Use of Cervical Approach for Insertion of the Impella 5.5 Ventricular Assist Device (Abiomed) in Pediatric Patients: Cohort Study.

Mohammed Absi, Andrew J Gienapp, Cihangir Buyukgoz, Shyam Sathanandam, Umar Boston
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Abstract

Background: Impella 5.5 ventricular assist device (VAD) insertion is typically done via the axillary artery or directly through the aorta; however, an axillary artery must be ≥6 mm in diameter, which excludes many pediatric patients who do not meet this criterion. The innominate artery is a larger vessel that can better accommodate the Impella VAD in pediatric patients. Outcomes of this technique were compared with other pediatric patients undergoing the standard axillary artery cannulation.

Methods: The Heart Center at Le Bonheur Children's Hospital recently adopted the trans-innominate cervical approach for insertion of the Impella 5.5 VAD. We performed a retrospective cohort study comparing these cases to data collected from cases using an axillary approach found in the Advanced Cardiac Therapies Improving Outcomes Network database. Comparisons between preoperative characteristics, postoperative course, adverse events, anticoagulation, and clinical outcomes for these two groups were analyzed.

Results: Thirty-nine patients were implanted via the axillary approach; seven patients were implanted via the transinnominate cervical approach at our institution. Patients inserted via the trans-innominate approach had fewer days on the device (median, 8 [range, 3-24]), postimplant intensive care unit days (16 [3-24]), and hospital length of stay (14 [3-28]) compared with axillary insertion patients (12.5 [6.75-29.2], 58.5 [12.5-43.5], and 32 [19.7-83.5], respectively). Trans-innominate patients had fewer adverse events than axillary patients.

Conclusions: Trans-innominate cervical approach for insertion of the Impella 5.5 VAD is safe with low rates of adverse events in pediatric patients. As miniaturization of VAD therapy continues to evolve, this technique may provide greater application of these devices for even smaller children.

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在儿科患者中使用颈入路置入Impella 5.5心室辅助装置(Abiomed):队列研究
背景:Impella 5.5心室辅助装置(VAD)的插入通常通过腋窝动脉或直接通过主动脉;然而,腋窝动脉必须直径≥6mm,这就排除了许多不符合这一标准的儿科患者。无名动脉是一种更大的血管,可以更好地容纳儿科患者的Impella VAD。该技术的结果与其他接受标准腋窝动脉插管的儿童患者进行了比较。方法:Le Bonheur儿童医院心脏中心最近采用经无名颈入路置入Impella 5.5 VAD。我们进行了一项回顾性队列研究,将这些病例与先进心脏治疗改善预后网络数据库中使用腋窝入路的病例收集的数据进行比较。比较两组患者的术前特点、术后过程、不良事件、抗凝治疗及临床结果。结果:39例患者经腋窝入路植入;本院有7例患者经经颈椎入路植入。与腋窝置入患者(分别为12.5[6.75-29.2]、58.5[12.5-43.5]和32[19.7-83.5])相比,经经无名氏入路置入的患者使用器械的天数(中位数为8[范围,3-24])、植入后重症监护病房天数(16[3-24])和住院时间(14[3-28])更短。跨无名患者的不良事件少于腋窝患者。结论:经宫颈入路置入Impella 5.5 VAD是安全的,儿科患者不良事件发生率低。随着VAD治疗的小型化不断发展,这项技术可能为这些设备提供更大的应用,甚至是更小的儿童。
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