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Get Free AccessBackground Severe forms of dengue, the most important arboviral infection of man, are associated with haemorrhagic disease and a generalised vascular leak syndrome. The importance of dengue as a cause of neurological disease is uncertain. Methods During 1995, all patients with suspected CNS infections admitted to a referral hospital in southern Vietnam were investigated by culture, PCR, and antibody measurement in serum and CSF for dengue and other viruses. Findings Of 378 patients, 16 (4·2%) were infected with dengue viruses, compared with four (1·4%) of 286 hospital controls (odds ratio [95% CI] 3·1 [1·7–5·8]). Five additional dengue positive patients with CNS abnormalities were studied subsequently. No other cause of CNS infection was identified. Seven infections were primary dengue, 13 secondary, and one was not classified. Ten patients had dengue viruses isolated or detected by PCR, and three had dengue antibody in the CSF. 12 of the 21 had no characteristic features of dengue on admission. The most frequent neurological manifestations were reduced consciousness and convulsions. Nine patients had encephalitis. No patient died, but six had neurological sequelae at discharge. Phylogenetic analysis of the four DEN-2 strains isolated mapped them with a DEN-2 strain isolated from a patient with dengue haemorhagic fever, and with other strains previously isolated in southern Vietnam. Interpretation In dengue endemic areas patients with encephalitis and encephalopathy should be investigated for this infection, whether or not they have other features of the disease.
Tom Solomon, Nguyen Minh Dung, David W. Vaughn, Rachel Kneen, Le Thi Thu Thao, Boonyos Raengsakulrach, Hà Thị Loan, Nicholas Day, Jeremy Farrar, Khin Saw Aye Myint, Mary Warrell, William James, A Nisalak, Sir Nicholas White (2000). Neurological manifestations of dengue infection. The Lancet, 355(9209), pp. 1053-1059, DOI: 10.1016/s0140-6736(00)02036-5.
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Type
Article
Year
2000
Authors
14
Datasets
0
Total Files
0
Language
English
Journal
The Lancet
DOI
10.1016/s0140-6736(00)02036-5
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