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短暂性脑缺血发作症状后检测到大型设备相关血栓。

Large Device-Related Thrombus Detected following Symptoms of Transient Ischemic Attack.

作者信息

Lawani Osayi, Baptista Edward

机构信息

University of Houston College of Medicine/HCA Houston Healthcare, USA.

Vital Heart & Vein, USA.

出版信息

Case Rep Cardiol. 2021 Nov 23;2021:9195984. doi: 10.1155/2021/9195984. eCollection 2021.

Abstract

As an independent risk factor for stroke, atrial fibrillation has been shown to be associated with a fivefold increase in the cause of embolic stroke in comparison to healthy individuals without atrial fibrillation. This risk may be compounded by other factors; however, the main probable cause of stroke leading from atrial fibrillation is thrombus formation in the left atrial appendage. In patients for whom anticoagulation is contraindicated, left atrial appendage occlusion has become a leading alternative option for therapeutic prevention of thromboembolism and stroke in patients with this condition. Unfortunately, these devices (particularly the WATCHMAN) have been associated with a 3-6% incidence of intracardiac thrombus development postimplantation. Some risk factors for the development of device-related thrombus are high platelet count, permanent atrial fibrillation, resistance to clopidogrel, and prior transient ischemic attack or stroke. Despite following an anticoagulant regimen, thrombus formation was reported in 5.6% of participants of a randomized clinical trial, and further analysis showed that some of these patients continued to develop either ischemic stroke or thromboembolism five years later as compared to patients without initial thrombus development. We present a case of an elderly male with prior history of stroke and transient ischemic attack who developed a large device-related thrombus five months following WATCHMAN FLX™ implantation. Currently, there are no specific recommendations on the management of this rare complication; however, we discuss possible consideration of initially prolonging anticoagulation therapy following implantation for high-risk individuals, as there is an increased possibility for thrombus formation in this population. Management options should continue to be studied for therapeutic benefit in streamlining postprocedural therapy and improve future outcomes in the use of left atrial appendage occlusion devices, as well as continual thrombus prevention.

摘要

作为中风的一个独立危险因素,与无房颤的健康个体相比,房颤已被证明与栓塞性中风病因增加五倍有关。其他因素可能会使这种风险加剧;然而,房颤导致中风的主要可能原因是左心耳血栓形成。对于抗凝治疗禁忌的患者,左心耳封堵已成为治疗性预防此类患者血栓栓塞和中风的主要替代选择。不幸的是,这些装置(尤其是WATCHMAN)植入后心内血栓形成的发生率为3%-6%。与装置相关血栓形成的一些危险因素包括血小板计数高、永久性房颤、对氯吡格雷耐药以及既往短暂性脑缺血发作或中风。尽管遵循抗凝方案,但在一项随机临床试验的参与者中,有5.6%报告有血栓形成,进一步分析表明,与最初无血栓形成的患者相比,其中一些患者在五年后仍继续发生缺血性中风或血栓栓塞。我们报告一例老年男性病例,该患者有中风和短暂性脑缺血发作病史,在植入WATCHMAN FLX™ 五个月后发生了与装置相关的大血栓。目前,对于这种罕见并发症的管理尚无具体建议;然而,我们讨论了对于高危个体在植入后最初延长抗凝治疗的可能考虑,因为该人群血栓形成的可能性增加。应继续研究管理选项,以获得简化术后治疗的治疗益处,并改善使用左心耳封堵装置的未来结果以及持续预防血栓。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22e4/8632399/d92c7fd83132/CRIC2021-9195984.001.jpg

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