Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:

Ординатура / Офтальмология / Английские материалы / Shields Textbook of Glaucoma, 6th edition_Allingham, Damji, Freedman_2010

.pdf
Скачиваний:
2
Добавлен:
28.03.2026
Размер:
44.54 Mб
Скачать

1 - Cellular and Molecular Biology of Aqueous Humor Dynamics

Page 195 of 225

color is not indicated it is understood to be white).

 

Figure 5.19 Goldmann manual perimeter. A: Patient's side, showing headres (H), fixation target (F), and projection device for test objects (P). B: Operator's side, showing telescope for fixation monitoring (T) and visual field chart (C) for locating and recording position of test objects.

Suprathreshold static perimetry can be performed by turning the disc-shaped test object from the black to the white side or by using a self-illuminating target with an on-off switch. Specific locations at which the patient fails to see the target are then evaluated further with kinetic techniques.

The tangent screen has the advantages of low cost and simplicity of operation. However, reproducibility of the fields, which is essential in managing patients with glaucoma, is limited by variations in background lighting and stimulus value of the targets, and by difficulty in monitoring fixation. Furthermore, it does not include the peripheral field, where early glaucomatous defects may appear. Arc and Bowl Perimeters

With these instruments, both the central and peripheral fields of vision can be examined. The screen of the perimeter may be a curved ribbon of metal (arc perimeter) or bowl shaped. The latter is preferable for glaucoma examinations, and the prototype is the Goldmann perimeter (Fig. 5.19) (327). Other similar instruments have been compared with the Goldmann unit,

P.113

with variable results (328). The bowl of the Goldmann perimeter has a radius of 300 mm and extends 95% to each side of fixation. The target is projected onto the bowl, and the stimulus value of the test object can be varied by changing the size or the intensity. Arbitrary designations for each value variable are usually printed on the visual field chart, with O-V for size, and 1-4 for intensity. An isopter,

therefore, might be designated as “I2e,” which indi cates a test object size of 0.25 mm2 and an intensity of 10 millilamberts. The examiner can monitor the patient's fixation through a telescope in the center of the bowl. The Goldmann perimeter can be used for both kinetic and static visual field testing. The

1 - Cellular and Molecular Biology of Aqueous Humor Dynamics

Page 196 of 225

Tübingen perimeter has been designed exclusively fo r the measurement of static threshold (profile) fields and consists of a bowl-type screen and stationary test objects with variable light intensity (329, 330).

Figure 5.20 In-depth technique with Goldmann-type perimeter in which the visual field has been plotted with five targets. The size and stimulus of the corresponding isopters are shown in the table in the lower right of the figure. This demonstrates a normal visual field.

Specific Techniques for Manual Perimetry

In the context of glaucoma detection and management, manual kinetic visual field testing has two basic aspects: (a) screening techniques to detect the presence of glaucomatous field loss, and (b) in-depth techniques to more accurately determine the extent of the damage and to follow the fields for evidence of progressive change.

Screening Techniques

Armaly developed a method of visual field screening for glaucoma that was modified by Drance and associates and is commonly referred to as selective perimetry, or the Armaly-Drance technique (331, 332, 333 and 334). The basic concept is to test those areas in the visual field that have the highest probability of showing glaucomatous defects. The technique uses Goldmann-type perimeter with suprathreshold static perimetry to test for central field defects and both suprathreshold static and kinetic perimetry to examine the peripheral field, with emphasis on the nasal and temporal periphery. This technique revealed a high sensitivity and specificity, which made it suitable for clinical and survey screening (332, 334). An additional modification is to use the V4e isopter nasally to rule out crowding of the peripheral nasal isopters (45).

Another technique for use with Goldmann-type perimeters uses three suprathreshold targets in three concentric zones from fixation in accordance with the normal physiologic sensitivity gradient (335). Other investigators have developed protocols to significantly reduce the number of test points without sacrificing sensitivity or specificity by concentrating the testing in those portions of the field where a defect is most likely to be found (336, 337).

In-Depth Techniques

1 - Cellular and Molecular Biology of Aqueous Humor Dynamics Page 197 of 225

When a glaucomatous field defect is suspected by use of a screening technique, the physician has two choices. The patient can be asked to return another day for a repeated screening field or an in-depth study. In many cases, however, it is more practical to proceed with the in-depth test at the time the defect is detected. The principle of in-depth field testing is to map out the size and shape of all scotomas and complete isopters by using the central threshold target and two or more additional targets of greater stimulus value (Fig. 5.20). However, automated static perimetry has certainly more value in studying areas of known loss for the depth and shape of the scotoma and for subtle evidence of progressive damage in serial fields.

KEY POINTS

The normal visual field may be depicted as a three-dimensional contour, representing areas of relative retinal sensitivity and characterized by a peak at the point of fixation, an absolute depression corresponding to the optic nerve head (blind spot), and a sloping of the remaining areas to the boundaries of the field.

Early glaucomatous damage may produce a generalized depression of this contour, which can be demonstrated with several psychophysical tests.

P.114

The more specific visual field changes of glaucoma, however, are localized defects that correspond to loss of retinal nerve fiber bundles, and include paracentral and arcuate scotomas above and below fixation and steplike defects along the nasal midline (nasal step).

Instruments used to measure the field of vision (perimeters) may have static or kinetic targets, which can be controlled automatically or manually. The targets are presented against a background that is bowl shaped or flat (tangent screen), with the former units providing more reliable measurements.

Comparative studies indicate that automated static perimeters, particularly those using new enhanced testing algorithms, are more sensitive than manual perimeters are at detecting and following glaucomatous visual field loss.

REFERENCES

1.Anderson DR, Patella VM. Automated Static Perimetry. St. Louis: Mosby; 1999.

2.Hart WM Jr, Burde RM. Three-dimensional topography of the central visual field. Sparing of foveal sensitivity in macular disease. Ophthalmology. 1983;90(8):1028-1038.

3.Armaly MF. The size and location of the normal blind spot. Arch Ophthalmol. 1969;81(2):192-201.

4.Jonas JB, Gusek GC, Fernandez MC. Correlation of the blind spot size to the area of the optic disk and parapapillary atrophy. Am J Ophthalmol. 1991;111(5):559-565.

5.LeBlanc EP, Becker B. Peripheral nasal field defects. Am J Ophthalmol. 1971;72(2):415-419.

6.Werner EB, Beraskow J. Peripheral nasal field defects in glaucoma. Ophthalmology. 1979;86 (10):1875-1878.

7.Armaly MF. Visual field defects in early open angle glaucoma. Trans Am Ophthalmol Soc. 1971;69:147-162.

8.Armaly MF. Selective perimetry for glaucomatous defects in ocular hypertension. Arch Ophthalmol. 1972;87(5) 518-524.

9.Schulzer M, Mikelberg FS, Drance SM. A study of the value of the central and peripheral isoptres in assessing visual field progression in the presence of paracentral scotoma measurements. Br J Ophthalmol. 1987; 71(6):422-427.

10.Caprioli J, Spaeth GL. Static threshold examination of the peripheral nasal visual field in glaucoma. Arch Ophthalmol. 1985; 103(8): 1150-1154.

11.Stewart WC, Shields MB, Ollie AR. Peripheral visual field testing by automated kinetic perimetry in glaucoma. Arch Ophthalmol. 1988; 106(2):202-206.

12.Miller KN, Shields MB, Ollie AR. Automated kinetic perimetry with two peripheral isopters in

1 - Cellular and Molecular Biology of Aqueous Humor Dynamics

Page 198 of 225

glaucoma. Arch Ophthalmol. 1989;107(9):1316-1320.

13.Ballon BJ, Echelman DA, Shields MB, et al. Peripheral visual field testing in glaucoma by automated kinetic perimetry with the Humphrey Field Analyzer. Arch Ophthalmol. 1992;110(12):17301732.

14.Harrington DO. The Bjerrum Scotoma. Am J Ophthalmol. 1965;59: 646-656.

15.Gramer E, Gerlach R, Krieglstein GK, et al. Topography of early glaucomatous visual field defects in computerized perimetry [ in German]. Klin Monatsbl Augenheilkd. 1982; 180(6):515-523.

16.Mikelberg FS, Drance SM. The mode of progression of visual field defects in glaucoma. Am J Ophthalmol. 1984;98(4):443-445.

17.Hart WM Jr, Becker B. The onset and evolution of glaucomatous visual field defects. Ophthalmology. 1982;89(3):268-279.

18.Drance SM. The glaucomatous visual field. Br J Ophthalmol. 1972; 56(3): 186-200.

19.Haefliger IO, Flammer J. Fluctuation of the differential light threshold at the border of absolute scotomas. Comparison between glaucomatous visual field defects and blind spots. Ophthalmology. 1991;98(10): 1529-1532.

20.Mikelberg FS, Schulzer M, Drance SM, et al. The rate of progression of scotomas in glaucoma. Am J Ophthalmol. 1986;101(1): 1-6.

21.Harrington DO. Differential diagnosis of the arcuate scotoma. Invest Ophthalmol Vis Sci. 1969;8 (1):96-105.

22.Kitazawa Y, Yamamoto T. Glaucomatous visual field defects: their characteristics and how to detect them. Clin Neurosci. 1997;4(5): 279-283.

23.Trobe JD. Chromophobe adenoma presenting with a hemianopic temporal arcuate scotoma. Am J Ophthalmol. 1974;77(3):388-392.

24.Drance SM. The glaucomatous visual field. Invest Ophthalmol Vis Sci. 1972;11(2):85-96.

25.Lau LI, Liu CJ, Chou JC, et al. Patterns of visual field defects in chronic angle-closure glaucoma with different disease severity. Ophthalmology. 2003;110(10):1890-1894.

26.Bonomi L, Marraffa M, Marchini G, et al. Perimetric defects after a single acute angle-closure glaucoma attack. Graefes Arch Clin Exp Ophthalmol. 1999;237(11):908-914.

27.Lynn JR. Correlation of pathogenesis, anatomy, and patterns of visual loss in glaucoma. In: Symposium on Glaucoma. St. Louis: Mosby; 1975:151.

28.Gilpin LB, Stewart WC, Shields MB, et al. Hemianopic offsets in the visual field of patients with glaucoma. Graefes Arch Clin Exp Ophthalmol. 1990;228(5):450-453.

29.Damgaard-Jensen L. Demonstration of peripheral hemiopic border steps by static perimetry. Acta Ophthalmol. 1977;55(5):815-817.

30.Anctil JL, Anderson DR. Early foveal involvement and generalized depression of the visual field in glaucoma. Arch Ophthalmol. 1984; 102(3):363-370.

31.Stamper RL. The effect of glaucoma on central visual function. Trans Am Ophthalmol Soc. 1984;82:792-826.

32.Drance SM. Diffuse visual field loss in open-angle glaucoma. Ophthalmology. 1991;98(10):15331538.

33.Lachenmayr BJ, Drance SM, Chauhan BC, et al. Diffuse and localized glaucomatous field loss in light-sense, flicker and resolution perimetry. Graefes Arch Clin Exp Ophthalmol. 1991;229(3):267-273.

34.Lachenmayr BJ, Drance SM, Airaksinen PJ. Diffuse field loss and diffuse retinal nerve-fiber loss in glaucoma. Ger J Ophthalmol. 1992;1(1):22-25.

35.Polo V, Larrosa JM, Pinilla I, et al. Glaucomatous damage patterns by short-wavelength automated perimetry (SWAP) in glaucoma suspects. Eur J Ophthalmol. 2002;12(1):49-54.

36.Samuelson TW, Spaeth GL. Focal and diffuse visual field defects: their relationship to intraocular pressure. Ophthalmic Surg. 1993;24(8): 519-525.

37.Lachenmayr BJ, Drance SM. Diffuse field loss and central visual function in glaucoma. Ger J Ophthalmol. 1992;1(2):67-73.

38.Chauhan BC, LeBlanc RP, Shaw AM, et al. Repeatable diffuse visual field loss in open-angle

1 - Cellular and Molecular Biology of Aqueous Humor Dynamics

Page 199 of 225

glaucoma. Ophthalmology. 1997;104(3):532-538.

39.Henson DB, Artes PH, Chauhan BC. Diffuse loss of sensitivity in early glaucoma. Invest Ophthalmol Vis Sci. 1999;40(13):3147-3151.

40.Heijl A. Lack of diffuse loss of differential light sensitivity in early glaucoma. Acta Ophthalmol. 1989;67(4):353-360.

41.Asman P, Heijl A. Diffuse visual field loss and glaucoma. Acta Ophthalmol. 1994;72(3):303-308.

42.Langerhorst CT, van den Berg TJ, Greve EL. Is there general reduction of sensitivity in glaucoma? Int Ophthalmol. 1989;13(1-2):31-35.

43.Hart WM Jr, Yablonski M, Kass MA, et al. Quantitative visual field and optic disc correlates early in glaucoma. Arch Ophthalmol. 1978; 96(12):2209-2211.

44.Flammer J, Eppler E, Niesel P. Quantitative perimetry in the glaucoma patient without local visual field defects [in German]. Graefes Arch Clin Exp Ophthalmol. 1982;219(2):92-94.

45.de Oliveira Rassi M, Shields MB. Crowding of the peripheral nasal isopters in glaucoma. Am J Ophthalmol. 1982;94(1):4-10.

46.Singh K, de Frank MP, Shults WT, et al. Acute idiopathic blind spot enlargement. A spectrum of disease. Ophthalmology. 1991;98(4):497-502.

47.Khorram KD, Jampol LM, Rosenberg MA. Blind spot enlargement as a manifestation of multifocal choroiditis. Arch Ophthalmol. 1991; 109(10):1403-1407.

48.Watzke RC, Shults WT. Clinical features and natural history of the acute idiopathic enlarged blind spot syndrome. Ophthalmology. 2002;109(7): 1326-1335.

49.Drance SM. The early field defects in glaucoma. Invest Ophthalmol Vis Sci. 1969;8(1):84-91.

50.Horton JC, Adams DL. The cortical representation of shadows cast by retinal blood vessels. Trans Am Ophthalmol. Soc 2000;98:33-38.

51.Colenbrander MC. The early diagnosis of glaucoma. Ophthalmologica. 1971;162(4):276-280.

52.Schiefer U, Benda N, Dietrich TJ, et al. Angioscotoma detection with fundus-oriented perimetry. A study with dark and bright stimuli of different sizes. Vision Res. 1999;39(10):1897-1909.

P.115

53.Benda N, Dietrich T, Schiefer U. Models for the description of angioscotomas. Vision Res. 1999;39 (10):1889-1896.

54.Safran AB, Halfon A, Safran E, et al. Angioscotomata and morphological features of related vessels in automated perimetry. Br J Ophthalmol. 1995;79(2):118-124.

55.Brais P, Drance SM. The temporal field in chronic simple glaucoma. Arch Ophthalmol. 1972;88 (5):518-522.

56.Pennebaker GE, Stewart WC. Temporal visual field in glaucoma: a re-evaluation in the automated perimetry era. Graefes Arch Clin Exp Ophthalmol. 1992;230(2):111-114.

57.Boden C, Sample PA, Boehm AG, et al. The structure-function relationship in eyes with glaucomatous visual field loss that crosses the horizontal meridian. Arch Ophthalmol. 2002;120(7):907-

58.Lichter PR, Ravin JG. Risks of sudden visual loss after glaucoma surgery. Am J Ophthalmol. 1974;78(6):1009-1013.

59.Caprioli J, Sears M, Miller JM. Patterns of early visual field loss in openangle glaucoma. Am J Ophthalmol. 1987;103(4):512-517.

60.Hitchings RA, Anderton SA. A comparative study of visual field defects seen in patients with lowtension glaucoma and chronic simple glaucoma. Br J Ophthalmol. 1983;67(12):818-821.

61.Caprioli J, Spaeth GL. Comparison of visual field defects in the low-tension glaucomas with those in the high-tension glaucomas. Am J Ophthalmol. 1984;97(6):730-737.

62.Drance SM. The visual field of low tension glaucoma and shock-induced optic neuropathy. Arch Ophthalmol. 1977;95(8):1359-1361.

63.Motolko M, Drance SM, Douglas GR. Visual field defects in low-tension glaucoma. Comparison of defects in low-tension glaucoma and chronic open angle glaucoma. Arch Ophthalmol. 1982;100

1 - Cellular and Molecular Biology of Aqueous Humor Dynamics

Page 200 of 225

(7):1074-1077.

64.Zeiter JH, Shin DH, Juzych MS, et al. Visual field defects in patients with normal-tension glaucoma and patients with high-tension glaucoma. Am J Ophthalmol. 1992;114(6):758-763.

65.Bhandari A, Crabb DP, Poinoosawmy D, et al. Effect of surgery on visual field progression in normal-tension glaucoma. Ophthalmology. 1997; 104(7):1131-1137.

66.Collaborative Normal-Tension Glaucoma Study Group. Comparison of glaucomatous progression between untreated patients with normal-tension glaucoma and patients with therapeutically reduced intraocular pressures. Am J Ophthalmol. 1998;126(4):487-497.

67.Radius RL, Maumenee AE. Visual field changes following acute elevation of intraocular pressure. Trans Sect Ophthalmol Am Acad Ophthalmol Otolaryngol. 1977;83(1):61-68.

68.McNaught EI, Rennie A, McClure E, et al. Pattern of visual damage after acute angle-closure glaucoma. Trans Ophthalmol Soc UK. 1974; 94(2):406-415.

69.Drance SM. Studies in the susceptibility of the eye to raised intraocular pressure. Arch Ophthalmol. 1962;68:478-485.

70.Tsamparlakis JC. Effects of transient induced elevation of the intraocular pressure on the visual field. Br J Ophthalmol. 1964;48:237-249.

71.Scott AB, Morris A. Visual field changes produced by artificially elevated intraocular pressure. Am J Ophthalmol. 1967;63(2):308-312.

72.Armaly MF. Effect of corticosteroids on intraocular pressure and fluid dynamics. III. Changes in visual function and pupil size during topical dexamethasone application. Arch Ophthalmol. 1964;71: 636-644.

73.Kolker AE, Becker B, Mills DW. Intraocular pressure and visual fields: effects of corticosteroids. Arch Ophthalmol. 1964;72:772-782.

74.LeBlanc RP, Stewart RH, Becker B. Corticosteroid provocative testing. Invest Ophthalmol Vis Sci. 1970;9(12):946-948.

75.Hart WM Jr, Becker B. Visual field changes in ocular hypertension. A computer-based analysis. Arch Ophthalmol. 1977;95(7):1176-1179.

76.Trible JR, Anderson DR. Factors associated with intraocular pressure-induced acute visual field depression. Arch Ophthalmol. 1997;115(12): 1523-1527.

77.Drance SM. The disc and the field in glaucoma. Ophthalmology. 1978; 85(3):209-214.

78.Zeyen TG, Caprioli J. Progression of disc and field damage in early glaucoma. Arch Ophthalmol. 1993;111(1):62-65.

79.Hoskins HD Jr, Gelber EC. Optic disk topography and visual field defects in patients with increased intraocular pressure. Am J Ophthalmol. 1975;80(2):284-290.

80.Shutt HK, Boyd TA, Salter AB. The relationship of visual fields, optic disc appearances and age in non-glaucomatous and glaucomatous eyes. Can J Ophthalmol 1967;2(2):83-90.

81.Drance SM. Correlation between optic disc changes and visual field defects in chronic open-angle glaucoma. Trans Sect Ophthalmol Am Acad Ophthalmol Otolaryngol. 1976;81(2):224-226.

82.Hitchings RA, Spaeth GL. The optic disc in glaucoma II: correlation of the appearance of the optic disc with the visual field. Br J Ophthalmol. 1977;61(2):107-113.

83.Quigley HA, Addicks EM, Green WR. Optic nerve damage in human glaucoma. III. Quantitative correlation of nerve fiber loss and visual field defect in glaucoma, ischemic neuropathy, papilledema, and toxic neuropathy. Arch Ophthalmol. 1982;100(1):135-146.

84.Quigley HA, Dunkelberger GR, Green WR. Retinal ganglion cell atrophy correlated with automated perimetry in human eyes with glaucoma. Am J Ophthalmol. 1989;107(5):453-464.

85.Kerrigan-Baumrind LA, Quigley HA, Pease ME, et al. Number of ganglion cells in glaucoma eyes compared with threshold visual field tests in the same persons. Invest Ophthalmol Vis Sci. 2000;41 (3):741-748.

86.Read RM, Spaeth GL. The practical clinical appraisal of the optic disc in glaucoma: the natural history of cup progression and some specific disc-field correlations. Trans Am Acad Ophthalmol Otolaryngol. 1974; 78(2):OP255-OP274.

1 - Cellular and Molecular Biology of Aqueous Humor Dynamics

Page 201 of 225

87.Gloster J. Quantitative relationship between cupping of the optic disc and visual field loss in chronic simple glaucoma. Br J Ophthalmol. 1978;62(10):665-669.

88.Hitchings RA, Anderton S. Identification of glaucomatous visual field defects from examination of monocular photographs of the optic disc. Br J Ophthalmol. 1983;67(12):822-825.

89.Nyman K, Tomita G, Raitta C, et al. Correlation of asymmetry of visual field loss with optic disc topography in normal-tension glaucoma. Arch Ophthalmol. 1994;112(3):349-353.

90.Weinreb RN, Shakiba S, Sample PA, et al. Association between quantitative nerve fiber layer measurement and visual field loss in glaucoma. Am J Ophthalmol. 1995;120(6):732-738.

91.Airaksinen PJ, Drance SM, Douglas GR, et al. Neuroretinal rim areas and visual field indices in glaucoma. Am J Ophthalmol. 1985;99(2):107-110.

92.Guthauser U, Flammer J, Niesel P. The relationship between the visual field and the optic nerve head in glaucomas. Graefes Arch Clin Exp Ophthalmol. 1987;225(2):129-132.

93.Caprioli J, Miller JM. Correlation of structure and function in glaucoma. Quantitative measurements of disc and field. Ophthalmology. 1988; 95(6):723-727.

94.Jonas JB, Gusek GC, Naumann GO. Optic disc morphometry in chronic primary open-angle glaucoma. II. Correlation of the intrapapillary morphometric data to visual field indices. Graefes Arch Clin Exp Ophthalmol. 1988;226(6):531-538.

95.Sommer A, Miller NR, Pollack I, et al. The nerve fiber layer in the diagnosis of glaucoma. Arch Ophthalmol. 1977;95(12):2149-2156.

96.Sommer A, Pollack I, Maumenee AE. Optic disc parameters and onset of glaucomatous field loss. II. Static screening criteria. Arch Ophthalmol. 1979;97(8):1449-1454.

97.Airaksinen PJ, Drance SM, Douglas GR, et al. Visual field and retinal nerve fiber layer comparisons in glaucoma. Arch Ophthalmol. 1985; 103(2):205-207.

98.Drance SM, Airaksinen PJ, Price M, et al. The correlation of functional and structural measurements in glaucoma patients and normal subjects. Am J Ophthalmol. 1986;102(5):612-616.

99.Okado K, Minato T, Miyaji S. A method for contrasting control visual fields in the Humphrey Field Analyzer and monochromatic turned-over fundus photographs. Jpn J Ophthalmol. 1988;30:925.

100.Airaksinen PJ, Heijl A. Visual field and retinal nerve fibre layer in early glaucoma after optic disc haemorrhage. Acta Ophthalmol. 1983; 61(2):186-194.

101.Katz J, Sommer A. Similarities between the visual fields of ocular hypertensive and normal eyes. Arch Ophthalmol. 1986;104(11):1648-1651.

102.Armaly MF. The correlation between appearance of the optic cup and visual function. Trans Am Acad Ophthalmol Otolaryngol. 1969;73(5):898-913.

103.Funk J, Bornscheuer C, Grehn F. Neuroretinal rim area and visual field in glaucoma. Graefes Arch Clin Exp Ophthalmol. 1988;226(5):431-434.

104.Choplin NT, Sherwood MB, Spaeth GL. The effect of stimulus size on the measured threshold values in automated perimetry. Ophthalmology. 1990;97(3):371-374.

105.Johnson CA, Keltner JL. Optimal rates of movement for kinetic perimetry. Arch Ophthalmol. 1987;105(1):73-75.

106.Schiefer U, Strasburger H, Becker ST, et al. Reaction time in automated kinetic perimetry: effects of stimulus luminance, eccentricity, and movement direction. Vision Res. 2001;41(16):2157-2164.

107.Portney GL, Krohn MA. The limitations of kinetic perimetry in early scotoma detection. Ophthalmology. 1978;85(3):287-293.

P.116

108.Agarwal HC, Gulati V, Sihota R. Visual field assessment in glaucoma: comparative evaluation of manual kinetic Goldmann perimetry and automated static perimetry. Indian J Ophthalmol. 2000;48(4): 301-306.

109.Ourgaud M. Static circular perimetry in open-angle glaucoma [in French]. J Fr Ophtalmol. 1982;5 (6-7):387-391.

110.Katz J, Tielsch JM, Quigley HA, et al. Automated perimetry detects visual field loss before manual

1 - Cellular and Molecular Biology of Aqueous Humor Dynamics

Page 202 of 225

Goldmann perimetry. Ophthalmology. 1995; 102(1):21-26.

111.McLean IM, Mueller E, Buttery RG, et al. Visual field assessment and the Austroads driving standard. Clin Experiment Ophthalmol 2002;30(1):3-7.

112.Klewin KM, Radius RL. Background illumination and automated perimetry. Arch Ophthalmol. 1986;104(3):395-397.

113.Drum B, Armaly MF, Huppert W. Scotopic sensitivity loss in glaucoma. Arch Ophthalmol. 1986;104(5):712-717.

114.Stirling RJ, Pawson P, Brimlow GM, et al. Patients with ocular hypertension have abnormal point scotopic thresholds in the superior hemifield. Invest Ophthalmol Vis Sci. 1996;37(8):1608-1617.

115.Lindenmuth KA, Skuta GL, Rabbani R, et al. Effects of pupillary constriction on automated perimetry in normal eyes. Ophthalmology. 1989;96(9):1298-1301.

116.McCluskey DJ, Douglas JP, O'Connor PS, et al. The effect of pilocarpine on the visual field in normals. Ophthalmology. 1986;93(6): 843-846.

117.Heuer DK, Anderson DR, Feuer WJ, et al. The influence of decreased retinal illumination on automated perimetric threshold measurements. Am J Ophthalmol. 1989;108(6):643-650.

118.Edgar DF, Crabb DP, Rudnicka AR, et al. Effects of dipivefrin and pilocarpine on pupil diameter, automated perimetry and LogMAR acuity. Graefes Arch Clin Exp Ophthalmol. 1999;237(2):117-124.

119.Lindenmuth KA, Skuta GL, Rabbani R, et al. Effects of pupillary dilation on automated perimetry in normal patients. Ophthalmology. 1990; 97(3):367-370.

120.Spry PG, Johnson CA. Senescent changes of the normal visual field: an age-old problem. Optom Vis Sci. 2001;78(6):436-441.

121.Haas A, Flammer J, Schneider U. Influence of age on the visual fields of normal subjects. Am J Ophthalmol. 1986;101(2):199-203.

122.Jaffe GJ, Alvarado JA, Juster RP. Age-related changes of the normal visual field. Arch Ophthalmol. 1986;104(7):1021-1025.

123.Johnson CA, Adams AJ, Lewis RA. Evidence for a neural basis of age-related visual field loss in normal observers. Invest Ophthalmol Vis Sci. 1989;30(9):2056-2064.

124.Heuer DK, Anderson DR, Knighton RW, et al. The influence of simulated light scattering on automated perimetric threshold measurements. Arch Ophthalmol. 1988;106(9):1247-1251.

125.Chen PP, Budenz DL. The effects of cataract extraction on the visual field of eyes with chronic open-angle glaucoma. Am J Ophthalmol. 1998; 125(3):325-333.

126.The AGIS Investigators. The advanced glaucoma intervention study, 6: effect of cataract on visual field and visual acuity. Arch Ophthalmol. 2000;118(12):1639-1652.

127.Bigger JF, Becker B. Cataracts and open-angle glaucoma. The effect of cataract extraction on visual fields. Am J Ophthalmol. 1971;1(1 pt 2): 335-340.

128.Smith SD, Katz J, Quigley HA. Effect of cataract extraction on the results of automated perimetry in glaucoma. Arch Ophthalmol. 1997;115(12): 1515-1519.

129.Hayashi K, Hayashi H, Nakao F, et al. Influence of cataract surgery on automated perimetry in patients with glaucoma. Am J Ophthalmol. 2001;132(1):41-46.

130.Wood JM, Wild JM, Smerdon DL, et al. Alterations in the shape of the automated perimetric profile arising from cataract. Graefes Arch Clin Exp Ophthalmol. 1989;227(2):157-161.

131.Guthauser U, Flammer J. Quantifying visual field damage caused by cataract. Am J Ophthalmol. 1988;106(4):480-484.

132.Radius RL. Perimetry in cataract patients. Arch Ophthalmol. 1978; 96(9):1574-1579.

133.Ruben JB, Lewis RA, Johnson CA, et al. The effect of Goldmann applanation tonometry on automated static threshold perimetry. Ophthalmology. 1988;95(2):267-270.

134.Weinreb RN, Perlman JP. The effect of refractive correction on automated perimetric thresholds. Am J Ophthalmol. 1986;101 (6):706-709.

135.Heuer DK, Anderson DR, Feuer WJ, et al. The influence of refraction accuracy on automated perimetric threshold measurements. Ophthalmology. 1987;94(12):1550-1553.

136.Goldstick BJ, Weinreb RN. The effect of refractive error on automated global analysis program G-

1 - Cellular and Molecular Biology of Aqueous Humor Dynamics

Page 203 of 225

1. Am J Ophthalmol. 1987;104(3):229-232.

137.Koller G, Haas A, Zulauf M, et al. Influence of refractive correction on peripheral visual field in static perimetry. Graefes Arch Clin Exp Ophthalmol. 2001;239(10):759-762.

138.Drance SM, Berry V, Hughes A. Studies in the reproducibility of visual field areas in normal and glaucomatous subjects. Can J Ophthalmol. 1966;1(1):14-23.

139.Heijl A, Lindgren G, Olsson J. The effect of perimetric experience in normal subjects. Arch Ophthalmol. 1989;107(1):81-86.

140.Werner EB, Krupin T, Adelson A, et al. Effect of patient experience on the results of automated perimetry in glaucoma suspect patients. Ophthalmology. 1990;97(1):44-48.

141.Wild JM, Dengler-Harles M, Searle AE, et al. The influence of the learning effect on automated perimetry in patients with suspected glaucoma. Acta Ophthalmol. 1989;67(5):537-545.

142.Marra G, Flammer J. The learning and fatigue effect in automated perimetry. Graefes Arch Clin Exp Ophthalmol. 1991;229(6):501-504.

143.Zulauf M, Flammer J, Signer C. The influence of alcohol on the outcome of automated static perimetry. Graefes Arch Clin Exp Ophthalmol. 1986;224(6):525-528.

144.Trobe JD, Acosta PC, Shuster JJ, et al. An evaluation of the accuracy of community-based perimetry. Am J Ophthalmol. 1980;90(5):654-660.

145.Heijl A, Drance SM. Changes in differential threshold in patients with glaucoma during prolonged perimetry. Br J Ophthalmol. 1983; 67(8):512-516.

146.Fujimoto N, Adachi-Usami E. Fatigue effect within 10 degrees visual field in automated perimetry. Ann Ophthalmol. 1993;25(4):142-144.

147.Hudson C, Wild JM, O'Neill EC. Fatigue effects during a single session of automated static threshold perimetry. Invest Ophthalmol Vis Sci. 1994;35(1):268-280.

148.Asman P, Fingeret M, Robin A, et al. Kinetic and static fixation methods in automated threshold perimetry. J Glaucoma. 1999;8(5):290-296.

149.Wabbels B, Kolling G. Automated kinetic perimetry using different stimulus velocities [in German]. Ophthalmologe. 2001;98(2):168-173.

150.Britt JM, Mills RP. The black hole effect in perimetry. Invest Ophthalmol Vis Sci. 1988;29(5):795-

151.Desjardins D, Anderson DR. Threshold variability with an automated LED perimeter. Invest Ophthalmol Vis Sci. 1988;29(6):915-921.

152.Wilensky JT, Mermelstein JR, Siegel HG. The use of different-sized stimuli in automated perimetry. Am J Ophthalmol. 1986;101(6):710-713.

153.Zalta AH. Use of a central 10 degrees field and size V stimulus to evaluate and monitor small central islands of vision in end stage glaucoma. Br J Ophthalmol. 1991;75(3):151-154.

154.Li SG, Spaeth GL, Scimeca HA, et al. Clinical experiences with the use of an automated perimeter (Octopus) in the diagnosis and management of patients with glaucoma and neurologic diseases. Ophthalmology. 1979; 86(7):1302-1316.

155.Schmied U. Automatic (Octopus) and manual (Goldmann) perimetry in glaucoma. Graefes Arch Clin Exp Ophthalmol. 1980;213(4): 239-244.

156.Wilensky JT, Joondeph BC. Variation in visual field measurements with an automated perimeter. Am J Ophthalmol. 1984;97(3):328-331.

157.Beck RW, Bergstrom TJ, Lichter PR. A clinical comparison of visual field testing with a new automated perimeter, the Humphrey Field Analyzer, and the Goldmann perimeter. Ophthalmology. 1985;92(1):77-82.

158.Trope GE, Britton R. A comparison of Goldmann and Humphrey automated perimetry in patients with glaucoma. Br J Ophthalmol. 1987; 71(7):489-493.

159.Brenton RS, Argus WA. Fluctuations on the Humphrey and Octopus perimeters. Invest Ophthalmol Vis Sci. 1987;28(5):767-771.

160.Mills RP, Hopp RH, Drance SM. Comparison of quantitative testing with the Octopus, Humphrey, and Tubingen perimeters. Am J Ophthalmol. 1986;102(4):496-504.

1 - Cellular and Molecular Biology of Aqueous Humor Dynamics

Page 204 of 225

161.King D, Drance SM, Douglas GR, et al. The detection of paracentral scotomas with varying grids in computed perimetry. Arch Ophthalmol. 1986;104(4):524-525.

162.Weber J, Dobek K. What is the most suitable grid for computer perimetry in glaucoma patients? Ophthalmologica. 1986;192(2):88-96.

163.Gramer E, Althaus G, Leydhecker W. The importance of grid density in automatic perimetry: a clinical study. Z Prakt Augenheilkd. 1986; 7:197.

164.Seamone C, LeBlanc R, Rubillowicz M, et al. The value of indices in the central and peripheral visual fields for the detection of glaucoma. Am J Ophthalmol. 1988;106(2):180-185.

165.Henson DB, Artes PH. New developments in supra-threshold perimetry. Ophthalmic Physiol Opt. 2002;22(5):463-468.

P.117

166.Artes PH, McLeod D, Henson DB. Response time as a discriminator between trueand falsepositive responses in suprathreshold perimetry. Invest Ophthalmol Vis Sci. 2002;43(1):129-132.

167.Fankhauser F, Funkhouser A, Kwasniewska S. Evaluating the applications of the spatially adaptive program (SAPRO) in clinical perimetry: part I. Ophthalmic Surg. 1986;17(6):338-342.

168.Asman P, Britt JM, Mills RP, et al. Evaluation of adaptive spatial enhancement in suprathreshold visual field screening. Ophthalmology. 1988;95(12):1656-1662.

169.Stewart WC, Shields MB, Ollie AR. Full threshold versus quantification of defects for visual field testing in glaucoma. Graefes Arch Clin Exp Ophthalmol. 1989;227(1):51-54.

170.Araujo ML, Feuer WJ, Anderson DR. Evaluation of baseline-related suprathreshold testing for quick determination of visual field nonprogression. Arch Ophthalmol. 1993;111(3):365-369.

171.Flanagan JG, Wild JM, Trope GE. Evaluation of FASTPAC, a new strategy for threshold estimation with the Humphrey Field Analyzer, in a glaucomatous population. Ophthalmology. 1993;100 (6):949-954.

172.Mills RP, Barnebey HS, Migliazzo CV, et al. Does saving time using FASTPAC or suprathreshold testing reduce quality of visual fields? Ophthalmology. 1994;101(9):1596-1603.

173.O'Brien C, Poinoosawmy D, Wu J, et al. Evaluation of the Humphrey FASTPAC threshold program in glaucoma. Br J Ophthalmol. 1994; 78(7):516-519.

174.Glass E, Schaumberger M, Lachenmayr BJ. Simulations for FASTPAC and the standard 4-2 dB full-threshold strategy of the Humphrey Field Analyzer. Invest Ophthalmol Vis Sci. 1995;36(9):18471854.

175.Bengtsson B, Olsson J, Heijl A, et al. A new generation of algorithms for computerized threshold perimetry, SITA. Acta Ophthalmol Scand. 1997;75(4):368-375.

176.Bengtsson B, Heijl A. SITA Fast, a new rapid perimetric threshold test. Description of methods and evaluation in patients with manifest and suspect glaucoma. Acta Ophthalmol Scand. 1998;76(4):431-

177.Bengtsson B, Heijl A. Evaluation of a new perimetric threshold strategy, SITA, in patients with manifest and suspect glaucoma. Acta Ophthalmol Scand. 1998;76(3):268-272.

178.Wild JM, Pacey IE, O'Neill EC, et al. The SITA perimetric threshold algorithms in glaucoma. Invest Ophthalmol Vis Sci. 1999;40(9): 1998-2009.

179.Bengtsson B, Heijl A. Comparing significance and magnitude of glaucomatous visual field defects using the SITA and Full Threshold strategies. Acta Ophthalmol Scand. 1999;77(2):143-146.

180.Sharma AK, Goldberg I, Graham SL, et al. Comparison of the Humphrey Swedish interactive thresholding algorithm (SITA) and full threshold strategies. J Glaucoma. 2000;9(1):20-27.

181.Budenz DL, Rhee P, Feuer WJ, et al. Sensitivity and specificity of the Swedish interactive threshold algorithm for glaucomatous visual field defects. Ophthalmology. 2002;109(6):1052-1058.

182.Budenz DL, Rhee P, Feuer WJ, et al. Comparison of glaucomatous visual field defects using standard full threshold and Swedish interactive threshold algorithms. Arch Ophthalmol. 2002;120 (9):1136-1141.

183.Remky A, Arend O. Clinical experiences with the “ Swedish interactive threshold

Соседние файлы в папке Английские материалы