Fluoroquinolone Versus Nonfluoroquinolone Treatment of Bloodstream Infections Caused by Chromosomally Mediated AmpC-Producing Enterobacteriaceae

被引:3
作者
Gunter, Sarah Grace [1 ,2 ]
Barber, Katie E. [3 ]
Wagner, Jamie L. [3 ]
Stover, Kayla R. [3 ,4 ]
机构
[1] Univ Mississippi, Dept Pharm, Med Ctr, Jackson, MS 39216 USA
[2] Grandview Med Ctr, Dept Pharm, Birmingham, AL 35243 USA
[3] Univ Mississippi, Dept Pharm Practice, Sch Pharm, Jackson, MS 39216 USA
[4] Univ Mississippi, Div Infect Dis, Med Ctr, Jackson, MS 39216 USA
来源
ANTIBIOTICS-BASEL | 2020年 / 9卷 / 06期
关键词
AmpC; beta-lactamases; fluoroquinolones; beta-lactams; bacteremia; GRAM-NEGATIVE BACTERIA; CLINICAL-OUTCOMES; BETA-LACTAMASE; ALTERNATIVE ANTIBIOTICS; CARBAPENEM; EPIDEMIOLOGY; CITROBACTER; SERRATIA; THERAPY;
D O I
10.3390/antibiotics9060331
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: Chromosomally mediated AmpC-producing Enterobacteriaceae (CAE) display high susceptibility to fluoroquinolones; minimal clinical data exist supporting comparative clinical outcomes. The objective of this study was to compare treatment outcomes between fluoroquinolone and nonfluoroquinolone definitive therapy of bloodstream infections caused by CAE. Methods: This retrospective cohort assessed adult patients with positive blood cultures for CAE that received inpatient treatment for >= 48 h. The primary outcome was difference in clinical failure between patients who received fluoroquinolone (FQ) versus non-FQ treatment. Secondary endpoints included microbiological cure, infection-related length of stay, 90-day readmission, and all-cause inpatient mortality. Results: 56 patients were included in the study (31 (55%) received a FQ as definitive therapy; 25 (45%) received non-FQ). All non-FQ patients received a beta-lactam (BL). Clinical failure occurred in 10 (18%) patients, with 4 (13%) in the FQ group and 6 (24%) in the BL group (p= 0.315). Microbiological cure occurred in 55 (98%) patients. Median infection-related length of stay was 10 (6-20) days, with a significantly longer stay occurring in the BL group (p= 0.002). There was no statistical difference in 90-day readmissions between groups (7% FQ vs. 17% BL;p= 0.387); one patient expired. Conclusion: These results suggest that fluoroquinolones do not adversely impact clinical outcomes in patients with CAE. When alternatives to beta-lactam therapy are needed, fluoroquinolones may provide an effective option.
引用
收藏
页码:1 / 9
页数:9
相关论文
共 30 条
[1]   Reemergence of gram-negative health care-associated bloodstream infections [J].
Albrecht, Svenja J. ;
Fishman, Neil O. ;
Kitchen, Jennifer ;
Nachamkin, Irving ;
Bilker, Warren B. ;
Hoegg, Cindy ;
Samel, Carol ;
Barbagallo, Stephanie ;
Arentzen, Judy ;
Lautenbach, Ebbing .
ARCHIVES OF INTERNAL MEDICINE, 2006, 166 (12) :1289-1294
[2]  
Centers for Disease Control and Prevention, 2019 AR THREATS REP
[3]   Clinical and microbiological characteristics of bloodstream infections due to AmpC β-lactamase producing Enterobacteriaceae: an active surveillance cohort in a large centralized Canadian region [J].
Chaubey, Vikas P. ;
Pitout, Johann D. D. ;
Dalton, Bruce ;
Gregson, Daniel B. ;
Ross, Terry ;
Laupland, Kevin B. .
BMC INFECTIOUS DISEASES, 2014, 14
[4]   Piperacillin-Tazobactam versus Other Antibacterial Agents for Treatment of Bloodstream Infections Due to AmpC β-Lactamase-Producing Enterobacteriaceae [J].
Cheng, Lucy ;
Nelson, Brian C. ;
Mehta, Monica ;
Seval, Nikhil ;
Park, Sarah ;
Giddins, Marla J. ;
Shi, Qiuhu ;
Whittier, Susan ;
Gomez-Simmonds, Angela ;
Uhlemann, Anne-Catrin .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2017, 61 (06)
[5]   Effect of Differences in MIC Values on Clinical Outcomes in Patients with Bloodstream Infections Caused by Gram-Negative Organisms Treated with Levofloxacin [J].
DeFife, Robyn ;
Scheetz, Marc H. ;
Feinglass, Joe M. ;
Postelnick, Michael J. ;
Scarsi, Kimberly K. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2009, 53 (03) :1074-1079
[6]   Multicenter, Observational Cohort Study Evaluating Third-Generation Cephalosporin Therapy for Bloodstream Infections Secondary to Enterobacter, Serratia, and Citrobacter Species [J].
Derrick, Caroline ;
Bookstaver, P. Brandon ;
Lu, Zhiqiang K. ;
Bland, Christopher M. ;
King, S. Travis ;
Stover, Kayla R. ;
Rumley, Kathey ;
MacVane, Shawn H. ;
Swindler, Jenna ;
Kincaid, Scott ;
Branan, Trisha ;
Cluck, David ;
Britt, Benjamin ;
Pillinger, Kelly E. ;
Jones, Bruce M. ;
Fleming, Virginia ;
DiMondi, V. Paul ;
Estrada, Sandy ;
Crane, Brad ;
Odle, Brian ;
Al-Hasan, Majdi N. ;
Justo, Julie Ann .
ANTIBIOTICS-BASEL, 2020, 9 (05)
[7]   Epidemiology and Mechanisms of Resistance of Extensively Drug Resistant Gram-Negative Bacteria [J].
Eichenberger, Emily M. ;
Thaden, Joshua T. .
ANTIBIOTICS-BASEL, 2019, 8 (02)
[8]   Evaluation of Clinical Outcomes in Patients with Bloodstream Infections Due to Gram-Negative Bacteria According to Carbapenem MIC Stratification [J].
Esterly, John S. ;
Wagner, Jamie ;
McLaughlin, Milena M. ;
Postelnick, Michael J. ;
Qi, Chao ;
Scheetz, Marc H. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2012, 56 (09) :4885-4890
[9]   AmpC β-lactamase among Enterobacteriaceae: A new insight [J].
Etemadi, Shima ;
Leylabadlo, Hamed Ebrahimzadeh ;
Ghotaslou, Reza .
GENE REPORTS, 2020, 19
[10]   Epidemiology and Clinical Outcomes of Multidrug-resistant, Gram-negative Bloodstream Infections in a European Tertiary Pediatric Hospital During a 12-month Period [J].
Folgori, Laura ;
Livadiotti, Susanna ;
Carletti, Michaela ;
Bielicki, Julia ;
Pontrelli, Giuseppe ;
Degli Atti, Marta Luisa Ciofi ;
Bertaina, Chiara ;
Lucignano, Barbara ;
Ranno, Stefania ;
Carretto, Edoardo ;
Muraca, Maurizio ;
Sharland, Mike ;
Bernaschi, Paola .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2014, 33 (09) :929-932