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肺炎链球菌作为医院感染病原体:耐青霉素菌株时代的治疗

Streptococcus pneumoniae as an agent of nosocomial infection: treatment in the era of penicillin-resistant strains.

作者信息

Paradisi F, Corti G, Cinelli R

机构信息

Infectious Disease Unit, University of Florence School of Medicine, Italy.

出版信息

Clin Microbiol Infect. 2001;7 Suppl 4:34-42. doi: 10.1046/j.1469-0691.2001.00056.x.

Abstract

Streptococcus pneumoniae is a well-known agent of community-acquired infections such as sinusitis, otitis media, pneumonia, bacterial meningitis, bacteremia and acute exacerbations of chronic bronchitis. However, the role of S. pneumoniae as a cause of nosocomial infections of respiratory tract, bloodstream and central nervous system is more and more recognized, primarily in high-risk patients with depression of their immune function. Therapy of pneumococcal infections is made difficult by the emergence and spread of bacterial resistance to penicillin and other beta-lactams as well as to a number of antimicrobials such as macrolides, chloramphenicol, tetracyclines and sulfonamides. This epidemiological situation is a cause for concern world-wide, but it primarily affects some European countries, North America, South Africa and the Far East. The main consequence on therapeutic grounds is that in severe infections such as bacterial meningitis, the addition of vancomycin to a third-generation cephalosporin is advisable while awaiting laboratory test results, even in areas with low prevalence of penicillin-resistant pneumococci. However, a beta-lactam agent can also be a valid choice in the presence of potentially lethal infections such as pneumonia or in the case of penicillin intermediately resistant isolates. In recent years, new alternative molecules have been introduced into clinical practice for therapy of infections caused by penicillin-resistant pneumococci. In both in vivo and in vitro studies, drugs of the classes of fluoroquinolones (levofloxacin, moxifloxacin, gatifloxacin), streptogramins (quinupristin/dalfopristin) and oxazolidinones (linezolid) have shown good microbiologic and clinical efficacy against penicillin-resistant pneumococci. In this era of world-wide spread of penicillin-resistant pneumococci, use of polysaccaride or conjugated vaccines is highly recommended.

摘要

肺炎链球菌是社区获得性感染的常见病原体,可引起鼻窦炎、中耳炎、肺炎、细菌性脑膜炎、菌血症以及慢性支气管炎急性加重等疾病。然而,肺炎链球菌作为呼吸道、血流及中枢神经系统医院感染病原体的作用日益受到认可,主要见于免疫功能低下的高危患者。肺炎链球菌对青霉素和其他β-内酰胺类药物以及多种抗菌药物(如大环内酯类、氯霉素、四环素类和磺胺类)产生耐药并出现传播,给肺炎链球菌感染的治疗带来了困难。这种流行病学情况在全球范围内令人担忧,但主要影响一些欧洲国家、北美、南非和远东地区。从治疗角度来看,主要后果是在严重感染(如细菌性脑膜炎)中,即使在青霉素耐药肺炎链球菌患病率较低的地区,在等待实验室检测结果时,建议在第三代头孢菌素基础上加用万古霉素。然而,对于潜在致命性感染(如肺炎)或青霉素中介耐药菌株感染,β-内酰胺类药物也可能是有效的选择。近年来,新的替代药物已被引入临床实践,用于治疗耐青霉素肺炎链球菌引起的感染。在体内和体外研究中,氟喹诺酮类(左氧氟沙星、莫西沙星、加替沙星)、链阳菌素类(奎奴普丁/达福普汀)和恶唑烷酮类(利奈唑胺)药物对耐青霉素肺炎链球菌均显示出良好的微生物学和临床疗效。在耐青霉素肺炎链球菌全球传播的时代,强烈建议使用多糖疫苗或结合疫苗。

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