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Microbiology and Pathogenesis !!navigator!!

Influenza A, B, and C viruses are RNA viruses and members of the family Orthomyxoviridae that have different nucleoprotein (NP) and matrix (M) protein antigens. Influenza A and B viruses are major human pathogens and are morphologically similar; influenza B infection is associated with less severe disease than influenza A infection, and influenza C virus causes subclinical disease.

Epidemiology !!navigator!!

Influenza outbreaks occur each year but vary in extent and severity. Influenza A epidemics occur almost exclusively during the winter months in temperate climates but take place year-round in the tropics. These epidemics begin abruptly, peak over 2-3 weeks, last 2-3 months, and then subside rapidly.

  • Global pandemics (the most recent of which took place in 2009 and was due to an A/H1N1 virus) occur, by definition, at multiple locations; they carry high attack rates (10-20% of the general population), extend beyond normal seasonality patterns, and are due in part to the propensity of the H and N antigens to undergo periodic antigenic variation.
    • - Major changes (which are restricted to influenza A viruses) are called antigenic shifts and are associated with pandemics.
    • - Minor variations are called antigenic drifts.
  • Avian influenza viruses (e.g., A/H5N1) cause sporadic human cases, but sustained human-to-human transmission has not been observed; infection is linked to direct contact with infected poultry.
  • Swine can sustain simultaneous infection with swine, human, and avian influenza viruses; these multiple-virus infections facilitate reassortment of genetic segments of different viruses. For example, the pandemic A/H1N1 virus of 2009-2010 represented a quadruple reassortment among swine, avian, and human influenza viruses.
  • Interpandemic outbreaks of influenza are associated with an average of 226,000 hospitalizations and 23,000 excess deaths per year in the United States. Chronic cardiopulmonary disease and old age are the most prominent risk factors for severe illness.

Clinical Manifestations !!navigator!!

Influenza has a wide spectrum of clinical presentations, ranging from a mild illness resembling the common cold to severe prostration with relatively few respiratory symptoms. The classic description involves the abrupt onset of headache, fever, chills, myalgia, and malaise in the setting of respiratory symptoms (e.g., cough, sore throat).

  • Pts typically defervesce within 2-3 days, but respiratory symptoms accompanied by substernal pain can persist for 1 week. Postinfluenzal asthenia may persist for weeks, particularly in the elderly.
  • Complications of influenza (pneumonia and extrapulmonary manifestations) are more common among pts <5 and >65 years old, pregnant women, and pts with chronic disorders (e.g., cardiopulmonary disease, diabetes, renal diseases, hemoglobinopathies, or immunosuppression).
    • - Pneumonia: Primary influenza pneumonia is the least common but most severe of the pneumonic complications, most often affecting pts with mitral stenosis and pregnant women. Pts have progressive pulmonary disease and high titers of virus in respiratory secretions.
  • Secondary bacterial pneumonia is usually due to Streptococcus pneumoniae, Staphylococcus aureus, or Haemophilus influenzae and presents as the reappearance of fever and respiratory symptoms after 2-3 days of clinical improvement.
  • The most common pneumonic complication involves aspects of viral and bacterial pneumonia.
    • - Extrapulmonary complications: Reye's syndrome, myositis, rhabdomyolysis, myoglobinuria, and CNS disease (e.g., encephalitis, transverse myelitis, Guillain-Barré syndrome) can occur as complications of influenza infection.
  • Reye's syndrome is a serious complication in children that is associated with influenza B virus (and less commonly with influenza A virus), varicella-zoster virus, and aspirin therapy for the antecedent viral infection.

Laboratory Findings !!navigator!!

Reverse-transcription PCR of respiratory samples (e.g., throat swabs, nasopharyngeal washes, sputum) is the most sensitive and specific technique for detecting influenza.

  • Rapid tests that detect viral antigens yield results quickly, can sometimes distinguish influenza A and B viruses, and are relatively specific but variably sensitive.
  • Serologic testing requires the availability of acute- and convalescent-phase sera and is useful only retrospectively.

Treatment: Influenza

  • See Table 101-1 for specific treatment of influenza.
    • - Antiviral agents have been tested in young adults with uncomplicated influenza but not in the treatment or prevention of complications associated with influenza.
    • - If started within 2 days of illness due to a susceptible virus (with possible efficacy up to 5 days after onset of symptoms), the neuraminidase inhibitors (oseltamivir and zanamivir) and the adamantane agents (amantadine and rimantadine) reduce the duration of signs and symptoms by 1-1.5 days and ~50%, respectively.
    • - An IV formulation of peramivir, a neuraminidase inhibitor, has recently been approved by the FDA; an IV formulation of zanamivir is in clinical trials.
    • - Zanamivir may exacerbate bronchospasm in asthmatic pts, while oseltamivir has been associated with nausea and vomiting (reactions whose incidence is reduced if the drug is given with food) and with neuropsychiatric side effects in children.
    • - Amantadine causes mild CNS side effects (e.g., jitteriness, anxiety, insomnia, difficulty concentrating) in ~5-10% of pts; rimantadine has fewer CNS side effects.
  • For uncomplicated influenza in individuals at low risk for complications, symptom-based rather than antiviral therapy may be considered.

Prophylaxis !!navigator!!

Annual vaccination with either an inactivated or a live attenuated vaccine is the main public health measure for prevention of influenza.

  • Vaccine strains are generated from influenza A and B viruses that have circulated during the previous influenza season and whose circulation during the upcoming season is predicted.
    • - For inactivated vaccines, 50-80% protection against influenza is expected if the vaccine virus and the currently circulating viruses are closely related.
    • - Influenza vaccination is currently recommended for all individuals >6 months of age.
  • Chemoprophylaxis against influenza (Table 101-1) should be reserved for individuals at high risk of complications who have had close contact with a pt sick with influenza. Chemoprophylaxis can be administered simultaneously with inactivated—but not with live—vaccine.


Outline

Outline

Section 7. Infectious Diseases