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

Clinical Infectious Diseases - Tập 48 Số 1 - Trang 1-12 - 2009
Helen W. Boucher1, George H. Talbot2, John S. Bradley3,4, John E. Edwards5,6,7, David N. Gilbert8, Louis B. Rice9,10, Michael Scheld11, Brad Spellberg5,6,7, John G. Bartlett12
1Division of Geographic Medicine and Infectious Diseases, Tufts University and Tufts Medical Center, Boston, Massachusetts
2Talbot Advisors, Wayne, Pennsylvania
3Division of Infectious Diseases, Rady Children's Hospital , San Diego
4University of California at San Diego, San Diego
5Division of Infectious Diseases, Harbor—University of California at Los Angeles (UCLA) Medical Center, Los Angeles California
6Los Angeles Biomedical Research Institute, Torrance
7The David Geffen School of Medicine at UCLA, Los Angeles, California
8Division of Infectious Diseases, Providence Portland Medical Center and Oregon Health Sciences University, Portland
9Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio
10Medical Service, Louis Stokes Cleveland Veterans Administration Medical Center, Cleveland, Ohio
11Department of Medicine, University of Virginia School of Medicine, Charlottesville
12Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland

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10.1128/AAC.01169-07

10.1086/533452

10.1086/524891

10.1016/j.ajic.2004.10.001

10.1086/499367

10.1086/533590

10.1016/j.ijantimicag.2006.12.012

10.1086/421495

10.1086/588048

10.1086/429323

10.1016/S1473-3099(08)70018-5

10.1086/499819

PhRMA: medicines in development for infectious diseases. Washington, DC: Pharmaceutical Research and Manufacturers of America, 2007.

10.1086/420937

10.1517/13543784.16.2.137

Theravance announces positive results from phase 2 clinical study with investigational antibiotic in patients with complicated skin and skin structure infections: TD-1792 achieves primary endpoint. South San Francisco, CA: Theravance, 2007.

10.1086/526527

10.1086/587896

10.1086/379015

FDA issues approvable letter for ceftobiprole, a new anti-MRSA broad-spectrum antibiotic. 18 March 2008 ed. Basel, Switzerland: Basilea Pharmaceutica, 2008.

Theravance receives additional information regarding FDA cancellation of Advisory Committee Meeting. South San Francisco, CA: Theravance, 2008.

Food and Drug Administration. Advisory Committee Calendar. Available at: http://www.fda.gov/oc/advisory/accalendar/2008/2008ACcalendar.html#November. Accessed 13 November 2008.

United States Food and Drug Administration. Doripenem. Available at: http://www.fda.gov/cder/rdmt/InternetNME07.htm. Accessed 13 November 2008.

JS Solomkin, O Umeh, J Jiang, et al. Doripenem vs. meropenem with an option for oral step-down therapy in the treatment of complicated intra-abdominal infections [abstract L-487]. In: Proceedings of the 47th Interscience Conference on Antimicrobial Agents and Chemotherapy (Chicago, IL). Washington, DC: American Society of Microbiology, 2007.

Chastre J, 2008, Crit Care Med, 36, 1089, 10.1097/CCM.0b013e3181691b99

Johnson & Johnson. FDA requires additional information on DORIBAX for treatment of hospital-acquired pneumonia. Langhorne, PA: Johnson & Johnson, 2008.

10.1586/14787210.6.1.39

10.1128/AAC.49.8.3239-3250.2005

PTK 0796 completed a randomized, evaluator200 patient phase 2 complicated skin and skin structure infection (cSSSI) clinical study with IV and oral step-down therapy compared to Zyvox. Boston: Paratek, 2007.

Macone A, Donatelli J, Dumont T, Levy S, Tanaka S. In-vitro activity of PTK0796 against gram-positive and gram-negative organisms. In: Proceedings of the 43rd Interscience Conference on Antimicrobial Agents and Chemotherapy (Chicago, IL). Washington, DC: American Society of Microbiology, 2003.

Traczewski M, Brown S. PTK0796: in vitro potency and spectrum of activity compared to ten other antimicrobial compounds. In: Proceedings of the 43rd Interscience Conference on Antimicrobial Agents and Chemotherapy (Chicago, IL). Washington, DC: American Society of Microbiology, 2003.

Sahm D, Draghi D, Thornsberry C. Activity of ME1036, a novel anti-MRSA carbapenem, against gram-positive and gram-negative pathogens. In: Proceedings of the 46th Interscience Conference on Antimicrobial Agents and Chemotherapy (San Francisco, CA). Washington, DC: American Society of Microbiology, 2006.

Kurazono M, Hirai Y, Takahata S, etal Efficacy of ME1036 against Enterobacteriaceae harboring a variety of beta-lactamases including ESBLs [abstract F-331]. In: Proceedings of the 44th Interscience Conference on Antimicrobial Agents and Chemotherapy. Washington, DC: American Society of Microbiology, 2004:197.

Brown SD, Traczewski MM. ME1036: in vitro potency and spectrum of activity [abstract F1-342]. In: Proceedings of the 47th Interscience Conference on Antimicrobial Agents and Chemotherapy (Chicago, IL). Washington, DC: American Society of Microbiology, 2007.

Pace J, Stevens T, Hamrick J, Hoban D, Bouchillon S, Xerri L. PZ-601 susceptibility of gram-positive pathogens causative for systemic and respiratory infections [abstract F1-230]. In: Proceedings of the 46th Interscience Conference on Antimicrobial Agents and Chemotherapy (San Francisco, CA). Washington, DC: American Society of Microbiology, 2006.

Pace J, Stevens T, Hoban D, etal PZ-601 susceptibility of important gram-negative bacterial species causative for community-acquired pneumonia (CAP), complicated skin and skin structure infections (cSSSI), and intra-abdominal infections (IAI) [abstract F1-229]. In: Proceedings of the 46th Interscience Conference on Antimicrobial Agents and Chemotherapy (San Francisco, CA). Washington, DC: American Society of Microbiology, 2006.

Protez pharmaceuticals to be acquired by Novartis. Malvern, PA: Protez Pharmaceuticals, 2008.

Page M, Desarbre E, Geier C, Hofer B. Activity of BAL30376 against gram-negative bacteria [abstract F1-229]. In: Proceedings of the 47th Interscience Conference on Antimicrobial Agents and Chemotherapy (Chicago, IL). Washington, DC: American Society of Microbiology, 2007.

Bowker K, Noel AR, MacGowan A, Walsh TR. In vitro potency of BAL30376 against gram-negative bacilli (GNB) [abstract F1-313]. In: Proceedings of the 47th Interscience Conference on Antimicrobial Agents and Chemotherapy (Chicago, IL). Washington, DC: American Society of Microbiology, 2007.

Schmitt-Hoffmann A, Gebhardt K, Gaucher B, Desarbre E, Page M. Efficacy of BAL30376 in a murine model of gram-negative sepsis [abstract F1-315]. In: Proceedings of the 47th Interscience Conference on Antimicrobial Agents and Chemotherapy (Chicago, IL). Washington, DC: American Society of Microbiology, 2007.

Ishii Y, Sugihara S, Tateda K, Yamaguchi K. In vitro synergistic effects of combinations of CP3242, as a novel metallo-beta-lactamase inhibitor, and carbapenems against carbapenemase producing organisms [abstract F1-331]. In: Proceedings of the 47th Interscience Conference on Antimicrobial Agents and Chemotherapy (Chicago, IL). Washington, DC: American Society of Microbiology, 2007.

Osaki Y, Morinaka A, Mikuniya K, etal CP3242, a novel metallo-beta-lactamase inhibitor: in vitro and in vivo efficacy against clinically isolated metallo-beta-lactamase-producing P. aeruginosa [abstract F1-332]. In: Proceedings of the 47th Interscience Conference on Antimicrobial Agents and Chemotherapy (Chicago, IL). Washington, DC: American Society of Microbiology, 2007.

Muto Y, Matsumoto K, Morinaka A, etal CP3242, a novel metallo-beta-lactamase inhibitor: pharmacokinetics and in vivo pharmacodynamic activities against metallo-beta-lactamase-producing P. aeruginosa in a murine thigh infection model [abstract F1-333]. In: Proceedings of the 47th Interscience Conference on Antimicrobial Agents and Chemotherapy (Chicago, IL). Washington, DC: American Society of Microbiology, 2007.

10.1128/AAC.00096-06

10.1128/AAC.00570-07

10.1016/j.jpeds.2007.04.060

10.1097/01.inf.0000180504.66437.1f

10.1086/421946

10.1086/520192

10.1097/01.idc.0000226868.52136.24

10.1086/523588

10.1592/phco.26.3.347

10.1086/533593

10.1086/587893

10.1086/586746

10.1128/AAC.50.4.1599-1602.2006

10.1086/520655

10.1016/S0140-6736(01)05410-1

10.1016/S1473-3099(08)70041-0

10.1056/NEJMra041359

10.1128/AAC.50.4.1257-1262.2006

10.1093/jac/dkm318

10.1097/CCM.0b013e31816a130d

10.1001/archinte.165.12.1430

10.1046/j.1469-0691.2002.00401.x

10.1086/522288

10.1086/497831

10.1016/j.tim.2006.07.008

10.1128/CMR.18.4.657-686.2005

10.1093/jac/dki175

10.1086/512370

10.1086/522287

10.1056/NEJMra070741

10.1128/AAC.01464-06

10.1086/529198

10.1086/431672

10.1592/phco.27.7.980

10.1093/jac/dkl441

10.1128/AAC.01198-06

Maroko R, Cooper A, Dukart G, Dartois N, Gandjini H. Results of phase 3 study comparing a tigecycline (TGC) regimen with an imipenem/cilastatin (IMI) regimen in treatment of patients (Pts) with hospital-acquired pneumonia (HAP). In: Proceedings of the 47th Interscience Conference on Antimicrobial Agents and Chemotherapy (Chicago, IL). Washington, DC: American Society of Microbiology, 2007.

10.1001/jama.289.7.885

10.1128/AAC.46.9.2920-2925.2002

10.1089/mdr.2006.12.223

10.1016/j.diagmicrobio.2006.02.009

Lin YC, 2006, J Microbiol Immunol Infect, 39, 67

10.1128/AAC.49.2.776-778.2005

10.1016/j.diagmicrobio.2005.06.010

10.1016/j.jinf.2008.01.003

10.1126/science.321.5887.356

10.1038/nrd2618

GlaxoSmithKline and Mpex Pharmaceuticals form alliance to develop novel efflux pump inhibitors for use against serious gram-negative infections. London, and San Diego: GlaxoSmithKline, 2008.

Novexel and Forest Laboratories announce license agreement for NXL104, a novel broad-spectrum beta lactamase inhibitor. Paris: Novexel, 2008.

FDA guidance documents. Rockville, MD: US Food and Drug Administration, 2008. Available at: http://www.fda.gov/cder/guidance/. Accessed 13 November 2008.

Clinical trial design for community-acquired pneumonia: public workshop, January 17-18, 2008. Rockville, MD: US Food and Drug Administration, 2008. Available at: http://www.fda.gov/CDER/meeting/CAP/presentations.htm. Accessed 13 November 2008.

10.1086/591411

10.1086/591389

Wellcome Trust and GlaxoSmithKline announce partnership to target drug-resistant hospital infections. Oxford, UK: Wellcome Trust, 2007.