Is antibiotic cycling the answer to preventing the emergence of bacterial resistance in the intensive care unit?

被引:67
作者
Kollef, Marin H. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Internal Med, Barnes Jewish Hosp,Pulm & Crit Care Div, St Louis, MO 63110 USA
关键词
D O I
10.1086/504484
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antibiotic resistance has emerged as an important determinant of mortality for patients in the intensive care unit (ICU) setting. This is largely due to the increasing presence of pathogenic microorganisms with resistance to existing antibiotic agents, resulting in the administration of inappropriate treatment. Escalating antibiotic resistance has also been associated with greater overall health care costs, as a result of prolonged hospitalizations and convalescence associated with failure of antibiotic treatment, the need to develop new antibiotic agents, and the implementation of broader infection control and public health interventions aimed at curbing the spread of antibiotic-resistant pathogens. Antibiotic cycling has been advocated as a tool to reduce the occurrence of antibiotic resistance, especially in the ICU setting. Unfortunately, the cumulative evidence to date suggests that antibiotic cycling has limited efficacy for preventing antibiotic resistance. Nevertheless, a strategy whereby multiple or all classes of antibiotics are available for use (i.e., antibiotic heterogeneity) can be part of a broader effort aimed at curtailing antibiotic resistance within ICUs. Such efforts should be routine, given the limited availability of new antibiotic drug classes for the foreseeable future.
引用
收藏
页码:S82 / S88
页数:7
相关论文
共 80 条
[1]   Doxycycline is a cost-effective therapy for hospitalized patients with community-acquired pneumonia [J].
Ailani, RK ;
Agastya, G ;
Ailani, RK ;
Mukunda, BN ;
Shekar, R .
ARCHIVES OF INTERNAL MEDICINE, 1999, 159 (03) :266-270
[2]   Modification of empiric antibiotic treatment in patients with pneumonia acquired in the intensive care unit [J].
AlvarezLerma, F ;
Pellus, AM ;
Sanchez, BA ;
Ortiz, EP ;
Jorda, R ;
Barcenilla, F ;
Maravi, E ;
Galvan, B ;
Palomar, M ;
Serra, J ;
Bermejo, B ;
Mateu, A ;
Quintana, E ;
Palacios, MS ;
Giral, R ;
Gonzalez, V ;
Lerma, FA ;
Mesa, JL ;
Melgarejo, JA ;
Martinez, J ;
Insausti, J ;
Olaechea, P ;
Chanovas, M ;
Gilabert, A ;
Junquera, C ;
Valles, J ;
Palacios, F ;
Calvo, R ;
Mesalles, E ;
Nava, J ;
Santos, A ;
Armengol, S ;
Marzo, D .
INTENSIVE CARE MEDICINE, 1996, 22 (05) :387-394
[3]   Antimicrobial resistance in isolates from inpatients and outpatients in the united states: Increasing importance of the intensive care unit [J].
Archibald, L ;
Phillips, L ;
Monnet, D ;
McGowan, JE ;
Tenover, F ;
Gaynes, R .
CLINICAL INFECTIOUS DISEASES, 1997, 24 (02) :211-215
[4]  
Bailey TC, 1997, PHARMACOTHERAPY, V17, P277
[5]   Ecological theory suggests that antimicrobial cycling will not reduce antimicrobial resistance in hospitals [J].
Bergstrom, CT ;
Lo, M ;
Lipsitch, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (36) :13285-13290
[6]   Multi-resistant Gram-negative bacilli:: from epidemics to endemics [J].
Cantón, R ;
Coque, TM ;
Baquero, F .
CURRENT OPINION IN INFECTIOUS DISEASES, 2003, 16 (04) :315-325
[7]   Epidemiology and control of antibiotic resistance in the intensive care unit [J].
Carlet, J ;
Ben Ali, A ;
Chalfine, A .
CURRENT OPINION IN INFECTIOUS DISEASES, 2004, 17 (04) :309-316
[8]   Methicillin-resistant Staphylococcus aureus (MRSA) with reduced susceptibility to glycopeptides (GISA) in 63 French general hospitals [J].
Cartolano, GL ;
Cheron, M ;
Benabid, D ;
Leneveu, M ;
Boisivon, A .
CLINICAL MICROBIOLOGY AND INFECTION, 2004, 10 (05) :448-451
[9]   Effectiveness of combination antimicrobial therapy for Pseudomonas aeruginosa bacteremia [J].
Chamot, E ;
El Amari, EB ;
Rohner, P ;
Van Delden, C .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (09) :2756-2764
[10]   Comparison of 8 vs 15 days of antibiotic therapy for ventilator-associated pneumonia in adults - A randomized trial [J].
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 .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 290 (19) :2588-2598