Treatment for infections with carbapenem-resistant Enterobacteriaceae: what options do we still have?
© The Author(s) 2014
Published: 27 June 2014
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© The Author(s) 2014
Published: 27 June 2014
The global spread of carbapenem-resistant Enterobacteriaceae (CRE) is increasingly becoming a major challenge in clinical and public health settings. To date, the treatment for serious CRE infections remains difficult. The intelligent use of antimicrobials and effective infection control strategies is crucial to prevent further CRE spread. Early consultation with experts in the treatment of infections with multidrug-resistant organisms is valuable in patient management. This brief review will focus on the current, yet limited, treatment options for CRE infections.
Characteristics associated with carbapenemase-producing organisms commonly encountered in clinical practice
Found commonly in
Klebsiella pneumoniae, Escherichia coli
First isolated in US in 1996; now endemic in US, Colombia, Brazil, Argentina, Poland, Italy, Greece, Israel, and China 
All beta-lactams; often also fluoroquinolones and aminoglycosides 
K. pneumoniae, E. coli
First isolated in Sweden from a traveler previously hospitalized in New Delhi; large environmental reservoirs in India, Pakistan, Middle East, and the Balkans ; recent ERCP-related nosocomial outbreak associated with infected endoscopes reported in Chicago, IL 
Plasmids carry resistance genes to all beta-lactams, aminoglycosides, macrolides, rifampin, and trimethoprim- sulfamethoxazole 
First identified in Turkey in 2003; multiple nosocomial outbreaks reported since then throughout the world 
Carbapenems are no longer fully effective in the CRE epidemic. The paucity of novel antimicrobials in development escalates the antimicrobial resistance problem, severely reducing the available therapeutic choices. In this review, we will summarize the main treatment options used in clinical practice as well as the few antimicrobials currently in development. For issues related to the epidemiology, detection, and prevention of infections with CRE, the reader is referred to several excellent reviews published on this topic [6, 10].
The optimal treatment of infections with CRE is uncertain, as most data come from retrospective case series and anecdotal case reports; few prospective studies or randomized controlled trials are published on this topic. Since carbapenem-producing organisms are often resistant to other antimicrobial classes in addition to most beta-lactams, additional susceptibility testing to antimicrobials such as colistin, fosfomycin, tigecycline, aztreonam, and rifampin is needed [11, 12]. Consultations from experts in the treatment of infections with multidrug-resistant organisms may also prove valuable in patient management. The following antimicrobial therapies have been used with various levels of success in the treatment of CRE infections.
Colistin (polymyxin E) is an old bactericidal antibiotic with cationic detergent properties. It disrupts the outer cell membrane of the Gram-negative bacilli by binding to the lipid A component of the lipopolysaccharide, causing leakage of cytoplasmic contents and bacterial cell death . The antibacterial spectrum includes most of the Enterobacteriaceae (Escherichia coli, Klebsiella, Salmonella, Shigella, and Enterobacter), Pseudomonas, Acinetobacter, and Stenotrophomonas species. However, colistin is not active against Burkholderia cepacia, Serratia marcescens, Moraxella catarrhalis, pathogenic Neisseria spp, Proteus spp, Providencia spp, or Morganella morganii . Colistin is also not active in vitro against anaerobes and aerobic Gram-positive cocci.
Dosing recommendations for colistin-based products available for parenteral use in critically ill patients
Product type a
Colistin base activity
Loading dose: 270 mg colistin base
(150 mg vials)
Maintenance dose: 135 mg colistin base every 12 hours
Loading dose: 9 million IU
(1 and 2 million IU vials)
Maintenance dose: 4.5 million IU every 12 hours
The importance of combination therapy is also suggested by several other retrospective studies. In a cohort of patients with bloodstream infections caused by K. pneumoniae carbapenemase (KPC)-producing organisms, none of the 14 patients treated with colistin in combination with one or more antimicrobials (tigecycline ± carbapenem ± gentamicin) died, whereas four of the seven patients treated with colistin alone died from their infection . Similarly, colistin-polymyxin B combined with carbapenem had a mortality of 12.5% (1 out of 6) versus 66.7% (8 out of 12) in a study of patients with bacteremia caused by KPC-producing K. pneumoniae bacteremia . Finally, in a large retrospective study of 125 patients with KPC-producing K. pneumoniae sepsis from three hospitals in Italy, the combination of colistin with tigecycline and extended-infusion meropenem (2 g IV infused over 3 hours every 8 hours) had the lowest mortality (13%) versus 50% mortality for those patients receiving colistin monotherapy .
The most common adverse event with colistin is nephrotoxicity, which can develop in up to half of the patients treated with high parenteral doses but which seems to be reversible in most cases [20, 24]. Reports of resistance to colistin among KPC-producing K. pneumoniae strains [25, 26], though rare, are concerning, especially for combination treatment regimens where colistin is intended as the major active component.
Polymyxin B differs from colistin by one amino acid . In contrast to colistin, however, it is administered as its active form and thus achieves higher plasma concentrations faster, making the need for a loading dose less stringent . Polymyxin B is not cleared by the kidney and therefore does not require renal dose adjustment . The clinical experience with polymyxin B in treatment of CRE infections is limited to small case series. Bergamasco and colleagues , in their description of a KPC-producing K. pneumoniae nosocomial outbreak among solid organ transplant patients, reported a survival rate of 67% (6 out of 9) for the patients treated with polymyxin B alone or in combination with tigecycline or carbapenem. These patients with pneumonia, bloodstream, urinary tract, or skin and soft tissue infections were given a polymyxin B dose of 25,000 or 15,000 IU/kg for a creatinine clearance of at least 50 mL/minute or less than 50 mL/minute, respectively. As is true for colistin, polymyxin B used in combination therapy for severe infections may be more effective, especially when one considers the possibility of resistance development during monotherapy. In this regard, Lee and colleagues  described the emergence of resistance to polymyxin B for three out of 12 patients treated with polymyxin B for their KPC-producing K. pneumoniae bloodstream infections; in contrast, none of the four patients treated with polymyxin B in combination with tigecycline developed resistance during therapy .
Treatment regimens and outcomes of various infections with carbapenemase-producing organisms reported in the literature
Colistina + tigecyclineb
Tigecycline + gentamicinc
Colistin + tigecycline + meropenemd
Colistin + carbapenem
Tigecycline + carbapenem
Tigecycline + aminoglycoside
Tigecyclinef + gentamicing ± fosfomycinh
Tigecycline plus colistini ± fosfomycin
3/14 (21 %)
KPC K. pneumoniae
Colistin + aminoglycoside
Colistin plus carbapenem
KPC K. pneumoniae
VAP ± bacteremia
Fosfomycink + colistin
Fosfomycin + gentamicin
Fosfomycin + piperacillin/tazobactam
KPC K. pneumoniae
Fosfomycinl + colistin
Fosfomycin + tigecycline
KPC K. pneumoniae
UTI (including colonization)
Recently, a double-carbapenem combination (ertapenem-doripenem) has been proposed as a potential treatment strategy for KPC-producing bacteria [38, 39]. Data come from in vitro experiments on a murine animal model  as well as in vivo. Regarding the latter, three patients with bacteremia or urinary tract infection (UTI) caused by pan-resistant KPC-producing K. pneumoniae  and one ICU patient with bacteremia and sepsis caused by colistin-resistant KPC-producing K. pneumoniae were reported to have been successfully treated with a double-carbapenem combination . Most recently, Karaiskos and colleagues  reported treating 14 patients with bacteremias and UTIs, including two patients with septic shock caused by KPC-producing K. pneumoniae with double-carbapenems therapy, as follows: 1 g ertapenem IV daily, followed 1 hour later by meropenem at 2 g every 8 hours infused over 3 hours. All treated patients experienced clinical and microbiological cure at 1-month follow-up, although four patients experienced a recurrence of their UTI . Nevertheless, since the clinical experience with this salvage therapy is still limited, concerns for promoting further carbapenem resistance remain , and the MICs of many carbapenem-producing organisms are sufficiently high to render carbapenems ineffective, this treatment strategy is not routinely recommended for clinical practice at the present time.
Tigecycline has been shown to have in vitro activity against multidrug-resistant Enterobacteriaceae isolates . Tigecycline has been used in the treatment of infections with CRE primarily as an adjuvant drug in combination therapy (Table 3) [43–45]. However, the clinical experience with tigecycline has been somewhat disappointing, especially for severe infections such as bloodstream infections or nosocomial pneumonias, for which the drug does not have US Food and Drug Administration (FDA) approval. For example, Kontopidou and colleagues , in their study of 127 ICU patients with bacteremias or ventilator-associated pneumonias caused by carbapenem-resistant K. pneumoniae, found that patients treated with tigecycline, especially as monotherapy (at doses of 100 to 200 mg/day), had the highest failure rates compared with other drug combinations. Most patients treated with tigecycline in this cohort had an MIC of 2 μg/mL (which is the cutoff for susceptibility) and severe infections with high Acute Physiology and Chronic Health Evaluation II scores, which may explain why tigecycline was ineffective . Post-approval meta-analyses have shown that tigecycline had lower cure rates and higher mortality compared with other treatment regimens in pooled randomized controlled trials of various infectious syndromes [47–49]. When evaluated in a randomized controlled trial of hospital-acquired pneumonia, tigecycline plus ceftazidime was inferior to vancomycin and imipenem-cilastatin for the treatment of ventilator-associated pneumonia . The problem may be related to the low plasma serum concentrations achieved by the dose recommended by the manufacturer (100 mg loading dose followed by a maintenance dose of 50 mg every 12 hours), which is likely ineffective against pathogens with an MIC of between 0.4 and 1 mg/L. Higher doses have been used in clinical practice . In fact, a recent phase 2 randomized controlled trial of patients with hospital-acquired pneumonia studied higher doses of tigecycline (150 mg loading followed by 75 mg every 12 hours, and 200 mg loading followed by 100 mg maintenance dose every 12 hours) versus imipenem/cilastatin. Clinical cure rates were the highest in the arm with the highest dose regimen of tigecycline, whereas the safety profile was similar to that of the lower dose regimens . Nevertheless, in 2010, the FDA added a warning regarding the risk of increased mortality with tigecycline treatment, especially for non-approved indications such as hospital- or ventilator-associated pneumonias (found at ). This safety concern was upgraded to a stronger Boxed Warning in 2013, after analysis of 10 clinical trials of tigecycline use for FDA-approved indications, including trials conducted after drug approval, still showed a higher (0.6%) risk of death for patients treated with tigecycline versus other antimicrobials (found at ). As a result, many clinicians have chosen tigecycline-based regimens only when other therapies were not available. The low concentration of tigecycline in the urine further limits the use of this antimicrobial for the treatment of UTIs. Unless more compelling evidence of improved clinical outcomes in well-designed studies of high-dose tigecycline becomes available, tigecycline monotherapy is not routinely recommended for severe infections such as bacteremia or hospital-acquired pneumonia.
Fosfomycin is another old broad-spectrum antibiotic that inhibits bacterial cell wall synthesis and has in vitro activity against CRE [12, 55]. The oral formulation achieves high concentrations in the urine and is usually effective in the treatment of non-complicated UTIs . The IV formulation (fosfomycin disodium) is not available in the US and other countries, although it has been used successfully in Greece, mostly as an adjuvant drug in combination therapies . For example, a study of 11 critically ill patients with nosocomial infections caused by KPC K. pneumoniae were treated with IV fosfomycin (2 to 4 g every 6 hours) in combination with colistin (n = 6), gentamicin (n = 3), and piperacillin/tazobactam (n = 1). All patients were reported to have good treatment-related microbiological and clinical outcomes, while the all-cause hospital mortality was 18.2% (two patients) . The emergence of resistance to fosfomycin during therapy for bacteremia with KPC K. pneumoniae has been reported and is especially concerning since fosfomycin was used as an adjunct in combination therapy in these cases . Recently, parenteral fosfomycin administered in combination with colistin or tigecycline was studied in a prospective observational multicenter trial in 11 ICUs in Europe. In total, 41 patients with bacteremia or ventilator-associated pneumonia caused by carbapenemase-producing K. pneumoniae were treated with a median dose of 24 g of fosfomycin per day for a total of 14 days. Microbiological cure was reported in 56.5% of cases, with an all-cause 28-day mortality of 43.5% and emergence of resistance in three patients .
Several parenteral antimicrobial therapies are currently under investigation for the treatment of multidrug-resistant Gram-negative infections, including CRE. Ceftazidime-avibactam (a new beta-lactamase inhibitor) is active against extended-spectrum beta-lactamase-producing organisms, some resistant Pseudomonas aeruginosa strains, and CRE of the KPC type, but not against metallo-beta-lactamases such as New Delhi metallo-beta-lactamase and verona integron-encoded metallo-beta-lactamase. It is currently undergoing phase 3 studies for complicated UTI and intra-abdominal infections . Ceftaroline-avibactam, entering phase 3 trials, is similarly active against KPC-producing strains, but not against P. aeruginosa or other metallo-beta-lactamase-producing organisms. Neither one of these drugs in development has activity against Acinetobacter species [6, 59]. Imipenem in combination with another novel beta-lactamase inhibitor, MK-7655, appears active in vitro against serine carbapenemase-producing organisms and against P. aeruginosa, but not against metallo-carbapenemase-producing organisms or Acinetobacter baumannii . Plazomycin (ACHN-490), a new aminoglycoside currently in development, has activity against isolate-producing KPC enzymes and does not seem susceptible to the same resistance mechanisms present in older aminoglycosides, although it does not have activity against strains that harbor 16S ribosomal methylases. It has completed phase 2 trials . Biapenem/RPX7009 (Carbavance; Rempex Pharmaceuticals, Inc., San Diego, CA, USA), a carbapenem combined with a novel boronate inhibitor, currently in phase 1 trials, appears active in vitro against KPC-producing organisms and other class A carbapenemases, including resistant Pseudomonas and Acinetobacter strains, although it is not active against class B and D carbapenemases [6, 61]. Eravacycline is a novel tetracycline that is not susceptible to efflux resistance mechanisms or to the protection of the ribosomal target that renders older tetracyclines ineffective. It has in vitro activity against KPC-producing bacteria but not against non-fermenters .
None of the antimicrobials currently in development has activity against the entire spectrum of carbapenemase-producing Gram-negative bacteria. The mortality associated with the failure rates from the current salvage therapies highlighted above is disconcerting. The treatment of serious infections with CRE remains an enormous challenge. A concerted global commitment to the intelligent use of antimicrobials, better antibiotic stewardship, the implementation of effective infection control strategies, and the development of more effective therapies are desperately needed.
This article is part of a series on Antibiotic resistance in the ICU, edited by Steven Opal. Other articles in this series can be found at http://ccforum.com/series/antibioticresistance.
US Food and Drug Administration
Klebsiella pneumoniae carbapenemase
Minimum inhibitory concentration
Urinary tract infection.
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