Aamir Saad, Gravino Gilbert, Abdelsalam Nasr, Chandran Arun
Department of Neuroradiology, Walton Centre for Neurology and Neurosurgery, Liverpool, UK.
Interv Neuroradiol. 2025 Sep 8:15910199251372502. doi: 10.1177/15910199251372502.
ObjectiveThis study aims to determine the outcomes of nickel allergic patients who underwent a trial of forearm arterial stenting with a nickel-based stent, with follow-up to assess for an allergic reaction. In the absence of adverse effects, patients had their intracranial aneurysm treatment with a nickel-based cerebrovascular device.MethodsA retrospective analysis was performed on patients who had an allergy to nickel, with an intracranial aneurysm who underwent treatment with a permanently implanted nickel-containing device. Nickel allergy was established by clinical history and dedicated patch testing. Outcomes such as in-stent thrombosis or any intracranial complications were recorded.ResultsOver a 10-year period, there were 18 patients who had a peripheral stent without development of in-stent stenosis, thrombosis or occlusion. One patient developed a cutaneous allergic reaction to the peripheral stent and their intracranial procedure was with a nitinol-free device.Of 17 patients who underwent intracranial treatment with a nitinol device, there was one patient who developed a postoperative complication of fish-mouthing of the device which has been reported in patients with a nickel contact allergy, but further studies are warranted to establish a causative relationship. Another patient omitted prescribed antiplatelet medication and occluded their stent. The remaining fifteen patients developed no complications with aneurysm occlusion on imaging.ConclusionPatients with a nickel allergy who would be eligible for endovascular treatment could benefit from trial peripheral arterial stenting. This provides an alternative approach to avoid unnecessarily eliminating endovascular treatment options with nickel-containing devices from which these patients may potentially still benefit.
目的
本研究旨在确定接受镍基支架前臂动脉支架置入试验的镍过敏患者的治疗结果,并进行随访以评估过敏反应。在无不良反应的情况下,患者使用镍基脑血管装置进行颅内动脉瘤治疗。
方法
对镍过敏且患有颅内动脉瘤并接受永久性植入含镍装置治疗的患者进行回顾性分析。通过临床病史和专门的斑贴试验确定镍过敏。记录支架内血栓形成或任何颅内并发症等结果。
结果
在10年期间,有18例患者接受了外周支架置入,未出现支架内狭窄、血栓形成或闭塞。1例患者对外周支架发生皮肤过敏反应,其颅内手术使用了不含镍钛诺的装置。
在17例接受镍钛诺装置颅内治疗的患者中,有1例患者出现了装置鱼嘴样术后并发症,这种情况在镍接触过敏患者中已有报道,但需要进一步研究以确定因果关系。另1例患者未按规定服用抗血小板药物,导致支架闭塞。其余15例患者影像学检查显示动脉瘤闭塞无并发症。
结论
符合血管内治疗条件的镍过敏患者可能从试验性外周动脉支架置入中获益。这提供了一种替代方法,避免不必要地排除这些患者可能仍能从中获益且含镍装置的血管内治疗选择。