission GCS score were more likely to require surgical intervention (26.5% for a GCS score of 9 but only 12.2% for a GCS score of 15). A patient with a GCS score of 9 was also significantly more likely to require ventilatory support (p < 0.0001) when compared to a patient with a GCS score of 15 ([Table 5]).

Table 5

Proportion of patients requiring surgery and ventilation for each GCS score of 9 to 15. Each is compared against a GCS score of 15 for statistical significance

GCS Score

Ventilation

Surgery

Yes

n (%)

Univariate

p value

Yes

n (%)

Univariate

p value

9

140/298 (47)

<0.00001

79/298 (26.5)

<0.00001

10

87/265 (32)

<0.00001

61/265 (23)

<0.00008

11

79/282 (28)

<0.00001

65/282 (23)

<0.00006

12

29/123 (23.6)

<0.00001

23/123 (18.7)

<0.056

13

63/281 (22.5)

<0.00001

58/281 (20.6)

<0.001

14

50/294 (17)

<0.00002

50/294 (17)

<0.00002

15

38/517 (7.3)

63/517 (12.2)

Seventy-one patients had a local injury to one or both eyes and therefore only 1,989 patients were included in the analysis for anisocoria. A little more than 20% of patients with a GCS score of 9 had clinically detected pupillary asymmetry, while this was less than 5% in patients with a GCS score of 15 ([Table 6]).

Table 6

Proportion of patients with anisocoria in each GCS score ranging from 9 to 15. Each group is compared against the GCS score of 15 for statistical significance

GCS score

Pupillary anisocoria

n (%)

Univariate

p value

9

64/293 (21.8)

<0.00001

10

35/255 (13.7)

<0.00001

11

37/276 (13.5)

<0.00002

12

11/119 (9.3)

<0.06

13

28/265 (10.6)

<0.002

14

21/282 (7.5)

0.12

15

24/499 (4.8)


#

Discussion

When the severity of head injury was initially categorized into severe, moderate, and mild, a GCS score of 13 was considered a moderate TBI.[15] This was changed later by the ATLS group with a GCS score of 13 being classified as a mild TBI. Defining an injury as mild implies that most patients in this category will not require significant interventions. Although the majority of patients with TBI who present to the hospital will fall under this “mild” category, there are no clear guidelines for managing these patients in the emergency department. Some authors consider a GCS score 15 alone as mild head injury, with evidence suggesting that injuries in patients with GCS score of 13 and 14 tend to be more severe.[16] In a meta-analysis of 24 studies that included 24,249 patients with a GCS score of 15, Geijerstam et al found that the mortality rate was 0.1% and complication rate was about 0.9%.[17] Norwood et al reported that a prehospital GCS score of ≤14 most reliably predicted the need for patient hospitalization after motor vehicle collisions.[11] Culotta et al reported that patients with an admission GCS scores of 13 were significantly more likely to have abnormal CT scans and were more likely to require neurosurgical intervention within the first 24 hours than were those with GCS scores of 14 or 15. Those with GCS score of 14 were more likely to have an abnormal CT and require an intervention than those with GCS score of 15. They concluded that patients with GCS scores of 13 and 14 should be segregated from those with a GCS score of 15.[16] Stein and Ross reported that nearly 40% of patients with a GCS score of 13 have a CT abnormality and 10% require surgical intervention; hence, they suggested these patients should be classified as moderate rather than mild in severity and risk.[18] Mena et al also found that a GCS score of 13 classified as moderate TBI predicted mortality better than when classified as mild TBI in a regression model.[7]

Most of these studies have been performed in an attempt to decide whether a patient with a GCS score of 13 should be classified as mild or moderate. None of them, however, have clearly delineated the differences in the approach to patients depending on whether they are classified as mild or moderate, and the only conclusion is that patients with a GCS score of 15 generally do not require as much attention as the other patients. Our data show that the risk of mortality and poor outcome increase with decreasing GCS score, as does the likelihood of having asymmetric pupils and requiring surgery or ventilation. The probability of a good outcome and return to work improves with increasing GCS score. We also have data that we have not included for reasons of clarity showing that the patients with a lower GCS score have progressively higher Rotterdam CT scores and need for tracheostomy.

In all these data, there is no step between two GCS scores that could indicate a point at which the patients can be categorized into moderate or mild. Instead we have a continuum where the variables and outcome change in practically a linear fashion as the GCS score increases or decreases, making this division into moderate and mild TBI an artificial construct with no definite influence on treatment required or the outcome.


#

Limitations

This study deals only with patients who were admitted to our hospital and not all patients with TBI who were referred to neurosurgery in the emergency department. The decision to admit a patient is made on our criteria that reflect the available resources, and this decision-making process may not be the same in other institutions. This could be an explanation for the comparatively higher mortality and need for aggressive treatment in our patients with a GCS score of 15, since the majority of the milder injuries were not admitted. However, we believe that even if the proportions differ, the overall trend will be the same in all hospitals.


#

Conclusion

The admission GCS score linearly correlates with mortality, outcome, and intensity of treatment required for TBI patients with a GCS score of ≥9. The classification of TBI patients into moderate and mild based on the admission GCS score does not provide guidance of any practical value, and TBI patients may be more usefully classified based on the admission GCS score into severe and not severe groups.


#
#

Conflict of Interest

None declared.

Note

This article was presented at NEUROTRAUMA 2022.


Authors' Contributions

Conception and design were done by M.J., A.P.A., and G.S. Drafting of the article was done by G.S. and M.J. Statistical analysis was performed by T.M.. M.J. is the guarantor.


  • References

  • 1 Dewan MC, Rattani A, Gupta S. et al. Estimating the global incidence of traumatic brain injury. J Neurosurg 2018; 130 (04) 1-18
  • 2 Gururaj G. Epidemiology of traumatic brain injuries: Indian scenario. Neurol Res 2002; 24 (01) 24-28
  • 3 Teasdale G, Jennett B. Assessment of coma and impaired consciousness. A practical scale. Lancet 1974; 2 (7872): 81-84
  • 4 Rowley G, Fielding K. Reliability and accuracy of the Glasgow Coma Scale with experienced and inexperienced users. Lancet 1991; 337 (8740): 535-538
  • 5 Bullock R. Management and prognosis of severe traumatic brain injury. Part 1 Guideline for the management of severe traumatic brain injury. J Neurotrauma 2000; 17: 451-553
  • 6 Perel P, Arango M, Clayton T. et al; MRC CRASH Trial Collaborators. Predicting outcome after traumatic brain injury: practical prognostic models based on large cohort of international patients. BMJ 2008; 336 (7641): 425-429
  • 7 Mena JH, Sanchez AI, Rubiano AM. et al. Effect of the modified Glasgow Coma Scale score criteria for mild traumatic brain injury on mortality prediction: comparing classic and modified Glasgow Coma Scale score model scores of 13. J Trauma 2011; 71 (05) 1185-1192 , discussion 1193
  • 8 Kortbeek JB, Al Turki SA, Ali J. et al. Advanced trauma life support, 8th edition, the evidence for change. J Trauma 2008; 64 (06) 1638-1650
  • 9 Smits M, Dippel DW, de Haan GG. et al. External validation of the Canadian CT Head Rule and the New Orleans Criteria for CT scanning in patients with minor head injury. JAMA 2005; 294 (12) 1519-1525
  • 10 Stiell IG, Clement CM, Rowe BH. et al. Comparison of the Canadian CT Head Rule and the New Orleans Criteria in patients with minor head injury. JAMA 2005; 294 (12) 1511-1518
  • 11 Norwood SH, McAuley CE, Berne JD, Vallina VL, Creath RG, McLarty J. A prehospital Glasgow coma scale score < or = 14 accurately predicts the need for full trauma team activation and patient hospitalization after motor vehicle collisions. J Trauma 2002; 53 (03) 503-507
  • 12 Fearnside M, McDougall P. Moderate head injury: a system of neurotrauma care. Aust N Z J Surg 1998; 68 (01) 58-64
  • 13 Stein SC, Ross SE. Moderate head injury: a guide to initial management. J Neurosurg 1992; 77 (04) 562-564
  • 14 Wilson JT, Pettigrew LE, Teasdale GM. Structured interviews for the Glasgow Outcome Scale and the extended Glasgow Outcome Scale: guidelines for their use. J Neurotrauma 1998; 15 (08) 573-585
  • 15 Miller JD. Minor, moderate and severe head injury. Neurosurg Rev 1986; 9 (1–2): 135-139
  • 16 Culotta VP, Sementilli ME, Gerold K, Watts CC. Clinicopathological heterogeneity in the classification of mild head injury. Neurosurgery 1996; 38 (02) 245-250
  • 17 af Geijerstam JL, Britton M. Mild head injury: mortality and complication rate—meta-analysis of findings in a systematic literature review. Acta Neurochir (Wien) 2003; 145 (10) 843-850 , discussion 850
  • 18 Stein SC, Ross SE. The value of computed tomographic scans in patients with low-risk head injuries. Neurosurgery 1990; 26 (04) 638-640

Address for correspondence

Mathew Joseph, MCh
Department of Neurological sciences, Christian Medical College
Vellore 632004, Tamil Nadu
India   

Publikationsverlauf

Artikel online veröffentlicht:
25. April 2023

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  • References

  • 1 Dewan MC, Rattani A, Gupta S. et al. Estimating the global incidence of traumatic brain injury. J Neurosurg 2018; 130 (04) 1-18
  • 2 Gururaj G. Epidemiology of traumatic brain injuries: Indian scenario. Neurol Res 2002; 24 (01) 24-28
  • 3 Teasdale G, Jennett B. Assessment of coma and impaired consciousness. A practical scale. Lancet 1974; 2 (7872): 81-84
  • 4 Rowley G, Fielding K. Reliability and accuracy of the Glasgow Coma Scale with experienced and inexperienced users. Lancet 1991; 337 (8740): 535-538
  • 5 Bullock R. Management and prognosis of severe traumatic brain injury. Part 1 Guideline for the management of severe traumatic brain injury. J Neurotrauma 2000; 17: 451-553
  • 6 Perel P, Arango M, Clayton T. et al; MRC CRASH Trial Collaborators. Predicting outcome after traumatic brain injury: practical prognostic models based on large cohort of international patients. BMJ 2008; 336 (7641): 425-429
  • 7 Mena JH, Sanchez AI, Rubiano AM. et al. Effect of the modified Glasgow Coma Scale score criteria for mild traumatic brain injury on mortality prediction: comparing classic and modified Glasgow Coma Scale score model scores of 13. J Trauma 2011; 71 (05) 1185-1192 , discussion 1193
  • 8 Kortbeek JB, Al Turki SA, Ali J. et al. Advanced trauma life support, 8th edition, the evidence for change. J Trauma 2008; 64 (06) 1638-1650
  • 9 Smits M, Dippel DW, de Haan GG. et al. External validation of the Canadian CT Head Rule and the New Orleans Criteria for CT scanning in patients with minor head injury. JAMA 2005; 294 (12) 1519-1525
  • 10 Stiell IG, Clement CM, Rowe BH. et al. Comparison of the Canadian CT Head Rule and the New Orleans Criteria in patients with minor head injury. JAMA 2005; 294 (12) 1511-1518
  • 11 Norwood SH, McAuley CE, Berne JD, Vallina VL, Creath RG, McLarty J. A prehospital Glasgow coma scale score < or = 14 accurately predicts the need for full trauma team activation and patient hospitalization after motor vehicle collisions. J Trauma 2002; 53 (03) 503-507
  • 12 Fearnside M, McDougall P. Moderate head injury: a system of neurotrauma care. Aust N Z J Surg 1998; 68 (01) 58-64
  • 13 Stein SC, Ross SE. Moderate head injury: a guide to initial management. J Neurosurg 1992; 77 (04) 562-564
  • 14 Wilson JT, Pettigrew LE, Teasdale GM. Structured interviews for the Glasgow Outcome Scale and the extended Glasgow Outcome Scale: guidelines for their use. J Neurotrauma 1998; 15 (08) 573-585
  • 15 Miller JD. Minor, moderate and severe head injury. Neurosurg Rev 1986; 9 (1–2): 135-139
  • 16 Culotta VP, Sementilli ME, Gerold K, Watts CC. Clinicopathological heterogeneity in the classification of mild head injury. Neurosurgery 1996; 38 (02) 245-250
  • 17 af Geijerstam JL, Britton M. Mild head injury: mortality and complication rate—meta-analysis of findings in a systematic literature review. Acta Neurochir (Wien) 2003; 145 (10) 843-850 , discussion 850
  • 18 Stein SC, Ross SE. The value of computed tomographic scans in patients with low-risk head injuries. Neurosurgery 1990; 26 (04) 638-640