Department of Pediatrics, Juntendo University Urayasu Hospital.
Department of Pediatrics, Juntendo University Faculty of Medicine.
Tohoku J Exp Med. 2021 Apr;253(4):275-281. doi: 10.1620/tjem.253.275.
Sepsis and septic shock are associated with high mortality and neurodevelopmental impairment in preterm infants. Recently, endotoxin and mediator removal using a polymyxin B-immobilized fiber column for direct hemoperfusion (PMX-DHP) has been used for the management of septic shock even in neonates. Although early withdrawal from shock with PMX-DHP contributes to survival, its effect on neurodevelopment after discharge is unclear. This study aimed to examine short-term neurodevelopmental impairment in preterm infants with septic shock who were treated with PMX-DHP. We retrospectively assessed five infants who received treatment with PMX-DHP (median 25.5 [interquartile range: 24.8-28.3] weeks and 817 [interquartile range: 667-954] g). Neurodevelopmental outcomes were assessed with the Kyoto Scale of Psychological Development 2001 at a median 34.5 (interquartile range: 29.5-44.5) months of corrected age after discharge. The short-term neurodevelopmental prognosis of preterm infants treated with PMX-DHP for septic shock was delayed (overall developmental quotient < 70) with an average quotient of 57.3. Furthermore, four (80%) of five patients presented with intraventricular hemorrhage and another four (80%) with periventricular leukomalacia. In conclusion, preterm infants with septic shock treated with PMX-DHP had unsatisfactory short-term neurodevelopmental outcomes. Hence, the effect of PMX-DHP in improving neurodevelopmental prognosis even in preterm infants with septic shock should be further evaluated.
败血症和感染性休克与早产儿死亡率和神经发育损害相关。最近,使用聚亚甲基蓝固定纤维柱直接血液灌流(PMX-DHP)清除内毒素和介质已用于治疗败血症性休克,甚至可用于新生儿。尽管 PMX-DHP 早期撤机有助于存活,但对出院后神经发育的影响尚不清楚。本研究旨在检查接受 PMX-DHP 治疗的败血症性休克早产儿的短期神经发育损害。我们回顾性评估了 5 名接受 PMX-DHP 治疗的婴儿(中位数 25.5[四分位距:24.8-28.3]周和 817[四分位距:667-954]g)。出院后中位数 34.5(四分位距:29.5-44.5)个月时,使用京都心理发育量表 2001 评估神经发育结局。PMX-DHP 治疗败血症性休克的早产儿短期神经发育预后延迟(总体发育商<70),平均商数为 57.3。此外,5 名患儿中有 4 名(80%)存在脑室周围出血,4 名(80%)存在脑室周围白质软化。总之,接受 PMX-DHP 治疗的败血症性休克早产儿的短期神经发育结局并不理想。因此,PMX-DHP 改善败血症性休克早产儿神经发育预后的效果应进一步评估。