Evaluation of the Antiviral Response to Zanamivir Administered Intravenously for Treatment of Critically Ill Patients With Pandemic Influenza A (H1N1) Infection

Abstract

A retrospective nationwide study on the use of intravenous (IV) zanamivir in patients receiving intensive care who were pretreated with oseltamivir in the Netherlands was performed. In 6 of 13 patients with a sustained reduction of the viral load, the median time to start IV zanamivir was 9 days (range, 4-11 days) compared with 14 days (range, 6-21 days) in 7 patients without viral load reduction (P = .052). Viral load response did not influence mortality. We conclude that IV zanamivir as late add-on therapy has limited effectiveness. The effect of an immediate start with IV zanamivir monotherapy or in combination with other drugs need to be evaluated.

Keywords

antiviral agents, critical illness, netherlands, viral load result, infection, influenzavirus a, mortality, zanamivir, oseltamivir, pandemics, influenza a virus, h1n1 subtypeswine, influenza

Citation

van der Vries, E 2011, 'Evaluation of the Antiviral Response to Zanamivir Administered Intravenously for Treatment of Critically Ill Patients With Pandemic Influenza A (H1N1) Infection', Journal of Infectious Diseases, vol. 204, no. 5, 21844304, pp. 777-782. https://doi.org/10.1093/infdis/jir397