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Does Intensive Treatment Select for Praziquantel Resistance in High-Transmission Settings? Parasitological Trends and Treatment Efficacy Within a Cluster-Randomized Trial

BACKGROUND: Praziquantel mass drug administration (MDA) is recommended in schistosomiasis-endemic areas. Animal models demonstrate Schistosoma parasite resistance to praziquantel after repeated exposure. METHODS: We conducted a parasitological survey in 26 fishing communities in Uganda after 4 years...

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Autores principales: Tushabe, John Vianney, Lubyayi, Lawrence, Sserubanja, Joel, Kabuubi, Prossy, Abayo, Elson, Kiwanuka, Samuel, Nassuuna, Jacent, Kaweesa, James, Corstjens, Paul, van Dam, Govert, Sanya, Richard E, Ssenyonga, William, Tukahebwa, Edridah Muheki, Kabatereine, Narcis B, Elliott, Alison M, Webb, Emily L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148002/
https://www.ncbi.nlm.nih.gov/pubmed/32296727
http://dx.doi.org/10.1093/ofid/ofaa091
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author Tushabe, John Vianney
Lubyayi, Lawrence
Sserubanja, Joel
Kabuubi, Prossy
Abayo, Elson
Kiwanuka, Samuel
Nassuuna, Jacent
Kaweesa, James
Corstjens, Paul
van Dam, Govert
Sanya, Richard E
Ssenyonga, William
Tukahebwa, Edridah Muheki
Kabatereine, Narcis B
Elliott, Alison M
Webb, Emily L
author_facet Tushabe, John Vianney
Lubyayi, Lawrence
Sserubanja, Joel
Kabuubi, Prossy
Abayo, Elson
Kiwanuka, Samuel
Nassuuna, Jacent
Kaweesa, James
Corstjens, Paul
van Dam, Govert
Sanya, Richard E
Ssenyonga, William
Tukahebwa, Edridah Muheki
Kabatereine, Narcis B
Elliott, Alison M
Webb, Emily L
author_sort Tushabe, John Vianney
collection PubMed
description BACKGROUND: Praziquantel mass drug administration (MDA) is recommended in schistosomiasis-endemic areas. Animal models demonstrate Schistosoma parasite resistance to praziquantel after repeated exposure. METHODS: We conducted a parasitological survey in 26 fishing communities in Uganda after 4 years of quarterly (13 communities) or annual (13 communities) praziquantel MDA, with Schistosoma infection detected by single-stool-sample Kato-Katz. A test of cure was done in participants who were positive on both urine circulating cathodic antigen test and 3-sample Kato-Katz. We calculated cure rates (CRs) and egg reduction rates (ERRs) based on 3-sample Kato-Katz and infection intensity using worm-specific circulating anodic antigen (CAA) in blood, comparing these between quarterly and annually treated participants. RESULTS: Single-sample Kato-Katz Schistosoma mansoni prevalence was 22% in 1,056 quarterly treated participants and 34% in 1,030 annually treated participants (risk ratio, 0.62; 95% confidence interval [CI], 0.40 to 0.94). Among 110 test-of-cure participants, CRs were 65% and 51% in annually and quarterly treated villages, respectively (odds ratio, 0.65; 95% CI, 0.27 to 1.58); ERRs were 94% and 81% (difference, –13%; 95% CI, –48% to 2%). There was no impact of quarterly vs annual praziquantel on S. mansoni by CAA. CONCLUSIONS: In this schistosomiasis hot spot, there was little evidence of decreased praziquantel efficacy. However, in the absence of alternative therapies, there remains a need for continued vigilance of praziquantel efficacy in the MDA era.
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spelling pubmed-71480022020-04-15 Does Intensive Treatment Select for Praziquantel Resistance in High-Transmission Settings? Parasitological Trends and Treatment Efficacy Within a Cluster-Randomized Trial Tushabe, John Vianney Lubyayi, Lawrence Sserubanja, Joel Kabuubi, Prossy Abayo, Elson Kiwanuka, Samuel Nassuuna, Jacent Kaweesa, James Corstjens, Paul van Dam, Govert Sanya, Richard E Ssenyonga, William Tukahebwa, Edridah Muheki Kabatereine, Narcis B Elliott, Alison M Webb, Emily L Open Forum Infect Dis Major Article BACKGROUND: Praziquantel mass drug administration (MDA) is recommended in schistosomiasis-endemic areas. Animal models demonstrate Schistosoma parasite resistance to praziquantel after repeated exposure. METHODS: We conducted a parasitological survey in 26 fishing communities in Uganda after 4 years of quarterly (13 communities) or annual (13 communities) praziquantel MDA, with Schistosoma infection detected by single-stool-sample Kato-Katz. A test of cure was done in participants who were positive on both urine circulating cathodic antigen test and 3-sample Kato-Katz. We calculated cure rates (CRs) and egg reduction rates (ERRs) based on 3-sample Kato-Katz and infection intensity using worm-specific circulating anodic antigen (CAA) in blood, comparing these between quarterly and annually treated participants. RESULTS: Single-sample Kato-Katz Schistosoma mansoni prevalence was 22% in 1,056 quarterly treated participants and 34% in 1,030 annually treated participants (risk ratio, 0.62; 95% confidence interval [CI], 0.40 to 0.94). Among 110 test-of-cure participants, CRs were 65% and 51% in annually and quarterly treated villages, respectively (odds ratio, 0.65; 95% CI, 0.27 to 1.58); ERRs were 94% and 81% (difference, –13%; 95% CI, –48% to 2%). There was no impact of quarterly vs annual praziquantel on S. mansoni by CAA. CONCLUSIONS: In this schistosomiasis hot spot, there was little evidence of decreased praziquantel efficacy. However, in the absence of alternative therapies, there remains a need for continued vigilance of praziquantel efficacy in the MDA era. Oxford University Press 2020-03-12 /pmc/articles/PMC7148002/ /pubmed/32296727 http://dx.doi.org/10.1093/ofid/ofaa091 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Major Article
Tushabe, John Vianney
Lubyayi, Lawrence
Sserubanja, Joel
Kabuubi, Prossy
Abayo, Elson
Kiwanuka, Samuel
Nassuuna, Jacent
Kaweesa, James
Corstjens, Paul
van Dam, Govert
Sanya, Richard E
Ssenyonga, William
Tukahebwa, Edridah Muheki
Kabatereine, Narcis B
Elliott, Alison M
Webb, Emily L
Does Intensive Treatment Select for Praziquantel Resistance in High-Transmission Settings? Parasitological Trends and Treatment Efficacy Within a Cluster-Randomized Trial
title Does Intensive Treatment Select for Praziquantel Resistance in High-Transmission Settings? Parasitological Trends and Treatment Efficacy Within a Cluster-Randomized Trial
title_full Does Intensive Treatment Select for Praziquantel Resistance in High-Transmission Settings? Parasitological Trends and Treatment Efficacy Within a Cluster-Randomized Trial
title_fullStr Does Intensive Treatment Select for Praziquantel Resistance in High-Transmission Settings? Parasitological Trends and Treatment Efficacy Within a Cluster-Randomized Trial
title_full_unstemmed Does Intensive Treatment Select for Praziquantel Resistance in High-Transmission Settings? Parasitological Trends and Treatment Efficacy Within a Cluster-Randomized Trial
title_short Does Intensive Treatment Select for Praziquantel Resistance in High-Transmission Settings? Parasitological Trends and Treatment Efficacy Within a Cluster-Randomized Trial
title_sort does intensive treatment select for praziquantel resistance in high-transmission settings? parasitological trends and treatment efficacy within a cluster-randomized trial
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148002/
https://www.ncbi.nlm.nih.gov/pubmed/32296727
http://dx.doi.org/10.1093/ofid/ofaa091
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