Rapid Diagnosis of Infection in the Critically Ill, a Multicenter Study of Molecular Detection in Bloodstream Infections, Pneumonia, and Sterile Site Infections

被引:148
作者
Vincent, Jean-Louis [1 ]
Brealey, David [2 ,3 ]
Libert, Nicolas [4 ]
Abidi, Nour Elhouda [5 ]
O'Dwyer, Michael [6 ]
Zacharowski, Kai [7 ]
Mikaszewska-Sokolewicz, Malgorzata [8 ]
Schrenzel, Jacques [9 ]
Simon, Francois [10 ]
Wilks, Mark [6 ]
Picard-Maureau, Marcus [11 ]
Chalfin, Donald B. [12 ]
Ecker, David J. [12 ]
Sampath, Rangarajan [12 ]
Singer, Mervyn [2 ,3 ]
机构
[1] Univ Libre Bruxelles, Erasme Hosp, Dept Intens Care, Brussels, Belgium
[2] Univ Coll Hosp, Univ Coll London Hosp NIHR Biomed Res Ctr, Div Crit Care, London, England
[3] Univ Coll Hosp, Bloomsbury Inst Intens Care Med, London, England
[4] Val de Grace Mil Hosp, Dept Anesthesiol & Crit Care, Paris, France
[5] Univ Hosp Geneva, Dept Anesthesiol Pharmacol & Intens Care, Intens Care Unit, Geneva, Switzerland
[6] Queen Mary Univ London & Barts Hlth NHS Trust, Barts & London Sch Med & Dent, London, England
[7] Univ Frankfurt Klinikum, Klin Anesthesiol Intens Med & Schmerztherapie, Frankfurt, Germany
[8] Med Univ Warsaw, Clin Anaesthesia & Intens Care 1, Warsaw, Poland
[9] Univ Hosp Geneva, Dept Internal Med, Infect Dis Serv, Genom Res Lab, Geneva, Switzerland
[10] St Louis Univ Hosp, Dept Microbiol, Paris, France
[11] Abbott GmbH & Co KG, Wiesbaden, Germany
[12] Abbott, Ibis Biosci, Carlsbad, CA USA
关键词
critically ill; culture-independent; early diagnosis; infection; microbiology; molecular detection; MASS-SPECTROMETRY; CULTURE ASSAY; IDENTIFICATION; PCR; BACTERIA; SEPSIS; PATHOGENS; SYSTEM; YEASTS; IMPACT;
D O I
10.1097/CCM.0000000000001249
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: Early identification of causative microorganism(s) in patients with severe infection is crucial to optimize antimicrobial use and patient survival. However, current culture-based pathogen identification is slow and unreliable such that broad-spectrum antibiotics are often used to insure coverage of all potential organisms, carrying risks of overtreatment, toxicity, and selection of multidrug-resistant bacteria. We compared the results obtained using a novel, culture-independent polymerase chain reaction/electrospray ionization-mass spectrometry technology with those obtained by standard microbiological testing and evaluated the potential clinical implications of this technique. Design: Observational study. Setting: Nine ICUs in six European countries. Patients: Patients admitted between October 2013 and June 2014 with suspected or proven bloodstream infection, pneumonia, or sterile fluid and tissue infection were considered for inclusion. Interventions: None. Measurements and Main Results: We tested 616 bloodstream infection, 185 pneumonia, and 110 sterile fluid and tissue specimens from 529 patients. From the 616 bloodstream infection samples, polymerase chain reaction/electrospray ionization-mass spectrometry identified a pathogen in 228 cases (37%) and culture in just 68 (11%). Culture was positive and polymerase chain reaction/electrospray ionization-mass spectrometry negative in 13 cases, and both were negative in 384 cases, giving polymerase chain reaction/electrospray ionization-mass spectrometry a sensitivity of 81%, specificity of 69%, and negative predictive value of 97% at 6 hours from sample acquisition. The distribution of organisms was similar with both techniques. Similar observations were made for pneumonia and sterile fluid and tissue specimens. Independent clinical analysis of results suggested that polymerase chain reaction/electrospray ionization-mass spectrometry technology could potentially have resulted in altered treatment in up to 57% of patients. Conclusions: Polymerase chain reaction/electrospray ionization-mass spectrometry provides rapid pathogen identification in critically ill patients. The ability to rule out infection within 6 hours has potential clinical and economic benefits.
引用
收藏
页码:2283 / 2291
页数:9
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