Department of Ophthalmology, Nasser Ibrahim Al-Rashid Orbital Vision Research Center, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida, USA.
Department of Mechanical and Aerospace Engineering, University of Miami, Coral Gables, Florida, USA.
Am J Ophthalmol. 2020 Dec;220:27-36. doi: 10.1016/j.ajo.2020.06.032. Epub 2020 Jul 22.
A proof-of-concept workflow study for the fabrication of custom orbital exenteration prostheses via automated noncontact scanning, 3D printing, and silicone casting.
Noncomparative, interventional case series.
Setting: Single-center institutional study. StudyPopulation: Three patients who have discontinued wearing of the ocularist-made exenteration prosthesis due to altered fit, discoloration, or material degradation. InterventionProcedure: A digital representation of the exenteration socket and contralateral periocular region was captured through noncontact facial topography mapping. Digital construction of the anterior prosthesis surface was based on the mirrored image of the contralateral side, and the posterior surface contour was based on orbital cavity geometry. The anterior and posterior surface details were digitally merged. A 2-piece mold was designed and produced in a 3D printer. Colorimetry was used to create a custom blend of pigments for incorporation into the Shore 40 silicone elastomer to generate a prosthesis that approximates the patient's skin tone. MainOutcomeMeasures: Prosthesis symmetry, skin tone match, comfort of wear, and appearance.
The first copy of every 3D-printed orbital prosthesis using this fabrication workflow produced good symmetry, color match, and prosthesis fit. In one case, the recontoured second copy with improved prosthesis edge-to-skin interface was made without the patient present.
A noncontact 3D scanning, computer-aided design, 3D printing, and silicone casting for fabrication of orbital prosthesis was developed and validated. This production workflow has the potential to provide an efficient, standardized, reproducible exenteration prosthesis and to overcome the principal barriers to an affordable custom prosthesis worldwide: access and cost.
通过自动化非接触式扫描、3D 打印和硅橡胶铸模来制作定制眼眶内容物摘除义眼的概念验证工作流程研究。
非对照、介入性病例系列研究。
设置:单中心机构研究。研究人群:三位因适配性改变、变色或材料降解而停止佩戴义眼制造商制作的眼眶内容物摘除义眼的患者。干预程序:通过非接触式面部拓扑图测绘捕获眼眶内容物摘除窝和对侧眼眶区域的数字表示。前义眼表面的数字构建基于对侧的镜像,而后部表面轮廓则基于眼眶腔几何形状。将前、后表面细节进行数字合并。设计并使用 3D 打印机制作 2 件式模具。比色法用于创建自定义颜料混合物,以掺入 Shore 40 硅橡胶弹性体中,生成接近患者肤色的义眼。主要观察指标:义眼对称性、肤色匹配、佩戴舒适度和外观。
使用这种制造工作流程制作的每个 3D 打印眼眶义眼的第一份副本都具有良好的对称性、颜色匹配和义眼适配。在一个病例中,使用改进的义眼边缘与皮肤接口的重新塑形的第二份副本在患者未在场的情况下制作。
开发并验证了一种用于制作眼眶义眼的非接触式 3D 扫描、计算机辅助设计、3D 打印和硅橡胶铸造技术。这种生产工作流程有可能提供一种高效、标准化、可重复的眼眶内容物摘除义眼,并克服全球范围内负担得起的定制义眼的主要障碍:可及性和成本。