Sir,
Pandrug-resistant Klebsiella pneumoniae that produces New Delhi MBL (NDM) is increasingly reported worldwide.1 These strains contain multiple β-lactamase genes but also may have acquired resistance to last-resort options such as colistin and tigecycline. Combining aztreonam and avibactam is potentially effective in MDR, NDM-producing Enterobacterales.2 Avibactam inhibits class A, C and D ESBLs, cephalosporinases and carbapenemases, while aztreonam is stable to hydrolysis by class B MBLs such as NDM. Until this drug combination becomes available, one could combine aztreonam and ceftazidime/avibactam to treat serious infections with such strains. A small number of studies have reported on 13 patients with serious infections with NDM-producing Enterobacterales who were successfully treated with aztreonam and ceftazidime/avibactam.3–7 Evidence of clinical efficacy and safety is therefore limited at present. Also, aztreonam for IV use is not registered and readily available in many countries, including the Netherlands. We describe successful rescue treatment of a patient with sepsis due to a pandrug-resistant, NDM-producing K. pneumoniae using aztreonam powder for nebulizer solution as IV therapy in combination with ceftazidime/avibactam.
A woman in her sixties who had received a kidney transplant 2 months earlier underwent routine urinary culture screening. The culture grew K. pneumoniae resistant to all antimicrobial classes (Table 1). An in-house carbapenemase PCR showed that the strain carried an NDM carbapenemase gene. As she was asymptomatic, no treatment was started, but 9 days later she presented signs and symptoms of a kidney transplant pyelonephritis. We regarded aztreonam combined with ceftazidime/avibactam as the only promising treatment option for the pandrug-resistant K. pneumoniae. However, it was not clear whether we could import aztreonam for IV use to the Netherlands within a reasonable time. As the patient’s condition deteriorated, we decided to administer aztreonam powder for nebulizer solution intravenously (1000 mg three-times daily, prepared from 14 vials of 75 mg, in extended infusion) in combination with ceftazidime/avibactam (2000 + 500 mg three-times daily by continuous infusion). The subsequent day the blood culture became positive with the pandrug-resistant K. pneumoniae. Immunosuppressive therapy was reduced and the patient received supportive care for sepsis. Her condition improved within 1 day after the start of combination therapy and she recovered completely with 14 days of therapy without signs of adverse events. Aztreonam for IV solution was imported from France 11 days after our urgent request to the Dutch Government. The patient had one mild pyelonephritis recurrence with the same strain and unchanged susceptibility pattern 1 month later and recovered with the same treatment. She consented to the publication of this report.
Table 1.
Phenotypic characteristics of the pandrug-resistant K. pneumoniae
| Method | Antimicrobial | MIC (mg/L) | Interpretationa | |
|---|---|---|---|---|
| Single susceptibility testing | ||||
| Vitek-2® | ||||
| amoxicillin/clavulanic acid | ≥32 | resistant | ||
| cefotaxime | ≥64 | resistant | ||
| ceftazidime | ≥64 | resistant | ||
| cefoxitin | ≥64 | resistant | ||
| ciprofloxacin | ≥4 | resistant | ||
| trimethoprim/ sulfamethoxazole | ≥320 | resistant | ||
| gentamicin | ≥16 | resistant | ||
| imipenem | ≥16 | resistant | ||
| meropenem | ≥16 | resistant | ||
| nitrofurantoin | 256 | resistant | ||
| piperacillin/tazobactam | ≥128 | resistant | ||
| tobramycin | ≥16 | resistant | ||
| Gradient test | ||||
| amikacin | >256 | resistant | ||
| aztreonam | >256 | resistant | ||
| ceftazidime/avibactam | >256 | resistant | ||
| ceftolozane/tazobactam | >256 | resistant | ||
| doripenem | >32 | resistant | ||
| eravacycline | 4 | resistant | ||
| fosfomycin | >256 | resistant | ||
| imipenem | >32 | resistant | ||
| meropenem | >32 | resistant | ||
| plazomicin | >256 | unknown | ||
| sulbactam | >256 | unknown | ||
| tigecycline | 6 | resistant | ||
| Broth microdilution | ||||
| colistin | 16 | resistant | ||
|
| ||||
|
MIC mg/L |
||||
| Antimicrobial | single | combined with aztreonam | Interpretationb | |
|
| ||||
| Gradient test superposition | ||||
| amoxicillin/clavulanic acid | >256 | 12 | synergy | |
| ceftazidime/avibactam | >256 | 0.5 | synergy | |
| ceftolozane/tazobactam | >256 | 48 | synergy | |
| colistin | 8 | 12 | no synergy | |
| meropenem | >32 | 16 | synergy | |
| piperacillin/tazobactam | >256 | 32 | synergy | |
According to EUCAST (www.eucast.org).
Synergy was defined as the occurrence of an inhibition zone when an antimicrobial was combined with aztreonam.
Table 1 shows phenotypic characteristics of the isolate. We assessed in vitro synergy by using gradient test superposition as previously described in this journal.5 We compared MICs of the gradient test superposition with MICs of single gradient tests. We only found clinically relevant synergy (i.e. inhibition of the strain at drug concentrations below the breakpoints of both antimicrobials with gradient test superposition compared with single gradient tests) when combining aztreonam and ceftazidime/avibactam (Table 1).
Next-generation sequencing (HiSeq 2500 sequencer, BaseClear, Leiden, the Netherlands) reads were uploaded to the European nucleotide archive (accession number PRJEB33296) and used to perform resistome and replicome composition analysis (ResFinder, version 2.1, PlasmidFinder, version 1.3). These analyses showed that the isolate (MLST ST15) carried the blaNDM-1 carbapenemase gene, as well as the blaCMY-6, blaCTX-M-15, blaOXA-1, blaOXA-10, blaSHV-28 β-lactamase genes and aac(3)-IIa, aac(6′)Ib-3 resistance genes, among others, conferring resistance to all β-lactams, aminoglycosides and fluoroquinolones. Similar to a previously described comparable strain, we did not identify resistance genes conferring resistance to colistin and tigecycline.1
We considered carefully before using aztreonam powder for nebulizer solution as off-label and unlicensed IV therapy. Aztreonam powder for nebulizer solution is a sterile product, without any additives that are known to be harmful. Also, it has a similar composition to the IV product. We expected that the benefits of the product, i.e. potential survival and no other treatment alternatives, weighed against potential risks of the product, i.e. unexpected side effects. Before providing aztreonam powder for nebulizer solution intravenously, we asked for consent from the patient and the medical director of our hospital.
In conclusion, we report successful rescue treatment of a patient with sepsis due to a pandrug-resistant, NDM-producing K. pneumoniae using aztreonam powder for nebulizer solution as IV therapy in combination with ceftazidime/avibactam and reducing immunosuppressive therapy. As such strains have been reported worldwide, we request the pharmaceutical industry to make aztreonam for IV use and ceftazidime/avibactam readily available in all countries. When aztreonam for IV use is not registered in a country, our case demonstrates that rescue treatment with aztreonam powder for nebulizer solution as IV therapy may be considered after careful assessment of the potential benefits and harms. Future studies are awaited to define the efficacy and safety of the promising treatment combination of aztreonam and avibactam in patients with serious infections due to pandrug-resistant, NDM-producing K. pneumoniae and other Enterobacterales.
Acknowledgements
We presented this study in March 2019 at the Scientific Spring Meeting 2019 from the Dutch Society of Medical Microbiology, Arnhem, the Netherlands.
Funding
This study was carried out as part of our routine work.
Transparency declarations
None to declare.
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