Glaucoma Department, Galician Institute of Ophthalmology, Santiago de Compostela, La Coruña, Spain.
Acta Ophthalmol. 2010 Aug;88(5):541-52. doi: 10.1111/j.1755-3768.2009.01595.x. Epub 2009 Oct 2.
This study aims to identify progression factors in patients with primary open-angle glaucoma (POAG), including the effects of treatment with dorzolamide 2% or brinzolamide 1%, each added to timolol 0.5%.
A sample of 161 POAG patients were prospectively randomized to receive either dorzolamide 2% (DT) or brinzolamide 1% (BT) b.i.d., each added to timolol 0.5%, during a 60-month, evaluator-masked study. Progression was determined by perimetric criteria. Factors associated with visual field progression were estimated using a conditional Cox hazard model with patient intraclass correlation and were expressed as hazard ratios (HRs) with 95% confidence intervals (95% CIs).
Predictive baseline factors were lower diastolic blood pressure (DBP), lower mean arterial pressure (MAP), antihypertensive treatment, lower end-diastolic velocity (EDV) in the ophthalmic artery (OA) and short posterior ciliary artery (SPCA), and a higher resistivity index (RI) in the OA and SPCA. Progression risk decreased by approximately 30% and 20% with each centimetre per second increase of EDV in the OA and SPCA, respectively, from baseline to the last follow-up visit. Each RI decrease (or increase) of 0.01 unit in the OA or SPCA was associated with an approximate 20% decrease (or increase) in risk for progression. In a multivariate analysis, progression risk was significantly lower in eyes treated with DT (HR=0.65, 95% CI 0.41-0.90) compared with those treated with BT.
Progression increased with lower DBP, lower MAP, antihypertensive medication, lower EDV in the OA and SPCA, and higher RI in the OA and SPCA. The risk for progression in patients treated with DT was half that in patients treated with BT.
本研究旨在确定原发性开角型青光眼(POAG)患者的进展因素,包括使用多佐胺 2%或布林佐胺 1%联合噻吗洛尔 0.5%治疗的效果。
对 161 例 POAG 患者进行前瞻性随机分组,分别接受多佐胺 2%(DT)或布林佐胺 1%(BT),每天 2 次,联合噻吗洛尔 0.5%,进行为期 60 个月、评估者盲法的研究。通过视野检查标准确定进展情况。使用条件 Cox 风险模型和患者类内相关系数来估计与视野进展相关的因素,并以风险比(HR)和 95%置信区间(95%CI)表示。
预测性基线因素为舒张压(DBP)较低、平均动脉压(MAP)较低、抗高血压治疗、眼动脉(OA)和睫状后短动脉(SPCA)舒张末期流速(EDV)较低,以及 OA 和 SPCA 阻力指数(RI)较高。OA 和 SPCA 的 EDV 从基线到最后一次随访每增加 1 厘米/秒,进展风险分别降低约 30%和 20%。OA 和 SPCA 的 RI 每降低(或增加)0.01 单位,进展风险分别降低(或增加)约 20%。多变量分析显示,与 BT 治疗组相比,DT 治疗组的进展风险显著降低(HR=0.65,95%CI 0.41-0.90)。
DBP、MAP、抗高血压药物、OA 和 SPCA 的 EDV 降低以及 OA 和 SPCA 的 RI 升高,与进展风险增加相关。DT 治疗组患者的进展风险是 BT 治疗组的一半。