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Circulating complement proteins for differentiation of SIRS and sepsis
Critical Care volume 7, Article number: P031 (2003)
Introduction
The systemic inflammatory response of the body to invading microorganisms, termed sepsis, leads to profound activation of the complement (C) system. The main proinflammatory properties of the complement system can be attributed to the anaphylatoxins C3a, C4a, C5a. These polypeptides are generated after proteolytic cleavage of the α-chain of C3, C4 or C5. The present study was conducted to determine serum complement 3 and 4 levels for differentiation in patients with SIRS and sepsis, in comparison with C-reactive protein (CRP), thrombocyte and leukocyte counts.
Method
Fifty-eight patients with SIRS and 41 patients with sepsis were admitted to the study. Blood samples were taken at the first day of intensive care unit for analysis of C3, C4, CRP, thrombocyte and leukocyte counts.
Results
Thrombocyte count was significantly lower in septic patients (mean ± SE: 179,975 ± 14,932, P = 0.005) compared with SIRS patients (243,165 ± 16,243). The plasma concentrations of CRP, C3 and C4 level were not different between groups. The power of parameters to discriminate between septic and SIRS patients was determined in a receiver operating characteristic analysis. Thrombocyte was the best analysis to differentiate between both populations with a maximal sensitivity and specificity (Table 1).
Discussion
In this study, C3, C4 and CRP had poor sensitivity and specificity for the differentiation of SIRS and sepsis. Because of the complex pathophysiology involved, it is likely that not a single mediator but a panel of different inflammatory mediators will ultimately predict the outcomes of individual patients.
References
Selberg O, Hecker H, Martin M, et al.: Crit Care Med 2000, 28: 2793-2798. 10.1097/00003246-200008000-00019
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Sungurtekin, H., BalcĂ˝, C. & Sungurtekin, U. Circulating complement proteins for differentiation of SIRS and sepsis. Crit Care 7 (Suppl 2), P031 (2003). https://doi.org/10.1186/cc1920
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DOI: https://doi.org/10.1186/cc1920