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Risk factors for colonisation by Multidrug-Resistant bacteria in critical care units
被引:3
|作者:
Garcia-Parejo, Yolanda
[1
]
Gonzalez-Rubio, Jesus
[2
,3
]
Guerrero, Jesus Garcia
[1
]
Sango, Ana Gomez-Juarez
[1
]
Escribano, Jose Miguel Cantero
[1
]
Najera, Alberto
[2
,3
]
机构:
[1] Albacete Univ, Dept Prevent Med & Publ Hlth, Teaching Hosp Complex, Albacete 02006, Spain
[2] Univ Castilla La Mancha, Fac Med Albacete, Dept Med Sci, Albacete, Spain
[3] Univ Castilla La Mancha, Ctr Biomed Res CRIB, Albacete, Spain
关键词:
Antimicrobial Resistance;
Critical Patient Units;
Healthcare-Associated Infections;
Intensive Care;
Multidrug-Resistant Bacteria;
Nosocomial Infections;
Zero-Resistance Project;
LACTAMASE-PRODUCING ENTEROBACTERIACEAE;
ANTIMICROBIAL RESISTANCE;
ANTIBIOTIC-RESISTANCE;
INFECTIONS;
ASSOCIATION;
PREVENTION;
STRATEGIES;
ADMISSION;
NEED;
SEX;
D O I:
10.1016/j.iccn.2024.103760
中图分类号:
R4 [临床医学];
学科分类号:
1002 ;
100602 ;
摘要:
Introduction: Antimicrobial resistance is a major public health challenge recognised by the WHO as an urgent global healthcare concern. Patients in Intensive Care Units (ICUs) are particularly prone to colonisation and/or infection by multidrug-resistant organisms (MDROs). Objectives: Delineate the epidemiological characteristics and risk factors for MDROs colonisation in mixed ICUs and Resuscitation Units by focusing on initial and nosocomial colonisation. Material and Methods: A descriptive observational study with analytical elements. It uses the Zero-Resistance register from the Preventive Medicine Service of the Albacete General University Hospital (Spain) from April 2016 to December 2021. It identifies the risk factors for MDROs colonisation. Results: Of 7,541 cases, 61.0 % with initial colonisation had risk factors for MDROs versus 34.0 % not colonised upon hospitalisation (p < 0.001). Significant risk factors for initial colonisation included hospitalisation for >= 5 days within the last 3 months, prior MDROs colonisation/infection and institutionalization. No significant risk factor differences were found for nosocomial colonisation. An association between longer ICU stays and nosocomial colonisation (p < 0.001) was noted. Conclusions: Significant risk factors for initial MDROs colonisation were hospitalisation for >= 5 days in the last 3 months, prior MDROs colonisation/infection and institutionalisation. Longer ICU stays increased the nosocomial colonisation risk. Implications for Clinical Practice: This study underscores the importance to early identify and manage patients at risk for MDROs colonisation in ICUs. By recognising factors (i.e. previous hospitalisations, existing colonisation or infection, impact of prolonged ICU stay), healthcare providers can implement targeted strategies to mitigate the spread of MDROs; e.g. enhanced surveillance, stringent infection control measures and judicious antibiotics use. Our findings highlight the need for a comprehensive approach to manage antimicrobial resistance in critical care settings to ultimately improve patient outcomes and reduce MDROs burden in hospitals.
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