Progression to severe visual impairment and blindness in POAG patients: pace and risk factors-a cohort study using German health claims data.
BMJ Open Ophthalmol
; 7(1): e000838, 2022.
Article
em En
| MEDLINE
| ID: mdl-35136840
ABSTRACT
OBJECTIVE:
Glaucoma is a leading cause of severe visual impairment and blindness (SVI/B) worldwide. Hence, it is of utmost importance to explore relevant risk factors and study the pace of progression to SVI/B. METHODS ANDANALYSIS:
We used a random sample of 250 000 persons from administrative individual-level health records of the Allgemeine Ortskrankenkassen between 2004 and 2015. We identified 3535 primary open-angle glaucoma (POAG) patients aged 55 and older and followed them for up to 10 years. Monocular and binocular SVI/B were defined by the ICD-10 classifications H54.0 and H54.4. Ophthalmological and chronic disease risk factors were analysed by applying a multivariable Cox proportional hazard model.RESULTS:
The risk of SVI/B in POAG patients was significantly increased by the presence of specific additional eye diseases such as secondary glaucoma (HR 3.08, p<0.001), retinal vascular occlusion (HR 3.00, p<0.001) or age-related macular degeneration (AMD) (HR 2.26, p<0.001). The risk was highest in the first 2 years after the POAG diagnosis and significantly decreased after the fifth year (HR 0.36, p=0.002). Ocular injuries, other ocular diseases, non-ophthalmological comorbidities, and age and sex had no significant influence (p>0.05).CONCLUSION:
Although progression to SVI/B is relatively rare in POAG patients in Germany, one must be aware of additional risk factors, such as secondary glaucoma, retinal vascular occlusion and AMD. Regular ophthalmological examinations help prevent the progression of SVI/B, especially in the first years after the POAG diagnosis. Specific, targeted, and timely treatments for the other eye diseases could help prevent or delay SVI/B.Palavras-chave
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Base de dados:
MEDLINE
Assunto principal:
Glaucoma de Ângulo Aberto
/
Baixa Visão
Idioma:
En
Ano de publicação:
2022
Tipo de documento:
Article