Leptospirosis in Emergency Medicine Workup
- Author: Judith Green-McKenzie, MD, MPH; Chief Editor: Rick Kulkarni, MD more...
Laboratory Studies
Definitive diagnosis is suggested by isolation of the organism by culture or a positive result on the microscopic agglutination test (MAT). An example of this is shown in the image below.
Darkfield microscopy of leptospiral microscopic agglutination test. (This image is in the public domain and thus free of any copyright restrictions. Courtesy of the Centers for Disease Control/Mrs. M. Gatton.) Only specialized laboratories perform serologic tests; hence, the decision to treat should not be delayed while waiting for the test results.
- Cultures
- Isolating the organism by culture allows definitive diagnosis.
- Leptospires remain viable in anticoagulated blood for as long as 11 days; hence, specimens can be mailed to a reference laboratory for culture. The infecting serovar can be isolated only by culture.
- Blood cultures may be negative if drawn too early or too late. Leptospires may not be detected in the blood until 4 days after the onset of symptoms (7-14 d after exposure). Once the immune system is activated, blood cultures may again become negative.
- Leptospires may be isolated from the cerebrospinal fluid (CSF) within the first 10 days.
- Leptospires may be isolated from the urine for several weeks after the initial infection. In some patients, urine cultures may remain positive for months or years after the onset of illness. Positive urine cultures may take as long as 8 weeks to grow.
- MAT
- A 4-fold rise in convalescent titers is considered a positive result.
- A presumed diagnosis is made by observing an antibody titer of greater than or equal to 1:100 in the MAT in conjunction with symptoms consistent with the disease.
- The MAT uses a battery of live leptospiral strains.
- The antibody response does not reach detectable levels until the second week of illness, and it can be affected by treatment.
- Macroscopic slide agglutination test
- This test allows a presumptive diagnosis.
- Clinical illness consistent with leptospirosis must be present to support the diagnosis.
- This test, which uses killed antigen, is useful for screening but is not specific.
- Other tests: Other tests include an indirect hemagglutination test, a microcapsule agglutination test, an immunoglobulin M (IgM) enzyme-linked immunoabsorbent assay (ELISA), and a dark-field examination of blood or urine.
- More recently, rapid commercial tests have been made available, such as the Dip-S-Ticks (PanBio, Inc; Baltimore, Maryland), which detects leptospira antibodies.
- Nucleic acid amplification (polymerase chain reaction [PCR])–based techniques have been developed to diagnose leptospirosis. PCR-based techniques are unable to identify the infecting serovar. This factor reduces its epidemiologic and public health value
- The dark-field examination frequently leads to misdiagnosis and should not be used.
- The ELISA uses a broadly reactive antigen and is a standard serologic procedure, as is the MAT.[9] Because it detects IgM, it may be useful for diagnosis of new infections within 3-5 days.
- Laboratory studies (general)
- In patients with mild disease, elevated erythrocyte sedimentation rates and peripheral leukocytosis (3,000-26,000 x 109/L) with a left shift are noted.
- Aminotransferases may be mildly elevated up to 200 U/L; serum bilirubin and alkaline phosphatase levels may also be elevated.
- Urinalysis may reveal the following:
- Proteinuria may be present.
- Leukocytes, erythrocytes, hyaline casts, and granular casts may be present in the urinary sediment.
- CSF studies may reveal the following:
- When the CNS becomes involved, polymorphonuclear leukocytes initially predominate and are later replaced by monocytes.
- CSF protein may be normal or elevated, whereas glucose levels remain normal.
- CSF pressure is normal, but a lumbar puncture can relieve the headache.
- Laboratory studies (Weil disease)
- Patients may exhibit mild thrombocytopenia (as many as 50%), which is often accompanied by renal failure.
- Azotemia and renal failure are other prominent characteristics.
- Marked leukocytosis may be present.
- Prothrombin times may be elevated.
- Creatine phosphokinase (CPK) levels are elevated in as many as 50% of patients; acutely, jaundice in Weil disease is associated with very high CPK level, but transaminases are only modestly elevated.
Imaging Studies
- In severe disease, a patchy alveolar pattern may be revealed on lung radiography findings, corresponding to alveolar hemorrhage.
- Most radiographic changes occur in the periphery of the lower lobes.
Other Tests
- Electrocardiographic (ECG) abnormalities are common during the leptospiremic phase of Weil syndrome.
- In severe cases, congestive heart failure and cardiogenic shock may occur.
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