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玻璃体内注射组织型纤溶酶原激活剂和膨胀性气体治疗黄斑下出血

Management of submacular hemorrhage with intravitreal injection of tissue plasminogen activator and expansile gas.

作者信息

Chen Christine Y, Hooper Claire, Chiu Daniel, Chamberlain Matthew, Karia Niral, Heriot Wilson J

机构信息

Ocular Genetics Unit, Eye Research Australia, University of Melbourne, East Melbourne, Victoria, Australia.

出版信息

Retina. 2007 Mar;27(3):321-8. doi: 10.1097/01.iae.0000237586.48231.75.

Abstract

PURPOSE

To evaluate the clinical outcome of intravitreal tissue plasminogen activator (tPA) and expansile gas injection as a minimally invasive treatment for submacular hemorrhage (SMH).

METHODS

This study was a retrospective clinical case series examining 104 eyes that received an intravitreal injection of 30-100 mcg of tPA and expansile gas (SF6 or C3F8) for SMH. The main outcomes evaluated were visual acuities (VA), anatomic displacement of submacular blood, and surgical complications.

RESULTS

: A total of 85, 77, and 81 eyes were available at 1 week, 3 months, and 12 months follow up, respectively. Postoperatively, > or = 2 Snellen lines improvement were achieved in 43/85 eyes (51%) at 1 week, 49/77 eyes (63%) at 3 months, and 52/81 eyes (64%) at 12 months. Postoperative VA improvement was significantly associated with preoperative VA, submacular blood displacement, and the underlying cause of SMH. Diagnostic postoperative angiogram and clinical examination were possible at 8.2 +/- 7.4 weeks and 9.5 +/- 7.4 weeks, respectively. The observed complications included breakthrough vitreous hemorrhage in 8 eyes (8%) and retinal detachment in 3 eyes (3%).

CONCLUSIONS

In this retrospective series, intravitreal injection of tPA and expansile gas was shown to be a safe and effective technique that can improve VA in most eyes with SMH and assist in the diagnosis of the underlying cause.

摘要

目的

评估玻璃体内注射组织型纤溶酶原激活剂(tPA)联合膨胀性气体注入作为黄斑下出血(SMH)微创治疗的临床疗效。

方法

本研究为回顾性临床病例系列,研究对象为104只接受玻璃体内注射30 - 100 mcg tPA及膨胀性气体(六氟化硫或八氟环丁烷)治疗SMH的眼睛。评估的主要指标包括视力(VA)、黄斑下血液的解剖移位及手术并发症。

结果

分别有85只、77只和81只眼睛在1周、3个月和12个月随访时可进行评估。术后,1周时85只眼中有43只(51%)视力提高≥2行Snellen视力表,3个月时77只眼中有49只(63%),12个月时81只眼中有52只(64%)。术后视力提高与术前视力、黄斑下血液移位及SMH的潜在病因显著相关。术后诊断性血管造影和临床检查分别在8.2±7.4周和9.5±7.4周可行。观察到的并发症包括8只眼(8%)发生玻璃体出血突破和3只眼(3%)发生视网膜脱离。

结论

在这个回顾性系列研究中,玻璃体内注射tPA联合膨胀性气体被证明是一种安全有效的技术,可改善大多数SMH患者的视力,并有助于诊断潜在病因。

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