EUROMEDICA 

Hanover

23-24  Mai 2011

Advanced methods of diagnosis,
treatment and prophylactics

European Academy of Natural Sciences, Hanover

European Scientific Society, Hanover


M.I Yeghiazaryan
G.R. Hakobyan
THE DIAGNOSTIC VALUE OF PROCALCITONIN IN PATIENTS WITH DIAGNOSED SEPSIS
University Clinical Hospital N1, Yerevan, Armenia

The increasing interest to sepsis is conditioned with the high level of morbidity and mortality, which occurs as a result of delayed diagnostics. Therefore, the searching of early informative markers of systemic inflammation is quite actual.

Goal of study: To evaluate the diagnostic value of procalcitonin (PCT) in patients with diagnosed sepsis.

Methods: We investigated the level of PCT in 90 patients with sepsis in intensive care unit. Among them 73.3% (n=66) were males and 26.7% (n=24) were females, mean age compiled 43.8±17.1 years, mortality – 28.9% (n=26), the severity of condition according to APACHE II scale was 14.3±6.9, duration of hospitalization – 18.1±18.8 (2-116) days; main diagnosis on admission – polytrauma – 33.3% (n=30), peritonitis – 11.1% (n=10), gynecological pathology – 6.7% (n=6), and pneumonia – 48.8% (n=44).

For establishment of sepsis diagnosis the classification of ACCP\SCCM (Bone R.C., 1992) was used. PCT concentration in plasma was calculated during the establishment of diagnosis. Diagnostic levels were as following: <0.5 ng/ml – sepsis is excepted, 0.5-2.0 ng/ml – infection and sepsis are possible, 2.0-10.0 ng/ml – high probability of sepsis, >10.0 ng/ml – probability of sever sepsis, septic shock and polyorganic dysfunction.

Results According to the data obtained the levels of PCT were as follows: < 0,5 ng/ml - 48,9% (n=22); ≥ 0,5 - < 2,0 ng/ml - 11,1% (n=5); ≥ 2,0 - < 10,0 ng/ml - 20% (n=9) and > 10 ng/ml - 20% (n=9).

Discussion: In these categories the correlatrion of diagnosis by PCT is revealed in 40% (n=36) of cases, meanwhile, in 60% (n=54) of cases sepsis was diagnosed basing on ACCP\SCCM classification. Data obtained concerning the values of PCT testify that PCT is not a universal biochemical marker of the acute phase of inflammation.

Conclusion: The levels of PCT marker do not correspond to the clinical-microbiological bases of sepsis diagnosis, which testifies the need of further investigations in this area.