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Recommendation of Antimicrobial Dosing Optimization During Continuous Renal Replacement Therapy
Continuous Renal Replacement Therapy (CRRT) is more and more widely used in patients for various indications recent years. It is still intricate for clinicians to decide a suitable empiric antimicrobial dosing for patients receiving CRRT. Inappropriate doses of antimicrobial agents may lead to treat...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7273837/ https://www.ncbi.nlm.nih.gov/pubmed/32547394 http://dx.doi.org/10.3389/fphar.2020.00786 |
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author | Li, Lu Li, Xin Xia, Yanzhe Chu, Yanqi Zhong, Haili Li, Jia Liang, Pei Bu, Yishan Zhao, Rui Liao, Yun Yang, Ping Lu, Xiaoyang Jiang, Saiping |
author_facet | Li, Lu Li, Xin Xia, Yanzhe Chu, Yanqi Zhong, Haili Li, Jia Liang, Pei Bu, Yishan Zhao, Rui Liao, Yun Yang, Ping Lu, Xiaoyang Jiang, Saiping |
author_sort | Li, Lu |
collection | PubMed |
description | Continuous Renal Replacement Therapy (CRRT) is more and more widely used in patients for various indications recent years. It is still intricate for clinicians to decide a suitable empiric antimicrobial dosing for patients receiving CRRT. Inappropriate doses of antimicrobial agents may lead to treatment failure or drug resistance of pathogens. CRRT factors, patient individual conditions and drug pharmacokinetics/pharmacodynamics are the main elements effecting the antimicrobial dosing adjustment. With the development of CRRT techniques, some antimicrobial dosing recommendations in earlier studies were no longer appropriate for clinical use now. Here, we reviewed the literatures involving in new progresses of antimicrobial dosages, and complied the updated empirical dosing strategies based on CRRT modalities and effluent flow rates. The following antimicrobial agents were included for review: flucloxacillin, piperacillin/tazobactam, ceftriaxone, ceftazidime/avibactam, cefepime, ceftolozane/tazobactam, sulbactam, meropenem, imipenem, panipenem, biapenem, ertapenem, doripenem, amikacin, ciprofloxacin, levofloxacin, moxifloxacin, clindamycin, azithromycin, tigecycline, polymyxin B, colistin, vancomycin, teicoplanin, linezolid, daptomycin, sulfamethoxazole/trimethoprim, fluconazole, voriconazole, posaconzole, caspofungin, micafungin, amphotericin B, acyclovir, ganciclovir, oseltamivir, and peramivir. |
format | Online Article Text |
id | pubmed-7273837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72738372020-06-15 Recommendation of Antimicrobial Dosing Optimization During Continuous Renal Replacement Therapy Li, Lu Li, Xin Xia, Yanzhe Chu, Yanqi Zhong, Haili Li, Jia Liang, Pei Bu, Yishan Zhao, Rui Liao, Yun Yang, Ping Lu, Xiaoyang Jiang, Saiping Front Pharmacol Pharmacology Continuous Renal Replacement Therapy (CRRT) is more and more widely used in patients for various indications recent years. It is still intricate for clinicians to decide a suitable empiric antimicrobial dosing for patients receiving CRRT. Inappropriate doses of antimicrobial agents may lead to treatment failure or drug resistance of pathogens. CRRT factors, patient individual conditions and drug pharmacokinetics/pharmacodynamics are the main elements effecting the antimicrobial dosing adjustment. With the development of CRRT techniques, some antimicrobial dosing recommendations in earlier studies were no longer appropriate for clinical use now. Here, we reviewed the literatures involving in new progresses of antimicrobial dosages, and complied the updated empirical dosing strategies based on CRRT modalities and effluent flow rates. The following antimicrobial agents were included for review: flucloxacillin, piperacillin/tazobactam, ceftriaxone, ceftazidime/avibactam, cefepime, ceftolozane/tazobactam, sulbactam, meropenem, imipenem, panipenem, biapenem, ertapenem, doripenem, amikacin, ciprofloxacin, levofloxacin, moxifloxacin, clindamycin, azithromycin, tigecycline, polymyxin B, colistin, vancomycin, teicoplanin, linezolid, daptomycin, sulfamethoxazole/trimethoprim, fluconazole, voriconazole, posaconzole, caspofungin, micafungin, amphotericin B, acyclovir, ganciclovir, oseltamivir, and peramivir. Frontiers Media S.A. 2020-05-29 /pmc/articles/PMC7273837/ /pubmed/32547394 http://dx.doi.org/10.3389/fphar.2020.00786 Text en Copyright © 2020 Li, Li, Xia, Chu, Zhong, Li, Liang, Bu, Zhao, Liao, Yang, Lu and Jiang http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Li, Lu Li, Xin Xia, Yanzhe Chu, Yanqi Zhong, Haili Li, Jia Liang, Pei Bu, Yishan Zhao, Rui Liao, Yun Yang, Ping Lu, Xiaoyang Jiang, Saiping Recommendation of Antimicrobial Dosing Optimization During Continuous Renal Replacement Therapy |
title | Recommendation of Antimicrobial Dosing Optimization During Continuous Renal Replacement Therapy |
title_full | Recommendation of Antimicrobial Dosing Optimization During Continuous Renal Replacement Therapy |
title_fullStr | Recommendation of Antimicrobial Dosing Optimization During Continuous Renal Replacement Therapy |
title_full_unstemmed | Recommendation of Antimicrobial Dosing Optimization During Continuous Renal Replacement Therapy |
title_short | Recommendation of Antimicrobial Dosing Optimization During Continuous Renal Replacement Therapy |
title_sort | recommendation of antimicrobial dosing optimization during continuous renal replacement therapy |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7273837/ https://www.ncbi.nlm.nih.gov/pubmed/32547394 http://dx.doi.org/10.3389/fphar.2020.00786 |
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