4.6 Article

Ceftazidime-Avibactam versus Colistin for the Treatment of Infections Due to Carbapenem-Resistant Enterobacterales: A Multicenter Cohort Study

期刊

INFECTION AND DRUG RESISTANCE
卷 15, 期 -, 页码 211-221

出版社

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IDR.S349004

关键词

ceftazidime-avibactam; colistin; colistimethate sodium; carbapenem-resistant Enterobacterales

资金

  1. King Saud University, Riyadh, Saudi Arabia [RSP-2021/74]
  2. Deanship of Scientific Research at Umm Al-Qura University [19-MED-1-03-0006]

向作者/读者索取更多资源

This study compared the safety and effectiveness of CAZ-AVI and colistin-based regimen in treating CRE infections. The results showed that CAZ-AVI was associated with a higher clinical cure rate and a lower incidence of AKI.
Background: The aim of this study was to compare the safety and effectiveness of ceftazidime-avibactam (CAZ-AVI) to colistinbased regimen in the treatment of infections caused by carbapenem-resistant Enterobacterales (CRE). Methods: This was a retrospective, multicenter, observational cohort study of inpatients who received either CAZ-AVI or intravenous colistin for treatment of infections due to CRE. The study was conducted in 5 tertiary care hospitals in Saudi Arabia. Main study outcomes included in-hospital mortality, clinical cure at end of treatment, and acute kidney injury (AKI). Univariate analysis and multivariate logistic regression model were conducted to assess the independent impact of CAZ-AVI on the clinical outcome. Results: A total of 230 patients were included in this study: 149 patients received CAZ-AVI and 81 patients received colistin-based regimen. Clinical cure (71% vs 52%; P = 0.004; OR, 2.29; 95% CI, 1.31-4.01) was significantly more common in patients who received CAZ-AVI. After adjusting the difference between the two groups, treatment with CAZ-AVI is independently associated with clinical cure (adjusted OR, 2.75; 95% CI, 1.28-5.91). In-hospital mortality (35% vs 44%; P = 0.156; OR, 0.67; 95% CI, 0.39-1.16) was lower in patients who received CAZ-AVI but the difference was not significant. AKI (15% vs 33%; P = 0.002; OR, 0.37; 95% CI, 0.19-0.69) was significantly less common in patients who received CAZ-AVI. Conclusion: CAZ-AVI is associated with higher rate of clinical cure and lower rate of AKI compared to colistin. Our findings support the preferential use of CAZ-AVI over colistin-based regimen for treating these infections.

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