Fatality Predictors In Traumatic Brain Injury

Résumé

Background: Traumatic brain injury is a global health problem, it is a major cause of devastating neurological sequelae and significant mortality. The underlying physiological events traumatic brain injury are most likely responsible for the poor clinical outcomes seen. The changes in changes in traumatic brain injury lead to a reduction in cerebral blood flow and cerebral perfusion resulting in cerebral ischaemia. The inflammatory response in traumatic brain injury coupled with oxidative stress changes cause a reduction in the endogenous anti-oxidants and dysfunction of the blood brain barrier function. An understanding of the natural history of oxidative stress and inflammatory changes in traumatic brain injury can help design appropriate management protocols to reduce the mortality and morbidity in these patients. While Glasgow Coma Score at admission was utilised in the initial evaluation of the state of consciousness of the traumatic brain injury patients, the Glasgow Outcome Score was used in assessing the clinical outcomes. This study utilizes clinical and biomarker profiles to evaluate and assess the functional outcomes in patients with moderate to severe TBI. Aim of the study: The aim of this study was to identify potential clinical parameters and biomarkers that were predictive of fatality in patients with moderate to severe traumatic brain injury. This study not only attempts to identify key predictors of fatality  from among clinical parameters, oxidative stress and inflammatory biomarkers in patients with moderate and severe traumatic brain injury and to defines the duration of survival in these patients. Methods: Patients with moderate to severe traumatic brain injury were admitted and managed at the Nelson Mandela Academic Hospital March 2014-March 2016. At admission  patient demographics including age and sex  were recorded. the Glasgow Coma Score was assessed and recorded. All these patients underwent neurosurgical intervention and intensive care management for the traumatic brain injury. Blood and cerebrospinal fluid were sampled for evaluation of oxidative stress and inflammatory biomarkers during the initial 7 days in the intensive care unit but on day 14 only blood was sampled. During follow up at 2 weeks and 12 weeks the Glasgow outcome score was evaluated. Results: Of the 64-patient’s fatality was observed in 12.5% of them. The analysis for fatality was done using Receiver operative curves, Cox regression and Kaplan Meier analysis methods of analysis.There was a significant association between the age of the patients, anti-oxidants, proinflammatory markers  and admission Glasgow Coma Score with fatality. Conclusion: Besides the admission Glasgow Coma Score, low anti-oxidant levels and elevated serum interleukin-1β levels were associated with fatal outcomes.