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A Prospective, Holistic, Multicenter Approach to Tracking and Understanding Bloodstream Infections in Pediatric Hematology-Oncology Patients
被引:18
|作者:
Gaur, Aditya H.
[1
]
Bundy, David G.
[2
]
Werner, Eric J.
[3
]
Hord, Jeffrey D.
[4
]
Miller, Marlene R.
[5
]
Tang, Li
[1
]
Lawlor, John P.
[6
]
Billett, Amy L.
[7
]
机构:
[1] St Jude Childrens Res Hosp, 332 N Lauderdale St, Memphis, TN 38105 USA
[2] Med Univ South Carolina, Charleston, SC USA
[3] Childrens Specialty Grp, Norfolk, VA USA
[4] Akron Childrens Hosp, Akron, OH USA
[5] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[6] Childrens Hosp Assoc, Washington, DC USA
[7] Dana Farber Boston Childrens Canc & Blood Disorde, Boston, MA USA
来源:
关键词:
CELL TRANSPLANT PATIENTS;
ACUTE MYELOID-LEUKEMIA;
CARE;
COMPLICATIONS;
SURVEILLANCE;
DEFINITION;
CENTERS;
CANCER;
RATES;
D O I:
10.1017/ice.2017.57
中图分类号:
R1 [预防医学、卫生学];
学科分类号:
1004 ;
120402 ;
摘要:
OBJECTIVE. To assess the burden of bloodstream infections (BSIs) among pediatric hematology-oncology (PHO) inpatients, to propose a comprehensive, all-BSI tracking approach, and to discuss how such an approach helps better inform within-center and across-center differences in CLABSI rate. DESIGN. Prospective cohort study. SETTING. US multicenter, quality-improvement, BSI prevention network. PARTICIPANTS. PHO centers across the United States who agreed to follow a standardized central-line maintenance care bundle and track all BSI events and central-line days every month. METHODS. Infections were categorized as CLABSI (stratified by mucosal barrier injury related, laboratory-confirmed BSI [MBI-LCBI] versus non MBI-LCBI) and secondary BSI, using National Healthcare Safety Network (NHSN) definitions. Single positive blood cultures (SPBCs) with NHSN defined common commensals were also tracked. RESULTS. Between 2013 and 2015, 34 PHO centers reported 1,110 BSIs. Among them, 708 (63.8%) were CLABSIs, 170 (15.3%) were secondary BSIs, and 232 (20.9%) were SPBCs. Most SPBCs (75%) occurred in patients with profound neutropenia; 22% of SPBCs were viridans group streptococci. Among the CLABSIs, 51% were MBI-LCBI. Excluding SPBCs, CLABSI rates were higher (88% vs 77%) and secondary BSI rates were lower (12% vs 23%) after the NHSN updated the definition of secondary BSI (P <.001). Preliminary analyses showed across-center differences in CLABSI versus secondary BSI and between SPBC and CLABSI versus non-CLABSI rates. CONCLUSIONS. Tracking all BSIs, not just CLABSIs in PHO patients, is a patient-centered, clinically relevant approach that could help better assess across-center and within-center differences in infection rates, including CLABSI. This approach enables informed decision making by healthcare providers, payors, and the public.
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页码:690 / 696
页数:7
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