Evaluation of Two Different Strategies for Schistosomiasis Screening in High-Risk Groups in a Non-Endemic Setting

Other authors

Institut Català de la Salut

[Roade L] Servei de Medicina Interna, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Sulleiro E, Zarzuela F, Goterris L] Servei de Microbiologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. PROSICS Barcelona, Barcelona, Spain. [Bocanegra C, Salvador F, Treviño B, Serre-Delcor N, Oliveira-Souto I, Aznar ML, Pou D, Sánchez-Montalvà A, Bosch-Nicolau P, Espinosa-Pereiro J, Molina I] Unitat de Medicina Tropical i Salut Internacional Drassanes-Vall d'Hebron Hospital Universitari, Barcelona, Spain. Servei de Malalties Infeccioses, Vall d'Hebron Hospital Universitari, Barcelona, Spain. PROSICS Barcelona, Barcelona, Spain

Vall d'Hebron Barcelona Hospital Campus

Publication date

2023-03-01T11:23:42Z

2023-03-01T11:23:42Z

2023-01-06

Abstract

Diagnosis; Non-endemic; Schistosomiasis


Diagnóstico; No endémico; Esquistosomiasis


Diagnòstic; No endèmic; Esquistosomiasi


A consensus on the recommended screening algorithms for schistosomiasis in asymptomatic high-risk subjects in non-endemic areas is lacking. The objective of this study was to evaluate the real-life performance of direct microscopy and ELISA serology for schistosomiasis screening in a high-risk population in a non-endemic setting. A retrospective cohort study was conducted in two out-patient Tropical Medicine units in Barcelona (Spain) from 2014 to 2017. Asymptomatic adults arriving from the Sub-Saharan region were included. Schistosomiasis screening was conducted according to clinical practice following a different strategy in each setting: (A) feces and urine direct examination plus S. mansoni serology if non-explained eosinophilia was present and (B) S. mansoni serology plus uroparasitological examination as the second step in case of a positive serology. Demographic, clinical and laboratory features were collected. Schistosomiasis cases, clinical management and a 24 month follow-up were recorded for each group. Four-hundred forty individuals were included. The patients were mainly from West African countries. Fifty schistosomiasis cases were detected (11.5% group A vs. 4 % group B, p = 0.733). When both microscopic and serological techniques were performed, discordant results were recorded in 18.4% (16/88). Schistosomiasis cases were younger (p < 0.001) and presented eosinophilia and elevated IgE (p < 0.001) more frequently. Schistosomiasis is a frequent diagnosis among high-risk populations. Serology achieves a similar performance to direct diagnosis for the screening of schistosomiasis in a high-risk population.

Document Type

Article


Published version

Language

English

Publisher

MDPI

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Tropical Medicine and Infectious Disease;8(1)

https://doi.org/10.3390/tropicalmed8010044

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Attribution 4.0 International

http://creativecommons.org/licenses/by/4.0/

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