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Journal of Clinical Microbiology, March 2000, p. 1081-1084, Vol. 38, No. 3
Epidemiology Branch, Communicable Disease
Division, Hawaii State Department of Health, Honolulu, Hawaii
968131; Medical Microbiology Branch,
State Laboratories Division, Hawaii State Department of Health,
Pearl City, Hawaii 967822; and CDC/WHO
Collaborating Center for Leptospirosis, Meningitis and Special
Pathogens Branch, Division of Bacterial and Mycotic Diseases, National
Center for Infectious Diseases, Centers for Disease Control and
Prevention, Atlanta, Georgia 303333
Received 14 October 1999/Returned for modification 7 December
1999/Accepted 20 December 1999
Timely diagnosis of leptospirosis is important to ensure a
favorable clinical outcome. The definitive serologic assay, the microscopic agglutination test (MAT), requires paired sera and is not
useful for guiding early clinical management. The only screening test
approved for use in the United States, the indirect hemagglutination
assay (IHA), has not undergone extensive field evaluation. To assess
the performance of the leptospirosis IHA in Hawaii, serum from patients
evaluated for leptospirosis between 1992 and 1997 were tested with the
IHA at the Hawaii State Laboratories Division and with the MAT at the
Centers for Disease Control and Prevention. Leptospirosis was
considered confirmed by a fourfold rise in MAT titer and/or a positive
culture. A total of 92 (41%) of 226 specimens from 114 persons with
confirmed leptospirosis were found positive by IHA. Only 18 (15%) of
119 specimens obtained within 14 days of onset were IHA positive,
compared to 74 (69%) of 107 specimens collected more than 14 days
after onset (P <0.001). Repeat testing ultimately resulted
in 78 (68%) of the confirmed cases having at least one specimen found
positive by IHA. Thirteen different presumptive infecting serogroups
were identified among 251 specimens with an MAT titer of
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Evaluation of the Indirect Hemagglutination Assay
for Diagnosis of Acute Leptospirosis in Hawaii
200 and
obtained from persons with confirmed or probable leptospirosis. Fifty
(68%) of 73 specimens with Icterohaemorrhagiae as the presumptive
infecting serogroup were found positive by IHA, compared to 44 (47%)
of 93 specimens with Australis as the presumptive infecting serogroup
(P, 0.01). The IHA test was positive for 3 (1%) of 236 specimens from 154 persons without leptospirosis. The sensitivity of
the leptospirosis IHA in Hawaii was substantially below figures
reported previously, particularly early in the course of illness,
limiting its usefulness for diagnosing acute infection. Since the
presumptive infecting serogroup affected IHA results and the prevalence
of serovars varies with geography, the performance of the IHA should be
assessed locally. More sensitive leptospirosis screening tests are
needed in Hawaii.
*
Corresponding author. Mailing address: Hawaii State
Department of Health, 1250 Punchbowl St., Room 444, Honolulu, HI 96813. Phone: (808) 586-4586. Fax: (808) 586-8347. E-mail:
pveffler{at}mail.health.state.hi.us.
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