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   Delta Procalcitonin Is a Better Indicator of Infection Than Absolute Procalcitonin Values in Critically Ill Patients: A Prospective Observational Study  
   
نویسنده tr�sy d. ,t�nczos k. ,n�meth m. ,hankovszky p. ,lovas a. ,mikor a. ,hajd� e. ,osztroluczki a. ,fazakas j. ,moln�r z.
منبع journal of immunology research - 2016 - دوره : 2016 - شماره : 0
چکیده    Purpose. to investigate whether absolute value of procalcitonin (pct) or the change (delta-pct) is better indicator of infection in intensive care patients. materials and methods. post hoc analysis of a prospective observational study. patients with suspected new-onset infection were included in whom pct,c-reactive protein (crp),temperature,and leukocyte (wbc) values were measured on inclusion (t 0) and data were also available from the previous day (t - 1). based on clinical and microbiological data,patients were grouped post hoc into infection- (i-) and noninfection- (ni-) groups. results. of the 114 patients,85 (75%) had proven infection. pct levels were similar at t - 1: i-group (median [interquartile range]): 1.04 [0.40-3.57] versus ni-group: 0.53 [0.16-1.68],p = 0.444. by t 0 pct levels were significantly higher in the i-group: 4.62 [1.91-12.62] versus 1.12 [0.30-1.66],p = 0.018. the area under the curve to predict infection for absolute values of pct was 0.64 [95% ci = 0.52-0.76],p = 0.022; for percentage change: 0.77 [0.66-0.87],p < 0.001; and for delta-pct: 0.85 [0.78-0.92],p < 0.001. the optimal cut-off value for delta-pct to indicate infection was 0.76 ng/ml (sensitivity 80 [70-88]%,specificity 86 [68-96]%). neither absolute values nor changes in crp,temperature,or wbc could predict infection. conclusions. our results suggest that delta-pct values are superior to absolute values in indicating infection in intensive care patients. this trial is registered with clinicaltrials.gov identifier: nct02311816. � 2016 domonkos tr�sy et al.
آدرس faculty of medicine,department of anaesthesiology and intensive therapy,university of szeged,6 semmelweis street,szeged, Hungary, faculty of medicine,department of anaesthesiology and intensive therapy,university of szeged,6 semmelweis street,szeged, Hungary, faculty of medicine,department of anaesthesiology and intensive therapy,university of szeged,6 semmelweis street,szeged, Hungary, faculty of medicine,department of anaesthesiology and intensive therapy,university of szeged,6 semmelweis street,szeged, Hungary, faculty of medicine,department of anaesthesiology and intensive therapy,university of szeged,6 semmelweis street,szeged, Hungary, faculty of medicine,department of anaesthesiology and intensive therapy,university of szeged,6 semmelweis street,szeged, Hungary, faculty of medicine,division of infectious diseases,first department of internal medicine,university of szeged,szeged, Hungary, faculty of medicine,department of anaesthesiology and intensive therapy,university of szeged,6 semmelweis street,szeged, Hungary, faculty of medicine,department of transplantation and surgery,semmelweis university,budapest, Hungary, faculty of medicine,department of anaesthesiology and intensive therapy,university of szeged,6 semmelweis street,szeged, Hungary
 
     
   
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