Ceftazidime-Avibactam as Salvage Therapy for Infections Caused by Enterobacteriales Coresistant to Carbapenems and Polymyxins.
Thais GuimarãesSimone A NouérRoberta C R MartinsLauro V Perdigão NetoWillames M B S MartinsAna Clara Narciso BarbosaAdriana L P FerreiraSilvia F CostaAna C GalesPublished in: Antimicrobial agents and chemotherapy (2019)
In this article, we report a case series of patients with infections caused by Enterobacteriales coresistant to carbapenems and polymyxins who were treated with ceftazidime/avibactam (CAZ-AVI) salvage therapy on a compassionate-use protocol. We enrolled 29 adult patients in 3 centers that had an infection due to a resistant microorganism and for whom the treatments available were considered ineffective, treated them with CAZ-AVI, and assessed clinical and microbiological cure at the end of treatment and all-cause mortality at 14 days and 30 days. The antimicrobial susceptibility profile was determined using broth microdilution, and total genomic DNA was sequenced. Twelve (41.4%) patients had bacteremia, and 48.3% (14/29) of the infections were treated with combination therapy. All strains were producers of KPC-2 and were susceptible to CAZ-AVI (MIC90, 1 μg/ml). Clinical success was high (24/29 [82.7%; 95% confidence interval, 64.2 to 94.2%]), even for the bacteremic cases (75%). The 14-day and 30-day mortality rates were 9/29 (31%) and 15/29 (51.7%), respectively. The 14-day mortality rate for pneumonia was the same as that for bloodstream infections (33.3%) and although not significant, we found that patients with renal impairment that received adjusted doses of CAZ-AVI had high mortality (4/9 [44%]; P = 0.22). We concluded that CAZ-AVI is an option for the treatment of severe infections due to difficult-to-treat drug-resistant Enterobacteriales.
Keyphrases
- combination therapy
- drug resistant
- gram negative
- multidrug resistant
- newly diagnosed
- klebsiella pneumoniae
- cardiovascular events
- end stage renal disease
- acinetobacter baumannii
- escherichia coli
- chronic kidney disease
- gene expression
- single molecule
- circulating tumor
- cardiovascular disease
- acute respiratory distress syndrome
- dna methylation
- extracorporeal membrane oxygenation
- patient reported outcomes
- genome wide
- mechanical ventilation
- drug induced