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Assessment of antigenemia among children in four hotspots of filarial endemic districts of Nepal during post-MDA surveillance
BACKGROUND: Sixty-three out of 77 districts reported lymphatic filariasis (LF) endemic in Nepal. Mass drug administration (MDA) with diethylcarbamazine (DEC) and albendazole (ALB) treatment program was continued for 6 to 11 rounds in these districts. Nepal government has stopped the MDA program base...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464004/ https://www.ncbi.nlm.nih.gov/pubmed/37620918 http://dx.doi.org/10.1186/s41182-023-00538-4 |
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author | Mehta, Pramod Kumar Maharjan, Mahendra |
author_facet | Mehta, Pramod Kumar Maharjan, Mahendra |
author_sort | Mehta, Pramod Kumar |
collection | PubMed |
description | BACKGROUND: Sixty-three out of 77 districts reported lymphatic filariasis (LF) endemic in Nepal. Mass drug administration (MDA) with diethylcarbamazine (DEC) and albendazole (ALB) treatment program was continued for 6 to 11 rounds in these districts. Nepal government has stopped the MDA program based on the transmission assessment survey (TAS) report of 2014 and 2018 indicating Wuchereria bancrofti antigenemia prevalence < 2%. But the persistence of low levels of the circulating filarial antigen (CFA) in some foci of four endemic districts of Central Nepal, i.e., 0.4% in Dhading, 0.7% in Mahottari, 0.21% in Lalitpur and 1.2% in Bara district could responsible for enhancing the risk of infection resurgence. Hence the present study was designed to assess antigenic prevalence using Filariasis Test Strip (Alere, Scarborough ME) in children born after MDA in hotspot areas of four endemic districts of Central Nepal. RESULTS: The present study covers 70% children of the eligible population. The result revealed significantly high CFA prevalence in hotspots of Mahottari district belonging to the Terai region and Dhading district belonging to the hilly region, i.e., 13% and 10%, respectively, compared to baseline prevalence and TAS report. While in Lalitpur district and Bara district CFA prevalence was still found to be less than 2%. A higher number of MDA rounds covered in hotspots were found significantly associated with the low antigenic prevalence of W. bancrofti. Whereas median treatment coverage and inter-quartile range (IQR) in study districts were not found significantly associated with CFA prevalence. Although the clinical manifestation of hydrocele (1%) was found in all four study districts, it was not due to the W. bancrofti infection. CONCLUSIONS: Two hotspot regions, one each from the Terai (Mahottari) and hilly (Dhading) districts were found highly prevalent with CFA and significantly associated with the number of MDA rounds but were not associated with treatment coverage and IQR. Higher CFA prevalence was observed in hotspots where baseline prevalence was high together indicating that rounds of MDA program need to be extended further in these hotspot regions of endemic districts. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41182-023-00538-4. |
format | Online Article Text |
id | pubmed-10464004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104640042023-08-30 Assessment of antigenemia among children in four hotspots of filarial endemic districts of Nepal during post-MDA surveillance Mehta, Pramod Kumar Maharjan, Mahendra Trop Med Health Research BACKGROUND: Sixty-three out of 77 districts reported lymphatic filariasis (LF) endemic in Nepal. Mass drug administration (MDA) with diethylcarbamazine (DEC) and albendazole (ALB) treatment program was continued for 6 to 11 rounds in these districts. Nepal government has stopped the MDA program based on the transmission assessment survey (TAS) report of 2014 and 2018 indicating Wuchereria bancrofti antigenemia prevalence < 2%. But the persistence of low levels of the circulating filarial antigen (CFA) in some foci of four endemic districts of Central Nepal, i.e., 0.4% in Dhading, 0.7% in Mahottari, 0.21% in Lalitpur and 1.2% in Bara district could responsible for enhancing the risk of infection resurgence. Hence the present study was designed to assess antigenic prevalence using Filariasis Test Strip (Alere, Scarborough ME) in children born after MDA in hotspot areas of four endemic districts of Central Nepal. RESULTS: The present study covers 70% children of the eligible population. The result revealed significantly high CFA prevalence in hotspots of Mahottari district belonging to the Terai region and Dhading district belonging to the hilly region, i.e., 13% and 10%, respectively, compared to baseline prevalence and TAS report. While in Lalitpur district and Bara district CFA prevalence was still found to be less than 2%. A higher number of MDA rounds covered in hotspots were found significantly associated with the low antigenic prevalence of W. bancrofti. Whereas median treatment coverage and inter-quartile range (IQR) in study districts were not found significantly associated with CFA prevalence. Although the clinical manifestation of hydrocele (1%) was found in all four study districts, it was not due to the W. bancrofti infection. CONCLUSIONS: Two hotspot regions, one each from the Terai (Mahottari) and hilly (Dhading) districts were found highly prevalent with CFA and significantly associated with the number of MDA rounds but were not associated with treatment coverage and IQR. Higher CFA prevalence was observed in hotspots where baseline prevalence was high together indicating that rounds of MDA program need to be extended further in these hotspot regions of endemic districts. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41182-023-00538-4. BioMed Central 2023-08-24 /pmc/articles/PMC10464004/ /pubmed/37620918 http://dx.doi.org/10.1186/s41182-023-00538-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Mehta, Pramod Kumar Maharjan, Mahendra Assessment of antigenemia among children in four hotspots of filarial endemic districts of Nepal during post-MDA surveillance |
title | Assessment of antigenemia among children in four hotspots of filarial endemic districts of Nepal during post-MDA surveillance |
title_full | Assessment of antigenemia among children in four hotspots of filarial endemic districts of Nepal during post-MDA surveillance |
title_fullStr | Assessment of antigenemia among children in four hotspots of filarial endemic districts of Nepal during post-MDA surveillance |
title_full_unstemmed | Assessment of antigenemia among children in four hotspots of filarial endemic districts of Nepal during post-MDA surveillance |
title_short | Assessment of antigenemia among children in four hotspots of filarial endemic districts of Nepal during post-MDA surveillance |
title_sort | assessment of antigenemia among children in four hotspots of filarial endemic districts of nepal during post-mda surveillance |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464004/ https://www.ncbi.nlm.nih.gov/pubmed/37620918 http://dx.doi.org/10.1186/s41182-023-00538-4 |
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