The African eye worm: current understanding of the epidemiology, clinical disease, and treatment of loiasis

Standard

The African eye worm: current understanding of the epidemiology, clinical disease, and treatment of loiasis. / Ramharter, Michael; Butler, Joanna; Mombo-Ngoma, Ghyslain; Nordmann, Tamara; Davi, Saskia Dede; Zoleko Manego, Rella.

in: LANCET INFECT DIS, Jahrgang 24, Nr. 3, 03.2024, S. e165-e178.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ReviewForschung

Harvard

APA

Vancouver

Bibtex

@article{29591a6291eb4947bbf17eabfe6d4274,
title = "The African eye worm: current understanding of the epidemiology, clinical disease, and treatment of loiasis",
abstract = "Loa loa, the African eye worm, is a filarial pathogen transmitted by blood-sucking flies of the genus Chrysops. Loiasis primarily affects rural populations residing in the forest and adjacent savannah regions of central and west Africa, where more than 20 million patients are chronically infected in medium and high transmission regions. For a long time, loiasis has been regarded as a relatively benign condition. However, morbidity as measured by disability-adjusted life-years lost might be as high as 400 per 100 000 residents, and the population attributable fraction of death is estimated at 14·5% in highly endemic regions, providing unequivocal evidence for the substantial disease burden that loiasis exerts on affected communities. The clinical penetrance of loiasis is variable and might present with the classic signs of eye worm migration or transient Calabar swellings, but might include common, unspecific symptoms or rare but potentially life-threatening complications. Although adult worm migration seems most closely linked to symptomatic disease, high levels of microfilaraemia are associated with clinically important complications and death. Loiasis remains difficult to diagnose, treat, and control due to an absence of reliable point-of-care diagnostic assays, safe and efficacious drugs, and cost-effective prevention strategies. This Review summarises the major advances in our understanding of loiasis made over the past decade and highlights the many gaps that await to be addressed urgently.",
author = "Michael Ramharter and Joanna Butler and Ghyslain Mombo-Ngoma and Tamara Nordmann and Davi, {Saskia Dede} and {Zoleko Manego}, Rella",
note = "Copyright {\textcopyright} 2023 Elsevier Ltd. All rights reserved.",
year = "2024",
month = mar,
doi = "10.1016/S1473-3099(23)00438-3",
language = "English",
volume = "24",
pages = "e165--e178",
journal = "LANCET INFECT DIS",
issn = "1473-3099",
publisher = "Lancet Publishing Group",
number = "3",

}

RIS

TY - JOUR

T1 - The African eye worm: current understanding of the epidemiology, clinical disease, and treatment of loiasis

AU - Ramharter, Michael

AU - Butler, Joanna

AU - Mombo-Ngoma, Ghyslain

AU - Nordmann, Tamara

AU - Davi, Saskia Dede

AU - Zoleko Manego, Rella

N1 - Copyright © 2023 Elsevier Ltd. All rights reserved.

PY - 2024/3

Y1 - 2024/3

N2 - Loa loa, the African eye worm, is a filarial pathogen transmitted by blood-sucking flies of the genus Chrysops. Loiasis primarily affects rural populations residing in the forest and adjacent savannah regions of central and west Africa, where more than 20 million patients are chronically infected in medium and high transmission regions. For a long time, loiasis has been regarded as a relatively benign condition. However, morbidity as measured by disability-adjusted life-years lost might be as high as 400 per 100 000 residents, and the population attributable fraction of death is estimated at 14·5% in highly endemic regions, providing unequivocal evidence for the substantial disease burden that loiasis exerts on affected communities. The clinical penetrance of loiasis is variable and might present with the classic signs of eye worm migration or transient Calabar swellings, but might include common, unspecific symptoms or rare but potentially life-threatening complications. Although adult worm migration seems most closely linked to symptomatic disease, high levels of microfilaraemia are associated with clinically important complications and death. Loiasis remains difficult to diagnose, treat, and control due to an absence of reliable point-of-care diagnostic assays, safe and efficacious drugs, and cost-effective prevention strategies. This Review summarises the major advances in our understanding of loiasis made over the past decade and highlights the many gaps that await to be addressed urgently.

AB - Loa loa, the African eye worm, is a filarial pathogen transmitted by blood-sucking flies of the genus Chrysops. Loiasis primarily affects rural populations residing in the forest and adjacent savannah regions of central and west Africa, where more than 20 million patients are chronically infected in medium and high transmission regions. For a long time, loiasis has been regarded as a relatively benign condition. However, morbidity as measured by disability-adjusted life-years lost might be as high as 400 per 100 000 residents, and the population attributable fraction of death is estimated at 14·5% in highly endemic regions, providing unequivocal evidence for the substantial disease burden that loiasis exerts on affected communities. The clinical penetrance of loiasis is variable and might present with the classic signs of eye worm migration or transient Calabar swellings, but might include common, unspecific symptoms or rare but potentially life-threatening complications. Although adult worm migration seems most closely linked to symptomatic disease, high levels of microfilaraemia are associated with clinically important complications and death. Loiasis remains difficult to diagnose, treat, and control due to an absence of reliable point-of-care diagnostic assays, safe and efficacious drugs, and cost-effective prevention strategies. This Review summarises the major advances in our understanding of loiasis made over the past decade and highlights the many gaps that await to be addressed urgently.

U2 - 10.1016/S1473-3099(23)00438-3

DO - 10.1016/S1473-3099(23)00438-3

M3 - SCORING: Review article

C2 - 37858326

VL - 24

SP - e165-e178

JO - LANCET INFECT DIS

JF - LANCET INFECT DIS

SN - 1473-3099

IS - 3

ER -