Qiu Han, Gao Ting, Qian Tianyang, Cao Yun, Cheng Guoqiang, Wang Laishuan
Department of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
Key Laboratory of Neonatal Disease, Ministry of Health, Shanghai, China.
Transl Pediatr. 2022 Dec;11(12):1899-1907. doi: 10.21037/tp-22-70.
Hyperammonemia due to inherited metabolic disease can lead to neurological sequelae and death in neonates. Metabolite scavenger (MS) administration and dialysis can be helpful. We aim at analyzing the factors affecting short-term survival in neonates with hyperammonemia.
We conducted a retrospective study including all neonates with hyperammonemia admitted to the neonatal intensive care unit (NICU) of the Children's Hospital of Fudan University between April 2013 and June 2020.
Sixty-two neonates were enrolled in the study. Of these, 32 neonates were included in the non-survival group, and 30 neonates in the survival group. Compared to the survival group, the non-survival group had a higher peak ammonia level (882.2 . 433.4 µmol/L) (P=0.002), a shorter length of stay (5.7 . 22.3 d) (P<0.000), and higher rates of acidosis (19 . 10) (P=0.047), electrolyte disturbance (15 . 6) (P=0.033), coma (12 . 2) (P=0.005), and invasive mechanical ventilation (28 . 8) (P=0.000). A longer length of stay was the most significant protective factors in the multivariate logistic regression analysis, followed by MS administration. Factors of invasive mechanical ventilation, Δ<0 (Δ= last ammonia level - first ammonia level), coma and electrolyte disturbance established a risk score model that performed well in survival analysis. Area under ROC curve for survival length of hyperammonemia combined with peak ammonia levels was 0.737 (95% CI: 0.603-0.870).
MS administration is an effective treatment method for hyperammonemia in neonates, and increasing the length of stay in the NICU could help improve short-term survival. Further intervention should be administered when peak ammonia levels >406.5 µmol/L.
遗传性代谢疾病所致高氨血症可导致新生儿出现神经后遗症甚至死亡。给予代谢物清除剂(MS)及进行透析可能会有所帮助。我们旨在分析影响高氨血症新生儿短期生存的因素。
我们进行了一项回顾性研究,纳入了2013年4月至2020年6月期间复旦大学附属儿科医院新生儿重症监护病房(NICU)收治的所有高氨血症新生儿。
62例新生儿纳入本研究。其中,32例新生儿进入非存活组,30例新生儿进入存活组。与存活组相比,非存活组的氨峰值水平更高(882.2. 433.4 μmol/L)(P = 0.002),住院时间更短(5.7. 22.3天)(P < 0.000),酸中毒发生率更高(19. 10)(P = 0.047),电解质紊乱发生率更高(15. 6)(P = 0.033),昏迷发生率更高(12. 2)(P = 0.005),有创机械通气发生率更高(28. 8)(P = 0.000)。在多因素逻辑回归分析中,较长的住院时间是最显著的保护因素,其次是给予MS。有创机械通气、Δ<0(Δ=末次氨水平 - 首次氨水平)、昏迷和电解质紊乱等因素建立了一个在生存分析中表现良好的风险评分模型。高氨血症生存时长联合氨峰值水平的ROC曲线下面积为0.737(95%CI:0.603 - 0.870)。
给予MS是治疗新生儿高氨血症的有效方法,延长在NICU的住院时间有助于提高短期生存率。当氨峰值水平>406.5 μmol/L时应进行进一步干预。