Relationship between immunosuppression and intensive care unit-acquired colonization and infection related to multidrug-resistant bacteria: a prospective multicenter cohort study

被引:20
|
作者
Kreitmann, Louis [1 ,2 ]
Vasseur, Margot [1 ]
Jermoumi, Sonia [1 ]
Perche, Juliette [3 ]
Richard, Jean-Christophe [4 ]
Wallet, Florent [5 ,6 ]
Chabani, Myriam [2 ]
Nourry, Emilie [2 ]
Garcon, Pierre [7 ]
Zerbib, Yoann [8 ]
Van Grunderbeeck, Nicolas [9 ]
Vinsonneau, Christophe [10 ]
Preda, Cristian [11 ,12 ]
Labreuche, Julien [13 ]
Nseir, Saad [1 ,14 ]
机构
[1] CHU Lille, Med Intens Reanimat, F-59000 Lille, France
[2] Hosp Civils Lyon, Hop Edouard Herriot, Med Intens Reanimat, F-69437 Lyon 03, France
[3] Hop Roubaix, Serv Reanimat, Roubaix, France
[4] Hosp Civils Lyon, Hop Croix Rousse, Med Intens Reanimat, F-69004 Lyon, France
[5] Hosp Civils Lyon, Grp Hosp Sud, Serv Reanimat, F-69637 Pierre Benite, France
[6] Claude Bernard Lyon Univ, Ctr Int Rech Infectiol CIRI, ENS Lyon, CNRS UMR5308,INSERM U1111, Villeurbanne, France
[7] Grand Hop Est Francilien, Reanimat, Site Marne La Vallee, Jossigny, France
[8] Ctr Hosp Univ Amiens Picardie, Med Intens Reanimat, Amiens, France
[9] Ctr Hosp Lens, Serv Reanimat Polyvalente, Lens, France
[10] Hop Bethune, Intens Care Unit, F-62408 Bethune, France
[11] Grp Hop Inst Catholique Lille, Dept Med Res, Biostat, Lille, France
[12] Univ Lille, Lab Paul Painleve, CNRS UMR 8524, F-59000 Lille, France
[13] CHU Lille, Dept Biostat, F-59000 Lille, France
[14] Univ Lille, CNRS, Inserm U1285, UMR 8576 UGSF, F-59000 Lille, France
关键词
Intensive Care Unit; Antimicrobial resistance; Cross infection; Immunocompromised host; Patient isolation; CLINICAL-PRACTICE GUIDELINES; LACTAMASE-PRODUCING ENTEROBACTERIACEAE; DISEASES SOCIETY; RISK-FACTORS; DIAGNOSIS; OUTCOMES; MANAGEMENT; THERAPY; UPDATE; ADULTS;
D O I
10.1007/s00134-022-06954-0
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Purpose: The impact of immunosuppression on intensive care unit (ICU)-acquired colonization and infection related to multidrug-resistant (MDR) bacteria (ICU-MDR-col and ICU-MDR-inf, respectively) is unknown. Methods: We carried out an observational prospective cohort study in 8 ICUs in France (all with single-bed rooms and similar organizational characteristics). All consecutive patients with an ICU stay > 48 h were included, regardless of immune status, and followed for 28 days. Patients underwent systematic screening for colonization with MDR bacteria upon admission and every week subsequently. Immunosuppression was defined as active cancer or hematologic malignancy, neutropenia, solid-organ transplant, use of steroids or immunosuppressive drugs, human immunodeficiency virus infection and genetic. The primary endpoint was the incidence rate of a composite outcome including ICU-MDR-col and/or ICU-MDR-inf. Results: 750 patients (65.9% males, median age 65 years) were included, among whom 264 (35.2%) were immunocompromised. Reasons for ICU admission, severity scores and exposure to invasive devices and antibiotics during ICU stay were comparable between groups. After adjustment for center and pre-specified baseline confounders, immunocompromised patients had a lower incidence rate of ICU-MDR-col and/or ICU-MDR-inf (adjusted incidence ratio 0.68, 95% CI 0.52-0.91). When considered separately, the difference was significant for ICU-MDR-col, but not for ICU-MDR-inf. The distribution of MDR bacteria was comparable between groups, with a majority of Enterobacteriacae resistant to third-generation cephalosporins (similar to 74%). Conclusion: Immunocompromised patients had a significantly lower incidence rate of a composite outcome including ICU-MDR-col and/or ICU-MDR-inf. This finding points to the role of contact precautions and isolation measures, and could have important implications on antibiotic stewardship in this population.
引用
收藏
页码:154 / 165
页数:12
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