AJTMH ASTMH MEMBERSHIP INFORMATION: astmh@astmh.org
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am. J. Trop. Med. Hyg., 59(2), 1998, pp. 275-278
Copyright © 1998 by The American Society of Tropical Medicine and Hygiene

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Rossi, C.
Right arrow Articles by Henchal, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rossi, C.
Right arrow Articles by Henchal, E.
Related Collections
Right arrow Dengue
Right arrow Flaviviruses
Right arrow Arboviruses
American Journal of Tropical Medicine and Hygiene, Vol 59, Issue 2, 275-278
Copyright © 1998 by American Society of Tropical Medicine and Hygiene

Research Articles


Laboratory diagnosis of acute dengue fever during the United Nations Mission in Haiti, 1995-1996

CA Rossi, JJ Drabick, JM Gambel, W Sun, TE Lewis, and EA Henchal

We evaluated laboratory methods to confirm a clinical diagnosis of dengue. Acute sera were collected from personnel (n = 414) supporting the United Nations Mission in Haiti and presenting with febrile illness consistent with dengue fever or no apparent underlying cause. Dengue virus was recovered from 161 of 379 acute sera by inoculation into C6/36 cell culture. While 93 of 414 acute sera had detectable IgM antibodies, the IgM capture ELISA (MAC ELISA) had a sensitivity of only 13% compared with the virus isolation gold standard. If presumptive dengue fever cases were identified by both virus isolation and the presence of IgM, virus isolation and the MAC ELISA had clinical sensitivities of 69% and 40%, respectively. This study suggests that a combination of laboratory methods that target virus or subviral components as well as anti-viral IgM antibodies may be necessary for sensitive laboratory diagnosis with acute sera.


This article has been cited by other articles:


Home page
CVIHome page
S.-J. L. Wu, H. Paxton, B. Hanson, C. G. Kung, T. B. Chen, C. Rossi, D. W. Vaughn, G. S. Murphy, and C. G. Hayes
Comparison of Two Rapid Diagnostic Assays for Detection of Immunoglobulin M Antibodies to Dengue Virus
Clin. Vaccine Immunol., January 1, 2000; 7(1): 106 - 110.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
T. Laue, P. Emmerich, and H. Schmitz
Detection of Dengue Virus RNA in Patients after Primary or Secondary Dengue Infection by Using the TaqMan Automated Amplification System
J. Clin. Microbiol., August 1, 1999; 37(8): 2543 - 2547.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1998 by the American Society of Tropical Medicine and Hygiene.