Novel pandemic influenza A (H1N1) and community-associated methicillin-resistant Staphylococcus aureus pneumonia

被引:17
|
作者
Chung, Doo Ryeon [1 ]
Huh, Kyungmin [2 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Infect Dis, Seoul 135710, South Korea
[2] Armed Forces Capital Hosp, Div Infect Dis, Songnam, South Korea
基金
新加坡国家研究基金会;
关键词
anti-bacterial agents; bacterial drug resistance; bacterial pneumonia; coinfection; linezolid; vancomycin; ALVEOLAR MACROPHAGE PHAGOCYTOSIS; INFECTIOUS-DISEASES-SOCIETY; PANTON-VALENTINE LEUKOCIDIN; DESORPTION IONIZATION-TIME; STREPTOCOCCUS-PNEUMONIAE; ACQUIRED PNEUMONIA; UNITED-STATES; NOSOCOMIAL PNEUMONIA; BACTERIAL PNEUMONIA; RESPIRATORY-TRACT;
D O I
10.1586/14787210.2015.999668
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Postinfluenza bacterial pneumonia is a leading cause of influenza-associated death, and Staphylococcus aureus and Streptococcus pneumoniae have been important pathogens that have caused pneumonia since the influenza pandemic in 1919. Emergence of novel influenza A (H1N1) pdm09 and the concomitant global spread of community-associated methicillin-resistant S. aureus (CA-MRSA) have led to increasing prevalence of CA-MRSA pneumonia following influenza infection. Such an epidemiologic change poses a therapeutic challenge due to a high risk of inappropriate empiric antimicrobial therapy and poor clinical outcomes. Early diagnosis and initiation of appropriate antimicrobial therapy for post-influenza bacterial pneumonia have become even more important in the era of CA-MRSA. Therefore, novel molecular diagnostic techniques should be applied to more readily diagnose MRSA pneumonia.
引用
收藏
页码:197 / 207
页数:11
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