Research Article

Emergency Department Management Metrics for Severe Pediatric Traumatic Brain Injury

Maple Bohan Liu1, Tanya Holt2, Gregory Hansen2*

1College of Medicine, Department of Pediatrics, University of Saskatchewan, Saskatoon, Canada

2Jim Pattison Children’s Hospital, Division of Pediatric Intensive Care, Saskatoon, Canada

Corresponding Author*: Gregory Hansen, Jim Pattison Children’s Hospital. 103 Hospital Drive. Pediatric Intensive Care Unit. Saskatoon, Saskatchewan, Canada.

Received Date: 28 September 2021

Accepted Date: 07 October, 2021

Published Date: 11 October 2021

Citation: Liu MB, Holt T, Hansen G. (2021) Emergency Department Management Metrics for Severe Pediatric Traumatic Brain Injury. Emerg Med Inves 6: 10112. DOI: 10.29011/2475-5605.010112


Background: As the majority of severe pediatric traumatic brain injuries (TBI) are received and managed in the emergency department (ED), the ED trauma center is vital to optimizing management. This study aimed to evaluate current management guidelines, and to recognize other high-risk components of TBI management.

Methods: A retrospective chart review was conducted solely at the Jim Pattison Children’s Hospital in Saskatoon, Canada. Data pertaining to severe pediatric brain injury in emergency department included transport to trauma center, injury severity, indicators for raised intracranial pressure, airway and breathing, circulation, disability/central nervous system, complications, and outcome scores.

Results: A total of 56 charts were included in the study population. Mean age of patient population was 14.3 years of age, with 76% being male. Thirty four percent of patients received a blood gas within 15 minutes of admission, and 20% received intervention to correct PCO2. Of the seven patients who received hyperosmolar therapy, three were based on computed tomography (CT) findings and four were based clinically. For 95% of patients, the position of the bed was not documented, and just 4% of patients had head of bed elevated to 30 degrees. Sixty four percent of patients were accompanied by a physician with airway expertise during CT.

Conclusion: Building on current TBI guidelines, timeliness of PCO2 retrieval and improvements for targeted hyperosmolar therapy were noted. Two other potential areas for improving management included deliberate considerations for head of bed positioning and personnel accompanying patients undergoing CT.

Keywords: Brain injuries; Children; Traumatic; Quality improvement


Traumatic brain injury (TBI) is the leading cause of residual disability and injury-related mortality in North American children [1-4]. Consequently, it is crucial to understand prognostic factors involved in improving outcomes that can be implemented in the management of this patient population. Although risk factors and mortality in adult TBI have been well studied, evidence in children is less robust [5]. Adherence to severe TBI guidelines [6] in pediatrics has been associated with higher discharge survival and improved Glasgow Outcome Scale (GOS) scores [5]. The emergency department (ED) is an important consideration [2], as it receives and provides timely management to the majority of injuries. To date, there have been two multi-center studies that examined ED adherence to pediatric TBI guidelines. A large multi-center study from Argentina observed 6 ED adherence parameters relating to hypoxia, hypotension, disability, and hyperosmolar therapy [7]. The second was the Pediatric Guideline Adherence and Outcomes Study (PEGASUS) group who included five ED adherence measures relating to management of hypoxia, hypotension, temperature, and hyperosmolar therapy [4]. Although the group from Argentina did not a find significant association between adherence to pediatric TBI guidelines and improved survival and outcome scores, the PEGASUS group did demonstrate a positive association [4,7]. Evaluating ED management of severe pediatric TBI with the aforementioned parameters may be missing key elements of care. This retrospective study aimed to expand on published ED adherence parameters through the application of current TBI guidelines [6] and recognition of high-risk components of TBI management in children. Areas of management addressed included; airway and breathing, circulation, disability, investigations, and specific neuroprotective therapies. We hypothesized that areas of ED management could be improved, in a province that has significant barriers regarding lengthy interfacility transports from rural, remote, and isolated communities [8]. 

Materials and Methods

Study Center

This study was a retrospective chart review that was conducted at the Jim Pattison Children’s Hospital (JPCH) in Saskatoon, Canada.

Population and criteria

Eligible individuals were identified through medical records and a Pediatric Intensive Care Unit (PICU) registry. Inclusion criteria included: patients ≤ 18 years, severe TBI defined as Glasgow Coma Scale (GCS) score of ≤ 8 prior to triage in the JPCH ED, injury from 2010 to 2018, Head Abbreviated Injury Scale (AIS) score of ≥ 3, TBI ICD codes (800-801.9, 803-804.9, 850-854.1, or 959.01) and triaged in the ED. Increased intracranial pressure (ICP) at the ED was defined by i) craniotomy with 12 hours of admission; or, ii) herniation syndrome or midline shift > 5 mm on neuroimaging; or, iii) raised ICP monitoring of > 20 mm cm H2O within 12 hours of admission. Exclusion criteria included death prior to arrival of ED.

Emergency Department Metrics

An exhaustive list of potential management indicators was created by a pediatric neurointensivist and neurosurgeon with experience in traumatic brain injury. Indicators and metrics were considered if they were consistent with TBI guidelines, clinically relevant, and accessible through a retrospective chart review. It was then vetted through a focus group which comprised of 3 pediatric intensivists, two neurosurgeons, and four emergency physicians. Modifications to the list ensued, followed by a final focus group review. Items required a 75% majority to be included. The final metrics included: a) position of head of bed (HOB); b) position of head (C-spine precaution); c) time of first temperature check; d) temperature treated in 30 minutes if <36 or >37.5°C; e) hypoxia treated in 30 minutes after onset; f) systemic hypotension [SBP < 70 + 2 (age) or MAP < 40 + 1.5 (age)] treated within 30 minutes of admission; g) blood gas CO2 obtained within 15 minutes of admission; h) ETCO2 monitoring; i) blood gas CO2 corrected within 5 minutes if <35 or >40; j) clinical seizures treated within 10 minutes of onset; k) timing of admission to labs including glucose, CBC, differential and electrolytes; l) timing of admission to computed tomography (CT); m) complications in CT (i.e. herniation, unplanned extubation); n) personnel with patient in CT; o) indications to administer hyperosmolar therapy; and, p) timing of admission to either neurosurgical operating room or PICU.


Patient identifiers included age, weight, gender, and mechanism of injury (including motor vehicular collision, fall, pedestrian vs. vehicle, gunshot, assault, bicycle). Pre-trauma center metrics included time of injury to arrival at trauma center, distance of scene to trauma center (if beyond urban emergency medical services catchment), and mode of transport (ground, fixed wing, helicopter EMS). Injury severity was documented with Head AIS and Pediatric Risk of Mortality (PRISM) score. Raised ICP at trauma center was defined as craniotomy within 12 hours of admission, raised ICP > 20 cm H2O within one hour of placement, and ED neuroimaging suggesting herniation syndrome or midline shift > 5 mm). ED TBI metrics were discussed above. Outcomes included: day 1 mortality, mortality, comfort care at admission, length of PICU stay, length of hospital stay, and GOS scores of survivors.

Statistical Methods

All analyses were be done using SPSS software. Discrete variables were reported as percentages, and continuous variables were reported as median and interquartile ranges.


Of the 57 charts identified through the registry, a total of 56 charts were included in the study population. Patient demographics, mechanism of injury and first responder data are summarized in Table 1. Metrics for airway, breathing, circulation and disability are summarized in Table 2. Of note, 34% (n=19) of patients received a blood gas within 15 minutes of admission and 20% (n=11) received interventions to achieve PCO2 between 35-40mmHg. Conversely, with regard to hypotension, the majority received corrective intervention within 15 minutes of identification. The HOB was elevated to 30 degrees for 4% (n=2) of patients, and was not documented for most (95%). Thirteen percent (n=7) of patients demonstrated radiographic signs of herniation on CT. Metrics for CT, and therapies directed at raised ICP is summarized in Table 3. Among the 8 patients (14.3%) who died in hospital, 5 died on day one of hospital stay. Four patients (7.1%) required comfort care on discharge. Length of PICU stay and hospital admission averaged 9.5 (SD 8.3) and 22.9 (SD 24.6) days, respectively. Median GOS on discharge was 3 (range 3 to 5).


The purpose of this study was to evaluate application of standard therapy guidelines and recognize other risk factors with regard to the management of severe pediatric TBI in the ED. Two key findings from this study relate to metrics outlined in current TBI guidelines; timeliness for retrieval of first PCO2, and indications for hyperosmolar therapy. Two non-guideline metrics showed that the HOB was not elevated in a large majority of our patients, and an inconsistent presence of physicians with airway expertise accompanying patients to the CT scanner. One of the deficiencies we reported was a timely retrieval of PCO2. Cerebral blood flow varies proportionally with PCO2 and is the most important factor that balances ICP exacerbation with adequate cerebral oxygenation [9]. Although most patients received EtCO2 monitoring within fifteen minutes of ED admission, a blood gas was obtained in only 34% of our patients during this time, and even fewer received corrections to maintain target normocapnia. Targeted ventilation in the ED has been well documented for optimal discharge outcomes in patients with normocarbia (PaCO2=36-45mmHg), and increased mortality with hypocapnia and hypercapnia (PaCO2 ≤35mmHg, and ≥46mmHg, respectively) [9]. As important, EtCO2 is not an adequate initial surrogate for PCO2 in pediatric patients with severe TBI, but its trend can be useful between PCO2 retrieval times [10,11]. This study also gathered data around hyperosmolar therapy administration based on clinical and radiological signs of raised ICP. Although the gold standard for ICP monitoring is placement of an intracranial monitor, it is obviously not feasible during the initial resuscitation in the ED [12,13]. The most challenging part of targeted hyperosmolar therapy in severe TBI has been the proper identification of increased ICP. Thirteen of our patients received hyperosmolar therapy, with an even split between CT and clinical indication for its use. Clinically changes in Glasgow Coma Scale, pupillary reactivity, and herniation syndrome are often late signs of raised ICP. Radiographically, a CT scan can be inconclusive in quantifying ICP after severe TBI [13,14], unless obvious criteria have been met. Together, they point to the utility of more novel techniques of reliably and rapidly estimating ICPs , such as transcranial dopplers or ultrasonography of optic nerve sheath diameters [12].

Adult ED management guidelines by the Seattle International Brain Injury Consensus Conference included elevation of HOB to 30-45o as an intervention [15]. HOB elevation can have beneficial effects on raised ICP by facilitating cerebral blood flow, increasing cerebrospinal fluid drainage, and maximizing cerebral venous return [16,17]. Although our study found that only 4% of patients had their HOB elevated, current pediatric TBI guidelines do not address this potential therapy. One hesitation may have been adherence to spinal precautions, but reverse Trendelenburg should not cause spine flexion and allows for HOB elevation. Interestingly, the wide range of HOB elevation recommendations in adults is likely indicative of patient height variations and consequential hydrostatic differences between skull base and heart level [17]. Given the known beneficial effects of elevating the HOB including lowering ICP as well as other multisystem effects in severe TBI [18,19], we recommend it as a high-level priority in the initial ED management with normotensive patients.

Finally, we identified that brain CT in the ED may require further considerations. Our study found that 5% of patients experienced adverse events during CT scan, with only 65% of patients being accompanied by a physician with airway expertise. However, a recent national study examined CT practice standards for severe pediatric TBI across tertiary care centers in Canada, and found that over half of the respondents experienced an adverse event in CT [20]. These events, including airway complications may be avoided with the correct care team at bedside.

Major limitations in this study included the small population cohort, the nature of chart reviews, variability in pre-hospital care and a single trauma center cohort. Inherent in a chart-review, data collection relies on accurate chronicling, thus calling to question the certainty regarding absence of the expected management versus failure of documentation. This limitation was especially important regarding HOB position. Lastly, patients arrived to the tertiary care hospital with previous management outside of our documentation parameters. The scope of this study did not include pre-hospital management that may have affected ED management protocols on arrival.


This study compared ED management of pediatric severe TBI to guidelines, as well as novel parameters shown to affect TBI outcomes in adults. Although there are many areas of adherence to current recommendations, we would suggest further considerations around time metrics for obtaining PCO2, non-invasive bedside evaluations for raised ICP, raised HOB with normotensive patients, and medical personnel for CT scanning.

Availability of Data and Materials

All data are available from the corresponding author upon request.




GH and TH conceptualized the study. ML collected data and wrote the initial manuscript. GH conducted data analysis and interpretation. GH approved the final manuscript. All authors read and approved the final manuscript.

Ethics Approval

Ethics approval was obtained from the University of Saskatchewan Health Research Ethics Board (IRB).


Not applicable.

Conflict of Interest Statement

The authors declare no conflicts of interests.


Age in years*

14.3 ± 4.6

Male sex, n(%)

43 (76)

Mechanism of injury

MVC (%)

25 (45)

Fall, n (%)

4 (7)

Pedestrian vs vehicle, n (%)

5 (9)

Recreational vehicle, n (%)

5 (9)

Sports related, n (%)

3 (5)

Gunshot, n (%)

1 (2)

Other, n (%)

9 (16)

First responder data


4 (2-5)


12 (7-17)

Location in km*

161.8 ± 125.3

Lowest GCS+

3 (3-6)

Air transport (%)

30 (54)

Ground transport (%)

26 (46)

Intubated prior to arrival (%)

42 (75)

Event to ED (minutes)*

233.1 ± 117.1

*mean ± standard deviation; +median (interquartile range). AIS = abbreviated injury scale, ED = Emergency Department, GCS = Glasgow Coma Scale, MVC = motor vehicle collision, PRISM = Pediatric Risk of Mortality Score.

Table 1: Patient characteristics and first responder data (n = 56).



Intubated in ED, n (%)

12 (21)

Time of intubation in minutes*

22.1 ± 14.7

Hypoxia, n (%)

3 (5)

Hypoxia treated, n (%)

2 (67)

Blood gas within 15 min., n (%)

19 (34)

If no blood gas within 15min., how long in minutes*

39.7 ± 26.8

EtCO2 obtained, n (%)

37 (66)

If EtCO2 obtained, how long after intubation in minutes

13.9 ± 25.2

CO2 corrected, n (%)

11 (20)


Systolic hypotension, n (%)

9 (16.)

Systolic hypotension corrected within 15min., n (%)

6 of 9 (67)

MAP hypotension, n (%)

7 (13)

MAP hypotension corrected within 15min., n (%)

7 of 7 (100)


Pupils checked, n (%)

48 (86)

Time of pupil check in minutes*

4.8 ± 12.1

GCS checked, n (%)

55 (98)

Position of bed not documented, n (%)

53 (95)

Position of bed 30 degrees, n (%)

2 (4)

C-spine precautions, n (%)

54 (96)

Temperature checked, n (%)

43 (77)

Time of temperature check in minutes*

21.7 ± 35.2

Abnormal temperature treated, n (%)

6 (11)

Clinical seizures, n (%)

4 (7)

If seizures, when treatment initiated in minutes*

6.5 ± 5.2


Labs taken, n (%)

53 (95)

Time to first labs in minutes*

31.5 ± 29.4

*mean ± standard deviation. ED = emergency department; EtCO2 = end-tidal CO2; GCS = Glasgow Coma Scale; MAP = mean arterial pressure.

Table 2: Measures for airway, breathing, circulation, disability (n = 56).

Indicators of raised ICP


Herniation, n (%)

5 (8.9)

Midline shift, n (%)

2 (3.8)

Emergent craniotomy, n (%)

6 (10.7)


Time to CT in minutes*

77 ± 29.1

Personnel: not charted, n (%)

31 (55.4)

Personnel: MD with airway expertise, n (%)

16 of 25 (64)

Complications in CT, n (%)

3 (5.4)

Hyperosmolar therapy

Therapy provided, n (%)

7 (12.5)

Time to hyperosmolar therapy in min.

38.6 ± 15.2

Indication: CT findings, n (%)

3 (42.9)

Indication: clinical, n (%)

4 (47.1)

Operating room

Time to neurosurgical OR in minutes

114 ± 80.7

*mean ± standard deviation. ICP = intracranial pressure; OR = operating room.

Table 3: Patient data regarding intracranial pressures and therapies (n = 56).


  1. Keenan HT, Bratton SL. (2006) Epidemiology and outcomes of pediatric traumatic brain injury. Dev Neurosci 28: 256-263.
  2. Langlois JA, Rutland-Brown W, Thomas KE. (2005) The incidence of traumatic brain injury among children in the United States: differences by race. J Head Trauma Rehabil 20: 229-238.
  3. Coronado VG, Xu L, Basavaraju SV, McGuire LC, Wald MM, Faul MD, et al. (2011) Surveillance for traumatic brain injury-related deaths - United States, 1997-2007. MMWR Surveill Summ 60: 1-32.
  4. Vavilala MS, Kernic MA, Wang J, Kannan N, Mink RB, Wainwright MS, et al. (2014) Acute care clinical indicators associated with discharge outcomes in children with severe traumatic brain injury. Crit Care Med 42: 2258-2266.
  5. Amagasa S, Tsuji S, Matsui H, Uematsu S, Moriya T, Kinoshita K (2018) Prognostic factors of acute neurological outcomes in infants with traumatic brain injury. Childs Nerv Syst 34: 673-680.
  6. Kochanek PM, Tasker RC, Carney N, Totten AM, Adelson PD, Selden NR, et al. (2019) Guidelines for the Management of Pediatric Severe Traumatic Brain Injury, Third Edition: Update of the Brain Trauma Foundation Guidelines. Pediatr Crit Care Med 20: S1-S82.
  7. Vavilala MS, Lujan SB, Qiu Q, Petroni GJ, Ballarini NM, Guadagnoli N, et al. (2016) Benchmarking prehospital and emergency department care for Argentine Children with traumatic brain injury: for the South American guideline adherence group. PLoS ONE 11: e0166478.
  8. Hansen G, Vallance JK. (2015) Ventilation Monitoring in Severe Pediatric Traumatic Brain Injury at Nontrauma Centers. Air Med J 34: 278- 282.
  9. Ramaiah VK, Sharma D, Ma L, Prathep S, Hoffman NG, Vavilala MS. (2013) Admission oxygenation and ventilation parameters associated with discharge survival in severe pediatric traumatic brain injury. Childs Nerv Syst 29: 629-634.
  10. Hansen G, Vallance JK (2015) Ventilation monitoring for severe pediatric traumatic brain injury during interfacility transport. Int J Emerg Med 8: 41.
  11. Martinon C, Duracher C, Blanot S, Escolano S, De Agostini M, Périé-Vintras AC, et al. (2011) Emergency tracheal intubation of severely head-injured children: changing daily practice after implementation of national guidelines. Pediatr Crit Care Med 12: 65 - 70.
  12. Narayan V, Mohammed N, Savardekar AR, Patra DP, Notarianni C, Nanda A. (2018) Noninvasive intracranial pressure monitoring for severe traumatic brain injury in children: a concise update on current methods. World Neurosurg 114: 293-300.
  13. Pappu S, Lerma J, Khraishi T (2016) Brain CT to assess intracranial pressure in patients with traumatic brain Injury. J Neuroimaging 26: 37-40.
  14. Vavilala MS, Lujan SB, Qiu Q, Bell MJ, Ballarini NM, Guadagnoli N, et al. (2017) Intensive care treatments associated with favorable discharge outcomes in Argentine children with severe traumatic brain injury: for the South American Guideline Adherence Group. PLoS One 12: e0189296.
  15. Miles DK, Ponisio MR, Colvin R, Limbrick D, Greenberg JK, Brancato C. et al. (2020) Predictors of intracranial hypertension in children undergoing ICP monitoring after severe traumatic brain injury. Childs Nerv Syst 36: 1453-1460.
  16. Tasker RC (2012) Intracranial pressure: influence of head-of-bed elevation, and beyond. Pediatr Crit Care Med 13: 116-117.
  17. Agbeko RS, Pearson S, Peters MJ, McNames J, Goldstein B (2012) Intracranial pressure and cerebral perfusion pressure responses to head elevation changes in pediatric traumatic brain injury. Pediatr Crit Care Med 13: e39- 47.
  18. Bennett TD, Statler KD, Korgenski EK, Bratton SL (2012) Osmolar therapy in pediatric traumatic brain injury. Crit Care Med 40: 208- 215.
  19. Fan JY (2004) Effect of backrest position on intracranial pressure and cerebral perfusion pressure in individuals with brain injury: a systematic review. J Neurosci Nurs 36: 278-288.
  20. Yoo G, Leach A, Woods R, Holt T, Hansen G (2020) Computed tomography practice standards for severe pediatric traumatic brain injury in the emergency department: a national survey. J Child Adol Trauma 14: 271-276.

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