An Electronic Frailty Index Based on Deficit Accumulation May Predict Glaucomatous Visual Field Progression.

Clinical ophthalmology (Auckland, N.Z.) Pub Date : 2025-02-05 eCollection Date: 2025-01-01 DOI:10.2147/OPTH.S503177
Walter Duy, Nicholas Pajewski, Jeff D Williamson, Atalie C Thompson
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Abstract

Purpose: To investigate whether an electronic frailty index (eFI) is associated with visual field loss in glaucoma.

Patients and methods: We identified 1163 subjects ≥65 years old with glaucoma (1082 right eyes and 1042 left eyes) who had a calculable baseline eFI, and who had reliable visual fields at baseline and final follow-up. Multivariable linear regression models adjusting for demographic and clinical variables were used to assess the association between eFI and mean deviation at baseline and the change in mean deviation over time in each eye.

Results: Being pre-frail or frail was not associated with baseline MD, except in the right eye where being pre-frail was associated with a higher baseline MD. Increasing level of eFI was negatively correlated with change in MD (p<0.05 both eyes), but not baseline MD. Moreover, being frail was significantly associated with a more significant decline in MD in both eyes (Right eye: Beta -0.89, 95% CI (-1.71, -0.063), p=0.035; Left eye: Beta -1.25, 95% CI (-2.17, -0.34), p=0.007). Notably, baseline IOP was not associated with MD at baseline or the change in MD in the multivariable models.

Conclusion: Glaucoma patients who are frail may be at higher risk of experiencing visual field decline, independent of baseline IOP. Future studies should investigate whether interventions to improve frailty can decrease risk of glaucoma progression.

基于缺陷积累的电子衰弱指数可以预测青光眼的视野进展。
目的:探讨电子衰弱指数(eFI)与青光眼患者视野丧失的关系。患者和方法:我们确定了1163名≥65岁的青光眼患者(1082只右眼和1042只左眼),他们有可计算的基线eFI,并且在基线和最终随访时具有可靠的视野。采用调整人口统计学和临床变量的多变量线性回归模型来评估eFI与基线平均偏差以及每只眼睛平均偏差随时间的变化之间的关系。结果:体弱或体弱与基线MD无关,除了右眼体弱与较高的基线MD相关。eFI水平的增加与MD的变化呈负相关(结论:体弱的青光眼患者可能有更高的经历视野下降的风险,独立于基线IOP。未来的研究应该调查改善虚弱的干预措施是否可以降低青光眼进展的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
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