Literature DB >> 12834367

Clinical role of beta-lactam/beta-lactamase inhibitor combinations.

Nelson Lee1, Kwok-Yung Yuen, Cyrus R Kumana.   

Abstract

The use of beta-lactamase inhibitors in combination with beta-lactam antibiotics is currently the most successful strategy to combat a specific resistance mechanism. Their broad spectrum of activity originates from the ability of respective inhibitors to inactivate a wide range of beta-lactamases produced by Gram-positive, Gram-negative, anaerobic and even acid-fast pathogens. Clinical experience confirms their effectiveness in the empirical treatment of respiratory, intra-abdominal, and skin and soft tissue infections. There is evidence to suggest that they are efficacious in treating patients with neutropenic fever and nosocomial infections, especially in combination with other agents. beta-Lactam/beta-lactamase inhibitor combinations are particularly useful against mixed infections. Their role in treating various multi-resistant pathogens such as Acinetobacter species and Stenotrophomonas maltophilia are gaining importance. Although, generally, they do not constitute reliable therapy against extended-spectrum beta-lactamase producers, their substitution in place of cephalosporins appears to reduce emergence of the latter pathogens. Similarly, their use may also curtail the emergence of other resistant pathogens such as Clostridium difficile and vancomycin-resistant enterococci. beta-Lactam/beta-lactamase inhibitor combinations are generally well tolerated and their oral forms provide effective outpatient therapy against many commonly encountered infections. In certain scenarios, they could even be more cost-effective than conventional combination therapies. With the accumulation of so much clinical experience, their role in the management of infections is now becoming more clearly defined.

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Year:  2003        PMID: 12834367     DOI: 10.2165/00003495-200363140-00006

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  81 in total

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4.  Clavulanate induces expression of the Pseudomonas aeruginosa AmpC cephalosporinase at physiologically relevant concentrations and antagonizes the antibacterial activity of ticarcillin.

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Journal:  Antimicrob Agents Chemother       Date:  1999-04       Impact factor: 5.191

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Journal:  Eur J Clin Microbiol Infect Dis       Date:  1992-11       Impact factor: 3.267

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Authors:  C E Thorburn; S J Knott; D I Edwards
Journal:  Antimicrob Agents Chemother       Date:  1998-08       Impact factor: 5.191

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  17 in total

1.  Antimicrobial peptide isolated from Bacillus amyloliquefaciens K14 revitalizes its use in combinatorial drug therapy.

Authors:  Sudip Regmi; Yun Hee Choi; Yoon Seok Choi; Mi Ri Kim; Jin Cheol Yoo
Journal:  Folia Microbiol (Praha)       Date:  2016-10-27       Impact factor: 2.099

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Authors:  Pius S Padayatti; Anjaneyulu Sheri; Monica A Totir; Marion S Helfand; Marianne P Carey; Vernon E Anderson; Paul R Carey; Christopher R Bethel; Robert A Bonomo; John D Buynak; Focco van den Akker
Journal:  J Am Chem Soc       Date:  2006-10-11       Impact factor: 15.419

3.  Comparative Evaluation of the in-vitro Activity of Six β-lactam/β-lactamase Inhibitor Combinations against Gram Negative Bacilli.

Authors:  Smita Sood
Journal:  J Clin Diagn Res       Date:  2013-02-01

4.  GW779439X and Its Pyrazolopyridazine Derivatives Inhibit the Serine/Threonine Kinase Stk1 and Act As Antibiotic Adjuvants against β-Lactam-Resistant Staphylococcus aureus.

Authors:  Adam J Schaenzer; Nathan Wlodarchak; David H Drewry; William J Zuercher; Warren E Rose; Carla A Ferrer; John-Demian Sauer; Rob Striker
Journal:  ACS Infect Dis       Date:  2018-08-15       Impact factor: 5.084

Review 5.  Combination therapies for combating antimicrobial resistance.

Authors:  Michael A Fischbach
Journal:  Curr Opin Microbiol       Date:  2011-09-06       Impact factor: 7.934

6.  Effect of the inhibitor-resistant M69V substitution on the structures and populations of trans-enamine beta-lactamase intermediates.

Authors:  Monica A Totir; Pius S Padayatti; Marion S Helfand; Marianne P Carey; Robert A Bonomo; Paul R Carey; Focco van den Akker
Journal:  Biochemistry       Date:  2006-10-03       Impact factor: 3.162

7.  Antifolate activity of epigallocatechin gallate against Stenotrophomonas maltophilia.

Authors:  María Dolores Navarro-Martínez; Enma Navarro-Perán; Juan Cabezas-Herrera; Joaquín Ruiz-Gómez; Francisco García-Cánovas; José Neptuno Rodríguez-López
Journal:  Antimicrob Agents Chemother       Date:  2005-07       Impact factor: 5.191

8.  β-Lactamase inhibition by 7-alkylidenecephalosporin sulfones: allylic transposition and formation of an unprecedented stabilized acyl-enzyme.

Authors:  Elizabeth A Rodkey; David C McLeod; Christopher R Bethel; Kerri M Smith; Yan Xu; Weirui Chai; Tao Che; Paul R Carey; Robert A Bonomo; Focco van den Akker; John D Buynak
Journal:  J Am Chem Soc       Date:  2013-12-03       Impact factor: 15.419

Review 9.  Antibiotics from microbes: converging to kill.

Authors:  Michael A Fischbach
Journal:  Curr Opin Microbiol       Date:  2009-08-18       Impact factor: 7.934

10.  Inhibition of flucloxacillin tubular renal secretion by piperacillin.

Authors:  Cornelia B Landersdorfer; Carl M J Kirkpatrick; Martina Kinzig; Jürgen B Bulitta; Ulrike Holzgrabe; Fritz Sörgel
Journal:  Br J Clin Pharmacol       Date:  2008-11       Impact factor: 4.335

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