Mycoplasmal Pneumonia Workup

  • Author: Michael Joseph Bono, MD, FACEP; Chief Editor: Robert E O'Connor, MD, MPH   more...
 
Updated: Mar 29, 2011
 

Approach Considerations

Laboratory tests are generally of limited benefit in mycoplasmal pneumonia, as they tend to be nonspecific or within the normal range. For example, elevated erythrocyte sedimentation rates (ESR) may be present but are nonspecific. The white blood cell (WBC) count is generally not helpful in this condition, because results may be normal or elevated, and, although hemolytic anemia has been described, it is rare.

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Radiography

Chest radiographic findings vary, but abnormalities are usually more striking than the findings upon physical examination. Bronchopneumonia often involves a single lower lobe, although lobar consolidation is rare. Platelike atelectasis is noted as thin, flat areas of collapsed lung and is often seen on a lateral image of the chest. Pleural effusions develop in less than 20% of patients; when present, they can be seen on lateral decubitus films.

Reticulonodular or interstitial infiltrates, primarily in the lower lobes, may resemble other diseases with granulomatous pathology, such as tuberculosis, mycoses, and sarcoidosis; hilar adenopathy is sometimes mistaken for malignancy.

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CT Scanning

High-resolution computed tomography (CT) scans of the chest are more sensitive than chest radiography in elucidating lung disease.[16]

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Sputum Culture

Sputum Gram stains and cultures are usually not helpful, because M pneumoniae lacks a cell wall and cannot be stained. In fact, M pneumoniae is difficult to culture and requires 7-21 days to grow; culturing is successful in only 40-90% of cases and does not provide information to guide patient management.

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Serology

Serum cold agglutination is a nonspecific test for M pneumoniae, but findings are positive in 50-70% of patients after 7-10 days of infection. Serology tests that demonstrate a 4-fold or greater increase or decrease in paired sera titers or a single titer greater than or equal to 1:32 supports the diagnosis of mycoplasmal pneumonia. A quick bedside test can be performed by partially filling a purple-top tube with blood and placing it in ice; a positive finding is one in which "grains of sand" appear on the glass portion of the tube.

Cold agglutinin tests can be obtained from diagnostic laboratories. A negative result does not exclude infection, and this test may be affected by cross-reactions with other pathogens, such as adenovirus, Epstein-Barr virus, and measles viruses.

Other serologic tests include complement fixation, enzyme-linked immunoassay, and indirect hemagglutination. All of these have acceptable sensitivity and specificity.

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Polymerase Chain Reaction

Polymerase chain reaction (PCR) has been shown to accurately diagnose atypical pneumonia.[17] This test has been used for epidemiologic studies but is not currently used in most clinical settings. Real-time PCR is a promising test that allows detection of M pneumoniae DNA in all phases of infection, including early periods when the serum may be negative for antibody.[18, 19]

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DNA Probes

A radiolabeled DNA probe detects M pneumoniae ribosomal RNA in respiratory secretions with 90% sensitivity.

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Eosinophil Cationic Protein

The role of eosinophil cationic protein (ECP) has been studied in M pneumoniae infection and asthma, in which ECP levels have been found to be increased.[20] This protein may play a role in damage to the respiratory epithelium and accelerated hypersensitivity in the respiratory system, although more studies are required.

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Contributor Information and Disclosures
Author

Michael Joseph Bono, MD, FACEP  Professor of Emergency Medicine, Associate Director of Emergency Medicine Residency Program, Department of Emergency Medicine, Eastern Virginia Medical School

Michael Joseph Bono, MD, FACEP is a member of the following medical societies: Alpha Omega Alpha, American College of Emergency Physicians, American Heart Association, Medical Society of Virginia, and Society for Academic Emergency Medicine

Disclosure: Nothing to disclose.

Specialty Editor Board

Joseph A Salomone III, MD  Associate Professor and Attending Staff, Truman Medical Centers, University of Missouri-Kansas City School of Medicine; EMS Medical Director, Kansas City, Missouri

Joseph A Salomone III, MD is a member of the following medical societies: American Academy of Emergency Medicine, National Association of EMS Physicians, and Society for Academic Emergency Medicine

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD  Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Senior Pharmacy Editor, eMedicine

Disclosure: eMedicine Salary Employment

Paul Blackburn, DO, FACOEP, FACEP  Program Director, Department of Emergency Medicine, Maricopa Medical Center; Assistant Professor, Department of Surgery, University of Arizona College of Medicine

Paul Blackburn, DO, FACOEP, FACEP is a member of the following medical societies: American College of Emergency Physicians, American College of Osteopathic Emergency Physicians, American Medical Association, and Arizona Medical Association

Disclosure: Nothing to disclose.

Chief Editor

Robert E O'Connor, MD, MPH  Professor and Chair, Department of Emergency Medicine, University of Virginia Health System

Robert E O'Connor, MD, MPH is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, American College of Physician Executives, American Heart Association, American Medical Association, Medical Society of Delaware, National Association of EMS Physicians, Society for Academic Emergency Medicine, and Wilderness Medical Society

Disclosure: Nothing to disclose.

References
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Diagram of the Mollicutes class, to which the Mycoplasma genus belongs.
 
 
 
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