Efficacy and safety of ascending doses of praziquantel against Schistosoma haematobium infection in preschool-aged and school-aged children: a single-blind randomised controlled trial

被引:14
|
作者
Coulibaly, Jean T. [1 ,2 ,3 ]
Panic, Gordana [1 ,2 ]
Yapi, Richard B. [4 ]
Kovac, Jana [1 ,2 ]
Barda, Beatrice [1 ,2 ]
N'Gbesso, Yves K. [5 ]
Hattendorf, Jan [2 ,6 ]
Keiser, Jennifer [1 ,2 ]
机构
[1] Swiss Trop & Publ Hlth Inst, Dept Med Parasitol & Infect Biol, CH-4002 Basel, Switzerland
[2] Univ Basel, Basel, Switzerland
[3] Univ Felix Houphouet Boigny, Unite Format & Rech Biosci, Abidjan, Cote Ivoire
[4] Ctr Suisse Rech Sci, Abidjan, Cote Ivoire
[5] Ctr Sante Urbain Azaguie, Dept Agboville, Azaguie, Cote Ivoire
[6] Swiss Trop & Publ Hlth Inst, Dept Epidemiol & Publ Hlth, Basel, Switzerland
来源
BMC MEDICINE | 2018年 / 16卷
基金
欧洲研究理事会;
关键词
Efficacy; Praziquantel; Preschool-aged children; Schistosoma haematobium; School-aged children; AFRICAN INFANTS; MANSONI; SCHOOLCHILDREN; METAANALYSIS; REINFECTION; RISK;
D O I
10.1186/s12916-018-1066-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Despite decades of experience with praziquantel treatment in school-aged children (SAC) and adults, we still face considerable knowledge gaps relevant to the successful treatment of preschool-aged children (PSAC). This study aimed to assess the efficacy and safety of escalating praziquantel dosages in PSAC infected with Schistosoma haematobium. Methods: We conducted a randomised, dose-finding trial in PSAC (2-5 years) and as comparator a cohort of SAC (6-15 years) infected with S. haematobium in Cote d'Ivoire. A total of 186 PSAC and 195 SAC were randomly assigned to 20, 40 or 60 mg/kg praziquantel or placebo. The nature of the dose-response relationship in terms of cure rate (CR) was the primary objective. Egg reduction rate (ERR) and tolerability were secondary outcomes. CRs and ERRs were assessed using triplicate urine filtration over 3 consecutive days. Available-case analysis was performed including all participants with primary endpoint data. Results: A total of 170 PSAC and 174 SAC received treatment. Almost 90% of PSAC and three quarters of SAC were lightly infected with S. haematobium. Follow-up data were available for 157 PSAC and 166 SAC. In PSAC, CRs of praziquantel were 85.7% (30/35), 78.0% (32/41) and 68.3% (28/41) at 20, 40 and 60 mg/kg and 47.5% (19/40) for placebo. In SAC, CRs were 10.8% for placebo (4/37), 55.6% for 20 mg/kg (25/45), 68.3% for 40 mg/kg (28/41) and 60.5% for 60 mg/kg (26/43). ERRs based on geometric means ranged between 96.5% (60 mg/kg) and 98.3% (20 mg/kg) in PSAC and between 97.6% (20 mg/kg and 60 mg/kg) and 98.6% (40 mg/kg) in SAC. Adverse events were mild and transient. Conclusions: Praziquantel revealed dose-independent efficacy against light infections of S. haematobium. Over the dose range tested, praziquantel displayed a ceiling effect with the highest response for 20 mg/kg in PSAC. In SAC maximum efficacy was obtained with 40 mg/kg praziquantel. Further investigations are required in children with moderate to heavy infections.
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页数:10
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