Tröger Birte, Härtel Christoph, Buer Jan, Dördelmann Michael, Felderhoff-Müser Ursula, Höhn Thomas, Hepping Nico, Hillebrand Georg, Kribs Angela, Marissen Janina, Olbertz Dirk, Rath Peter-Michael, Schmidtke Susanne, Siegel Jens, Herting Egbert, Göpel Wolfgang, Steinmann Joerg, Stein Anja
Department of Pediatrics at the University of Lübeck, Lübeck, Germany.
Institute of Medical Microbiology, University of Duisburg-Essen, Essen, Germany.
PLoS One. 2016 Jul 29;11(7):e0159821. doi: 10.1371/journal.pone.0159821. eCollection 2016.
In the German Neonatal Network (GNN) 10% of very-low-birth weight infants (VLBWI) suffer from blood-culture confirmed sepsis, while 30% of VLBWI develop clinical sepsis. Diagnosis of sepsis is a difficult task leading to potential over-treatment with antibiotics. This study aims to investigate whether the results of blood multiplex-PCR (SeptiFast®) for common sepsis pathogens are relevant for clinical decision making when sepsis is suspected in VLBWI.
We performed a prospective, multi-centre study within the GNN including 133 VLBWI with 214 episodes of suspected late onset sepsis (LOS). In patients with suspected sepsis a multiplex-PCR (LightCycler SeptiFast MGRADE-test®) was performed from 100 μl EDTA blood in addition to center-specific laboratory biomarkers. The attending neonatologist documented whether the PCR-result, which was available after 24 to 48 hrs, had an impact on the choice of antibiotic drugs and duration of therapy.
PCR was positive in 110/214 episodes (51%) and blood culture (BC) was positive in 55 episodes (26%). Both methods yielded predominantly coagulase-negative staphylococci (CoNS) followed by Escherichia coli and Staphylococcus aureus. In 214 BC-PCR paired samples concordant results were documented in 126 episodes (59%; n = 32 were concordant pathogen positive results, n = 94 were negative in both methods). In 65 episodes (30%) we found positive PCR results but negative BCs, with CoNS being identified in 43 (66%) of these samples. Multiplex-PCR results influenced clinical decision making in 30% of episodes, specifically in 18% for the choice of antimicrobial therapy and in 22% for the duration of antimicrobial therapy.
Multiplex-PCR results had a moderate impact on clinical management in about one third of LOS-episodes. The main advantage of multiplex-PCR was the rapid detection of pathogens from micro-volume blood samples. In VLBWI limitations include risk of contamination, lack of resistance testing and high costs. The high rate of positive PCR results in episodes of negative BC might lead to overtreatment of infants which is associated with risk of mortality, antibiotic resistance, fungal sepsis and NEC.
在德国新生儿网络(GNN)中,10%的极低出生体重儿(VLBWI)患有血培养确诊的败血症,而30%的VLBWI发生临床败血症。败血症的诊断是一项艰巨的任务,可能导致抗生素的过度治疗。本研究旨在调查当怀疑VLBWI患有败血症时,针对常见败血症病原体的血液多重聚合酶链反应(SeptiFast®)结果是否与临床决策相关。
我们在GNN内进行了一项前瞻性、多中心研究,纳入了133例VLBWI,发生214次疑似晚发型败血症(LOS)发作。在疑似败血症的患者中,除了中心特定的实验室生物标志物外,还从100μl乙二胺四乙酸(EDTA)血样中进行了多重聚合酶链反应(LightCycler SeptiFast MGRADE检测®)。主治新生儿科医生记录24至48小时后获得的聚合酶链反应结果是否对抗生素药物的选择和治疗持续时间有影响。
214次发作中有110次(51%)聚合酶链反应呈阳性,血培养(BC)有55次(26%)呈阳性。两种方法检出的主要是凝固酶阴性葡萄球菌(CoNS),其次是大肠杆菌和金黄色葡萄球菌。在214对血培养-聚合酶链反应配对样本中,126次发作(59%;n = 32为病原体阳性结果一致,n = 94两种方法均为阴性)记录到结果一致。在65次发作(30%)中,我们发现聚合酶链反应结果为阳性但血培养为阴性,其中43份(66%)样本鉴定出CoNS。多重聚合酶链反应结果在30%的发作中影响了临床决策,具体而言,在18%的发作中影响了抗菌治疗的选择,在22%的发作中影响了抗菌治疗的持续时间。
多重聚合酶链反应结果在约三分之一的LOS发作中对临床管理有中度影响。多重聚合酶链反应的主要优点是能从微量血样中快速检测病原体。在VLBWI中,其局限性包括污染风险、缺乏耐药性检测和成本高。血培养阴性发作中聚合酶链反应阳性率高可能导致婴儿过度治疗,这与死亡风险、抗生素耐药性、真菌败血症和坏死性小肠结肠炎有关。