Staphylococcal Meningitis Workup

  • Author: Lawrence A Zumo, MD; Chief Editor: Karen L Roos, MD   more...
 
Updated: Mar 29, 2011
 

Approach Considerations

CoNS is a normal inhabitant of the human skin and mucous membranes. Patients most at risk for CoNS infection frequently have a disruption in their host defense mechanisms due to surgery, foreign body placement, or immunosuppression. Because CoNS is a common contaminant of cultures, the diagnostic definition of adult CoNS meningitis is different from that of meningitis caused by other common pathogens and is therefore defined by a more strict criteria.

To see complete information on Meningitis, please go to the main article by clicking here.

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Lab Studies

Complete Blood Cell Count

Complete blood cell (CBC) count with differential demonstrates polymorphonuclear leukocytosis with left shift.

Cerebrospinal Fluid Analysis

CSF analysis is the diagnostic test of choice for suspected meningitis. CSF lactate dehydrogenase (LDH) appears to be diagnostic and has a prognostic value in bacterial meningitis. Increase in total LDH is observed consistently in bacterial meningitis, mostly due to increases in fractions 4 and 5, which are derived from granulocytes. LDH fractions 1 and 2, derived presumably from brain tissue, are elevated only slightly in bacterial meningitis but rise sharply in patients who develop neurologic sequelae.

Leukocyte count in the CSF ranges from 250-100,000/µL. Counts above 50,000 raise the possibility of a brain abscess having ruptured into a ventricle. Neutrophils predominate early in infection, but mononuclear cells (lymphocytes, plasma cells, histiocytes) steadily increase as the infection continues.

Protein content is higher than 45 mg/dL in greater than 90% of cases. In most cases, the protein ranges from 100 to 500 mg/dL. Glucose content is usually diminished to below 40 mg/dL or to less than 40% of blood glucose level. Gram stain of CSF sediment permits identification of the causative agent in most cases.

Blood Cultures

Blood cultures should always be obtained. They are positive in 40-60% of patients with Haemophilus influenzae, meningococcal, or pneumococcal meningitis, but data are scarce for staphylococcal meningitis. Blood cultures may provide the only definite clue as to the causative agent if CSF cultures are negative and if more sophisticated diagnostic identification procedures are not readily available.

Polymerase Chain Reaction

Because of earlier antibiotic intervention in patients presenting with signs suggestive of bacterial meningitis, a noted rise occurs in culture-negative CSF and blood cultures in some laboratories. This makes the use of a non–culture-based system to detect and identify the causal agents increasingly important. It is here that the 16S rRNA polymerase chain reaction (PCR) becomes a valuable molecular tool to aid in the detection on nonculturable etiologic agents of meningitis.

With the advent of polyacrylamide gel electrophoresis (PAGE) to separate mixed 16S rRNA amplicons prior to sequencing without the need of cloning, the PCR technique is increasingly being used to augment staphylococci identification.

16S rRNA genes exist in all bacteria and accumulate mutations at a slow constant rate over time; therefore, they may be used as "molecular clocks." Highly variable portions of the 16S rRNA sequence provide unique signatures to any bacterium and useful information about relationships between them. These properties provide important aids in microbiologic diagnostics, especially in equivocal cases.

Complement and Immunoglobulin levels

Complement levels and immunoglobulin levels should be part of the evaluation of every patient with bacterial meningitis.

Antibody levels

Antibody levels should be monitored and pneumococcal and meningococcal vaccines should be given to patients with recurrent bacterial meningitis, because this is common in persons with previous head trauma, skull fracture, or dural CSF leak, as well as in patients with deficiencies of any of the complement components or hypogammaglobulinemia.

Additional Laboratory Tests

Other laboratory methods for identification of causative organisms include counterimmunoelectrophoresis (CIE), radioimmunoassay (RIA), latex particle agglutination (LPA), and enzyme-linked immunosorbent assay (ELISA).

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Imaging Studies

Radiography

Chest radiographs are important because they may show an abscess or pneumonitis, an important consideration for infants and immunocompromised patients. Sinus and skull radiographs may show the presence of cranial osteomyelitis, paranasal sinusitis, or mastoiditis.

Computed Tomography Scanning

Computed tomography (CT) scans of the head are usually normal but may reveal nonspecific cerebral edema or show previous neurosurgical interventions. CT scans reveal eroding skull lesions and routes for bacterial invasion (eg, mastoiditis, sinusitis, tumors, sinus wall defects, brain abscess, subdural empyema).

In patients with immunosuppression or with focal findings, papilledema, or other signs of increased intracranial pressure, a CT scan of the head must be done before the spinal tap to detect mass lesions that could result in herniation. Patients with space-occupying lesions do not undergo lumbar puncture because the withdrawal of CSF removes counterpressure from below, thus increasing the effect of compression from above and exacerbating the brain shift already present. A CT scan should be preceded by blood cultures and the initiation of antibiotic therapy.

Magnetic Resonance Imaging

Magnetic resonance imaging (MRI) with contrast enhancement may demonstrate cortical reactions, including infarctions, hydrocephalus, and meningeal exudates. The role of MRI with contrast T1 and T2 sequences is not well established.

Echocardiography

Transthoracic and transesophageal echocardiograms are helpful for the evaluation of endocarditis. Negative tests do not rule out endocarditis, since neither technique is sensitive enough to detect small vegetations, which may require more than 10 days to develop. (Blood cultures and peripheral manifestations also help to point to staphylococcal endocarditis as the source of meningitis.)

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Procedures

Lumbar Puncture

CSF pressure is elevated consistently (>180 mm H2 O), but pressures greater than 400 mm H2 O suggest the potential for herniation.

Cerebrospinal Fluid YKL-40 levels

YKL-40, a member of the family 18 glycosyl hydrolases, is secreted by activated neutrophils and macrophages and may function in tissue inflammation and remodeling. This is a useful adjunct, since CNS infections are characterized by an inflammatory response within the subarachnoidal space or brain parenchyma. However, preliminary research findings to date do not show a definite positive correlation with levels of CSF YKL-40 levels as they have shown with other forms of purulent meningitis.

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Histologic Findings

Pia-arachnoiditis with edema and microinfarcts is observed. Polymorphonuclear leukocytes fill the subarachnoid space in severely affected areas and are found predominantly around the leptomeningeal blood vessels in less severe cases. In fulminant meningitis, the inflammatory cells infiltrate the walls of the leptomeningeal veins and produce a venulitis that can lead to venous occlusion and subsequent hemorrhagic infarction of the underlying brain.

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Contributor Information and Disclosures
Author

Lawrence A Zumo, MD  Neurologist, Private Practice

Lawrence A Zumo, MD is a member of the following medical societies: American Academy of Neurology, American College of Physicians, American Medical Association, and Southern Medical Association

Disclosure: Nothing to disclose.

Coauthor(s)

Alan Greenberg, MD  Director, Associate Professor, Department of Internal Medicine, Jersey City Medical Center, Seton Hall University

Alan Greenberg, MD is a member of the following medical societies: Alpha Omega Alpha and American College of Physicians

Disclosure: Nothing to disclose.

Specialty Editor Board

Norman C Reynolds Jr, MD  Neurologist, Veterans Affairs Medical Center of Milwaukee; Clinical Professor, Medical College of Wisconsin

Norman C Reynolds Jr, MD is a member of the following medical societies: American Academy of Neurology, Association of Military Surgeons of the US, Movement Disorders Society, Sigma Xi, and Society for Neuroscience

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

Florian P Thomas, MD, MA, PhD, Drmed  Director, Spinal Cord Injury Unit, St Louis Veterans Affairs Medical Center; Director, National MS Society Multiple Sclerosis Center; Director, Neuropathy Association Center of Excellence, Professor, Department of Neurology and Psychiatry, Associate Professor, Institute for Molecular Virology, and Department of Molecular Microbiology and Immunology, St Louis University School of Medicine

Florian P Thomas, MD, MA, PhD, Drmed is a member of the following medical societies: American Academy of Neurology, American Neurological Association, American Paraplegia Society, Consortium of Multiple Sclerosis Centers, and National Multiple Sclerosis Society

Disclosure: Nothing to disclose.

Chief Editor

Karen L Roos, MD  John and Nancy Nelson Professor of Neurology, Professor of Neurological Surgery, Department of Neurology, Indiana University School of Medicine

Karen L Roos, MD is a member of the following medical societies: American Academy of Neurology and American Neurological Association

Disclosure: Nothing to disclose.

References
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  9. Faville RJ, Zaske DE, Kaplan EL, et al. Staphylococcus aureus endocarditis. Combined therapy with vancomycin and rifampin. JAMA. Oct 27 1978;240(18):1963-5. [Medline].

  10. Acar JF, Goldstein FW, Duval J. Use of rifampin for the treatment of serious staphylococcal and gram-negative bacillary infections. Rev Infect Dis. Jul-Aug 1983;5 Suppl 3:S502-6. [Medline].

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