A new simplified predictive model for mortality in methicillin-resistant Staphylococcus aureus bacteremia

被引:6
作者
Jorgensen, Sarah C. J. [1 ]
Lagnf, Abdalhamid M. [1 ]
Bhatia, Sahil [1 ]
Rybak, Michael J. [1 ,2 ,3 ]
机构
[1] Wayne State Univ, Eugene Applebaum Coll Pharm & Hlth Sci, Antiinfect Res Lab, 259 Mack Ave, Detroit, MI 48201 USA
[2] Detroit Med Ctr, Dept Pharm, Detroit, MI 48201 USA
[3] Wayne State Univ, Sch Med, Detroit, MI 48202 USA
关键词
Methicillin-resistant Staphylococcus aureus; Bacteremia; Risk stratification; APACHE II; Pitt bacteremia score; CLINICAL-FEATURES; RISK-FACTORS; INFECTIONS; VANCOMYCIN; THERAPY; ENDOCARDITIS; CRITERIA; OUTCOMES;
D O I
10.1007/s10096-018-03464-0
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Adjustment for confounding is important in observational methicillin-resistant Staphylococcus aureus bacteremia (MRSAB) studies due to the wide spectrum of disease severity and baseline health status that patients present with. The objectives of this study were to develop a simplified MRSAB-specific scoring model to estimate the risk of 30-day all-cause mortality and to compare its performance to the APACHE II and Pitt Bacteremia scores. Retrospective, singe-center, cohort study in adults with MRSAB 2008 to 2018. Independent predictors of mortality were identified through multivariable logistic regression. A scoring model was derived using a regression coefficient-based scoring method. Discriminatory ability was assessed using the c statistic. A total of 455 patients were included. Thirty-day mortality was 16.3%. The MRSAB score consisted of six variables: age, respiratory rate, Glasgow Coma scale, renal failure, hospital-acquired MRSAB, and infective endocarditis or lower respiratory tract infection source. The score demonstrated very good discrimination (c statistic 0.8662, 95% CI 0.824-0.909) and was superior to the APACHE II (P = 0.043) and the Pitt bacteremia (P < 0.001) scores. A weighted combination of six independent variables routinely measured in patients with MRSAB can be used to predict, with high discrimination, 30-day all-cause mortality. External validation is required before widespread use.
引用
收藏
页码:843 / 850
页数:8
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