- •Table of Contents
- •Preface
- •History
- •Epidemiology of angle closure glaucoma
- •Anatomy and biometry
- •Pathophysiology of angle-closure glaucoma
- •Classification
- •Screening for angle-closure glaucoma
- •Gonioscopy
- •Provocative test
- •Ultrasound biomicroscopy
- •Anterior segment optical coherence tomography
- •New approaches to visualize the anterior chamber angle
- •Optic nerve and visual field examinations
- •Acute angle closure
- •Intermittent angle closure
- •Chronic angle closure
- •Occludable angles
- •Plateau iris
- •Lens-associated angle closure
- •Secondary angle-closure glaucoma
- •Malignant glaucoma
- •Medical treatment
- •Laser iridotomy
- •Argon laser peripheral iridoplasty (ALPI)
- •Trabeculectomy
- •Goniosynechialysis
- •Combined surgery
- •Paracentesis
- •Index of Authors
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Ultrasound biomicroscopy
Yukitaka Uji
Department of Ophthalmology, Mie University School of Medicine, Tsu, Japan
Introduction
In the treatment of glaucoma, testing the anterior chamber angle is essential. While gonioscopy is the most common method, ultrasound biomicroscopy (UMB)1 is useful for assessing areas that cannot be examined by gonioscopy, such as the ciliary body, inside the iris, the posterior chamber, inside filtering blebs following filtering surgery, or the outflow tract for aqueous humor inside the sclera or cases that are difficult to examine using gonioscopy, such as narrow-angle glaucoma. This chapter describes UBM images for common glaucoma conditions.
UBM Characteristics
The following characteristics make UBM suitable for the treatment of glaucoma: 1) a high resolution of 50 μm at a frequency of 50 MHz; 2) cross-sections of the angle can be captured without lighting, so changes in iris shape with or without light can be ascertained; 3) observation is independent of corneal opacity; 4) dynamic changes can be recorded; 5) the technique is noninvasive and can be repeated numerous times; and 6) UBM images can be automatically quantified. However, unlike gonioscopy, UBM cannot detect mild differentiation failure, pigmentation, inflammatory exudate or neovascularization in the angle. Hence, following slitlamp microscopy or gonioscopy, UBM should be performed to compensate for the shortcomings of gonioscopy.
Equipment
The present article deals with UBM model 840 (Humphrey Instruments, San Leandro, CA) and UD-1000/6000 (UBM probe: UD-6010) (Tomey Corporation, Nagoya, Japan)2 (Fig. 1). Both systems are based on water immersion and use an eye cup
Address for correspondence: Yukitaka Uji, Professor, Department of Ophthalmology, Mie University School of Medicine, 2-174,Edobashi, Tsu, 514-8507, Japan. E-mail:uji@clin.medic.mie-u.ac.jp
Angle Closure Glaucoma, pp. 79–90
edited by Chul Hong and Tetsuya Yamamoto
© 2007 Kugler Publications, Amsterdam, The Netherlands
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Fig. 1. Left: UD-1000/6000 ultrasound machine and UD-6010 probe. A protective cap covers the probe tip. Right: Model 840 conventional UBM machine and probe.
Fig. 2. Left: Testing using UD-6010 and an eye cup. Right: Testing using Model 840 and an eye cup.
for testing (Fig. 2). Ultrasonic frequency is 50 MHz for Model 840 and 40 MHz for UD-6010. Model 840 uses mechanical linear scanning while UD-6010 uses magnetic linear scanning, and while no marked difference is apparent, the scanning range is 5 mm wide × 5 mm deep for Model 840 and 9 mm wide × 6 mm deep for UD6010. The UD-6010 is thus capable of capturing a larger area from the pupillary
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margin to the ciliary body, and allows easy analysis of the posterior pole past the ciliary body. With UD-1000/6000(probe:UD-6010), static images can be stored using compact flash cards, facilitating subsequent imaging processing.
UBM Images
Quality of UBM images
If a probe is positioned perpendicular to the cornea, UBM images show the anterior and posterior surfaces of the cornea as clear reflective lines, along with the scleral spur of the angle (Fig. 3). If the probe is not positioned well, these structures cannot be clearly seen. This is an important point in assessing image quality.
Fig. 3. UBM image clarity and probe angle. Left (UBM image): With proper probe angle, clear reflective lines are seen for the anterior and posterior surfaces of the cornea (arrows). Schwalbe's line is apparent (black triangle). Right (UBM image): Improper probe angle.
Comparison of gonioscopy and UBM images
An UBM-image of the angle merely represents a cross-section, and at this point of time, only captures a single cross-section of 360˚ of the angle at a specific point in time. UBM does not replace gonioscopy, and comparison of results with slit-lamp microscopy or gonioscopy remains important. Figure 4 compares images from a normal eye between UBM and gonioscopy. With UBM, the scleral spur is the only reference point seen on all images, and represents the cross point between inner surface of the cornea and the boundary between ciliary body and sclera. If the probe angle is appropriate, Schwalbe's line can also be seen nearest to the angle recess of the high-intensity reflective line for the inner surface of the cornea. On normal UBM images, the iris is mildly convex in the anterior direction or flat, and the ciliary sulcus is seen between ciliary processes and iris.
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Fig. 4. Comparison of gonioscopy and UBM images.
UBM findings in relative pupillary block
Unlike gonioscopy, which requires lighting, the angle can be observed by UBM without lighting, as is the case with a darkroom test. Figure 5 shows UBM images of relative pupillary block (PRB) captured using the two machines for UBM. With both machines, the iris was pushed up due to increased posterior segment pressure by pupillary block. In addition, angle closure that is absent in bright light may occur in the dark due to pupillary dilatation. In this example, the ciliary sulcus was clearly seen.3
Fig. 5. UBM images of relative pupillary block captured using the two machines in a patient with primary angle-closure glaucoma. Above: with lighting. Below: without lighting. The ciliary sulcus is apparent (arrow).
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UBM findings of plateau iris configuration
Figure 6 shows plateau iris configuration (PIC), and while the anterior segment was not shallow, unlike pupillary block, the iris was flat and displayed a thick root. Due to the ciliary process that rotated anteriorly, the iris was pushed up and the ciliary sulcus was lost. In this patient, gonioscopy was difficult to perform, and because the shape of the ciliary body was unique, UBM was extremely useful as a diagnostic tool.4
Fig. 6. UBM image of plateau iris configuration in a patient with primary angle-closure glaucoma. The ciliary sulcus is unclear (arrow). The ciliary body can be seen (asterisk).
UBM images before and after laser iridotomy in relative pupillary block
Figure 7 compares UBM images before and after laser iridotomy (LI). LI widened the angle recess, and the iris that initially arched anteriorly became flattened. In this manner, changes in the iris and angle due to surgery can be seen on cross sections.5
Indentation UBM
Indentation UBM is an imaging technique to observe the angle by compressing the contralateral cornea using the gonioscopy probe to move the aqueous humor and push down on the iris. With this technique, apposition closure can be differentiated from adhesive closure. The same effect can be achieved by observing the eye by applying slight pressure using a small eye cup, and we have thus performed pressure UBM using an eye cup with a built-in compressor to safely and easily compress the cornea.6 When angle closure is detected by UBM with lighting,, use of this eye cup allows differentiation of appositional angle closure (Fig. 8) from synechial angle closure (Fig. 9). In other words, compression cannot push and
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Fig. 7. UBM images before and after laser iridotomy (LI) in a patient with relative pupillary block.
Fig. 8. Indentation UBM in a patient with appositional angle closure. Appositional closure (triangles). Direction of aqueous humor pressure (arrows).
widen iridocorneal adhesion during synechial angle closure. In the case of PIC, compression does not change the shape of the iris root, but state of the angle recess can be observed (Fig. 10).7
Iris observation
Angle closure caused by umbrella iris can increase ocular pressure. Whether umbrella iris is caused by a cyst or solid tumor can be assessed on UBM cross-sections of the iris (Fig. 11).8 Reverse pupillary block can be seen in patients with pigment dispersion syndrome, where the iris is flexed posteriorly (Fig. 11).9
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Fig. 9. Indentation UBM in a patient with synechial angle closure. Synechial closure (triangles). Direction of aqueous humor pressure (arrows).
Fig. 10. Indentation UBM in a patient with plateau iris configuration. Direction of aqueous humor pressure is shown (arrows).
UBM images following filtering surgery
Following trabeculectomy, the outflow tract under a scleral flap, inside the filtering bleb, the ciliary body and back surface of the iris cannot be observed optically, but these structures can be assessed by UBM (Figs. 12-14) . This is useful for postoperative management, reoperation and transconjunctival needling procedure under a scleral flap.10 In addition, following trabeculectomy with MMC, filtering blebs are usually assessed by slit lamp microscopy, but this is sometimes difficult. With UBM, patients can be classified into the following four types: low-reflective type where intensity inside a filtering bleb is low, and ocular pressure control is favorable; high-reflective type where intensity of a filtering bleb is high, and the bleb
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Fig. 11. Above left: Umbrella iris caused by an iris cyst (asterisk). Above right: Umbrella iris caused by an iris tumor (asterisk). Below: A posteriorly flexed iris in pigment dispersion syndrome (From Dr. Hiroshi Ishikawa’s data).
Fig. 12. A UBM image following trabeculectomy. Scleral flap (black arrow), iridectomy (white arrow) and conjunctival filtering bleb (asterisk) are shown.
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Fig. 13. A UBM image following trabeculectomy. The aqueous humor outflow tract under the scleral flap (arrow) and high-intensity filtering bleb (asterisk) are shown.
Fig. 14. UBM images of filtering blebs following trabeculectomy with MMC. L: low reflective; H: high reflective; F: flattened; and E: encapsulated.
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is clearly seen; flattened type where a filtering bleb is not seen, and ocular pressure control is poor; and encapsulated type where tissue under the scleral flap is scarred and surrounded by Tenon's capsule, blocking function as a filtering bleb11). This type of information is important for planning therapy for patients with poor ocular pressure control.
UBM images of the ciliary body
As the ciliary body is difficult to observe through the pupil, cross-sectional imaging by UBM is useful for pathological clarification and therapy planning. Figure 15 shows a patient with malignant glaucoma12 following filtering surgery. The anterior segment was shallow, and the ciliary process rotated anteriorly and then compressed against the iris. Supraciliary effusion was confirmed. Figure 16 shows a patient with uveal effusion complicated by narrow angle and supraciliary effusion. UBM is also useful for assessing ciliary body dissection or rupture caused by other blunt traumas, supraciliary effusion at low ocular pressure following filtering surgery,13 or dissection of the ciliary body or choroid in Harada's disease14 or following laser photocoagulation in diabetic retinopathy.
Fig. 15. A UBM image of malignant glaucoma. Supraciliary effusion (white arrow), anterior segment loss (black arrow) and ciliary body (asterisk) are shown.
Quantitative UBM
Measurement of the degree of anterior chamber angle opening is significant in the therapy of closed angle glaucoma. Estimating an angle opening by gonioscopy is subjective and generally gross. But UBM is much better suited for objective measurements and evaluation of the anatomy and pathophysiology of the anterior segment. Pavlin et al.3 proposed several parameters to measure the anterior segment. Angle opening distance (AOD500) is defined as the length of the line drawn from the point
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Fig. 16. Shallow anterior segment and narrow angle in a patient with uveal effusion. Supraciliary effusion (arrow) and ciliary body (asterisk) are shown.
Fig. 17. Parameters to measure the angle. Left: Angle opening distance (AOD500) and angle (θ1). Right: Angle recess area (ARA).
on the endothelial surface 500 μm anterior to the scleral spur to the iris surface perpendicular to the corneal endothelial surface. The trabecular/iris angle (θ1) is measured with the apex in the iris recess and the arms passing through the point 500 μm from the scleral spur and the point perpendicularly opposite on the iris. In addition to these, Pavlin et al.3 presented other parameters to measure the iris and ciliary body configuration, such as the iris thickness, trabecular-ciliary process distance (TCPD), the angle at which the iris leaves the lens surface (θ2), etc.
Ishikawa et al.15,16 introduced angle recess area (ARA) to estimate the anterior chamber angle width. ARA is defined as a triangular area bordered by the anterior iris surface, corneal endothelium, and a line perpendicular to the corneal endothelium drawn from a point 750 μm anterior to the scleral spur to the iris surface. This method faithfully reflects irregularities of iris contour and curvature.
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Summary
UBM is capable of generating high-resolution cross-sectional images of the anterior segment and depicting areas that cannot be detected optically. This technique can also be performed without lighting, which is important for testing narrow angle glaucoma. UBM is thus useful for the diagnosis and treatment of glaucoma, but should be combined with techniques such as gonioscopy to maximize usefulness.
References
1.Pavlin CJ, Harasiewicz K, Sherar MD, Foster FS: Clinical use of ultrasound biomicroscopy. Ophthalmology 1991;98:287-95.
2.Sugimoto K, Uji Y, Ito K, Miura K, Matsunaga K, Furuta M, Ogo M: Usefulness of new probe UD-6010 for ultrasound biomicroscopy. Eye 2005;22:1411-4.
3.Pavlin CJ, Harasiewicz K, Foster S: Ultrasound biomicroscopy of anterior segment structures in normal and glaucomatous eyes. Am J Ophthalmol 1992;113:381-9.
4.Pavlin CJ, Ritch R, Foster FS: Ultrasound biomicroscopy in plateau iris syndrome. Am J Ophthalmol 1992;113:390-5.
5.Liebmann JM, Ritch R: Laser iridotomy. Ophthalmic Surg Lasers 1996;27:209-27.
6.Matsunaga K, Ito K, Esaki K, Sugimoto K, Sano T, Miura K, Sasoh M, Uji Y: Evaluation of eyes with relative papillary block by indentation ultrasound biomicroscopy gonioscopy. Am J Ophthalmol 2004;137:552-4.
7.Matsunaga K, Ito K, Esaki K, Sugimoto T, Sano K, Miura K, Sasoh M, Uji Y: Evaluation and comparison of indentation ultrasound biomicroscopy gonioscopy in relative papillary block, peripheral anterior synechia, and plateau iris configuration. J Glaucoma 2004;13:516-9.
8.Marigo FA, Esaki K, Finger PT, Ishikawa H, Green field DS, Liebmann JM, Ritch R: Differential diagnosis of anterior segment cysts by ultrasound biomicroscopy. Ophthalmology 1999;106:2131-5.
9.Breingan PJ, Esaki K, Ishikawa H, Liebmann JM, Greenfield DS, Ritch R: Iridolenticular contact decreases following laser iridotomy for pigment dispersion syndrome. Arch Ophthalmol 1999;117:325-8.
10.Mistlberger A, Esaki K, Liebmann JM, Ritch R: A slit-lamp needling filtration procedure for uncontrolled glaucoma in pseudophakic and aphakic eyes. Ophthalmic Surg Lasers 1999;30:23740.
11.Yamamoto T, Sakuma T, Kitazawa Y: An ultrasound biomicroscopic study of filtering blebs after mitomycin C trabeculectomy. Ophthalmology 1995;102:1770-6.
12.Trope GE, Pavlin CJ, Bau A, Baumal CR, Foster FS: Malignant glaucoma. Clinical and ultrasound biomicroscopic features. Ophthalmology 1994;101:1030-5.
13.Sugimoto K, Ito K, Esaki K, Miyamura M, Sasoh M, Uji Y: Supraciliochoroidal fluid at a early stage after trabeculectomy. Jpn J Ophthalmol 2002;46:548-52.
14.Maruyama Y, Kimura Y, Kishi S, Shimizu K: Serous detachment of the ciliary body in Harada disease. Am J Ophthalmol 1998;125:666-72.
15.Ishikawa H, Uji Y, Emi K:A new method of quantifying angle measurements based on ultrasound biomicroscopy. Atarashii Ganla(J Eye)1995;12:957-60.
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