Can mass drug administration lead to the sustainable control of schistosomiasis?
- PMID: 25070942
- DOI: 10.1093/infdis/jiu416
Can mass drug administration lead to the sustainable control of schistosomiasis?
Abstract
Background: In the Philippines, the current national control strategy for schistosomiasis is annual mass drug administration (MDA) with 40 mg/kg of praziquantel in all schistosomiasis-endemic villages with a prevalence ≥10%.
Methods: A cross-sectional survey of schistosomiasis was conducted in 2012 on 18 221 individuals residing in 22 schistosomiasis-endemic villages in the province of Northern Samar. The prevalence of schistosomiasis, intensity of Schistosoma infection, and morbidity of disease were assessed.
Results: Despite an active schistosomiasis-control program in Northern Samar for >30 years, which included a MDA campaign in the last 5 years, the mean prevalence of schistosomiasis among 10 435 evaluated subjects was 27.1% (95% confidence interval [CI], 26.3%-28.0%), and the geometric mean intensity of infection among 2832 evaluated subjects was 17.2 eggs per gram of feces (95% CI, 16.4-18.1). Ultrasonography revealed high levels of schistosomiasis-induced morbidity in the schistosomiasis-endemic communities. Left lobe liver enlargement (≥70 mm) was evident in 89.3% of subjects. Twenty-five percent of the study population had grade II/III liver parenchyma fibrosis, and 13.3% had splenomegaly (≥100 mm).
Conclusions: MDA on its own was insufficient to control the prevalence of schistosomiasis, intensity of Schistosoma infection, or morbidity of the disease. Alternative control measures will be needed to complement the existing national MDA program.
Keywords: control; elimination; mass drug administration (MDA); schistosomiasis.
© The Author 2014. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.
Comment in
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Mass drug administration (MDA) for schistosomiasis.J Infect Dis. 2015 Mar 1;211(5):848-9. doi: 10.1093/infdis/jiu506. Epub 2014 Sep 9. J Infect Dis. 2015. PMID: 25205633 No abstract available.
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Reply to Wang and Liang.J Infect Dis. 2015 Mar 1;211(5):849-50. doi: 10.1093/infdis/jiu507. Epub 2014 Sep 9. J Infect Dis. 2015. PMID: 25205635 No abstract available.
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