Prevalence and risk factors associated with lymphatic filariasis in American Samoa after mass drug administration

Tropical Medicine and Health - Tập 45 - Trang 1-10 - 2017
Shaun P. Coutts1, Jonathan D. King2, Molisamoa Pa’au3, Saipale Fuimaono3, Joseph Roth4, Mary Rose King5, Patrick J. Lammie6, Colleen L. Lau7, Patricia M. Graves8
1College of Public Health, Medical and Veterinary Sciences, James Cook University, Cairns, Australia
2Department of Control of Neglected Tropical Diseases, World Health Organization, Geneva, Switzerland
3American Samoa Department of Health, Pago Pago, American Samoa
4Office of Public Health Preparedness and Response, Centers for Disease Control and Prevention, Atlanta, USA
5Independent Nursing Consultant, Geneva, Switzerland
6Neglected Tropical Diseases Support Center, The Task Force for Global Health, Atlanta, USA
7Department of Global Health, Research School of Population Health, Australian National University, Canberra, Australia
8Australian Institute of Tropical Health and Medicine and College of Public Health, Medical and Veterinary Sciences, James Cook University, Cairns, Australia

Tóm tắt

In 2000, American Samoa had 16.5% prevalence of lymphatic filariasis (LF) antigenemia. Annual mass drug administration (MDA) was conducted using single-dose albendazole plus diethylcarbamazine from 2000 to 2006. This study presents the results of a 2007 population-based PacELF C-survey in all ages and compares the adult filarial antigenemia results of this survey to those of a subsequent 2010 survey in adults with the aim of improving understanding of LF transmission after MDA. The 2007 C-survey used simple random sampling of households from a geolocated list. In 2007, the overall LF antigen prevalence by immunochromatographic card test (ICT) for all ages was 2.29% (95% CI 1.66–3.07). Microfilaremia prevalence was 0.27% (95% CI 0.09–0.62). Increasing age (OR 1.04 per year, 95% CI 1.02–1.05) was significantly associated with ICT positivity on multivariate analysis, while having ever taking MDA was protective (OR 0.39, 95% CI 0.16–0.96). The 2010 survey used a similar spatial sampling design. The overall adult filarial antigenemia prevalence remained relatively stable between the surveys at 3.32% (95% CI 2.44–4.51) by ICT in 2007 and 3.23 (95% CI 2.21–4.69) by Og4C3 antigen in 2010. However, there were changes in village-level prevalence. Eight village/village groupings had antigen-positive individuals identified in 2007 but not in 2010, while three villages/village groupings that had no antigen-positive individuals identified in 2007 had positive individuals identified in 2010. After 7 years of MDA, with four rounds achieving effective coverage, a representative household survey in 2007 showed a decline in prevalence from 16.5 to 2.3% in all ages. However, lack of further decline in adult prevalence by 2010 and fluctuation at the village level showed that overall antigenemia prevalence at a broader scale may not provide an accurate reflection of ongoing transmission at the village level.

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