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Association of late‐onset neonatal sepsis with late neurodevelopment in the first two years of life of preterm infants with very low birth weight

机译:出生体重很低的早产儿出生后头两年的新生儿败血症与晚期神经发育的关系

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Objective To establish the influence of late‐onset sepsis on neurodevelopment of preterm infants with very low birth weight (VLBW), according to the etiologic agent. Method This was a cohort of newborns with birth weight < 1,500g and gestational age less than 32 weeks, admitted to the institutional intensive care unit (ICU) with up to 48hours of life, and followed‐up at the outpatient follow‐up clinic for preterm infants with VLBW until 2 years of corrected age. Exclusion criteria: death within the first 72hours of life, congenital malformations and genetic syndromes, children with congenital infection by the human immunodeficiency virus (HIV), congenital infection (STORCH), presence of early‐onset spesis and cases with more than one pathogen growth in blood cultures. Septic and non‐septic infants were compared regarding neonatal outcomes and mortality. Neurodevelopment was assessed using the Bayley Scale (BSDI‐II) at 18 to 24 months of corrected age. Results 411 preterm infants with VLBW were eligible; the mean gestational age was 29 ± 2.2 weeks and mean birth weight was 1,041 ± 281grams. Late‐onset sepsis occurred in 94 preterm infants with VLBW (22.8%). VLBW infants with Gram‐positive infection showed motor deficit when compared to the non‐septic group, 68.8% vs. 29.3%, respectively (OR 6; 1.6‐21.8, p = 0.006); the cognitive development was similar between the groups. The overall mortality rate from infection was 26.7%; considering the pathogens, the rates were 18.7% for coagulase‐negative Staphylococcus, 21.8% for Gram‐positive bacteria, and 50% for Gram‐negative bacteria and fungi. Conclusion Neonatal sepsis has a significant influence on late neurodevelopment at 2 years of corrected age in preterm infants with VLBW, and Gram‐positive infections are associated with motor deficit.
机译:目的根据病原学,确定晚期脓毒症对极低出生体重(VLBW)早产儿神经发育的影响。方法这是一组新生儿,出生体重<1,500g,胎龄小于32周,入院重症监护病房(ICU),寿命长达48小时,并在门诊随访诊所进行随访。患有VLBW的早产儿,直到2岁的校正年龄。排除标准:生命的前72小时内死亡,先天性畸形和遗传综合症,患有人类免疫缺陷病毒(HIV)的先天性感染的儿童,先天性感染(STORCH),早发性麻痹的存在以及病原体生长超过一个的病例在血液文化中。比较了败血症和非败血症婴儿的新生儿结局和死亡率。在18至24个月的校正年龄时,使用Bayley量表(BSDI-II)评估神经发育。结果411例VLBW早产儿符合条件。平均胎龄为29±2.2周,平均出生体重为1,041±281克。 94例VLBW早产儿发生迟发败血症(22.8%)。与非脓毒症组相比,患有革兰氏阳性感染的VLBW婴儿分别显示出运动缺陷,分别为68.8%和29.3%(OR 6; 1.6-21.8,p = 0.006);两组之间的认知发展相似。感染造成的总死亡率为26.7%;考虑到病原体,凝固酶阴性葡萄球菌的发生率为18.7%,革兰氏阳性细菌的发生率为21.8%,革兰氏阴性细菌和真菌的发生率为50%。结论新生儿败血症对VLBW早产儿在校正年龄2岁时的晚期神经发育有重要影响,革兰氏阳性感染与运动功能障碍有关。

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