Abstract
The pattern of vascular tone seen in patients with the sepsis syndrome is generally, and certainly in the early stages, one of reduced peripheral vascular resistance, often with a normal or elevated cardiac output (Siegel et al. 1971; Groeneveld et al. 1986; Thijs and Groeneveld 1988). This loss of vascular tone can be persistent (‘unrelenting hypotension’: Thijs et al. 1987) and is one of the major causes of death in these patients (Parker et al. 1984). Circulating endotoxin (lipopolysaccharide; LPS) is an important component of human shock pathogenesis; indeed, the administration of small doses of endotoxin to human volunteers results in a cardiovascular pattern identical to that seen early in septic shock (Parrillo, 1989).
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Fleming, I. et al. (1991). Mechanisms of Vascular Impairment During Endotoxaemia with Special Reference to the Role of the L-arginine Pathway. In: Schlag, G., Redl, H., Siegel, J.H., Traber, D.L. (eds) Shock, Sepsis, and Organ Failure. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-76511-7_16
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