Intestinal Infection of Multi-Resistant NDM-Producing K. pneumoniae in a Patient with NK/T Lymphoma – Case Study
The incidence of NDM-producing Klebsiella pneumoniae is increasing worldwide. NDM beta-lactamase is a significant cause of multidrug resistance in enterobacteria to various antibiotics, including carbapenems. Currently, the most suitable approach for the treatment of intestinal infections caused by NDM-producing K. pneumoniae is considered to be the combination of ceftazidime/avibactam with aztreonam. The following case study also illustrates its use in more complicated cases.
Case Description
A 62-year-old man diagnosed with NK/T lymphoma was hospitalized in August 2021 in the hematology department for autologous stem cell transplantation. On the 3rd day post-procedure, he developed fever and diarrhea. Empirical antibiotic therapy with imipenem/cilastatin at a dose of 500 mg IV every 6 hours and teicoplanin at a dose of 400 mg IV every 12 hours was initiated. However, after 2 days of treatment, the patient remained febrile and had watery diarrhea. On the 5th day post-transplant, the initial combination of antibiotics was replaced with tigecycline at a dose of 100 mg IV every 12 hours and cefoperazone/sulbactam at a dose of 2 g every 8 hours. Due to the development of septic shock, the patient was transferred to the ICU on the 6th day post-transplant.
Here, the antibiotic therapy was changed once again. A combination of imipenem/cilastatin 500 mg IV every 4 hours and ceftazidime/avibactam (CAZ/AVI) at a dose of 2.5 g IV every 8 hours was administered. After 3 days of ICU hospitalization, Klebsiella pneumoniae was detected in both blood cultures and stool samples. The use of the CARBA5 immunological qualitative test confirmed the presence of a New Delhi metallo-beta-lactamase (NDM) producing variant of K. pneumoniae resistant to carbapenems. Based on this finding, a combination of CAZ/AVI 2.5 g IV every 8 hours with aztreonam (ATM) at a dose of 2 g IV every 8 hours was initiated. Shortly after starting this targeted antibiotic therapy, the patient's clinical condition significantly improved and the septical state receded.
Discussion
The presence of metallo-dependent beta-lactamase (MBL) NDM-1 enables bacteria to hydrolyze nearly all beta-lactam antibiotics. ATM belongs to a group of beta-lactam antibiotics that are active against MBL-producing microorganisms, but it is subject to hydrolysis by bacteria producing extended-spectrum beta-lactamases (ESBL). Avibactam can protect ATM from hydrolysis by class A and C beta-lactamases.
The bactericidal effect of the combination of CAZ/AVI with ATM was demonstrated by Marshall et al. on 17 of 21 enterobacteria isolates producing MBL. After 24 hours, the colony-forming units (CFUs) decreased by nearly 4log10. In vitro, synergistic action of ATM and CAZ/AVI against 40 multi-resistant MBL and serine beta-lactamase producing strains of K. pneumoniae was demonstrated. The efficacy of this combination was also found using MIC test strips on 15 clinical isolates of NDM-producing K. pneumoniae. Further prospective studies highlighted significantly lower mortality rates in patients treated with a combination of antibiotics compared to those receiving monotherapy alone.
Several other case studies of successful treatment with the combination of ATM and CAZ/AVI have also been published. In one case, it involved a patient with aplastic anemia, agranulocytosis, and hematogenic sepsis following chemotherapy. Another case demonstrated the treatment of sepsis and successful intestinal decolonization in a patient with thrombotic thrombocytopenic purpura (TTP) complicated by a nosocomial SARS-CoV-2 infection.
(kali)
Sources:
1. Liu S., Lin Q., Ouyang L et al. Successful treatment of ceftazidime/avibactam combined with aztreonam in the NDM-producing Klebsiella pneumoniae bloodstream and intestinal infections in an NK/T lymphoma patient with agranulocytopenia during autologous hematopoietic stem cell transplantation: a case report. Eur J Clin Microbiol Infect Dis 2022 Nov 12: 1–4, doi: 10.1007/s10096-022-04523-3.
2. Marshall S., Hujer A. Mm, Rojas L. J. et al. Can ceftazidime-avibactam and aztreonam overcome β-lactam resistance conferred by metallo-β-lactamases in enterobacteriaceae? Antimicrob Agents Chemother 2017; 61 (4): e02243-16, doi: 10.1128/AAC.02243-16.
3. Maraki S., Mavromanolaki V. E., Moraitis P. et al. Ceftazidime-avibactam, meropenem-vaborbactam, and imipenem-relebactam in combination with aztreonam against multidrug-resistant, metallo-β-lactamase-producing Klebsiella pneumoniae. Eur J Clin Microbiol Infect Dis 2021; 40 (8): 1755–1759, doi: 10.1007/s10096-021-04197-3.
4. Bocanegra-Ibarias P., Camacho-Ortiz A., Garza-González E. et al. Aztreonam plus ceftazidime-avibactam as treatment of NDM-1-producing Klebsiella pneumoniae bacteraemia in a neutropenic patient: Last resort therapy? J Glob Antimicrob Resist 2020; 23: 417–419, doi: 10.1016/j.jgar.2020.10.019.
5. Perrotta F., Perrini M. P. Successful treatment of Klebsiella pneumoniae NDM sepsis and intestinal decolonization with ceftazidime/avibactam plus aztreonam combination in a patient with TTP complicated by SARS-CoV-2 nosocomial infection. Medicina (Kaunas) 2021; 57 (5): 424, doi: 10.3390/medicina57050424.
Did you like this article? Would you like to comment on it? Write to us. We are interested in your opinion. We will not publish it, but we will gladly answer you.