术中输血是儿童心脏手术后脑损伤的危险因素:一项前瞻性观察研究

A. Ivkin, E. Grigoryev, D. G. B. D. G. Balakhnin, I. I. Chermnykh
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引用次数: 0

摘要

供体血液成分能够启动系统性炎症反应综合征(SIRS),并增强神经炎症和随后的脑损伤。目的:探讨输血对儿童先天性心脏缺陷矫正术中脑损伤发展的影响。材料与方法:78例患者,年龄1 ~ 78月龄,体重3.3 ~ 21.5 kg。所有患者均在体外循环下进行了室间隔缺损矫正。所有患者被分为不输血组和输血组。研究脑损伤标志物(S-100-β蛋白、神经元特异性烯醇化酶(NSE)和胶质纤维酸性蛋白(GFAP))和SIRS(白细胞介素1 (ILb-1)、6 (IL-6)、10 (IL-10)和肿瘤坏死因子α (TNF-α))。在三个控制点研究标志物:1 -手术开始前,2 -体外循环结束后立即,3 -手术结束后16小时。结果:两组患者血液中大部分标志物的浓度峰值均出现在第2个控制点。输血组在第2个控制点各脑损伤指标S-100-β蛋白(ng/ml)分别为509.90[379.30-871.70]和717.10[517.90-1195.33],差异有统计学意义(χ = 0.024);分析了无(ng / ml) - 17.55(11.19 - -26.41)和34.05(17.06 - -44.90)(р= 0023);GFAP (ng/ml) - 0.1190[0.1135-0.1245]和0.1231[0.1138-0.1493]。脑损伤指标与SIRS存在相关性,其中NSE与TNF-α在第3个控制点的相关性最强,Rho = 0.43 (p = 0.0001)。S-100-β蛋白与输血量在第2、3个控制点存在相关性(Rho = 0.48, p = 0.00065), Rho = 0.36, p = 0.01330。结论:已证实输血事实和红细胞剂量对儿童心脏手术中脑损伤发展的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intraoperative transfusion is a risk factor for cerebral injury after cardiac surgery in children: a prospective observational study
INTRODUCTION: Donor blood components are able to initiate a systemic inflammatory response syndrome (SIRS) and potentiate neuroinflammation with subsequent cerebral damage. OBJECTIVE: To study the effect of transfusion on the development of cerebral damage during the surgical correction of congenital heart defects in children. MATERIALS AND METHODS: 78 patients aged from 1 to 78 months, weighing from 3.3 to 21.5 kg, were studied. All patients underwent correction of a septal defect under cardiopulmonary bypass. All patients were divided to group 1 — without the use of transfusion and group 2 — with the use of red blood cell transfusion. Cerebral damage markers (S-100-β protein, neuron-specific enolase (NSE) and glial fibrillar acidic protein (GFAP)) and SIRS (interleukins 1 (ILb-1), 6 (IL-6), 10 (IL-10) and tumor necrosis factor alpha (TNF-α) were studied. Markers ware studied at three control points: 1 — before the start of surgery, 2 — immediately after end of cardiopulmonary bypass, 3 — 16 hours after the end of the operation. RESULTS: The peak concentration of most markers in the blood in both groups of patients was noted at the 2nd control point. The concentration of all markers of cerebral damage was significantly higher in the transfusion group at the 2nd control point: S-100-β protein (ng/ml) — 509.90 [379.30–871.70] and 717.10 [517.90–1195.33] (р = 0.024); NSE (ng/ml) — 17.55 [11.19–26.41] and 34.05 [17.06–44.90] (р = 0,023); GFAP (ng/ml) — 0.1190 [0.1135–0.1245] and 0.1231 [0.1138–0.1493]. Correlations were found between markers of cerebral damage and SIRS, the strongest of which was the relationship between NSE and TNF-α at the 3rd control point — Rho = 0.43 (p = 0.0001). A correlation of S-100-β protein with transfusion volume was observed at the 2nd (Rho = 0.48, p = 0.00065) and 3rd control points (Rho = 0.36, p = 0.01330). CONCLUSIONS: The influence of the fact of transfusion and the dose of red blood cell on the development of cerebral damage during cardiac surgery in children has been proven.
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