CC BY-NC-ND 4.0 · Asian J Neurosurg
DOI: 10.1055/s-0044-1788062
Research Article

Clinical Outcome and Predictors of Traumatic Cervical Injury: A Prospective Observational Study

1   Department of Neurosurgery, King George's Medical University, Lucknow, Uttar Pradesh, India
,
1   Department of Neurosurgery, King George's Medical University, Lucknow, Uttar Pradesh, India
,
1   Department of Neurosurgery, King George's Medical University, Lucknow, Uttar Pradesh, India
,
Ankur Bajaj
1   Department of Neurosurgery, King George's Medical University, Lucknow, Uttar Pradesh, India
› Author Affiliations
Funding None.
 

Abstract

Introduction Traumatic cervical spine injuries (CSIs) have an incidence of 1.7 to 8% among traumatic brain injury (TBI) patients and should be a pivotal part of its neurological examination. Prognosis of cervical spine insult in TBI depends on several epidemiological and clinical factors which need to be considered during the management of these injuries. This study aims to analyze the outcomes of patients with CSI and its associated predictors.

Material and Methods A prospective observational study was conducted among 63 patients of traumatic CSI admitted at a tertiary care center of Lucknow, Uttar Pradesh, India. All patients underwent a clinical assessment using the American Spinal Injury Association, Functional Independence Measure (FIM), and Barthel Index scoring and grading at admission, 1, and 4 months, respectively. All patients at the facility underwent magnetic resonance imaging (MRI). Midsagittal T1- and T2-weighted sequences were used to measure the degree of spinal cord injury (SCI) impairment. Patients were followed for outcome assessment.

Results There was a significant difference in the median values of Barthel Index and mean values of FIM preoperatively and at 4 months' follow-up. There was a significant improvement in the neurological outcome of the patients after admission, at 1, and 4 months' follow-up. Out of the 30 patients who had improvement in the neurological outcome, majority (26) had edema present in less than equal to 2 segments and this was statistically significant. The overall FIM score was significantly higher among those with ≤ 2 segment edema as compared with those with > 2 segments.

Conclusion The study concludes that incomplete injury, edema on MRI imaging less than equal to 2 segments, and no listhesis are predictors of neurological and functional improvement in patients with traumatic cervical spinal injuries.


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Introduction

Traumatic cervical spine injuries (CSIs) result from falls, road traffic accidents, penetrating injuries or blunt trauma, and injuries related to sports and diving.[1] Globally, they contribute to almost half of all the spinal injuries and are emerging as a major cause of long-term disability because of the neurological impairment due to the magnitude of cervical spine insult and delay in its identification.[2] Patients with traumatic brain injury have a documented incidence of CSI that varies from 1.7 to 8% and hence should be a pivotal part of neurological examination in traumatic injuries.[3]

Early identification and prompt treatment play a crucial role in the outcome of traumatic CSIs. These injuries require both surgical as well as conservative management. Conservative management mainly involves the use of a cervical collar or halo for neck stabilization. Surgical management is needed in cases of surgical decompression.[4] [5] With the advent of advance emergency medical care, there has been a paradigm shift in the management of these injuries, moving away from conservative methods toward cord decompression, spine stabilization, early mobilization, and rehabilitation.[6] This results in early recovery of these patients with better functional and neurological outcome.

However, prognosis depends on several epidemiological and clinical factors which need to be considered during the management of these injuries. Factors like age, gender, mode or level of injury, extent of edema, etc. are crucial determinants of the outcome.[7] However, not much has been explored in this domain as the prevalence of isolated traumatic CSIs seem to be low when compared with other spinal injuries. But they can consequently cause adverse repercussions among the patients if robust action is not taken. Hence, this study aims to analyze the outcomes of patients with CSI and its associated predictors.


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Materials and Methods

Study Design and Setting

This study was a prospective observational study that included all patients with cervical spinal injuries who presented at the emergency department within 1 week of the injury and underwent surgical management at the Department of Neurosurgery, King George's Medical University in Lucknow, Uttar Pradesh, India. The study received approval from the Institutional Ethics Committee [Number 128/Ethics/2020].


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Study Participants

Patients who came within a week of their cervical spinal injuries spanning from C1 to C7 were included in this study. Exclusion criteria for the research included patients with significant autonomic disorders, such as systolic blood pressure less than 40, had correlated thoracolumbar and brain injuries, penetrating injuries, underwent conservative management, and arrival to the institution after 7 days following the injury.


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Sample Size

For the purpose of sample size estimation, the study used was Srinivas et al.[8]

Sample size formula used was n = ([Zα /2][2]*p(1–p))/d 2, where Zα /2 is the critical value of the normal distribution at α/2 (for a confidence level of 95%, α = 0.05, and the critical value of 1.96), p is the proportion of patients with traumatic CSI and of American Spinal Injury Association (ASIA) grade D with significant neurological improvement (value 83.3%), and d is the margin of error for desired precision (10%). At 95% confidence interval, the required minimum sample size was 54 patients. Taking 10% loss to follow-up, the total sample size calculated was 59 patients. So a total of 63 patients were enrolled in the study.


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Data Collection

After obtaining written informed consent from the patient or their guardian, all patients underwent a clinical assessment using the ASIA scoring and grading system. In addition to clinical characteristics, the study also considered demographic variables including age, gender, injury type, and chronology. All patients at the facility underwent magnetic resonance imaging (MRI). Midsagittal T1- and T2-weighted sequences were used to measure the degree of spinal cord injury (SCI) impairment. Based on the length of time of the traumatic incident and the MRI, the MRI results were divided into two groups: (1) contusion and (2) edema. The vertebral bodies and discs were used to segregate the midsagittal area of the MRI to objectively estimate the length of the lesion (edema/contusion). The SCI apart from routine axial, coronal, and sagittal T1 and T2 imaging, some special sequences are required depending on the clinical need like in T2-weighted image (T2WI) (gradient echo, susceptibility weighted imaging sequence are more sensitive for hemorrhage, while short tau inversion recovery are more sensitive to ligamentous injury).

In spinal cord swelling, sagittal T1WI focal cord enlargement is seen without signal changes, in spinal cord edema, changes like cord swelling with high T2 signal intensity is seen, and in spinal cord contusion, thick hyperintense T2 signal rim is seen around small central hypointense T1 signal with blooming on T2WI.[9]

The adjacent disc was regarded as a third segment in addition to the upper and lower vertebral body segments. This led to the classification of edema as (1) 2 segments and (2) > 2 segments. The National Spinal Cord Injury Study II advised injecting methylprednisolone into patients who came within 8 hours of the injury (n = 2). Based on the date of the operation after the accident, the patients were arbitrarily split into two groups: early (1 week) and late (> 1 week). A team of neurosurgeons from the department established the preoperative plan during the preoperative phase.

Surgery indicates if there was instability, dislocation, canal stenosis, and spinal cord compression. Anterior cervical discectomy/corpectomy has been the most used surgical procedure, which was described by Cloward and Robinson and Smith in 1958. This procedure is done under general anesthesia technique and the patient is positioned in a supine position. A longitudinal or vertical surgical incision was made medial to the sternocleidomastoid muscle at the targeted level of decompression, followed by superficial dissections through the fascia and platysma muscle, retraction of the tracheoesophageal complex medially and the sternocleidomastoid with the carotid sheath laterally. A deep dissection by splinting the longus colli muscles and anterior longitudinal ligament to expose the vertebral body was done. This was followed by decompression of the targeted level by removal of the affected disc level, fractured bone, and osteophytes. The bone graft was then applied followed by plate and screws.[10]

An impartial supervising senior specialist recognized that surgical decompression was performed until the dura became visible, without any intervening disc or posterior longitudinal ligament. In the outpatient department, each of these patients received routine follow-up care. A change of one or more grades in the ASIA grade between the admission date and the 4-month follow-up was considered an improvement. The Functional Independence Measure (FIM) scale was used to evaluate functional grade at both the 4-month follow-up and admission.


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Statistical Analysis

The data was evaluated using SPSS 24.0. The study data were presented in a descriptive summary including frequencies, percentages, graphs, means, and standard deviation. To assess statistical significance at the 5% level of significance, probability (p) was determined. The Kolmogorov–Smirnov test was used to determine the data's normality. The chi-square test was used to analyze categorical data. Continuous variables were calculated using the independent t-test. Paired t-test was used to compare FIM and Barthel Index at various follow-ups. ASIA grades were observed at various follow-ups using the Friedman test.


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Results

Majority (26.9%) of the study participants were in the age group of 31 to 40 years. Maximum were males (88.9%). The most common mode of CSI was due to fall from height (46.03%). Most (25.4%) of the study participants presented to the hospital between 6 and 24 hours postinjury. More than half of the participants had incomplete injury. Note that 71.4% underwent operative management. Note that 22.2% had grade 1 listhesis, followed by 12.7, 19.0, 9.5, and 1.6% with grade 2, 3, 4, and 5 listhesis, respectively. Approximately 50.8% patients had edema in the MRI findings. The extent of edema was ≤ 2 segments in maximum (68.3%) patients. Only 6.3 and 17.5% patients had locked and parched facet, respectively ([Table 1]).

Table 1

Baseline parameters of the study participants

Parameters

N = 63

%

Age (y)

Up to 20

3

4.76

21–30

22

34.9

31–40

17

26.9

41–50

15

23.8

51–60

6

9.64

Gender

Male

56

88.9

Female

7

11.1

Mode of injury

Fall from height

29

46.03

Road traffic accident (RTA)

24

38.1

Hit by animal

2

3.17

Assault

3

4.76

Other

5

7.94

Injury to hospital presentation time

Within 6 h

4

6.34

6–24 h

16

25.4

24–48 h

10

15.9

48–72 h

11

17.5

72 h—1 wk

7

14.3

> 1 wk

13

20.6

Cervical immobilization used during transportation

Yes

40

61.9

No

23

38.1

Type of injury

Complete

28

44.4

Incomplete

34

54.0

Normal

1

1.6

Level of injury

Upper (C2–C4)

11

81

Lower (C5–C7)

51

19

Management

Operative

45

71.4

Conservative

18

28.6

Listhesis

No listhesis

22

34.9

Grade 1

14

22.2

Grade 2

8

12.7

Grade 3

12

19.0

Grade 4

6

9.5

Grade 5

1

1.6

MRI finding

Normal

7

11.1

Edema

32

50.8

Contusion

24

38.1

Extent of edema

≤ 2 segments

43

68.3

> 2 segments

20

31.7

Locked facet/joint

Yes

4

6.3

No

59

93.7

Parched facet/joint

Yes

11

17.5

No

52

82.5

Abbreviation: MRI, magnetic resonance imaging.


There was a significant difference in the median values of preoperative Barthel Index and at 4 months' follow-up ([Table 2]).

Table 2

Functional outcome of the study participants

Functional outcome

Median (IQR)

25th percentile

75th percentile

p-Value[a]

Barthel Index preoperative

5.0 (8)

0

8

0.0001

Barthel Index at 4 months' follow-up

6.0 (10)

0

10

Note: p-Value <0.05 are significant.


Abbreviation: IQR, interquartile range.


a Wilcoxon sign rank test.


There was a significant difference in the mean values of FIM score preoperatively and 4 months' follow-up ([Table 3]).

Table 3

Comparison of preoperative FIM and at 4 months' follow-up

FIM

Mean ± SD

95% confidence interval

p-Value[a]

Lower

Upper

Preoperative

41.76 ± 27.16

–18.58

–6.98

0.0001

4 months' follow-up

54.54 ± 41.90

Note: p-Value <0.05 are significant.


Abbreviations: FIM, Functional Independence Measure; SD, standard deviation.


a Paired t-test.


There was a significant improvement in the neurological outcome of the patients after admission, at 1, and 4 months' follow-up. At admission, 28 patients were in grade A but at 4 months, only 14 patients were in grade A. Out of the 15, 11, and 8 patients in grade B, C, and D, only 2, 3, and 15 patients were in the same grades, respectively, at 4 months ([Table 4]).

Table 4

Neurological outcome of the study participants

ASIA grade

A

B

C

D

E

At admission (N = 63)

28 (44.4)

15 (23.8)

11 (17.5)

8 (12.7)

1 (1.6)

1 months' follow-up (n = 50)[a]

14 (28)

12 (24)

13 (26)

10 (20)

1 (2)

4 months' follow-up (n = 47)[b]

12 (25.5)

2 (4.3)

3 (6.4)

15 (31.9)

8 (17.02)

Abbreviations: ASIA, American Spinal Injury Association; LAMA, leave against medical advice.


a Expired (11) and LAMA (2).


b Expired (14) and LAMA (2).


At 4 months, 49.8% patients had neurological improvement, 27.9% had no improvement, and 22.3% had expired ([Fig. 1]).

Zoom Image
Fig. 1 Neurological outcome at 4 months (American Spinal Injury Association [ASIA] grade).

Among the 30 patients who showed neurological improvement, 28 had incomplete injury, 26 had edema, 29 patients had extent of edema in less than equal to 2 segments, and 16 had no listhesis and all these were significantly associated with the neurological improvement ([Table 5]).

Table 5

Predictors of neurological outcome among the study participants

ASIA grade at 4 months

Parameters

Improved

n = 30 (%)

Not improved

n = 17 (%)

Expired

n = 14 (%)

p-Value

Age (y)

1–20

1 (3.3)

1 (5.9)

1 (7.1)

0.393

21–30

9 (30)

10 (58.8)

2 (9.1)

31–40

10 (33.3)

2 (11.8)

5 (35.7)

41–50

6 (20)

3 (17.6)

4 (28.6)

51–60

4 (13.3)

1 (5.9)

2 (14.3)

Sex

Male

27 (90)

16 (94.1)

11 (78.6)

0.377[a]

Female

3 (10)

1 (5.9)

3 (21.4)

Mode of injury

Fall from height

11 (36.7)

9 (52.9)

9 (64.3)

0.238

Road traffic injury

13 (43.3)

7 (41.2)

4 (28.6)

Hit by animal

0 (0)

1 (5.9)

1 (7.1)

Assault

2 (6.7)

0 (0.0)

0 (0)

Others

4 (13.3)

0 (0.0)

0 (0)

Injury to hospital presentation time

Within 6 h

2 (6.7)

1 (5.9)

1 (7.1)

0.455

6–24 h

19 (36.7)

2 (11.8)

3 (21.4)

24–48 h

2 (6.7)

5 (29.4)

4 (28.6)

48–72 h

6 (20)

2 (11.8)

3 (21.4)

> 72 h

3 (10)

4 (23.5)

2 (14.3)

> 1 wk

6 (20)

3 (17.6)

1 (7.1)

Mobilization

Yes

19 (63.3)

10 (58.8)

11 (78.6)

0.483[a]

No

11 (36.7)

7 (41.2)

3 (21.4)

Type of injury

Complete

1 (3.3)

12 (70.6)

13 (92.9)

0.0001

Incomplete

28 (93.3)

5 (29.4)

1 (7.1)

Normal

1 (3.3)

0 (0)

0 (0)

Level of injury

Upper

11 (36.7)

16 (94.1)

4 (28.6)

0.026 [a]

Lower

19 (63.3)

1 (5.9)

10 (71.4)

Management

Conservative

17 (56.7)

3 (17.6)

10 (71.4)

0.388[a]

Operative

13 (43.3)

14 (82.4)

4 (28.6)

MRI finding

None

4 (13.3%)

3 (17.6)

0 (0.0%)

0.0001

Edema

26 (86.7%)

6 (35.3)

0 (0.0%)

Contusion

0 (0.0%)

8 (47.1)

14 (100.0)

Extent of edema

≤ 2 segments

29 (96.7%)

9 (52.9)

4 (28.6)

0.0001 [a]

> 2 segments

1 (3.3%)

8 (47.1)

10 (71.4)

Listhesis

No listhesis

16 (53.3)

4 (23.5)

2 (14.3)

0.0001

Grade 1

10 (33.3)

3 (17.6)

1 (7.1)

Grade 2

3 (10)

4 (23.5)

0 (0)

Grade 3

1 (3.3)

4 (23.5)

6 (42.9)

Grade 4

0 (0)

2 (11.8)

4 (28.6)

Grade 5

0 (0)

0 (0)

1 (7.1)

Locked facet/joint

Yes

3 (10)

1 (5.9)

0

0.802

No

27 (90)

16 (94.1)

14 (100)

Parched facet/joint

Yes

2 (6.7)

6 (35.3)

2 (14.3)

0.033 [a]

No

28 (93.3)

11 (64.7)

12 (85.7)

Abbreviation: MRI, magnetic resonance imaging.


Note: p < 0.05 is significant (bold).


a Chi-square test, rest is Fischer's exact test.


The mean FIM score of patients with incomplete injury was significantly higher than those with complete injury. Those with lower level of injury had higher FIM score than the upper level of injury and this was statistically significant. Those with conservative management had higher FIM scores as compared with those with operative management, and this was significant. Those with edema had significantly higher FIM scores as compared with those with contusion. Those with extent of edema up to less than equal to 2 segments had higher FIM scores than those with ≥ 2 segments, and this was highly significant ([Table 6]).

Table 6

Predictors of functional outcome among the study participants

FIM score at 4 months

Parameters

Mean ± SD

95% CI

p-Value

Lower

Upper

Age (y)

1–20

42.33 ± 51.033

–84.44

169.11

0.665[a]

21–30

53.50 ± 37.011

37.09

69.91

31–40

54.71 ± 42.880

32.66

76.75

41–50

47.86 ± 43.661

22.65

73.07

51–60

76.00 ± 52.170

27.75

124.25

Sex

Male

56.45 ± 41.640

45.30

67.60

0.311

Female

39.29 ± 44.022

–1.43

80.00

Mode of injury

Fall from height

43.90 ± 40.381

28.82

58.98

0.075[a]

Road traffic injury

63.38 ± 42.033

45.63

81.12

Hit by animal

11.00 ± 15.556

–128.77

150.77

Assault

76.67 ± 50.964

–49.94

203.27

Others

86.50 ± 16.823

59.73

113.27

Injury to hospital presentation time

Within 6 h

45.40 ± 52.046

–19.22

110.02

0.237[a]

6–24 h

70.25 ± 41.282

48.25

92.25

24–48 h

31.36 ± 32.500

9.53

53.20

48–72 h

52.18 ± 42.249

23.80

80.56

> 72 h

49.33 ± 42.790

16.44

82.22

> 1 wk

65.64 ± 41.752

37.59

93.69

Mobilization

Yes

53.35 ± 42.113

39.88

66.82

0.769

No

56.61 ± 42.375

38.28

74.93

Type of Injury

Complete

42.73 ± 38.983

31.02

54.45

0.0001

Incomplete

84.06 ± 34.304

67.00

101.11

Level of Injury

Upper

42.73 ± 38.983

31.02

54.45

0.0001

Lower

84.06 ± 34.304

67.00

101.11

Management

Operative

47.67 ± 38.888

35.98

59.35

0.038

Conservative

71.72 ± 45.274

49.21

94.24

MRI findings

None

88.71 ± 21.132

69.17

108.26

0.0001[a]

Edema

80.88 ± 27.392

71.00

90.75

Contusion

9.46 ± 12.755

4.07

14.84

Extent of edema

≤ 2 segments

70.63 ± 38.033

58.92

82.33

0.0001

> 2 segments

19.95 ± 26.172

7.70

32.20

Listhesis

Listhesis

46.66 ± 40.429

33.90

59.42

0.125[a]

Fracture

69.36 ± 41.094

45.63

93.08

Listhesis/fracture

69.36 ± 41.094

45.63

93.08

Abbreviations: CI, confidence interval; FIM, Functional Independence Measure; MRI, magnetic resonance imaging; SD, standard deviation.


Note: p-value < 0.05 is significant (bold).


a One-way analysis of variance test, rest all is independent t-test.


The overall FIM score and mean scores of self-care, sphincter control, locomotion, communication, and cognitive was higher among those with ≤ 2 segment edema as compared with those with > 2 segments. There was a highly significant association between overall FIM scores and all its components with the extent of edema ([Table 7]).

Table 7

Association of Functional Independence Measure scores at 4 months with number of segments of injury

Functional Independence Measure scores

Mean

95% CI of the difference

p-Value

 ≤ 2 segment

> 2 segment

Lower

Upper

 Overall FIM

 70.63

19.95

 31.857

 69.499

0.0001

 Self-care

 25.47

5.05

 13.007

 27.823

0.0001

 Sphincters

 6.35

1.30

 2.791

 7.307

0.0001

 Locomotion

 11.26

2.85

 4.672

 12.139

0.0001

 Communication

 11.47

5.45

 3.175

 8.855

0.0001

 Cognitive

 15.67

5.65

 5.714

 14.335

0.0001

Note: p-Value <0.05 are significant.


Abbreviation: FIM, Functional Independence Measure.


Out of the 30 patients who had improvement in the neurological outcome, majority (26) had edema present in less than equal to 2 segments and this was statistically significant ([Table 8]).

Table 8

Association of extent of edema in the MRI with the neurological outcome

Extent of edema in MRI

 Neurological outcome

 p-Value

 Improved

 n = 30

 Not improved

 n = 17

 Expired

 n = 14

 No edema/contusion

 ≤ 2 segment

 3 (75.0%)

 8 (72.7%)

 4 (28.6%)

 0.059

 > 2 segment

 1 (25.0%)

 3 (27.3%)

 10 (71.4%)

 Edema present

 < 2 segment

 26 (100.0%)

 1 (16.7%)

0 (0)

0.0001

 > 2 segment

 0 (0.0%)

 5 (83.3%)

0 (0)

Note: p-Value <0.05 are significant.


Abbreviation: MRI, magnetic resonance imaging.



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Discussion

CSIs are a common cause of SCI and can lead to significant neurological and functional impairment.[11] [12] Various factors determine the outcome of these injuries and need to be understood well for better prognosis and longevity of life of the sufferers. The following study has followed patients of traumatic CSI postmanagement to determine the neurological and functional outcome as well as assess its associated factors.

The neurological outcome assessed by ASIA grade improved significantly in our study from admission to 4 months' follow-up. This was in consensus with the study by Srinivas et al, who also observed improvement in the ASIA grade among almost half of the patients with cervical SCI.[8] Hitti et al in their study have explained that neurological recovery depends on nonmodifiable factors like sociodemographic information and underlying comorbidity and modifiable factors like timing of surgery, delay in stabilization, progressive edema, or ischemia, etc. and in few cases, the cause is iatrogenic where patients underwent reoperation.[13] Our study has also shown that the rate of improvement was least in ASIA grade A. This was in concordance with Vazquez et al who studied 173 traumatic cervical SCI patients and concluded that the rate of improvement was least in ASIA grade A patients, and none of them were functional. In contrast, incomplete injury patients had better recovery.[14]

Significant predictors of neurological improvement in our study were type of injury, presence of edema on MRI, segments involved in injury ≤ 2, and grading of listhesis. Based on these variables, functional outcome (FIM score) was also highly significant. This finding was in concordance with the study by Srinivas et al, who found similar results with cervical injuries that were incomplete (grades C and D), lower cervical injuries (C5–C7), and those exhibiting edema in MRI experiencing greater improvements compared with the individuals with complete, upper cervical injuries (at or above C4), and contusion in the MRI. They also reported that patients with no abnormality on MRI improved to ASIA grade E irrespective of their neurological status at admission.[8] Hence, our study clearly depicts an association of MRI findings (absence of edema and number of segments involved) with the neurological outcome. Moreover, strong association was observed between presence of edema and number of segments involved with the neurological outcome. MRI is a gold standard imaging test for acute spinal trauma. Boldin et al studied the neurological recovery predictive value of MRI findings in 29 patients with acute cervical SCI and a median follow-up of 35 months. Length of edema was the only predictive measure of retaining SCI. Each millimeter increase in the length of edema entailed an increased rate of retaining a complete SCI (p = 0.017).[15] The resolution of spinal cord edema after SCI with subsequent MRI examinations has been reported previously in the literature.[16] Martínez-Pérez et al found that edema larger than 36 mm was significantly (p = 0.006) associated with a poor neurological outcome.[10] Hence, length of edema can serve as a proxy indicator of prognosis of traumatic CSIs.[17]

Advancing age was associated with poor neurological and functional recovery in our study. It has been hypothesized that advancing age has a negative impact on neurological improvement,[18] [19] as it reduces neural plasticity which deteriorates the neurologic recovery.[20] Similarly, other researchers have examined the impact of age and initial neurological status on ambulation recovery in patients with incomplete injuries. They concluded that patients classified as ASIA grade D had an excellent prognosis for achieving independent ambulation regardless of age. However, for patients classified as ASIA grade C, the likelihood of recovering ambulation was influenced by age, with a 42% improvement rate observed in individuals under the age of 50.[9] [21] [22] [23]

The following study has highlighted various determinants of neurological and functional outcome among patients with traumatic CSI which will play a key role in clinical decision making of a neurosurgeon. However, a small sample size limits the generalizability of the results, along with no uniformity in imaging and timing of surgery.


#

Conclusion

The study concludes that incomplete injury, edema on MRI imaging less than equal to 2 segments, and no listhesis are predictors of neurological and functional improvement in patients with traumatic cervical spinal injuries. Overall mean FIM score was higher in those who had less than 2 segments of edema on MRI, with no adverse outcome.


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Conflict of Interest

None declared.

  • References

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  • 2 Kumar R, Lim J, Mekary RA. et al. Traumatic spinal injury: global epidemiology and worldwide volume. World Neurosurg 2018; 113: e345-e363
  • 3 Leucht P, Fischer K, Muhr G, Mueller EJ. Epidemiology of traumatic spine fractures. Injury 2009; 40: 166-172
  • 4 Lomaz MB, Netto LA, Filho MS, Alves AP, De Tavares Canto FR. Epidemiological profile of patients with traumatic spinal fracture. Coluna/Columna 2017; 16: 224-227
  • 5 Aleem IS, DeMarco D, Drew B. et al. The burden of spine fractures in India: a prospective multicentre study. Global Spine J 2017; 7: 325-333
  • 6 Singh G, Prakash R, Bhatti V, Mahen A. Spinal cord injury in organizational setup-a hospital based descriptive study. J Mar Med Soc. 2019; 21: 46-50
  • 7 Birua GJS, Munda VS, Murmu NN. Epidemiology of spinal injury in north east India: a retrospective study. Asian J Neurosurg 2018; 13: 1084-1086
  • 8 Srinivas B, Rajesh A, Purohit A. Factors affecting outcome of acute cervical spine injury: a prospective study. Asian J Neurosurg 2017; 12 (03) 416-423
  • 9 Katzberg RW, Benedetti PF, Drake CM. et al. Acute cervical spine injuries: prospective MR imaging assessment at a level 1 trauma centre. Radiology 1999; 213 (01) 203-212
  • 10 Martínez-Pérez R, Cepeda S, Paredes I, Alen JF, Lagares A. MRI prognostication factors in the setting of cervical spinal cord injury secondary to trauma. World Neurosurg 2017; 101: 623-632
  • 11 Schousboe JT. Epidemiology of vertebral fractures. J Clin Densitom 2016; 19: 8-22
  • 12 den Ouden LP, Smits AJ, Stadhouder A, Feller R, Deunk J, Bloemers FW. Epidemiology of spinal fractures in a level one trauma center in the Netherlands: a 10 years review. Spine 2019; 44: 732-739
  • 13 Hitti FL, McShane BJ, Yang AI. et al. Predictors of neurological outcome following subaxial cervical spine trauma. Cureus 2019; 11 (12) e6402
  • 14 Vazquez XM, Rodriguez MS, Peñaranda JM, Concheiro L, Barus JI. Determining prognosis after spinal cord injury. J Forensic Leg Med 2008; 15: 20-23
  • 15 Boldin C, Raith J, Fankhauser F, Haunschmid C, Schwantzer G, Schweighofer F. Predicting neurologic recovery in cervical spinal cord injury with postoperative MR imaging. Spine 2006; 31 (05) 554-559
  • 16 Tarawneh AM, D'Aquino D, Hilis A, Eisa A, Quraishi NA. Can MRI findings predict the outcome of cervical spinal cord injury? A systematic review. Eur Spine J 2020; 29: 2457-2464
  • 17 Wenger M, Adam PJ, Alarcón F, Markwalder TM. Traumatic cervical instability associated with cord oedema and temporary quadriparesis. Spinal Cord 2003; 41 (09) 521-526
  • 18 Singh R, Sharma S, Mittal R, Sharma A. Traumatic spinal cord injuries in Haryana: an epidemiological study. Indian J Community Med 2003; 13: 184-186
  • 19 Grauer JN, Vaccaro AR, Lee JY. et al. The timing and influence of MRI on the management of patients with cervical facet dislocations remains highly variable: a survey of members of the spine trauma study group. J Spinal Disord Tech 2009; 22: 96-99
  • 20 Hadley MN, Walters BC. The case for the future role of evidence-based medicine in the management of cervical spine injuries, with or without fractures. J Neurosurg Spine 2019; 31: 457-463
  • 21 Gelb DE, Hadley MN, Aarabi B. et al. Initial closed reduction of cervical spinal fracture-dislocation injuries. Neurosurgery 2013; 72: 73-83
  • 22 Passias PG, Poorman GW, Segreto FA. et al. Traumatic fractures of the cervical spine: analysis of changes in incidence, cause, concurrent injuries, and complications among 488,262 patients from 2005 to 2013. World Neurosurg 2018; 110: e427-e437
  • 23 Jain M, Mohanty CR, Doki SK. et al. Traumatic spine injuries in Eastern India: a retrospective observational study. Int J Crit Illn Inj Sci 2021; 11 (02) 79

Address for correspondence

Suresh Kumar Jaiswal, MCh, DNB, MS, 105
Department of Neurosurgery, King George's Medical University, Lucknow 226003, Uttar Pradesh
India   

Publication History

Article published online:
11 July 2024

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  • References

  • 1 World Health Organization. Injuries and Violence: The Facts. World health Organization. 2014 . Accessed September 30, 2020 at: https://www.who.int/violence_injury_prevention/media/news/2015/Injury_violence_facts_2014/en
  • 2 Kumar R, Lim J, Mekary RA. et al. Traumatic spinal injury: global epidemiology and worldwide volume. World Neurosurg 2018; 113: e345-e363
  • 3 Leucht P, Fischer K, Muhr G, Mueller EJ. Epidemiology of traumatic spine fractures. Injury 2009; 40: 166-172
  • 4 Lomaz MB, Netto LA, Filho MS, Alves AP, De Tavares Canto FR. Epidemiological profile of patients with traumatic spinal fracture. Coluna/Columna 2017; 16: 224-227
  • 5 Aleem IS, DeMarco D, Drew B. et al. The burden of spine fractures in India: a prospective multicentre study. Global Spine J 2017; 7: 325-333
  • 6 Singh G, Prakash R, Bhatti V, Mahen A. Spinal cord injury in organizational setup-a hospital based descriptive study. J Mar Med Soc. 2019; 21: 46-50
  • 7 Birua GJS, Munda VS, Murmu NN. Epidemiology of spinal injury in north east India: a retrospective study. Asian J Neurosurg 2018; 13: 1084-1086
  • 8 Srinivas B, Rajesh A, Purohit A. Factors affecting outcome of acute cervical spine injury: a prospective study. Asian J Neurosurg 2017; 12 (03) 416-423
  • 9 Katzberg RW, Benedetti PF, Drake CM. et al. Acute cervical spine injuries: prospective MR imaging assessment at a level 1 trauma centre. Radiology 1999; 213 (01) 203-212
  • 10 Martínez-Pérez R, Cepeda S, Paredes I, Alen JF, Lagares A. MRI prognostication factors in the setting of cervical spinal cord injury secondary to trauma. World Neurosurg 2017; 101: 623-632
  • 11 Schousboe JT. Epidemiology of vertebral fractures. J Clin Densitom 2016; 19: 8-22
  • 12 den Ouden LP, Smits AJ, Stadhouder A, Feller R, Deunk J, Bloemers FW. Epidemiology of spinal fractures in a level one trauma center in the Netherlands: a 10 years review. Spine 2019; 44: 732-739
  • 13 Hitti FL, McShane BJ, Yang AI. et al. Predictors of neurological outcome following subaxial cervical spine trauma. Cureus 2019; 11 (12) e6402
  • 14 Vazquez XM, Rodriguez MS, Peñaranda JM, Concheiro L, Barus JI. Determining prognosis after spinal cord injury. J Forensic Leg Med 2008; 15: 20-23
  • 15 Boldin C, Raith J, Fankhauser F, Haunschmid C, Schwantzer G, Schweighofer F. Predicting neurologic recovery in cervical spinal cord injury with postoperative MR imaging. Spine 2006; 31 (05) 554-559
  • 16 Tarawneh AM, D'Aquino D, Hilis A, Eisa A, Quraishi NA. Can MRI findings predict the outcome of cervical spinal cord injury? A systematic review. Eur Spine J 2020; 29: 2457-2464
  • 17 Wenger M, Adam PJ, Alarcón F, Markwalder TM. Traumatic cervical instability associated with cord oedema and temporary quadriparesis. Spinal Cord 2003; 41 (09) 521-526
  • 18 Singh R, Sharma S, Mittal R, Sharma A. Traumatic spinal cord injuries in Haryana: an epidemiological study. Indian J Community Med 2003; 13: 184-186
  • 19 Grauer JN, Vaccaro AR, Lee JY. et al. The timing and influence of MRI on the management of patients with cervical facet dislocations remains highly variable: a survey of members of the spine trauma study group. J Spinal Disord Tech 2009; 22: 96-99
  • 20 Hadley MN, Walters BC. The case for the future role of evidence-based medicine in the management of cervical spine injuries, with or without fractures. J Neurosurg Spine 2019; 31: 457-463
  • 21 Gelb DE, Hadley MN, Aarabi B. et al. Initial closed reduction of cervical spinal fracture-dislocation injuries. Neurosurgery 2013; 72: 73-83
  • 22 Passias PG, Poorman GW, Segreto FA. et al. Traumatic fractures of the cervical spine: analysis of changes in incidence, cause, concurrent injuries, and complications among 488,262 patients from 2005 to 2013. World Neurosurg 2018; 110: e427-e437
  • 23 Jain M, Mohanty CR, Doki SK. et al. Traumatic spine injuries in Eastern India: a retrospective observational study. Int J Crit Illn Inj Sci 2021; 11 (02) 79

Zoom Image
Fig. 1 Neurological outcome at 4 months (American Spinal Injury Association [ASIA] grade).