巴西新诊断青光眼患者的临床概况

Rafaela Costa de Aranda Lima , Franklin Roberto Dutra de Souza , Frederico de Miranda Cordeiro , Tiago dos Santos Prata , Carolina P.B. Gracitelli , Isabela Vianello Valle , Carla Nagamine Urata , Luciana Arce Alencar de Andrade , Ricardo Y. Abe
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引用次数: 0

摘要

目的描述新诊断青光眼患者的临床特征,确定与青光眼晚期相关的危险因素。设计回顾性多中心研究。方法我们纳入了来自巴西不同地区的6个医疗中心的18岁以上新诊断的青光眼患者。我们应用逻辑回归评估比值比(OR),以确定患者在诊断时出现青光眼晚期的危险因素。结果共纳入523例青光眼患者。确诊时平均年龄64.5岁(±12.4岁),以白人居多(82.94%)。我们发现20%的患者在诊断时病情已进展,低视力患病率为4.21%。在多变量logistic回归中,我们发现老年患者[比值比(OR) = 1.04 /年;95%置信区间(CI): 1.02-1.06;P & lt;0.001)和基线时眼压(IOP)较高的患者(OR = 1.08 / mmHg;95% ci: 1.04-1.12;P & lt;0.001)在诊断时出现晚期疾病的风险更高。相比之下,正常张力性青光眼患者(OR = 0.13;95% ci: 0.00-00.20;P = 0.024)在诊断时出现晚期疾病的风险较低。523例患者中,366例(70.2%)诊断为原发性开角型青光眼(POAG)。在POAG患者亚组中,我们发现老年患者(OR = 1.04 /年;95% ci: 1.01-1.06;P = 0.001),基线时IOP较高的患者(OR = 1.09 / mmHg;95% ci: 1.04-1.15;P & lt;0.001)和高度近视患者(球面等效值<;-6屈光度;或轴向长度>;如果是假晶状体,则为26.5 mm) (OR = 3.39;95% ci: 1.35-8.42;P = 0.009)在诊断时出现晚期疾病的风险较高。结论20%的患者在诊断时病情已进展,其中低视力的患病率为4.21%。我们已经表明,年龄较大和基线时IOP高的患者在诊断时出现进展性青光眼的风险更高。在POAG亚组中,我们发现基线时IOP高、年龄较大和高度近视的患者在诊断时出现晚期青光眼的风险更高,这突出了监测具有这些临床特征的患者的重要性。
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Clinical profile of newly diagnosed glaucoma patients in Brazil

Purpose

Describe clinical characteristics of newly diagnosed glaucoma patients and identify risk factors associated with advanced stage of glaucoma.

Design

Retrospective multicenter study.

Methods

We included patients over 18 years old with newly diagnosed glaucoma in 6 medical centers from different regions of Brazil. We applied logistic regression to assess odds ratios (OR) to identify risk factors for the patient to present advanced stage of glaucoma at diagnosis.

Results

We included a total of 523 glaucoma patients. Mean age at the time of diagnosis was 64.5 years (± 12.4 years), with the majority being Caucasian (82.94 %). We found that 20 % of patients had advanced disease at diagnosis, with a low vision prevalence of 4.21 %. In the multivariable logistic regression, we found that older patients [odds ratio (OR) = 1.04 per year; 95 % confidence interval (CI):1.02–1.06; P < 0.001) and patients with higher intraocular pressure (IOP) at baseline (OR = 1.08 per mmHg; 95 % CI: 1.04–1.12; P < 0.001) were at higher risk to present advanced disease at diagnosis. In contrast, normal tension glaucoma patients (OR = 0.13; 95 % CI: 0.00–00.20; P = 0.024) had lower risk to present advanced disease at diagnosis. From the total of 523 patients, 366 (70.2 %) were diagnosed with primary open angle glaucoma (POAG). Within this subgroup of POAG patients, we found that older patients (OR = 1.04 per year; 95 % CI:1.01–1.06; P = 0.001), patients with higher IOP at baseline (OR = 1.09 per mmHg; 95 % CI: 1.04–1.15; P < 0.001) and patients with high myopia (spherical equivalent < -6 diopters, if phakic; or axial length > 26.5 mm, if pseudophakic) (OR = 3.39; 95 % CI: 1.35–8.42; P = 0.009) were at higher risk to present advanced disease at diagnosis.

Conclusions

We found that 20 % of patients had advanced disease at diagnosis, with a low vision prevalence of 4.21 %. We have showed that patients with older age and high IOP at baseline were at higher risk to present advance glaucoma at diagnosis. Within the subgroup of POAG, we found that patients with high IOP at baseline, older age, and high myopia were at higher risk of presenting advanced glaucoma at diagnosis, highlighting the importance of monitoring patients with these clinical characteristics.
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