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Clinical efficacy of dalbavancin for the treatment of acute bacterial skin and skin structure infections (ABSSSI)
Acute bacterial skin and skin structure infections (ABSSSI) are a common disease causing patients to seek treatment through the health care system. With the continued increase of drug-resistant bacterial pathogens, these infections are becoming more difficult to successfully cure. Lipoglycopeptides...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4907732/ https://www.ncbi.nlm.nih.gov/pubmed/27354809 http://dx.doi.org/10.2147/TCRM.S86330 |
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author | Leuthner, Kimberly D Buechler, Kristin A Kogan, David Saguros, Agafe Lee, H Stephen |
author_facet | Leuthner, Kimberly D Buechler, Kristin A Kogan, David Saguros, Agafe Lee, H Stephen |
author_sort | Leuthner, Kimberly D |
collection | PubMed |
description | Acute bacterial skin and skin structure infections (ABSSSI) are a common disease causing patients to seek treatment through the health care system. With the continued increase of drug-resistant bacterial pathogens, these infections are becoming more difficult to successfully cure. Lipoglycopeptides have unique properties that allow the drug to remain active toward both common and challenging pathogens at the infected site for lengthy periods of time. Dalbavancin, a new lipoglycopeptide, provides two unique dosing regimens for the treatment of ABSSSI. The original regimen of 1,000 mg intravenous infusion followed by a 500 mg intravenous infusion after a week has been shown as safe and effective in multiple, randomized noninferiority trials. These studies also demonstrated that dalbavancin was similar to standard regimens in terms of both safety and tolerability. Recently a single 1,500 mg dose was demonstrated to be equivalent to the dalbavancin two-dose regimen for treating ABSSSI. With the introduction of dalbavancin, clinicians have the option to provide an intravenous antimicrobial agent shown to be as effective as traditional therapies, without requiring admission into the hospitals or prescribing a medication which may not be utilized optimally. Further understanding of dalbavancin and its unusual properties can provide unique treatment situations with potential benefits for both the patient and the overall health care system, which should be further explored. |
format | Online Article Text |
id | pubmed-4907732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49077322016-06-28 Clinical efficacy of dalbavancin for the treatment of acute bacterial skin and skin structure infections (ABSSSI) Leuthner, Kimberly D Buechler, Kristin A Kogan, David Saguros, Agafe Lee, H Stephen Ther Clin Risk Manag Review Acute bacterial skin and skin structure infections (ABSSSI) are a common disease causing patients to seek treatment through the health care system. With the continued increase of drug-resistant bacterial pathogens, these infections are becoming more difficult to successfully cure. Lipoglycopeptides have unique properties that allow the drug to remain active toward both common and challenging pathogens at the infected site for lengthy periods of time. Dalbavancin, a new lipoglycopeptide, provides two unique dosing regimens for the treatment of ABSSSI. The original regimen of 1,000 mg intravenous infusion followed by a 500 mg intravenous infusion after a week has been shown as safe and effective in multiple, randomized noninferiority trials. These studies also demonstrated that dalbavancin was similar to standard regimens in terms of both safety and tolerability. Recently a single 1,500 mg dose was demonstrated to be equivalent to the dalbavancin two-dose regimen for treating ABSSSI. With the introduction of dalbavancin, clinicians have the option to provide an intravenous antimicrobial agent shown to be as effective as traditional therapies, without requiring admission into the hospitals or prescribing a medication which may not be utilized optimally. Further understanding of dalbavancin and its unusual properties can provide unique treatment situations with potential benefits for both the patient and the overall health care system, which should be further explored. Dove Medical Press 2016-06-07 /pmc/articles/PMC4907732/ /pubmed/27354809 http://dx.doi.org/10.2147/TCRM.S86330 Text en © 2016 Leuthner et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Leuthner, Kimberly D Buechler, Kristin A Kogan, David Saguros, Agafe Lee, H Stephen Clinical efficacy of dalbavancin for the treatment of acute bacterial skin and skin structure infections (ABSSSI) |
title | Clinical efficacy of dalbavancin for the treatment of acute bacterial skin and skin structure infections (ABSSSI) |
title_full | Clinical efficacy of dalbavancin for the treatment of acute bacterial skin and skin structure infections (ABSSSI) |
title_fullStr | Clinical efficacy of dalbavancin for the treatment of acute bacterial skin and skin structure infections (ABSSSI) |
title_full_unstemmed | Clinical efficacy of dalbavancin for the treatment of acute bacterial skin and skin structure infections (ABSSSI) |
title_short | Clinical efficacy of dalbavancin for the treatment of acute bacterial skin and skin structure infections (ABSSSI) |
title_sort | clinical efficacy of dalbavancin for the treatment of acute bacterial skin and skin structure infections (absssi) |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4907732/ https://www.ncbi.nlm.nih.gov/pubmed/27354809 http://dx.doi.org/10.2147/TCRM.S86330 |
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