Dynamics of <it>Schistosoma haematobium </it>egg output and associated infection parameters following treatment with praziquantel in school-aged children

<p>Abstract</p> <p>Background</p> <p>Praziquantel is the drug of choice in preventive chemotherapy targeting schistosomiasis. Increasing large-scale administration of praziquantel requires monitoring of drug efficacy to detect early signs of development of resistance. S...

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Main Authors: Stete Katarina, Krauth Stefanie J, Coulibaly Jean T, Knopp Stefanie, Hattendorf Jan, Müller Ivan, Lohourignon Laurent K, Kern Winfried V, N’Goran Eliézer K, Utzinger Jürg
Format: Article
Language:English
Published: BMC 2012-12-01
Series:Parasites & Vectors
Subjects:
Online Access:http://www.parasitesandvectors.com/content/5/1/298
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spelling doaj-e3aa60a9a7db4fc8b7471edd8f44084f2020-11-24T21:11:28ZengBMCParasites & Vectors1756-33052012-12-015129810.1186/1756-3305-5-298Dynamics of <it>Schistosoma haematobium </it>egg output and associated infection parameters following treatment with praziquantel in school-aged childrenStete KatarinaKrauth Stefanie JCoulibaly Jean TKnopp StefanieHattendorf JanMüller IvanLohourignon Laurent KKern Winfried VN’Goran Eliézer KUtzinger Jürg<p>Abstract</p> <p>Background</p> <p>Praziquantel is the drug of choice in preventive chemotherapy targeting schistosomiasis. Increasing large-scale administration of praziquantel requires monitoring of drug efficacy to detect early signs of development of resistance. Standard protocols for drug efficacy monitoring are necessary. Here, we determined the optimal time point for praziquantel efficacy assessment against <it>Schistosoma haematobium</it> and studied the dynamics of infection parameters following treatment.</p> <p>Methods</p> <p>Ninety school-aged children from south Côte d’Ivoire with a parasitologically confirmed <it>S. haematobium</it> infection were treated with a single oral dose of praziquantel (40 mg/kg) and followed up for 62 days post-treatment. Urine samples were collected on 23 schooldays during this period and were subjected to visual examination (macrohaematuria), urine filtration and microscopy (<it>S. haematobium</it> eggs) and reagent strip testing (microhaematuria, proteinuria and leukocyturia).</p> <p>Results</p> <p>Observed cure and egg reduction rates were highly dependent on the time point post-treatment. Egg reduction rates were high (>97%) in weeks 3–9 post-treatment. Cure rates were highest in weeks 6 (92.9%) and 9 (95.0%) post-treatment. The prevalence of infection-associated parameters decreased after treatment, reaching a minimum of 2.4% in weeks 5 (proteinuria) and 7 (leukocyturia) post-treatment, and 16.3% at the end of week 8 (microhaematuria). Macrohaematuria disappeared between weeks 3 and 6 post-treatment.</p> <p>Conclusions</p> <p>For monitoring praziquantel efficacy against <it>S. haematobium</it>, we recommend that the cure rate is assessed at week 6 post-treatment. The egg reduction rate can be evaluated earlier, from day 14 post-treatment onwards. Reagent strips are a useful additional tool for evaluating treatment outcomes in areas with high endemicity, preferably at weeks 5 and 6 post-treatment. The delayed decrease of microhaematuria confirms that lesions in the urinary tract persist longer than egg excretion post-treatment.</p> http://www.parasitesandvectors.com/content/5/1/298Schistosomiasis<it>Schistosoma haematobium</it>PraziquantelDrug efficacyMacrohaematuriaMicrohaematuriaProteinuriaLeukocyturiaSchool-aged childrenCôte d’Ivoire
collection DOAJ
language English
format Article
sources DOAJ
author Stete Katarina
Krauth Stefanie J
Coulibaly Jean T
Knopp Stefanie
Hattendorf Jan
Müller Ivan
Lohourignon Laurent K
Kern Winfried V
N’Goran Eliézer K
Utzinger Jürg
spellingShingle Stete Katarina
Krauth Stefanie J
Coulibaly Jean T
Knopp Stefanie
Hattendorf Jan
Müller Ivan
Lohourignon Laurent K
Kern Winfried V
N’Goran Eliézer K
Utzinger Jürg
Dynamics of <it>Schistosoma haematobium </it>egg output and associated infection parameters following treatment with praziquantel in school-aged children
Parasites & Vectors
Schistosomiasis
<it>Schistosoma haematobium</it>
Praziquantel
Drug efficacy
Macrohaematuria
Microhaematuria
Proteinuria
Leukocyturia
School-aged children
Côte d’Ivoire
author_facet Stete Katarina
Krauth Stefanie J
Coulibaly Jean T
Knopp Stefanie
Hattendorf Jan
Müller Ivan
Lohourignon Laurent K
Kern Winfried V
N’Goran Eliézer K
Utzinger Jürg
author_sort Stete Katarina
title Dynamics of <it>Schistosoma haematobium </it>egg output and associated infection parameters following treatment with praziquantel in school-aged children
title_short Dynamics of <it>Schistosoma haematobium </it>egg output and associated infection parameters following treatment with praziquantel in school-aged children
title_full Dynamics of <it>Schistosoma haematobium </it>egg output and associated infection parameters following treatment with praziquantel in school-aged children
title_fullStr Dynamics of <it>Schistosoma haematobium </it>egg output and associated infection parameters following treatment with praziquantel in school-aged children
title_full_unstemmed Dynamics of <it>Schistosoma haematobium </it>egg output and associated infection parameters following treatment with praziquantel in school-aged children
title_sort dynamics of <it>schistosoma haematobium </it>egg output and associated infection parameters following treatment with praziquantel in school-aged children
publisher BMC
series Parasites & Vectors
issn 1756-3305
publishDate 2012-12-01
description <p>Abstract</p> <p>Background</p> <p>Praziquantel is the drug of choice in preventive chemotherapy targeting schistosomiasis. Increasing large-scale administration of praziquantel requires monitoring of drug efficacy to detect early signs of development of resistance. Standard protocols for drug efficacy monitoring are necessary. Here, we determined the optimal time point for praziquantel efficacy assessment against <it>Schistosoma haematobium</it> and studied the dynamics of infection parameters following treatment.</p> <p>Methods</p> <p>Ninety school-aged children from south Côte d’Ivoire with a parasitologically confirmed <it>S. haematobium</it> infection were treated with a single oral dose of praziquantel (40 mg/kg) and followed up for 62 days post-treatment. Urine samples were collected on 23 schooldays during this period and were subjected to visual examination (macrohaematuria), urine filtration and microscopy (<it>S. haematobium</it> eggs) and reagent strip testing (microhaematuria, proteinuria and leukocyturia).</p> <p>Results</p> <p>Observed cure and egg reduction rates were highly dependent on the time point post-treatment. Egg reduction rates were high (>97%) in weeks 3–9 post-treatment. Cure rates were highest in weeks 6 (92.9%) and 9 (95.0%) post-treatment. The prevalence of infection-associated parameters decreased after treatment, reaching a minimum of 2.4% in weeks 5 (proteinuria) and 7 (leukocyturia) post-treatment, and 16.3% at the end of week 8 (microhaematuria). Macrohaematuria disappeared between weeks 3 and 6 post-treatment.</p> <p>Conclusions</p> <p>For monitoring praziquantel efficacy against <it>S. haematobium</it>, we recommend that the cure rate is assessed at week 6 post-treatment. The egg reduction rate can be evaluated earlier, from day 14 post-treatment onwards. Reagent strips are a useful additional tool for evaluating treatment outcomes in areas with high endemicity, preferably at weeks 5 and 6 post-treatment. The delayed decrease of microhaematuria confirms that lesions in the urinary tract persist longer than egg excretion post-treatment.</p>
topic Schistosomiasis
<it>Schistosoma haematobium</it>
Praziquantel
Drug efficacy
Macrohaematuria
Microhaematuria
Proteinuria
Leukocyturia
School-aged children
Côte d’Ivoire
url http://www.parasitesandvectors.com/content/5/1/298
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