Kuhn Jessica E, Pareja Zabala Maria C, Chavez Maria Mateo, Almodóvar Melvin, Mulinari Leonardo A, Sainathan Sandeep, de Rivero Vaccari Juan Pablo, Wang Kevin K, Muñoz Pareja Jennifer C
University of Miami Miller School of Medicine, Miami, Florida.
Department of Pediatrics Medical College of Wisconsin, Milwaukee, Wisconsin.
Pediatr Neurol. 2023 Nov;148:44-53. doi: 10.1016/j.pediatrneurol.2023.06.024. Epub 2023 Jul 6.
Congenital heart disease (CHD) affects roughly 40,000 children annually. Despite advancements, children undergoing surgery for CHD are at an increased risk for adverse neurological outcomes. At present, there is no gold standard for the diagnosis of cerebral injury during the perioperative period.
To determine the utility of brain injury biomarkers in children undergoing cardiac surgery.
We searched PUBMED, EMBASE, LILACS, EBSCO, ClinicalTrials.gov, Cochrane Databases, and OVID interface to search MEDLINE through July 2021 and assessed the literature following the snowball method. The search terms used were "congenital heart disease," "cardiopulmonary bypass," "biomarkers," "diagnosis," "prognosis," and "children." No language or publication date restrictions were used. Papers studying inflammatory and imaging biomarkers were excluded. The risk of bias, strengths, and limitations of the study were reported. Study was registered in PROSPERO ID: CRD42021258385.
A total of 1449 articles were retrieved, and 27 were included. Eight neurological biomarkers were examined. Outcomes assessed included prognosis of poor neurological outcome, mortality, readmission, and diagnosis of brain injury. Results from these studies support that significant perioperative elevations in brain injury biomarkers in cerebrospinal fluid and serum, including S100B, GFAP, NSE, and activin A, may be diagnostic of real-time brain injury and serve as an independent predictor of adverse neurological outcomes in patients with CHD undergoing cardiopulmonary bypass.
There are limited homogeneous data in the field, limiting the generalizability and comparability of the results. Further large-scale longitudinal studies addressing neurological biomarkers in children undergoing CHD corrective surgery are required to support the routine use of neuronal biomarkers in this population.
先天性心脏病(CHD)每年大约影响40000名儿童。尽管取得了进展,但接受CHD手术的儿童出现不良神经结局的风险增加。目前,围手术期脑损伤的诊断尚无金标准。
确定脑损伤生物标志物在接受心脏手术儿童中的效用。
我们检索了PUBMED、EMBASE、LILACS、EBSCO、ClinicalTrials.gov、Cochrane数据库和OVID界面,以检索截至2021年7月的MEDLINE,并采用滚雪球法评估文献。使用的检索词为“先天性心脏病”、“体外循环”、“生物标志物”、“诊断”、“预后”和“儿童”。未设语言或出版日期限制。排除研究炎症和成像生物标志物的论文。报告了研究的偏倚风险、优势和局限性。该研究已在PROSPERO注册,编号为:CRD42021258385。
共检索到1449篇文章,纳入27篇。检查了八种神经生物标志物。评估的结局包括不良神经结局的预后、死亡率、再入院率和脑损伤的诊断。这些研究结果支持,脑脊液和血清中脑损伤生物标志物在围手术期显著升高,包括S100B、GFAP、NSE和激活素A,可能诊断实时脑损伤,并可作为接受体外循环的CHD患者不良神经结局的独立预测指标。
该领域同质数据有限,限制了结果的普遍性和可比性。需要进一步开展大规模纵向研究,以探讨接受CHD矫正手术儿童的神经生物标志物,以支持在该人群中常规使用神经元生物标志物。