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Endemic/pandemic worldwide every 3–5 y.
Outbreaks likely during summer and early fall.
Affects persons of all ages.
Long incubation periods of 1–3 wk.
Transmitted person to person via aerosols.
Frequent in closed and semiclosed communities.
Common cause of upper and lower respiratory infections.
Up to 40% of community-acquired pneumonias, “walking pneumonia.”
Up to 5% of bronchiolitis in children.
3–10% of adults may develop bronchopneumonia.
Clinical manifestations similar to Chlamydophila pneumonia, Streptococcus pneumonia, and respiratory viruses.
Fulminant pneumonia may occur in children with sickle cell disease (functional asplenism), Down syndrome, and immunosuppressive conditions.
Extrapulmonary complications in 25% of pts infected with Mycoplasma pneumoniae.
No periop risk data; hemolytic anemia, DIC, and cross-reacting cold agglutinins are of concern, especially if CPB is required.
Hyper-reactive airway disease.
Multisystem organ dysfunction
Clinical manifestations of respiratory involvement are mediated by activity of cytoadherence on the airway epithelium and include
Sore throat, hoarseness, fever, cough (pertussis-like).
May play a role in asthma, COPD.
Conjunctivitis, headache, chills, coryza, myalgias, earache, and generalized malaise are common.
Extrapulmonary manifestations are the result of direct invasion or immune reactivity.
Dx:
Hx and clinical manifestations: Unspecific upper respiratory symptoms.
CXR: Diffuse reticular infiltrates in perihilar and lower lobe regions; bilateral in 20% of cases.
Pathology: Ulceration, edema, ciliary loss, bronchioalveolar inflammatory cell infiltration.
Culture: Incubation period of several wk; sensitivity around 60%; not practical for routine diagnosis.
Serology: Current or recent infection likely if antibody titer increase ≥fourfold.
Cold agglutinins: IgM within 1–2 wk after initial infection; titers ≥1:32 correlate with severity of lung involvement.
PCR: RNA-amplification techniques are highly sensitive and indicate viable bacterium.
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