2008-2009 Influenza Season Week 40, ending October 4, 2008
(All data are preliminary and may change as more reports are received.)The Centers for Disease Control and Prevention’s (CDC) Influenza Division collects and analyzes surveillance data year-round and produces a weekly report on U.S. influenza activity from October through May. The U.S. influenza surveillance system consists of information in five different categories collected from nine different data sources.
From week 21 through week 39 (weeks ending May 18 – September 27), WHO and NREVSS laboratories located in all 50 states and Washington DC tested 25,031 specimens for influenza and 179 (0.7%) were positive. Influenza positive tests were reported from all nine public health surveillance regions during the summer. Of the positive results, 6 (3.4%) were influenza A (H1) viruses, 21 (11.7%) were influenza A (H3) viruses, 80 (44.7%) were influenza A viruses that were not subtyped, and 72 (40.2%) were influenza B viruses. More than half (63%) of these isolates were tested from mid-May through late July. Of the 40 influenza viruses reported during September (weeks 36-39), one (2.5%) was an influenza A (H1) virus, four (10.0%) were influenza A (H3) viruses, 29 (72.5%) were influenza A viruses that were not subtyped, and six (15.0%) were influenza B viruses.
Since September 30, 2007, WHO and NREVSS laboratories have tested a total of 218,493 specimens for influenza viruses and 39,407 (18.0%) were positive. Among the 39,407 influenza viruses, 28,091 (71.3%) were influenza A viruses and 11,316 (28.7%) were influenza B viruses. Eight thousand two hundred seventy-two (29.4%) of the 28,091 influenza A viruses have been subtyped: 2,173 (26.3%) were influenza A (H1) viruses and 6,099 (73.7%) were influenza A (H3) viruses.
During week 40, WHO and NREVSS laboratories reported 1,123 specimens tested for influenza viruses, eight of which were positive: five influenza A viruses that were not subtyped (Mountain, Pacific, South Atlantic and West South Central regions) and three influenza B virus (Mountain and South Atlantic regions).

A small number of isolates were available for antigenic characterization during the summer. CDC antigenically characterized six isolates collected from May 18 – September 27, including four influenza A (H1), one influenza A (H3), and one influenza B viruses. All six viruses are antigenically similar to the components selected for the 2008-09 influenza vaccine (A/Brisbane/59/2007-like (H1N1), A/Brisbane/10/2007-like (H3N2), and B/Florida/04/2006-like).
No novel influenza A virus infections were reported during the summer of 2008 or for week 40.
In the United States, two groups of antiviral drugs have been approved by FDA for use in treating or preventing influenza virus infections. These two groups of antiviral drugs are: neuraminidase inhibitors (oseltamivir and zanamivir) and adamantanes (amantadine and rimantadine). A description of these drugs can be found at: http://www.cdc.gov/flu/protect/antiviral/index.htm.
A small number of isolates collected since May 18 were sent to CDC for antiviral resistance testing during the summer.
Neuraminidase Inhibitor Antiviral Drugs: CDC performed antiviral resistance testing on 10 influenza A and B viruses collected since May 18. Two of the six influenza A (H1N1) viruses tested were found to be resistant to oseltamivir. No oseltamivir resistance has been detected in influenza A (H3N2) or influenza B viruses, and all tested viruses retain their sensitivity to zanamivir. Additional information on antiviral resistance can be found at: http://www.cdc.gov/flu/about/qa/antiviralresistance.htm
Adamantane Antiviral Drugs:Six influenza A viruses collected since May 18 have been tested for adamantane resistance. The one influenza A (H3N2) virus tested and one of the five influenza A (H1N1) viruses tested were resistant to the adamantanes. The adamantanes are not effective against influenza B viruses.
Based on the level of oseltamivir resistance observed in only one influenza subtype, H1N1, and the persisting high levels of resistance to the adamantanes in H3N2 viruses, CDC continues to recommend the use of oseltamivir and zanamivir for the treatment or prevention of influenza. Use of amantadine or rimantadine is not recommended. Guidance on influenza antiviral use can be found at: http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5606a1.htm
No influenza-associated pediatric deaths were reported for week 40.

No influenza-associated pediatric deaths were reported for week 40.

Laboratory-confirmed influenza-associated hospitalizations are monitored in two population-based surveillance networks: the Emerging Infections Program (EIP) and the New Vaccine Surveillance Network (NVSN). EIP and NVSN estimated rates of hospitalization for influenza will be reported every two weeks starting later this season.
During week 40, 0.8% of patient visits reported through the US Outpatient Influenza-like Illness Surveillance Network (ILINet), formally known as the US Influenza Sentinel Provider Surveillance Network, were due to influenza-like illness (ILI). This percentage is less than the national baseline of 2.4%. On a regional level, the percentage of visits for ILI ranged from 0.3% to 1.6%. All nine regions reported percentages of visits for ILI below their respective region-specific baselines.

During week 40 the following influenza activity was reported: