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Cure of recurring Klebsiella pneumoniae carbapenemase-producing Klebsiella pneumoniae septic shock episodes due to complicated soft tissue infection using a ceftazidime and avibactam-based regimen: a case report

  • 1Email author,
  • 2,
  • 3,
  • 4,
  • 1,
  • 1,
  • 1,
  • 1,
  • 1,
  • 1,
  • 1,
  • 3,
  • 4 and
  • 2
Journal of Medical Case Reports201913:20

https://doi.org/10.1186/s13256-018-1934-2

  • Received: 16 January 2018
  • Accepted: 25 November 2018
  • Published:
Open Peer Review reports

Abstract

Background

Infections caused by multidrug-resistant Enterobacteriaceae are hard to treat and life-threatening due to reduced therapeutic options. Systemic infections caused by Klebsiella pneumoniae carbapenemase-producing Klebsiella pneumoniae strains have increased in many European regions, becoming frequent in many clinical settings, and are associated with high mortality. The co-formulation of ceftazidime, a third-generation cephalosporin, with avibactam, a new suicide inhibitor beta-lactamase inhibitor able to block most Klebsiella pneumoniae carbapenemases, has been recently licensed, with promising results in patients with limited or absent therapeutic options. Little is known, however, as to the efficacy of such a combination in patients with soft tissue infections caused by multidrug-resistant Klebsiella pneumoniae carbapenemase-producing strains of Klebsiella pneumoniae.

Case presentation

A Caucasian 53-year-old man with paraplegia suffered multiple vertebral fractures due to a car crash. He was treated with external fixators that became infected early after insertion and were repeatedly and inefficiently treated with multiple antibiotics. He suffered repeated septic episodes caused by Klebsiella pneumoniae carbapenemase-producing Klebsiella pneumoniae strains with a multidrug-resistant profile. Meropenem, tigecycline, and colistin combinations allowed only temporary improvements, but septic shock episodes recurred, in spite of removal of infected external fixators. After approval of pre-marketing prescription by our local Ethics Committee, full clinical resolution was obtained with a compassionate treatment using meropenem and ceftazidime/avibactam in combination for 16 days.

Conclusions

Our experience provides additional evidence that ceftazidime/avibactam, possibly in combination with meropenem rescued by avibactam, may be an efficacious treatment option also for complicated skin and soft tissue infections caused by multidrug-resistant strains of Klebsiella pneumoniae carbapenemase-producing Klebsiella pneumoniae.

Keywords

  • Sepsis
  • Klebsiella pneumoniae carbapenemase (KPC)-producing Klebsiella pneumoniae
  • Treatment

Introduction

Systemic infections caused by Gram-negative multidrug-resistant (MDR) Enterobacteriaceae are nowadays frequently hard to treat and life-threatening worldwide due to reduced therapeutic options [1]. Klebsiella pneumoniae carbapenemase (KPC)-producing Klebsiella pneumoniae (KPC-Kp) strains are endemic in most Italian regions and selection of nearly panresistant strains has become frequent in many clinical settings [2]. In particular, patients with difficult or delayed infectious source control may present with recurring infections and relapsing septic episodes, whose treatment may become increasingly difficult due to stepwise selection of bacterial strains with worsening resistance profiles. In such cases, effective source control may turn out to be useless even in immunocompetent patients, if clearance of residual infectious foci is impossible due to bacterial resistance [3]. In this scenario, availability of new therapeutic options may be crucial for patients’ rescue in the event of overwhelming septic recurrences. Recently, the US Food & Drug Administration/European Medicines Agency’s (FDA/EMA) release of a fixed dose combination of avibactam, a new carbapenemase inhibitor, and ceftazidime ushered expectation that at least some severe infections due to KPC-Kp may find a rescue option [4]. Experiences on the off-label use of such a combination for indications outside those included in clinical trials, however, are so far scanty. Here we present the case of an immunocompetent patient with vertebral traumatic fractures treated with multiple indwelling fixators, who became infected with a KPC-Kp strain early in the postoperative period. He could be rescued with the compassionate introduction of avibactam/ceftazidime as a last chance combination regimen after effective source control.

Case presentation

Our patient is a Caucasian 53-year-old, otherwise healthy, man with paraplegia since his recent car crash causing multiple vertebral fractures and a D7 lesion. He was admitted at the Infectious Diseases Unit due to low grade intermittent fever, severe back pain, and high (7.5 ng/mL) procalcitonin (PCT) levels in spite of the absence of any other sign of sepsis or septic shock. Repeated blood cultures (BCs), however, all turned positive for a single infecting strain of KPC-Kp (Table 1). Strains were molecularly typed as KPC II positive, with limited therapeutic options (Table 2). He was treated with meropenem, tigecycline, and colistin, in accordance with local protocols for KPC-Kp (Table 2). At that time, he refused any surgical management as he had been treated at another Italian center for his previous three septic episodes following insertion of fixators. In those circumstances, due to recent vertebral stabilization, he had been treated with single shot removal and replacement surgery for infected fixators, followed by early relapse of infection signs. After 18 days of treatment in our ward, the infection apparently resolved, with negative control BCs, and normal C-reactive protein (CRP) and PCT levels. He was discharged to home, with the indication to monitor infection relapse twice weekly, while starting his rehabilitation protocol. After 2 weeks, with normal PCT levels, his CRP had risen to 79 mg/L. He complained of worsening back pain. After 10 days, he was re-hospitalized on emergency due to recurrent sepsis. His BCs were again positive for KPC-Kp (Table 1). Treatment was restarted with the same combination based on the available resistance profile (Table 2). Treatment was again efficacious, and on the 12th day he accepted his transfer to the Neurosurgery Unit for removal of fixators (Fig. 1). It was explained to him that control neuroimaging studies allowed a two-step procedure, aimed at a definitive cure of infection prior to possible reinsertion of fixators. He was given the same antibiotic treatment for residual source control after surgery for 21 days (Table 2). He was once more discharged to home as neurosurgeons considered reinsertion of fixators unnecessary. After 35 days, he was readmitted with recurring sepsis. BCs revealed progression of the resistance phenotype of his KPC-Kp isolates (Table 1). A rescue treatment was provided with all available, potentially useful antibiotics, including gentamycin and colistin (Table 2). Clinical remission was obtained after 14 days of treatment, but septic shock recurred 6 days after treatment discontinuation. He presented with a relapse of hyperpyrexia (42 °C), hypotension, severe leukocytosis with white blood cells (WBC) 38,000, drop in platelet counts (nadir 46,000/mm3), and rapidly ensuing renal failure with creatinine nadir of 4.4 mg/dL and liver failure with alanine aminotransferase (ALT) nadir of 456 U/L.
Table 1

Evolving phenotypes of isolated Klebsiella strains from our patient

Antibiotics

April 10, 2016

July 23, 2016

December 27, 2016

January 19, 2017

Klebsiella pneumoniae

Klebsiella pneumoniae

Klebsiella pneumoniae

Enterobacter aerogenes

Klebsiella pneumoniae

Amikacin

Resistant

Resistant

Resistant

Susceptible

Resistant

Amoxicillin-clavulanic acid

Resistant

Resistant

Resistant

Resistant

Resistant

Ampicillin

Resistant

Resistant

Resistant

Resistant

Resistant

Cefepime

Resistant

Resistant

Resistant

Susceptible

Resistant

Cefotaxime

Resistant

Resistant

Resistant

Susceptible

Resistant

Ceftazidime

Resistant

Resistant

Resistant

Susceptible

Resistant

Ciprofloxacin

Resistant

Resistant

Resistant

Susceptible

Resistant

Colistin

Susceptible

Susceptible

Resistant

Susceptible

Resistant

Ertapenem

Resistant

Resistant

Resistant

Susceptible

Resistant

Fosfomycin

Susceptible

Susceptible

Resistant

Susceptible

Resistant

Gentamicin

Intermediate

Intermediate

Intermediate

Susceptible

Intermediate

Imipenem

Resistant

Resistant

Resistant

Susceptible

Resistant

Meropenem

Resistant

Resistant

Resistant

Susceptible

Resistant

Piperacillin/tazobactam

Resistant

Resistant

Resistant

Susceptible

Resistant

Tigecycline

Intermediate

Intermediate

Resistant

Susceptible

Intermediate

Trimethoprim/sulfamethoxazole

Resistant

Resistant

Resistant

Susceptible

Resistant

Table 2

Combination regimens used to treat ensuing septic episodes in our patient

Date of hospitalization in Infectious Diseases Unit

Microbiological data

Combination therapy

Doses

Timing of therapy

10 April 2016

(first septic episode)

KPC-producing Klebsiella pneumoniae

isolates on BCs

Tigecycline

Meropenem

Colistin

LD 100 mg + 50 mg/12 hours

LD 2gr + 2gr/8 hours

LD 9 MU + 4.5 MU/8 hours

18 days

June 2016

Re-hospitalization for the second septic episode

KPC-producing Klebsiella pneumoniae on BCs

Tigecycline

Meropenem

Colistin

LD 100 mg + 50 mg/12 hours

LD 2gr + 2gr/8 hours

LD 9 MU + 4.5 MU/12 hours

12 days before surgical management for fixators’ removal

Continuing hospitalization after surgical treatment

 

Same combination therapy as above

 

21 days

December. 2016

Third septic recurrence with hospitalization

KPC-producing Klebsiella pneumoniae and Enterobacter aerogenes isolates on BC

Tigecycline

Meropenem

Colistin

Gentamycin

LD 100 mg + 50 mg/12 hours

LD 2gr + 2gr/8 hours

LD 9 MU +  4.5 MU/8 hours

14 days

Septic shock/MOF after discontinuation of therapy

(January 2017)

KPC-producing Klebsiella pneumoniae with a progression of a resistance phenotype isolates on BC

Avibactam/ceftazidime

(compassionate use)

Tigecycline

Meropenem

Gentamycin

2gr/8 hours

LD 100 mg + 50 mg/12 hours

LD 2gr + 2gr/8 hours

LD 7 mg/kg per day (480 mg) + 5 mg/kg per day (350 mg/24 hours)

16 days

BCs blood cultures, KPC Klebsiella pneumoniae carbapenemase, LD loading dose, MOF multiple organ failure, MU monitor unit

Fig. 1
Fig. 1

Vertebral and paravertebral infectious foci detected at vertebral magnetic resonance imaging after neurosurgical intervention for final removal of indwelling fixators

During his last hospital stay, our patient was positive for other microbiological culture assays: susceptible Candida albicans from an epicutaneous catheter and BCs; susceptible Pseudomonas aeruginosa from urine cultures, and susceptible Staphylococcus hominis from BCs. All viral tests performed were negative: cytomegalovirus (CMV) DNA in whole blood samples; Epstein–Barr virus (EBV) DNA in whole blood samples; serum hepatitis B surface antigen (HBsAg), and hepatitis C virus (HCV) antibodies, as recommended by national and local guidelines for opt out tests before surgical interventions. Respiratory pathogens were not tested in the absence of clinical or radiological suspicion of lung involvement at any time during his clinical course. HCV antibodies and the HBsAg were assayed with chemiluminescent immunoassays; antibiotic susceptibility was assayed with Vitek® (bioMérieux). An Xpert® Carba-R (Cepheid; Sunnyvale, USA) was used for rapid detection of resistance to carbapenems. Molecular tests for EBV and CMV were performed with ELITe MGB® Kits for real-time polymerase chain reaction (PCR) kits (Turin, Italy). Altered mentation and clonal involuntary movements at upper limbs completed the presenting picture. Lactates from arterial blood rose to 4 mmol. Septic shock support was provided, including fluid resuscitation, noradrenaline, and albumin support. The best possible antibiotic rescue regimen, that is the same regimen as 20 days earlier, was established in accordance with available microbiological data (Tables 1 and 2). Meanwhile, compassionate use of avibactam/ceftazidime was requested and authorized on emergency by the local Ethical Board. A new treatment regimen was started on day 5, including avibactam/ceftazidime, meropenem, gentamycin, and tigecycline. This treatment provided rapid and stable control of sepsis, with normal inflammation indexes on day 10. The regimen was continued for 16 days. Microbiological evidence of in vitro efficacy of the combination of ceftazidime, avibactam, and meropenem was provided. Our patient was discharged on day 31 to a local rehabilitation facility, with remarkable improvements. He was finally discharged home after 56 days. His PCT, CRP, and control BCs were all negative 40 days after discharge. His last follow-up visit was on December 5, 2017, with persistently normal clinical and laboratory parameters.

Discussion and conclusion

Our patient was a previously healthy man, surviving a car crash with paraparesis due to a D7 spinal lesion. Due to multiple vertebral fractures, multiple fixators were positioned along his spine, with ensuing early infective complications. His skin and soft tissue infections never resolved until definitive removal of fixators, nor were they resolved when residual infection was repeatedly treated with suboptimal regimens for his deep-seated KPC-Kp infection. In fact, combination antibiotic regimens including gentamycin, meropenem, tigecycline, and colistin, all delivered at the recommended doses and for expanded periods of time as recommended in the recent international literature for such critical infections [5], were only able to provide short spells of remission, with apparent remission of sepsis indexes. His last relapsing infection episode, in particular, was a frank septic shock with reversible multiorgan failure, prompting us to plead for compassionate use of avibactam/ceftazidime. Recent literature data suggested that avibactam may be efficacious on most strains of KPC-Kp [6], and this looked appealing in our case, although his infection site was not included in available clinical trials. As avibactam-containing combinations were experimented on a limited subset of possible clinical conditions, including nosocomial pneumonia, abdominal infections, and complicated urinary tract infections [4, 7, 8], little is known at present on the potential benefit that complicated and long-lasting soft tissue infections, with a possible bone involvement as in the case of our patient, may draw from introduction of avibactam/ceftazidime or avibactam/ceftazidime including rescue antibiotic combinations. Meropenem has a good soft tissue penetration [9], and it provided repeated transient benefit for this patient when included in previous regimens at high dose and protracted infusion times. Avibactam provided in the fixed dose combination with ceftazidime was likely to potentiate meropenem efficacy in our case. Microbiological evidence of avibactam efficacy could be obtained on recent isolates from our patient. Although direct evidence for in vitro enhanced combination efficacy could not be obtained, it is likely that the infusion of meropenem for expanded times in sequence with avibactam/ceftazidime may have greatly helped to reach the target of clinical eradication. Other susceptible pathogens evidenced by microbiological assays were easily controlled by standard prescribed treatments.

As to the duration of treatment, we doubted whether a second shipment of the drug should be requested in view of clinical success. Most literature evidence would suggest that longer duration of treatment beyond 2 weeks in the absence of signs of residual infection would not be of benefit [10]. In fact, control MR imaging showed remarkable improvement of lesions, in the absence of the need for further infection control surgery.

Our experience therefore provides a useful piece of evidence that avibactam-containing regimens may support treatment of KPC-Kp susceptible strains also in extreme circumstances, such as recurrent sepsis and septic shock episodes from soft tissue infections with delayed surgical source control.

Abbreviations

BC: 

Blood culture

CMV: 

Cytomegalovirus

CRP: 

C-reactive protein

EBV: 

Epstein–Barr virus

HBsAg: 

Hepatitis B surface antigen

HCV: 

Hepatitis C virus

KPC: 

Klebsiella pneumoniae carbapenemase

KPC-Kp: 

Klebsiella pneumoniae carbapenemase-producing Klebsiella pneumoniae

PCT: 

Procalcitonin

Declarations

Acknowledgements

We are greatly indebted to all the nurses of Infectious Diseases Unit (Pescara General Hospital, Pescara, Italy) for their support.

Funding

There was no funding for this case report.

Availability of data and materials

All data generated or analyzed during this study are included in this published article.

Authors’ contributions

GP, AF, and DCC contributed to drafting and preparation of the manuscript; AC, AA, GP, FDM, PC, AP, and AF made substantial contributions to clinical decision-making processes; EP, VS, GDI, and PF performed laboratory analyses; AS, EP, TS, and GDI critically revised and complemented the manuscript. All authors read and approved the final version.

Ethics approval and consent to participate

Compassionate use of ceftazidime/avibactam combination for our patient was approved by the local Ethics Committee “Regione Abruzzo, Comitato Etico per la ricerca biomedica delle provicie di Chieti e Pescara.”

Consent for publication

Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Competing interests

The authors declare that they have no competing interests.

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Authors’ Affiliations

(1)
Infectious Diseases Unit, Pescara General Hospital, Via Fonte Romana 8, 65124 Pescara, Italy
(2)
Anaesthesia and Intensive Care Unit, Pescara General Hospital, Pescara, Italy
(3)
Clinical Pathology Unit, Pescara General Hospital, Pescara, Italy
(4)
Microbiology and Virology Unit, Pescara General Hospital, Pescara, Italy

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Copyright

© The Author(s). 2019

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