Abstract

BackgroundSchistosoma haematobium infections are responsible for significant urinary tract (UT) complications. Schistosomiasis control programs aim to reduce morbidity, yet the extent of morbidity in preschool-aged children and the impact of treatment on morbidity reduction are not well studied.MethodologyOur study was embedded in a randomized, placebo-controlled, single-blind trial in Côte d’Ivoire, which evaluated the efficacy and safety of three doses (20, 40 and 60 mg/kg) of praziquantel in school-aged (SAC) and preschool-aged (PSAC) children infected with S. haematobium. Enrolled children were invited to participate in an ultrasound examination prior and six months after treatment. At these time points 3 urine samples were collected for parasitological and clinical examinations.Principal findings162 PSAC and 141 SAC participated in the ultrasound examination at baseline, of which 128 PSAC and 122 SAC were present at follow-up. At baseline 43% (70/162) of PSAC had UT morbidity, mostly at bladder level and 7% had hydronephrosis. 67% (94/141) of SAC revealed mainly moderate UT pathology, 4% presented pseudopolyps on the bladder wall, and 6% had pyelectasis. At follow up, 45% of PSAC and 58% of SAC were S. haematobium positive, mostly harboring light infection intensities (41% and 51%, respectively). Microhematuria was present in 33% of PSAC and 42% of SAC and leukocyturia in 53% and 40% of PSAC and SAC, respectively. 50% (64/128) of PSAC and 58% (71/122) of SAC presented urinary tract morbidity, which was mainly mild. A significant correlation (p<0.05) was observed between praziquantel treatment and reversal of S. haematobium induced morbidity. Progression of UT pathology decreased with increasing praziquantel dosages. A worsening of morbidity was observed among children in the placebo group.Conclusion/SignificanceBladder morbidity is widespread among PSAC. Praziquantel treatment is significantly associated with the reversal of S. haematobium induced morbidity, which underscores the importance of preventive chemotherapy programs. These programs should be expanded to PSAC to prevent or decrease the prevalence of morbidity in young children. This trial is registered as an International Standard Randomized Controlled Trial, number ISRCTN15280205.

Highlights

  • Schistosomiasis primarily caused by Schistosoma haematobium, S. japonicum and S. mansoni is a significant public health problem in low-income tropical and subtropical countries

  • People get infected with the parasite through contact with fresh water and children are at major risk

  • After treatment 50% of preschoolaged children (PSAC) and 58% of school-aged children (SAC) still had pathology linked to the infection

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Summary

Introduction

Schistosomiasis primarily caused by Schistosoma haematobium, S. japonicum and S. mansoni is a significant public health problem in low-income tropical and subtropical countries. It is an ancient disease with first reports on schistosomiasis dating back 4000 years ago [1]. Adult S. haematobium settle in the Ultrasound in schistosomiasis venous plexus of the genito-urinary tract of the infected host and produce fertilized eggs. Evidence suggests that morbidity is caused by the trapping of eggs within the urinary and genital tract, which induce a granulomatous host immune response. The granuloma formation induces a chronic inflammation resulting in disease manifestations. Schistosoma haematobium infections are responsible for significant urinary tract (UT) complications. Schistosomiasis control programs aim to reduce morbidity, yet the extent of morbidity in preschool-aged children and the impact of treatment on morbidity reduction are not well studied

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