Abstract:Objective To discuss the initial expression of serum procalcitonin (PCT) in patients with severe traumatic brain injury (TBI) and determine the potential value of PCT to predict the neurological outcome.Methods A retrospective analysis was made on patients admitted due to severe TBI (GCS≤8 points) from July 2011 to August 2012.Mortality and neurological outcome of the survivors were determined using Glasgow outcome scale (GOS) at 6 months after TBI.Results A total of 52 patients (39 males and 13 females),at median age of 38 years (range,15-65 years) were included in the study.Twenty-eight patients had good outcome (GOS of grade Ⅳ-Ⅴ),whereas 24 patients had poor outcome or died (GOS of grade Ⅰ-Ⅲ).Within 24 hours after TBI,serum PCT level was significantly higher in patients with bad outcome compared to those with good outcome (0.778 ng/ml:0.094 ng/ml,P <0.01).Enhanced PCT level presented a close correlation with the poor outcome (r =0.657,P <0.01).Area under the receiver operating characteristic curve (ROC) was 0.879 [95% CI (0.757,1.000)].A cutoff value of 0.2 ng/ml had a sensitivity of 100% and a specificity of 72.2%.Once the PCT level was superior to 4.7 ng/ml,none of the patients regained consciousness.Conclusion PCT is a simple and effective method for prediction of the outcome after severe TBI.
[4]Marshall LF, Marshall SB,Klauber MR,et al.The diagnosis of head injury requires a classification based on computed axial tomography. J Neurotrauma,1992,9 (Suppl 1):S287-S292.
[5]Amantini A, Grippo A, Fossi S, et al. Predicion of ‘awakening’and outcome in prolonged acute coma from severe traumatic brain injury: evidence for validity of short latency SEPs. Clin Neurophysiol, 2005, 116(1):229-235.
[6]Hinzman JM, Thomas TC, Quintero JE, et al. Disruptions in the regulation of extracellular glutamate by neurons and glia in the rat striatum two days after diffuse brain injury. J Neurotrauma, 2012, 29(6):1197-1208.
[7]Mondello S,Akinyi L,Buki A,et al.Clinical utility of serum levels of ubiquitin c-terminal hydrolase as a biomarker for severe traumatic brain injury. Neurosurgery, 2012, 70(3):666-675.
[10]Bouadma L, Luyt CE, Tubach F, et al. Use of procalcitonin to reduce patients’ exposure to antibiotics in intensive care units (PRORATA trial): a multicentre randomised controlled trial. Lancet, 2010, 375 (9713):463-474.
[11]Nobre V, Harbarth S, Graf JD, et al. Use of procalcitonin to shorten antibiotic treatment duration in septic patients: a randomized trial. Am J Respir Crit Care Med, 2008, 177(5):498-505.
[12]Mongardon N, Lemiale V, Perbet S, et al. Value of procalcitonin for diagnosis of early onset pneumonia in hypothermia-treated cardiac arrest patients. Intensive Care Med, 2010, 36(1):92-99.
[13]Schuetz P, Affolter B, Hunziker S, et al. Serum procalcitonin, C-reactive protein and white blood cell levels following hypothermia after cardiac arrest: a retrospective cohort study. Eur J Clin Invest, 2010, 40(4):376-381.
[15]Dalla Libera AL, Regner A, de Paoli J, et al. IL-6 polymorphism associated with fatal outcome in patients with severe traumatic brain injury. Brain Inj, 2011, 25(4) :365-369.
[16]Mellerqärd P,Äneman O,Sjöqren F,et al.Differences in cerebral extracellular response of interleukin-1β, interleukin-6, and interleukin-10 after subarachnoid hemorrhage or severe head trauma in humans.Neurosurgery,2011,68(1):12-19.
[19]Oberhoffer M, Stonans I, Russwurm S, et al. Procalcitonin expression in Human peripheral blood mononuclear cells and its mudalution by lipopolysaccharides and sepsis related cytokines in vitro. J Lab Clin Med, 1999, 134(1):49-55.
[20]Whang KT,Vath SD,Becker KL,et al. Procalcitonin and proinflammatory cytokine interactions in sepsis. Shock, 2000, 14(1):73-78.
[21]Becker KL,Snider R,Nylen ES.Procalcitonin in sepsis and systemic inflammation: a harmful biomarker and a therapeutic target. Br J Pharmacol,2010,159(2):253-264.