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既往接受过滤过手术的患者在使用药物性房水抑制剂治疗后出现低眼压和睫状体脉络膜脱离。

Hypotony and ciliochoroidal detachment following pharmacologic aqueous suppressant therapy in previously filtered patients.

作者信息

Vela M A, Campbell D G

出版信息

Ophthalmology. 1985 Jan;92(1):50-7. doi: 10.1016/s0161-6420(85)34060-5.

Abstract

This is the first report describing the syndrome of hypotony and ciliochoroidal detachment following pharmacologic aqueous suppressant therapy in previously filtered eyes. Four patients had a history of advanced primary open-angle glaucoma treated with multiple medical therapies, including timolol for 11 to 36 months. They then underwent filtration surgery, which failed in two cases. Timolol and/or acetazolamide therapy was instituted 1 to 18 months following surgery. The patients then developed hypotony and ciliochoroidal detachment, which resolved spontaneously after cessation of the pharmacologic aqueous suppressant therapy. In three of the cases, the episode of hypotony and ciliochoroidal detachment recurred after a second challenge with timolol and/or acetazolamide therapy. Inflammation, tumor, wound leakage, retinal detachment and cyclodialysis cleft were excluded. A mechanism of formation of ciliochoroidal detachment in this syndrome is proposed. Long-term timolol therapy followed by filtration surgery and its attendant postoperative hypotony and ciliochoroidal detachment sensitizes the ciliary epithelium. Subsequent pharmacologic aqueous suppressant therapy results in almost total reduction of aqueous production, causing hypotony and ciliochoroidal detachment.

摘要

这是首篇描述曾接受滤过手术的眼睛在使用药物性房水生成抑制剂治疗后出现低眼压和睫状体脉络膜脱离综合征的报告。4例患者有晚期原发性开角型青光眼病史,接受过多种药物治疗,包括使用噻吗洛尔11至36个月。之后他们接受了滤过手术,其中2例手术失败。术后1至18个月开始使用噻吗洛尔和/或乙酰唑胺治疗。患者随后出现低眼压和睫状体脉络膜脱离,在停用药物性房水生成抑制剂治疗后自行缓解。其中3例在再次使用噻吗洛尔和/或乙酰唑胺治疗后,再次出现低眼压和睫状体脉络膜脱离。排除了炎症、肿瘤、伤口渗漏、视网膜脱离和睫状体分离。本文提出了该综合征中睫状体脉络膜脱离的形成机制。长期使用噻吗洛尔治疗后进行滤过手术及其伴随的术后低眼压和睫状体脉络膜脱离使睫状体上皮致敏。随后的药物性房水生成抑制剂治疗几乎完全抑制了房水生成,导致低眼压和睫状体脉络膜脱离。

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