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[Diagnostics and therapy for normal tension glaucoma].

Abstract

Pooled data from "The Baltimore Eye Survey", "The Blue Mountains Eye Study", "The Beaver Dam Eye Study", "The Rotterdam Study" and "The Melbourne VIP" showed a strong age-dependent prevalence of open angle glaucoma. Patients younger than 60 years have a prevalence of open angle glaucoma of less than 1 %. Beginning with the age of 60 the prevalence increases exponentially. The prevalence of open angle glaucoma in persons in the 8(th) age decade reaches up to 5 %. Among these patients, 30-50 % have normal intraocular pressure. The diagnostics and therapy for open angle glaucoma with normal intraocular pressure (IOP), also called normal tension glaucoma, is a complex and often interdisciplinary challenge. Established causative factors for developing a glaucomatous optic nerve atrophy in normal tension glaucoma are: relatively increased IOP, older age, non-dippers (0-10 %) or extreme dippers (> 20 %) concerning nocturnal arterial blood pressure drop, small vessel disease with cardiovascular disease and cerebral microgliosis (white matter lesions), decreased blood flow in the optic nerve head, extreme dip of the optic nerve head blood flow in the morning, cerebral blood flow dysregulation and the epsilon4-allele polymorphism of the apolipoprotein E-gene. Clinical pathways are presented for the diagnostics and therapy for normal tension glaucoma.

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BibTeXRIS

D Baleanu, G Michelson. 2005. [Diagnostics and therapy for normal tension glaucoma].. https://doi.org/10.1055/s-2005-858741

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Screening for prevention of optic nerve damage due to chronic open angle glaucoma.

BACKGROUND: Open angle glaucoma (OAG) is a primary, progressive optic neuropathy; the onset is without symptoms and progression occurs silently until the advanced stages of the disease, when it affects central vision. The blindness caused by OAG is irreversible. It has often been assumed to be a condition that fulfils the criteria for population screening, although this has not been supported by other in-depth non-systematic reviews. The focus of this review was to examine the evidence for the effectiveness of screening for OAG. OBJECTIVES: To determine the impact of screening for OAG compared with opportunistic case findings or current referral practices on the prevalence of and the degree of optic nerve damage due to OAG in screened and unscreened populations. SEARCH STRATEGY: We included any randomised controlled trial (RCT) evaluating population-based screening programmes for OAG with a minimum one year follow up. We searched the Cochrane Central Register of Controlled Trials (CENTRAL) on The Cochrane Library (which contains the Cochrane Eyes and Vision Trials Register) (Issue 1, 2006), MEDLINE (1950 to February 2006) and EMBASE (1988 to February 2006). We also searched the National Research Register (Issue 1, 2006) and Zetoc for grey literature (29 June 2006). There were no language or date restrictions in the electronic searches. SELECTION CRITERIA: We planned to include RCTs, including cluster RCTs. DATA COLLECTION AND ANALYSIS: Two review authors independently assessed the study abstracts identified by the electronic searches. We did not find any trials that met the inclusion criteria. MAIN RESULTS: As no trials were identified, no formal analysis was performed. AUTHORS' CONCLUSIONS: On the basis of current evidence, population-based screening for chronic OAG cannot be recommended, although much can be done to improve awareness and encourage at risk individuals to seek testing. In wealthy countries with equitable access to high quality eye care and health education, blindness from chronic OAG should become increasingly rare; much greater challenges face poor and emerging economies and countries where there are substantial health and wealth inequalities. Effectiveness of screening for OAG can be established only by high quality RCTs.

Glaucoma, Open-Angle↗

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Glaucoma, Open-Angle↗