Literature DB >> 32179519

Ceftobiprole Activity against Bacteria from Skin and Skin Structure Infections in the United States from 2016 through 2018.

Robert K Flamm1, Leonard R Duncan2, Kamal A Hamed3, Jennifer I Smart3, Rodrigo E Mendes1, Michael A Pfaller1,4.   

Abstract

Ceftobiprole medocaril is an advanced-generation cephalosporin prodrug that has qualified infectious disease product status granted by the US FDA and is currently being evaluated in phase 3 clinical trials in patients with acute bacterial skin and skin structure infections (ABSSSIs) and in patients with Staphylococcus aureus bacteremia. In this study, the activity of ceftobiprole and comparators was evaluated against more than 7,300 clinical isolates collected in the United States from 2016 through 2018 from patients with skin and skin structure infections. The major species/pathogen groups were S. aureus (53%), Enterobacterales (23%), Pseudomonas aeruginosa (7%), beta-hemolytic streptococci (6%), Enterococcus spp. (4%), and coagulase-negative staphylococci (2%). Ceftobiprole was highly active against S. aureus (MIC50/90, 0.5/1 mg/liter; 99.7% susceptible by EUCAST criteria; 42% methicillin-resistant S. aureus [MRSA]). Ceftobiprole also exhibited potent activity against other Gram-positive cocci. The overall susceptibility of Enterobacterales to ceftobiprole was 84.8% (>99.0% susceptible for isolate subsets that exhibited a non-extended-spectrum β-lactamase [ESBL] phenotype). A total of 74.4% of P. aeruginosa, 100% of beta-hemolytic streptococci and coagulase-negative staphylococci, and 99.6% of Enterococcus faecalis isolates were inhibited by ceftobiprole at ≤4 mg/liter. As expected, ceftobiprole was largely inactive against Enterobacterales that contained ESBL genes and Enterococcus faecium Overall, ceftobiprole was highly active against most clinical isolates from the major Gram-positive and Gram-negative skin and skin structure pathogen groups collected at U.S. medical centers participating in the SENTRY Antimicrobial Surveillance Program during 2016 to 2018. The broad-spectrum activity of ceftobiprole, including potent activity against MRSA, supports its further evaluation for a potential ABSSSI indication.
Copyright © 2020 American Society for Microbiology.

Entities:  

Keywords:  ABSSSI; MRSA; SSTI; ceftobiprole; cephalosporin; skin; surveillance

Mesh:

Substances:

Year:  2020        PMID: 32179519      PMCID: PMC7269461          DOI: 10.1128/AAC.02566-19

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  27 in total

1.  Comparative activity of ceftobiprole against Gram-positive and Gram-negative isolates from Europe and the Middle East: the CLASS study.

Authors:  Gian M Rossolini; Matthew S Dryden; Roman S Kozlov; Alvaro Quintana; Robert K Flamm; Jörg M Läuffer; Emma Lee; Ian Morrissey
Journal:  J Antimicrob Chemother       Date:  2011-01       Impact factor: 5.790

Review 2.  Complicated skin and soft tissue infection.

Authors:  Matthew S Dryden
Journal:  J Antimicrob Chemother       Date:  2010-11       Impact factor: 5.790

3.  Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America.

Authors:  Dennis L Stevens; Alan L Bisno; Henry F Chambers; E Patchen Dellinger; Ellie J C Goldstein; Sherwood L Gorbach; Jan V Hirschmann; Sheldon L Kaplan; Jose G Montoya; James C Wade
Journal:  Clin Infect Dis       Date:  2014-07-15       Impact factor: 9.079

4.  In vitro activity of ceftobiprole against frequently encountered aerobic and facultative Gram-positive and Gram-negative bacterial pathogens: results of the CANWARD 2007-2009 study.

Authors:  Andrew Walkty; Heather J Adam; Michel Laverdière; James A Karlowsky; Daryl J Hoban; George G Zhanel
Journal:  Diagn Microbiol Infect Dis       Date:  2011-03       Impact factor: 2.803

5.  In vitro and in vivo properties of Ro 63-9141, a novel broad-spectrum cephalosporin with activity against methicillin-resistant staphylococci.

Authors:  P Hebeisen; I Heinze-Krauss; P Angehrn; P Hohl; M G Page; R L Then
Journal:  Antimicrob Agents Chemother       Date:  2001-03       Impact factor: 5.191

6.  Binding of ceftobiprole and comparators to the penicillin-binding proteins of Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Streptococcus pneumoniae.

Authors:  Todd A Davies; Malcolm G P Page; Wenchi Shang; Ted Andrew; Malgosia Kania; Karen Bush
Journal:  Antimicrob Agents Chemother       Date:  2007-04-30       Impact factor: 5.191

Review 7.  Cephalosporins in clinical development.

Authors:  Malcolm G P Page
Journal:  Expert Opin Investig Drugs       Date:  2004-08       Impact factor: 6.206

8.  The Importance of Antimicrobial Resistance Monitoring Worldwide and the Origins of SENTRY Antimicrobial Surveillance Program.

Authors:  Andrew S Fuhrmeister; Ronald N Jones
Journal:  Open Forum Infect Dis       Date:  2019-03-15       Impact factor: 3.835

9.  A prospective, multicenter, observational study of complicated skin and soft tissue infections in hospitalized patients: clinical characteristics, medical treatment, and outcomes.

Authors:  Benjamin A Lipsky; Gregory J Moran; Lena M Napolitano; Lien Vo; Susan Nicholson; Myoung Kim
Journal:  BMC Infect Dis       Date:  2012-09-25       Impact factor: 3.090

10.  Incidence, microbiology, and patient characteristics of skin and soft-tissue infections in a U.S. population: a retrospective population-based study.

Authors:  Gary Thomas Ray; Jose Antonio Suaya; Roger Baxter
Journal:  BMC Infect Dis       Date:  2013-05-30       Impact factor: 3.090

View more
  1 in total

1.  The antimicrobial activity of ceftobiprole against Methicillin-resistant Staphylococcus aureus and multi-drug resistant Pseudomonas aeruginosa: A large tertiary care university hospital experience in Riyadh, Saudi Arabia.

Authors:  Lamees A Altamimi; Leen A Altamimi; Ali M Somily
Journal:  Saudi Med J       Date:  2022-01       Impact factor: 1.422

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.