Defining the Breakpoint Duration of Staphylococcus aureus Bacteremia Predictive of Poor Outcomes

被引:109
作者
Minejima, Emi [1 ,2 ,3 ]
Mai, Nikki [1 ]
Bui, Nancy [1 ]
Mert, Melissa [4 ,5 ]
Mack, Wendy J. [4 ]
She, Rosemary C. [6 ]
Nieberg, Paul [7 ]
Spellberg, Brad [2 ,3 ,8 ]
Wong-Beringer, Annie [1 ,9 ]
机构
[1] Univ Southern Calif, Dept Clin Pharm, Sch Pharm, Los Angeles, CA 90089 USA
[2] Los Angeles Cty, Los Angeles, CA USA
[3] USC, Med Ctr, Los Angeles, CA USA
[4] USC, Keck Sch Med, Dept Prevent Med, Los Angeles, CA USA
[5] USC, Keck Sch Med, Clin & Translat Sci Inst, Los Angeles, CA USA
[6] USC, Keck Sch Med, Dept Pathol, Los Angeles, CA USA
[7] Huntington Hosp, Dept Med Infect Dis, Pasadena, CA USA
[8] USC, Dept Med, Keck Sch Med, Los Angeles, CA USA
[9] Huntington Hosp, Dept Pharm, Pasadena, CA USA
基金
美国国家卫生研究院;
关键词
S. aureus bacteremia; persistence; mortality; RISK-FACTORS; MORTALITY; PERSISTENCE; VANCOMYCIN; IDENTIFICATION; ENDOCARDITIS; STEWARDSHIP; THERAPY;
D O I
10.1093/cid/ciz257
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Persistent Staphylococcus aureus bacteremia (SAB) is defined based on varying duration in literature. The primary objective was to determine the risk of poor outcomes in relation to bacteremia duration. Methods: Multicenter, prospective, observational study of adult hospitalized patients with SAB. Medical records were reviewed for pertinent data. Patients were grouped by bacteremia duration: short (1-2 days), intermediate (3-6 days), and prolonged (>= 7 days) and compared for risk factors and outcomes. Results: Of 884 patients, 63% had short, 28% intermediate, and 9% prolonged bacteremia. Overall mean age was 57 years, and 70% were male. The prolonged group had the highest proportion of methicillin-resistant SAB (P < .0001). Choice of antibiotic therapy did not significantly affect bacteremia duration; however, time to source-control procedure was delayed in the prolonged and intermediate groups compared with the short group (3.5 vs 3 vs 1 day, P < .0001). Metastatic complications, length of stay, and 30-day mortality were progressively worse as bacteremia duration increased (P < .0001). Every continued day of bacteremia was associated with a relative risk of death of 1.16 (95% confidence interval, 1.10-1.22; P < .0001), with a significant increase in risk starting at 3 days as determined by receiver operating characteristic analysis. Conclusions: Optimal management of SAB should target bacterial clearance as soon as possible to minimize incremental risk of mortality with each day of positive blood culture. Delay in source control but not type of antistaphylococcal therapy was significantly associated with prolonged bacteremia and worse outcomes.
引用
收藏
页码:566 / 573
页数:8
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