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Review
. 2009 Feb;63(2):243-5.
doi: 10.1093/jac/dkn511. Epub 2008 Dec 18.

Temocillin revived

Affiliations
Review

Temocillin revived

David M Livermore et al. J Antimicrob Chemother. 2009 Feb.

Abstract

Resistance in Gram-negative pathogens is an increasing concern, with carbapenems often appearing as the only acceptable treatment option in serious infections. Reviving older compounds that have fallen into disuse may help to alleviate this burden. Temocillin (6-alpha-methoxy-ticarcillin) is resistant to most if not all classical and extended-spectrum beta-lactamases and to AmpC enzymes. It is also chemically stable, allowing administration by continuous infusion. Pharmacokinetic/pharmacodynamic analysis, aided by Monte-Carlo simulations, suggests a breakpoint of 8 mg/L for the registered maximum dosage of 4 g daily. Temocillin's weaknesses, explaining its limited previous use, are a lack of activity against Gram-positive organisms, anaerobes and Pseudomonas. In settings where these are unlikely or are covered by other agents, temocillin may be useful, potentially 'sparing' carbapenems and having little apparent potential to select for Clostridium difficile.

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Comment in

  • Clinical efficacy of temocillin.
    Gupta ND, Smith RE, Balakrishnan I. Gupta ND, et al. J Antimicrob Chemother. 2009 Aug;64(2):431-3. doi: 10.1093/jac/dkp208. Epub 2009 Jun 11. J Antimicrob Chemother. 2009. PMID: 19520716 No abstract available.

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