Evidence map›Paper›PMID 39994719›Full record

ArticleInfectious diseases of poverty2025

Safety and effectiveness of triple-drug therapy with ivermectin, diethylcarbamazine, and albendazole in reducing lymphatic filariasis prevalence and clearing circulating filarial antigens in Mombasa, Kenya.

Christabel Khaemba, Sammy M Njenga, Wyckliff P Omondi, Elvis Kirui, Margaret Oluka, Anastacia Guantai, Eleni Aklillu

Abstract read
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Article in Infectious diseases of poverty, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Christabel KhaembaDepartment of Global Public Health, Karolinska Institutet, Karolinska University Hospital, Tomtebodavägen 18A, 171 77, Stockholm, Sweden.
Sammy M NjengaKenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Wyckliff P OmondiMinistry of Health, National Neglected Tropical Diseases Program, Nairobi, Kenya.
Elvis KiruiMinistry of Health, National Public Health Laboratory, Nairobi, Kenya.
Margaret OlukaDepartment of Pharmacology and Pharmacognosy, School of Pharmacy, University of Nairobi, Nairobi, Kenya.
Anastacia GuantaiDepartment of Pharmacology and Pharmacognosy, School of Pharmacy, University of Nairobi, Nairobi, Kenya.
Eleni AklilluDepartment of Global Public Health, Karolinska Institutet, Karolinska University Hospital, Tomtebodavägen 18A, 171 77, Stockholm, Sweden. eleni.aklillu@ki.se.ORCID http://orcid.org/0000-0002-9788-0790

Funding

European and Developing Countries Clinical Trials Partnership CSA2016S-1618Styrelsen för Internationellt Utvecklingssamarbete CSA2016S-1618
6 · The paper itself

Abstract

backgroundIn 2018, Kenya introduced triple-drug therapy with ivermectin, diethylcarbamazine, albendazole (IDA) through mass drug administration (MDA) to accelerate the elimination of lymphatic filariasis (LF). This community-based surveillance study assessed the safety and effectiveness of IDA-MDA in reducing LF-antigenemia prevalence and circulating filarial antigens (CFA) clearance among LF infected individuals.

methodsA total of 8928 residents in Mombasa, Kenya, were screened for CFA using the Filarial Test Strip: 3464 were screened in 2018 and 5464 in 2021 after two annual IDA-MDA rounds. CFA-positive individuals in 2021 were re-tested at two and four months of post-MDA for CFA-clearance rates. Adverse events (AEs) associated with IDA-MDA were monitored via door-to-door visits on days 1, 2, and 7 post-MDA to document the incidence, type and risk factors. Efficacy outcomes included post-MDA LF-antigenemia prevalence reduction after two rounds of annual MDA and CFA clearance rate. Chi-square test compared proportions, and logistic regression analysis identified AE predictors.

resultsLF antigenemia prevalence significantly decreased from 1.39% (n = 48) in 2018 to 0.66% (n = 36) in 2021 [P < 0.001; 95% confidence interval (CI) for difference in proportions: 0.003-0.012]. CFA clearance rates were 63.2% (12/19, 95% CI: 41.0-80.1%) at 2 months and 68.4% (13/19, 95% CI: 46.0-86.6%) at 4 months post-MDA. Among 53 CFA-positive individuals monitored, the cumulative 7-day AE incidence was 37.7% (95% CI: 25.6-51.7), higher than the general population's 27.3% (95% CI: 26.4-28.2). Common AEs included nausea (11.3%), diarrhea (11.3%), abdominal pain (7.6%), and headache (5.7%). Risk factors for AEs included age, overweight status, concomitant medication use, chronic illness, and fasting before MDA.

conclusionsTriple therapy with IDA is safe and well-tolerated, with some mild-to-moderate and transient adverse events among LF-infected individuals. The high incidence of AEs highlights the need for safety monitoring during MDA. The significant reductions in LF antigenemia prevalence and high CFA clearance rates underscore IDA's effectiveness in reducing LF transmission, positioning it as a key strategy for eliminating LF as a public health problem by 2030.

Indexed as

AlbendazoleAntigens, HelminthDiethylcarbamazineElephantiasis, FilarialFilaricidesIvermectinAdolescentAdultAgedAnimalsChildChild, PreschoolDrug Therapy, CombinationFemaleHumansKenyaAlbendazoleAntigens, HelminthDiethylcarbamazineFilaricidesIvermectinActive safety surveillanceAdverse eventsAlbendazoleDiethylcarbamazineEfficacyIvermectinLymphatic filariasisMass drug administrationPositive participants

Identifiers

PMID39994719
PMCPMC11849337

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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.