Community-acquired pneumonia: the evolving challenge

被引:21
作者
Finch, R [1 ]
机构
[1] Univ Nottingham, City Hosp, Div Microbiol & Infect Dis, Nottingham NG5 1PB, England
关键词
D O I
10.1046/j.1469-0691.2001.0070s3030.x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Community-acquired pneumonia (CAP) is a common disorder that has been the focus of a major international research effort to define its epidemiology, etiology and management. The microbial etiology of CAP is complex and severity assessment is important in identifying at-risk populations as well as defining therapeutic strategies. Laboratory investigations rarely influence initial therapy, which remains empirical. Guidelines have been developed in many countries in response to the need to optimize management and outcomes. However, many of these guidelines have been based on expert opinion rather than robust evidence. New evidence-based guidelines have been developed that take into account disease severity, the local distribution of pathogens and their likely susceptibility to antimocrobials, and that include newer treatment options. Macrolide and fluroquinolone antimicrobials feature heavily in these new treatment recommendations. Promising new therapies continue to emerge that may offer advantages over fluroquinolones and macrolides, in particular with regard to the problem of resistance. Of these, the ketolides are of special interest. Telithromycin, the first ketolide antibacterial, has been evaluated in the treatment of >700 patients with CAP. A once-daily oral dose of telithromycin 800 mg for 7-10 days produces clinical and bacteriological success rates >90% and equivalent to standard comparator agents, whilst maintaining efficacy against resistant pathogens.
引用
收藏
页码:30 / 38
页数:9
相关论文
共 39 条
[1]   THE OUTCOME OF COMMUNITY ACQUIRED PNEUMONIA TREATED ON THE INTENSIVE-CARE UNIT [J].
ALKHAYER, M ;
JENKINS, PF ;
HARRISON, BDW .
RESPIRATORY MEDICINE, 1990, 84 (01) :13-16
[2]  
ANDREWS BE, 1987, Q J MED, V62, P195
[3]  
BARTLETT CLR, 1992, RESP MED, V86, P7
[4]   Community-acquired pneumonia in adults: Guidelines for management [J].
Bartlett, JG ;
Breiman, RF ;
Mandell, LA ;
File, TM .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (04) :811-838
[5]  
Bartlett John G., 2000, Clinical Infectious Diseases, V31, P347, DOI 10.1086/313954
[6]  
CARBON C, 2000, 40 INT C ANT AG CHEM, P490
[7]   Decreased susceptibility of Streptococcus pneumoniae to fluoroquinolones in Canada [J].
Chen, DK ;
McGeer, A ;
de Azavedo, JC ;
Low, DE .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (04) :233-239
[8]   Pharmacodynamic and pharmacokinetic considerations in antimicrobial selection: focus on telithromycin [J].
Drusano, G .
CLINICAL MICROBIOLOGY AND INFECTION, 2001, 7 :24-29
[9]   The Alexander Project 1996-1997:: latest susceptibility data from this international study of bacterial pathogens from community-acquired lower respiratory tract infections [J].
Felmingham, D ;
Grüneberg, RN .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2000, 45 (02) :191-203
[10]   Practical considerations and guidelines for the management of community-acquired pneumonia [J].
Finch, RG ;
Woodhead, MA .
DRUGS, 1998, 55 (01) :31-45