Detection of bacteraemia in critically ill patients using 16S rDNA polymerase chain reaction and DNA sequencing

被引:43
作者
Sleigh, J
Cursons, R
La Pine, M
机构
[1] Waikato Hosp, Dept Intens Care, Hamilton, New Zealand
[2] Univ Waikato, Dept Biol Sci, Hamilton, New Zealand
关键词
polymerase chain reaction; sepsis; intensive care;
D O I
10.1007/s001340100981
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: To confirm the sensitivity of the polymerase chain reaction PCR) technique (versus blood cultures) and to gain a better understanding of the incidence of true- and false-positive results when using this technique. Design: Observational study. Setting: Fourteen-bed, level 3 intensive care unit. Patients: Hundred twenty-six critically ill adult patients. Hundred ninety-seven blood culture and PCR samples taken as clinically indicated for suspected sepsis, according to routine ICU protocol. Measurements and results: The PCR product (16SrDNA: 341F-1195R) was sequenced and compared with a database of known species (Gene-bank) to identify the bacterial nucleic acid. The PCR or blood culture result was classified as a true-positive if there was other microbiological or clinical supporting evidence.
引用
收藏
页码:1269 / 1273
页数:5
相关论文
共 15 条
[1]   TOWARD AN EPIDEMIOLOGY AND NATURAL-HISTORY OF SIRS (SYSTEMIC INFLAMMATORY RESPONSE SYNDROME) [J].
BONE, RC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1992, 268 (24) :3452-3455
[2]   Prediction of microbial infection and mortality in medical patients with fever:: Plasma procalcitonin, neutrophilic elastase-α1-antitrypsin, and lactoferrin compared with clinical variables [J].
Bossink, AWJ ;
Groeneveld, ABJ ;
Thijs, LG .
CLINICAL INFECTIOUS DISEASES, 1999, 29 (02) :398-407
[3]   The use of polymerase chain reaction to detect septicemia in critically ill patients [J].
Cursons, RTM ;
Jeyerajah, E ;
Sleigh, JW .
CRITICAL CARE MEDICINE, 1999, 27 (05) :937-940
[4]   A one-year prospective study of nosocomial bacteraemia in ICU and non-ICU patients and its impact on patient outcome [J].
Garrouste-Orgeas, M ;
Chevret, S ;
Mainardi, JL ;
Timsit, JF ;
Misset, B ;
Carlet, J .
JOURNAL OF HOSPITAL INFECTION, 2000, 44 (03) :206-213
[5]   PCR PRIMERS AND PROBES FOR THE 16S RIBOSOMAL-RNA GENE OF MOST SPECIES OF PATHOGENIC BACTERIA, INCLUDING BACTERIA FOUND IN CEREBROSPINAL-FLUID [J].
GREISEN, K ;
LOEFFELHOLZ, M ;
PUROHIT, A ;
LEONG, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (02) :335-351
[6]   Broad-spectrum bacterial rDNA polymerase chain reaction assay for detecting amniotic fluid infection among women in premature labor [J].
Hitti, J ;
Riley, DE ;
Krohn, MA ;
Hillier, SL ;
Agnew, KJ ;
Krieger, JN ;
Eschenbach, DA .
CLINICAL INFECTIOUS DISEASES, 1997, 24 (06) :1228-1232
[7]   Rapid detection of Chlamydia pneumoniae by PCR-enzyme immunoassay [J].
Jantos, CA ;
Roggendorf, R ;
Wuppermann, FN ;
Hegemann, JH .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (07) :1890-1894
[8]  
Jones GR, 1996, QJM-MON J ASSOC PHYS, V89, P515
[9]   Comparison of 16S rRNA gene PCR and BACTEC 9240 for detection of neonatal bacteremia [J].
Jordan, JA ;
Durso, MB .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (07) :2574-2578
[10]   Rapid detection of neonatal sepsis using polymerase chain reaction [J].
Laforgia, N ;
Coppola, B ;
Carbone, R ;
Grassi, A ;
Mautone, A ;
Iolascon, A .
ACTA PAEDIATRICA, 1997, 86 (10) :1097-1099