New antibiotics and antimicrobial combination therapy for the treatment of gram-negative bacterial infections

被引:66
作者
Bassetti, Matteo [1 ]
Righi, Elda [1 ]
机构
[1] Santa Maria della Misericordia Univ Hosp, Div Infect Dis, Udine, Italy
关键词
combination regimens; gram-negative pathogens; multidrug resistance; new antibiotics; RESISTANT ACINETOBACTER-BAUMANNII; BLOOD-STREAM INFECTIONS; CRITICALLY-ILL PATIENTS; VIVO ANTIBACTERIAL ACTIVITIES; IN-VITRO ACTIVITY; CARBAPENEMASE-PRODUCING ENTEROBACTERIACEAE; VENTILATOR-ASSOCIATED PNEUMONIA; URINARY-TRACT-INFECTIONS; BETA-LACTAMASE INHIBITOR; KLEBSIELLA-PNEUMONIAE;
D O I
10.1097/MCC.0000000000000235
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Purpose of review Increasing rates of life-threatening infections due to multidrug-resistant (MDR) gram-negative bacteria, such as carbapenemase-producer strains, as well as pathogens that are resistant to all current therapeutic options, have been reported. The number of compounds that are currently being developed is still insufficient to control this global threat. We have reviewed the current available options for the treatment of MDR gram-negative infections, including combination regimens employing older antimicrobials and new compounds. Recent findings A limited number of large trials have assessed the treatment options for commonly encountered resistant pathogens (e.g., Klebsiella pneumoniae, Acinetobacter baumanii, Pseudomonas aeruginosa). Antimicrobials that were used in the past, such as colistin and fosfomycin, have been recently resumed and used in association with carbapenems, tigecycline, or aminoglycosides, showing a positive impact on clinical outcomes. New compounds belonging to various antimicrobial classes (e.g. beta-lactamase inhibitors, cephalosporins, glycyclines, aminoglycosides) have been investigated. Summary Only few new molecules have an adequate activity against MDR gram-negative pathogens, especially carbapenemase-producer strains. Among these, ceftozolane/tazobactam has been recently approved for clinical use. Other compounds, such as avibactam combinations, plazomicin, and eravacycline, have shown promising activity in phase 2 and 3 clinical trials.
引用
收藏
页码:402 / 411
页数:10
相关论文
共 92 条
[1]   Interventional strategies and current clinical experience with carbapenemase-producing Gram-negative bacteria [J].
Akova, M. ;
Daikos, G. L. ;
Tzouvelekis, L. ;
Carmeli, Y. .
CLINICAL MICROBIOLOGY AND INFECTION, 2012, 18 (05) :439-448
[2]   In vitro and bactericidal activities of ABT-492, a novel fluoroquinolone, against gram-positive and gram-negative organisms [J].
Almer, LS ;
Hoffrage, JB ;
Keller, EL ;
Flamm, RK ;
Shortridge, VD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (07) :2771-2777
[3]   Comparison of colistin-carbapenem, colistin-sulbactam, and colistin plus other antibacterial agents for the treatment of extremely drug-resistant Acinetobacter baumannii bloodstream infections [J].
Batirel, A. ;
Balkan, I. I. ;
Karabay, O. ;
Agalar, C. ;
Akalin, S. ;
Alici, O. ;
Alp, E. ;
Altay, F. A. ;
Altin, N. ;
Arslan, F. ;
Aslan, T. ;
Bekiroglu, N. ;
Cesur, S. ;
Celik, A. D. ;
Dogan, M. ;
Durdu, B. ;
Duygu, F. ;
Engin, A. ;
Engin, D. O. ;
Gonen, I. ;
Guclu, E. ;
Guven, T. ;
Hatipoglu, C. A. ;
Hosoglu, S. ;
Karahocagil, M. K. ;
Kilic, A. U. ;
Ormen, B. ;
Ozdemir, D. ;
Ozer, S. ;
Oztoprak, N. ;
Sezak, N. ;
Turhan, V. ;
Turker, N. ;
Yilmaz, H. .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2014, 33 (08) :1311-1322
[4]   Ceftaroline fosamil: a novel broad-spectrum cephalosporin with expanded anti-Gram-positive activity [J].
Biek, Donald ;
Critchley, Ian A. ;
Riccobene, Todd A. ;
Thye, Dirk A. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2010, 65 :iv9-iv16
[5]   Bad Bugs, No Drugs: No ESKAPE! An Update from the Infectious Diseases Society of America [J].
Boucher, Helen W. ;
Talbot, George H. ;
Bradley, John S. ;
Edwards, John E., Jr. ;
Gilbert, David ;
Rice, Louis B. ;
Scheld, Michael ;
Spellberg, Brad ;
Bartlett, John .
CLINICAL INFECTIOUS DISEASES, 2009, 48 (01) :1-12
[6]   Carbapenems [J].
Breilh, Dominique ;
Texier-Maugein, Jeannette ;
Allaouchiche, Bernard ;
Saux, Marie-Claude ;
Boselli, Emmanuel .
JOURNAL OF CHEMOTHERAPY, 2013, 25 (01) :1-17
[7]   Double-Carbapenem Therapy for Carbapenemase-Producing Klebsiella pneumoniae [J].
Bulik, Catharine C. ;
Nicolau, David P. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (06) :3002-3004
[8]   A FUNCTIONAL CLASSIFICATION SCHEME FOR BETA-LACTAMASES AND ITS CORRELATION WITH MOLECULAR-STRUCTURE [J].
BUSH, K ;
JACOBY, GA ;
MEDEIROS, AA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (06) :1211-1233
[9]   High rate of colistin resistance among patients with carbapenem-resistant Klebsiella pneumoniae infection accounts for an excess of mortality [J].
Capone, A. ;
Giannella, M. ;
Fortini, D. ;
Giordano, A. ;
Meledandri, M. ;
Ballardini, M. ;
Venditti, M. ;
Bordi, E. ;
Capozzi, D. ;
Balice, M. P. ;
Tarasi, A. ;
Parisi, G. ;
Lappa, A. ;
Carattoli, A. ;
Petrosillo, N. .
CLINICAL MICROBIOLOGY AND INFECTION, 2013, 19 (01) :E23-E30
[10]   Pharmacokinetics and Safety of Single and Multiple Doses of ACHN-490 Injection Administered Intravenously in Healthy Subjects [J].
Cass, Robert T. ;
Brooks, Carter D. ;
Havrilla, Nancy A. ;
Tack, Kenneth J. ;
Borin, Marie T. ;
Young, Don ;
Bruss, Jon B. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (12) :5874-5880