June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Factors that contribute to vision-related quality of life scores in patients with diabetic retinopathy
Author Affiliations & Notes
  • Roxanne Crosby-Nwaobi
    Florence Nightingale School of Nursing and Midwifery, King's College London, London, United Kingdom
  • Angus Forbes
    Florence Nightingale School of Nursing and Midwifery, King's College London, London, United Kingdom
  • Sobha Sivaprasad
    Laser and Retinal Unit, King's College Hospital, London, United Kingdom
  • Footnotes
    Commercial Relationships Roxanne Crosby-Nwaobi, None; Angus Forbes, None; Sobha Sivaprasad, Allergan (F), Bayer (F), Novartis (F)
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 1544. doi:
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      Roxanne Crosby-Nwaobi, Angus Forbes, Sobha Sivaprasad, South East London Diabetic Retinopathy study; Factors that contribute to vision-related quality of life scores in patients with diabetic retinopathy. Invest. Ophthalmol. Vis. Sci. 2013;54(15):1544.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: To determine the impact of severity of diabetic retinopathy (DR), visual acuity and diabetes related stress on vision related quality of life in patients with diabetic retinopathy.

Methods: 372 men and women with T2D were stratified by severity of DR into no retinopathy and proliferative diabetic retinopathy (PDR). Each subject underwent tests of diabetes related distress (PAID), vision-related quality of life (NEI-VFQ25), best corrected visual acuity (BCVA)[logMAR], ophthalmic and physical examination. Bivariate analysis between categories of DR; linear regression was conducted for the NEI-VFQ-25 by DR severity adjusting for age, gender, HbA1c and PAID were conducted using SPSS v17.

Results: The mean NEI-VFQ-25 for the PDR group was significantly lower when compared to the group with no retinopathy, 86.2±10.7 vs. 75.8±20.4, p=<0.001, where lower score=decreased vision-related quality of life. BCVA (0.09±0.13 vs. 0.19±0.21, p< 0.001) and HbA1c (8.0±1.8 vs. 8.7±2.0, p=0.007) were also significantly different between the two groups of retinopathy. PAID was not significant between the groups. NEI-VFQ-25 was inversely correlated to logMAR BCVA (r=-0.052, p<0.001) and PAID (r=-0.219, p<0.001). Gender differences were found for NEI-VFQ-25 by DR severity; men showed significantly higher NEI-VFQ-25 scores when compared to women (no retinopathy: 88.8±9.5 vs. 88.3±11.3, p=0.002 and PDR: 79.4±19.7 vs. 71.4±20.4, p=0.030). On full adjustment of the model, NEI-VFQ-25 was significantly associated with severity of retinopathy (no retinopathy: 84.3±1.1 vs. PDR: 79.0±191.2, p<0.001) with BCVA accounting for 20% of the variance in the model.

Conclusions: NEI-VFQ-25 is independently associated with severity of DR and visual acuity only accounts for 20% of the variance.

Keywords: 499 diabetic retinopathy • 669 quality of life • 464 clinical (human) or epidemiologic studies: risk factor assessment  
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