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CARDIOVASCULAR
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Volume 1, 1996, No 1 |
Abstract:
Procalcitonin (PCT), a 116 amino acid protein with identical
sequence to the precursor protein of the human calcitonin
hormone, is a new diagnostic parameter of bacterial infection and
systemic inflammation. High plasma concentrations of PCT are
induced in severe bacterial and fungal infection and in sepsis
and multiorgan dysfunction syndrome (MODS). Unlike C-reactive
protein (CRP), IL-6, or other parameters of the inflammatory
response, PCT is generally not induced by viral infections,
operation trauma, autoimmune or allergic disorders including
allograft rejection and in the initial phase of circulatory
failure. Hence, this parameter can be used for differential
diagnosis of bacterial and non-bacterial inflammation and to
assess the inflammatory reaction in sepsis and MODS. Increased
PCT plasma concentrations are always found in sepsis and MODS,
with high concentrations in the more severe states of disease. In
circulatory failure and SIRS without bacterial infection, PCT
values are less than in bacterial-induced septic shock, however,
they may increase in the course of the disease. After major
surgical procedures, only moderately increased PCT concentrations
are observed. Presently PCT is regarded more suitable than CRP or
other conventional indicators of inflammation to differentiate
acute microbial infections from viral or allograft rejection
following transplantation and immunosuppression. Since PCT
initially shows only a weak induction during cardiac failure, it
could be of prognostic value also in cardiac assist devices by
indicating patients with septic hypotension and poor prognosis.
To answer this question, prospective studies are warranted.
Keywords:
PCT, procalcitonin, bacterial inflammation, sepsis, infection,
immunomonitoring, transplantation, immunosuppression, cardiac
assist devices
Address for Correspondence:
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