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玻璃体内注射曲安奈德与眼压

Intravitreal triamcinolone acetonide and intraocular pressure.

作者信息

Smithen Lindsay M, Ober Michael D, Maranan Leandro, Spaide Richard F

机构信息

Vitreous, Retina, Macula Consultants of New York, and the LuEsther T. Mertz Retinal Research Center, Manhattan Eye, Ear, and Throat Hospital, New York, New York, USA.

出版信息

Am J Ophthalmol. 2004 Nov;138(5):740-3. doi: 10.1016/j.ajo.2004.06.067.

DOI:10.1016/j.ajo.2004.06.067
PMID:15531307
Abstract

PURPOSE

To analyze the incidence of intraocular pressure (IOP) elevation following intravitreal triamcinolone injection.

DESIGN

Retrospective observational case series.

METHODS

Charts of patients undergoing intravitreal triamcinolone injection in one clinical practice were reviewed. A pressure elevation was defined as a pressure of 24 mm Hg or higher during follow-up.

RESULTS

There were 89 patients with a mean age of 76.4 years. The mean baseline IOP was 14.9 mm Hg with a mean change of 8.0 mm Hg. Thirty-six patients (40.4%) experienced a pressure elevation to 24 mm Hg or higher at a mean of 100.6 days (SD = 83.1 day) after treatment. Of nonglaucomatous patients with baseline IOP of 15 mm Hg or above, 60.0% experienced a pressure elevation, compared with only 22.7% of those with baseline pressures below 15 mm Hg (relative risk = 2.1, P < .01). In glaucoma patients, 6 of 12 (50%) experienced a pressure elevation, and this elevation was not correlated with baseline pressure. Thirty-two patients (36.0%) received repeat injections, and there was no difference in the incidence of procedure elevation in patients receiving multiple injections versus those receiving a single injection. Pressure elevation was controlled with topical medications in all patients.

CONCLUSIONS

IOP elevation after intravitreal triamcinolone injection is common and may take an extended period of time to manifest. The proportion of patients who developed a pressure elevation to at least 24 mm Hg was much higher for those with baseline IOP 15 mm Hg or greater.

摘要

目的

分析玻璃体内注射曲安奈德后眼压升高的发生率。

设计

回顾性观察病例系列。

方法

回顾了在一个临床实践中接受玻璃体内注射曲安奈德的患者病历。眼压升高定义为随访期间眼压达到或高于24mmHg。

结果

共89例患者,平均年龄76.4岁。平均基线眼压为14.9mmHg,平均变化为8.0mmHg。36例患者(40.4%)在治疗后平均100.6天(标准差=83.1天)眼压升高至24mmHg或更高。基线眼压在15mmHg及以上的非青光眼患者中,60.0%出现眼压升高,而基线眼压低于15mmHg的患者中这一比例仅为22.7%(相对危险度=2.1,P<.01)。在青光眼患者中,12例中有6例(50%)出现眼压升高,且这种升高与基线眼压无关。32例患者(36.0%)接受了重复注射,接受多次注射的患者与接受单次注射的患者在眼压升高发生率上无差异。所有患者的眼压升高均通过局部用药得到控制。

结论

玻璃体内注射曲安奈德后眼压升高很常见,且可能需要较长时间才会显现。基线眼压在15mmHg或更高的患者中,眼压升高至至少24mmHg的比例要高得多。

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