Performance of clinical signs and symptoms, rapid and laboratory diagnostic tests for diagnosis of human African trypanosomiasis by passive screening in Guinea: a non-interventional, prospective cross-sectional study

Author:

Camara Oumou1,Camara Mamadou1,Falzon Laura Cristina2,Ilboudo Hamidou3,Kaboré Jacques4,Compaoré Charlie Franck Alfred4,Fèvre Eric Maurice2,Büscher Philippe5,Bucheton Bruno6,Lejon Veerle7ORCID

Affiliation:

1. Programme National de Lutte contre la Trypanosomiase Humaine Africaine

2. ILRI: International Livestock Research Institute

3. Institut de Recherche en Sciences de la Santé: Institut de Recherche en Sciences de la Sante

4. CIRDES: Centre International de Recherche-Developpement sur l'Elevage en zone Subhumide

5. Institute of Tropical Medicine: Instituut voor Tropische Geneeskunde

6. IRD: Institut de recherche pour le developpement

7. Institut de recherche pour le développement: Institut de recherche pour le developpement

Abstract

Abstract Background: Passive diagnosis of human African trypanosomiasis (HAT) at the health facility level is a major component of HAT control in Guinea. We examined which clinical signs and symptoms are associated with HAT, and assessed the performance of selected clinical presentations, of rapid diagnostic tests (RDT), and of laboratory tests on dried blood spots (DBS) for diagnosing HAT. Method: The study took place in 11 health facilities in Guinea, where 2345 clinical suspects were tested with RDTs HAT Sero-K-Set, rHAT Sero-Strip, and SD Bioline HAT. Seropositives underwent parasitological examination to confirm HAT and their DBS were tested in indirect ELISA/T.b. gambiense, trypanolysis, LAMP and m18S qPCR. Multivariable regression analysis assessed association of clinical presentation with HAT. Sensitivity, specificity, positive and negative predictive values of key clinical presentations, of the RDTs and of the DBS tests for HAT diagnosis were determined. Results: The HAT prevalence, as confirmed parasitologically, was 2.0% (1.5-2.7%). Odds ratios (OR) for HAT were increased for participants with swollen lymph nodes (OR 96.7), important weight loss (OR 20.4), severe itching (OR 45.9) or motor disorders (OR 4.5). Presence of at least one of these clinical presentations was 75.6% (73.8-77.4%) specific and 97.9% (88.9-99.9%) sensitive for HAT. HAT Sero-K-Set, rHAT Sero-Strip, and SD Bioline HAT were respectively 97.5% (96.8-98.1%), 99.4% (99.0-99.7%) and 97.9% (97.2-98.4%) specific, and 100% (92.5-100.0%), 59.6% (44.3-73.3%) and 93.8% (82.8-98.7%) sensitive for HAT. All DBS tests had specificities ≥ 92.9%. While LAMP and m18S qPCR sensitivities were below 50%, trypanolysis and ELISA/T.b. gambiense had sensitivities of 85.3% (68.9-95.0%) and 67.6% (49.5-82.6%). Conclusions: Presence of swollen lymph nodes, important weight loss, severe itching or motor disorders are simple but accurate clinical criteria for HAT referral in Guinea. Diagnostic performances of HAT Sero-K-Set and SD Bioline HAT are sufficient for referring positives to microscopy. Trypanolysis on DBS may discriminate HAT patients from false RDT positives. Trial registration: The trial was registered under NCT03356665 in clinicaltrials.gov (November 29, 2017, retrospectively registered https://clinicaltrials.gov/ct2/show/NCT03356665).

Publisher

Research Square Platform LLC

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