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Outcomes and associated factors of traumatic brain injury among adult patients treated in Amhara regional state comprehensive specialized hospitals

Abstract

Background

Globally, traumatic brain injury is the leading cause of death and disability which affects more than 69 million individuals a year.

Objective

This study aimed to assess the outcome and associated factors of traumatic brain injury among adult patients treated in Amhara regional state comprehensive specialized hospitals.

Method

Institutional-based cross-sectional study design was conducted from January 1, 2018, to December 30, 2020. A simple random sampling technique was used and a checklist was used to extract data between March 15 and April 15, 2021. The data were entered into Epi-data version 4.2 and exported to SPSS version 25 for analysis after being checked for consistency. Associated variables with outcomes of traumatic brain injury were determined by a binary logistic regression model. The degree of association was interpreted by using AOR and a 95% confidence interval with a p-value less than or equal to 0.05 at 95% CI was considered statistically significant.

Result

In this study road traffic injury was the most frequent cause of traumatic brain injuries among adult patients, accounting for 181 (37.5%), followed by assault, accounting for 117 (24.2%) which affects adult age groups. One-third of the participant had a moderate Glasgow coma scale of 174(36%). Only 128(26.8%) patients arrived within one hour. One hundred sixty, 160 (33.1%) of patients had a mild traumatic brain injury, whereas, 149(36%) of patients had a severe traumatic brain injury. Regarding computerized tomography scans findings, the hematoma was the most common (n = 163, 33.7%). Ninety-one, 91(18.8%) of participants had cerebrospinal fluid otorrhea, and, 92(19%) were diagnosed with a positive battle sign. The overall prevalence of unfavorable outcomes after traumatic brain injury was found to be 35.2% (95%CI (30.8–39.1). Having additional Injury, hypoxia, time to hospital presentation after 24 h, severe Glasgow Coma Scale, moderate Glasgow Coma Scale, tachypnea, bradypnea, and cerebrospinal fluid Othorrhea, were factors associated with unfavorable outcomes.

Conclusion and recommendation

In this study, the overall unfavorable outcome was experienced by about four out of every 10 victims of traumatic brain injury. Time of arrival > 24 h, low Glasgow coma scale, additional injury, Cerebrospinal fluid otorrhea, abnormal respiration, and hypoxia were significant predictors of unfavorable outcomes. To reduce the adverse effects of traumatic brain injury in adults, it is therefore desirable to guarantee safe road traffic flow and improve health care services.

Peer Review reports

Introduction

Traumatic brain injury is a disruption of the brain structure with its function caused by the application of an external source which is manifest as confusion, loss of consciousness, coma, or seizure [1]. Based on the World Health Organization (WHO) report RTA is the 8thleading reason of death, and each year 1.35 million people are estimated to die due to RTA [2]. Globally, TBI is estimated that affects 69 million individuals each year; low and middle-income countries (LMICS) have three times higher burden of TBI than high-income countries, according to the WHO report. Internationally, TBI is the leading cause of death and disability [3,4,5].

In the United States of America, TBI is the commonest cause of mortality and disabilities. Annually, more than 2.8 million TBI cases were recorded with a 2% of death rate. Among those who survived, most of them experience several short and long-term impacts throughout their lives including thinking ability, physical activity, and loss of sensation like hearing and sight, emotional abnormality like depression. Furthermore, it has also impacted the lives of their families and thereby community [6, 7]. Besides, it results in immediate disruption of the brain function or it has lifelong mental or physical complications, and annually it is estimated worldwide greater than 50 million people may suffer from TBI complications and about half of the world population is expected to get one or more TBI within the lifetime [8]. Furthermore, studies showed that patients with a history of brain injury were significantly related to the chance of developing Parkinson's disease, epilepsy, stroke, and other neurological diseases this association is more common in different countries [9,10,11].

Additionally, death after the occurrence of TBI had been reduced; but the greatest number of severe TBI required long-term rehabilitation and these patients are suffering from the complication of TBI, which also has a consequence on social and economic costs [12].

Several studies suggested that early prevention of TBI is important to save lives, minimize disabilities and reduce healthcare-related costs. Regarding prevention strategies, giving priority to road traffic safety was found to be successful in some countries. Inappropriate use of motor vehicles in LMIC, infrastructural problems, and unable to use safety measures was found to increase the occurrence of TBI [13,14,15]. Likewise in our country, the pooled prevalence of TBI was reported at 20% and it is the leading reason behind mortality and disability, since RTA is the commonest cause of TBI the federal government has proclaimed the rules and regulations about the prevention strategies, but still mortality and severe disability were significantly associated with RTA [16, 17]. The global incidence rate of traumatic brain injury TBI is estimated at 200 per 100 000 people per year with wide variation in developed and developing countries [18]. During the COVID-19 pandemic era the challenges in treatment of the TBI in such countries were tremendous [19]. A similar recent report from Ethiopia also showed road traffic injury was the commonest cause of TBI. Increasing availability of radiological imaging scans and early resuscitations and surgical interventions are abetting in decreasing the mortality in recent years [20]. Prevention of hypoxia and maintaining cerebral perfusion pressure are imperative for favorable outcome. Kohler et al. have suggested narrative interviews, participatory diagramming and discrete event simulation as one possible suite of methods deliverable within an international partnership for boosting of outcome in developing countries like Ethiopia [21]. Different studies found in Africa and our country Ethiopia suggested that TBI is the leading cause of death and disability in addition to this the main reason for TBI was RTA [22,23,24,25]. As is the case globally, traumatic brain injury is a leading cause of morbidity and mortality in Ethiopia [8]. Road traffic incidents (RTI) are the greatest cause of TBI and substantial efforts have been undertaken to reduce RTIs in Ethiopia [26].

Despite these measures, the high incidence of TBI remains a major cause of disability that requires further study and public health intervention. As far as the researcher's search no related study has been undertaken so far in the study area. Therefore, this study aimed to assess the outcome and its associated factors of TBI among Patients Treated for traumatic brain Injury at the comprehensive specialized hospitals of the Amhara region, Ethiopia. 2021.

Methods

Study design and study period

An institutional-based retrospective cross-sectional study design was conducted on TBI patients who visited the comprehensive specialized hospitals of the Amhara region hospitals from January 1, 2018, to December 30, 2020,

Study setting

The study was conducted in the comprehensive specialized hospitals of the Amhara national regional state in Ethiopia. Amhara national regional state is one of Ethiopia's federal republics, with an approximate land area of 170,000 square kilometers [41]. The territory is divided into 12 administrative zones, three city administrations, and 83 districts. According to the Ethiopian twelve-month report for 2020, the region's total population projection is 22,191,890 people (11,317,864 men and 10,874,026 women), and the Amhara national regional health bureau's annual performance report shows the region has 81 hospitals, 858 health centers, and 3560 health posts. Among hospitals eight of them are comprehensive specialized hospital; these are the University of Gondar, Dessie, Felege-Hiwot, Tibebe-Ghion, Debre-Markos, Waldiy, Debre Tabor, and Debebirhan comprehensive specialized hospital which serves the population within the region [42]. These hospitals provide surgical, medical, pediatric, maternal, and other types of care to their patients. These hospitals have specialty units for cardiology, respiratory, neurology, dermatology, and sexually transmitted diseases, as well as gastroenterology, infectious diseases, orthopedics, gynecology and obstetrics, hematology, and intensive care units. Five comprehensive specialized hospitals were chosen by simple random lottery methods from a total of eight Comprehensive Specialized Hospitals those are University of Gondar, Felege-Hiwot, Tibebe-Ghion, Debre-Markos, and Debre-Berhan compressive specialized hospital. Thus, all those eight comprehensive specialized hospitals serve the population found in the region [27]. These hospitals provide specialized outpatient and inpatient services in different departments including emergency, surgical, internal medicine, gynecology & obstetrics, psychiatry, intensive care units (neonatal, pediatrics, and adult surgical and medical), ophthalmology, pediatrics, and oncology. Each hospital provides services for an estimated five million population. The hospitals have their organized trauma or surgical emergency departments, surgical wards, and surgical intensive care units [28]. The University of Gondar comprehensive specialized hospital is a referral tertiary care center with more than 600 beds located in the Amhara region, Northwest Ethiopia with a catchment population of more than 8 million people. In addition to general medical services, it provides advanced subspecialty surgical services including cardiothoracic surgery, neurosurgery, hepato-pancreatic-biliary surgery, pediatric surgery, urogynecology, and gynecologic oncology surgical services. There are around 20 general and subspecialist surgeons, 5 orthopedic surgeons, 20 general and subspecialist gynecologists/obstetricians, one anesthesiologist, and more than 30 anesthesia providers. It has also around 100 beds dedicated to surgical patients and 30 beds dedicated to gynecologic cases. It has 7 major operation theaters, 2 minor ORs, 2 obstetric ORs, and 2 urogynecology procedures. It has a 6 bedded surgical ICU dedicated to trauma and post-operative patients. On normal days, the hospital handles more than 50 OPD surgical cases, 5–6 elective operations, 4–5 elective gynecologic procedures, and 8–10 surgical and 5–10 obstetric emergency operations each day on average. The hospital uses an HMIS patient data recording system at surgery and gynecologic OPDs, at each ward, and all operation theaters record each patient profile, and the data is reported to the HMIS center monthly and annually.

Population

Source population

The source population for this study was all patients presented with traumatic head injury attended in Amhara region comprehensive specialized hospitals.

Study population

Adult Patients presented in Amhara region comprehensive specialized hospitals, with the diagnosis of traumatic brain injury from January 1, 2018, to December 30, 2020, were the study population.

Eligibility criteria

Inclusion criteria

All records of TBI patients who visited the comprehensive specialized hospitals of the Amhara region from January 1, 2018, to December 30, 2020, whose ages were above 18 years, were included in this study.

Exclusion criteria

Incomplete charts like missed outcome record, GCS score, time to arrival, conservative management, and loss from the record office due to consultation, transfer, or any other medical reason like neurological dysfunction before the occurrence of TBI, and death on arrival were excluded.

Study variables

The dependent variable for this study is the Outcomes of Traumatic brain injury. The Independent variables are Socio-demographic factors( Age, sex, mode of arrival, source of referral, and area of residence), Patients condition at admission, Mechanism of injury, Time of arrival after injury, GCS on admission, the severity of the head injury, the occurrence of Co-existing injury, Type of co-existing injuries, comorbidity, pupillary reactivity, use of steroids, and Intervention taken, Clinical factors(Blood pressure, Respiratory rate, Pulse rate, O2 saturation, Blood glucose level, loss of consciousness, convulsion, battle sign, cerebrospinal fluid leakage, length of hospital stay and increase intracranial pressure), diagnostic factors, and CT-scan results.

Operational definitions and definition of terms

GOS-Glasgow coma Outcome Scale was a multi-dimensional scale that assesses various aspects of outcome which are listed below:-

  • Death (GOS category 1) – patients were certified for death

  • Vegetative state (GOS category 2)–the patient exhibited no obvious cortical function

  • Severe disability (GOS category 3) –patients were conscious but disabled, those patients could not perform any activity independently.

  • Moderate disability (GOS category 4) – (disabled but independent) Those patients were independent as far as daily life was concerned the disabilities found include varying degrees of dysphasia and hemiparesis.

  • Good recovery (GOS category 5)–Resumption of normal activities even though there may be minor neurological or psychological deficits

  • Unfavorable outcome – was for the patient with GOS scored 1–3

  • Favorable outcome – was for the patient with GOS scored 4 and 5

  • GCS- was used to assess the neurological status of the patient.

  • Mild traumatic brain injury:—was an injury to the head with a Glasgow coma scale between 13 and 15.

  • Moderate traumatic brain injury:—was an injury to the head with Glasgow coma scales between 9 and 13.

  • Severe traumatic brain injury:—was an injury to the head with a Glasgow coma scale less than or equal to 8.

Sample size determination

The sample size was determined by using EPI info Version 7 statistical software to determine a single population proportion formula by considering the following assumptions. Based on the previous study, the proportion outcome of TBI 25.1% was taken from a cross-sectional study conducted in Nekemte in 2020 [29].

P = proportion of unfavorable outcome was (25%).

Z α/2 = the corresponding Z score of 95% CI,

d = Margin of error (4%) and.

n = required Sample size

$$\begin{array}{c}\mathbf{n}=\frac{{(\mathbf{Z}\mathrm{\alpha }/2)}^{2}\times \mathbf{p}(1-\mathbf{p})}{{(\mathbf{d})}^{2}}\\ \mathbf{n}=\frac{{(1.96)}^{2}\times (1-0.25)}{{(0.04)}^{2}}\\ \mathbf{n}=450\end{array}$$

The final sample size by adding a 10% nonresponse rate was 495.

For the second objective, by taking some of the significantly associated variables with an unfavorable outcome the sample size was determined through double population proportion formula using version 7 Epi info software (Table 1).

Table 1 sample size determination by using factors associated with TBI

Sampling technique and procedures

The sample was selected with a simple random sampling technique thorough review of the patient's chart which is diagnosed with TBI for the last three years. The patient's medical record number was taken from the hospital ward registration book as a frame; the sample was proportionally allocated for each hospital. The final sample size of four hundred ninety-five was selected by using a simple random sampling method through the lottery method (Fig. 1).

Fig. 1
figure 1

Sampling procedure for the outcome and its associate factors of TBI among adults who were treated for a head injury at comprehensive specialized hospitals Amhara region

Data collection tools and procedures

The outcome and explanatory variables were collected through data extraction tool which was adopted from different literature [30,31,32,33,34,35]. And the data was recorded on structured checklists through a retrospective review of the patient charts. The data was collected by ten BSc nurses, after receiving one-day training on data collection tools and techniques. All the variables of interest were assessed accordingly. The questionnaire comprises five parts. Those socio-demographic factors, patient condition at admission, clinical profile, diagnostic factors, and outcome of TBI, Glasgow coma outcome scale (GOS) were used to assess the patient's outcome. This is a multidimensional outcome assessment scale it assessed the different aspects of outcomes. It has five categories based on that, GOS of I-III was considered as the unfavorable outcome, and GOS of IV, V was considered as a favorable outcome for statistical analysis which is taken through reviewing different studies [30, 31, 35]. This outcome assessment scale was introduced by Jennet and Bond in 1975. It has been widely used to describe the outcome of patients with a head injury. It has a high degree of validity (80%) and reliability (95%). The extraction tools for the assessment of associated factors are adapted from different related literature [29, 31, 33, 36].

Data quality control

Different measures were taken to assure the quality of the data. The first measure was giving training for data collectors (ten BSc nurses) on how to extract data using the data abstraction format prepared for the study. To assess the clarity of the variable, a pre-test was done at 5% (25 medical charts) of the calculated sample size two weeks before the actual data collection at the University of Gondar comprehensive specialized hospital, those charts were excluded from the final study to check the validity and reliability of the collected data. After the pre-test, Ambiguous words and concepts were corrected accordingly. Throughout the data collection, data collectors were supervised by five MSc nurses. The collected data were checked by the supervisor daily for completeness and finally, the collected data were reviewed and checked for completeness before data entry; the incomplete data was discarded.

Data processing and analysis

Data was checked manually, coded, and entered into Epi-Data Manager version 4.2, and it was exported to SPSS version 25 for analysis. Cross-tabulation was done to assess the distribution of favorable and unfavorable outcomes and the data was processed by carrying out simple descriptive statistics. The frequency with percentage distribution was used for categorical variables. Model goodness-of-fit was checked by the Hosmer–Lemeshow test. After checking the multi-collinearity each independent variable with a p-value < 0.25 in the bivariate analysis was included in multivariable logistic regression to control confounders. And finally, the variables which have an independent association with outcomes of TBI were identified based on AOR, with 95% CI and p-value less than 0.05 to measure the strength of association and identify statistical significance. Finally, the data was presented in the form of text, tables, and charts.

Results

Socio-demographic characteristics of the study participants

A total of 495 adult charts with the diagnosis of traumatic brain injury (TBI) were reviewed by using data extraction tools and included in the analysis with a response rate of 483(97.5%). Out of the total respondents, 296(61.2%) were male. The majority of the study participants 169(35%) were in the age group of 24–34 years. More than two-thirds 293(60.7%) were urban residents. More than two-thirds 293(60.7%) were urban residents. Out of the total 483 trauma patients, 320(66.2%) were transported to the hospital by ambulance followed by Bajaj 141(29.2%). Two hundred twenty-nine (47.4%) study participants were referred from the Health center followed by hospital 199(41.2%) (Table 2).

Table 2 Socio-demographic characteristics of favorable and unfavorable outcomes among adult patients in comprehensive specialized hospitals of Amhara regional state, Ethiopia 2021 (n = 483)

Patient’s condition on admission and treatment-related factors

A road traffic accident was the leading cause of injury 181(37.5%) followed by assault 117(24.2%). One-third 86(34.4%) of trauma patients sustained maxillofacial injury and nearly one-fourth 58(23.2%) of the study participants had an abdominal injury. Twenty-four (9.6%) of trauma patients had poly-trauma. In one hundred twenty-eight cases 132(27.3%) arrived at the health care facilities they received care from the scene greater than 24 h followed (by 26.8%) within 1 h, 106(21.9%), within 1–4 h, and 117(24.2%) 4–24 h from the incident regardless of the mode of arrival (Table 3).

Table 3 Patient's condition on the admission and treatment-related factors of favorable and unfavorable outcomes among adult patients treated in comprehensive specialized hospitals of Amhara regional state, Ethiopia 2021 (n = 483)

Clinical characteristics

A significant number of the respondents 314(65%) had a loss of consciousness. Of the total respondents, 91(18.8%) respondents had CSF otorrhea and from the total sample charts, 92(19%) were diagnosed with a positive battle sign (Table 4).

Table 4 Clinical characteristics of favorable and unfavorable outcomes among adult patients treated in comprehensive specialized hospitals of Amhara regional state, Ethiopia 2021 (n = 483)

Outcomes of traumatic brain injury

From the total of 483 respondents, the outcome of the patient after traumatic brain injury on discharge was assessed based on GOS, and a large number of respondents, 277(57.3%) had a good recovery and among those unfavorable outcomes, 120(24.8%) died. For better analysis, the above outcomes are divided into two categories by using GOS such as favorable outcomes (64.8%) which consist of moderate disability and good recovery, and Unfavorable outcomes (35.2%) which consist of death, vegetative state, and severe disability (Fig. 2).

Fig. 2
figure 2

Outcome of Traumatic brain injury among patients treated in comprehensive specialized hospitals of Amhara regional state, Ethiopia 2021

Factors associated with outcomes of traumatic brain injury

As can be noted from the result of the bivariable analysis, eleven of the twenty-six variables show a significant association with the unfavorable outcome at the 95% level of significance. Those eleven variables were entered in the multivariable logistic regression at 0.25 level of significance multivariable logistic regression was done by taking eleven variables into account simultaneously. Five variables that showed significant association with unfavorable outcomes in the bivariable analysis could not persist as significant in the multivariable analysis. In the multivariable logistic regression analysis, after controlling the possible confounders; additional injury, low GCS on admission, abnormal respiration (tachypnea and bradypnea), and time of arrival after 24 h, hypoxia, and CSF otorrhea were statistically significant with the unfavorable outcome at p-value < 0.05.

Having additional injury showed a significant association with unfavorable outcomes. The odds of having an unfavorable outcome from TBI were 4.8 times higher in those who had additional injury than the counterpart [AOR = 4.844; 95% CI [2.532- 9.267]. This study showed that the odds of having unfavorable outcomes from TBI were 4.6 times more associated in those hypoxemic patients than those who were in normal oxygen status [AOR = 4.615; 95% CI (2.608–8.169]. Patients who were attending the hospital after 24 h after injury were two times higher to develop unfavorable outcomes than those who arrived less than one hour [AOR = 2.041; 95% CI [1.073- 3.882]. The odds of having an unfavorable outcome are two folds higher among patients with severe Glasgow coma scale [AOR = 2.142; 95% CI (1.196- 3.836], likewise the odds of having unfavorable outcome from TBI were 2.2 times higher for those patients with moderate Glasgow coma scale [AOR = 2.276;95% CI (1.308- 3.960] as compared to those who had mild Glasgow coma scale. The finding of this study showed that the odds of having unfavorable outcomes from TBI were 2.8 times higher in those who had CSF Othorrhea as compared to those without CSF leakage [2.884; 95%CI (1.417–5.870] (Table 5).

Table 5 Bivariable and multivariable logistic regression analysis result for significant variables among adult patients treated for traumatic brain injury attending comprehensive specialized hospitals of Amhara regional state, Ethiopia 2021 (n = 483)

Discussion

In this study, the overall unfavorable outcome from TBI was 35.2%(n = 170) (95%CI(30.8–39.1), this study is consistent with the study conducted in Sudan at 31.4%. And with a study done at the University of Toledo Medical Center in Ohio 30% [37]. However, this finding was higher than a study conducted at Nekemte, Ethiopia 25.1% [29]. This discrepancy might be due to the difference in the number of hospitals included in the study and study period. The study conducted in Nekemte was conducted on a single referral hospital and it only includes two years of data, whereas the current study was done in all Amhara regional state comprehensive specialized hospitals and reviewed three years of data. This could cause a reasonable difference in the number of the outcome.

On the other hand, the finding of this study was lower than the study conducted in Kenya 55% [38], Austrian public hospitals 50% [39], Nepal 43.5% [40],, and Greece 40% [31]. This variation might be due to study subjects, the study subjects of the current study were all traumatic brain injury patients attending studied hospitals without specification of wards, but the study conducted in Kenya, Nepal, and Greece used study subjects under ICU department, patients under ICU have more chance of having an unfavorable outcome because, patients who are in life-threatening condition, serious infection, and severe injury are expected to admit to ICU department to get serious medical attention for 24 h and seven days and they would have a poor outcome after invasive procedures. In the current study, the likelihood of unfavorable outcomes from TBI is 4.6 times higher among patients with hypoxia than those who were in normal oxygen status. This finding agreed with the study done at Addis Ababa Tikur Anibesa specialized hospital, Ethiopia [41], Benin [42],, and Greece [31]. This is because hypoxia leads to a reduction in cerebral oxygen flow. So patients who had hypoxia may be complicated by cardiac arrest and small blood clots in the blood vessel consequently unfavorable outcomes [43].

And the odds of having unfavorable outcomes from TBI were 4.8 times higher in those who had additional injury than their counterpart. This study was consistent with the study employed in Nekemte referral hospital that suggested patients with additional injury had 5.8 times higher odds to have unfavorable outcomes [29]. And similar to a study conducted in Kenya that showed patients with additional injury had significantly associated with the unfavorable outcome. It might be the additional injury may cause patients to have other pathophysiologic reactions, such as neurologic shock due to pain from injuries, hypovolemia due to bleeding, hypotension, and other inflammatory reactions secondary to additional injury.

Regarding the mechanism of injury in TBI patients, road traffic injury was the commonest cause of traumatic brain injury which affected adult age groups 181(37.5%) followed by assault at 117(24.2%). These findings confirm what has been found and documented in South Africa, Zambia, Rwanda, and Europe [44,45,46,47,48,49,50].In contrast to this study, a study done in Norway the leading causes of TBI were falling down accidents, RTA, and assault [51].

In this study, 160 (33.1%) patients had mild traumatic brain injury the rest had moderate (n = 174, 30.8%)) to severe traumatic brain injury (n = 149, 36%). This study is comparable with a study conducted in Tanzania, England, and Nigeria [52,53,54]. Unlike that of Zambia where the number of operated patients was Moderate TBI [44].

In the current study, regarding CT scan findings, hematoma was the most common (n = 163, 33.7%). However, the study was conducted in Zambia, India, Tanzania, Ayder, Dilla University, and TASH Skull fracture followed by brain contusion [44, 52, 53, 55,56,57].

In this study, only 128(26.8%) patients came within one hour. Studies show that mortality will increase with incremental hours of patient arrival [58]. From the total of 483 participants, the outcome of the patient after traumatic brain injury on discharge was assessed based on GOS, and a large number of respondents, 277(57.3%) had a good recovery and among those unfavorable outcomes, 120(24.8%) died.

In this study, the overall unfavorable outcome from TBI was 35.2%( n = 170) (95%CI (30.8, 39.1). this study is lower than the Study conducted in Zambia, 58% of discharged TBI patients had a favorable GOS [44]. And higher than study conducted in Nekemte, Ethiopia (25.1%) were discharged with unfavorable outcome [59]. In this study, a relatively higher unfavorable outcome could be due to the absence of diagnostic imaging modality and Neurosurgery for moderate to severe TBI in the study area during the study period.

This study also revealed a severe and moderate type of head injury on admission was significantly associated with unfavorable outcomes. The odds of having unfavorable outcomes were 2.1 times higher for patients who had a severe Glasgow coma scale likewise, patients who had a moderate Glasgow coma scale had 2.2 times significantly associated with the unfavorable outcome as compared to those who had a mild Glasgow coma scale. This finding was in line with the study conducted in Addis Ababa [34], Nekemte referral hospital [29], Tunisia, Greece [31],, and the University of Toledo Medical Center in Ohio. For instance, the study done in Addis Ababa Tikur Anibesa and Nekemte referral hospitals showed that patients who had a low Glasgow coma scale on admission were 3.7 and 18.2 times higher chances to develop unfavorable outcomes respectively. This similarity might be due to an increased risk of secondary brain injury that leads to an increase in the risk of hematoma, brain edema, raised intracranial pressure, hypoxia, and hypotension for those patients who had severe and moderate Glasgow coma scale. Cerebrospinal fluid Othorrhea was significantly associated with unfavorable outcomes; the odds of having unfavorable outcomes from TBI were 2.8 times higher in those who had CSF otorrhea as compared to those without CSF leakage. This might be due to abnormal communication of the sterile subarachnoid space with the external environment, the patients may be at risk for meningitis, brain herniation, abnormal BP, and the first and most serious complication is spontaneous intracranial hypotension, where the pressure in the brain is severely decreased. Those complications may be the contributing factors to unfavorable outcomes [60].

This study finding showed that patients who were attending the hospital after 24 h after injury were two times higher chance to develop unfavorable outcomes than those who arrived less than one hour, this study is consistent with the study done at Dilla University referral hospital, Nekemte referral hospital [29], which indicates patients who arrived in hospital after 24 h had 4.7 and 16 times significantly associated with unfavorable outcome respectively as compared to those who arrived less than one hour and the study was similar with the study done in Kenya This can be explained timely diagnosis and management of the patients after traumatic brain injury is the key factor to prevent secondary brain injury through edema, hemorrhage, hypotension, and hypoxia.

Those patients who had tachypnea and bradypnea had a significant relationship with unfavorable outcomes. The odds of having unfavorable outcomes after TBI were 6.8 and 7.2 times high for those patients who had tachypnea and Bradypnea respectively. This might be because patients after traumatic brain injury have a chance to develop acute respiratory distress syndrome (ARDS), secondary to ARDS the patient may develop additional complications such as hypoxia, ischemia, and aspiration pneumonia. So having abnormal respiration is a leading cause to have unfavorable outcomes [61].

Limitation

In the current study lack of some predictors such as the occupation of the patients, alcohol consumption before the injury, and nursing care for patients after TBI, which was a strong predictor of TBI, were not recorded. This may underestimate the role of those variables on the outcome of TBI.

Conclusion and recommendation

In this study, the overall unfavorable outcome was experienced by about four out of every 10 victims of traumatic brain injury and time of arrival > 24 h, severe and moderate GCS on admission, having an additional injury, CSF otorrhea, abnormal respiration, and hypoxia were factors associated with the unfavorable outcome of traumatic brain injury among adults patients. Therefore our recommendation goes to upcoming researchers to use long-term longitudinal studies to better capture the recovery process and occurrence of late complications after TBI.

Availability of data and material

The datasets generated and/or analyzed during the current study are not publicly available due (we didn’t have an open data sharing agreement between study participants and investigators for their data to be shared publicly). However, Data are available from the authors upon reasonable request.

Abbreviations

TBI:

Traumatic brain injury

GOS:

Glasgow coma scale

AOR:

Adjusted odds ratio

CI:

Confidence interval

COR:

Crude odds ratio

LMIC:

Low- and middle-income countries

SPSS:

Statistical Package for Social Sciences

RTA:

Road traffic accident

WHO:

World health organization

ICU:

Intensive care unit

CSF:

Cerebrospinal fluid

CSA:

Central Statistical Agency

CSA:

Central Statistical Agency

ARDS:

Acute respiratory distress syndrome

TASH:

Tikur anibesa specialized hospital

OR:

Operation room

OPD:

Outpatient departments

HMIS:

Health Management Information Systems

BSc:

Bachelor of Science

MSC:

Master of Science

References

  1. Silver JM, McAllister TW, Arciniegas DB. Textbook of traumatic brain injury. American Psychiatric Pub. 2018.

  2. Organization WH. Global status report on road safety 2018: Summary. World Health Organization;2018.

  3. Organization WH. WHO Reveals Leading Causes of Death and Disability Worldwide: 2000–2019.

  4. Dewan MC, Rattani A, Gupta S, et al. Estimating the global incidence of traumatic brain injury. J Neurosurg. 2018;130(4):1080–97.

    PubMed  Google Scholar 

  5. Rubiano AM, Carney N, Chesnut R, Puyana JC. Global neurotrauma research challenges and opportunities. Nature. 2015;527(7578):S193–7.

    CAS  PubMed  Google Scholar 

  6. Taylor CA, Bell JM, Breiding MJ, Xu L. Traumatic brain injury–related emergency department visits, hospitalizations, and deaths—United States, 2007 and 2013. MMWR Surveill Summ. 2017;66(9):1.

    PubMed  PubMed Central  Google Scholar 

  7. James SL, Theadom A, Ellenbogen RG, et al. Global, regional, and national burden of traumatic brain injury and spinal cord injury, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016. The Lancet Neurology. 2019;18(1):56–87.

    Google Scholar 

  8. Maas AI, Menon DK, Adelson PD, et al. Traumatic brain injury: integrated approaches to improve prevention, clinical care, and research. Lancet Neurology. 2017;16(12):987–1048.

    PubMed  Google Scholar 

  9. Gardner RC, Burke JF, Nettiksimmons J, Goldman S, Tanner CM, Yaffe K. Traumatic brain injury in later life increases risk for P arkinson disease. Ann Neurol. 2015;77(6):987–95.

    PubMed  PubMed Central  Google Scholar 

  10. Crane PK, Gibbons LE, Dams- K, O’Connor, et al. Association between traumatic brain injury and late life neurodegenerative conditions and neuropathological findings. JAMA Neurol. 2016;73(9):1062–9.

    PubMed  PubMed Central  Google Scholar 

  11. Walsh S, Donnan J, Fortin Y, et al. A systematic review of the risks factors associated with the onset and natural progression of epilepsy. Neurotoxicology. 2017;61:64–77.

    PubMed  Google Scholar 

  12. Stocchetti N, Zanier ER. Chronic impact of traumatic brain injury on outcome and quality of life: a narrative review. Crit Care. 2016;20(1):1–10.

    Google Scholar 

  13. Toroyan T. Global status report on road safety 2015. Geneva: World Health Organization; 2015.

    Google Scholar 

  14. Organization WH. Global status report on road safety 2015. World Health Organization; 2015.

  15. Busko A, Hubbard Z, Zakrison T. Motorcycle-helmet laws and public health. N Engl J Med. 2017;376(13):1208–9.

    PubMed  Google Scholar 

  16. Indeshaw K. Pattern of head injury among patients presented to adult emergency department of Jimma University Teaching Hospital. Jimma: South West Ethiopia, Addis Ababa University; 2015.

    Google Scholar 

  17. Abate SM, Abafita BJ, Bekele T, Abate SM. The prevalence of traumatic brain injury among trauma patients in Ethiopia: systematic review and meta-analysis. 2020.

  18. Bryan-Hancock C, Harrison JJIP. The global burden of traumatic brain injury: preliminary results from the Global Burden of Disease Project. 2010;16(Suppl 1):A17-A17

  19. Rajalu BM, Devi BI, Shukla DP, et al. Traumatic brain injury during COVID-19 pandemic—time-series analysis of a natural experiment. BMJ Open. 2022;12(4):e052639.

    PubMed  Google Scholar 

  20. Hagos A, Tedla F, Tadele A, Zewdie A. Pattern and outcome of traumatic brain injury, addis ababa, Ethiopia: a cross-sectional hospital-based study. 2022;32(2):

  21. Kohler K, Myint PPN, Wynn S, et al. Systems approach to improving traumatic brain injury care in Myanmar: a mixed-methods study from lived experience to discrete event simulation. BMJ Open. 2022;12(5):e059935.

    PubMed  PubMed Central  Google Scholar 

  22. Baru A, Azazh A, Beza L. Injury severity levels and associated factors among road traffic collision victims referred to emergency departments of selected public hospitals in Addis Ababa, Ethiopia: the study based on the Haddon matrix. BMC Emerg Med. 2019;19(1):1–10.

    Google Scholar 

  23. Hordofa GG, Assegid S, Girma A, Weldemarium TD. Prevalence of fatality and associated factors of road traffic accidents among victims reported to Burayu town police stations, between 2010 and 2015 Ethiopia. J Transp Health. 2018;10:186–93.

    Google Scholar 

  24. Gardner A, Zafonte R. Neuroepidemiology of traumatic brain injury. Handb Clin Neurol. 2016;138:207–23.

    CAS  PubMed  Google Scholar 

  25. Wong J, Linn K, Shinohara R, Mateen F. Traumatic brain injury in Africa in 2050: a modeling study. Eur J Neurol. 2016;23(2):382–6.

    CAS  PubMed  Google Scholar 

  26. Persson AJAits. Road traffic accidents in Ethiopia: magnitude, causes and possible interventions. 2008;15:5–16.

  27. ARHB. Amhara National Regional Health Bureau: 9 month performance report 2020.

  28. Liyew B, DejenTilahun A, Kassew T. Knowledge, attitude, and associated factors towards physical assessment among nurses working in intensive care units: a multicenter cross-sectional study. Crit Care Res Pract. 2020;2020:9145105.

    PubMed  PubMed Central  Google Scholar 

  29. Kumara MG, Dhugasa MB. Factors affecting traumatic brain injury outcome among patients treated for head injury at surgical side, in Nekemte referral hospital, Oromia, Ethiopia. J Spine Neuroscie. 2020;1(2):1.

    Google Scholar 

  30. Jennett B, Bond M. Assessment of outcome after severe brain damage: a practical scale. Lancet. 1975;305(7905):480–4.

    Google Scholar 

  31. Grigorakos L, Alexopoulou A, Tzortzopoulou K, et al. Predictors of outcome in patients with severe traumatic brain injury. J Neurosci Clin Res. 2016;1(1):1–4.

    Google Scholar 

  32. Eaton J, Hanif AB, Grudziak J, Charles A. Epidemiology, management, and functional outcomes of traumatic brain injury in Sub-Saharan Africa. World neurosurgery. 2017;108:650–5.

    PubMed  Google Scholar 

  33. Opondo E, Mwangombe N. Outcome of severe traumatic brain injury at a critical care unit: a review of 87 patients. Ann Afr Surg. 2007;1.

  34. Brazinova A, Rehorcikova V, Taylor MS, et al. Epidemiology of traumatic brain injury in Europe: a living systematic review. J Neurotrauma. 2021;38(10):1411–40.

    PubMed  PubMed Central  Google Scholar 

  35. McMillan T, Wilson L, Ponsford J, Levin H, Teasdale G, Bond M. The Glasgow Outcome Scale—40 years of application and refinement. Nat Rev Neurol. 2016;12(8):477–85.

    PubMed  Google Scholar 

  36. Maas AI, Lingsma HF, Roozenbeek B. Predicting outcome after traumatic brain injury. Handb Clin Neurol. 2015;128:455–74.

    PubMed  Google Scholar 

  37. Baum J, Entezami P, Shah K, Medhkour A. Predictors of outcomes in traumatic brain injury. World neurosurgery. 2016;90:525–9.

    PubMed  Google Scholar 

  38. Rotich J, Raballah E, Maina D. Predictors of Outcome among Patients with Traumatic Brain Injury at MOI Teaching and Referral Hospital, Eldoret, Kenya.

  39. Majdan M, Brazinova A, Rusnak M, Leitgeb J. Outcome prediction after traumatic brain injury: comparison of the performance of routinely used severity scores and multivariable prognostic models. J Neurosci Rural Pract. 2017;8(1):20.

    PubMed  PubMed Central  Google Scholar 

  40. Kafle P, Khanal B, Yadav DK, Poudel D, Karki T, Cherian I. Head injury in Nepal: An institutional based prospective study on clinical profile, management and early outcome of traumatic brain injury in eastern part of Nepal. Birat J Health Sci. 2019;4(2):750–4.

    Google Scholar 

  41. Landes M, Venugopal R, Berman S, Heffernan S, Maskalyk J, Azazh A. Epidemiology, clinical characteristics and outcomes of head injured patients in an Ethiopian emergency centre. Afr J Emerg Medi. 2017;7(3):130–4.

    Google Scholar 

  42. Tobi K, Azeez A, Agbedia S. Outcome of traumatic brain injury in the intensive care unit: a five-year review. South African J Anaesth Analg. 2016;22(5):135–9.

    Google Scholar 

  43. Lee P, Chandel NS, Simon MC. Cellular adaptation to hypoxia through hypoxia inducible factors and beyond. Nat Rev Mol Cell Biol. 2020;21(5):268–83.

    CAS  PubMed  PubMed Central  Google Scholar 

  44. Mwala K, Munthali J, Chikoya LJMJoZ. Factors associated with Outcome in Patients Admitted with Traumatic Brain Injury at the University Teaching Hospital, Lusaka, Zambia. 2015;42(2):68-73

  45. Bailey CDJIHALBJoS. Love’s Short Practice of Surgery. 25th edn. NS Williams, CJK Bulstrode and PR O’Connell (eds) 283× 225 mm. 2008;95(10):1311–1311.

  46. Jennett B. Epidemiology of head injury. 1996;60(4):362.

  47. Arienta C, Caroli M, Balbi S. Management of head-injured patients in the emergency department: a practical protocol. Surg Neurol. 1997;48(3):213–9.

    CAS  PubMed  Google Scholar 

  48. Kraus JFJN. Epidemiology of head injury. 1996.

  49. Hitimana J, Perez M, Kinasha A, Kakande IJE, Surgery CAJo. Clinical presentation and outcome of neurosurgical conditions at Butare Teaching Hospital, Rwanda. 2009;14(1):50-56

  50. Zulu B, Mulaudzi T, Madiba T, Muckart DJI. Outcome of head injuries in general surgical units with an off-site neurosurgical service. 2007;38(5):576-583

  51. Heskestad B, Baardsen R, Helseth E, Romner B, Ingebrigtsen T. Incidence of hospital referred head injuries in Norway: a population based survey from the Stavanger region. Scand J Trauma Resusc Emerg Med. 2009;17(1):1–5.

    Google Scholar 

  52. Boniface R, Lugazia ER, Ntungi AM, Kiloloma O. Management and outcome of traumatic brain injury patients at Muhimbili Orthopaedic Institute Dar es Salaam. Tanzania Pan Afr Med J. 2017;26:140.

    PubMed  Google Scholar 

  53. Adogu PO, Egenti NB, Ubajaka CF, Anakwue JC, Ugezu AI. Epidemiological pattern and outcome of head injuries during festive and non-festive periods in a tertiary hospital, Nnewi, Nigeria. Int J Res Med Sci. 2015;3(10):1.

    Google Scholar 

  54. Dyer O. Covid-19: Many poor countries will see almost no vaccine next year, aid groups warn. 2020;371.

  55. Landes M, Venugopal R, Berman S, Heffernan S, Maskalyk J, Azazh A. Epidemiology, clinical characteristics and outcomes of head injured patients in an Ethiopian emergency centre. Afr J Emerg Med. 2017;7(3):130–4.

    PubMed  PubMed Central  Google Scholar 

  56. Eshete A, Taye F. Magnitude of severe head injury and its associated factors among head injury patients in gedeo zone, southern Ethiopia: a two-year retrospective study. Ethiop J Health Sci. 2018;28(3):323–30.

    PubMed  PubMed Central  Google Scholar 

  57. Gebrekirkos FA, Kidanu M, Tadesse A, Lerebo WJEMJ. Head injury admissions at a referral hospital in Ethiopia. 2017;55(3).

  58. Dinh MM, Bein K, Roncal S, Byrne CM, Petchell J, Brennan JJI. Redefining the golden hour for severe head injury in an urban setting: the effect of prehospital arrival times on patient outcomes. Injury. 2013;44(5):606–10.

    PubMed  Google Scholar 

  59. Kumara MG, Dhugasa MB. Factors affecting traumatic brain injury outcome among patients treated for head injury at surgical side, in Nekemte Referral Hospital, Oromia, Ethiopia. J Spine Neurosci. 2020;1(2):1.

    Google Scholar 

  60. Oh JW, Kim SH, Whang K. Traumatic cerebrospinal fluid leak: diagnosis and management. Korean J Neurotrauma. 2017;13(2):63–7.

    PubMed  PubMed Central  Google Scholar 

  61. Thompson BT, Chambers RC, Liu KD. Acute respiratory distress syndrome. N Engl J Med. 2017;377(6):562–72.

    CAS  PubMed  Google Scholar 

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Acknowledgements

The authors would like to thank the hospital administrative officials for their valuable information and cooperation and we are happy to thank data collectors for their collaboration throughout the data collection process.

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Contributions

S.G/M. conceived and designed the study, analyzed and interprets the data, and wrote the manuscript; B.T. contributed to the interpretation of data, re-analysis of results, reviewing the analysis, and language editing and prepared the final version of the manuscript. M.G.A. and B.L. advised the whole research paper, revised the proposal, data analysis, interpretation, and prepared figures. All authors reviewed the manuscript.

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Correspondence to Bikis Liyew.

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The research was approved by the health research ethics institutional review board (IRB) of the University of Gondar ethical clearance No S/N/168/7/2013 was given to the investigator preceding the data collection. Then an official permission letter was obtained from the administrative bodies of the comprehensive specialized hospitals and Confidentiality was kept during data collection, any recorded patient information was not been exposed to a third person. All methods were carried out following relevant guidelines and regulations, and informed consent was obtained from all concerned subjects following the Declaration of Helsinki.

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G/Michael, S., Terefe, B., Asfaw, M.G. et al. Outcomes and associated factors of traumatic brain injury among adult patients treated in Amhara regional state comprehensive specialized hospitals. BMC Emerg Med 23, 109 (2023). https://doi.org/10.1186/s12873-023-00859-x

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