There should be no ESKAPE for febrile neutropenic cancer patients: the dearth of effective antibacterial drugs threatens anticancer efficacy

被引:33
作者
Bow, E. J. [1 ,2 ,3 ,4 ]
机构
[1] Univ Manitoba, Dept Med Microbiol & Infect Dis, Winnipeg, MB, Canada
[2] Univ Manitoba, Dept Internal Med, Winnipeg, MB, Canada
[3] CancerCare Manitoba, Infect Control Serv, Winnipeg, MB R3E 0V9, Canada
[4] CancerCare Manitoba, Manitoba Blood & Marrow Transplant Programme, Winnipeg, MB R3E 0V9, Canada
关键词
multi-drug resistance; extended-spectrum; -lactamase; carbapenemase; Gram-negative bacilli; Gram-positive cocci; MRSA; VISA; INFECTIOUS-DISEASES SOCIETY; ANTIMICROBIAL RESISTANCE; ENTEROCOCCAL BACTEREMIA; CLINICAL-FEATURES; MORTALITY; THERAPY; HEALTH; RISK; CHALLENGES; EMERGENCE;
D O I
10.1093/jac/dks512
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The success of modern anticancer treatment is a composite function of enhanced efficacy of surgical, radiation and systemic treatment strategies and of our collective clinical abilities in supporting patients through the perils of their cancer journeys. Despite the widespread availability of antibacterial therapies, the threat of community- or healthcare facility-acquired bacterial infection remains a constant risk to patients during this journey. The rising prevalence of colonization by multidrug-resistant (MDR) bacteria in the population, acquired through exposure from endemic environments, antimicrobial stewardship and infection prevention and control strategies notwithstanding, increases the likelihood that such organisms may be the cause of cancer treatment-related infection and the likelihood of antibacterial treatment failure. The high mortality associated with invasive MDR bacterial infection increases the likelihood that many patients may not survive long enough to reap the benefits of enhanced anticancer treatments, thus threatening the societal investment in the cancer journey. Since cancer care providers arguably no longer have, and are unlikely to have in the foreseeable future, the antibacterial tools to reliably rescue patients from harms way, the difficult ethical debate over the risks and benefits of anticancer treatments must now be reopened.
引用
收藏
页码:492 / 495
页数:4
相关论文
共 50 条
[1]   Mucosal barrier injury: biology, pathology, clinical counterparts and consequences of intensive treatment for haematological malignancy: an overview [J].
Blijlevens, NMA ;
Donnelly, JP ;
De Pauw, BE .
BONE MARROW TRANSPLANTATION, 2000, 25 (12) :1269-1278
[2]   Attributable Mortality Rate for Carbapenem-Resistant Klebsiella pneumoniae Bacteremia [J].
Borer, Abraham ;
Saidel-Odes, Lisa ;
Riesenberg, Klaris ;
Eskira, Seada ;
Peled, Nejama ;
Nativ, Ronit ;
Schlaeffer, Francisc ;
Sherf, Michael .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2009, 30 (10) :972-976
[3]   Bad Bugs, No Drugs: No ESKAPE! An Update from the Infectious Diseases Society of America [J].
Boucher, Helen W. ;
Talbot, George H. ;
Bradley, John S. ;
Edwards, John E., Jr. ;
Gilbert, David ;
Rice, Louis B. ;
Scheld, Michael ;
Spellberg, Brad ;
Bartlett, John .
CLINICAL INFECTIOUS DISEASES, 2009, 48 (01) :1-12
[4]   Intestinal mucosal dysfunction and infection during remission-induction therapy for acute myeloid leukaemia [J].
Bow, E. J. ;
Meddings, J. B. .
LEUKEMIA, 2006, 20 (12) :2087-2092
[5]  
BOW EJ, 1987, CAN MED ASSOC J, V137, P397
[6]   Improving known classes of antibiotics: an optimistic approach for the future [J].
Bush, Karen .
CURRENT OPINION IN PHARMACOLOGY, 2012, 12 (05) :527-534
[7]   Tackling antibiotic resistance [J].
Bush, Karen ;
Courvalin, Patrice ;
Dantas, Gautam ;
Davies, Julian ;
Eisenstein, Barry ;
Huovinen, Pentti ;
Jacoby, George A. ;
Kishony, Roy ;
Kreiswirth, Barry N. ;
Kutter, Elizabeth ;
Lerner, Stephen A. ;
Levy, Stuart ;
Lewis, Kim ;
Lomovskaya, Olga ;
Miller, Jeffrey H. ;
Mobashery, Shahriar ;
Piddock, Laura J. V. ;
Projan, Steven ;
Thomas, Christopher M. ;
Tomasz, Alexander ;
Tulkens, Paul M. ;
Walsh, Timothy R. ;
Watson, James D. ;
Witkowski, Jan ;
Witte, Wolfgang ;
Wright, Gerry ;
Yeh, Pamela ;
Zgurskaya, Helen I. .
NATURE REVIEWS MICROBIOLOGY, 2011, 9 (12) :894-896
[8]   Clinical features associated with bacteremia due to heterogeneous vancomycin-intermediate Staphylococcus aureus [J].
Charles, PGP ;
Ward, PB ;
Johnson, PDR ;
Howden, BP ;
Grayson, ML .
CLINICAL INFECTIOUS DISEASES, 2004, 38 (03) :448-451
[9]   The relationship between antimicrobial resistance and patient outcomes: Mortality, length of hospital stay, and health care costs [J].
Cosgrove, SE .
CLINICAL INFECTIOUS DISEASES, 2006, 42 :S82-S89
[10]   Vancomycin dosage optimization in patients with malignant haematological disease by pharmacokineticpharmacodynamic analysis [J].
Gatta M.D.M.F.D. ;
Buelga D.S. ;
Navarro A.S. ;
Dominguez-Gil A. ;
García M.J. .
Clinical Pharmacokinetics, 2009, 48 (4) :273-280