Role of the microbiology laboratory in the diagnosis of lower respiratory tract infections

被引:55
作者
Reimer, LG
Carroll, KC
机构
[1] Vet Affairs Med Ctr, Dept Pathol 113, Salt Lake City, UT 84148 USA
[2] Univ Utah, Hlth Sci Ctr, Dept Med, Div Infect Dis, Salt Lake City, UT 84132 USA
[3] Univ Utah, Hlth Sci Ctr, Dept Pathol, Salt Lake City, UT 84132 USA
关键词
D O I
10.1086/514583
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The appropriate use of the clinical microbiology laboratory for diagnosing lower respiratory tract infections is controversial. As in clinical care, it is crucial to categorize the presenting illness properly as acute bronchitis, an acute exacerbation of chronic bronchitis, community-acquired pneumonia, or nosocomial pneumonia if diagnostic efforts to establish a microbial etiology are to be productive for the individual patient and affordable to society. The greatest potential benefit of microbiological investigations lies in the etiologic diagnosis of pneumonia. For community-acquired pneumonia, evaluation of a gram-stained smear of sputum in terms of both quality and microorganisms present can help guide initial therapy as well as aid interpretation of subsequent culture results. As discussed in this review, the role of the clinical microbiology laboratory in the etiologic diagnosis of nosocomial and complicated pneumonias is more extensive and, in addition to evaluation of respiratory secretions, may include cultures of blood, pleural fluid, and specimens obtained by bronchoscopy. However, a prerequisite for the use of all currently available tests is their deployment for patients with clinical and radiographic evidence of pneumonia.
引用
收藏
页码:742 / 748
页数:7
相关论文
共 49 条
[1]   DECISION-MAKING IN NOSOCOMIAL PNEUMONIA - AN ANALYTIC APPROACH TO THE INTERPRETATION OF QUANTITATIVE BRONCHOSCOPIC CULTURES [J].
BAKER, AM ;
BOWTON, DL ;
HAPONIK, EF .
CHEST, 1995, 107 (01) :85-95
[2]   Pneumonia in intubated trauma patients - Microbiology and outcomes [J].
Baker, AM ;
Meredith, JW ;
Haponik, EF .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 153 (01) :343-349
[3]  
BARRETTC.E, 1971, AM REV RESPIR DIS, V103, P845
[4]   COMMUNITY-ACQUIRED PNEUMONIA [J].
BARTLETT, JG ;
MUNDY, LM .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (24) :1618-1624
[5]  
BARTLETT JG, 1996, INFECT DIS CLIN PRAC, V5, P147
[6]   BRONCHOSCOPIC DIAGNOSIS OF PNEUMONIA [J].
BASELSKI, VS ;
WUNDERINK, RG .
CLINICAL MICROBIOLOGY REVIEWS, 1994, 7 (04) :533-&
[7]   MICROBIAL ETIOLOGY OF ACUTE PNEUMONIA IN HOSPITALIZED-PATIENTS [J].
BATES, JH ;
CAMPBELL, GD ;
BARRON, AL ;
MCCRACKEN, GA ;
MORGAN, PN ;
MOSES, EB ;
DAVIS, CM .
CHEST, 1992, 101 (04) :1005-1012
[8]   JUSTIFYING THE USE OF BLOOD CULTURES WHEN DIAGNOSING COMMUNITY-ACQUIRED PNEUMONIA [J].
BERK, SL .
CHEST, 1995, 108 (04) :891-892
[9]   THE VALUE OF THE SPUTUM GRAMS STAIN IN COMMUNITY-ACQUIRED PNEUMONIA [J].
BOERNER, DF ;
ZWADYK, P .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1982, 247 (05) :642-645
[10]   CLINICAL UTILITY OF BLOOD CULTURES IN ADULT PATIENTS WITH COMMUNITY-ACQUIRED PNEUMONIA WITHOUT DEFINED UNDERLYING RISKS [J].
CHALASANI, NP ;
VALDECANAS, MAL ;
GOPAL, AK ;
MCGOWAN, JE ;
JURADO, RL .
CHEST, 1995, 108 (04) :932-936