FPIN's Clinical Inquiries. What Is the Best Antiviral Agent for Influenza Infection? Searchable Question

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FPIN's Clinical Inquiries What Is the Best Antiviral Agent for Influenza Infection? Searchable Question What is the best antiviral treatment for influenza? Evidence-Based Answer Four antiviral agents have been approved by the U.S. Food and Drug Administration for the treatment of influenza infection: amantadine (Symmetrel), oseltamivir (Tamiflu), rimantadine (Flumadine), and zanamivir (Relenza). No head-to-head trials have compared the effectiveness of these agents, and no direct evidence exists regarding their relative efficacy. In the absence of specific contraindications, amantadine and rimantadine are preferred for use in most patients because these two agents cost less than the other two. Patients with renal insufficiency or a seizure disorder should not take amantadine, and patients with chronic obstructive pulmonary disease or asthma should not take zanamivir. [Strength of recommendation: C] Evidence Summary The efficacy of each agent has been studied individually. Two systematic reviews showed that amantadine and rimantadine reduced the duration of influenza A symptoms by about one day compared with placebo when the agents were given within 48 hours of symptom onset.1 Three systematic reviews found that zanamivir reduced the duration of influenza A fluenza B symptoms by about one day compared with placebo when it was given within 48 hours of symptom onset.2,3,4 Three systematic reviews also showed that oseltamivir was effective in reducing the duration of symptoms of influenza A fluenza B by one day compared with placebo. However, unlike the other agents, oseltamivir must be given within 36 hours of symptom onset.2,3,5 There is insufficient evidence regarding the effects of antiviral agents in reducing serious complications of influenza. One systematic review showed that oseltamivir reduced the incidence of otitis media following influenza in.3 Adverse effects of antiviral agents were addressed in a nonsystematic review by the Centers for Disease Control and Prevention (CDC) in their annual report on influenza.6 The CDC noted that in a six-week study of healthy adults taking amantadine, rimantadine, or placebo, the incidence of central nervous system (CNS) side effects such as anxiety, insomnia, and difficulty concentrating was 4 percent in the placebo group, 6 percent in the rimantadine group (at 200 mg

daily), and 13 percent in the amantadine group (at 200 mg daily). The CDC noted other studies that found more serious adverse effects such as delirium and seizures, but these adverse effects have occurred primarily in older patients taking amantadine for longer periods, patients with renal insufficiency or a comorbid seizure disorder. The neuraminidase inhibitors (i.e., oseltamivir, zanamivir) are not thought to cause CNS side effects. In one review2 comparing neuraminidase inhibitors with placebo, patients taking the inhibitors had an incidence of gastrointestinal symptoms of 12.7 percent compared with 4.9 percent in the placebo group (odds ratio [OR], 2.57; 95 percent confidence interval [CI], 1.19 to 5.52). The incidence of overall adverse effects in patients taking neuraminidase inhibitors was 37.6 percent versus 18 percent in the placebo group (OR, 2.59; 95 percent CI, 1.59 to 4.21).2 Asthma is a contraindication to the use of zanamivir because the latter may induce bronchospasms.6 Amantadine and rimantadine treat only influenza type A infection. However, the vast majority of influenza in the United States is type A. During the 2003-2004 influenza season, 99.4 percent of the reported cases were type A.7 The accompanying table compares the four antiviral agents.

Antiviral Agents for Treatment of Influenza Infection Age approved for Mechanism of Agent treatment action Amantadine Adults (Symmetrel) and Oseltamivir (Tamiflu) Adults and Rimantadine Adults (Flumadine) and Blocks activity of viral M2 protein Neuraminidase $67 for fiveday inhibitor (capsule) Blocks activity $22 for fiveday of viral M2 protein (tablet) Influenza Approximate viruses Route of cost* inhibited Usual dosage administration Side effects $14 for fiveday A 100 mg twice Oral (capsule and syrup) (capsule) daily for three to five days (reduced elderly patients, those with impairment, one to nine s of age) A, B 75 mg twice A days (reduced patients with impairment one to 13 s of age) 100 mg twice to seven days (reduced elderly patients, those with impairment, one to 10 s of age) CNS and GI symptoms (dose dependent) Oral (capsule GI symptoms and powder for oral suspension) Oral (tablet and syrup) CNS and GI symptoms

Zanamivir (Relenza) Adults and > seven s Neuraminidase $57 for one inhibitor inhaler, fiveday A, B Two inhalations (one 5-mg blister per inhalation for a total dose of 10 mg) twice days Oral inhalation (blisters of powder for inhalation using the Diskhaler device) Bronchospasm in patients with COPD or asthma CNS = central nervous system; GI = gastrointestinal; COPD = chronic obstructive pulmonary disease. *-Average wholesale cost, based on Red Book, Montvale, N.J.: Medical Economics Data, 2004. Recommendations from Others The CDC Advisory Committee on Immunization Practices (ACIP) recommends administration of one of the four antiviral agents within two days of influenza symptom onset. If given within this time period, these agents can reduce the duration of uncomplicated influenza in otherwise healthy adults. None of the four agents has been demonstrated to be effective in preventing serious influenza-related complications. The ACIP warns that the use of antiviral agents should not be considered a substitute for influenza vaccination.6 Clinical Commentary Because the four antiviral agents have similar efficacy, the family physician should consider cost, side effect profiles, spectrum of coverage, and patient's age when selecting an agent. Amantadine and rimantadine are less expensive and have a side effect profile similar to that of placebo. However, the use of amantadine should be avoided in patients 65 s and older, and in patients with renal insufficiency or a seizure disorder. Patients with asthma should not receive zanamivir. Although amantadine and rimantadine are limited in their spectrum of coverage, this is a relatively minor issue. Influenza type B is a mild illness and is not associated with epidemic outbreaks in the United States. HEATHER BITTNER FAGAN, M.D. AMY HOLLIHAN MOELLER, D.O. Christiana Care Health System, Family Medicine Residency Program Wilmington, Delaware REFERENCES 1. Jefferson T, Deeks JJ, Demicheli V, Rivetti D, Rudin M. Amantadine and rimantadine for preventing and treating influenza A in adults. Cochrane Database Syst Rev 2004;(3):CD001169. 2. Jefferson T, Demicheli V, Deeks JJ, Rivetti D. Neuraminidase inhibitors for preventing and treating influenza in healthy adults. Cochrane Database Syst Rev 2004(3):CD001265.

3. Matheson NJ, Symmonds-Abrahams M, Sheikh A, Shepperd S, Harnden A. Neuraminidase inhibitors for preventing and treating influenza in. Cochrane Database Syst Rev 2004;(3):CD002744. 4. Burls A, Clark W, Stewart T, Preston C, Bryan S, Jefferson T, et al. Zanamivir for the treatment of influenza in adults: a systematic review and economic evaluation. Health Technol Assess 2002;6(9):1-87. 5. Husereau DR, Brady B, McGeer A. Oseltamivir for the treatment of suspected influenza: a clinical and economic assessment. Technology report no. 21. Ottawa, Ont.: Canadian Coordinating Office for Health Technology Assessment, 2001. 6. Bridges CB, Harper SA, Fukuda K, Uyeki TM, Cox NJ, Singleton JA. Prevention and control of influenza. Recommendations of the Advisory Committee on Immunization Practices (ACIP) [published correction in MMWR Morb Mortal Wkly Rep 2003;52(22):526]. MMWR Recomm Rep 2003;52(RR-8):1-34. 7. Centers for Disease Control and Prevention. 2003-04 U.S. influenza season summary. Accessed online September 9, 2004, at: http://www.cdc.gov/flu/weekly/fluactivity.htm. Clinical Inquiries provide answers to questions submitted by practicing family physicians to the Family Practice Inquiries Network (FPIN). Members of the network select questions based on their relevance to family medicine. Answers are drawn from an approved set of evidence-based resources and undergo peer review. The strength of recommendations and the level of evidence for individual studies are rated using criteria developed by the Evidence-Based Medicine Working Group (http://www.cebm.net/levels_of_evidence.asp). This series of Clinical Inquiries is coordinated for American Family Physician by John Epling, M.D., State University of New York Upstate Medical University, Syracuse, N.Y. The complete database of evidence-based questions and answers is copyrighted by FPIN. If you are interested in submitting questions to be answered or writing answers for this series, go to http://www.fpin.org or contact CI2Editor@fpin.org. The authors indicate that they do not have any conflicts of interest. Sources of funding: none reported. Address correspondence by e-mail to Amy Hollihan Moeller, D.O., amyhollihan@hotmail.com. Reprints are not available from the authors. Copyright Family Practice Inquiries Network. Used with permission.