A triple-drug treatment regimen to accelerate elimination of lymphatic filariasis: From conception to delivery
- PMID: 33349879
- PMCID: PMC7753162
- DOI: 10.1093/inthealth/ihaa046
A triple-drug treatment regimen to accelerate elimination of lymphatic filariasis: From conception to delivery
Erratum in
-
Corrigendum to: SUPPLEMENT, Two Decades of Public Health Achievements in Lymphatic Filariasis (2000-2020): Reflections, Progress and Future Challenges.Int Health. 2021 Sep 3;13(5):492. doi: 10.1093/inthealth/ihab014. Int Health. 2021. PMID: 33749744 Free PMC article. No abstract available.
Abstract
The Global Programme to Eliminate Lymphatic Filariasis (LF) is using mass drug administration (MDA) of antifilarial medications to treat filarial infections, prevent disease and interrupt transmission. Almost 500 million people receive these medications each year. Clinical trials have recently shown that a single dose of a triple-drug combination comprised of ivermectin, diethylcarbamazine and albendazole (IDA) is dramatically superior to widely used two-drug combinations for clearing larval filarial parasites from the blood of infected persons. A large multicenter community study showed that IDA was well-tolerated when it was provided as MDA. IDA was rapidly advanced from clinical trial to policy and implementation; it has the potential to accelerate LF elimination in many endemic countries.
Keywords: elimination; ivermectin; lymphatic filariasis; mass drug administration; therapy.
© The Author(s) 2020. Published by Oxford University Press on behalf of Royal Society of Tropical Medicine and Hygiene.
References
-
- WHO . Progress report 2000–2009 and Strategic Plan 2010–2020 of the Global Programme to Eliminate Lymphatic Filariasis: Halfway Towards Eliminating Lymphatic Filariasis. Geneva: World Health Organization, 2010.
-
- Thomsen EK, Sanuku N, Baea Met al. . Efficacy, safety, and pharmacokinetics of coadministered diethylcarbamazine, albendazole, and ivermectin for treatment of bancroftian filariasis. Clin Infect Dis. 2016;62(3):334–41. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
