Orbit (Amsterdam, Netherlands) · 2026
Fixation of high-density porous polyethylene implant with cyanoacrylate tissue adhesive in orbital floor fracture.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Alsheikh Osama, Althaqib Rawan N, Aldufaileej Mohammed A, Alghaferi Laila S, Alsulaiman Hamad M
Аннотация
PURPOSE: Cyanoacrylate tissue adhesives have been used successfully in different branches of the medical field. The purpose of this study was to assess the safety and efficacy of porous polyethylene implant fixation with N-butyl cyanoacrylate tissue adhesive.
METHODS: A retrospective chart review was conducted for all patients with orbital floor fracture who underwent surgical repair with a high-density porous polyethylene (Medpor) implant fixated with N-butyl-2-cyanoacrylate tissue adhesive glue from January 2000-December 2018.
RESULTS: Thirty-seven patients were included. The median interval between trauma and surgery was 7 months (interquartile range, 0.7-24 months), and the median duration of the last follow-up also 7 months (interquartile range, 1.2-31 months). The indication for surgery was diplopia in 19 (51.3%) patients, enophthalmos in 22 (59.5%), limited ocular motility in 12 (29.7%), and combined canalicular laceration with orbital floor fracture in 1 (2.7%). Thirty-five (94.6%) patients showed either partial or complete improvement in their symptoms after surgery, either subjectively or objectively after the first operation, regardless of the presence of subsequent operations. No patient exhibited implant displacement or implant-related infections.
CONCLUSION: Overall, these findings suggest that N-butyl-2-cyanoacrylate fixation of high-density porous polyethylene implants for orbital floor fractures is safe and effective.
METHODS: A retrospective chart review was conducted for all patients with orbital floor fracture who underwent surgical repair with a high-density porous polyethylene (Medpor) implant fixated with N-butyl-2-cyanoacrylate tissue adhesive glue from January 2000-December 2018.
RESULTS: Thirty-seven patients were included. The median interval between trauma and surgery was 7 months (interquartile range, 0.7-24 months), and the median duration of the last follow-up also 7 months (interquartile range, 1.2-31 months). The indication for surgery was diplopia in 19 (51.3%) patients, enophthalmos in 22 (59.5%), limited ocular motility in 12 (29.7%), and combined canalicular laceration with orbital floor fracture in 1 (2.7%). Thirty-five (94.6%) patients showed either partial or complete improvement in their symptoms after surgery, either subjectively or objectively after the first operation, regardless of the presence of subsequent operations. No patient exhibited implant displacement or implant-related infections.
CONCLUSION: Overall, these findings suggest that N-butyl-2-cyanoacrylate fixation of high-density porous polyethylene implants for orbital floor fractures is safe and effective.