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[突尼斯人群原发性开角型青光眼进展的眼部危险因素]

[Ocular risk factors for progression of primary open angle glaucoma in the Tunisian population].

作者信息

Loukil I, Korchène N, Hachicha F, Wathek C, Bouguerra C, Mallouch N, Bhiri R, Hijazi A, Zouari B, El Afrit M A

机构信息

Service d'ophtalmologie, CHU La Rabta, 1007 Jabbari, Tunis, Tunisie.

出版信息

J Fr Ophtalmol. 2013 Apr;36(4):324-30. doi: 10.1016/j.jfo.2012.05.010. Epub 2012 Dec 5.

Abstract

PURPOSE

To evaluate intraocular pressure parameters and the role of other ocular risk factors in the progression of primary open angle glaucoma.

PATIENTS AND METHODS

We performed a retrospective analysis of long-term glaucomatous progression in 140 patients (280 eyes) with primary open angle glaucoma (POAG) between 1998 and 2009. After analyzing their disease progression, the eyes of our patients were divided into two groups: group 1 (G1) consisted of eyes with worsening of their POAG, and group 2 (G2) consisted of the eyes that remained stable. The indicators of progression studied were factors associated with glaucomatous optic neuropathy, other ocular risk factors, and treatment-related risk factors.

RESULTS

We found 188 eyes with stable visual fields (G2) and 92 eyes with glaucoma progression (G1), for a progression rate of 32.9%. Mean intraocular pressure (IOP) at diagnosis was statistically higher in the cases with progression, 22.78 mmHg vs. 19.9 mmHg for stable cases (P=0.03; OR=5.25). Higher final intraocular pressure (IOP) was also associated with progression (16.82 mmHg for G1 vs. 14.85 mmHg for G2; P=0.051). IOP less or equal to 12.75 mmHg was identified as the target pressure for our population. Progressed eyes also showed a statistically higher diurnal peak IOP (23.13 mmHg vs. 19.87 mmHg for G2; P=0.007). Long term IOP fluctuation was also predictive of progression (4.43 mmHg for G1 vs. 2.31 mmHg for G2; P=0.003). Eyes with initial visual field defect more than 8.2dB had 4.8 times the risk of progression (P=0.07). However, eyes diagnosed in an early glaucoma stage had four times the chance of maintaining a stable visual field (P=0.003). Statistically significant risk factors between the two groups also included: pseudoexfoliation (OR=2.84; P=0.05), cornea less than 505 μ (OR=10.89; P=0.005), topical beta blockers (P=0.003), and more than two topical medications (OR=3; P=0.003).

CONCLUSION

It is currently known that IOP lowering contributes to glaucoma stabilization. However, this single criterion remains insufficient, as other, particularly ocular, factors have been implicated in glaucoma progression. Identification of these risk factors allows for a better therapeutic approach toward these patients, so as to preserve their vision and quality of life.

摘要

目的

评估眼压参数以及其他眼部危险因素在原发性开角型青光眼进展中的作用。

患者与方法

我们对1998年至2009年间140例(280只眼)原发性开角型青光眼(POAG)患者的长期青光眼进展情况进行了回顾性分析。在分析他们的疾病进展后,我们将患者的眼睛分为两组:第1组(G1)为POAG病情恶化的眼睛,第2组(G2)为病情保持稳定的眼睛。所研究的进展指标包括与青光眼性视神经病变相关的因素、其他眼部危险因素以及与治疗相关的危险因素。

结果

我们发现188只眼视野稳定(G2),92只眼青光眼进展(G1),进展率为32.9%。进展组患者诊断时的平均眼压(IOP)在统计学上更高,进展组为22.78 mmHg,稳定组为19.9 mmHg(P = 0.03;OR = 5.25)。更高的最终眼压(IOP)也与进展相关(G1为16.82 mmHg,G2为14.85 mmHg;P = 0.051)。眼压小于或等于12.75 mmHg被确定为我们研究人群的目标眼压。进展组的眼睛在统计学上也显示出更高的日间眼压峰值(G2为19.87 mmHg,G1为23.13 mmHg;P = 0.007)。长期眼压波动也可预测进展(G1为4.43 mmHg,G2为2.31 mmHg;P = 0.003)。初始视野缺损超过8.2 dB的眼睛进展风险为4.8倍(P = 0.07)。然而,早期青光眼阶段诊断出的眼睛保持稳定视野的几率为4倍(P = 0.003)。两组之间具有统计学意义的危险因素还包括:假性剥脱(OR = 2.84;P = 0.05)、角膜厚度小于505 μ(OR = 10.89;P = 0.005)、局部使用β受体阻滞剂(P = 0.003)以及使用两种以上局部药物(OR = 3;P = 0.003)。

结论

目前已知降低眼压有助于青光眼病情稳定。然而,这一单一标准仍然不足,因为其他因素,尤其是眼部因素,也与青光眼进展有关。识别这些危险因素有助于对这些患者采取更好的治疗方法,从而保护他们的视力和生活质量。

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