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Evaluation of the Impact of Comorbidities on Omadacycline Pharmacokinetics

Omadacycline is approved in the United States for the treatment of patients with community-acquired bacterial pneumonia or acute bacterial skin and skin structure infections. Analyses were undertaken to evaluate pharmacokinetic differences among subjects or patients stratified by comorbidities. Diff...

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Autores principales: Trang, M., Lakota, E. A., Safir, M. C., Bhavnani, S. M., Friedrich, L., Steenbergen, J. N., McGovern, P. C., Tzanis, E., Rubino, C. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10112242/
https://www.ncbi.nlm.nih.gov/pubmed/36916956
http://dx.doi.org/10.1128/aac.02397-21
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author Trang, M.
Lakota, E. A.
Safir, M. C.
Bhavnani, S. M.
Friedrich, L.
Steenbergen, J. N.
McGovern, P. C.
Tzanis, E.
Rubino, C. M.
author_facet Trang, M.
Lakota, E. A.
Safir, M. C.
Bhavnani, S. M.
Friedrich, L.
Steenbergen, J. N.
McGovern, P. C.
Tzanis, E.
Rubino, C. M.
author_sort Trang, M.
collection PubMed
description Omadacycline is approved in the United States for the treatment of patients with community-acquired bacterial pneumonia or acute bacterial skin and skin structure infections. Analyses were undertaken to evaluate pharmacokinetic differences among subjects or patients stratified by comorbidities. Differences in clearance by smoking status, history of diabetes mellitus, chronic lung disease, hypertension, heart failure, or coronary artery disease were evaluated using a Welch two-sample t test. Smoking was the only significant comorbidity after correction for sex, with a clinically insignificant difference of 13%. Omadacycline dose adjustments based on these comorbidities do not appear to be warranted.
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spelling pubmed-101122422023-04-19 Evaluation of the Impact of Comorbidities on Omadacycline Pharmacokinetics Trang, M. Lakota, E. A. Safir, M. C. Bhavnani, S. M. Friedrich, L. Steenbergen, J. N. McGovern, P. C. Tzanis, E. Rubino, C. M. Antimicrob Agents Chemother Pharmacology Omadacycline is approved in the United States for the treatment of patients with community-acquired bacterial pneumonia or acute bacterial skin and skin structure infections. Analyses were undertaken to evaluate pharmacokinetic differences among subjects or patients stratified by comorbidities. Differences in clearance by smoking status, history of diabetes mellitus, chronic lung disease, hypertension, heart failure, or coronary artery disease were evaluated using a Welch two-sample t test. Smoking was the only significant comorbidity after correction for sex, with a clinically insignificant difference of 13%. Omadacycline dose adjustments based on these comorbidities do not appear to be warranted. American Society for Microbiology 2023-03-14 /pmc/articles/PMC10112242/ /pubmed/36916956 http://dx.doi.org/10.1128/aac.02397-21 Text en Copyright © 2023 Trang et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Pharmacology
Trang, M.
Lakota, E. A.
Safir, M. C.
Bhavnani, S. M.
Friedrich, L.
Steenbergen, J. N.
McGovern, P. C.
Tzanis, E.
Rubino, C. M.
Evaluation of the Impact of Comorbidities on Omadacycline Pharmacokinetics
title Evaluation of the Impact of Comorbidities on Omadacycline Pharmacokinetics
title_full Evaluation of the Impact of Comorbidities on Omadacycline Pharmacokinetics
title_fullStr Evaluation of the Impact of Comorbidities on Omadacycline Pharmacokinetics
title_full_unstemmed Evaluation of the Impact of Comorbidities on Omadacycline Pharmacokinetics
title_short Evaluation of the Impact of Comorbidities on Omadacycline Pharmacokinetics
title_sort evaluation of the impact of comorbidities on omadacycline pharmacokinetics
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10112242/
https://www.ncbi.nlm.nih.gov/pubmed/36916956
http://dx.doi.org/10.1128/aac.02397-21
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