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

E. van der Vries

    Research output: Contribution to journalArticleAcademicpeer-review

    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.
    Original languageEnglish
    Article number21844304
    Pages (from-to)777-782
    Number of pages6
    JournalJournal of Infectious Diseases
    Volume204
    Issue number5
    DOIs
    Publication statusPublished - 1 Sept 2011

    Keywords

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

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