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
[11]   Prognosis and outcomes of patients with community-acquired pneumonia - A meta-analysis [J].
Fine, MJ ;
Smith, MA ;
Carson, CA ;
Mutha, SS ;
Sankey, SS ;
Weissfeld, LA ;
Kapoor, WN .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 275 (02) :134-141
[12]   A prediction rule to identify low-risk patients with community-acquired pneumonia [J].
Fine, MJ ;
Auble, TE ;
Yealy, DM ;
Hanusa, BH ;
Weissfeld, LA ;
Singer, DE ;
Coley, CM ;
Marrie, TJ ;
Kapoor, WN .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (04) :243-250
[13]  
GARAU J, 5 INT C MACR AZ STRE, P65
[14]   Community-acquired pneumonia: The annual cost to the national health service in the UK [J].
Guest, JF ;
Morris, A .
EUROPEAN RESPIRATORY JOURNAL, 1997, 10 (07) :1530-1534
[15]  
HAGBERG L, 2000, 40 INT C ANT AG CHEM, P490
[16]   Management of community-acquired pneumonia in the era of pneumococcal resistance -: A report from the Drug-Resistant Streptococcus pneumoniae Therapeutic Working Group [J].
Heffelfinger, JD ;
Dowell, SF ;
Jorgensen, JH ;
Klugman, KP ;
Mabry, LR ;
Musher, DM ;
Plouffe, JF ;
Rakowsky, A ;
Schuchat, A ;
Whitney, CG .
ARCHIVES OF INTERNAL MEDICINE, 2000, 160 (10) :1399-1408
[17]   Impact of management guidelines on the outcome of severe community acquired pneumonia [J].
Hirani, NA ;
Macfarlane, JT .
THORAX, 1997, 52 (01) :17-21
[18]   Breakthrough sepsis in macrolide-resistant pneumococcal infection [J].
Jackson, MA ;
Burry, VF ;
Olson, LC ;
Duthie, SE ;
Kearns, GL .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1996, 15 (11) :1049-1051
[19]   Susceptibilities of Streptococcus pneumoniae and Haemophilus influenzae to 10 oral antimicrobial agents based on pharmacodynamic parameters:: 1997 US surveillance study [J].
Jacobs, MR ;
Bajaksouzian, S ;
Zilles, A ;
Lin, GR ;
Pankuch, GA ;
Appelbaum, PC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (08) :1901-1908
[20]   INCIDENCE OF COMMUNITY-ACQUIRED PNEUMONIA IN THE POPULATION OF 4 MUNICIPALITIES IN EASTERN FINLAND [J].
JOKINEN, C ;
HEISKANEN, L ;
JUVONEN, H ;
KALLINEN, S ;
KARKOLA, K ;
KORPPI, M ;
KURKI, S ;
RONNBERG, PR ;
SEPPA, A ;
SOIMAKALLIO, S ;
STEN, M ;
TANSKA, S ;
TARKIAINEN, A ;
TUKIAINEN, H ;
PYORALA, K ;
MAKELA, PH .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1993, 137 (09) :977-988