Bad Bugs, No Drugs: No ESKAPE! An Update from the Infectious Diseases Society of America

被引:3991
作者
Boucher, Helen W. [1 ,2 ]
Talbot, George H. [3 ]
Bradley, John S. [4 ,5 ]
Edwards, John E., Jr. [6 ,7 ,8 ]
Gilbert, David [9 ,10 ]
Rice, Louis B. [11 ,12 ]
Scheld, Michael [13 ]
Spellberg, Brad [6 ,7 ,8 ]
Bartlett, John [14 ]
机构
[1] Tufts Med Ctr, Div Geog Med & Infect Dis, Boston, MA 02111 USA
[2] Tufts Univ, Div Geog Med & Infect Dis, Boston, MA 02111 USA
[3] Talbot Advisors, Wayne, PA USA
[4] Rady Childrens Hosp San Diego, Div Infect Dis, San Diego, CA USA
[5] Univ Calif San Diego, San Diego, CA 92103 USA
[6] Harbor Univ Calif Los Angeles, Med Ctr, Div Infect Dis, Los Angeles, CA USA
[7] Los Angeles Biomed Res Inst, Torrance, CA USA
[8] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
[9] Providence Portland Med Ctr, Div Infect Dis, Portland, OR USA
[10] Oregon Hlth & Sci Univ, Portland, OR 97201 USA
[11] Louis Stokes Cleveland Vet Adm Med Ctr, Med Serv, Cleveland, OH USA
[12] Case Western Reserve Univ, Sch Med, Dept Med, Cleveland, OH 44106 USA
[13] Univ Virginia, Sch Med, Dept Med, Charlottesville, VA 22908 USA
[14] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
关键词
BLOOD-STREAM INFECTIONS; RESISTANT STAPHYLOCOCCUS-AUREUS; VENTILATOR-ASSOCIATED PNEUMONIA; GRAM-NEGATIVE BACTERIA; METALLO-BETA-LACTAMASE; INTENSIVE-CARE UNITS; KLEBSIELLA-PNEUMONIAE; DOUBLE-BLIND; ANTIMICROBIAL RESISTANCE; ACINETOBACTER-BAUMANNII;
D O I
10.1086/595011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The Infectious Diseases Society of America (IDSA) continues to view with concern the lean pipeline for novel therapeutics to treat drug-resistant infections, especially those caused by gram-negative pathogens. Infections now occur that are resistant to all current antibacterial options. Although the IDSA is encouraged by the prospect of success for some agents currently in preclinical development, there is an urgent, immediate need for new agents with activity against these panresistant organisms. There is no evidence that this need will be met in the foreseeable future. Furthermore, we remain concerned that the infrastructure for discovering and developing new antibacterials continues to stagnate, thereby risking the future pipeline of antibacterial drugs. The IDSA proposed solutions in its 2004 policy report," Bad Bugs, No Drugs: As Antibiotic R&D Stagnates, a Public Health Crisis Brews,"and recently issued a "Call to Action" to provide an update on the scope of the problem and the proposed solutions. A primary objective of these periodic reports is to encourage a community and legislative response to establish greater financial parity between the antimicrobial development and the development of other drugs. Although recent actions of the Food and Drug Administration and the 110th US Congress present a glimmer of hope, significant uncertainly remains. Now, more than ever, it is essential to create a robust and sustainable antibacterial research and development infrastructure-one that can respond to current antibacterial resistance now and anticipate evolving resistance. This challenge requires that industry, academia, the National Institutes of Health, the Food and Drug Administration, the Centers for Disease Control and Prevention, the US Department of Defense, and the new Biomedical Advanced Research and Development Authority at the Department of Health and Human Services work productively together. This report provides an update on potentially effective antibacterial drugs in the late-stage development pipeline, in the hope of encouraging such collaborative action.
引用
收藏
页码:1 / 12
页数:12
相关论文
共 97 条
[1]
Good clinical outcomes but high rates of adverse reactions during linezolid therapy for serious infections: a proposed protocol for monitoring therapy in complex patients [J].
Bishop, E ;
Melvani, S ;
Howden, BP ;
Charles, PGP ;
Grayson, ML .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (04) :1599-1602
[2]
Multicenter study to assess safety and efficacy of INH-A21 a donor-selected human staphylococcal immunoglobulin, for prevention of nosocomial infections in very low birth weight infants [J].
Bloom, B ;
Schelonka, R ;
Kueser, T ;
Walker, W ;
Jung, E ;
Kaufman, D ;
Kesler, K ;
Roberson, D ;
Patti, J ;
Hetherington, S .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2005, 24 (10) :858-866
[3]
Epidemiology of methicillin-resistant Staphylococcus aureus [J].
Boucher, Helen W. ;
Corey, G. Ralph .
CLINICAL INFECTIOUS DISEASES, 2008, 46 :S344-S349
[4]
Perspectives on daptomycin resistance, with emphasis on resistance in Staphylococcus aureus [J].
Boucher, Helen W. ;
Sakoulas, George .
CLINICAL INFECTIOUS DISEASES, 2007, 45 (05) :601-608
[5]
BOWKER K, 2007, P 47 INT C ANT AG CH
[6]
Emergence of carbapenem-resistant Klebsiella species possessing the class A carbapenem-hydrolyzing KPC-2 and inhibitor-resistant TEM-30 β-lactamases in New York City [J].
Bradford, PA ;
Bratu, S ;
Urban, C ;
Visalli, M ;
Mariano, N ;
Landman, D ;
Rahal, JJ ;
Brooks, S ;
Cebular, S ;
Quale, J .
CLINICAL INFECTIOUS DISEASES, 2004, 39 (01) :55-60
[7]
Carbapenemase-producing Klebsiella pneumoniae in Brooklyn, NY:: molecular epidemiology and in vitro activity of polymyxin B and other agents [J].
Bratu, S ;
Tolaney, P ;
Karumudi, U ;
Quale, J ;
Mooty, M ;
Nichani, S ;
Landman, D .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 56 (01) :128-132
[8]
Detection of KPC carbapenem-hydrolyzing enzymes in Enterobacter spp. from Brooklyn, New York [J].
Bratu, S ;
Landman, D ;
Alam, M ;
Tolentino, E ;
Quale, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (02) :776-778
[9]
Rapid spread of carbapenem-resistant Klebsiella pneumoniae in New York City -: A new threat to our antibiotic armamentarium [J].
Bratu, S ;
Landman, D ;
Haag, R ;
Recco, R ;
Eramo, A ;
Alam, M ;
Quale, J .
ARCHIVES OF INTERNAL MEDICINE, 2005, 165 (12) :1430-1435
[10]
Detection and spread of Escherichia coli possessing the plasmid-borne carbapenemase KPC-2 in Brooklyn, New York [J].
Bratu, Simona ;
Brooks, Steven ;
Burney, Sibte ;
Kochar, Sandeep ;
Gupta, Jyoti ;
Landman, David ;
Quale, John .
CLINICAL INFECTIOUS DISEASES, 2007, 44 (07) :972-975