Department of Pediatrics, Children's National Hospital, Washington, DC, USA.
Global Health Initiative, Children's National Hospital, Washington, DC, USA.
Malar J. 2024 Jan 19;23(1):28. doi: 10.1186/s12936-024-04843-z.
In children with cerebral malaria (CM) admission blood lactate has previously guided intravenous fluid therapy and been validated as a prognostic biomarker associated with death. The usefulness of post-admission measurements of blood lactate in children with CM is less clear. The strength of association between blood lactate and neurological sequelae in CM survivors, as well as the optimal duration of post-admission measurements of blood lactate to identify children at higher risk of adverse outcomes is unknown.
A retrospective cohort study of 1674 Malawian children with CM hospitalized from 2000 to 2018 who had blood lactate measurements every 6 h for the first 24 h after admission was performed. The strength of association between admission lactate or values measured at any time point in the first 24 h post-admission and outcomes (mortality and neurological morbidity in survivors) was estimated. The duration of time after admission that lactate remained a valid prognostic biomarker was assessed.
When lactate is analysed as a continuous variable, children with CM who have higher values at admission have a 1.05-fold higher odds (95% CI 0.99-1.11) of death compared to those with lower lactate values. Children with higher blood lactate at 6 h have 1.16-fold higher odds (95% CI 1.09-1.23) of death, compared to those with lower values. If lactate levels are dichotomized into hyperlactataemic (lactate > 5.0 mmol/L) or not, the strength of association between admission lactate and mortality increases (OR = 2.49, 95% CI 1.47-4.22). Blood lactate levels obtained after 18 h post-admission are not associated with outcomes. Similarly, the change in lactate concentrations through time during the first 24 h of hospital admission is not associated with outcomes. Blood lactate during hospitalization is not associated with adverse neurologic outcomes in CM survivors.
In children with CM, blood lactate is associated with death but not neurologic morbidity in survivors. To comprehensively estimate prognosis, blood lactate in children with CM should be assessed at admission and for 18 h afterwards.
在患有脑疟疾(CM)的儿童中,入院时的血乳酸曾指导过静脉输液治疗,并被验证为与死亡相关的预后生物标志物。CM 患儿入院后血乳酸测量的用途尚不清楚。CM 幸存者中血乳酸与神经后遗症之间的关联强度,以及确定发生不良结局风险较高的患儿所需的入院后血乳酸测量的最佳持续时间尚不清楚。
对 2000 年至 2018 年期间在马拉维住院的 1674 名患有 CM 的儿童进行了回顾性队列研究,这些儿童在入院后 24 小时内每 6 小时测量一次血乳酸。入院时的血乳酸或入院后 24 小时内任何时间点测量的血乳酸值与结局(幸存者的死亡率和神经发病率)之间的关联强度进行了评估。评估了入院后血乳酸仍然是有效的预后生物标志物的时间长度。
当血乳酸作为连续变量进行分析时,入院时血乳酸值较高的 CM 患儿死亡的几率是血乳酸值较低的患儿的 1.05 倍(95%CI 0.99-1.11)。与血乳酸值较低的患儿相比,入院后 6 小时血乳酸值较高的患儿死亡的几率高 1.16 倍(95%CI 1.09-1.23)。如果将血乳酸水平分为高乳酸血症(血乳酸>5.0mmol/L)或非高乳酸血症,入院时血乳酸与死亡率之间的关联强度增加(OR=2.49,95%CI 1.47-4.22)。入院后 18 小时后获得的血乳酸水平与结局无关。同样,入院后 24 小时内血乳酸浓度随时间的变化与结局无关。CM 幸存者住院期间的血乳酸与不良神经结局无关。
在患有 CM 的儿童中,血乳酸与死亡相关,但与幸存者的神经发病率无关。为了全面评估预后,应在入院时和入院后 18 小时评估 CM 患儿的血乳酸。