Jamie Rice In individuals under 45 years of age traumatic injuries are the leading cause of death, approximately fifty percent of which are head injuries (Unden, 43). The leading cause of death in children worldwide is traumatic brain injury. In the United States alone, children (individuals aged younger than 18 years old) account for approximately 7400 deaths, 60000 hospitalizations, and 600000 emergency room visits every year (Identification of Children at Very Low Risk of Clinacally-important Brain Injuries After Head Trauma: a Prospective Cohort Study). This makes the ability to diagnose the injury quickly a necessity. Computed tomography (CT) scans and magnetic resonance imaging (MRI) are used to determine the presence and severity of a traumatic brain injury as well as skull fractures and other severe injuries that could in the instance of head impact. It is argued, however, that these tests expose children to (in many cases) unnecessary radiation, which had the potential to cause malignancies. It is also argued that these two types of imaging are not sensitive enough for some brain injuries to be seen on the images produced. There is a need for an alternative method for quick diagnosis and a way to determine whether it is necessary for a child to undergo some form of neuroimaging. The following research explores the question: Is there a way to determine whether a pediatric patient needs a neurological scan and is there a method of diagnosing head trauma without scanning the brains of children? Biomarkers are the most researched alternative and aid for diagnosis of head injuries in children. This topic is important because head trauma in children can have many life threatening consequences. Children cannot be treated the same adults because they “have a more susceptible cranial vault due to thinner bones, large head-to-torso ratio, late development of air sinuses and differences in the immune system and in their capability of maintaining body temperature”(Alexiou, 403). In order to determine the severity of head traumas in pediatric patients many factors should be taken into account. A detailed history of the patient, loss of consciousness, seizures, and amnesia, should be recorded and a physical examination should be performed that involve assessment of patient’s airway, breathing and circulation, Glasgow coma scale scores (Glasgow coma scale is a 15 point test based on eye opening response, verbal response, and motor response(Rowlett)), the size or their pupils, the head and spine, and ears. Such extensive evaluations need to be done because there are many possible injuries that can result from head trauma. Skull fractures can be found in anywhere between two and twenty percent of children that experience head trauma. These fractures can be linear, depressed, diastatic, and of skull base. Children with head trauma can also have epidural hematoma, a collection of blood between the inner skull and dura mater, subdural hematoma, which results because of injury to the bridging cortical veins, intracerebral hematoma, and penetrating head trauma. (Alexiou) Physical examination, Glasgow Coma Scale scores, and computed tomography (CT) scan of the cranium are considered the current gold standards for diagnosing traumatic brain injury in children, even though these “standards” have a number of limitations in their ability to predict the neurological outcome and have a low sensitivity for detecting mild traumatic brain injury. This study is focusing on the use of the biochemical marker S-100B, a large number of studies have explored the S-100B as an analytical and predictive index of head trauma. S-100B is a calcium-binding protein produced by astrological cells that exerts extracellular functions so it is actively secreted. S-100B stimulates neuronal growth and enhances the survival of neurons during development and after injury. Piazza measured the range of S-100B concentration in children that experienced traumatic brain injury and the possible roles of the protein. “S-100B is a small diametric calcium-binding protein that is found in astroglial within the central nervous system.” Piazza’s studied fifteen children between the ages of one and fifteen years of age with head injury that were admitted to the emergency department within 12 hours of injury. The severity of their head injuries was determined by Glasgow coma scores. Nine patients had mild traumatic brain injury (TBI), two patients had moderate TBIs, and four patients had severe TBIs. The patients’ characteristics were recorded, as well as the time and cause of injury. Cerebral CT scans were performed at admission to the emergency department and after 48 hours. Blood samples were also obtained at the same time intervals, these samples were used to analyze the S-100B measurement in the patients’ bodies. The lower detection level was .02 µg/l. Six of the fifteen children analyzed had heightened levels (greater than .3µg/l) of S-100B in their systems. In three out of the four cases the concentration of the protein remained elevated for at least 48 hours. The result of this study showed a trend towards increasing levels of the protein with increased severity of the head injury. The serum concentrations of S-100B was higher in children with a score of eight or less in Glasgow coma scale test, the lower the score the more severe the head injury. Although the results of this investigation showed that there is a correlation between the severity of head injuries and the levels of the S-100B protein, the conductors of this research conclude that the role of S-100B is not yet cleared and it is not a reliable prognostic index. (Piazza, 258-260, 262) Undén performed a similar study with a fourteen-year-old male and a seventeen-yearold male. In the case of the 14-year-old he was sent home after visiting a primary care center with no substantial symptoms and was sent home. The next morning he could not be waken and he was rushed to the hospital. At the hospital the child underwent a CT scan which showed “a skull fracture with a massive epidural hematoma with signs of a cerebral herniation” (Undén, 44). His S-100B levels were measured at .2µg/l. The 17-year-old suffered a massive epidural hematoma after a blunt head injury. The hematoma was rather large and resulted in possible cerebral herniation. S-100B levels were .14µg/l three and a half hours after the initial injury and .10µg/l six hours after the injury. Undén suggests that S-100B is the most promising biomarker to date. This protein has a high negative predictive value, which means there are minimal numbers of false negatives produced when measurements of S-100B are used to determine. Undén also stated the faults of using the biomarker in clinical use. S-100B has a very short halflife, so if a patient has samples taken too late there is the possibility of a reading that suggests a less serious injury. Even in the case if the 17-year-old the concentration of S-100B was not a good indicator of “the most feared of complications after head injury.” This is extremely important because a misdiagnosis of epidural hematoma can be harmful consequences. Undén concludes that he showed that S-100B does not always detect intracranial hematomas, even when serum is taken shortly after the head impact. A study was conducted to determine when it is necessary for a child to undergo two CT scans. The study was conducted on patients aged 0 to 21 years who had initial and subsequent head imaging studies performed at a participating children’s hospital and their initial scan documented. Patients were excluded if they had transferred to a participating hospital with a cranial injury confirmed by a CT scan performed elsewhere, a second image of the brain injury was not performed, they were treated to manage hypertension before the second CT scan was performed, and if the patient had a history or diagnosis of a bleeding disorder, neurological disorder, or bone metabolism disorder. Forty-seven patients were involved in the study, of these patients, only 5 had to undergo surgical intervention when the results of the second CT scan were produced. Of the five, four were infants that suffered nonaccidental trauma and had follow up MRIs performed. The fifth child suffered a closed head injury while sledding which cause an epidural hematoma without mass effect. The other 42 children remained stable. This study was concluded by the researcher stating that children that do not require surgery may not benefit from serial brain imaging, but a larger study would need to be performed in order to determine who can be exempt from neuroimaging. (Schnellinger) Tang researches the when to image children and what can actually be found by a CT scan. CT scans are the “first-line investigation” for head trauma in pediatric patients, even though MRIs may be more sensitive and effective in finding the full extent of the injuries. In cases of minimal head trauma, the patient may be discharged and given head injury advice from the medical professional that saw them. Patients with moderate to severe head trauma, loss of consciousness for more than five minutes, or focal neurological deficit should be sent for an urgent CT scan. Ambiguity is caused when there is an in between case, where patients cannot be considered mild nor severe and are less than moderately injured. There is no clear consensus on where to draw the line for CT scans. Positive findings are seen in less than ten percent of patients that are screened and approximately 0.5% require surgical intervention. The indications for a CT scan in a child younger than 16 years of age with head trauma include: 1. Witnessed unconsciousness >5 min. 2. Amnesia >5 min.4 3. Abnormal drowsiness 4. Three or more discrete episodes of vomiting 5. Clinical suspicion of nonaccidental injury 6. Posttraumatic seizure in absence of history of epilepsy 7. GCS score <14 in a child or GCS score <15 in infants in the emergency department 8. Suspicion of open/depressed skull fracture or tense frontanelle 9. Clilical evidence of base of skull fracture 10. Focal neurological deficit 11. Bruise, swelling or laceration >5 cm in infants 12. High impact head trauma The National Institute for Health and Clinical Excellence guidelines recommends that the Children’s Head injury Algorithm for the Prediction of Important Clinical Excellence guidelines shown above be followed. Minor head injuries account for the largest percentage of children seen for head trauma and the concerns for exposing them to unnecessary radiation has increased. Although children absorb a lower dose of radiation for a CT scan of the head than adults do, the effective dose can be up to four times greater in a neonate (a child four weeks old or younger). If the tube current could be decreased, the dose of radiation could decrease by up to fifty-eight percent. CT scans are useful for finding very serious brain conditions due to head traumas hematoma is more commonly due to a dural vein tear, it is imperative to diagnose an extradural hematoma because it could be due to a middle meningeal artery. (Tang) Based on the research that I studied, it can be concluded that the biomarker S-100B cannot be used in clinical practice. The half-life of S-100B is very short, therefore the concentrations decrease very quickly. If a patient is not taken to the hospital within a few hours of the injury there may be no information gained from taking samples and the patient would get a CT scan regardless of whether serum samples were taken. The protein S-100B does has been shown to make accurate predictions to the severity of head traumas, but in realistic situations, patients would not be seen by a medical professional in time to be tested for concentration levels of the protein. S-100B has a very high negative predictive value, yet since it is not 100% accurate it cannot be cleared for clinical use. Although there specifications for what a child’s symptoms should be in order to undergo some sort of neuroimaging, many pediatric patients still experience unnecessary scanning. From the research I conducted, I can conclude that there are possible ways to reduce the number or neurological scans performed on children, but methods have not been implemented because they may not be practical for clinical use and rare cases of overlooked severity of a head injury. Works Cited Alexiou, George A, George Sfakianos, and Neofytos Prodromou. “Pediatric Head Trauma.” Journal of Emergencies, Trauma, and Shock 4.3 (2011): 403-408. MEDLINE with Full Text. Web. 2 Nov. 2011. Ashwal, Stephen, Barbara A. Holshouser, and Karen A. Tong. “Use of Advanced Neoroimaging Techniques in the Evaluation of Pediatric Trauma Brain Injury.” Developmental Neuroscience 28 (2006): 309-326. MEDLINE with Full Text. Web. 2 Nov. 2011. Berger, Rachel Pardes, et al. “Serum Biomarkers after Traumatic and Hypoxemic Brain Injuries: Insight into the Biochemical Reseonse of the Pediatric Brain to Inflicted Brain Injury.” Developmental Neuroscience 28 (2006): 327-335. MEDLINE with Full Text. 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