Fever of unknown origin (Proceedings)
Nov 01, 2009
CVC IN SAN DIEGO PROCEEDINGS
Fever of Unknown Origin (FUO) is defined in human medicine as an illness of more than 3 weeks duration, with a fever 1.5 °F above normal body temperature on multiple occasions, the cause of which remains uncertain after 1 week of in-hospital investigation.1 In veterinary medicine, the term is much more loosely applied to any patient with a sustained or episodic fever without a readily apparent cause after routine laboratory testing. Fever of unknown origin tends to be a challenging clinical entity in veterinary medicine, frequently necessitating diagnostic testing that is labor intensive, expensive, invasive, and time consuming. Despite this, causes of fever may still go undiagnosed. Understanding the pathophysiology and varied causes of fever is critical to successful management of these frustrating cases.
The febrile response is a "complex physiologic reaction to disease, involving a cytokine mediated rise in core temperature, generation of acute phase reactants, and activation of numerous physiologic, endocrinologic, and immunologic systems." Fever develops when exogenous or endogenous stimuli such as endotoxin, viral, bacterial rickettsial, or fungal agents, tumor antigens, tissue necrosis, or immune-mediated diseases induce mononuclear cells to release endogenous pyrogens. The pyrogens most commonly associated with febrile responses include interleukins (IL-1 and IL-6), tumor necrosis factor (TNF), and interferon. Exogenous antigens taken up by Kupffer cells in the liver, or endogenous pyrogens entering the central nervous system at the anterior hypothalamus elevate the thermoregulatory setpoint through upregulation of prostaglandin E2. Alteration of the hypothalamic "thermostat" in this way triggers physiologic mechanisms such as shivering and vasoconstriction that increase heat production and conservation within the body.
Animal experimental models evaluating the effect of fever on survival during infection suggest that mild to moderate fevers benefit the host, and may improve survival during sepsis. Increased temperature is known to induce change in phagocytic cells and lymphocytes, stimulate release of interferon, and induce the heat shock response. This heat shock response leads to the production of heat shock proteins (HSPs) that serve to protect against cell death from a variety of stressors, including endotoxemia. Additionally, increasing temperature may lower minimum inhibitory concentrations of antibiotics, progressively increasing their antimicrobial activity. Severe fever (>106 °F) may become dangerous however, as a result of altered cellular metabolism and direct thermal damage to a variety of tissues (ie. Heatstroke).