- Research article
- Open Access
- Open Peer Review
Rotational stability of the AcrySof SA60TT toric intraocular lenses: A cohort study
© Zuberbuhler et al; licensee BioMed Central Ltd. 2008
- Received: 17 October 2007
- Accepted: 06 May 2008
- Published: 06 May 2008
To evaluate the rotational stability of the three types of AcrySof SA60TT toric intraocular lenses (Alcon, Switzerland) in cataract surgery after the first postoperative week.
A retrospective study of 44 eyes in 33 patients. All patients underwent similar uncomplicated phacoemulsification cataract surgery. Seven eyes with corneal astigmatism of less than 1.5 D were implanted with the AcrySof SA60T3 intraocular lens. Seventeen eyes with astigmatism between 1.5 D and 2.25 D received the SA60T4 intraocular lens, and 20 eyes with more than 2.25 D of corneal astigmatism received the SA60T5 intraocular lens. Intraoperatively, the axis of the toric lens was aligned to the steepest axis of the corneal astigmatism. Main outcome measure was the postoperative position of the lens, assessed at 1 week and 3 months, using a specially designed angle measuring eyepiece for the slit lamp.
There was no significant difference in the rotational stability of the three types of toric intraocular lenses. Overall, the postoperative rotation was within 5 degrees in 95% and within 2 degrees in 68% of eyes. The mean absolute rotation was 2.2 ± 2.2 degrees. No lens showed more than 9 degrees of rotation, and no lens required secondary repositioning. There was no trend for either clockwise or anti-clockwise rotation. The surgical procedure did not change the corneal astigmatism.
Once placed to it's position, each of the three types of the AcrySof SA60TT toric intraocular lenses demonstrate rotational stability in the capsular bag.
- Slit Lamp
- Rotational Stability
- Corneal Astigmatism
- Cylinder Power
Corneal astigmatism above 1.5 D occurs in 19% of patients . Implanting a toric intraocular lens (IOL) offers the possibility of correcting not only spherical equivalent refraction, but also astigmatism during phacoemulsification cataract surgery. The AcrySof SA60TT toric series of IOLs (Alcon, Switzerland) is made of hydrophobic Acrylate and shares the same biconvex single-piece design as the AcrySof SA60AT monofocal IOL (Alcon, Switzerland). The toric IOL differs in that there is a toric component located on the posterior surface of the lens optic. The optic is marked with 3 peripheral dots that indicate the cylindrical axis of the lens and so enables its correct alignment with the steepest axis of the corneal astigmatism during surgery. The AcrySof toric IOL is available in 3 types with different cylinder powers: 1.5 D (SA60T3), 2.25 D (SA60T4) and 3.0 D (SA60T5).
The success of a toric IOL can be judged not only by its ability to reduce refractive astigmatism immediately postoperatively, but also by its ability to maintain a stable position in the capsular bag in the longer term. However, many surgeons have stopped using toric IOLs because of reported positional instability . The most frequent cause of IOL rotation following uncomplicated cataract surgery is because of capsular bag shrinkage due to fibrosis . The majority of this occurs within the first three months after implantation . Even a small rotational deviation of the toric IOL from its intended axis can result in large reduction of the astigmatic correction . For example, a deviation of 10 degrees minimizes the potential correction by 35%.
The aim of this study was to evaluate the postoperative rotational stability of the three types of AcrySof SA60TT toric IOLs in standard cataract surgery between the first postoperative week and the third month.
This is a retrospective cohort study of 44 eyes of 33 patients. The eyes all had corneal astigmatism of 1 to 5 D, and between July 2006 and March 2007 received an AcrySof toric intraocular lens during cataract surgery. Exclusion criteria were axial length of less than 22 mm, zonular weakness, a change in refractive astigmatism of more than 0.5 D within the 3 months prior to surgery, and coexisting maculopathy or glaucoma.
Eyes with a corneal astigmatism (Orbscan, Carl Zeiss, Germany) of less than 1.5 D were implanted with the AcrySof SA60T3 IOL, eyes with a corneal astigmatism between 1.5 D and 2.25D were implanted with the SA60T4 IOL, and eyes showing a corneal astigmatism of more than 2.25 D were implanted with the SA60T5 IOL. A total of 44 eyes of 33 patients were recruited.
Biometry was performed with the IOL Master (Carl Zeiss, Germany), using the Haigis formula for the IOL power calculation and the company's recommended A-constant of 118.4 for the toric IOL. The target postoperative spherical equivalent was aimed to emmetropia.
Preoperatively, the steepest axis of the corneal astigmatism, determined by Orbscan topography was marked at the corneal limbus with a marker pen, using an angle measuring eyepiece on a BQ900 slit lamp (Haag Streit, Switzerland). Cataract surgery was performed by a single surgeon (EH) at the Vista Klinik, Binningen, Switzerland under topical local anesthesia. Each patient underwent the same technique with a 2.8 mm superior clear limbal incision, continuous curvilinear capsulorhexis, phacoemulsification with cleaver technique and bimanual irrigation/aspiration. The toric IOL was implanted into the capsular bag with a Monarch II injector and a B-Cartridge. Subsequently, the IOL was rotated with a second instrument, so that the cylindrical axis of the lens was aligned with the limbal marks of the corneal astigmatism. All patients were prescribed a combination of tobramicin and dexamethasone eye drops 4 times daily for 4 weeks.
At 1 week and 3 months postoperatively all patients underwent best-corrected distance visual acuity, subjective refraction and slit lamp examination. The postoperative corneal astigmatism was assessed by Orbscan topography at 3 months.
For the measurement of the axis of the toric lens the pupil was dilated to enable the peripheral dots on the optic to become visible. A specially designed eyepiece, replacing one of the 10× eyepieces, was inserted in the slit lamp. Looking through the eyepiece, a spirit level, a horizontal line, a black measurement line and a circular scale in the periphery with single degree steps could be seen. With the spirit level the horizontal line could be adjusted to the horizontal axis. A virtual reference line was used, formed by the line between the pupils of patient's eyes, to provide a patient's reference. This reference line was aligned with the horizontal line of the eyepiece at each follow-up to guarantee reproducible measuring conditions. The black measurement line then could be rotated into the axis of the toric IOL. The angle between the black measurement line and the horizontal line represented the angle of the toric IOL. The angle could be read on the peripheral scale in degrees.
Statistical analysis was performed using SPSS Software (SPSS Inc., Chicago, IL, USA). For comparative statistics the Wilcoxon matched-pairs test was used and for independent samples and the Mann-Whitney U-test was used. For association statistics the Spearman rank correlation test was applied. P-values less than 0.05 were considered statistically significant.
Patient demographics, best-corrected distance visual acuity, refractive astigmatism and corneal astigmatism before and three months after implantation of a AcrySof SA60TT toric intraocular lens (SA60T3, SA60T4 or SA60T5 type).
Mean ± SD
66 ± 9
71 ± 14
72 ± 13
71 ± 13
52 to 76
35 to 88
35 to 86
35 to 88
Mean BCDVA (LogMAR) ± SD
0.28 ± 0.22
0.27 ± 0.15
0.30 ± 0.17
0.28 ± 0.17
Mean SE (D) ± SD
-1.90 ± 3.27
-1.60 ± 3.38
-1.50 ± 3.15
-1.60 ± 3.19
Mean refractive astigmatism (D) ± SD*
1.86 ± 0.83
2.24 ± 0.83
2.98 ± 1.07
Mean corneal astigmatism (D) ± SD†
1.40 ± 0.55
1.95 ± 0.56
3.06 ± 0.74
Mean BCDVA (LogMAR) ± SD
0.00 ± 0.06
-0.02 ± 0.04
0.05 ± 0.15
0.01 ± 0.11
Mean SE (D) ± SD
-0.75 ± 0.95
-0.80 ± 1.44
-0.38 ± 1.26
-0.61 ± 1.28
Mean refractive astigmatism (D) ± SD*
0.43 ± 0.59
0.22 ± 0.26
0.89 ± 1.29
Mean corneal astigmatism (D) ± SD†
1.54 ± 0.51
1.85 ± 0.50
3.19 ± 0.93
The corneal astigmatism did not significantly change following surgery (p = 0.17 for SA60T3; p = 0.98 for SA60T4; p = 0.26 for SA60T5). The mean reduction in refractive astigmatism was 1.43 D for the SA60T3 IOL, 2.02D for the SA60T4 IOL, and 2.09D for the SA60T5 IOL. A reduction of at least 1 D was achieved in 71% of eyes receiving a SA60T3 IOL, a reduction of at least 1.5 D was achieved in 65% of eyes receiving a SA60T4 IOL, and a reduction of at least 2 D was achieved in 61% of eyes receiving a SA60T5 IOL. There was no correlation between the rotation of the lens and the amount or the change in refractive astigmatism (p = 0.931).
At three months, 90% of eyes were within 1.0 D and 81% of eyes within 0.5 D of the target spherical equivalent. Ninety-six percent of eyes gained one or more Snellen line of best-corrected distance visual acuity (BCDVA); 82% of eyes gained two or more Snellen lines of BCDVA. One eye lost one line of BCDVA.
No complication was encountered during the intra- and postoperative course. None of the lenses required secondary alignment.
This is the first study to report the rotational stability of the AcrySof SA60TT toric IOL in a series of 44 cases 3 months after implantation in cataract surgery.
Absolute rotation and direction of rotation of the AcrySof SA60TT toric intraocular lenses between the one week and three months follow-up after implantation in standard cataract surgery.
Absolute rotation (degrees)
Mean ± SD
1.6 ± 1.0*
3.3 ± 2.4*
1.5 ± 2.0*
2.2 ± 2.2
0 to 3
0 to 9
0 to 7
0 to 9
Direction of rotation, n (%)
In this series, the largest rotation of the toric IOL was 9 degrees, seen in one eye only. No specific cause was identified for this large deviation and the patient did not require secondary repositioning of the lens because of visual satisfaction. One eye lost a single line of BCDVA because of a disadvantageous change in the regularity of the corneal astigmatism. No reason could be found for this anomaly. This patient was managed conservatively.
A toric lens has to be implanted using an astigmatically neutral procedure: a technique that will have no effect on the preoperative corneal astigmatism . This study demonstrated no significant change in corneal astigmatism from the preoperative assessment to the 3 month postoperative assessment. Caution should be exercised while implanting and rotating the toric lens in the capsular bag so as not to cause capsular damage. Very small eyes, eyes with zonular instability or floppy capsules (post-vitrectomy eyes) may be considered a relative contraindication.
Except for the SA60T5, the AcrySof SA60TT lenses reduced refractive astigmatism as expected. The manufacturer's data claim that the cylinder power of the SA60T5 IOL is 0.75 diopters higher at the IOL plane, and 0.51 D higher at the corneal plane, than the SA60T4. However, the results of this study show a mean difference in refractive cylinder power between the two types of only 0.1 D. Theoretically, this could be due to errors in our refractive data. Further studies with a longer follow-up are necessary to analyze the refractive outcome of the toric IOLs.
Different methods can be used to accurately determine the position of a toric IOL. Weinand et al.  and Becker et al.  analyzed digital and conventional photographs, taken preoperative and postoperative through the slit lamp and operating microscope. This method with photographs in retrograde illumination has become the 'gold standard' for evaluating the centration and axial positioning of a toric intraocular lens. Viestenz et al. [11, 12] and Quentin et al.  used the method of simultaneous slide projection to evaluate the rotation of the toric lens. This method has shown superior accuracy in calculating the rotational stability, because it respects the autorotation of the eye which has shown to be up to 11.5 degrees (mean of 2.3 degrees) [12, 14]. The negative side of the methods with photographs or slides is the increased time consume and demand for specific equipment. In this study, we choose the eyepiece measuring device because it was only a postoperative analysis of the toric lens axis. The device was easy and fast to handle and allowed the ophthalmologist to perform axis measurements at any follow-up, even in busy clinics. It also showed good reproducibility when the patient's head was correctly aligned with the eyepiece and the slit lamp. Because the eyepiece provided data with one degree precision, this unit was used for the study, too. The precision of one degree steps, of course is on the optimistic side, and needs to be set in relation to the errors occurring from autorotation and head dislocation. For comparisons of misalignments of the toric lens, analyzing preoperative and postoperative axis, respecting parallaxes and cyclorotation, we recommend to use the superior technique of simultaneous slide projection.
In conclusion, the three types of AcrySof SA60TT toric IOLs demonstrated no significant rotation three months after implantation. The surgical technique used for implantation did not significantly change the axis of corneal astigmatism.
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