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dc.contributor.authorChappuis, F
dc.contributor.authorLoutan, L
dc.contributor.authorSimarro, P
dc.contributor.authorLejon, V
dc.contributor.authorBüscher, P
dc.date.accessioned2008-07-24T15:13:59Z
dc.date.available2008-07-24T15:13:59Z
dc.date.issued2005-01
dc.identifier.citationOptions for field diagnosis of human african trypanosomiasis. 2005, 18 (1):133-46 Clin. Microbiol. Rev.en
dc.identifier.issn0893-8512
dc.identifier.pmid15653823
dc.identifier.doi10.1128/CMR.18.1.133-146.2005
dc.identifier.urihttp://hdl.handle.net/10144/33072
dc.description.abstractHuman African trypanosomiasis (HAT) due to Trypanosoma brucei gambiense or T. b. rhodesiense remains highly prevalent in several rural areas of sub-Saharan Africa and is lethal if left untreated. Therefore, accurate tools are absolutely required for field diagnosis. For T. b. gambiense HAT, highly sensitive tests are available for serological screening but the sensitivity of parasitological confirmatory tests remains insufficient and needs to be improved. Screening for T. b. rhodesiense infection still relies on clinical features in the absence of serological tests available for field use. Ongoing research is opening perspectives for a new generation of field diagnostics. Also essential for both forms of HAT is accurate determination of the disease stage because of the high toxicity of melarsoprol, the drug most widely used during the neurological stage of the illness. Recent studies have confirmed the high accuracy of raised immunoglobulin M levels in the cerebrospinal fluid for the staging of T. b. gambiense HAT, and a promising simple assay (LATEX/IgM) is being tested in the field. Apart from the urgent need for better tools for the field diagnosis of this neglected disease, improved access to diagnosis and treatment for the population at risk remains the greatest challenge for the coming years.
dc.language.isoenen
dc.publisherThe American Society for Microbiologyen
dc.rightsArchived on this site with kind permission from the American Society for Microbiologyen
dc.subject.meshAnimalsen
dc.subject.meshAntibodies, Protozoanen
dc.subject.meshAntigens, Protozoanen
dc.subject.meshCerebrospinal Fluiden
dc.subject.meshHumansen
dc.subject.meshPolymerase Chain Reactionen
dc.subject.meshTrypanosoma brucei gambienseen
dc.subject.meshTrypanosoma brucei rhodesienseen
dc.subject.meshTrypanosomiasis, Africanen
dc.titleOptions for field diagnosis of human african trypanosomiasis.en
dc.contributor.departmentTravel and Migration Medicine Unit, Geneva University Hospital, 24 rue Micheli-du-Crest, 1211 Geneva 14, Switzerland. francois.chappuis@hcuge.chen
dc.identifier.journalClinical Microbiology Reviewsen
refterms.dateFOA2019-03-04T11:28:35Z
html.description.abstractHuman African trypanosomiasis (HAT) due to Trypanosoma brucei gambiense or T. b. rhodesiense remains highly prevalent in several rural areas of sub-Saharan Africa and is lethal if left untreated. Therefore, accurate tools are absolutely required for field diagnosis. For T. b. gambiense HAT, highly sensitive tests are available for serological screening but the sensitivity of parasitological confirmatory tests remains insufficient and needs to be improved. Screening for T. b. rhodesiense infection still relies on clinical features in the absence of serological tests available for field use. Ongoing research is opening perspectives for a new generation of field diagnostics. Also essential for both forms of HAT is accurate determination of the disease stage because of the high toxicity of melarsoprol, the drug most widely used during the neurological stage of the illness. Recent studies have confirmed the high accuracy of raised immunoglobulin M levels in the cerebrospinal fluid for the staging of T. b. gambiense HAT, and a promising simple assay (LATEX/IgM) is being tested in the field. Apart from the urgent need for better tools for the field diagnosis of this neglected disease, improved access to diagnosis and treatment for the population at risk remains the greatest challenge for the coming years.


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