Mycoplasma pneumoniae Infection


Risk

  • 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.

Perioperative Risks

  • No periop risk data; hemolytic anemia, DIC, and cross-reacting cold agglutinins are of concern, especially if CPB is required.

  • Hyper-reactive airway disease.

Worry About

  • Multisystem organ dysfunction

Overview

  • 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.

You're Reading a Preview

Become a Clinical Tree membership for Full access and enjoy Unlimited articles

Become membership

If you are a member. Log in here