Abstract:Objective: To evaluate the effects of delayed vs early fluid resuscitation on cerebral hemodynamics after severe head injury and uncontrolled hemorrhagic shock.
“…Slices were incubated in 2% 2,3,5-triphenyltetrazolium chloride (TTC) (SigmaChemical Co., St. Louis, MO) to detect nonviable tissue. 20 Lesion size was measured with computer-assisted image analysis software ImageJ (National Institutes of Health, Bethesda, MD). Brain swelling was calculated by comparing the injured hemisphere with the uninjured hemisphere [(ipsilateral hemisphere's volume / contralateral hemisphere's volume) j 1] Â 100.…”
Section: Calculation Of Brain Lesion and Swellingmentioning
In a clinically realistic combined TBI + HS model, early administration of plasma products decreases brain lesion size and edema. LSP is as effective as FFP, while offering many logistic advantages.
“…Slices were incubated in 2% 2,3,5-triphenyltetrazolium chloride (TTC) (SigmaChemical Co., St. Louis, MO) to detect nonviable tissue. 20 Lesion size was measured with computer-assisted image analysis software ImageJ (National Institutes of Health, Bethesda, MD). Brain swelling was calculated by comparing the injured hemisphere with the uninjured hemisphere [(ipsilateral hemisphere's volume / contralateral hemisphere's volume) j 1] Â 100.…”
Section: Calculation Of Brain Lesion and Swellingmentioning
In a clinically realistic combined TBI + HS model, early administration of plasma products decreases brain lesion size and edema. LSP is as effective as FFP, while offering many logistic advantages.
“…Models that have tried to explain the effects of posttraumatic hypotension have done so more commonly in larger animals such as pigs and cats relatively to rodents. It is worth nothing that many and several studies have been conducted on the effects of fluid resuscitation strategies after traumatic brain injury44-50 while posttraumatic hypotensive effects have been poorly dealt with in the laboratory environment. Majority of these animal models of TBI have been able to include parameters such as intracranial pressure monitoring, cerebral blood flow, oxygen delivery and so on but very few have been able to be compared with secondary insults, hence it is easy to speculate that these models have been limited in their capacity to specifically explain the mechanisms of neuronal damage intensified by secondary insults leading to some of the failures pertaining to translating laboratory results to the bedside.…”
Section: Limiting Factors In Tbi Animal Modelsmentioning
Experimental modeling of traumatic brain injury (TBI) in animals has identified several potential means and interventions that might have beneficial applications for treating traumatic brain injury clinically. Several of these interventions have been applied and tried with humans that are at different phases of testing (completed, prematurely terminated and others in progress). The promising results achieved in the laboratory with animal models have not been replicated with human trails as expected. This review will highlight some insights and significance attained via laboratory animal modeling of TBI as well as factors that require incorporation into the experimental studies that could help in translating results from laboratory to the bedside. Major progress has been made due to laboratory studies; in explaining the mechanisms as well as pathophysiological features of brain damage after TBI. Attempts to intervene in the cascade of events occurring after TBI all rely heavily on the knowledge from basic laboratory investigations. In looking to discover treatment, this review will endeavor to sight and state some central discrepancies between laboratory models and clinical scenarios.
“…In comparison to colloids, crystalloids were shown to produce more cerebral edema in TBI patients. [1819] It is likely that in severe head injury patients (with disrupted BBB), edema formation would be even worse with the further use of crystalloids. The high oncotic pressure of colloids decreases the cerebral edema formation and is also associated with improvement in the mean arterial blood pressure (MABP), having low infused volume, and decreased neuronal death.…”
Trauma is a leading cause of death worldwide and traumatic brain injury is one of the commonest injuries associated with it. The need for urgent resuscitation is warranted for prevention of secondary insult to brain. However, the choice of fluid in such cases is still a matter of conflict. The literature does not provide enough data pertaining to role of colloids in head injury patients. In this article, we have tried to explore the present role of colloid resuscitation in patient with head injury.
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