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Neuraminidase Inhibitor Therapy in a Military Population

Overview
Journal J Clin Virol
Specialty Microbiology
Date 2015 May 12
PMID 25959151
Citations 1
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Abstract

Background: Although neuraminidase inhibitors (NI) are the mainstay of treatment for influenza infection, prescribing practice for these agents is not well described. Additionally, benefit is contested.

Objectives: We examined provider prescriptions of NI during the 2009 pandemic and post-pandemic periods. We also evaluated the effectiveness of NI in reducing severity of influenza infection.

Study Design: Data on NI prescription and severity of influenza infection were compiled in healthy pediatric and adult beneficiaries enrolled in a prospective study of influenza like illness conducted at five military medical centers over five years. Subjects underwent nasal swabs to determine viral etiology of their infection. Demographic, medication and severity data were collected. Subjects with positive influenza were included.

Results: Two hundred sixty three subjects were influenza positive [38% [H1N1] pdm09, 38.4% H3N2, and 20.5% B); 23.9% were treated with NI. NI were initiated within 48h in 63% of treated subjects. Although NI use increased over the five years of the study, early use declined. Most measures for severity of illness were not significantly reduced with NI; adults treated within 48h had only a modest reduction in duration and severity of some of their symptoms.

Conclusions: NI use in our population is increasing, but early use is not. NI use resulted in no reduction in complications of illness. Resolution of symptoms and reduction in severity of some symptoms were slightly better in adults who were treated early. These modest benefits do not support routine treatment with NI in otherwise healthy individuals with influenza.

Citing Articles

The Acute Respiratory Infection Consortium: A Multi-Site, Multi-Disciplinary Clinical Research Network in the Department of Defense.

Coles C, Millar E, Burgess T, Ottolini M Mil Med. 2019; 184(Suppl 2):44-50.

PMID: 31778194 PMC: 6886571. DOI: 10.1093/milmed/usz174.

References
1.
Witkop C, Duffy M, Macias E, Gibbons T, Escobar J, Burwell K . Novel Influenza A (H1N1) outbreak at the U.S. Air Force Academy: epidemiology and viral shedding duration. Am J Prev Med. 2009; 38(2):121-6. DOI: 10.1016/j.amepre.2009.10.005. View

2.
Uyeki T . Antiviral treatment for patients hospitalized with 2009 pandemic influenza A (H1N1). N Engl J Med. 2009; 361(23):e110. DOI: 10.1056/NEJMopv0910738. View

3.
Ling L, Chow A, Lye D, Tan A, Krishnan P, Cui L . Effects of early oseltamivir therapy on viral shedding in 2009 pandemic influenza A (H1N1) virus infection. Clin Infect Dis. 2010; 50(7):963-9. DOI: 10.1086/651083. View

4.
Morgan O, Bramley A, Fowlkes A, Freedman D, Taylor T, Gargiullo P . Morbid obesity as a risk factor for hospitalization and death due to 2009 pandemic influenza A(H1N1) disease. PLoS One. 2010; 5(3):e9694. PMC: 2837749. DOI: 10.1371/journal.pone.0009694. View

5.
Grijalva-Otero I, Talavera J, Solorzano-Santos F, Vazquez-Rosales G, Vladislavovna-Doubova S, Perez-Cuevas R . Critical analysis of deaths due to atypical pneumonia during the onset of the influenza A (H1N1) virus epidemic. Arch Med Res. 2010; 40(8):662-8. DOI: 10.1016/j.arcmed.2009.10.010. View