Risk factors for acquisition of OXA-48-producing Klebsiella pneumonia among contact patients: a multicentre study

被引:16
作者
Hilliquin, D. [1 ]
Le Guern, R. [2 ]
Seegers, V. Thepot [3 ,4 ]
Neulier, C. [5 ]
Lomont, A. [6 ]
Marie, V. [7 ,8 ]
Legeay, C. [1 ]
Merrer, J. [5 ]
Lepelletier, D. [9 ,10 ]
Rogues, A. M. [7 ,8 ]
Grandbastien, B. [2 ]
Lucet, J. C. [6 ]
Zahar, J. R. [11 ,12 ]
机构
[1] CHU Angers, Unite Prevent & Lutte Infect Nosocomiales, Angers, France
[2] CHRU Lille, Serv Gest Risque Infectieux & Vigilances, Lille, France
[3] Pole Biometrie, Inst Cancerol Ouest, Dept Biostat, Angers, France
[4] Univ Angers, SFR ICAT, Angers, France
[5] CH Andre Mignot, Serv Prevent Risque Infectieux, Versailles, France
[6] AP HP, Bichat Claude Bernard Hop, Infect Control Unit, Paris, France
[7] Grp Hosp Pelllegrin, Serv Hyg Hosp, Bordeaux, France
[8] Univ Bordeaux, INSERM, U1219, Bordeaux, France
[9] CHU Nantes, Serv Bacteriol Hyg Hosp, Nantes, France
[10] Univ Nantes, Equipe Emergente, Lab MiHAR, Nantes, France
[11] Univ Paris 13, Sorbonne Paris Cite, IAME, UMR 1137, Paris, France
[12] Grp Hosp Paris Seine St Denis, AP HP, Dept Microbiol Clin, Unite Controle & Prevent Risque Infectieux, Bobigny, France
关键词
Carbapenemases; Carbapenemase-producing; Enterobacteriaceae; Risk factors; Screening; OXA-48; Contact patients; CARBAPENEM-RESISTANT ENTEROBACTERIACEAE; INFECTION; OUTBREAK; SPREAD; IMPACT; TIME;
D O I
10.1016/j.jhin.2017.08.024
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Cohorting carbapenemase-producing Enterobacteriaceae (CPE) carriers during hospitalization limits in-hospital spreading. Aim: To identify risk factors for CPE acquisition among contacts of an index patient in non-cohorted populations. Methods: A multicentre retrospective matched case-control study was conducted in five hospitals. Each contact patient (case) who acquired Klebsiella pneumoniae (KP)-OXA-48 from an index patient was compared to three contact (controls) with the same index patients matched with hospitalization in the same unit and similar exposure times. Findings: Fifty-one secondary cases and 131 controls were included. By univariate analysis, exposure time (odds ratio: 1.06; 95% confidence interval: 1.02-1.1; P = 0.006), concomitant infection at admission (3.23; 1.42-7.35; P = 0.005), antimicrobial therapy within the last month before hospitalization (2.88; 1.34-6.2; P = 0.007), antimicrobial therapy during the exposure time (5.36; 2.28-12.6; P < 0.001), use of at least one invasive procedure (2.99; 1.25-7.15; P = 0.014), number of invasive procedures (1.52; 1.05-2.19; P = 0.025), and geographical proximity (2.84; 1.15-7.00; P = 0.023) were associated with CPE acquisition. By multivariate analysis, antimicrobial therapy during the exposure time (odds ratio: 6.36; 95% confidence interval: 2.46-16.44; P < 0.001), at least one invasive procedure (2.92; 1.04-8.17; P = 0.041), and geographical proximity (3.69; 1.15-11.86; P = 0.028) were associated with acquisition. Conclusion: In this study, geographical proximity, invasive procedure, and antimicrobial therapy during exposure time were significantly associated with KP-OXA-48 acquisition. (C) 2017 The Healthcare Infection Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:253 / 259
页数:7
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