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Inflammatory response syndrome, systemic

In rare cases of a systemic release, kinins have the potential to cause severe hypotension. Uncontrolled activation of the contact system (Fig. 3) is thought to trigger a massive formation of kinins under certain pathological conditions [3]. For instance, this situation is seen in patients with underlying diseases such as systemic inflammatory response syndrome (SIRS) due to sepsis or trauma. SIRS progression is accompanied by depletion of contact system factors and low levels of H-kininogen and plasma kallikrein are indicative of a... [Pg.675]

Sepsis is a continuum of physiologic stages characterized by infection, systemic inflammation, and hypoperfusion with widespread tissue injury.1 The American College of Chest Physicians and the Society of Critical Care Medicine developed definitions to utilize for sepsis (Table 79—l).2 They provide physiologic parameters categorizing patients as having bacteremia, infection, systemic inflammatory response syndrome (SIRS), sepsis, severe sepsis, septic shock, or multiple-organ-dysfunction syndrome (MODS).2 Standardized definitions have been developed for infections in critically ill patients.3... [Pg.1185]

Sepsis The systemic inflammatory response syndrome and documented infection (culture or Gram stain of blood, sputum, urine, or normally sterile body fluid positive for pathogenic microorganisms Severe sepsis Sepsis associated with organ dysfunction, hypoperfusion, or hypotension (systolic blood pressure less than 90 mm Hg). Hypoperfusion and perfusion abnormalities may include, but are not limited to, lactic acidosis, oliguria, or acute alteration in mental status. [Pg.1186]

According to the patient s parameters what does he have (i.e., systemic inflammatory response syndrome, sepsis, or septic shock) ... [Pg.1190]

Focus efforts on distinguishing sepsis from systemic inflammatory response syndrome, since identification and treatment of an infection should be initiated as soon as possible (with antibiotics or surgical drainage). [Pg.1196]

Kaneider NC, Agarwal A, Leger AJ, Kuliopulos A. Reversing systemic inflammatory response syndrome with chemokine receptor pepducins. Nat Med 2005 11 661-665. [Pg.82]

Systemic inflammatory response syndrome The systemic inflammatory response to a wide variety of severe clinical insults. The response is manifested by two or more of the following conditions Temperature >38°C or <36°C Heart rate >90 beats/min... [Pg.58]

Pathological findings frequently observed in organs of patients who have died of sepsis include disseminated intravascular coagulation (DIC), manifested as diffuse thrombotic occlusions in the entire microvascular system, associated with alterations in the hemostatic mechanism and clinical signs of hemorrhagic diathesis. Many observations indicate that DIC contributes to the major symptoms of the systemic inflammatory response syndrome (SIRS), which frequently complicate sepsis (HI, H2, H3, T6). [Pg.76]

D5. Darville, T Giroir, B and Jacobs, R., The systemic inflammatory response syndrome (SIRS) immunology and potential immunotherapy. Infection 21,279-290 (1993). [Pg.112]

G3. Gando, S., Kameue, T., Nanzaki, S and Nakanishi, Y., Cytokines, soluble thrombomodulin and disseminated intravascular coagulation in patients with systemic inflammatory response syndrome. Thomb. Res. 80,519-526 (1995). [Pg.115]

Patients predicted to follow a severe course require treatment of any cardiovascular, respiratory, renal, and metabolic complications. Aggressive fluid resuscitation is essential to correct intravascular volume depletion and maintain blood pressure. IV colloids may be required because fluid losses are rich in protein. Drotrecogin alfa may benefit patients with pancreatitis and systemic inflammatory response syndrome. IV potassium, calcium, and magnesium are used to correct deficiency states. Insulin is used to treat hyperglycemia. Patients with necrotizing pancreatitis may require antibiotics and surgical intervention. [Pg.320]

Definitions of terms related to sepsis are given in Table 45-1. Physiologically similar systemic inflammatory response syndrome can be seen even in the absence of identifiable infection. [Pg.500]

Systemic inflammatory response syndrome secondary to infection. [Pg.501]

Compensatory physiologic response to systemic inflammatory response syndrome that is considered secondary to the actions of antiinflammatory cytokine mediators. [Pg.501]

Sepsis What the pathogen does to the patient. For example, a patient with gram-negative bacillary pneumonia may receive a perfectly adequate course of antibiotic chemotherapy, only to succumb to systemic inflammatory response syndrome (SIRS), an exaggerated and counterproductive release of inflammatory cytokines. [Pg.510]

Lissauer, M.E., et al. (2007) Coagulation and complement protein differences between septic and uninfected systemic inflammatory response syndrome patients. / Tmuma. 62, 1082-92 discussion 1092-4. [Pg.212]

Noradrenaline is used to treat shock-like conditions associated with peripheral vasodilatation, e.g. sepsis, systemic inflammatory response syndrome (SIRS), neurogenic shock. The rationale of its use in sepsis and SIRS is to counteract the vasodilatory effects of nitric oxide. Following the surgical removal of phaeochromocytoma and similar tumours, noradrenaline is often given to maintain blood pressure in the initial period. During and after cardiac surgery, it may be used to optimise haemodynamic parameters in combination with other drugs, such as phosphodi-esterase inhibitors. Dose... [Pg.152]

Rangel-Frausto MS, Pittet D, Costigan M, Hwang T, Davis CS, Wenzel RP (1995) The natural history of the systemic inflammatory response syndrome (SIRS). A prospective study. JAMA 273(2) 117-123... [Pg.230]

Ogura H, Tanaka H, Koh T, Fujita K, Fujimi S, Nakamori Y, Hosotsubo H, Kuwagata Y, Shimazu T, Sugimoto H. Enhanced production of endothelial microparticles with increased binding to leukocytes in patients with severe systemic inflammatory response syndrome. J Traum 2004 56 823-830. [Pg.158]

H7. Hietaranta, A., Kemppainen, E., Puolakkainen, P., Sainio, V., Haapiainen, R., Peuravuori, H., Kivilaakso, E., and Nevalainen, T., Extracellular phospholipases A2 in relation to systemic inflammatory response syndrome (SIRS) and systemic complications in severe acute pancreatitis. Pancreas 18, 385-391 (1999). [Pg.74]

Raper, S. E., Chirmule, N., Lee, F. S., Wivel, N. A., Bagg, A., Gao, G. P., Wilson, J. M. and Batshaw, M. L. (2003). Fatal systemic inflammatory response syndrome in a ornithine transcarbamylase deficient patient following adenoviral gene transfer. Mol. Genet. Metab. 80, 148-158. [Pg.273]


See other pages where Inflammatory response syndrome, systemic is mentioned: [Pg.676]    [Pg.295]    [Pg.203]    [Pg.207]    [Pg.1082]    [Pg.1186]    [Pg.1196]    [Pg.73]    [Pg.57]    [Pg.501]    [Pg.501]    [Pg.417]    [Pg.561]    [Pg.316]    [Pg.208]    [Pg.220]    [Pg.145]    [Pg.149]    [Pg.51]    [Pg.68]    [Pg.266]    [Pg.467]   
See also in sourсe #XX -- [ Pg.481 , Pg.2131 ]




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