Yao Sarah, Chong Shu-Ling, Allen John Carson, Dang Hongxing, Ming Meixiu, Chan Lawrence C N, Gan Chin Seng, Ji Jian, Fan Lijia, Kurosawa Hiroshi, Lee Jan Hau
Department of Emergency Medicine, KK Women's and Children's Hospital, Singapore, Singapore.
Duke-NUS Medical School, Singapore.
Transl Pediatr. 2023 Mar 31;12(3):344-353. doi: 10.21037/tp-22-443. Epub 2023 Mar 9.
To study the association in moderate and severe pediatric traumatic brain injury (TBI) between hyperglycemia, hyperlactatemia, acidosis and unfavorable outcome, as assessed by Pediatric Cerebral Performance Category (PCPC) on discharge from the pediatric intensive care unit (PICU).
Children <16 years old with TBI and Glasgow Coma Scale (GCS) ≤13 in an Asian multi-center PICU TBI cohort from January 2014 to October 2017 were included in this study. We defined unfavorable outcome as PCPC ≥3-moderate disability, severe disability, vegetative state, and death. We performed logistic regression to investigate the association between metabolic changes with unfavorable outcome. We divided hyperglycemia (glucose >11.1 mmol/L) during PICU admission into early-onset (within 24 h), late-onset (beyond 48 h) and persistent (throughout first 72 h).
Among the 305 children analyzed, 136 (44.6%) had unfavorable outcome. Children with unfavorable outcome were more likely to have early hyperglycemia (75/136, 55.1% 33/169, 19.5%; P<0.001), high lactate levels >2.0 mmol/L (74/136, 54.4% 56/169, 32.5%; P<0.001) and initial acidosis (85/136, 62.5% 78/169, 56.1%; P=0.003) compared to those with favorable outcome. After adjusting for gender, GCS ≤8 and presence of polytrauma, early hyperglycemia [adjusted odds ratio (aOR) =3.68, 95% CI: 2.12-6.39, P<0.001] and late hyperglycemia (aOR =13.30, 95% CI: 1.64-107.8, P=0.015] were independently associated with unfavorable outcome. All children with persistent hyperglycemia died.
We described unfavorable outcome in pediatric TBI especially with persistent hyperglycemia. Future trials should investigate the causal relationship between glycemic trends, early intervention and outcome in this cohort.
研究小儿重症监护病房(PICU)出院时,根据小儿脑功能表现分类(PCPC)评估的中度和重度小儿创伤性脑损伤(TBI)中高血糖、高乳酸血症、酸中毒与不良结局之间的关联。
纳入2014年1月至2017年10月在亚洲多中心PICU TBI队列中年龄<16岁、格拉斯哥昏迷量表(GCS)≤13的TBI患儿。我们将不良结局定义为PCPC≥3——中度残疾、重度残疾、植物状态和死亡。我们进行逻辑回归分析,以研究代谢变化与不良结局之间的关联。我们将PICU住院期间的高血糖(血糖>11.1 mmol/L)分为早发性(24小时内)、晚发性(48小时后)和持续性(最初72小时内持续存在)。
在分析的305名儿童中,136名(44.6%)有不良结局。与结局良好的儿童相比,结局不良的儿童更可能出现早发性高血糖(75/136,55.1%对33/169,19.5%;P<0.001)、乳酸水平>2.0 mmol/L(74/136,54.4%对56/169,32.5%;P<0.001)和初始酸中毒(85/136,62.5%对78/169,56.1%;P=0.003)。在调整性别、GCS≤8和多发伤的存在后,早发性高血糖[调整后的优势比(aOR)=3.68,95%置信区间:2.12 - 6.39,P<0.001]和晚发性高血糖(aOR =13.30,95%置信区间:1.64 - 107.8,P=0.015)与不良结局独立相关。所有持续性高血糖的儿童均死亡。
我们描述了小儿TBI尤其是持续性高血糖的不良结局。未来的试验应研究该队列中血糖趋势、早期干预与结局之间的因果关系。