Division of Neonatology, Department of Paediatrics, University Maternity Hospital Limerick (UMHL), Limerick, Ireland.
Department of Clinical Microbiology, University Hospital Limerick (UHL), Limerick, Ireland.
J Matern Fetal Neonatal Med. 2021 Mar;34(5):780-786. doi: 10.1080/14767058.2019.1617687. Epub 2019 Jul 30.
Blood culture (BC) remains gold standard for the evaluation and diagnosis of neonatal sepsis. Time when BC becomes positive and the type of microorganism isolated are crucial in deciding the antimicrobial management. Likely pathogenicity of organisms growing in BC could potentially be predicted based on the "time to positivity" (TTP). We aimed to estimate the predictive value of isolating a likely pathogenic organism depending on TTP; evaluate the aetiological trend and neonatal mortality rate due to culture-proven neonatal sepsis for over a decade and verify whether the application of a "" to discontinue empiric antibiotics in well newborn infants with negative BC would be safe. Retrospective review of BC results over a 14-year period from a regional neonatal unit in Ireland. Laboratory data were independently extracted in relation to BC results from the laboratory information management system (LIMS-iLAB). Neonatal mortality data were collected from multiple sources. Statistical analysis included logistic regression, chi-square, and Mann-Whitney -test. Over a 14-year period 11,432 neonatal BC specimens were incubated of which 605 (5.3%) turned positive. Overall, the commonest organism grown was coagulase-negative (CoNS), 416 (68.8%). Main pathogenic organisms were 23 (3.8%), spp. 22 (3.6%), 21 (3.5%), (GBS) 18 (3.0%), and species 9 (1.5%). Gram-negative organisms had the shortest TTP, with spp. having a median TTP of 10 h and 11 h. For Gram-positives, GBS had a median TTP of 12 h, species 14 h, with growing at a median time of 15 h. All of the spp. and other Coliforms were detected within 24 h, with, 95.2% of , 94.4% of GBS, 95.5% of , and 95.7% of , flagging positive in 24 h. Using logistic regression the omnibus test of the coefficients in the resulting model was significant ( < .001). Our observed coefficient () for TTP was 0.144; shorter the TTP higher was the likelihood of isolating a pathogenic organism, with an odds ratio (OR) of 1.155. We also report a relatively low blood culture proven sepsis-specific neonatal mortality rate of 0.403/1000 live births and in all such instances observed TTP was less than 24 h. Duration of this study exceeds that of most of the neonatal blood culture TTP analysis published to-date. A shorter TTP is an important adjunct to suggest the growth of a pathogenic organism while managing suspected neonatal sepsis. TTP if < 24 h would not necessarily confirm the growth of a highly pathogenic organism; however, if a positive growth is likely to happen for a significant neonatal pathogen, in more than 98% the TTP would be within 24 h. This offers the clinician more of negative predictive value than a positive one; when there is no growth in BC. Our observation on TTP reiterate the National Institute of Health and Care Excellence (NICE) guideline of discontinuation of empiric antibiotics after 36 h in and clinically well and BC negative newborn infants.
血培养(BC)仍然是评估和诊断新生儿败血症的金标准。BC 变为阳性的时间和分离出的微生物类型对于决定抗菌药物管理至关重要。根据“阳性时间”(TTP),生长在 BC 中的可能致病生物的可能致病性可以预测。我们旨在根据 TTP 估计分离可能致病生物的预测值;评估过去十年因培养证实的新生儿败血症导致的病因趋势和新生儿死亡率,并验证在没有 BC 阴性的健康新生儿中应用“”停止经验性抗生素是否安全。对爱尔兰一个地区新生儿病房 14 年期间的 BC 结果进行回顾性审查。实验室数据是从实验室信息管理系统(LIMS-iLAB)中独立提取与 BC 结果相关的信息。新生儿死亡率数据来自多个来源。统计分析包括逻辑回归、卡方检验和曼-惠特尼 U 检验。在 14 年期间,共孵育了 11432 份新生儿 BC 标本,其中 605 份(5.3%)呈阳性。总体而言,最常见的生长菌是凝固酶阴性葡萄球菌(CoNS),共 416 株(68.8%)。主要的致病生物是 23 株(3.8%), spp. 22 株(3.6%), 21 株(3.5%), (GBS)18 株(3.0%)和 9 株(1.5%)。革兰氏阴性菌的 TTP 最短,其中 spp. 的中位 TTP 为 10 小时, 为 11 小时。对于革兰氏阳性菌,GBS 的中位 TTP 为 12 小时, 种的中位 TTP 为 14 小时,中位时间为 15 小时。所有 spp.和其他肠杆菌科在 24 小时内被检测到,其中,95.2%的 ,94.4%的 GBS,95.5%的 ,95.7%的 ,在 24 小时内呈阳性。使用逻辑回归,对模型中产生的系数进行全系数检验具有统计学意义(<0.001)。我们观察到的 TTP 系数()为 0.144;TTP 越短,分离出致病生物的可能性就越高,优势比(OR)为 1.155。我们还报告了相对较低的血培养证实的败血症特异性新生儿死亡率为 0.403/1000 活产儿,在所有这些情况下,观察到的 TTP 均小于 24 小时。本研究的持续时间超过了迄今为止发表的大多数新生儿血培养 TTP 分析。较短的 TTP 是一个重要的辅助手段,可以提示在疑似新生儿败血症的治疗中生长出一种致病性生物体。如果 TTP<24 小时,则不一定能确认高度致病性生物体的生长;然而,如果一种阳性生长很可能发生在一种重要的新生儿病原体中,那么超过 98%的 TTP 将在 24 小时内发生。这为临床医生提供了比阳性结果更大的阴性预测值;当 BC 中没有生长时。我们对 TTP 的观察结果重申了国家卫生与保健卓越研究所(NICE)的指南,即在 36 小时后停止经验性抗生素治疗,对于临床情况良好且 BC 阴性的新生儿。