Literature DB >> 10221472

Carbapenems and monobactams: imipenem, meropenem, and aztreonam.

W C Hellinger1, N S Brewer.   

Abstract

Imipenem and meropenem, members of the carbapenem class of beta-lactam antibiotics, are among the most broadly active antibiotics available for systemic use in humans. They are active against streptococci, methicillin-sensitive staphylococci, Neisseria, Haemophilus, anaerobes, and the common aerobic gram-negative nosocomial pathogens including Pseudomonas. Resistance to imipenem and meropenem may emerge during treatment of P. aeruginosa infections, as has occurred with other beta-lactam agents; Stenotrophomonas maltophilia is typically resistant to both imipenem and meropenem. Like the penicillins, the carbapenems have inhibitory activity against enterococci. In general, the in vitro activity of imipenem against aerobic gram-positive cocci is somewhat greater than that of meropenem, whereas the in vitro activity of meropenem against aerobic gram-negative bacilli is somewhat greater than that of imipenem. Daily dosages may range from 0.5 to 1 g every 6 to 8 hours in patients with normal renal function; the daily dose of meropenem, however, can be safely increased to 6 g. Infusion-related nausea and vomiting, as well as seizures, which have been the main toxic effects of imipenem, occur no more frequently during treatment with meropenem than during treatment with other beta-lactam antibiotics. The carbapenems should be considered for treatment of mixed bacterial infections and aerobic gram-negative bacteria that are not susceptible to other beta-lactam agents. Indiscriminate use of these drugs will promote resistance to them. Aztreonam, the first marketed monobactam, has activity against most aerobic gram-negative bacilli including P. aeruginosa. The drug is not nephrotoxic, is weakly immunogenic, and has not been associated with disorders of coagulation. Aztreonam may be administered intramuscularly or intravenously; the primary route of elimination is urinary excretion. In patients with normal renal function, the recommended dosing interval is every 8 hours. Patients with renal impairment require dosage adjustment. Aztreonam is used primarily as an alternative to aminoglycosides and for the treatment of aerobic gram-negative infections. It is often used in combination therapy for mixed aerobic and anaerobic infections. Approved indications for its use include infections of the urinary tract or lower respiratory tract, intra-abdominal and gynecologic infections, septicemia, and cutaneous infections caused by susceptible organisms. Concurrent initial therapy with other antimicrobial agents is recommended before the causative organism has been determined in patients who are seriously ill or at risk for gram-positive or anaerobic infection.

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Year:  1999        PMID: 10221472     DOI: 10.4065/74.4.420

Source DB:  PubMed          Journal:  Mayo Clin Proc        ISSN: 0025-6196            Impact factor:   7.616


  10 in total

1.  Microdialysis study of imipenem distribution in the intraperitoneal fluid of rats with or without experimental peritonitis.

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Journal:  Antimicrob Agents Chemother       Date:  2006-01       Impact factor: 5.191

Review 2.  Antianaerobic antimicrobials: spectrum and susceptibility testing.

Authors:  Itzhak Brook; Hannah M Wexler; Ellie J C Goldstein
Journal:  Clin Microbiol Rev       Date:  2013-07       Impact factor: 26.132

3.  Kinetics of imipenem distribution into the peritoneal fluid of patients with severe peritonitis studied by microdialysis.

Authors:  Claire Dahyot-Fizelier; Sandrine Lefeuvre; Leila Laksiri; Sandrine Marchand; Ronald J Sawchuk; William Couet; Olivier Mimoz
Journal:  Clin Pharmacokinet       Date:  2010-05       Impact factor: 6.447

4.  Amino acid residues that contribute to substrate specificity of class A beta-lactamase SME-1.

Authors:  Fahd K Majiduddin; Timothy Palzkill
Journal:  Antimicrob Agents Chemother       Date:  2005-08       Impact factor: 5.191

Review 5.  Use of pharmacodynamic principles to optimise dosage regimens for antibacterial agents in the elderly.

Authors:  Ayman M Noreddin; Virginia Haynes
Journal:  Drugs Aging       Date:  2007       Impact factor: 3.923

Review 6.  Pharmacokinetics of meropenem in patients with renal failure and patients receiving renal replacement therapy.

Authors:  F Thalhammer; W H Hörl
Journal:  Clin Pharmacokinet       Date:  2000-10       Impact factor: 6.447

7.  Amino acid sequence requirements at residues 69 and 238 for the SME-1 beta-lactamase to confer resistance to beta-lactam antibiotics.

Authors:  Fahd K Majiduddin; Timothy Palzkill
Journal:  Antimicrob Agents Chemother       Date:  2003-03       Impact factor: 5.191

8.  Identification, characterization, and regulation of a cluster of genes involved in carbapenem biosynthesis in Photorhabdus luminescens.

Authors:  Sylviane Derzelle; Eric Duchaud; Frank Kunst; Antoine Danchin; Philippe Bertin
Journal:  Appl Environ Microbiol       Date:  2002-08       Impact factor: 4.792

9.  Mathematical model predicts anti-adhesion-antibiotic-debridement combination therapies can clear an antibiotic resistant infection.

Authors:  Paul A Roberts; Ryan M Huebinger; Emma Keen; Anne-Marie Krachler; Sara Jabbari
Journal:  PLoS Comput Biol       Date:  2019-07-23       Impact factor: 4.475

10.  Ribosome-Targeting Antibiotics Impair T Cell Effector Function and Ameliorate Autoimmunity by Blocking Mitochondrial Protein Synthesis.

Authors:  Luís Almeida; Ayesha Dhillon-LaBrooy; Carla N Castro; Nigatu Adossa; Guilhermina M Carriche; Melanie Guderian; Saskia Lippens; Sven Dennerlein; Christina Hesse; Bart N Lambrecht; Luciana Berod; Leif Schauser; Bruce R Blazar; Markus Kalesse; Rolf Müller; Luís F Moita; Tim Sparwasser
Journal:  Immunity       Date:  2020-11-24       Impact factor: 31.745

  10 in total

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