Infectious disease: how to manage Gram-positive and Gram-negative pathogen conundrums with dual beta-lactam therapy

被引:2
作者
FakhriRavari, Alireza [1 ]
Simiyu, Brenda [2 ]
Morrisette, Taylor [3 ,4 ]
Dayo, Yewande [5 ]
Abdul-Mutakabbir, Jacinda C. [1 ,6 ]
机构
[1] Loma Linda Univ, Sch Pharm, Dept Pharm Practice, Loma Linda, CA USA
[2] West Jefferson Med Ctr, Dept Pharm Serv, Marrero, LA USA
[3] Med Univ South Carolina, Coll Pharm, Dept Clin Pharm & Outcomes Sci, Charleston, SC USA
[4] Med Univ South Carolina, Shawn Jenkins Childrens Hosp, Dept Pharm Serv, Charleston, SC USA
[5] Ochsner Hlth, Dept Syst Pharm Serv, New Orleans, LA USA
[6] Loma Linda Univ, Sch Med, Dept Basic Sci, Loma Linda, CA USA
关键词
antimicrobial resistance; beta-lactam; combination therapy; double carbapenem therapy; dual therapy; Gram-; negative; Gram-positive; DOUBLE-CARBAPENEM REGIMEN; IN-VITRO ACTIVITY; PENICILLIN-BINDING PROTEINS; AMPICILLIN PLUS CEFTRIAXONE; BLOOD-STREAM INFECTIONS; STAPHYLOCOCCUS-AUREUS; ACINETOBACTER-BAUMANNII; PSEUDOMONAS-AERUGINOSA; ENTEROCOCCUS-FAECALIS; ANTIBIOTIC-RESISTANCE;
D O I
10.7573/dic.2021-8-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Antimicrobial resistance is a global public health threat due to its associated increase in mortality, and the most appropriate treatment algorithms for resistant and persistent Gram-positive and Gram-negative infections have yet to be elucidated. Whilst combination therapy has been touted as a viable method to overcome prominent resistant mechanisms represented amongst these microbes, the optimal agents to utilize remains controversial. Beta-lactams have a safe profile and are bactericidal against most Gram-positive and Gram-negative microorganisms. Thus, the use of dual betalactam therapy to overcome multidrug-resistant pathogens is of supreme interest. This article reviews the mechanisms of beta-lactam resistance in Gram-positive and Gram-negative bacteria, discusses the rationale for dual beta-lactam use against multidrug-resistant infections (and other scenarios in which this strategy may be most utilized in clinical practice), explores the available in vitro, in vivo and clinical data, and provides considerations for the use of dual beta-lactam therapy against Enterococcus faecalis, Listeria monocytogenes, Staphylococcus aureus, Enterobacterales, Pseudomonas aeruginosa and Acinetobacter baumannii pathogens.
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页数:18
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共 130 条
[81]  
Montero M, 2018, ANTIMICROB AGENTS CH, V62, DOI [10.1128/AAC.00026-18, 10.1128/aac.00026-18]
[82]  
Moody R, 2021, J Med Res Innov, V5, DOI [10.32892/jmri.243, DOI 10.32892/JMRI.243]
[83]   Clinical Presentation, Etiology, and Outcome of Infective Endocarditis in the 21st Century [J].
Murdoch, David R. ;
Corey, G. Ralph ;
Hoen, Bruno ;
Miro, Jose M. ;
Fowler, Vance G., Jr. ;
Bayer, Arnold S. ;
Karchmer, Adolf W. ;
Olaison, Lars ;
Pappas, Paul A. ;
Moreillon, Philippe ;
Chambers, Stephen T. ;
Chu, Vivian H. ;
Falco, Vicenc ;
Holland, David J. ;
Jones, Philip ;
Klein, John L. ;
Raymond, Nigel J. ;
Read, Kerry M. ;
Tripodi, Marie Francoise ;
Utili, Riccardo ;
Wang, Andrew ;
Woods, Christopher W. ;
Cabell, Christopher H. .
ARCHIVES OF INTERNAL MEDICINE, 2009, 169 (05) :463-473
[84]  
Nath S K, 1995, Can J Infect Dis, V6, P21
[85]   What's New in the Treatment of Enterococcal Endocarditis? [J].
Nigo, Masayuki ;
Munita, Jose M. ;
Arias, Cesar A. ;
Murray, Barbara E. .
CURRENT INFECTIOUS DISEASE REPORTS, 2014, 16 (10)
[86]  
O'Neill J., 2016, Review on antimicrobial resistance: tackling drug-resistant infections globally: final report and recommendations
[87]   Enterococcal endocarditis in Sweden, 1995-1999: Can shorter therapy with aminoglycosides be used? [J].
Olaison, L ;
Schadewitz, K .
CLINICAL INFECTIOUS DISEASES, 2002, 34 (02) :159-166
[88]   In Vitro Responses of Acinetobacter baumannii to Two- and Three-Drug Combinations following Exposure to Colistin and Doripenem [J].
Oleksiuk, Louise M. ;
Hong Nguyen, M. ;
Press, Ellen G. ;
Updike, Cassaundra L. ;
O'Hara, Jessica A. ;
Doi, Yohei ;
Clancy, Cornelius J. ;
Shields, Ryan K. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2014, 58 (02) :1195-1199
[89]   Bactericidal and synergistic activity of double-carbapenem regimen for infections caused by carbapenemase-producing Klebsiella pneumoniae [J].
Oliva, A. ;
Gizzi, F. ;
Mascellino, M. T. ;
Cipolla, A. ;
D'Abramo, A. ;
D'Agostino, C. ;
Trinchieri, V. ;
Russo, G. ;
Tierno, F. ;
Iannetta, M. ;
Mastroianni, C. M. ;
Vullo, V. .
CLINICAL MICROBIOLOGY AND INFECTION, 2016, 22 (02) :147-153
[90]   Therapeutic strategy for pandrug-resistant Klebsiella pneumoniae severe infections: short-course treatment with colistin increases the in vivo and in vitro activity of double carbapenem regimen [J].
Oliva, Alessandra ;
Mascellino, Maria T. ;
Cipolla, Alessia ;
D'Abramo, Alessandra ;
De Rosa, Annalisa ;
Savinelli, Stefano ;
Ciardi, Maria Rosa ;
Mastroianni, Claudio M. ;
Vullo, Vincenzo .
INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2015, 33 :132-134