New antimicrobial options for the management of complicated intra-abdominal infections

被引:36
作者
Leone, Sebastiano [1 ]
Damiani, Giovanni [2 ]
Pezone, Ilaria [3 ]
Kelly, Molly E. [4 ]
Cascella, Marco [5 ]
Alfieri, Aniello [6 ]
Pace, Maria C. [6 ]
Fiore, Marco [6 ]
机构
[1] San Giuseppe Moscati Hosp, Div Infect Dis, I-83100 Avellino, Italy
[2] Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Dept Pathophysiol & Transplantat, I-20122 Milan, Italy
[3] San Giuseppe Moscati Hosp, Dept Pediat, I-81031 Aversa Ce, Italy
[4] Case Western Reserve Univ, Sch Med, Cleveland, OH 44106 USA
[5] Ist Nazl Tumori IRCCS Fdn G Pascale, Div Anesthesia & Pain Med, Dept Support Clin Act & Crit Area, I-80131 Naples, Italy
[6] Univ Campania Luigi Vanvitelli, Dept Anaesthesiol Surg & Emergency Sci, I-80138 Naples, Italy
关键词
Intra-abdominal infections; Antimicrobial resistance; Antimicrobial therapy; New antimicrobial agents; CEFTAZIDIME/AVIBACTAM PLUS METRONIDAZOLE; IN-VITRO ACTIVITY; DOUBLE-BLIND; HOSPITALIZED ADULTS; ESCHERICHIA-COLI; URINARY-TRACT; EFFICACY; SAFETY; MEROPENEM; CEFTOLOZANE/TAZOBACTAM;
D O I
10.1007/s10096-019-03533-y
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Complicated intra-abdominal infections (cIAIs) are a common cause of morbidity and mortality in surgical patients. Optimal management of cIAI requires early source control in combination with adequate antimicrobial treatment and aggressive fluid resuscitation. cIAIs are mainly caused by Gram-negative bacilli and anaerobes. Broad-spectrum single-agent or combination drug regimens against these microorganisms are the mainstay of therapy. However, development of antimicrobial resistance has become an increasingly large concern: multidrug-resistant organisms are associated with a higher rate of inadequate antimicrobial therapy, which in turn is associated with higher mortality rate, longer hospital stay, and increased cost compared to adequate antimicrobial therapy. In this mini-review, we discuss the effectiveness of several new antimicrobial agents, recently approved or in advanced phases of clinical development, for the treatment of cIAIs, including the new beta-lactam and beta-lactamase inhibitor combinations (ceftolozane/tazobactam, ceftazidime/avibactam, meropenem/vaborbactam, imipenem/cilastatin/relebactam, aztreonam/avibactam), siderophore cephalosporins (cefiderocol), aminoglycosides (plazomicin), and tetracyclines (eravacycline).
引用
收藏
页码:819 / 827
页数:9
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