Recently, the use of multifocal and toric IOLs has increased the need for obtaining well-centered round CCCs. Because an anterior capsulotomy is usually not perfectly circular, several methods to facilitate the completion of CCC have been devised.
6–8 Several studies have reported that femtosecond laser capsulotomies show better IOL centration with better circularity after surgery than manual CCCs.
9–12 However, it is difficult to create a perfectly sized anterior capsulorhexis that is also perfectly centered in relation to the lens. Some useful methods are available to locate a well-centered capsulotomy in the anterior lens capsule, such as the use of an eyecage device
13 or algorithms that provide a SCC or PC during FACS. Clinically, surgeons locate the CCC to the center of the limbus or dilated pupil, but the eyecage device shows only an indirect center relative to the limbus. In contrast, FACS is not used worldwide for economic reasons or because of its limitations when performing surgery in small pupils or shallow anterior chambers.
In this study, we used OCT, MRI, and anterior segment photographs to investigate which anatomical structure most closely matches the preoperative lens center and provides perfect concordance with the postoperative IOL center. Recently, several studies have attempted to perform ideal well-centered CCCs, but the results were analyzed only during the postoperative period. To our knowledge, this is the first study to determine the relative anatomical location before cataract surgery using sectional anterior segment images.
Our study showed that the AC and SCC tended to be the centers closest to the IOL center on the lens equatorial plane. The AC and SCC were also concentrated around the IOL center without outlier points. The next nearest center was the PC, whereas the LC was widely dispersed and too far from the IOL center. In conclusion, the best landmark for crystalline lens centering is either the AC or SCC. Of these two exact landmarks, the AC is more useful because nearly all of the commercially available anterior segment OCTs or ultrasounds can provide a clear angle image.
A limitation of our study is that the SCC and IOL center do not perfectly coincide with the crystalline lens center; they are only estimated values that can be used as substitutes for the lens center. To increase accuracy, we excluded tilted photographs, and we analyzed photographs of patients who showed maintenance of even capsular contracture around the whole optic edge after 2 to 6 months. The mean postoperative best-corrected visual acuity was logMAR 0.04 ± 0.09 (n = 76) at 2 months after cataract surgeries. Although there were no significant differences in postoperative vision according to the CCC center chosen, postoperative IOL position could be affected by decentering or tilting of the IOL or contraction of CCC. Further long-term follow-up studies for visual prognosis involving subjective vision, refractive error, and high-order aberration should be performed, because a relationship may exist between the CCC center and visual prognosis after cataract surgery.
To improve the shortcomings of OCT scans, which cannot show retro-iris structures, we rechecked the relationships among centers in pig eyes ex vivo using MRI. In contrast to other well-established ophthalmologic imaging methods, MRI provides true anatomical proportions independent of the absorption and optical characteristics of the tissues. In a prior study by Langner et al.,
14 7.1 T MRI to assess the anterior segment of the eye was effective for discriminating microstructures such as the angle, sulcus, and lens equator. In this study, we used high-resolution 9.4 Tesla MRI with an orbit coil and set the sectional thickness to be as thin as possible to avoid artifacts and to improve image quality. The 9.4 T MRI is more powerful than 7.1 T MRI, and its use in humans is not permitted for safety reasons. In the MR images, we found the exact location of the lens equator directly, and the center closest to the lens center was the AC; the PC was significantly farther away than the AC. We tried to perform MRI in human eyes in vivo in the early stage, but finally we did not succeed because of poor image quality. Several factors such as high cost, microsaccades (i.e., involuntary eye movements), and motion artifacts from continuous breathing were significant problems in a previous human MR imaging study,
15 and we experienced the same problems. However, when we performed MRI in pig eyes ex vivo rather than in human eyes, we showed that the lens center was closer to the AC than PC.
The next question we addressed was why the AC is superior to the limbus or PC. Our results can be interpreted in two ways. First, because the limbus is not perfectly circular but rather is an ovoid-shaped structure, the horizontal corneal diameter is approximately 0.8 mm greater than the vertical diameter.
16 The presence of pannus can also interfere with the estimation of the true center prior to performing capsulorhexis. Second, there is a significant shift in the location of the PC with increasing dilation, with the lateral position coming closer to the center of the cornea at its maximal dilation. A previous study showed that the PC shifts temporally as the pupil dilates, with a mean motion distance of 0.133 mm between the mesopic and photopic conditions.
17 With pharmacologic dilation, the PC shifts in every direction, primarily inferotemporally, relative to the corneal reflex.
18
The equator of the crystalline lens hangs from the ciliary body via zonular fibers, and the borderline between the anterior aspect of the iris and the corneal endothelial surface is the angle. Thus, anatomically, the angle could be a better representative of the lens equator than the pupil margin or limbus because of its geometric location. In addition, the angle has an advantage over the pupil because it is not influenced by pharmacologic dilation. A previous study reported that the corneal diameter is significantly correlated with the lens diameter (correlation coefficient = 0.711;
P < 0.001),
19 and there are possible close relationships between size and location for the lens, angle, and corneal structures.
The Catalys system produces three-dimensional spectral-domain OCT images with a wavelength of 830 nm and axial and lateral resolutions of 30 and 15 μm, respectively. This technique can show every structure covered by a liquid optic interface whose clear aperture is 13.5 mm. Because the depth of field is also large, OCT scans can include the corneal epithelium to the posterior capsule of the lens. To show the center of the CCC during FACS, automated surface mapping algorithms may calculate the scanned capsule line along the anterior and posterior capsules. In contrast, anterior segment OCTs commonly used in the field of ophthalmology have transverse scan ranges of 10 to 16 mm, scan depths of 2 to 6 mm, and resolutions of 5 to 60 μm. Despite their good resolution, they are limited by their relatively smaller field of view in a single scan compared to the OCT Catalys system. Commonly used systems cannot show the scanned capsule curvature because the images that they produce lack the posterior lens capsule. Ultrasound biomicroscopes have several applications because of their probe characteristics, but in general, only the newest vesions can show the whole cornea and lens. However, despite the limitations mentioned above, all ultrasound biomicroscopes and commercially available OCTs can show the “angle structure” clearly; therefore, information regarding the AC could be applied during CCC procedures in every clinical condition.
Placement of enucleated pig eyes in perfluorocarbon minimized the effect of gravity. Under this condition, our ex vivo study showed the true anatomical structures without deviations. In contrast, human eyes imaged in vivo under the docking state using a patient interface may be distorted by external pressure. However, the results of our study coincided with two opposite extreme conditions. Thus, our method can be used in real conditions under gravity or other pressures arising from the patient interface or nearby soft tissues.
In conclusion, if surgeons cannot find the location of the lens equator under the surgical microscope because of the iris structure, they can determine the exact location of the lens center from the AC in OCT scans taken before surgery. This method is as useful as SCC. If surgeons perform CCC based on the AC, the postoperative capsulotomy center will be close to the real center of the lens. Other landmarks such as the pupil or limbus center are less accurate than the AC. If a surgical microscope fused with OCT is developed, surgeons will be able to determine the center of the CCC in real time by overlaying the point of the anterior capsule on the surgeon's view.