Early-onset sepsis: a predictive model based on maternal risk factors

被引:26
作者
Puopolo, Karen M. [1 ,2 ]
Escobar, Gabriel J. [3 ,4 ]
机构
[1] Brigham & Womens Hosp, Dept Newborn Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Kaiser Permanente Northern Calif, Div Res, Oakland, CA USA
[4] Kaiser Permanente Med Ctr, Dept Pediat, Walnut Creek, CA USA
关键词
Bayesian statistics; intrapartum antibiotics; neonatal early-onset sepsis; neonatal infection; risk prediction; B STREPTOCOCCAL DISEASE; NEONATAL SEPSIS; PREVENTION; MANAGEMENT; INFECTION; BURDEN;
D O I
10.1097/MOP.0b013e32835e1f96
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Purpose of review Neonatal early-onset sepsis (EOS) is a very low-incidence, but potentially fatal condition among term and late preterm newborns. EOS algorithms based on risk-factor threshold values result in evaluation and empiric antibiotic treatment of large numbers of uninfected newborns, leading to unnecessary antibiotic exposures and maternal/infant separation. Ideally, risk stratification should be quantitative, employ information conserving strategies, and be readily transferable to modern comprehensive electronic medical records. Recent findings We performed a case-control study of infants born at or above 34 weeks' gestation with blood culture-proven EOS. We defined the relationship of established predictors to the risk of EOS, then used multivariate analyses and split validation to develop a predictive model using objective data. The model provides an estimation of sepsis risk that can identify the same proportion of EOS cases by evaluating fewer infants, as compared with algorithms based on subjective diagnoses and cut-off values for continuous predictors. Summary An alternative approach to EOS risk assessment based only on objective data could decrease the number of infants evaluated and empirically treated for EOS, compared with currently recommended algorithms. Prospective evaluation is needed to determine the accuracy and safety of using the sepsis risk model to guide clinical decision-making.
引用
收藏
页码:161 / 166
页数:6
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