경구용 항생제 Cefditoren의 주요 호흡기 감염균에대한 시험관내 항균력 비교
In Vitro Activity of Cefditoren against Respiratory Pathogens
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목 적 : Cefditoren은 경구용 3세대 cephalosporin 계열의 항생제로서, 특히 호흡기 병원균에 효과적인 것으로 알려져 있다. 본 연구는 지역사회 획득 폐렴의 주요 원인균인 S. pneumoniae, H. influenzae와 M. catarrhalis에 대한 cefditoren의 항생제 감수성을 기존의 항생제와 비교 평가하는데 그 목적이 있다.재료 및 방법 : 임상 환자의 검체로부터 분리한 총 208개의 임상 균주(S. pneumoniae 117주, H. influenzae 60주, M. catarrhalis 31주)를 대상으로 NCCLS 지침에 따라서 액체 배지 희석법(broth microdilution method)과 한천 배지 희석법(agar dilution method)을 사용하여 MIC를 측정하고 기존의 β-lactam 계열 항생제, clarithromycin 및 신세대 fluoroquinolone제 등과 비교하였다.결 과 : Cefditoren (MIC50/90, 0.5/1 g/mL)은 다른 β- lactam 계열 항생제 (MIC50/90, 4-64/16-128 g/mL)와 clarithromycin (MIC50/90, >32/>32 g/mL)에 비해서 pneumococci에 대해 8-128배 더 강력한 항균력을 보였다. Cefditoren은 fluoroquinolone에 비해 다소 높은 MIC를 보였으나 ceftriaxone에 상응하였다. 즉, cefditoren은 PISP/PRSP를 포함한 대부분의 균주(97.4%)를 1 g/mL 이하의 농도에서 억제하였고 심지어 quinolone 내성 pneumococci 2균주에 대해서도 우수한 항균력을 보였다 (MIC 0.5 g/mL). Cefditoren은 또한 β-lactamase 생성 및 ampicillin 내성 여부와 상관 없이 모든 H. influenzae (MIC50/90, 0.03/0.06 g/mL)와 M. catarrhalis (MIC50/90, 0.03/0.05 g/mL) 분리주에 낮은 MIC를 보였다.결 론:호흡기 감염증은 원인 균 규명이 다른 감염증에 비해 어렵고 따라서 경험적 항생제의 적절한 선택이 더욱 강조되는데 cefditoren이 호흡기 감염 환자의 외래 치료 시 특히 PISP/PRSP 또는 β-lactamase 생성 균주에 의한 감염이 우려되는 경우 훌륭한 선택제로 고려될 수 있겠다.
Abstract
Background : Cefditoren is a third generation orally administered cephalosporin with excellent activity against respiratory pathogens. This study was performed to determine the comparative antibacterial activity of cefditoren against clinical isolates of respiratory tract infection. Materials and Methods : According to the NCCLS guideline, in vitro activities of cefditoren and other antibiotics were tested against respiratory pathogens including 117 isolates of Streptococcus pneumoniae, 60 isolates of Haemophilus influenzae, and 31 isolates of Moraxella catarrhalis. Results : The level of cefditoren activity against S. pneumoniae (MIC50/90, 0.5/1 µg/mL) was superior to amoxicillin±clavulanate (MIC50/90, 4/16 µg/mL), clarithromycin (MIC50/90, >32/>32 µg/mL), and most of the marketed cephalosporins (MIC50/90, 8-64/16-128 µg/mL). Although the MIC of cefditoren was relatively higher than those of new fluoroquinolone agents (MIC50/90, 0.03-1/0.06-1 µg/mL), it was comparable to ceftriaxone (MIC50/90, 0.5/1 µg/mL). In addition, cefditoren was active against two quinolone resistant pneumococci strains with MIC of 0.5 µg/mL. In detail, cefditoren was active against pneumococci strains with MIC50 and MIC90 values of 0.015/0.12, 0.12/0.5, and 0.5/1 µg/mL for penicillin-susceptible, -intermediate, and -resistant pneumococci, respectively. Cefditoren was also active against all respiratory isolates of H. influenzae (MIC50/90, 0.03/0.06 µg/mL) and M. catarrhalis (MIC50/90, 0.03/0.05 µg/mL) irrespective of β-lactamase production or ampicillin resistance. Conclusion : Cefditoren is considered to be a good option for outpatient treatment of respiratory infections, particulary if there is concern about S. pneumoniae infection with decreased susceptibility to penicillin or β-lactamase producing organisms.
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