Arterial Thrombosis Following Umbilical Artery Catheterization: Visualising Uncommon Neonatal Intensive Care Unit (NICU) Complications

Q3 Medicine
Andrea Calandrino, Alessia Pepe, Francesco Vinci, Luca Antonio Ramenghi
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Abstract

Background

Right internal iliac artery (RIIA) thrombosis is an extremely rare but serious complication associated with umbilical artery catheter (UAC) malposition in neonates in the Neonatal Intensive Care Unit (NICU). Timely diagnosis and appropriate management are essential to prevent long-term sequelae.

Case Report

We present the case of a term neonate with hypoxic–ischaemic encephalopathy (HIE), who developed RIIA thrombosis secondary to UAC malposition, highlighting the role of bedside Doppler ultrasound in diagnosis and monitoring, and the success of a conservative therapeutic approach.

Discussion

A term male neonate with HIE was undergoing therapeutic hypothermia when violaceous macular skin lesions appeared on the right buttock and loin shortly after UAC insertion. Imaging confirmed malposition of the catheter in the RIIA. The catheter was promptly removed, and the patient was closely monitored both clinically and with serial Doppler ultrasounds. Approximately 6 h after catheter removal, Doppler ultrasound revealed a clot in the RIIA. The patient was managed conservatively with continuous infusion of unfractionated heparin (10 IU/kg/h) and topical anti-inflammatory therapy. The skin lesions resolved within 36 h, and Doppler at 48 h post-removal confirmed re-established arterial flow. No invasive interventions were required. This case underscores the importance of careful catheter placement and the utility of bedside Doppler ultrasound in detecting and monitoring vascular complications. Moreover, prompt recognition and conservative treatment of arterial thrombosis can result in optimal outcomes, even in neonates with complex clinical conditions such as birth asphyxia.

Abstract Image

脐动脉置管后动脉血栓形成:观察新生儿重症监护病房(NICU)罕见并发症
背景:右髂内动脉(RIIA)血栓形成是新生儿重症监护病房(NICU)新生儿脐动脉导管(UAC)错位引起的一种极为罕见但严重的并发症。及时诊断和适当管理对预防长期后遗症至关重要。我们报告一例足月新生儿缺氧缺血性脑病(HIE),继发于UAC位错并发RIIA血栓形成,强调床边多普勒超声在诊断和监测中的作用,以及保守治疗方法的成功。一名患有HIE的足月男婴在接受低温治疗时,在UAC插入后不久,右臀部和腰部出现紫色黄斑皮肤病变。影像学证实导管在RIIA位置不正确。立即拔除导管,并对患者进行临床和连续多普勒超声密切监测。拔管后约6小时,多普勒超声显示RIIA有血块。患者给予持续输注未分离肝素(10 IU/kg/h)和局部抗炎治疗。皮肤病变在36小时内消退,去除后48小时多普勒证实动脉血流重新建立。不需要侵入性干预。这个病例强调了小心放置导管的重要性,以及床边多普勒超声在检测和监测血管并发症中的作用。此外,及时识别和保守治疗动脉血栓形成可以获得最佳的结果,即使在新生儿复杂的临床情况,如出生窒息。
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来源期刊
Australasian Journal of Ultrasound in Medicine
Australasian Journal of Ultrasound in Medicine Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.90
自引率
0.00%
发文量
40
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