Rapid diagnostic tests for non-malarial febrile illness in the tropics

• Published in: Clinical microbiology and infection Vol. 19; no. 5; pp. 422 - 431
• Main Authors: Chappuis, F., Alirol, E., d’Acremont, V., Bottieau, E., Yansouni, C.P.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.05.2013; Elsevier Limited
• Subjects: African trypanosomiasis; Antibodies - blood; brucellosis; dengue; Diagnostic Tests, Routine - methods; fever; Fever of Unknown Origin - diagnosis; Humans; Immunoassay - methods; Infections; Leptospira; leptospirosis; Malaria; rapid diagnostic tests; Sensitivity and Specificity; Tropical Climate; Tropical diseases; Tropical Medicine - methods; tropics; typhoid; visceral leishmaniasis; Africa; leptospirosis; typhoid; tropics; brucellosis; rapid diagnostic tests; fever; dengue; visceral leishmaniasis; African trypanosomiasis
• ISSN: 1198-743X; 1469-0691
• DOI: 10.1111/1469-0691.12154

The recent roll-out of rapid diagnostic tests (RDTs) for malaria has highlighted the decreasing proportion of malaria-attributable illness in endemic areas. Unfortunately, once malaria is excluded, there are few accessible diagnostic tools to guide the management of severe febrile illnesses in low resource settings. This review summarizes the current state of RDT development for several key infections, including dengue fever, enteric fever, leptospirosis, brucellosis, visceral leishmaniasis and human African trypanosomiasis, and highlights many remaining gaps. Most RDTs for non-malarial tropical infections currently rely on the detection of host antibodies against a single infectious agent. The sensitivity and specificity of host-antibody detection tests are both inherently limited. Moreover, prolonged antibody responses to many infections preclude the use of most serological RDTs for monitoring response to treatment and/or for diagnosing relapse. Considering these limitations, there is a pressing need for sensitive pathogen-detection-based RDTs, as have been successfully developed for malaria and dengue. Ultimately, integration of RDTs into a validated syndromic approach to tropical fevers is urgently needed. Related research priorities are to define the evolving epidemiology of fever in the tropics, and to determine how combinations of RDTs could be best used to improve the management of severe and treatable infections requiring specific therapy.