Abstract |
Comparative antibacterial activity of imipenem (IPM), panipenem (PAPM), meropenem (MEPM) and biapenem (BIPM) was determined against 288 clinical isolates of P. aeruginosa collected from various hospitals in 2000. The order of activity by comparison of MIC50/MIC80/MIC90 was: MEPM (1/4/8 micrograms/ml) > BIPM (1/4/16 micrograms/ml) > IPM (2/4/16 micrograms/ml) > PAPM (8/16/32 micrograms/ml). Moreover, the order of activity against 75 strains of P. aeruginosa (MIC of CAZ, AZT was > or = 16 micrograms/ml and MIC of IPM, MEPM was < or = 8 micrograms/ml) by comparison of MIC50/MIC80/MIC90 was: BIPM (1/2/8 micrograms/ml) > or = MEPM (1/4/8 micrograms/ml) > or = IPM (2/2/8 micrograms/ml) > PAPM (8/16/16 micrograms/ml). Judging from both correlation between the MICs of carbapenems and relationship between class C beta-lactamase activity and drug susceptibility of carbapenems, it becomes apparent that carbapenems, especially BIPM and MEPM will be useful for treatment of antipseudomonal cephem resistant pseudomonas infection.
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Authors | M Hikida, S Terashima, Y Sato, R Okamoato, M Inoue |
Journal | The Japanese journal of antibiotics
(Jpn J Antibiot)
Vol. 54
Issue 11
Pg. 571-9
(Nov 2001)
ISSN: 0368-2781 [Print] Japan |
PMID | 11828603
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- Carbapenems
- Thienamycins
- Imipenem
- beta-Lactamases
- Meropenem
- panipenem
- biapenem
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Topics |
- Carbapenems
(pharmacology)
- Drug Resistance, Microbial
- Imipenem
(pharmacology)
- Meropenem
- Pseudomonas aeruginosa
(drug effects, enzymology)
- Thienamycins
(pharmacology)
- beta-Lactamases
(metabolism)
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