Intravenous peramivir vs oral oseltamivir in high-risk emergency department patients with influenza: Results from a
Yu-Hsiang Hsieh1, Andrea F Dugas1, Frank LoVecchio2
1Department of Emergency Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Background:
Peramivir offers a single-dose intravenous (IV) treatment option for influenza (vs 5-day oral dosing for oseltamivir). We sought to compare outcomes of emergency department (ED) patients at high risk for influenza complications treated with IV peramivir vs oral oseltamivir.
Methods:
During the 2015-16 and 2016-17 influenza seasons, adult patients in two US EDs were randomized to either oral oseltamivir or IV peramivir treatment group. Eligibility included positive molecular influenza test; met CDC criteria for antiviral treatment; able to provide informed consent and agree to follow-up assessment. Outcomes were measured by clinical end-point indicators, including FLU-PRO Score, Ordinal Scale, Patient Global Impression on Severity Score, and Karnofsky Performance Scale for 14 days. Non-inferior t test was performed to assess comparative outcomes between the two groups.
Results:
Five hundred and seventy-five (68%) of 847 influenza-positive patients were approached. Two hundred and eighty-four met enrollment criteria and 179 were enrolled; of these 95 (53%) were randomized to peramivir, and 84 to oseltamivir. Average FLU-PRO score at baseline was similar (peramivir: 2.67 vs oseltamivir: 2.52); the score decreased over time for both groups (day 5: peramivir: 1.71 vs oseltamivir: 1.62; day 10: peramivir: 1.48 vs oseltamivir: 1.37; day 14: peramivir: 1.40 vs oseltamivir: 1.33; all P < .05 for significantly non-inferior). Influenza-related complications were similar between two groups (All: peramivir: 31% vs oseltamivir: 21%, P > .05; pneumonia: peramivir: 11% vs oseltamivir: 14%, P > .05).
Conclusions:
Clinical outcomes of influenza-infected patients treated with single-dose IV peramivir were comparable to those treated with oral oseltamivir, suggesting potential utility of peramivir for influenza-infected patients in the ED.
Insights
Single-dose intravenous peramivir demonstrated comparable clinical outcomes to oral oseltamivir for high-risk influenza patients in the emergency department. This suggests peramivir is a viable alternative treatment option for influenza.
Area of Science:
- Infectious Diseases
- Pharmacology
- Clinical Medicine
Background:
- Influenza treatment traditionally involves 5-day oral oseltamivir.
- Peramivir offers a single-dose intravenous (IV) alternative for influenza management.
- This study evaluated peramivir versus oseltamivir in high-risk emergency department patients.
Purpose of the Study:
- To compare clinical outcomes in emergency department patients with influenza receiving IV peramivir versus oral oseltamivir.
- To assess the efficacy and safety of single-dose IV peramivir against a standard oral antiviral regimen.
Main Methods:
- Randomized trial in two US emergency departments during 2015-17 influenza seasons.
- Adult patients with confirmed influenza were randomized to peramivir or oseltamivir.
- Clinical outcomes measured using FLU-PRO, Ordinal Scale, Patient Global Impression, and Karnofsky Performance Scale over 14 days.
Main Results:
- 179 patients enrolled (95 peramivir, 84 oseltamivir) with similar baseline characteristics.
- Both groups showed significant improvement in FLU-PRO scores over 14 days, with non-inferiority demonstrated for peramivir.
- Influenza-related complications, including pneumonia, were similar between the peramivir and oseltamivir groups.
Conclusions:
- Single-dose IV peramivir achieved comparable clinical outcomes to oral oseltamivir in high-risk influenza patients.
- Peramivir presents a potentially useful alternative for influenza treatment in the emergency department setting.
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