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Antimicrobial Resistance Surveillance and New Drug Development
Surveillance represents an important informational tool for planning actions to monitor emerging antimicrobial resistance. Antimicrobial resistance surveillance (ARS) programs may have many different designs and can be grouped in 2 major categories based on their main objectives: (1) public health A...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419994/ https://www.ncbi.nlm.nih.gov/pubmed/30895210 http://dx.doi.org/10.1093/ofid/ofy345 |
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author | Sader, Helio S Rhomberg, Paul R Fuhrmeister, Andrew S Mendes, Rodrigo E Flamm, Robert K Jones, Ronald N |
author_facet | Sader, Helio S Rhomberg, Paul R Fuhrmeister, Andrew S Mendes, Rodrigo E Flamm, Robert K Jones, Ronald N |
author_sort | Sader, Helio S |
collection | PubMed |
description | Surveillance represents an important informational tool for planning actions to monitor emerging antimicrobial resistance. Antimicrobial resistance surveillance (ARS) programs may have many different designs and can be grouped in 2 major categories based on their main objectives: (1) public health ARS programs and (2) industry-sponsored/product-oriented ARS programs. In general, public health ARS programs predominantly focus on health care and infection control, whereas industry ARS programs focus on an investigational or recently approved molecule(s). We reviewed the main characteristics of industry ARS programs and how these programs contribute to new drug development. Industry ARS programs are generally performed to comply with requirements from regulatory agencies responsible for commercial approval of antimicrobial agents, such as the US Food and Drug Administration, European Medicines Agency, and others. In contrast to public health ARS programs, which typically collect health care and diverse clinical data, industry ARS programs frequently collect the pathogens and perform the testing in a central laboratory setting. Global ARS programs with centralized testing play an important role in new antibacterial and antifungal drug development by providing information on the emergence and dissemination of resistant organisms, clones, and resistance determinants. Organisms collected by large ARS programs are extremely valuable to evaluate the potential of new agents and to calibrate susceptibility tests once a drug is approved for clinical use. These programs also can provide early evaluations of spectrum of activity and postmarketing trends required by regulatory agencies, and the programs may help drug companies to select appropriate dosing regimens and the appropriate geographic regions in which to perform clinical trials. Furthermore, these surveillance programs provide useful information on the potency and spectrum of new antimicrobial agents against indications and organisms in which clinicians have little or no experience. In summary, large ARS programs, such as the SENTRY Antimicrobial Surveillance Program, contribute key data for new drug development. |
format | Online Article Text |
id | pubmed-6419994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64199942019-03-20 Antimicrobial Resistance Surveillance and New Drug Development Sader, Helio S Rhomberg, Paul R Fuhrmeister, Andrew S Mendes, Rodrigo E Flamm, Robert K Jones, Ronald N Open Forum Infect Dis Supplement Article Surveillance represents an important informational tool for planning actions to monitor emerging antimicrobial resistance. Antimicrobial resistance surveillance (ARS) programs may have many different designs and can be grouped in 2 major categories based on their main objectives: (1) public health ARS programs and (2) industry-sponsored/product-oriented ARS programs. In general, public health ARS programs predominantly focus on health care and infection control, whereas industry ARS programs focus on an investigational or recently approved molecule(s). We reviewed the main characteristics of industry ARS programs and how these programs contribute to new drug development. Industry ARS programs are generally performed to comply with requirements from regulatory agencies responsible for commercial approval of antimicrobial agents, such as the US Food and Drug Administration, European Medicines Agency, and others. In contrast to public health ARS programs, which typically collect health care and diverse clinical data, industry ARS programs frequently collect the pathogens and perform the testing in a central laboratory setting. Global ARS programs with centralized testing play an important role in new antibacterial and antifungal drug development by providing information on the emergence and dissemination of resistant organisms, clones, and resistance determinants. Organisms collected by large ARS programs are extremely valuable to evaluate the potential of new agents and to calibrate susceptibility tests once a drug is approved for clinical use. These programs also can provide early evaluations of spectrum of activity and postmarketing trends required by regulatory agencies, and the programs may help drug companies to select appropriate dosing regimens and the appropriate geographic regions in which to perform clinical trials. Furthermore, these surveillance programs provide useful information on the potency and spectrum of new antimicrobial agents against indications and organisms in which clinicians have little or no experience. In summary, large ARS programs, such as the SENTRY Antimicrobial Surveillance Program, contribute key data for new drug development. Oxford University Press 2019-03-15 /pmc/articles/PMC6419994/ /pubmed/30895210 http://dx.doi.org/10.1093/ofid/ofy345 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Supplement Article Sader, Helio S Rhomberg, Paul R Fuhrmeister, Andrew S Mendes, Rodrigo E Flamm, Robert K Jones, Ronald N Antimicrobial Resistance Surveillance and New Drug Development |
title | Antimicrobial Resistance Surveillance and New Drug Development |
title_full | Antimicrobial Resistance Surveillance and New Drug Development |
title_fullStr | Antimicrobial Resistance Surveillance and New Drug Development |
title_full_unstemmed | Antimicrobial Resistance Surveillance and New Drug Development |
title_short | Antimicrobial Resistance Surveillance and New Drug Development |
title_sort | antimicrobial resistance surveillance and new drug development |
topic | Supplement Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419994/ https://www.ncbi.nlm.nih.gov/pubmed/30895210 http://dx.doi.org/10.1093/ofid/ofy345 |
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