Clinical feature | Risk of developing long-term neuropsychological sequelae | Comments |
Intraventricular haemorrhage | ||
Prolonged post-traumatic amnesia | High risk associated with PTA >1 week determined by prospective assessment*. | |
Surgical intervention required | ||
Presence of ischaemic brain injury | ||
Anoxia | Neuropsychological risk depends on the period and severity of anoxia. | |
Evidence of diffuse axonal injury on MRI | The more widespread the injury, the more widespread the associated cognitive deficit is likely to be. | |
Elevated ICP | The more elevated and longer the duration, the higher the risk. | |
Presence of midline shift | ||
Evidence of inflammatory response | ||
Evidence of sulcal effacement | Duration and extent is an important determinant of associated deficit. | |
Evidence of contusions | May result in focal deficits, particularly if damage remains evident on later neuroradiology (MRI). | |
Abnormalities suggestive of traumatic axonal injuries evident on DTI | May be associated with reduced processing speed or focal deficits. These abnormalities can also be present with no neuropsychological correlates. |
Incomplete neuropsychological recovery likely.
Some long-term neuropsychological sequelae likely.
Possibility of some long.
Flags are cumulative.
*Reports of prolonged post-traumatic amnesia gained retrospectively must be carefully evaluated. If indicating significant brain trauma, there should also be an evident corroborative sign and symptoms.
DTI, diffusion tensor imaging; ICP, intracranial pressure; PTA, post-traumatic amnesia.