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High risk of early sub-therapeutic penicillin concentrations after intramuscular benzathine penicillin G injections in Ethiopian children and adults with rheumatic heart disease

INTRODUCTION: Intramuscular benzathine penicillin G (BPG) injections are a cornerstone of secondary prophylaxis to prevent acute rheumatic fever (ARF) and rheumatic heart disease (RHD). Uncertainties regarding inter-ethnic and preparation variability, and target exposure profiles of BPG injection ar...

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Autores principales: Ketema, Ezra B., Gishen, Nigus Z., Hailu, Abraha, Leul, Abadi, Hadgu, Abera, Hagos, Kiflom, Berhane, Samual, Tsega, Temesgen, Page-Sharp, Madhu, Davis, Timothy ME, Moore, Brioni, Batty, Kevin T., Carapetis, Jonathan, Salman, Sam, Manning, Laurens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195421/
https://www.ncbi.nlm.nih.gov/pubmed/34115748
http://dx.doi.org/10.1371/journal.pntd.0009399
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author Ketema, Ezra B.
Gishen, Nigus Z.
Hailu, Abraha
Leul, Abadi
Hadgu, Abera
Hagos, Kiflom
Berhane, Samual
Tsega, Temesgen
Page-Sharp, Madhu
Davis, Timothy ME
Moore, Brioni
Batty, Kevin T.
Carapetis, Jonathan
Salman, Sam
Manning, Laurens
author_facet Ketema, Ezra B.
Gishen, Nigus Z.
Hailu, Abraha
Leul, Abadi
Hadgu, Abera
Hagos, Kiflom
Berhane, Samual
Tsega, Temesgen
Page-Sharp, Madhu
Davis, Timothy ME
Moore, Brioni
Batty, Kevin T.
Carapetis, Jonathan
Salman, Sam
Manning, Laurens
author_sort Ketema, Ezra B.
collection PubMed
description INTRODUCTION: Intramuscular benzathine penicillin G (BPG) injections are a cornerstone of secondary prophylaxis to prevent acute rheumatic fever (ARF) and rheumatic heart disease (RHD). Uncertainties regarding inter-ethnic and preparation variability, and target exposure profiles of BPG injection are key knowledge gaps for RHD control. METHODS: To evaluate BPG pharmacokinetics (PK) in patients receiving 4-weekly doses in Ethiopia, we conducted a prospective cohort study of ARF/RHD patients attending cardiology outpatient clinics. Serum samples were collected weekly for one month after injection and assayed with a liquid chromatography-mass spectroscopy assay. Concentration-time datasets for BPG were analyzed by nonlinear mixed effects modelling using NONMEM. RESULTS: A total of 190 penicillin concentration samples from 74 patients were included in the final PK model. The median age, weight, BMI was 21 years, 47 kg and 18 kg/m(2), respectively. When compared with estimates derived from Indigenous Australian patients, the estimate for median (95% confidence interval) volume of distribution (V/F) was lower (54.8 [43.9–66.3] l.70kg(-1)) whilst the absorption half-life (t(1/2-abs2)) was longer (12.0 [8.75–17.7] days). The median (IQR) percentage of time where the concentrations remained above 20 ng/mL and 10 ng/mL within the 28-day treatment cycle was 42.5% (27.5–60) and 73% (58.5–99), respectively. CONCLUSIONS: The majority of Ethiopian patients receiving BPG as secondary prophylaxis to prevent RHD do not attain target concentrations for more than two weeks during each 4-weekly injection cycle, highlighting the limitations of current BPG strategies. Between-population variation, together with PK differences between different preparations may be important considerations for ARF/RHD control programs.
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spelling pubmed-81954212021-06-21 High risk of early sub-therapeutic penicillin concentrations after intramuscular benzathine penicillin G injections in Ethiopian children and adults with rheumatic heart disease Ketema, Ezra B. Gishen, Nigus Z. Hailu, Abraha Leul, Abadi Hadgu, Abera Hagos, Kiflom Berhane, Samual Tsega, Temesgen Page-Sharp, Madhu Davis, Timothy ME Moore, Brioni Batty, Kevin T. Carapetis, Jonathan Salman, Sam Manning, Laurens PLoS Negl Trop Dis Research Article INTRODUCTION: Intramuscular benzathine penicillin G (BPG) injections are a cornerstone of secondary prophylaxis to prevent acute rheumatic fever (ARF) and rheumatic heart disease (RHD). Uncertainties regarding inter-ethnic and preparation variability, and target exposure profiles of BPG injection are key knowledge gaps for RHD control. METHODS: To evaluate BPG pharmacokinetics (PK) in patients receiving 4-weekly doses in Ethiopia, we conducted a prospective cohort study of ARF/RHD patients attending cardiology outpatient clinics. Serum samples were collected weekly for one month after injection and assayed with a liquid chromatography-mass spectroscopy assay. Concentration-time datasets for BPG were analyzed by nonlinear mixed effects modelling using NONMEM. RESULTS: A total of 190 penicillin concentration samples from 74 patients were included in the final PK model. The median age, weight, BMI was 21 years, 47 kg and 18 kg/m(2), respectively. When compared with estimates derived from Indigenous Australian patients, the estimate for median (95% confidence interval) volume of distribution (V/F) was lower (54.8 [43.9–66.3] l.70kg(-1)) whilst the absorption half-life (t(1/2-abs2)) was longer (12.0 [8.75–17.7] days). The median (IQR) percentage of time where the concentrations remained above 20 ng/mL and 10 ng/mL within the 28-day treatment cycle was 42.5% (27.5–60) and 73% (58.5–99), respectively. CONCLUSIONS: The majority of Ethiopian patients receiving BPG as secondary prophylaxis to prevent RHD do not attain target concentrations for more than two weeks during each 4-weekly injection cycle, highlighting the limitations of current BPG strategies. Between-population variation, together with PK differences between different preparations may be important considerations for ARF/RHD control programs. Public Library of Science 2021-06-11 /pmc/articles/PMC8195421/ /pubmed/34115748 http://dx.doi.org/10.1371/journal.pntd.0009399 Text en © 2021 Ketema et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ketema, Ezra B.
Gishen, Nigus Z.
Hailu, Abraha
Leul, Abadi
Hadgu, Abera
Hagos, Kiflom
Berhane, Samual
Tsega, Temesgen
Page-Sharp, Madhu
Davis, Timothy ME
Moore, Brioni
Batty, Kevin T.
Carapetis, Jonathan
Salman, Sam
Manning, Laurens
High risk of early sub-therapeutic penicillin concentrations after intramuscular benzathine penicillin G injections in Ethiopian children and adults with rheumatic heart disease
title High risk of early sub-therapeutic penicillin concentrations after intramuscular benzathine penicillin G injections in Ethiopian children and adults with rheumatic heart disease
title_full High risk of early sub-therapeutic penicillin concentrations after intramuscular benzathine penicillin G injections in Ethiopian children and adults with rheumatic heart disease
title_fullStr High risk of early sub-therapeutic penicillin concentrations after intramuscular benzathine penicillin G injections in Ethiopian children and adults with rheumatic heart disease
title_full_unstemmed High risk of early sub-therapeutic penicillin concentrations after intramuscular benzathine penicillin G injections in Ethiopian children and adults with rheumatic heart disease
title_short High risk of early sub-therapeutic penicillin concentrations after intramuscular benzathine penicillin G injections in Ethiopian children and adults with rheumatic heart disease
title_sort high risk of early sub-therapeutic penicillin concentrations after intramuscular benzathine penicillin g injections in ethiopian children and adults with rheumatic heart disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195421/
https://www.ncbi.nlm.nih.gov/pubmed/34115748
http://dx.doi.org/10.1371/journal.pntd.0009399
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