在护理点使用三维打印来处理面膜坏死性筋膜炎的复杂伤口:一个病例报告。

IF 3.2 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING 3D printing in medicine Pub Date : 2023-02-23 DOI:10.1186/s41205-022-00166-4
Sarah C Nyirjesy, Ryan T Judd, Yazen Alfayez, Peter Lancione, Brian Swendseid, Natalia von Windheim, Stephen Nogan, Nolan B Seim, Kyle K VanKoevering
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引用次数: 1

摘要

背景:复杂的面部创伤由于靠近重要结构而难以稳定。我们提出了一个病例,在病人特定的伤口夹板制造使用计算机辅助设计和三维打印在护理点,以允许伤口稳定设置的半面坏死性筋膜炎。我们还描述了美国食品和药物管理局扩大医疗器械应急使用机制的过程和实施。病例介绍:一名58岁女性,颈部及半面部出现坏死性筋膜炎。多次清创后,患者病情仍然危重,伤口床组织血管性差,无健康肉芽组织的迹象,担心向右眼眶、纵隔和气管前软组织进一步破裂,尽管延长了插管时间,但仍无法进行气管造口术。负压伤口真空被认为可以改善愈合,但靠近眼睛会引起牵引力损伤导致视力丧失的担忧。作为一种解决方案,根据食品和药物管理局的医疗设备紧急使用扩展通道机制,我们设计了一种三维打印的、患者专用的硅胶伤口夹板,通过CT扫描,使伤口真空固定在夹板上,而不是眼睑上。经过5天的夹板辅助真空治疗,伤口床稳定,无脓残留,肉芽组织发育健康,无眼睛或下眼睑损伤。在持续的真空治疗下,伤口收缩,以便于1个月后进行安全的气管切开术、释放呼吸机、口服吸入,并使用胸肌筋膜肌瓣和旁正中额瓣进行半面部重建。在六个月的随访中,她的伤口愈合和眶周功能良好。结论:患者特异性的三维打印技术是一种创新的解决方案,可以促进负压伤口治疗靠近脆弱结构的安全放置。本报告还展示了定制设备在护理点制造的可行性,以优化头颈部的复杂伤口管理,并描述了美国食品和药物管理局医疗设备应急使用机制的成功使用。
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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Use of 3-dimensional printing at the point-of-care to manage a complex wound in hemifacial necrotizing fasciitis: a case report.

Background: Complex facial wounds can be difficult to stabilize due to proximity of vital structures. We present a case in which a patient-specific wound splint was manufactured using computer assisted design and three-dimensional printing at the point-of-care to allow for wound stabilization in the setting of hemifacial necrotizing fasciitis. We also describe the process and implementation of the United States Food and Drug Administration Expanded Access for Medical Devices Emergency Use mechanism.

Case presentation: A 58-year-old female presented with necrotizing fasciitis of the neck and hemiface. After multiple debridements, she remained critically ill with poor vascularity of tissue in the wound bed and no evidence of healthy granulation tissue and concern for additional breakdown towards the right orbit, mediastinum, and pretracheal soft tissues, precluding tracheostomy placement despite prolonged intubation. A negative pressure wound vacuum was considered for improved healing, but proximity to the eye raised concern for vision loss due to traction injury. As a solution, under the Food and Drug Administration's Expanded Access for Medical Devices Emergency Use mechanism, we designed a three-dimensional printed, patient-specific silicone wound splint from a CT scan, allowing the wound vacuum to be secured to the splint rather than the eyelid. After 5 days of splint-assisted vacuum therapy, the wound bed stabilized with no residual purulence and developed healthy granulation tissue, without injury to the eye or lower lid. With continued vacuum therapy, the wound contracted to allow for safe tracheostomy placement, ventilator liberation, oral intake, and hemifacial reconstruction with a myofascial pectoralis muscle flap and a paramedian forehead flap 1 month later. She was eventually decannulated and at six-month follow-up has excellent wound healing and periorbital function.

Conclusions: Patient-specific, three-dimensional printing is an innovative solution that can facilitate safe placement of negative pressure wound therapy adjacent to delicate structures. This report also demonstrates feasibility of point-of-care manufacturing of customized devices for optimizing complex wound management in the head and neck, and describes successful use of the United States Food and Drug Administration's Expanded Access for Medical Devices Emergency Use mechanism.

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