Evidence map›Paper›PMID 42030349›Full record

ArticlePLOS global public health2026

Impact of mass drug administration with Ivermectin, Diethylcarbamazine, and Albendazole in elimination of lymphatic filariasis in five districts of Nepal.

Ram Kumar Mahato, Gokarna Dahal, Yadu Chandra Ghimire, Rudra Prasad Marasini, David T S Hayman, Kaliannagounder Krishnamoorthy, Sunil Raj Sharma, Dipak Sah, Ram Balak Ray, Radha Subedi and 15 more

Abstract read
In one paragraph

Article in PLOS global public health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors.

Ram Kumar MahatoEpidemiology and Disease Control Division, Teku, Kathmandu, Nepal.ORCID https://orcid.org/0000-0001-5006-6516
Gokarna DahalEpidemiology and Disease Control Division, Teku, Kathmandu, Nepal.
Yadu Chandra GhimireEpidemiology and Disease Control Division, Teku, Kathmandu, Nepal.
Rudra Prasad MarasiniEpidemiology and Disease Control Division, Teku, Kathmandu, Nepal.
David T S HaymanMolecular Epidemiology and Public Health Laboratory, Infectious Disease Research Centre, Hopkirk Research Institute, Massey University, Palmerston North, New Zealand.ORCID https://orcid.org/0000-0003-0087-3015
Kaliannagounder KrishnamoorthyICMR-Vector Control Research Centre, Puducherry, India.ORCID https://orcid.org/0000-0003-4249-8890
Sunil Raj SharmaVector Borne Disease Research and Training Center, Hetauda, Makwanpur, Nepal.
Dipak SahVector Borne Disease Research and Training Center, Hetauda, Makwanpur, Nepal.
Ram Balak RayVector Borne Disease Research and Training Center, Hetauda, Makwanpur, Nepal.
Radha SubediVector Borne Disease Research and Training Center, Hetauda, Makwanpur, Nepal.
Keshav Raj PanditVector Borne Disease Research and Training Center, Hetauda, Makwanpur, Nepal.
Sudip Raj KhatiwadaRTI International, Act to End NTDs | East, Kathmandu, Nepal.
Achut Babu OjhaRTI International, Act to End NTDs | East, Kathmandu, Nepal.
Saroj MahasethRTI International, Act to End NTDs | East, Kathmandu, Nepal.
Deepak Bahadur MahataRTI International, Act to End NTDs | East, Kathmandu, Nepal.
Molly BradyRTI International, Act to End NTDs | East, Research Triangle Park, North Carolina, United States of America.
Clara R Burgert-BruckerRTI International, Act to End NTDs | East, Research Triangle Park, North Carolina, United States of America.
Briana StoneRTI International, Act to End NTDs | East, Research Triangle Park, North Carolina, United States of America.ORCID https://orcid.org/0000-0002-0792-3356
Ashna ParajuliEpidemiology and Disease Control Division, Teku, Kathmandu, Nepal.ORCID https://orcid.org/0009-0001-4441-9263
Satya Raj PaudelFAIRMED Foundation, Kathmandu, Nepal.ORCID https://orcid.org/0009-0001-4767-602X
Bhim Prakash DevkotaDepartment of Health Services, Teku, Kathmandu, Nepal.ORCID https://orcid.org/0009-0003-3090-6698
Chandra Bhal JhaEpidemiology and Disease Control Division, Teku, Kathmandu, Nepal.
Krishna Prasad PaudelMinistry of Health and Population, Ramshahpath, Kathmandu, Nepal.
Bhim Prasad SapkotaMinistry of Health and Population, Ramshahpath, Kathmandu, Nepal.ORCID https://orcid.org/0000-0001-7104-5968
Bijay BajracharyaCenter For Health and Disease Studies, Nepal.ORCID https://orcid.org/0000-0003-2476-821X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nepal aims to eliminate lymphatic filariasis (LF) by 2030. Mass drug administration (MDA) has ceased in 53 of the 64 endemic districts. Following failure to pass the pre-Transmission Assessment Survey of antigenemia prevalence, five districts completed two rounds of MDA using a three-drug regimen (Ivermectin, Diethylcarbamazine, and Albendazole; IDA) and achieved over 65% coverage of the total population in 2023 and 2024. An Epidemiological Monitoring Survey (EMS) was conducted to evaluate IDA's impact. A cross-sectional EMS was conducted 9 months post-MDA in 11 evaluation units (EUs) across five districts, using two sites per EU (n = 22). A total of 6,829 individuals aged ≥20 years were sampled via multi-stage methods, with ≥300 blood samples per site. Data on demographics and MDA participation were collected. LF antigen testing was followed by night blood microfilariae testing in antigen-positive samples. Analysis included non-parametric tests, logistic and mixed-effects models accounting for site-level clustering, and penalized regression (lasso and ridge) to assess predictor importance and manage multicollinearity. Nine of 11 EUs passed EMS. Two EUs in Kapilvastu failed due to ≥1% microfilariae prevalence in at least one site. Microfilariae prevalence was negatively correlated with site MDA coverage (p-value 0.04), but not antigen prevalence (p-value 0.8). Overall, 4.63% of participants were antigen-positive and 0.34% were microfilariae-positive (ratio 14:1). Being female (OR 0.12; 95% CI: 0.04-0.36) and participation in latest MDA round (OR 0.34; 95% CI: 0.15-0.77) were associated with lower microfilariae prevalence. Suboptimal impact of MDA was observed in two EUs based on microfilariae prevalence and may reflect insufficient treatment compliance. Two additional rounds of MDA with directly observed treatment are recommended to improve adherence. Female sex and participation in the most recent MDA round were associated with reduced odds of microfilaremia. Targeted strategies focusing on men and other identified risk groups may enhance program effectiveness.

Identifiers

PMID42030349
PMCPMC13108797

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.