Temocillin revived

被引:102
作者
Livermore, David M. [1 ]
Tulkens, Paul M. [2 ,3 ]
机构
[1] Hlth Protect Agcy, Ctr Infect, Antibiot Resistance Monitoring & Reference Lab, London NW9 5EQ, England
[2] Univ Catholique Louvain, Unite Pharmacol Cellulaire & Mol, B-1200 Brussels, Belgium
[3] Univ Catholique Louvain, Ctr Pharm Clin, B-1200 Brussels, Belgium
关键词
IN-VITRO ACTIVITY; IMPAIRED RENAL-FUNCTION; METALLO-BETA-LACTAMASE; ESCHERICHIA-COLI; PHARMACOKINETICS; INFECTIONS; ENTEROBACTERIACEAE; CEFTAZIDIME; VOLUNTEERS; PENICILLIN;
D O I
10.1093/jac/dkn511
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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.
引用
收藏
页码:243 / 245
页数:3
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