Department of Pediatrics and Child Health, Weill Bugando School of Medicine, P.O. Box 1464, Mwanza, Tanzania.
Department of Microbiology and Immunology, Weill Bugando School of Medicine, P.O. Box 1464, Mwanza, Tanzania.
Int J Med Microbiol. 2018 Oct;308(7):803-811. doi: 10.1016/j.ijmm.2018.06.012. Epub 2018 Jul 2.
The study was conducted to establish predictors of extended-spectrum beta-lactamase-producing Enterobacteriaceae (ESBL-PE) neonatal sepsis and mortality in a tertiary hospital, Tanzania. Between July and December 2016, blood culture was performed in neonates with clinical features of sepsis and neonates/mothers/guardians were screened for ESBL colonization. Selected isolates underwent whole genome sequencing to investigate relatedness. Logistic regression analysis was performed to determine predictors for ESBL-PE associated neonatal sepsis and mortality. Neonatal ESBL-PE sepsis was detected in 32(10.5%) of the 304 neonates investigated. Neonatal ESBL-PE sepsis was independently predicted by admission at the Intensive care Unit and positive mother and neonate ESBL-PE colonization. Deaths occurred in 55(18.1%) of neonates. Neonates infected with ESBL-PE, admitted at ICU, increased age and those transferred from other centres had significantly high mortality rates. Gram-negative bacteria formed the majority (76%) of the isolates, of which 77% were ESBL-PE. Virulent Klebsiella pneumoniae ST45 carrying bla were commonly isolated from neonates. Klebsiella pneumoniae (ST45) were the predominant cause of ESBL-PE neonatal sepsis and mortality. Improved infection control and antibiotic stewardship are crucial in controlling the spread of resistant strains. Rapid diagnostic tests to detect ESBL-PE in low-income countries are needed to guide treatment and reduce ESBL-PE-associated mortality.
本研究旨在确定坦桑尼亚一家三级医院中产超广谱β-内酰胺酶(ESBL)肠杆菌科(ESBL-PE)新生儿败血症和死亡的预测因素。2016 年 7 月至 12 月,对具有败血症临床特征的新生儿进行血培养,并对新生儿/母亲/监护人进行 ESBL 定植筛查。选择的分离株进行全基因组测序以调查相关性。采用逻辑回归分析确定与 ESBL-PE 相关的新生儿败血症和死亡率的预测因素。在 304 名接受调查的新生儿中,发现 32 例(10.5%)新生儿患有 ESBL-PE 败血症。新生儿 ESBL-PE 败血症的独立预测因素是入住重症监护病房和母亲及新生儿 ESBL-PE 定植阳性。55 例(18.1%)新生儿死亡。感染 ESBL-PE 的新生儿、入住 ICU、年龄较大以及从其他中心转来的新生儿死亡率显著较高。革兰氏阴性菌是分离株的主要(76%)组成部分,其中 77%为 ESBL-PE。毒力较强的肺炎克雷伯菌 ST45 携带 bla,常从新生儿中分离出来。肺炎克雷伯菌(ST45)是导致 ESBL-PE 新生儿败血症和死亡的主要原因。改善感染控制和抗生素管理对于控制耐药菌株的传播至关重要。在低收入国家需要快速诊断试验来检测 ESBL-PE,以指导治疗并降低 ESBL-PE 相关死亡率。