4.7 Article

Safety Surveillance of Mass Praziquantel and Albendazole Co-Administration in School Children from Southern Ethiopia: An Active Cohort Event Monitoring

Journal

JOURNAL OF CLINICAL MEDICINE
Volume 11, Issue 21, Pages -

Publisher

MDPI
DOI: 10.3390/jcm11216300

Keywords

safety surveillance; pharmacovigilance; praziquantel; albendazole; school children; preventive chemotherapy; cohort event monitoring; schistosomiasis; STH; Ethiopia; drug safety

Funding

  1. European and Developing Countries Clinical Trials Partnership (EDCTP) 2 program - European Union (PROFORMA project [CSA2016S-1618]
  2. Swedish International Development Cooperation Agency (SIDA)

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Preventive chemotherapy with praziquantel and albendazole co-administration is a global strategy to eliminate schistosomiasis and soil-transmitted helminth. This study conducted active safety surveillance to assess the adverse events following the mass drug administration of praziquantel and albendazole in school children. The results showed that the treatment was generally safe, but children infected with parasites were more likely to experience adverse events.
Preventive chemotherapy (PC) with praziquantel and albendazole co-administration to all at-risk populations is the global intervention strategy to eliminate schistosomiasis and soil-transmitted helminth (STH) from being public health problems. Due to weak pharmacovigilance systems, safety monitoring during a mass drug administration (MDA) is lacking, especially in sub-Saharan Africa. We conducted large-scale active safety surveillance to identify the incidence, types, severity, and associated risk factors of adverse events (AEs) following praziquantel and albendazole MDA in 5848 school children (5-15 years old). Before MDA, 1484 (25.4%) children were prescreened for S. mansoni and STH infections, of whom 71.8% were infected with at least one parasite; 34.5% (512/1484) had S. mansoni and 853 (57.5%) had an STH infection. After collecting the baseline socio-demographic, clinical, and medical data, including any pre-existing clinical symptoms, participants received single dose praziquantel and albendazole MDA. Treatment-associated AEs were actively monitored on days 1 and 7 of the MDA. The events reported before and after the MDA were cross-checked and verified to identify MDA-associated AEs. The cumulative incidence of experiencing at least one type of MDA-associated AE was 13.3% (95% CI = 12.5-14.2%); 85.5%, 12.4%, and 1.8% of reported AEs were mild, moderate, and severe, respectively. The proportion of experiencing one, two, or >= three types of AEs was 57.7%, 34.1%, and 8.2%, respectively. The cumulative incidence of AEs in S. mansoni- and (17.0%) and STH (14.1%)-infected children was significantly higher (p < 0.001, chi(2) = 15.0) than in non-infected children (8.4%). Headache, abdominal pain, vomiting, dizziness, and nausea were the most common AEs. Being female, older age, having S. mansoni or STH infection were significant predictors of MDA-associated AEs. In summary, praziquantel and albendazole co-administration is generally safe and tolerable. MDA-associated AEs are mostly mild-to-moderately severe and transient. The finding of few severe AEs and significantly high rates of AEs in helminth-infected children underscores the need to integrate pharmacovigilance in MDA programs, especially in high schistosomiasis and STH endemic areas.

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