Department of Pediatrics at the University of Lübeck, Lübeck, Germany.
PLoS One. 2012;7(6):e38304. doi: 10.1371/journal.pone.0038304. Epub 2012 Jun 29.
We evaluated blood culture-proven sepsis episodes occurring in microclusters in very-low-birth-weight infants born in the German Neonatal Network (GNN) during 2009-2010.
Thirty-seven centers participated in GNN; 23 centers enrolled ≥50 VLBW infants in the study period. Data quality was approved by on-site monitoring. Microclusters of sepsis were defined as occurrence of at least two blood-culture proven sepsis events in different patients of one center within 3 months with the same bacterial species. For microcluster analysis, we selected sepsis episodes with typically cross-transmitted bacteria of high clinical significance including gram-negative rods and Enterococcus spp.
In our cohort, 12/2110 (0.6%) infants were documented with an early-onset sepsis and 235 late-onset sepsis episodes (≥72 h of age) occurred in 203/2110 (9.6%) VLBW infants. In 182/235 (77.4%) late-onset sepsis episodes gram-positive bacteria were documented, while coagulase negative staphylococci were found to be the most predominant pathogens (48.5%, 95%CI: 42.01-55.01). Candida spp. and gram-negative bacilli caused 10/235 (4.3%, 95%CI: 1.68% -6.83%) and 43/235 (18.5%) late-onset sepsis episodes, respectively. Eleven microclusters of blood-culture proven sepsis were detected in 7 hospitals involving a total 26 infants. 16/26 cluster patients suffered from Klebsiella spp. sepsis. The median time interval between the first patient's Klebsiella spp. sepsis and cluster cases was 14.1 days (interquartile range: 1-27 days). First patients in the cluster, their linked cases and sporadic sepsis events did not show significant differences in short term outcome parameters.
Microclusters of infection are an important phenomenon for late-onset sepsis. Most gram-negative cluster infections occur within 30 days after the first patient was diagnosed and Klebsiella spp. play a major role. It is essential to monitor epidemic microclusters of sepsis in surveillance networks to adapt clinical practice, inform policy and further improve quality of care.
我们评估了 2009 年至 2010 年期间在德国新生儿网络(GNN)中出生的极低出生体重儿(VLBW)中发生的血液培养阳性败血症发作的微簇。
37 个中心参与了 GNN;23 个中心在研究期间招募了≥50 名 VLBW 婴儿。通过现场监测批准了数据质量。微簇败血症定义为在 3 个月内,同一中心的不同患者中至少发生两次血培养阳性败血症事件,且细菌种类相同。为了进行微簇分析,我们选择了具有高临床意义的典型交叉传播细菌的败血症发作,包括革兰氏阴性杆菌和肠球菌属。
在我们的队列中,12/2110(0.6%)名婴儿被记录为早发性败血症,235 例晚发性败血症(≥72 小时)发生在 2110 名 VLBW 婴儿中的 203 例。在 182/235(77.4%)例晚发性败血症中,记录了革兰氏阳性菌,而凝固酶阴性葡萄球菌被发现是最主要的病原体(48.5%,95%CI:42.01-55.01)。念珠菌和革兰氏阴性杆菌分别引起 10/235(4.3%,95%CI:1.68%-6.83%)和 43/235(18.5%)例晚发性败血症。在 7 家医院中检测到 11 个血液培养阳性败血症的微簇,共涉及 26 名婴儿。16/26 例簇患者患有克雷伯菌属败血症。首例克雷伯菌属败血症患者与簇病例之间的中位时间间隔为 14.1 天(四分位距:1-27 天)。集群中的首例患者、其关联病例和散发性败血症事件在短期预后参数方面无显著差异。
感染微簇是晚发性败血症的一个重要现象。大多数革兰氏阴性簇感染发生在首例患者确诊后的 30 天内,克雷伯菌属起主要作用。在监测网络中监测败血症的流行微簇,以适应临床实践、告知政策和进一步提高护理质量是至关重要的。