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Factors involved in initiation and regulation of complement lectin pathway influence postoperative outcome after pediatric cardiac surgery involving cardiopulmonary bypass

机译:涉及补体血凝素途径启动和调节的因素影响小儿心脏外科手术(体外循环)后的结局

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摘要

Congenital heart disease (CHD) often requires surgical intervention, and is sometimes associated with life-threatening post-operative complications. We have investigated some factors of the innate immune system involved in the initiation or regulation of complement lectin pathway activation (MASP-1, MASP-2 MASP-3, MAp19, MAp44, ficolin-3) and related them to complications and prognosis in 190 pediatric patients undergoing CHD repair with the use of cardiopulmonary bypass (CPB). Patients with MAp44 levels ≤1.81 µg/ml more frequently experienced low cardiac output syndrome (LCOS), renal insufficiency, systemic inflammatory response syndrome (SIRS) and multiorgan dysfunction (MODS). Low MASP-3 (≤5.18 µg/ml) and high MASP-1 (≥11.7 µg/ml) levels were often associated with fatal outcome. Low ficolin-3 concentrations (≤10.1 µg/ml) were more common among patients experiencing SIRS and MODS than in those without complications. However, patients suffering from SIRS and MODS with low ficolin-3 had a much better prognosis (91% survival vs. 37% among other patients; p = 0.007). A discriminating value of 12.7 µg/ml ficolin-3 yielded 8% vs. 60% mortality (p = 0.001). Our data extend the knowledge concerning involvement of proteins of the lectin pathway in development of post-CPB complications. The potential prognostic value of low preoperative MAp44 and high preoperative ficolin-3 seems promising and warrants independent confirmation.
机译:先天性心脏病(CHD)通常需要外科手术干预,有时还伴有危及生命的术后并发症。我们研究了与补体凝集素途径激活(MASP-1,MASP-2,MASP-3,MAp19,MAp44,ficolin-3)的启动或调控有关的先天免疫系统的一些因素,并将它们与190的并发症和预后相关使用体外循环(CPB)进行冠心病修复的小儿科患者。 MAp44水平≤1.81µg / ml的患者更常发生低心输出量综合征(LCOS),肾功能不全,全身性炎症反应综合征(SIRS)和多器官功能障碍(MODS)。低MASP-3(≤5.18μg/ ml)和高MASP-1(≥11.7μg/ ml)通常与致命结局有关。患有SIRS和MODS的患者比没有并发症的患者更常见低ficolin-3浓度(≤10.1μg/ ml)。但是,患有Ficolin-3低的SIRS和MODS患者的预后要好得多(存活率分别为91%和37%; p; = 0.007)。 ficolin-3的辨别值为12.7μg/ ml,可产生8%的死亡率和60%的死亡率(p = 0.001)。我们的数据扩展了有关凝集素途径蛋白参与CPB后并发症发展的知识。低术前MAp44和高术前Ficolin-3的潜在预后价值似乎很有希望,值得独立确认。

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