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The Value of Combining Blood Culture and SeptiFast Data for Predicting Complicated Bloodstream Infections Caused by Gram-Positive Bacteria or Candida Species

机译:结合血液培养和SeptiFast数据预测由革兰氏阳性细菌或念珠菌引起的复杂血流感染的价值

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摘要

Management of complicated bloodstream infections requires more aggressive treatment than uncomplicated bloodstream infections. We assessed the value of follow-up blood culture in bloodstream infections caused by Staphylococcus aureus, Enterococcus spp., Streptococcus spp., and Candida spp. and studied the value of persistence of DNA in blood (using SeptiFast) for predicting complicated bloodstream infections. Patients with bloodstream infections caused by these microorganisms were enrolled prospectively. After the first positive blood culture, samples were obtained every third day to perform blood culture and SeptiFast analyses simultaneously. Patients were followed to detect complicated bloodstream infection. The study sample comprised 119 patients. One-third of the patients developed complicated bloodstream infections. The values of persistently positive tests to predict complicated bloodstream infections were as follows: SeptiFast positive samples (sensitivity, 56%; specificity, 79.5%; positive predictive value, 54%; negative predictive value, 80.5%; accuracy, 72.3%) and positive blood cultures (sensitivity, 30.5%; specificity, 92.8%; positive predictive value, 64%; negative predictive value, 75.5%; accuracy, 73.9%). Multivariate analysis showed that patients with a positive SeptiFast result between days 3 and 7 had an almost 8-fold-higher risk of developing a complicated bloodstream infection. In S. aureus, the combination of both techniques to exclude endovascular complications was significantly better than the use of blood culture alone. We obtained a score with variables selected by the multivariate model. With a cutoff of 7, the negative predictive value for complicated bloodstream infection was 96.6%. Patients with a positive SeptiFast result between days 3 and 7 after a positive blood culture have an almost 8-fold-higher risk of developing complicated bloodstream infections. A score combining clinical data with the SeptiFast result may improve the exclusion of complicated bloodstream infections.
机译:与不复杂的血液感染相比,处理复杂的血液感染需要更积极的治疗。我们评估了后续血液培养在由金黄色葡萄球菌,肠球菌,链球菌和念珠菌引起的血液感染中的价值。并研究了血液中DNA的持久性(使用SeptiFast)对预测复杂的血液感染的价值。由这些微生物引起的血流感染患者前瞻性入组。首次阳性血液培养后,每三天获取一次样本,以同时进行血液培养和SeptiFast分析。跟踪患者以发现复杂的血液感染。该研究样本包括119名患者。三分之一的患者发生了复杂的血液感染。预测复杂的血液感染的持续阳性测试的值如下:SeptiFast阳性样品(敏感性为56%;特异性为79.5%;阳性预测值为54%;阴性预测值为80.5%;准确性为72.3%)和阳性血液培养(灵敏度为30.5%;特异性为92.8%;阳性预测值为64%;阴性预测值为75.5%;准确性为73.9%)。多因素分析显示,在第3天到第7天之间SeptiFast结果呈阳性的患者发生复杂的血液感染的风险几乎高8倍。在金黄色葡萄球菌中,排除血管内并发症的两种技术的结合明显优于单独使用血液培养。我们获得了一个由多元模型选择的变量的得分。截止值为7,复杂血液感染的阴性预测值为96.6%。血液培养阳性后第3天到第7天之间SeptiFast结果阳性的患者发生复杂的血液感染的风险要高将近8倍。将临床数据与SeptiFast结果相结合的评分可以改善排除复杂的血液感染的可能性。

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