Eptifibatide bolus dose postductal stenting intervention: A single-center experience.

IF 0.9 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Annals of Pediatric Cardiology Pub Date : 2024-11-01 Epub Date: 2025-04-24 DOI:10.4103/apc.apc_175_24
Rishika Mehta, Amitabha Chattopadhyay, Aritra Mukherji, Sanjiban Ghosh, Jayita Nandy Das, Pushpanjali Gupta
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引用次数: 0

Abstract

Objectives: Stent thrombosis, a potential complication of ductal stenting, is associated with high mortality. This is a catastrophic complication, which can occur acutely (within 24 h), subacutely (within 30 days), or late (≥30 days) after stent implantation, with rates between 0.8% and 25%. Oral antiplatelet drugs like aspirin have erratic and inconsistent absorption and antiplatelet effects in critically ill neonates. Intravenous (IV) glycoprotein IIb/IIIa inhibitors (GPIs) are antiplatelet agents with rapid effect (84% inhibition of platelet aggregation 15 min after bolus) that may help prevent this catastrophic complication.

Materials and methods: The study was conducted among 127 neonates with a median age of 1 month, of which 48% were male, undergoing ductal stenting procedures between January 2022 and March 2024 at our center who received an IV eptifibatide bolus of 180 µg/kg immediately postprocedure. Dosing simulations were generated based on extrapolation from the adult model. The primary outcome measures were stent thrombosis and bleeding events, whereas the secondary outcomes included platelet count.

Results: Stent thrombosis occurred in one of the patients after prophylactic treatment with eptifibatide. Five patients experienced bleeding complications. Eight patients had thrombocytopenia, as thrombosis is prevented via the adenosine diphosphate pathway. The treatment did not affect serum creatinine and liver function.

Conclusion: IV GPIs are safe in neonates after a ductal stenting procedure as an adjunct to oral antiplatelet therapy. Dosing considerations should include age and renal function. Randomized trials are warranted to establish efficacy and compare with current anticoagulation practices.

依替巴肽大剂量导管支架置入术干预:单中心经验。
目的:支架血栓形成是导管支架置入术的潜在并发症,与高死亡率相关。这是一种灾难性的并发症,可在支架植入后急性(24小时内)、亚急性(30天内)或晚期(≥30天)发生,发生率在0.8%至25%之间。口服抗血小板药物如阿司匹林在危重新生儿中具有不稳定和不一致的吸收和抗血小板作用。静脉注射(IV)糖蛋白IIb/IIIa抑制剂(gpi)是一种快速起效的抗血小板药物(在注射后15分钟抑制血小板聚集84%),可能有助于预防这种灾难性并发症。材料和方法:研究对象为127名中位年龄为1个月的新生儿,其中48%为男性,于2022年1月至2024年3月在我中心接受导管支架置入术,术后立即静脉注射180µg/kg依替巴肽。剂量模拟是基于成人模型的外推得出的。主要结局指标是支架内血栓形成和出血事件,而次要结局包括血小板计数。结果:1例患者经依替巴肽预防性治疗后发生支架内血栓形成。5例患者出现出血并发症。8例患者有血小板减少症,因为血栓形成是通过二磷酸腺苷途径预防的。治疗不影响血清肌酐和肝功能。结论:静脉GPIs作为口服抗血小板治疗的辅助手段,在导管支架手术后的新生儿中是安全的。给药时应考虑年龄和肾功能。随机试验是必要的,以建立疗效和比较目前的抗凝实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Annals of Pediatric Cardiology
Annals of Pediatric Cardiology CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
1.40
自引率
14.30%
发文量
51
审稿时长
23 weeks
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