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对一种由膨体聚四氟乙烯制成的房水引流青光眼装置的评估。

Evaluation of an aqueous drainage glaucoma device constructed of ePTFE.

作者信息

Boswell C A, Noecker R J, Mac M, Snyder R W, Williams S K

机构信息

Department of Surgery, Section of Surgical Research, Arizona Health Sciences Center, Tucson, Arizona 85724, USA.

出版信息

J Biomed Mater Res. 1999;48(5):591-5. doi: 10.1002/(sici)1097-4636(1999)48:5<591::aid-jbm1>3.0.co;2-9.

DOI:10.1002/(sici)1097-4636(1999)48:5<591::aid-jbm1>3.0.co;2-9
PMID:10490671
Abstract

Aqueous drainage devices for the treatment of glaucoma are subject to the same limitations as most polymeric implants, namely a healing response comprised of chronic inflammation and fibrosis. The most widely used devices are currently made of silicone or polypropylene, materials that exhibit biocompatibility difficulties when they are implanted on the sclera underneath the conjunctiva of the eye. Decreased outflow of aqueous fluid to the conjunctival space caused by the development of a fibrous capsule around the device accounts for at least 20% of aqueous shunts failures. Clearly, the need exists to improve the healing response to aqueous drainage devices, and one approach is to develop new polymers or polymer modifications. Improved devices would elicit a limited fibrotic response while increasing neovascularization around the implant. Previous studies have indicated that denucleation markedly improves the healing characteristics and biocompatibility of expanded polytetrafluoroethylene (ePTFE). We reasoned that altering the design of drainage devices to allow the use of denucleated ePTFE in vivo might minimize fibrosis, thereby improving shunt function. We found that after 8 weeks in vivo, experimental shunt function was equivalent to the Baerveldt shunt, while there was less scarring with increased neovascularizatin. These findings suggest that ePTFE has potential as an improved, long-term alternative material for use in constructing glaucoma shunts.

摘要

用于治疗青光眼的房水引流装置与大多数聚合物植入物存在相同的局限性,即由慢性炎症和纤维化组成的愈合反应。目前使用最广泛的装置由硅酮或聚丙烯制成,当这些材料植入眼结膜下方的巩膜上时,会出现生物相容性问题。装置周围纤维囊的形成导致房水向结膜间隙的流出减少,这至少占房水分流失败的20%。显然,需要改善对房水引流装置的愈合反应,一种方法是开发新的聚合物或对聚合物进行改性。改进后的装置在增加植入物周围新生血管形成的同时,会引发有限的纤维化反应。先前的研究表明,去核显著改善了膨体聚四氟乙烯(ePTFE)的愈合特性和生物相容性。我们推断,改变引流装置的设计以允许在体内使用去核的ePTFE可能会使纤维化最小化,从而改善分流功能。我们发现,在体内8周后,实验性分流功能与Baerveldt分流相当,同时瘢痕形成较少,新生血管形成增加。这些发现表明,ePTFE有潜力作为一种改良的长期替代材料用于构建青光眼分流装置。

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引用本文的文献

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A new glaucoma drainage implant with the use of Polytetrafluoroethylene (PTFE). A pilot study.一种使用聚四氟乙烯(PTFE)的新型青光眼引流植入物。一项初步研究。
Rom J Ophthalmol. 2021 Apr-Jun;65(2):150-156. doi: 10.22336/rjo.2021.30.
2
A novel bilayered expanded polytetrafluoroethylene glaucoma implant creates a permeable thin capsule independent of aqueous humor exposure.一种新型双层膨体聚四氟乙烯青光眼植入物可形成一个独立于房水暴露的可渗透薄囊。
Bioeng Transl Med. 2020 Aug 22;6(1):e10179. doi: 10.1002/btm2.10179. eCollection 2021 Jan.
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A One-Year Follow-Up of Two Ahmed Glaucoma Valve Models (S2 and FP7) for Refractory Glaucoma: A Prospective Randomized Trial.
两种艾哈迈德青光眼引流阀型号(S2和FP7)用于难治性青光眼的一年随访:一项前瞻性随机试验
Clin Ophthalmol. 2020 Mar 4;14:693-705. doi: 10.2147/OPTH.S224653. eCollection 2020.
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Evaluation of tissue interactions with mechanical elements of a transscleral drug delivery device.评估巩膜给药装置机械元件与组织的相互作用。
Pharmaceutics. 2012 Mar 12;4(1):212-29. doi: 10.3390/pharmaceutics4010212.
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The Ahmed glaucoma valve in neovascular glaucoma (An AOS Thesis).阿赫迈德青光眼引流阀在新生血管性青光眼中的应用(一篇美国眼科学会论文)
Trans Am Ophthalmol Soc. 2009 Dec;107:325-42.