Human urogenital schistosomiasis in West and Sub-Saharan Africa migrants in Sardinia, Italy: A retrospective monocentric study.


Journal

Journal of infection in developing countries
ISSN: 1972-2680
Titre abrégé: J Infect Dev Ctries
Pays: Italy
ID NLM: 101305410

Informations de publication

Date de publication:
30 08 2022
Historique:
received: 19 06 2021
accepted: 25 03 2022
entrez: 13 9 2022
pubmed: 14 9 2022
medline: 16 9 2022
Statut: epublish

Résumé

Schistosoma (S.) haematobium is the aetiological agent of urogenital schistosomiasis endemic in Sub-Saharan Africa and the Middle East. Microhaematuria is strongly associated with schistosomiasis diagnosis. Praziquantel (PZQ) is the treatment of choice. We conducted a monocentric survey among African migrants from January 2017 to December 2018. The diagnosis of S. haematobium was performed by direct microscopic examination of urine. The treatment was PZQ 40 mg/Kg/die for three days. We enrolled 91 male patients with a median age of 20.2 years (IQR 18.9-23.4)]. Forty-five (49.5%) described a history of haematuria. Sixteen (17.6%) evidenced the presence of red blood cells (RBCs) during urine microscopy. Eighteen (19.8%) had urogenital schistosomiasis. Their median white blood count (WBC) was 5.15 x 109/L (IQR 4.45-6.08) and it was 6.37 x 109 /L (IQR 5.14-8.27), p = 0.009, after 15 days from treatment. Baseline eosinophil count was 0.5 x 109/L (IQR 0.3-0.6) and 0.7 x 109/L (IQR 0.2-1.9; p = 0.032). According to the univariate analysis, origin from Mali [odds ratio (OR) 3.6 (CI 1.2-10.9), p = 0.022] and microscopic evidence of RBCs [OR of 10.7 (CI 2.5-45.1), p = 0.001] were main predictors of urogenital schistosomiasis diagnosis. One (5.6%) treatment failure was registered. Three (16.7%) patients had bladder cancer. Detection of RBCs was a significant predictor of S. haematobium infection and could be used as a screening method in migrants coming from endemic areas. Early urogenital schistosomiasis diagnosis and ultrasound diagnostic tools are crucial for reducing the risk of potential neoplastic evolution.

Identifiants

pubmed: 36099381
doi: 10.3855/jidc.15492
doi:

Substances chimiques

Praziquantel 6490C9U457

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1359-1363

Informations de copyright

Copyright (c) 2022 Nicholas Geremia, Andrea De Vito, Vincenzo Lai, Vito Fiore, Elija Princic, Paola Rappelli, Giordano Madeddu, Sergio Babudieri.

Déclaration de conflit d'intérêts

No Conflict of Interest is declared

Auteurs

Nicholas Geremia (N)

Unit of Infectious Diseases, Department of Medical, Surgical and Experimental Science, University of Sassari, Sassari, Italy. nich.geremia@gmail.com.

Andrea De Vito (A)

Department of Biomedical Sciences, University of Sassari, Sassari, Italy.

Vincenzo Lai (V)

Mediterranean Center for Disease Control (MCDC), University of Sassari, Sassari, Italy.

Vito Fiore (V)

Unit of Infectious Diseases, Department of Medical, Surgical and Experimental Science, University of Sassari, Sassari, Italy.

Elija Princic (E)

Unit of Infectious Diseases, Department of Medical, Surgical and Experimental Science, University of Sassari, Sassari, Italy.

Paola Rappelli (P)

Department of Biomedical Sciences, University of Sassari, Sassari, Italy.

Giordano Madeddu (G)

Unit of Infectious Diseases, Department of Medical, Surgical and Experimental Science, University of Sassari, Sassari, Italy.

Sergio Babudieri (S)

Unit of Infectious Diseases, Department of Medical, Surgical and Experimental Science, University of Sassari, Sassari, Italy.

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