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CIDRAP: CDC updates advice on antiviral treatment for flu

Shiloh

Editor, Senior Moderator
Source: http://www.cidrap.umn.edu/cidrap/content/influenza/swineflu/news/jun2509tamiflu-brjw.html


CDC updates advice on antiviral treatment for flu

Lisa Schnirring * Staff Writer

Jun 25, 2009 (CIDRAP News) ? The US Centers for Disease Control and Prevention (CDC) today at the Advisory Committee on Immunization Practices meeting in Atlanta issued updated guidelines for treatment of influenza, including novel H1N1, suggesting basing antiviral selection on laboratory test results when possible.

The new guidance appears to be aimed at preventing the inadvertent prescription of oseltamivir (Tamiflu) for seasonal H1N1 infections, which have shown extensive resistance to oseltamivir in the United States and other parts of the world. The update was provided by CDC spokesman Tom Skinner.

According to the CDC update, only patients who test positive for influenza A/H3N2, pandemic H1N1, or B should receive oseltamivir. Zanamivir (Relenza) is preferred for patients who test positive for seasonal H1N1 influenza.

If a laboratory test is not performed or the test is negative but clinical suspicion remains, the preferred treatment is zanamivir or a combination of oseltamivir and rimantadine, which is an older drug of the adamantine class of antivirals. If testing indicates influenza A or unspecified influenza, the preferred treatment is also zanamivir or a combination of oseltamivir and rimantadine.

As with its earlier recommendation for novel H1N1 treatment, the CDC emphasized in today's updated guidance that treatment should be started as soon as possible after illness onset.

The CDC added a few more specifics to the list of people for whom antiviral treatment should be considered to include those who are hospitalized with influenza, have influenza with viral or bacterial pneumonia, or have influenza with a higher risk for complications, regardless or illness severity.

Seasonal flu strains, which typically wane this time of year, account for only a small fraction of currently circulating strains, the CDC said on Jun 19 in its surveillance update for the week ending Jun 13. More than 98% of subtyped influenza A viruses reported to the CDC were pandemic H1N1 strains. Seasonal H1N1 and H3N2 each accounted for only 0.8% of the viruses.

Last December the CDC changed its guidance about flu treatment after noting increased resistance to oseltamivir, the leading influenza drug. The new guidance added adamantanes back into the recommendations, suggesting zanamivir or oseltamivir plus rimantadine for patients suspected of having seasonal influenza A infections.

See also:

May 6 CDC interim antiviral recommendations for patients with novel H1N1 infections and their contacts

Dec 19, 2008, CIDRAP News story "With H1N1 resistance, CDC changes advice on flu drugs"

CDC weekly influenza update
 
Re: CIDRAP: CDC updates advice on antiviral treatment for flu

This is murky.

Why to insert the seasonal AH1N1 resistance to not using Tamiflu,
when such seasonal flu is supposed to not circulate now in USA (?)

There is more maybe, because in the same text it is inserted the dual somministration for new flu, instead of only Tamiflu:

#1:
"If a laboratory test is not performed or the test is negative but clinical suspicion remains, the preferred treatment is zanamivir or a combination of oseltamivir and rimantadine, which is an older drug of the adamantine class of antivirals. If testing indicates influenza A or unspecified influenza, the preferred treatment is also zanamivir or a combination of oseltamivir and rimantadine."
 
Re: CIDRAP: CDC updates advice on antiviral treatment for flu

Yes, interesting treatment update. I like to see the recommendation for Relenza (zanamivir) as a possible alternative to tamiflu. Also I like the recommendation for treating if there is a high level of suspicion. Physician judgement is needed here to not overtreat people that already have underlying medical problems and yet to promptly start treatment in these and other patients if they truly are showing influenza like symptoms. Also it would be important to know how robust and timely your supporting testing system is.

It would seem prudent to give the inhalational Relenza under the supervision of a physician especially for asthma patients or other patients with reactive airway disease because of the possible complication of bronchospasm.

It would be interesting to know if the investigational drug peramivir which is given intravenously is being tried in seriously ill patients...


http://www.cdc.gov/mmwr/preview/mmwrhtml/mm58d0428a1.htm?s_cid=mm58d0428a1_e

Update: Drug Susceptibility of Swine-Origin Influenza A (H1N1) Viruses, April 2009

Since April 21, 2009, CDC has reported cases of respiratory infection with a swine-origin influenza A (H1N1) virus (S-OIV) that is being spread via human-to-human transmission (1).

.......

Two NAIs, oseltamivir (Tamiflu [Hoffman-La Roche, Ltd, Basel, Switzerland]) and zanamivir (Relenza [GlaxoSmithKline, Stevenage, United Kingdom]) are FDA-approved drugs for use against type A and type B influenza infections (16). The two drugs differ structurally, resulting in oseltamivir being orally bioavailable, whereas zanamivir is not and must be inhaled (17,18). A third NAI, peramivir (BioCryst, Inc., Birmingham, Alabama), is formulated for intravenous administration and is undergoing clinical trials, and a fourth, called A-315675 (Abbott Laboratories, Abbott Park, Illinois) has only been investigated in preclinical studies.

......
 

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