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Treatment of Avian Influenza - Essay Example

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The essay "Treatment of Avian Influenza" focuses on the critical analysis of the major issues in the treatment of avian influenza. Avian influenza was not expected to cause disease in human beings. However, in 1997, an influenza epidemic broke out in Asia and North East Africa…
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Treatment of Avian Influenza
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The continuous effort by the World Health Organization resulted in the WHO declaring that the world was not ready to contain an influenza epidemic in 2005. The swine flu epidemic of 2009 made things look worse. Efforts since then had been consistently attempting to be ever-ready for an influenza epidemic by improving global surveillance and response capacity. The H5N1 avian flu virus was highly pathogenic and had caused disease widely in wild birds and poultry (CDC, 2009). It caused 408 human cases by February 2009. Guidance for testing suspected human cases infected with pathological avian flu with the H5N1 influenza virus was provided. Enhanced surveillance by local and national health care services was to continue. Cases were to be notified to the local and national authorities immediately after a presumptive diagnosis is made. Follow-up of cases was a necessity. In the US, information had to be transferred to the CDC (CDC, 2009).

Testing and reporting guidelines had been established by the CDC. A person diagnosed presumptively with avian flu had to be hospitalized because it could end fatally.  Another requirement for hospitalization was that the temperature of the patient would be equal to or more than 38°C. The patient could have any other respiratory illness like pneumonia or acute or severe respiratory illness (CDC, 2009). Potential exposures occurring within seven previous days could be a reason for admission in the following conditions. Direct contact with infected birds or animals or their feces was another reason for admission. Travel through a country with a history of the virus caused by exposure to any animal or bird, intimate contact with a person with influenza, close contact with a person who was a suspect, and working in a laboratory with a highly pathogenic live virus (CDC, 2009). The infection was spread through droplet infection when in close contact.

Clinicians needed to notify the local and higher authorities when a person was to be diagnosed using laboratory tests. Specific guidelines were also followed for the clinicians who performed the specimen collection and testing. Protective equipment for the clinicians was to be strictly used to prevent any contamination of the body parts of the suspected or confirmed person with H5N1 virus and when entering the room where aerosol-generating procedures have been used where such a patient was lying (CDC, 2009). The respiratory protector (N-95) filtering face mask, goggles, face shield, latex gloves, gown, and head covering were all included (CDC, 2009). In the absence of a particulate respirator, other certified respirators like the NIOSH-certified N-, R-, or P-class respirators could be used. The aerosol-generating procedures could be done only with the N-95 respirator or powered air-purifying respirators (CDC, 2009). Bronchoalveolar lavage was a high-risk aerosol-generating procedure that required excellent protection.  If the clinician had a beard, a loose-fitting respirator could be used. The virus could be detected from the bronchoalveolar lavage, oropharyngeal swabs, or endotracheal aspirate as these specimens usually had the virus. The nasopharyngeal swab contained lesser virus so a lower respiratory specimen should be taken (CDC, 2009). However nasopharyngeal swabs sufficed for detection of influenza viruses A and B. If most virus counts needed to be isolated, multiple respiratory specimens from the same patient could be taken on other days too. The specimen collection could be done by using swabs with a Dacron tip and an aluminium shaft. Immediate transfer was to be made into the sterile transport medium which was stored at the temperature of 4°C till the testing was done. Rapid tests were never to be used for the detection of influenza virus due to low sensitivity. Negative results with these low-sensitivity tests could not be believed to be negative for the presence of the virus H5N1 (CDC, 2009). A positive result did not exclude influenza. A virus or specify virus H5N1. The tests had to be specific.

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