Multicenter performance evaluation of the Unyvero IAI cartridge for detection of intra-abdominal infections

被引:0
作者
H. Ciesielczuk
M. Wilks
S. Castelain
M. Choquet
M. Morotti
E. Pluquet
V. Sambri
M. Tassinari
S. Zannoli
L. Cavalié
H. Dupont
H. Guet-Revillet
机构
[1] Barts Health NHS Trust,Department of Infection
[2] Queen Mary University of London,Blizard Institute
[3] Centre Hospitalier Universitaire Amiens Picardie,Microbiology Department, Centre de Biologie Humaine
[4] Université de Picardie Jules Verne,EA4294
[5] The Great Romagna Hub Laboratory,Unit of Microbiology
[6] University of Bologna,DIMES
[7] Institut Fédératif de Biologie,Laboratoire de Bactériologie
[8] Hôpital Purpan,Hygiène Hospitalière
[9] CHU de Toulouse,Pole D’Anesthesie
[10] Université de Picardie Jules Verne,Reanimation, Centre Hospitalier Universitaire Amiens Picardie
来源
European Journal of Clinical Microbiology & Infectious Diseases | 2018年 / 37卷
关键词
Intra-abdominal infections; Diagnostics; Antibiotic resistance; Multiplex PCR;
D O I
暂无
中图分类号
学科分类号
摘要
Intra-abdominal infections (IAIs) are one of the most common type of infections in patients with sepsis and an important cause of death in intensive care units. Early detection and treatment are necessary to reduce patient complications and improve outcomes. The Unyvero IAI Application (Curetis GmbH) is the first automated assay to rapidly and simultaneously identify a large panel of bacteria, fungi, toxins, and antibiotic resistance markers directly from IAI-related samples. The assay was evaluated in four European clinical laboratories in comparison to routine microbiological practices. A total of 300 clinical samples were tested with an overall sensitivity of 89.3% and specificity of 99.5%, while time to results was reduced by an average of about 17 h compared to identification (ID) results and 41 h compared to full antibiotic susceptibility testing (AST) results. The Unyvero IAI was able to detect additional microorganisms compared with culture, in particular anaerobes, with most detections confirmed by sequencing. The most frequent resistance markers detected were mecA/mecC (n = 25), aacA4 (n = 20), and blaCTX-M (n = 17) and carbapenemase genes were identified in nine specimens. Further studies are now required to determine the clinical impact of this new rapid test which could play a role in the successful treatment of IAI.
引用
收藏
页码:2107 / 2115
页数:8
相关论文
共 106 条
[1]  
Claridge JA(2014)Bacterial species-specific hospital mortality rate for intra-abdominal infections Surg Infect 15 194-199
[2]  
Banerjee A(2018)Epidemiology and risk factors for isolation of multi-drug-resistant organisms in patients with complicated intra-abdominal infections Surg Infect 19 264-272
[3]  
Kelly KB(2013)Metagenome-wide analysis of antibiotic resistance genes in a large cohort of human gut microbiota Nat Commun 4 2151-11
[4]  
Leukhardt WH(2013)Intestinal colonization resistance Immunology 138 1-2988
[5]  
Carter JW(2013)Distribution of extended-spectrum β-lactamases, AmpC β-lactamases, and carbapenemases among Enterobacteriaceae isolatescausing intra-abdominal infections in the Asia-Pacific region: results of the study for Monitoring Antimicrobial Resistance Trends (SMART) Antimicrob Agents Chemother 57 2981-61
[6]  
Haridas M(2015)Susceptibility trends and molecular characterization of Gram-negative bacilli associated with urinary tract infection and intra-abdominal infections in Jordan and Lebanon: SMART 2011-2013 Int J Infect Dis 35 56-925
[7]  
Malangoni MA(2015)Multicenter evaluation of the BioFire FilmArray gastrointestinal panel for etiologic diagnosis of infectious gastroenteritis J Clin Microbiol 53 915-3673
[8]  
Labricciosa FM(2014)Comparative evaluation of two commercial multiplex panels for detection of gastrointestinal pathogens by use of clinical stool specimens J Clin Microbiol 52 3667-728
[9]  
Sartelli M(2017)FilmArray GI panel performance for the diagnosis of acute gastroenteritis or hemorragic diarrhea BMC Microbiol 17 111-347
[10]  
Abbo LM(2015)Spectrum of enteropathogens detected by the FilmArray GI panel in a multicentre study of community-acquired gastroenteritis Clin Microbiol Infect 21 719-494