First-generation fluoroquinolone use and subsequent emergence of multiple drug-resistant bacteria in the intensive care unit

被引:88
作者
Nseir, S [1 ]
Di Pompeo, C
Soubrier, S
Delour, P
Lenci, H
Roussel-Delvallez, M
Onimus, T
Saulnier, F
Mathieu, D
Durocher, A
机构
[1] Reg Univ Ctr, Calmette Hosp, Intens Care Unit, Lille, France
[2] Reg Univ Ctr, Calmette Hosp, Bacteriol Lab, Lille, France
[3] Univ Lille 2, Med Assessment Lab, Lille, France
关键词
fluoroquinolones; multiple drug-resistant bacteria; intensive care unit; antibiotic resistance;
D O I
10.1097/01.CCM.0000152230.53473.A1
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: The objective of this study was to determine the relationship between fluoroquinolone (FQ) use and subsequent emergence of multiple drug-resistant bacteria (MRB) in the intensive care unit (ICU). Design. The authors conducted a prospective observational cohort study and a case control study. Setting: The study was conducted in a 30-bed ICU. Methods: All immunocompetent patients hospitalized for >48 hrs who did not receive antibiotics before ICU admission were eligible during a 15-month period. Routine MRB screening was performed at ICU admission and weekly thereafter. This screening included tracheal aspirate and nasal, anal, and axilla swabs. Univariate and multivariate analyses were used to determine risk factors for MRB emergence in the ICU. In addition, a case control study was performed to determine whether FQ use is associated with subsequent emergence of MRB. Results: Two hundred thirty-nine patients were included; 108 ICU-acquired MRB were isolated in 77 patients. FQ use and longer duration of antibiotic treatment were identified as independent risk factors for MB occurrence (odds ratio [95% confidence interval [CI] = 3.3[1.7-6.5], 1.1[1.0-1.2]; p < .001; respectively). One hundred thirty-five (56%) patients received FQ; matching was successful for 72(53%) of them. Number of MRB (40 vs. 15 per 1,000 ICU days; p = .019) and percentage of patients with MRB (40% vs. 22%; OR [95% CI] = 1.5[1.0-2.4]; p = .028) were significantly higher in cases than in controls. Although methicillin-resistant Staphylococcus aureus (26% vs. 12%; OR [95% CI] = 1.6[.6-2.9]; p = .028) and extending-spectrum beta-lactamase-producing Gram-negative bacilli (11% vs. 1%; OR [95% CI] = 4.7 [0.7-30.2]; p = .017) rates were higher in cases than in controls, ceftazidime or imipenem-resistant Pseudomonas aeruginosa (15% vs. 8%), Acinetobacter baumannii (1% vs. 5%), and Stenotrophomonas maltophilia (2% vs. 1%) rates were similar (p > .05) in case and control patients. Conclusion. FQ use and longer duration of antibiotic treatment are independently associated with MRB emergence. Reducing antimicrobial treatment duration and restricting FQ use could be suggested to control MRB spread in the ICU.
引用
收藏
页码:283 / 289
页数:7
相关论文
共 34 条
  • [1] Induction of fibronectin-binding proteins and increased adhesion of quinolone-resistant Staphylococcus aureus by subinhibitory levels of ciprofloxacin
    Bisognano, C
    Vaudaux, P
    Rohner, P
    Lew, DP
    Hooper, DC
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (06) : 1428 - 1437
  • [2] Antibiotic use and the prevalence of antibiotic resistance in bacteria from healthy volunteers in the Dutch community
    Bruinsma, N
    Stobberingh, E
    de Smet, P
    van den Bogaard, A
    [J]. INFECTION, 2003, 31 (01) : 9 - 14
  • [3] Comparison of 8 vs 15 days of antibiotic therapy for ventilator-associated pneumonia in adults - A randomized trial
    Chastre, J
    Wolff, M
    Fagon, JY
    Chevret, S
    Thomas, F
    Wermert, D
    Clementi, E
    Gonzalez, J
    Jusserand, D
    Asfar, P
    Perrin, D
    Fieux, F
    Aubas, S
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 290 (19): : 2588 - 2598
  • [4] Methicillin-resistant Staphylococcus aureus and antimicrobial use in Belgian hospitals
    Crowcroft, NS
    Ronveaux, O
    Monnet, DL
    Mertens, R
    [J]. INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 1999, 20 (01) : 31 - 36
  • [5] A CASE-CONTROL STUDY OF AN OUTBREAK OF INFECTIONS CAUSED BY KLEBSIELLA-PNEUMONIAE STRAINS PRODUCING CTX-1 (TEM-3) BETA-LACTAMASE
    DECHAMPS, C
    ROUBY, D
    GUELON, D
    SIROT, J
    SIROT, D
    BEYTOUT, D
    GOURGAND, JM
    [J]. JOURNAL OF HOSPITAL INFECTION, 1991, 18 (01) : 5 - 13
  • [6] Clinical impact of pneumonia caused by Acinetobacter baumannii in intubated patients:: A matched cohort study
    Garnacho, J
    Sole-Violan, J
    Sa-Borges, M
    Diaz, E
    Rello, J
    [J]. CRITICAL CARE MEDICINE, 2003, 31 (10) : 2478 - 2482
  • [7] CDC DEFINITIONS FOR NOSOCOMIAL INFECTIONS, 1988
    GARNER, JS
    JARVIS, WR
    EMORI, TG
    HORAN, TC
    HUGHES, JM
    [J]. AMERICAN JOURNAL OF INFECTION CONTROL, 1988, 16 (03) : 128 - 140
  • [8] Risk factors associated with nosocomial methicillin-resistant Staphylococcus aureus (MRSA) infection including previous use of antimicrobials
    Graffunder, EM
    Venezia, RA
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 49 (06) : 999 - 1005
  • [9] Risk factors for persistent carriage of methicillin-resistant Staphylococcus aureus
    Harbarth, S
    Liassine, N
    Dharan, S
    Herrault, P
    Auckenthaler, R
    Pittet, D
    [J]. CLINICAL INFECTIOUS DISEASES, 2000, 31 (06) : 1380 - 1385
  • [10] Excretion of ciprofloxacin in sweat and multiresistant Staphylococcus epidermidis
    Holby, N
    Jarlov, JO
    Kemp, M
    Tvede, M
    Bangsborg, JM
    Kjerulf, A
    Pers, C
    Hansen, H
    [J]. LANCET, 1997, 349 (9046) : 167 - 169