LOCAL AND SYSTEMIC INFLAMMATORY MEDIATOR RELEASE IN PATIENTS WITH ACUTE AND CHRONIC POSTTRAUMATIC OSTEOMYELITIS

Citation
B. Klosterhalfen et al., LOCAL AND SYSTEMIC INFLAMMATORY MEDIATOR RELEASE IN PATIENTS WITH ACUTE AND CHRONIC POSTTRAUMATIC OSTEOMYELITIS, The journal of trauma, injury, infection, and critical care, 40(3), 1996, pp. 372-378
Citations number
43
Categorie Soggetti
Emergency Medicine & Critical Care
Volume
40
Issue
3
Year of publication
1996
Pages
372 - 378
Database
ISI
SICI code
Abstract
The local and systemic release of thromboxane A(2), prostaglandin I-2, leukotriene B-4 (LTB(4)), tumor necrosis factor alpha (TNF-alpha), in terleukin-1 beta (IL-1 beta), interleukin-6 (IL-6), and interleukin-8 (IL-8) were studied before and after operation in 29 patients with acu te and 22 with chronic posttraumatic osteomyelitis, Twenty patients wi thout osteomyelitis, who underwent operations for fractures of the low er extremities, served as controls. Blood and tissue samples from the osteomyelitic and control groups were collected under defined conditio ns and mediators were determined by radioimmunoassay (thromboxane B-2, 6-keto-prostaglandin F-1 alpha, LTB(4)) or by enzyme-linked immunosor bent assay (TNF-alpha, IL-1 beta, IL-6, and IL-8). In addition, common parameters (leukocyte count, C-reactive protein, temperature) were me asured. The best correlation with acute disease activity was given by TNF-alpha, IL-6, IL-8, and LTB(4). Plasma levels of these mediators in acute osteomyelitis were significantly increased compared to chronic osteomyelitis and to controls, respectively. Tissue samples from the o steomyelitic focus shelved significantly increased levels for IL-8, IL -6, TNF-alpha, IL-1 beta, and LTB(4) in acute osteomyelitis, whereas t he values for TxB(2) and 6-keto-prostaglandin F-1 alpha were only slig htly increased compared to the chronic osteomyelitis group, This study describes the local and systemic liberation of various mediators in a cute and chronic posttraumatic osteomyelitis in detail for the first t ime and provides data for pre- and postoperative monitoring of disease activity and demonstrates new pathogenetic and therapeutic aspects of bane modulation in osteomyelitis.