Ceftazidime-Avibactam as Salvage Therapy for Infections Caused by Enterobacteriales Coresistant to Carbapenems and Polymyxins

被引:31
作者
Guimaraes, Thais [1 ]
Nouer, Simone A. [2 ]
Martins, Roberta C. R. [3 ]
Perdigao Neto, Lauro, V [3 ]
Martins, Willames M. B. S. [4 ]
Narciso Barbosa, Ana Clara [4 ]
Ferreira, Adriana L. P. [2 ,5 ]
Costa, Silvia F. [3 ]
Gales, Ana C. [4 ]
机构
[1] Univ Sao Paulo, Hosp Clin, Inst Cent, Sao Paulo, Brazil
[2] Univ Fed Rio de Janeiro, Sch Med, Rio De Janeiro, Brazil
[3] Univ Sao Paulo, Lab Bacteriol LIM 49, Sao Paulo, Brazil
[4] Univ Fed Sao Paulo, Escola Paulista Med, Div Infect Dis, Sao Paulo, Brazil
[5] DASA, Lab Diagnost Amer, Rio De Janeiro, Brazil
关键词
CRE; Enterobacteriales; KPC-Kp; extensively drug resistant; KLEBSIELLA-PNEUMONIAE; MORTALITY;
D O I
10.1128/AAC.00528-19
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 mu g/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.
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页数:6
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