Low Donald E, Felmingham David, Brown Steve D, Rangaraju Manickam, Nusrat Roomi
Department of Microbiology, Mount Sinai Hospital, University of Toronto, Toronto, Ont, Canada.
J Infect. 2004 Aug;49(2):115-25. doi: 10.1016/j.jinf.2004.03.009.
To investigate the correlation between in vitro susceptibility of isolates and clinical outcomes with telithromycin in respiratory tract infections.
The activity of telithromycin was determined by in vitro susceptibility testing of key respiratory tract pathogens isolated from patients with community-acquired pneumonia, acute exacerbations of chronic bronchitis or acute maxillary sinusitis enrolled in 14 Phase III/IV clinical trials evaluating the clinical efficacy of telithromycin.
In this pooled analysis, telithromycin mode minimum inhibitory concentration (MIC) and MIC90, respectively, were: 0.016 and 0.03 mg/l against Streptococcus pneumoniae (n=626); 0.03 and 0.5 mg/l for penicillin-resistant S. pneumoniae (n=56); 0.03 and 1 mg/l for erythromycin-resistant S. pneumoniae (n=81); 2 and 4 mg/l against Haemophilus influenzae (including beta-lactamase producers; n=627); both 0.12 mg/l for Moraxella catarrhalis (n=159) and both 0.25 mg/l for Staphylococcus aureus (n=124). Telithromycin (5 or 7-10 days) resulted in overall clinical and bacteriologic success rates of 88.1% (1593/1808) and 89% (1593/1789), respectively.
High levels of in vitro susceptibility to telithromycin are paralleled by high rates of clinical cure and bacteriologic eradication.
研究呼吸道感染分离株的体外药敏情况与使用泰利霉素的临床疗效之间的相关性。
从参与14项评估泰利霉素临床疗效的III/IV期临床试验的社区获得性肺炎、慢性支气管炎急性加重或急性上颌窦炎患者中分离出关键呼吸道病原体,通过体外药敏试验确定泰利霉素的活性。
在这项汇总分析中,泰利霉素对肺炎链球菌(n = 626)的最低抑菌浓度(MIC)和MIC90分别为0.016和0.03mg/l;对青霉素耐药的肺炎链球菌(n = 56)为0.03和0.5mg/l;对红霉素耐药的肺炎链球菌(n = 81)为0.03和1mg/l;对流感嗜血杆菌(包括产β-内酰胺酶菌株;n = 627)为2和4mg/l;对卡他莫拉菌(n = 159)均为0.12mg/l,对金黄色葡萄球菌(n = 124)均为0.25mg/l。泰利霉素(5天或7 - 10天)治疗的总体临床和细菌学成功率分别为88.1%(1593/1808)和89%(1593/1789)。
泰利霉素的体外高药敏水平与高临床治愈率和细菌清除率相关。