The location of CNV is defined in relation to the lesions distance to the geometric center of the foveal avascular zone (FAZ). Lesion of subfoveal CNV is under FAZ; lesion of juxtafoveal CNV occurs between 1μm and 199μm from the FAZ; extrafoveal CNV is defined as a lesion situated at least 200μm from the FAZ. Studies on eyes with subfoveal classic CNV (which could also have an occult CNV component) found the decrease of ≥3 lines of visual acuity in 60% to 80% of patients during two years’ followup. If CNV is not detected early and treated promptly, the rapid vision loss could have severe consequences for patients. Several studies on subfoveal classic CNV due to AMD indicated a poor prognosis for vision loss in this type of lesion. The data showed that the visual acuity loss in many AMD patients resulted from subfoveal classic CNV which occurs during the first two years after diagnosis. Visual acuity often deteriorates rapidly in eyes with juxtafoveal CNV, with most eyes (≥80%) losing at least 2 lines of visual acuity within two years and almost 90% losing 2 lines in five years. There is also a very high risk (≥90%) that untreated juxtafoveal lesions will progress to subfoveal lesions within five years. The studies on the natural course of extrafoveal classic CNV demonstrated a decrease of ≥3 lines of visual acuity in 56% to 86% of patients through two years of followup. There also appears to be a tendency for CNV to extend towards the center of FAZ (i.e., to become subfoveal in location). Some studies showed that extrafoveal occult CNV demonstrates a slower progression of visual loss than juxtafoveal classic CNV[5]. In the present study, there were 42 eyes of subfoveal CNV in which 30 eyes had visual acuity less than 0.1, 14 eyes of juxtafoveal CNV, 3 eyes of extrafoveal CNV. Clinically, CNV may be associated with subretinal fluid, subretinal hemorrhage, lipid exudation, or RPE detachment and finally with the development of fibrovascular disciform scars and loss of the outer retinal tissues. These events usually lead to progressive and variable amounts of irreversible central vision loss. In conclusion, suspected AMD patients are performed FFA, which will provide important information for AMD patients including early detected CNV, the quality and location of lesion confirmed, timely and appropriate treatment indicated. This will help to prevent or slow down the declining of visual acuity of AMD patients.
【参考文献】 1 WHO. Magnitude and causes of visual impairment. World Health Organization;2004
2 Wei M, Lei CT, Chen H, Fan YC. Analysis of the situation of visual disability of Sichuan Province. Int J Ophthalmol(Guoji Yanke Zazhi)2007;7(6):16521654
3 Bai ZL, Ren BC, Yang JG, He Y, Chen L, Sun NX . Epidemiological investigation on agerelated macular degeneration in rural area of Shaanxi Province, China. Int J Ophthalmol (Guoji Yanke Zazhi)2005;5(6):11141121
4 Ocular Fundus Diseases Study Group of Chinese Ophthalmological Society. Clinical diagnosis criteria of agerelated macular degeneration. Chin J Ophthalmol1987;23 (3): 2nd cover
5 Pauleikhoff D. Neovascular agerelated macular degeneration: Natural history and treatment outcomes. Retina 2005;25:10651084
6 Zhang X, Ren BC. Recent advance of the study on treatment for agerelated macular degeneration. Int J Ophthalmol (Guoji Yanke Zazhi)2007;7(6):16741676
7 Armbrecht AM, Aspinall PA, Dhillon B. A prospective study of visual function and quality of life following PDT in patients with wet age related macular degeneration. Br J Ophthalmol2004;88:12701273
8 Luibl V, Isas JM, Kayed R, Glabe CG, Langen R, Chen J. Drusen deposits associated with aging and agerelated macular degeneration contain nonfibrillar amyloid oligomers. J Clin Invest 2006;116:378385
9 Ambati J, Ambati BK, Yoo SH, Ianchulev S, Adamis AP. Agerelated macular degeneration: etiology, pathogenesis, and therapeutic strategies. Surv Ophthalmol2003;48:257293
10 Chopdar A, Chakravarthy U, Verma D. Age related macular degeneration. BMJ2003; 326:485488
11 Pauleikhoff D, Zuels S, Sheraidah GS, Marshall J, Wessing A, Bird AC. Correlation between biochemical composition and fluorescein binding of deposits in Bruchs membrane. Ophthalmology1992;99(10):15481553
12 Magnusson KP, Duan S, Sigurdsson H, Petursson H, Yang Z, Zhao Y, Bernstein PS, Ge J, Jonasson F, Stefansson E, Helgadottir G, Zabriskie NA, Jonsson T, Bj rnsson A, Thorlacius T, Jonsson PV, Thorleifsson G, Kong A, Stefansson H, Zhang K, Stefansson K, Gulcher JR. CFH Y402H confers similar risk of soft drusen and both forms of advanced AMD. PLoS Med2006;3(1):e5
13 Shahidi M, Blair NP, Mori M, Gieser J, Pulido JS. Retinal topography and thickness mapping in atrophic age related macular degeneration. Br J Ophthalmol2002;86:623626
14 Tang J, Foster CS. Agerelated macular degeneration: current trends and emerging treatments. Contemp Ophthalmol2007;6(4):15
15 Singh R, Kaiser PK. Advances in AMD imaging. Int Ophthalmol Clin2007;47(1):6574
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