Evaluation of the INCREMENT-CPE, Pitt Bacteremia and qPitt Scores in Patients with Carbapenem-Resistant Enterobacteriaceae Infections Treated with Ceftazidime-Avibactam

被引:20
作者
Jorgensen, Sarah C. J. [1 ]
Trinh, Trang D. [1 ,2 ]
Zasowski, Evan J. [1 ,3 ]
Lagnf, Abdalhamid M. [1 ]
Bhatia, Sahil [1 ]
Melvin, Sarah M. [1 ]
Simon, Samuel P. [4 ]
Rosenberg, Joshua R. [4 ]
Steed, Molly E. [5 ]
Estrada, Sandra J. [6 ,7 ]
Morrisette, Taylor [1 ,8 ]
Davis, Susan L. [1 ,9 ]
Rybak, Michael J. [1 ,10 ,11 ]
机构
[1] Wayne State Univ, Antiinfect Res Lab, Dept Pharm Practice, Eugene Applebaum Coll Pharm & Hlth Sci, Detroit, MI 48202 USA
[2] Univ Calif San Francisco, Dept Clin Pharm, Sch Pharm, Medicat Outcomes Ctr, San Francisco, CA 94143 USA
[3] Touro Univ Calif, Coll Pharm, Dept Clin Sci, Vallejo, CA USA
[4] Brooklyn Hosp, Brooklyn, NY USA
[5] Univ Kansas, Dept Pharm Practice, Sch Pharm, Kansas City, KS USA
[6] Lee Hlth, Dept Pharm, Ft Myers, FL USA
[7] T2 Biosyst Inc, Lexington, MA USA
[8] Univ Colorado, Skaggs Sch Pharm & Pharmaceut Sci, Dept Pharm, Aurora, CO USA
[9] Henry Ford Hosp, Dept Pharm, Detroit, MI 48202 USA
[10] Wayne State Univ, Dept Med, Detroit, MI 48202 USA
[11] Detroit Med Ctr, Dept Pharm, Detroit, MI USA
关键词
Carbapenem-resistant Enterobacteriaceae; Ceftazidime-avibactam; INCREMENT-CPE; Pitt bacteremia; MONOTHERAPY; OUTCOMES; THERAPY;
D O I
10.1007/s40121-020-00288-4
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background The aim of this study was to evaluate the predictive performance of the INCREMENT-CPE (ICS), Pitt bacteremia score (PBS) and qPitt for mortality among patients treated with ceftazidime-avibactam for carbapenem-resistant Enterobacteriaceae (CRE) infections. Methods Retrospective, multicenter, cohort study of patients with CRE infections treated with ceftazidime-avibactam between 2015 and 2019. The primary outcome was 30-day all-cause mortality. Predictive performance was determined by assessing discrimination, calibration and precision. Results In total, 109 patients were included. Thirty-day mortality occurred in 18 (16.5%) patients. There were no significant differences in discrimination of the three scores [area under the curve (AUC) ICS 0.7039, 95% CI 0.5848-0.8230, PBS 0.6893, 95% CI 0.5709-0.8076, and qPitt 0.6847, 95% CI 0.5671-0.8023; P > 0.05 all pairwise comparisons]. All scores showed adequate calibration and precision. When dichotomized at the optimal cut-points of 11, 3, and 2 for the ICS, PBS, and qPitt, respectively, all scores had NPV > 90% at the expense of low PPV. Patients in the high-risk groups had a relative risk for mortality of 3.184 (95% CI 1.35-8.930), 3.068 (95% CI 1.094-8.606), and 2.850 (95% CI 1.016-7.994) for the dichotomized ICS, PBS, and qPitt, scores respectively. Treatment-related variables (early active antibiotic therapy, combination antibiotics and renal ceftazidime-avibactam dose adjustment) were not associated with mortality after controlling for the risk scores. Conclusions In patients treated with ceftazidime-avibactam for CRE infections, mortality risk scores demonstrated variable performance. Modifications to scoring systems to more accurately predict outcomes in the era of novel antibiotics are warranted.
引用
收藏
页码:291 / 304
页数:14
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