From the Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, MI.
Cosm Medical Corp., Toronto, ON, Canada.
Urogynecology (Phila). 2023 Sep 1;29(9):732-739. doi: 10.1097/SPV.0000000000001346. Epub 2023 Mar 9.
Vaginal pessaries are an effective nonsurgical treatment for pelvic organ prolapse (POP) when properly fitted. However, pessary fitting and use are often unsuccessful or imperfect.
The objective of this study was to assess the feasibility of using patient-specific pessaries fabricated from three-dimensional (3D)-printed molds to improve POP symptoms and increase overall satisfaction of pessary treatment in patients using standard vaginal pessaries.
Patients undergoing POP treatment with standard vaginal pessaries were enrolled in this pilot prospective study. Patient-specific pessaries were designed and fabricated for each patient using patient input, physician input, and anatomic measurements from clinical assessment. Pessary fabrication involved injection of biocompatible liquid silicone rubber into 3D-printed molds followed by a biocompatible silicone coating. Pelvic organ prolapse symptomatic distress and pessary treatment satisfaction were evaluated before and after a 3-week patient-specific pessary home trial using the validated Pelvic Organ Prolapse Distress Inventory-6 form and a visual analog scale, respectively.
Eight women were included in this study. Changing from standard pessary to patient-specific pessary treatment was associated with an improvement in prolapse symptoms on the Pelvic Organ Prolapse Distress Inventory-6 (median change, -3.5; interquartile range, -5 to -2.5; P = 0.02) and an increase in overall pessary satisfaction on a visual analog scale (median change, +2.0; interquartile range, +1.0 to +3.0; P = 0.02). All patients reported either an improvement or no change in pessary ease of use, comfort, and the feeling of support provided by the pessary.
Patient-specific vaginal pessaries are a promising alternative to standard pessaries for alleviating POP symptoms and improving patient satisfaction with pessary use.
阴道子宫托是治疗盆腔器官脱垂(POP)的有效非手术方法,如果正确适配。然而,子宫托适配和使用往往不成功或不完美。
本研究旨在评估使用三维(3D)打印模具制造的个体化子宫托改善 POP 症状并提高使用标准阴道子宫托的患者对子宫托治疗总体满意度的可行性。
本研究纳入了正在接受标准阴道子宫托治疗的 POP 患者。为每位患者设计和制造了个体化子宫托,使用患者输入、医生输入和临床评估的解剖测量值。子宫托制造涉及将生物相容性液态硅橡胶注入 3D 打印模具中,然后进行生物相容性硅橡胶涂层处理。使用经过验证的盆腔器官脱垂困扰量表-6 表格和视觉模拟量表,分别在 3 周个体化子宫托家庭试用前后评估子宫托治疗的盆腔器官脱垂症状困扰和满意度。
本研究纳入了 8 名女性。从标准子宫托改为个体化子宫托治疗与盆腔器官脱垂困扰量表-6 评分中脱垂症状的改善相关(中位数变化,-3.5;四分位距,-5 至-2.5;P = 0.02),以及视觉模拟量表上整体子宫托满意度的提高(中位数变化,+2.0;四分位距,+1.0 至+3.0;P = 0.02)。所有患者均报告子宫托易用性、舒适度和支撑感得到改善或无变化。
个体化阴道子宫托是一种有前途的替代标准子宫托的方法,可缓解 POP 症状并提高患者对子宫托使用的满意度。