Traumatic brain injury is an alteration of brain function caused by an external force.
Acquired brain injuries can be traumatic or non-traumatic.
The leading causes of TBI are falls, assaults, and motor vehicle accidents.
Adults older than 75 are at the highest risk for TBI.
Hospitalizations and death from TBI is greatest in those older than 65.
The primary injury occurs immediately after the event. The brain tissue is damaged as a result of the force.
The secondary injury occurs after the primary injury. Cellular, molecular, and biochemical changes occur in the brain.
The secondary injury will eventually evolve into hypoxia, edema, and elevated ICP.
The primary injury is the result of brain tissue coming into contact with an internal or external object or rapid accelerations and decelerations of the brain.
A coup-contrecoup injury occurs when the brain hits both the front and back of the skull. This commonly occurs with car accidents.
Blast injuries result in a transient shock wave that causes damage. Typically, the vasculature of the brain is affected.
The secondary injury is also known as the metabolic cascade. There are changes in the neurochemical and metabolic components of the brain.
The metabolic cascade results in changes in cerebral blood flow, decreased access to energy stores, and decreased ability to heal.
The metabolic cascade begins immediately after injury, but changes will continue to occur for weeks after the event.
Hematoma is brain bleeding that leads to the collection of blood in brian tissues or empty spaces.
Hematomas are the result of contact injuries.
Epidural hematoma is blood outside the brain and the dura but under the skull.
Epidural hematomas will happen very quickly and will result in a large buildup of ICP.
Subdural hematoma is blood between the brain and the dura.
Subdural hematomas are slow as a vein is affected. It will take hours for the decline to occur.
Epidural hematomas affect an artery.
Hemorrhage occurs when an artery bursts with localized bleeding due to acceleration and deceleration forces.
Subarachnoid hemorrhage is bleeding within the layers of the dura, specifically under the arachnoid layer.
Intraventricular hemorrhage is bleeding into the ventricles. This is the most severe and has the worst prognosis.
Intraventricular hemorrhage will have a large increase of ICP in the entire brain.
Diffuse axonal injuries occur with shearing type injuries leading to disruption of neurofilaments.
Diffuse axonal injuries are typically caused by acceleration deceleration injuries.
The Glasgow coma scale is a clinical scale that measures level of consciousness and helps define/classify the severity of injury.
The GCS monitors and detects meaningful changes in neurobehavioral function.
A score of 3 to 8 on the GCS indicates severe TBI.
A scores of 9 to 12 on the GCS indicates moderate TBI.
A score of 13 to 15 on the GCS indicates mild TBI.
Anterograde amnesia is the inability to create new memories.
Post-traumatic amnesia is the time between the incident and when the patient is able to recall recent events.
Post-traumatic amnesia is the best indicator of severity after TBI.
Retrograde amnesia is the inability to remember events prior to the injury.
Loss of consciousness is a period of partial or total loss of awareness of self and surroundings.
Post-traumatic amnesia typically lasts 1 day or less for mild TBI.
Post-traumatic amnesia typically lasts 1 to 7 days for moderate TBI.
Post-traumatic amnesia typically lasts greater than 7 days for severe TBI.