Duke-NUS Medical School, 8 College Road, Singapore, 169857, Singapore.
Children's Intensive Care Unit, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore, 229899, Singapore.
Acta Neurochir (Wien). 2024 Feb 14;166(1):82. doi: 10.1007/s00701-024-05919-0.
We aimed to investigate the association between initial dysnatremia (hyponatremia and hypernatremia) and in-hospital mortality, as well as between initial dysnatremia and functional outcomes, among children with traumatic brain injury (TBI).
We performed a multicenter observational study among 26 pediatric intensive care units from January 2014 to August 2022. We recruited children with TBI under 18 years of age who presented to participating sites within 24 h of injury. We compared demographics and clinical characteristics between children with initial hyponatremia and eu-natremia and between those with initial hypernatremia and eu-natremia. We defined poor functional outcome as a discharge Pediatric Cerebral Performance Category (PCPC) score of moderate, severe disability, coma, and death, or an increase of at least 2 categories from baseline. We performed multivariable logistic regression for mortality and poor PCPC outcome.
Among 648 children, 84 (13.0%) and 42 (6.5%) presented with hyponatremia and hypernatremia, respectively. We observed fewer 14-day ventilation-free days between those with initial hyponatremia [7.0 (interquartile range (IQR) = 0.0-11.0)] and initial hypernatremia [0.0 (IQR = 0.0-10.0)], compared to eu-natremia [9.0 (IQR = 4.0-12.0); p = 0.006 and p < 0.001]. We observed fewer 14-day ICU-free days between those with initial hyponatremia [3.0 (IQR = 0.0-9.0)] and initial hypernatremia [0.0 (IQR = 0.0-3.0)], compared to eu-natremia [7.0 (IQR = 0.0-11.0); p = 0.006 and p < 0.001]. After adjusting for age, severity, and sex, presenting hyponatremia was associated with in-hospital mortality [adjusted odds ratio (aOR) = 2.47, 95% confidence interval (CI) = 1.31-4.66, p = 0.005] and poor outcome (aOR = 1.67, 95% CI = 1.01-2.76, p = 0.045). After adjustment, initial hypernatremia was associated with mortality (aOR = 5.91, 95% CI = 2.85-12.25, p < 0.001) and poor outcome (aOR = 3.00, 95% CI = 1.50-5.98, p = 0.002).
Among children with TBI, presenting dysnatremia was associated with in-hospital mortality and poor functional outcome, particularly hypernatremia. Future research should investigate longitudinal sodium measurements in pediatric TBI and their association with clinical outcomes.
本研究旨在探讨创伤性脑损伤(TBI)患儿入院时的初始血钠异常(低钠血症和高钠血症)与住院死亡率之间的关系,以及初始血钠异常与功能结局之间的关系。
我们进行了一项多中心观察性研究,纳入了 2014 年 1 月至 2022 年 8 月期间 26 家儿科重症监护病房的患儿。纳入年龄在 18 岁以下、受伤后 24 小时内就诊于参与研究机构的 TBI 患儿。我们比较了初始低钠血症和正常血钠组以及初始高钠血症和正常血钠组患儿的人口统计学和临床特征。我们将出院时的儿童脑功能预后评分(PCPC)为中度、重度残疾、昏迷和死亡,或与基线相比至少增加 2 级定义为不良功能结局。我们使用多变量逻辑回归分析死亡率和不良 PCPC 结局。
在 648 名患儿中,分别有 84 名(13.0%)和 42 名(6.5%)患儿出现低钠血症和高钠血症。与正常血钠组相比,初始低钠血症组[7.0(四分位距(IQR)=0.0-11.0)]和初始高钠血症组[0.0(IQR=0.0-10.0)]的 14 天无呼吸机天数更少,p 值分别为 0.006 和 p < 0.001。与正常血钠组相比,初始低钠血症组[3.0(IQR=0.0-9.0)]和初始高钠血症组[0.0(IQR=0.0-3.0)]的 14 天无 ICU 天数更少,p 值分别为 0.006 和 p < 0.001。在校正年龄、严重程度和性别后,入院时的低钠血症与住院死亡率相关[校正优势比(aOR)=2.47,95%置信区间(CI)=1.31-4.66,p=0.005]和不良结局相关[aOR=1.67,95%CI=1.01-2.76,p=0.045]。校正后,初始高钠血症与死亡率相关[aOR=5.91,95%CI=2.85-12.25,p<0.001]和不良结局相关[aOR=3.00,95%CI=1.50-5.98,p=0.002]。
在 TBI 患儿中,入院时的血钠异常与住院死亡率和不良功能结局相关,尤其是高钠血症。未来的研究应探讨儿科 TBI 患者的纵向钠测量及其与临床结局的关系。