AI Article Synopsis

  • The article reports on a study involving 29 adult patients with infections caused by carbapenem and polymyxin-resistant bacteria who were treated with ceftazidime/avibactam (CAZ-AVI) under a compassionate-use protocol.
  • The results showed a high clinical success rate of 82.7%, with notable effectiveness even in cases of bacteremia (75%).
  • However, the mortality rates were concerning, with 31% at 14 days and 51.7% at 30 days, particularly high among patients with renal impairment.

Article Abstract

In this article, we report a case series of patients with infections caused by 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 (MIC, 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%]; = 0.22). We concluded that CAZ-AVI is an option for the treatment of severe infections due to difficult-to-treat drug-resistant .

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761521PMC
http://dx.doi.org/10.1128/AAC.00528-19DOI Listing

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