To THE EDITOR—As West Nile virus (WNV) becomes widespread throughout the United States, larger cohort data allow investigators to more precisely identify determinants of clinical outcomes of disease. We commend Bode et al. [1] for uncovering additional factors associated with adverse events in patients hospitalized with WNV infection during an outbreak in 4 Colorado counties in 2003. In this population with high morbidity, multivariate analysis of the presence of rash as a prognostic factor for severe disease and mortality would have been of interest.
Two recent studies of large-scale outbreaks of WNV in the United States have highlighted this finding. In 2002, the Illinois Department of Public Health reported 884 cases of WNV infection and 66 deaths due to infection [2]. Rash was a common finding among all patients for whom information was available (301 [46%] of 654 patients), as well as among patients with neuroinvasive disease (151 [39%] of 390 patients). Among patients with reported rash, age-adjusted risks were significantly decreased for encephalitis (relative risk, 0.67; 95% CI, 0.53–0.84), encephalitis plus death (relative risk, 0.44; 95% CI, 0.21–0.92), and death (relative risk, 0.39; 95% CI, 0.19–0.81). In 2003, the Colorado Epartment of Public Health and Environment reported 2947 cases of WNV infection and 63 deaths due to infection throughout the entire state [3]. A total of 1564 patients (60%) had signs of rash among evaluable cases. Age-adjusted risks for meningitis (OR, 0.7; 95% CI, 0.6–0.9), encephalitis (OR, 0.5; 95% CI, 0.3–0.6), and death (OR, 0.3; 95% CI, 0.1–0.8) were also similarly decreased in patients with reported rash [4].
A characteristic rash typically appears transiently in a diffuse maculopapular pattern at the height of febrile symptoms [4–6]. Few studies have examined the histopathological characteristics of rash lesions in WNV infection. In 1 case series, skin biopsy revealed superficial perivascular lymphocytic infiltrates seen commonly in viral exanthems [6]. Whether the development of rash in WNV infection reflects a functional immunoprotective response to circulating viral antigens requires further investigation and validation. Future surveillance activities should include prospective studies assessing features of rash that might account for its apparent favorable effect against severe disease and mortality in WNV disease.
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