Polymyxins (colistin and polymyxin B) exert their bactericidal activity through interactions with lipid A on the outer membrane and are active against most gram-negative species with a few exceptions (e.g. Serratia marcescens, Proteus spp., Providencia spp.) Between colistin and polymyxin B, colistin is used more extensively worldwide due to its better availability. Among Acinetobacter clinical isolates collected from hospitals in the United States in 2010, 94.7% were susceptible to colistin [8]. Clinical data on the efficacy of colistin in the treatment of carbapenem-resistant A. baumannii infections are mostly observational, but data from several prospective, randomized studies addressing the efficacy of colistin-based combination therapy are also emerging.

Colistin maintains excellent activity against A. baumannii, but whether treatment of invasive infection due to A. baumannii with this agent alone is adequate has not been definitively established. In a retrospective study of patients with ventilator-associated pneumonia caused by A. baumannii who were treated according to susceptibility of the organism with colistin or imipenem, clinical cure and in-hospital mortality rates were comparable at 57% each and 61.9% and 64.2%, respectively, suggesting that colistin might be a reasonable alternative for imipenem [9]. On the other hand, in another study of invasive infections caused by carbapenem-resistant A. baumannii and treated with a polymyxin or ampicillin-sulbactam, therapy with a polymyxin was an independent risk factor for in-hospital mortality (odds ratio [OR]: 2.07, P = 0.041), but the medial daily dose of colistin was quite low compared with today's standards [10]. Overall, the limited data suggest that colistin likely has clinical efficacy comparable with carbapenem for invasive A. baumannii infection when an adequate dose is used [11].

Nebulized colistin is increasingly utilized in the management of acute A. baumannii infection, with or without intravenous colistin. In a case-control study conducted in Taiwan, patients with respiratory secretions growing MDR A. baumannii eradicated the organism sooner when they were given nebulized colistin, with or without intravenous colistin, compared with when no nebulized colistin therapy was given (8.2 days and 21.5 days; P < 0.001) [12]. However, there were no differences in the in-hospital mortality. In a randomized, open-label trial of 100 patients with MDR gram-negative pathogens including A. baumannii conducted in Thailand, favorable microbiological outcome was achieved significantly more frequently among those receiving both nebulized and intravenous colistin (60.9%) than among those receiving intravenous colistin only (38.2%; P = 0.03), but there was no difference in the rates of favorable clinical outcome in this study, either [13]. Nebulized colistin may therefore expedite microbiological eradication in the airways but has not been associated with clinical benefit.

Sulbactam is a β-lactamase inhibitor which also has intrinsic activity against Acinetobacter spp. including A. baumannii. Ampicillin-sulbactam susceptibility of 63.6% has been reported for Acinetobacter spp. isolates collected from U.S. hospitals in the early 2000s [14]. However, the susceptibility rate declined from 89% in 2003 to 40% in 2008 in one hospital system in the U.S. along with increased use of this agent [15]. Carbapenemases produced by A. baumannii, such as OXA-23, do not affect sulbactam. Therefore, some carbapenem-resistant strains remain susceptible to sulbactam, making it a potentially useful alternative.

A head-to-head comparison of ampicillin-sulbactam and colistin was made in a small randomized study, where 28 patients with ventilator-associated pneumonia due to XDR A. baumannii received either ampicillin-sulbactam (9 g of sulbactam/day) or colistin (270 mg colistin base activity [CBA]/day) [16]. The clinical response rates, bacteriological success rates, 14- and 28-day mortality rates and the rates of adverse events were all comparable between the two groups. These limited data suggest that sulbactam-containing regimens may have a role in the treatment of infections caused by carbapenem-resistant A. baumannii that remain susceptible to sulbactam.

Tigecycline is a glycylcycline derivative of minocycline which was designed to circumvent common tetracycline resistance mechanisms. It has unique pharmacokinetics with a large volume of distribution resulting in low serum peak concentration of 0.7 to 0.8 µg/mL after the standard loading dose of 100 mg [17]. The use of tigecycline for bacteremia is controversial for this reason. An infection-related mortality of 56% has been reported for patients with carbapenem-resistant A. baumannii bloodstream infection who were treated with tigecycline despite in vitro susceptibility in a small series [18]. In a larger case series on the use of tigecycline for XDR A. baumannii infections, 266 patients were treated with tigecycline alone or in combination with another agent (a carbapenem, expanded-spectrum cephalosporin or piperacillin-tazobactam), and 120 were treated with imipenem and sulbactam [19]. The patients who received tigecycline were less ill, evidenced by significantly lower rates of intensive care unit stay, febrile illness, abnormal serum creatinine and sepsis. There was no difference in 30-day mortality between the two groups, and a lower percentage of patients experienced unfavorable clinical outcome in the tigecycline group (30.8% and 50.0%; P < 0.001). On the other hand, in a series of 9 patients who received tigecycline for bacteremia due to tigecycline-susceptible, carbapenem-resistant A. baumannii, 5 (56%) deaths were related to bacteremia and 1 breakthrough carbapenem-resistant Acinetobacter baumannii bacteremia case was observed during therapy with tigecycline [18]. It has been suggested in a randomized study of hospital-acquired pneumonia that a higher dose of tigecycline (a loading dose of 200 mg followed by 100 mg instead of the approved 50 mg twice a day) may improve the clinical response rate without increasing adverse events, but there were too few patients with A. baumannii pneumonia in this study to draw definitive conclusions [20]. Overall, tigecycline may have a role in the definitive therapy of carbapenem-resistant A. baumannii infections when the patients are not severely ill, but it should probably be avoided for critically ill patients, at least as monotherapy.

Minocycline, like tigecycline, inhibits the 30S ribosomal subunits. It is more active against A. baumannii than doxycycline which is prone to efflux-mediated resistance. In a surveillance study of MDR A. baumannii isolates collected in the U.S., 72.1% were susceptible to minocycline despite a very low susceptibility rate to carbapenems (8.7%) [21]. Clinical data on the use of this agent are scarce. In a series of 8 military patients treated with oral minocycline for traumatic wound infections due to MDR A. baumannii, minocycline therapy resulted in clinical cure in 7 of the patients [22]. In another small series, 4 patients with ventilator-associated pneumonia due to XDR A. baumannii were treated with intravenous minocycline [23]. All 4 patients had clinical improvement, and 3 of them had microbiologic clearance as well. While clinical data are lacking, the compelling in vitro activity suggests that minocycline should be studied further in the context of de-escalation therapy given the availability of oral formulations.

Rifampin by itself is not considered for treatment of A. baumannii infection due to rapid emergence of resistance, but its potential role as an adjunct to other active agents has been explored. In an open-label, randomized trial comparing the efficacy of colistin and colistin plus rifampin for ventilator-associated pneumonia due to carbapenem-resistant A. baumannii, 22 patients were treated with colistin alone, and 21 patients were treated with the combination [24]. The baseline patient characteristics were largely comparable. The crude in-hospital mortality and pneumonia-related mortality were higher for the colistin group (72.7% and 63.6%) compared with the combination group (61.9% and 38.1%), though the differences did not reach statistical significance. No hepatotoxicity from rifampin was observed. Another study was conducted in Italy as a multicenter, open-label, randomized trial comparing the efficacy of colistin and colistin plus rifampin [25]. A total of 210 patients with life-threatening infection due to XDR, colistin-susceptible A. baumannii were enrolled. The baseline characteristics were again comparable between the groups. There was no mortality difference between the two groups (43.4% for the combination group, 42.9% for the colistin group), although the microbiologic eradication rate was significantly higher in the combination group (60.6% and 44.8%; P = 0.034). Hepatic dysfunction was more common in the combination group, but the difference was not statistically significant (20.8% and 11.9%; P = 0.13). These data suggest that the addition of rifampin to colistin may facilitate microbiological clearance of A. baumannii but is unlikely to convey clinical benefit in terms of improved patient survival.

Fosfomycin is not active against A. baumannii, but in vitro synergy has been reported between fosfomycin and colistin or sulbactam [26], and a pilot randomized controlled trial has been conducted comparing the efficacy of colistin and colistin plus fosfomycin for infections caused by carbapenem-resistant A. baumannii [27]. In this study of 94 patients, fosfomycin was given at 4 g every 12 hours intravenously, and therapy was given for 7 to 14 days. The two groups did not differ in favorable clinical outcomes (59.6% and 55.3%) or mortality at 28 days (46.8% and 57.4%), whereas microbiological eradication rates were significantly higher in the combination group (100% and 81.2%; P = 0.01). The small size of the study precludes definitive conclusions, and dosing of fosfomycin was relatively conservative. Nonetheless, this combination may merit further investigation given the trend for lower mortality in the combination group coupled with the favorable safety profile of fosfomycin.

In an observational study of 250 XDR A. baumannii bloodstream infections, 36 patients received colistin monotherapy and 214 patients received colistin-based combination therapy, including 102 with a carbapenem, 69 with ampicillin-sulbactam or sulbactam, and 43 with other agents [28]. The baseline characteristics were comparable among the 4 groups, and all isolates were susceptible to colistin. The in-hospital mortality rate was significantly lower in the colistin-based combination groups compared to the colistin monotherapy group (52.3 % and 72.2 %; P = 0.03), and the rate of microbiological eradication was significantly higher in the combination groups than the monotherapy group (79.9 % and 55.6 %; P = 0.001). In another observational study of 69 patients with solid organ transplantation who developed XDR A. baumannii infection, treatment with a combination of colistin and a carbapenem was an independent predictor of survival [29]. While these data are limited by the observational and retrospective nature of the studies they are derived from, they overall support the use of colistin-containing combination regimens for the treatment of invasive carbapenem-resistant and XDR A. baumannii infections.

Eravacycline is a novel fluorocycline with activity against gram-positive and gram-negative pathogens in vitro, including A. baumannii. Among 52 A. baumannii isolates displaying resistance to carbapenems, fluoroquinolones, and aminoglycosides, MIC_50/90 values of eravacycline were 0.5/2 µg/mL [30]. A phase 2, randomized, double-blind study was conducted to evaluate the efficacy and safety of eravacycline in comparison with ertapenem in patients with complicated intra-Habdominal infections [31]. The clinical success rates were 92.9% to 100% for those receiving eravacycline and 92.3% for those receiving ertapenem, respectively. The adverse event rates were 28.6% to 35.8% and 26.7%, respectively. The study however did not include infections due to A. baumannii.

Studies have shown that, despite the risk for nephrotoxicity in patients receiving colistin, colistin may be useful for salvage therapy of P. aeruginosa infection when therapeutic choices are severely limited due to resistance to commonly used agents, including carbapenems. A recent survey in the U.S. indicated 98.8% susceptibility of P. aeruginosa to this agent [32]. In a retrospective cohort study where colistin use in 23 critically ill patients with MDR P. aeruginosa infection was examined, favorable clinical response was observed in 14 patients (61%), with only 3 patients experiencing relapse of infection. Bacteremia was the only significant factor associated with treatment failure (P = 0.02) [33]. In another retrospective analysis of 258 episodes of MDR gram-negative infections, which included 68 cases caused by P. aeruginosa, higher daily doses of colistin were independently associated with better survival regardless of the pathogen [34]. Finally, in a retrospective cohort study of 95 cancer patients with MDR P. aeruginosa infections who were treated with either colistin or another anti-pseudomonal agent, a significantly higher clinical response rate was observed among patients who received colistin (P = 0.026) [35]. Although randomized studies are lacking, these data suggest that colistin is likely a viable alternative for the therapy of P. aeruginosa infections when other anti-pseudomonal agents are inactive or treatment with them has failed.

Nebulized colistin has been used in patients with P. aeruginosa respiratory tract infection, particularly in the setting of cystic fibrosis. This mode of delivery is used to achieve high drug levels in the respiratory tract while minimizing systemic adverse effects. In one retrospective cohort study, nebulized colistin was used alone in the treatment of 21 patients with pneumonia due to MDR A. baumannii or P. aeruginosa [36]. The overall clinical and microbiological response rates were 57% and 86%, respectively, and nephrotoxicity was not observed. Another prospective observational study compared the efficacy of nebulized colistin for 14 days plus 3 days of intravenous aminoglycoside for ventilator-associated pneumonia due to MDR P. aeruginosa or A. baumannii and 14 days of intravenous β-lactam therapy plus 3 days of intravenous aminoglycoside or fluoroquinolone for the same condition due to susceptible P. aeruginosa or A. baumannii [37]. In this study, 67% of those treated with nebulized colistin were clinically cured at the end of treatment compared with 66% treated with intravenous β-lactams, suggesting that nebulized colistin with a short course of intravenous aminoglycoside may be as efficacious as β-lactam-based intravenous therapy. These data suggest that nebulized colistin may be a useful adjunct to intravenous therapy in the treatment of P. aeruginosa, but whether it can be used alone in the management of pneumonia remains to be seen.

MICs of fosfomycin for P. aeruginosa cluster around 64 µg/mL, and its role in the management of carbapenem-resistant P. aeruginosa infections has been explored. In a series of 8 hospitalized patients with a urine culture growing carbapenem-resistant P. aeruginosa who were treated with fosfomycin, the microbiological cure rate was 38% after receiving an average of 2.9 fosfomycin doses per treatment course [38]. In a cohort study examining the outcome of 30 patients with P. aeruginosa infection treated with fosfomycin, 86.7% had favorable clinical outcomes [39]. In another observational case series, the outcomes of critically ill patients treated with fosfomycin for infections due to XDR, carbapenemase-producing gram-negative bacteria were examined [40]. Among the 17 patients with P. aeruginosa infection, the clinical success rate was 83.3% and the microbiological success rate was 66.7% at day 14. Finally, a recent retrospective study compared the outcomes of patients with hospital-acquired and ventilator-associated bacterial pneumonia due to P. aeruginosa with intermediate resistance to carbapenems who were treated with doripenem and fosfomycin or colistin and fosfomycin [41]. No differences were detected between the groups regarding clinical cure rates (60% and 58%), microbiological eradication rates (72% and 63%) and all-cause mortality (40% and 42%). These studies, while informative, did not address the specific clinical efficacy of fosfomycin in P. aeruginosa infections since an overwhelming majority received additional agents. A prospective study where patients would receive standard therapy with or without fosfomycin would be required to answer this question.

Among the agents in late-stage clinical development, ceftolozane-tazobactam (formerly CXA-201) is undergoing phase 3 studies for complicated urinary tract infection and complicated intra-abdominal infection. Ceftolozane is a novel anti-pseudomonal cephalosporin. This combination is active against P. aeruginosa, including many isolates that are resistant to carbapenems [42]. Ceftazidime-avibactam is also in phase 3 studies for the same indications. Avibactam (formerly NXL104) is a β-lactamase inhibitor which restores the activity of ceftazidime against class A, C, and some class D β-lactamase-producing gram-negative bacteria [43]. Ceftazidime-avibactam is active against some P. aeruginosa isolates that are resistant to carbapenems. However, it is not active against isolates producing MBL.

Tigecycline has been used either alone or in combination with another agent in a number of patients. In a series of 12 patients infected with MBL-producing K. pneumoniae and treated with tigecycline alone at the standard dose, the overall clinical response rate was 75% [49]. In a review of 10 clinical studies investigating the outcomes of infections due to carbapenem-resistant, ESBL-producing or MDR Enterobacteriaceae, 69.3% of the 33 reported patients treated with tigecycline achieved resolution of infection [50]. Uniquely low serum concentrations of tigecycline warrant caution when using this agent alone to treat documented or potential bacteremic infections, as discussed in 1.3. Highlighting this concern, a case with persistent breakthrough bacteremia due to a K. pneumoniae isolate producing both MBL and ESBL while on tigecycline therapy has been reported [51]. Furthermore, it is not recommended for the treatment of urinary tract infections due to its low urine concentration [52].

In vitro susceptibility of carbapenemase-producing Enterobacteriaceae isolates to colistin ranges between 80 and 100% worldwide [53]. Colistin is often the only agent against carbapenemase-producing Enterobacteriaceae that achieves adequate serum levels exceeding the MICs [54].

In a case series including 17 seriously ill patients, 12 patients were treated successfully with colistin alone or in combination with either a carbapenem or an active aminoglycoside [55]. In an outbreak of KPC-producing K. pneumoniae, infection was successfully treated in 12 patients with an antimicrobial regimen containing colistin either as the only active agent, or with an aminoglycoside, tigecycline, or carbapenem [56]. In a prospective observational study of 67 patients with bloodstream infection caused by MBL-producing K. pneumoniae, 12 received appropriate combination therapy with two active drugs (carbapenem in combination with either colistin or an active aminoglycoside), and 37 received appropriate therapy with one active drug (14 carbapenem, 15 colistin, and 8 an active aminoglycoside) [57]. Mortality rates were 8.3% for those who received combination therapy with two active drugs and 27% for those who received therapy with one active drug, suggesting these combinations, almost half of which included colistin, may be efficacious. However, the outcome was not stratified for the use of colistin.

More recently, 127 patients with infections due to carbapenem-resistant K. pneumoniae in intensive care units across Greece were studied, which primarily included central venous catheter-related bacteraemia and ventilator-associated pneumonia [58]. Resistance to colistin, tigecycline, gentamicin and amikacin was detected in 20%, 33%, 21% and 64% of the isolates, respectively. Fourteen-day mortality rates were as follows: colistin monotherapy, 23.1%; aminoglycoside monotherapy, 22.7%; tigecycline monotherapy, 31.3%; tigecycline plus aminoglycosides, 18.1%; colistin plus aminoglycosides, 11.7%; colistin plus tigecycline, 44.4%. Mortality from inappropriate therapy (i.e., no active agent) was 35.0%. As such, colistin is a key agent in the treatment of carbapenem-resistant K. pneumoniae, with available clinical data generally favoring combination therapy over monotherapy in general (see also 3.8.).

The use of aminoglycosides for KPC-producing K. pneumoniae infections was reviewed earlier by Hirsch and Tam [59]. The aminoglycosides were used, alone or in combination, in a total of 8 patients with a 75% success rate. They had pneumonia, bacteremia or urinary tract infection and were treated with gentamicin or amikacin, alone or in combination with ciprofloxacin or tetracycline. However, the small number of patients and the heterogeneity of patient conditions and regimens precluded interpretation of the outcome data.

In a study of bloodstream infections due to CRE among patients with hematologic malignancies, gram-negative antimicrobial therapy was initiated in response to fever and/or sepsis on the day of blood culture collection in nearly all patients [47]. Only 2 patients received empirical therapy with an agent to which the CRE isolate was susceptible in vitro, with both clearing bacteremia. Three patients died before susceptibility data were available and never received an active agent. Among the remaining patients, 10 patients received one active agent, of which amikacin was most common, and 5 patients received two active agents. The 7-day, 14-day and in-hospital mortality rates were 39%, 53% and 56%, respectively. All 10 deaths were CRE-related [47]. The high mortality rates are likely due to the severity of the underlying illnesses in this population, but it is also possible that effective monotherapy with amikacin also contributed to the suboptimal clinical outcome. Overall, there are not sufficient data to support the use of aminoglycosides monotherapy for the therapy of carbapenem-resistant K. pneumoniae infections.

Carbapenems are rarely used alone for treatment of carbapenem-resistant K. pneumoniae infections, but before the carbapenem breakpoints were lowered by the Clinical and Laboratory Standards Institute (CLSI) in 2010, some cases that were reported as susceptible to a carbapenem despite production of KPC were treated with carbapenem monotherapy.

The aforementioned review by Hirsch and Tam complied reports on a total of 19 patients who were treated with a carbapenem alone or in combination with another agent due to the apparent susceptible testing results for carbapenems [59]. Strikingly, only 6 of 15 patients treated with carbapenem monotherapy had clinical success. While infections from isolates with carbapenem MICs of ≤ 4 µg/mL may be treated with high-dose carbapenem alone from pharmacokinetic and pharmacodynamics standpoints [60], the proportion of isolates falling within this range is small, and there is a concern for inadequate response as changes in the porin function may further raise the carbapenem MICs [61]. Therefore, the existing data do not support the use of carbapenem alone for invasive carbapenem-resistant K. pneumoniae infections, but it is increasingly suggested that it should be part of combination regimens (also see 3.8.).

Fosfomycin is active against over 90% of KPC-producing K. pneumoniae when using the susceptibility breakpoint of 64 µg/mL [62]. In a retrospective study of 13 hospitalized patients with urine culture growing KPC-producing K. pneumoniae and treated with oral fosfomycin, patients received an average of 2.9 fosfomycin doses per treatment course, resulting in a microbiological cure rate of 46% [38]. In another study, intravenous fosfomycin in combination with colistin, gentamicin, or piperacillin-tazobactam resulted in a promising clinical success rate (100%) in the treatment of serious infections caused by carbapenem-resistant K. pneumoniae [63]. In a recent prospective case series, the outcomes of critically ill patients treated with fosfomycin for infections due to XDR, carbapenemase-producing gram-negative bacteria were examined [40]. Among 23 patients with monomicrobial K. pneumoniae infection, clinical success rate was 56.5% and microbial success rate was 65.2%, but most of them appear to have received fosfomycin in combination with another agent (colistin for the most part). These data suggest that benefit of fosfomycin in the treatment of infections caused by carbapenem-resistant K. pneumoniae may exist, but only in the context of combination therapy. It should also be kept in mind that fosfomycin resistance may emerge during therapy, even when combination therapy is used [64].

Temocillin is a 6-α-methoxy derivative of ticarcillin that is approved for clinical use in several European countries. It is relatively resistant to hydrolysis by class A β-lactamases including KPC [65]. The MICs of temocillin for KPC-producing K. pneumoniae ranged between 16 and 64 µg/mL, and production of KPC in itself does not influence the temocillin MICs [66]. The susceptibility breakpoints available from the British Society for Antimicrobial Chemotherapy (BSAC) are 32 µg/mL for urinary tract infection and 8 µg/mL for systemic infections. Therefore, while specific clinical data are lacking, it may have a role in the treatment of urinary tract infection due to CRE. Although the currently licensed dosage is 2 g intravenously twice daily, 2 g thrice daily regimen is under evaluation and may justify a higher breakpoint for systemic infections [65].

Since the clinical efficacy of β-lactam agents is pharmacokinetically predicted by time above MIC, an extended infusion or continuous infusion is a potential strategy to overcome higher carbapenem MICs in carbapenemase-producing gram-negative bacteria. The advantage of this approach has been suggested in immunocompetent and neutropenic murine thigh models [67]. A case of successful treatment of KPC-producing K. pneumoniae bacteremia with high-dose continuous infusion meropenem has been reported [68]. However, no other clinical data addressing the utility this approach specifically for the treatment of CRE infections are available at this time.

Studies addressing the clinical outcome of CRE infections have been reviewed recently by Tzouvelekis et al. [69]. Among 889 patients included in this analysis, 441 received combination therapy and 346 received monotherapy. The mortality rates were 27.4% for combination therapy and 38.7% for monotherapy (P < 0.001). The mortality rates for monotherapy were 40.1% for carbapenem, 41.1% for tigecycline and 42.8% for colistin. The mortality rates for combination therapy were 30.7% for carbapenem-sparing combinations and 18.8% for carbapenem-containing combinations, suggesting that the inclusion of a carbapenem in the combination may provide survival benefit. A large proportion of patients in this analysis were derived from four studies conducted in the U.S., Greece and Italy addressing the clinical outcome of carbapenemase-producing K. pneumoniae bacteremia, most of which were due to KPC producing isolates. In the study from the U.S., the outcomes of a total of 41 patients with bacteremia were examined [70]. The overall 28-day crude mortality rate was 39.0% in this cohort. In the multivariate analysis, definitive therapy with a combination regimen was independently associated with survival (odds ratio [OR]: 0.07, P = 0.02). The 28-day mortality was 13.3% in the combination therapy group compared with 57.8% in the monotherapy group (P = 0.01). Despite in vitro susceptibility, patients who received monotherapy with colistin, polymyxin B or tigecycline had a high mortality of 66.7%. In the first study from Greece, a total of 53 patients with bacteremia were identified and included [71]. The overall mortality was 52.8%, and the infection-related mortality was 20%. Appropriate antimicrobial therapy was administered to 35 patients. All 20 patients who received combination therapy (colistin plus tigecycline or tigecycline with gentamicin) had favorable clinical outcome. In contrast, 7 of 15 patients given appropriate monotherapy (colistin, tigecycline, gentamicin) died (P = 0.001). The study from Italy examined the clinical outcomes of 125 patients with bloodstream infections caused by KPC-producing K. pneumoniae [72]. The overall 30-day mortality rate was 41.6%. A significantly higher mortality rate was observed among patients treated with monotherapy (54.3%) compared with those who received combined therapy (34.1%; P = 0.02). Mortality rates with the most frequent combinations were 30% for colistin plus tigecycline and 50% for tigecycline plus gentamicin. Notably, definitive therapy with a triple combination of tigecycline, colistin, and meropenem was associated with increased survival (OR: 0.11, 95% CI: 0.02 to 0.69, P = 0.01). Finally, the second study from Greece examined the outcome of 205 patients with bacteremia due to carbapenemase-producing K. pneumoniae, 163 of which produced KPC [73]. The rate of resistance to colistin was high at 25.4%. Of 175 patients who received active definitive therapy, 103 received combination therapy and 72 received monotherapy. The 28-day mortality rates were 27.2% and 44.4%, respectively (P = 0.003). Additionally, a low mortality rate (19.3%) was seen among patients given carbapenem-containing combinations, and lower carbapenem MICs were associated with lower mortality, as in the study from Italy.

These data support the use of combination therapy that includes colistin and/or tigecycline along with a carbapenem in the therapy of invasive infections due to carbapenem-resistant K. pneumoniae. On the other hand, patients may fare well regardless of therapy for non-invasive infections such as uncomplicated urinary tract infection. In a retrospective study examining the clinical outcome of 21 patients with urinary tract infection due to carbapenem-resistant K. pneumoniae, 90% of them had clinical success regardless of therapy given, and the overall 30-day mortality was low at 6% [70]. Therefore, it is important to stratify cases into invasive (i.e. high mortality) and non-invasive (low mortality) infections and consider therapeutic approaches accordingly.

There are several new agents with activity against CRE in late clinical development that merit mention. Avibactam is a non-β-lactam β-lactamase inhibitor that is active against known Ambler class A and C β-lactamases with activity against some Ambler class D enzymes as well [74]. In vitro, avibactam inhibits the activity of Ambler class A (including ESBL and KPC), class C (i.e. AmpC), and some class D (including OXA-48) enzymes. It is not active against MBLs (e.g. NDM, VIM, IMP) due to the absence of the active-site serine residue in these enzymes, and it does not inhibit OXA-type carbapenemases produced by A. baumannii [75, 76]. Of note, avibactam has a potent inhibitory activity against KPC that is substantially greater than that of clavulanate and tazobactam [74, 77]. Ceftazidime-avibactam is currently in phase 3 trials for the treatment of complicated intra-abdominal infections and complicated urinary tract infections. Once approved, it is expected to play a role in the empiric monotherapy of invasive infections suspected to be caused by resistant Enterobacteriaceae pathogens, and also potentially as definitive therapy of KPC-producing Enterobacteriaceae infection.

Plazomicin is a novel aminoglycoside that is designed to resist most clinically relevant aminoglycoside modifying enzymes and holds promise for the treatment of infections caused by CRE, including KPC-producing K. pneumoniae [78]. It is currently undergoing a phase 3 superiority trial targeting CRE bacteremia and pneumonia, where plazomicin-based regimens will be compared with colistin-based regimens. It is however not active against many of the NDM-producing isolates due to the co-production of 16S ribosomal RNA methyltransferase.