有无磷酰胆碱涂层心肺搭桥回路的健康技术评估:关于心脏手术安全性和效率的回顾性研究

Life Pub Date : 2024-07-06 DOI:10.3390/life14070851
Ignazzo Condello, G. Nasso, Salvatore Scrivo, F. Fiore, G. Speziale
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The patient cohort was divided into two groups—30 patients whose CPB circuits were coated with phosphorylcholine (phosphorylcholine-coated group) and 30 patients who did not receive phosphorylcholine supplementation or circuit coating. Both groups underwent surgery with identical CPB circuit designs. We assessed the absence of adverse events, safety, and efficacy parameters, including blood loss, clotting, and the structural integrity of the CPB circuit. Additionally, we measured changes in mean albumin levels (g/dL), mean platelet counts (×109/L), and antithrombin III (ATIII) levels before and after CPB. Results: The retrospective analysis revealed an absence of adverse events in both groups. 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引用次数: 0

摘要

背景:磷酰胆碱已成为心肺旁路(CPB)回路的潜在辅助药物。磷酰胆碱是 CPB 循环的涂层,可增强生物相容性并减少血栓事件。然而,它对特定患者群体和手术结果的影响仍未得到充分探讨。材料和方法:在这项回顾性研究中,我们分析了使用 CPB 进行心脏手术的 60 名患者的数据,其中包括冠状动脉旁路移植术 (CABG)、二尖瓣修复术和主动脉瓣置换术各 20 例。患者队列分为两组--30 名患者的 CPB 电路涂有磷酰胆碱(磷酰胆碱涂敷组),30 名患者未接受磷酰胆碱补充或电路涂敷。两组患者均采用相同的 CPB 循环设计进行手术。我们评估了无不良事件、安全性和疗效参数,包括失血、凝血和 CPB 电路结构的完整性。此外,我们还测量了 CPB 前后平均白蛋白水平(g/dL)、平均血小板计数(×109/L)和抗凝血酶 III (ATIII) 水平的变化。结果:回顾性分析显示,两组患者均未发生不良事件。涂抹磷脂胆碱组与未涂抹磷脂胆碱组相比,平均白蛋白水平的δ变化有显著差异(0.87 ± 0.1 vs. 1.65 ± 0.2 g)。1.65 ± 0.2 g/dL,p 值 0.021)、平均血小板计数(42.251 ± 0.121 vs. 54.21 ± 0.194 × 109/L,p 值 0.049)和 ATIII 水平(16.85 ± 0.2 vs. 31.21 ± 0.3,p 值 0.017)的 delta 变化有显著差异。CPB 后围术期消耗的人体复合单位明显减少(3 对 12,P 值 0.019)。结论磷脂胆碱和非磷脂胆碱两组均未发生不良事件,这两种系统对先天性并发症是安全的。我们的研究结果表明,在心脏手术中,在 CPB 循环上使用磷酰胆碱涂层(不使用磷酰胆碱补充剂)与平均白蛋白水平、平均血小板计数和 ATIII 水平的有利变化相关。要全面阐明磷酸胆碱对患者预后和 CPB 循环性能的影响,还需要进一步的研究。
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Health Technology Assessment of Cardiopulmonary Bypass Circuit with and without Phosphorylcholine Coating: A Retrospective Study on Safety and Efficiency in Cardiac Surgery
Background: Phosphorylcholine has emerged as a potential adjunctive agent in cardiopulmonary bypass (CPB) circuits. Phosphorylcholine serves as a coating for the CPB circuit, potentially enhancing biocompatibility and reducing thrombotic events. However, its impact on specific patient populations and procedural outcomes remains underexplored. Materials and Methods: In this retrospective study, we analyzed data from 60 patients who underwent cardiac surgery with CPB, comprising 20 cases each of coronary artery bypass grafting (CABG), mitral valve repair, and aortic valve replacement. The patient cohort was divided into two groups—30 patients whose CPB circuits were coated with phosphorylcholine (phosphorylcholine-coated group) and 30 patients who did not receive phosphorylcholine supplementation or circuit coating. Both groups underwent surgery with identical CPB circuit designs. We assessed the absence of adverse events, safety, and efficacy parameters, including blood loss, clotting, and the structural integrity of the CPB circuit. Additionally, we measured changes in mean albumin levels (g/dL), mean platelet counts (×109/L), and antithrombin III (ATIII) levels before and after CPB. Results: The retrospective analysis revealed an absence of adverse events in both groups. In the phosphorylcholine-coated group compared to the non-phosphorylcholine-coated group, there was a notable difference in the delta change in mean albumin levels (0.87 ± 0.1 vs. 1.65 ± 0.2 g/dL, p-value 0.021), mean platelet counts (42.251 ± 0.121 vs. 54.21 ± 0.194 × 109/L, p-value 0.049), and ATIII levels (16.85 ± 0.2 vs. 31.21 ± 0.3 p-value 0.017). There was a notable reduction in the perioperative consumption of human complex units after CPB (3 vs. 12, p-value 0.019). Conclusions: Both groups, phosphorylcholine and non-phosphorylcholine, demonstrated the absence of adverse events and that the systems are safe for iatrogenic complication. Our findings suggest that the use of phosphorylcholine coating on the CPB circuit, in the absence of supplementary phosphorylcholine, in cardiac surgery is associated with favorable changes in mean albumin levels, mean platelet counts, and ATIII levels. Further research is warranted to elucidate the full extent of phosphorylcholine’s impact on patient outcomes and CPB circuit performance.
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