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PMID: 19095679 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Temocillin revived.

The Journal of antimicrobial chemotherapy ·Vol. 63 ·No. 2 ·2009-02-00 ·Pages 243-5

Livermore DM, Tulkens PM

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.

MeSH Terms
Anti-Bacterial Agents/administration & dosage,metabolism,pharmacokinetics,pharmacology Bacteria/drug effects Gram-Negative Bacterial Infections/drug therapy Humans Penicillins/administration & dosage,metabolism,pharmacokinetics,pharmacology beta-Lactamases/metabolism
Chemicals
Anti-Bacterial Agents Penicillins temocillin beta-Lactamases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Livermore David M
Antibiotic Resistance Monitoring and Reference Laboratory, Health Protection Agency Centre for Infections, 61 Colindale Avenue, London NW9 5EQ, UK. david.livermore@hpa.org.uk
Tulkens Paul M
Article Info
Journal
The Journal of antimicrobial chemotherapy
Abbr.
J Antimicrob Chemother
ISSN
1460-2091
Published
2009-02-00
Epub
2008-00-18
Pages
243-5
Language
English
Region
England
NLM ID
7513617
Subset
IM
Corrections
CommentIn
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